Guest guest Posted May 12, 2009 Report Share Posted May 12, 2009 Thank you Clarence. Good reminder to me re Hans Selye's book. My BP is stable, and K only being tested because I am off Spiro. On Wed, May 13, 2009 at 4:06 AM, lowerbp2 <lowerbp2@...> wrote: Yes but stress does its damage by biochemical mechanisms.You might want to read Hans Selye's book old but still good. Clarence E. Grim, BS, MS, MD On Tuesday, May 12, 2009, at 06:46AM, " Helen Drewe " <hdrewe@...> wrote:>Am due for k blood test again Friday. Will keep a chart re brain fog and low >K. Still think stress changes all my biochemistry. 2 deaths in my family in>last 2 months.>>On Tue, May 12, 2009 at 11:22 AM, Clarence Grim <lowerbp2@...> wrote: >>>>>>> Can you correlate with your K? CE Grim MD>>>> On May 11, 2009, at 4:47 PM, Helen Drew wrote:>>>>>>>> I agree Carol. I was working in Case Management 9 years ago when first >> diagnosed, and had to resign that position, because the brain fog was so>> severe. I had been working in Dementia care, and thought I was getting>> dementia. I have had episodes of brain fog over the years. I also times when >> I am very clear. Its an up and down thing. At present it is down.>>>> On Tue, May 12, 2009 at 9:22 AM, Carol Christie <carolch@...> >> wrote:>>>>>>>>>>> I have been taking clonazepam for only a few months. The mental>>> fogginess/confusion has been with me for about 5 years. My assessment is >>> that there is some correlation with the PA condition itself.>>> Carol>>>>>>>>> Clarence Grim wrote:>>> >>>> >>>> > I would discuss this with your sleep Dr and try being off clonazepam >>> > to assess its role in this. Were you on it before the problems emerged>>> > or after?>>> >>>> >>>> > CE Grim MD>>> > On May 10, 2009, at 10:03 PM, Carol Christie wrote: >>> >>>> >>>>> >>>>> >> Hello again Dr Grim. My current medications are>>> >> verapamil 240mg/day>>> >> spiro 50mg/day >>> >> clonazepam .5mg(as required)>>> >> vitamin D 2000iu/day>>> >> Carol>>> >>>>> >>>>> >> Clarence Grim wrote: >>> >> >>>> >> >>>> >> > Tell us all meds u>>> >> > Are taking.>>> >> >>>> >> > Tiped sad Send form mi >>> >> > iPhone ;-)>>> >> >>>> >> > May your pressure be low!>>> >> >>>> >> > CE Grim MD>>> >> > Specializing in Difficult >>> >> > Hypertension>>> >> >>>> >> > On May 10, 2009, at 10:48 PM, Carol Christie <carolch@...<carolch%40gil.com.au> >>>>>> >> <mailto:carolch%40gil.com.au <carolch%2540gil.com.au>> >>> >> > <mailto:carolch%40gil.com.au <carolch%2540gil.com.au>>> wrote: >>> >> >>>> >> > > I, too identify strongly with dealing with mental changes.>>> >> > > I thought my personal papers filing was only a few months behind. I >>> >> > > started sorting yesterday and found it had been a year since I had>>> >> > > filed/sorted things out.>>> >> > > I used to be meticulous in recording payments due/made etc. My >>> >> > > organisational skills have deteriorated badly.>>> >> > > Carol>>> >> > >>>> >> > >>>> >> > > Isa Hackett wrote: >>> >> > >>>>> >> > >>>>> >> > >> ->>> >> > >>>>> >> > >> I can identify with your challenges RE mental sharpness. It seems, >>> >> > >> especially within the past six or so months, that my language>>> >> > >> (vocabulary) is suffering. I also find myself making silly>>> mistakes. >>> >> > >> It makes things very hard with work. I often have to be " on " - and>>> I>>> >> > >> am very aware that I am not.>>> >> > >> >>> >> > >> I've also recently been diagnosed - actually, I still have the>>> >> > >> salt-loading test yet to confirm. I believe my father had PA and>>> will >>> >> > >> likely be tested for GRA. From what I have read, there is an>>> >> > >> increased>>> >> > >> risk of early stroke. My father began having small strokes in his >>> >> > >> 40's>>> >> > >> and died of a massive stroke in his early 5o's.>>> >> > >>>>> >> > >> Anyway, I encourage you to read as much as possible about GRA. >>> >> > >>>>> >> > >> DR Grim -are you aware of any differences in symptoms or treatment>>> ->>> >> > >> or>>> >> > >> follow-up for those with GRA? >>> >> > >>>>> >> > >> , you should know that there are lots of understanding, helpf>>> ul>>> >> > >> and experienced people on this board -welcome. >>> >> > >>>>> >> > >> Wishing you better health!>>> >> > >>>>> >> > >> >>> >> > >> >>> >> > >> Sent via BlackBerry from T-Mobile>>> >> > >>>>> >> > >> --->>> >> > >> ---------------------------------------------------------- >>> >> > >> *From*: Echols>>> >> > >> *Date*: Sun, 10 May 2009 19:17:24 -0700 (PDT)>>> >> > >> *To*: <hyperaldosteronism <hyperaldosteronism%40> >>>>>> >> <mailto:hyperaldosteronism%40<hyperaldosteronism%2540> >>> >>>> >> > <mailto:hyperaldosteronism%40<hyperaldosteronism%2540> >>> >>>>> >> > >> *Subject*: Re: Renewing Conn's journey>>> >> > >> I plan to check my history and talk with my dad (it may take me a >>> >> > >> little time though). I think I posted my story but I'll check my>>> past>>> >> > >> posts.>>> >> > >>>>> >> > >> --- >>> >> > >> ---------------------------------------------------------->>> >> > >> *From:* Clarence Grim <lowerbp2@... <lowerbp2%40mac.com> >>> >> <mailto:lowerbp2%40mac.com <lowerbp2%2540mac.com>> <mailto:>>> lowerbp2%40mac.com <lowerbp2%2540mac.com>>> >>>>>> >> > >> *To:* hyperaldosteronism <hyperaldosteronism%40> >>>>>> >> <mailto:hyperaldosteronism%40<hyperaldosteronism%2540> >>> >>>> >> > <mailto:hyperaldosteronism%40<hyperaldosteronism%2540> >>> >>>> >> > >> *Sent:* Sunday, May 10, 2009 1:34:25 AM>>> >> > >> *Subject:* Re: Renewing Conn's journey >>> >> > >>>>> >> > >> If you father had PA can you give us his story as well (check with>>> >> > >> him>>> >> > >> first of course). >>> >> > >>>>> >> > >>>>> >> > >> If he has clearly been diagnosed then it is likely that you and he>>> >> > >> have the same thing (assuming your have a Dx of PA that is clear >>> as>>> >> > >> well). You likely have GRA which is an autosomal dominate genetic>>> >> > >> cause of PA in which 1/2 of all your first degree relatives will >>> have>>> >> > >> it as well (on the average).>>> >> > >>>>> >> > >> Recommend you find out as much as you can about your FH of HTN, >>> low>>> >> > >> K,>>> >> > >> causes and age of death as far back as you can go.>>> >> > >>>>> >> > >> I am looking for the Dr. in ville and should get back with >>> you>>> >> > >> soon.>>> >> > >>>>> >> > >> Have you given us you complete story yet. I may have missed it as>>> >> > >> have been at the Am Soc of HTN meeting for last week. Lots of >>> things>>> >> > >> to report to the group.>>> >> > >>>>> >> > >>>>> >> > >> On May 9, 2009, at 10:18 PM, Echols wrote: >>> >> > >>>>> >> > >>>>>> >> > >>>>>> >> > >>>>>> >> > >>> D oc, I am closer to than I am Birmingham. To answer the >>> >> > >>> family history question, my father was diagnosed with PA in 2007>>> but>>> >> > >>> he stated that no CT was ran. It appears that the spiro is >>> lowering>>> >> > >>> my bp.>>> >> > >>> As far as my CT scan, would a scan of my renal arteries and>>> kidneys>>> >> > >>> reveal a bump? I am still suffering extreme fatigue and muscle >>> >> > >>> weakness and tingling in my extremities, headaches, mental>>> confusion>>> >> > >>> and cloudiness (harde to concentrate) , memory loss, language >>> >> > >>> difficulty. I also have intermittent pain in the region of my>>> coccyx>>> >> > >>> bone. Further, when I am surprised, or see something that causes >>> me>>> >> > >>> to cringe, I feel a tingling sensation in my lower back that>>> flows>>> >> > >>> down toward my rear pelvic region. >>> >> > >>> Doc, I agree with your comment as to other physicians do not>>> appear>>> >> > >>> to want to work with others to assist in the care of their >>> patients.>>> >> > >>> I don't know if it is pride or the fact that the concern of>>> >> > >>> keeping a>>> >> > >>> patient overrides the overall health of the & nbsp;patient. I have >>> >> > >>> the>>> >> > >>> same concerns in the legal profession. I have heard attorneys say>>> >> > >>> that " you can't help people " . The statement broke my heart. Last >>> I>>> >> > >>> checked, there were three (3) noble professions: Doctors, lawyers>>> >> > >>> and>>> >> > >>> ministers. We provide a service. Don't misunderstand me, doc, >>> this>>> >> > >>> is my livelihood and I am not apologizing for the salaries in our>>> >> > >>> respective professions. I pprovide a service and plan to receive >>> >> > >>> compensation for those services. My concerned is that we need to>>> >> > >>> keep>>> >> > >>> in my that we are providing " people " with those services. >>> >> > >>> I am not a complainer. I have been told that I am kind of stoic>>> in>>> >> > >>> nature. However, in my profession, I cannot afford to lose my >>> mental>>> >> > >>> edge or acuity. My job depends on it and I am on a quest to feel>>> >> > >>> better. Thanks for responding.>>> >> > >>> If the best doctors are in Birmingham, I will go there but if you >>> >> > >>> know someone in , that is closer. Thanks, Doc.>>> >> > >>>>>> >> > >>> --->>> >> > >>> --- >>> >> > >>> ---------------------------------------------------------->>> >> > >>> *From:* Clarence Grim <lowerbp2mac (DOT) com>>>> >> > >>> *To:* hyperaldosteronism >>> >> > >>> *Sent:* Friday, May 8, 2009 10:39:57 AM>>> >> > >>> *Subject:* Re: [hyperaldosteronism ] Renewing Conn's journey>>> >> > >>> >>> >> > >>> As you can see from our group's stories we need to increase the>>> >> > >>> knowledge base or every one who sees pts with high blood>>> pressure. >>> >> > >>> HTN + low K = PA.>>> >> > >>>>>> >> > >>> At some point we would like to have your complete story as well>>> if >>> >> > >>> you have time.>>> >> > >>>>>> >> > >>>>>> >> > >>>>>> >> > >>> Your aldo and renin confirm this Dx. >>> >> > >>>>>> >> > >>> If you have not read my article on the evolution of PA please do>>> >> > >>> so-and take to your Dr. I would be happy to work with him in your >>> >> > >>> care but most Drs don't seem to be interested. Which blows my>>> mind.>>> >> > >>>>>> >> > >>> Any family Hx of HTN and/or low K? >>> >> > >>>>>> >> > >>> If spiro works for BP and K and your are DASHing to the max that>>> >> > >>> essentially confirms the Dx. >>> >> > >>> If the first CT did not show a bump on the adrenal then others>>> will>>> >> > >>> not likely show anything.>>> >> > >>> >>> >> > >>>>>> >> > >>> Our basic approach here(based on 45 years of experience) is to>>> treat>>> >> > >>> with medications and DASH and if BP and K are controlled and >>> other>>> >> > >>> Sx>>> >> > >>> go away not to do any further D x tests at this stage.>>> >> > >>> If there is a single bump and Rx fails to get to feeling normal >>> >> > >>> then>>> >> > >>> would do AVS to see if the problem is unilateral or bilateral.>>> >> > >>>>>> >> > >>> I know folks in MS, in New Orleans and in Birmingham who >>> are>>> >> > >>> experts in PA. I would recommend you go to someone who has a lot>>> >> > >>> of>>> >> > >>> experience in this and has been doing it for some time. >>> >> > >>>>>> >> > >>>>>> >> > >>>>>> >> > >>>>>> >> > >>> Clarence Grim BS, MS, MD >>> >> > >>>>>> >> > >>> Clinical Professor of Medicine>>> >> > >>> Medical College of Wisconsin>>> >> > >>> Senior Consultant to Shared Care Research and Education >>> >> > >>> Consulting, Inc.>>> >> > >>>>>> >> > >>> Specializing in Difficult to control high blood pre ssure.>>> >> > >>> >>> >> > >>>>>> >> > >>>>>> >> > >>>>>> >> > >>>>>> >> > >>> On May 7, 2009, at 1:49 PM, Echols wrote: >>> >> > >>>>>> >> > >>>>>>> >> > >>>>>>> >> > >>>>>>> >> > >>>> Dr. Grim, I am an attorney in Mississippi and have just recently >>> >> > >>>> been diagnosed with PA. My family physician was attempting to>>> treat>>> >> > >>>> my extremely high bp to no avail and after nearly 3 years fina >>> lly>>> >> > >>>> told me that he did not have a clue as to what was going on and>>> >> > >>>> referred me to an internist. The internist specializes in >>> >> > >>>> hypertension. I really don't know how much the internist>>> >> > >>>> understands>>> >> > >>>> about PA but I am glad that he has at least heard of it after >>> I've>>> >> > >>>> suffered for about 15 or more years with nearly all the symptoms>>> >> > >>>> listed by others here. The internist ordered a blood workup and >>> my>>> >> > >>>> aldosterone levels were 3 times the normal amount and my renin>>> was>>> >> > >>>> undetected. No other tests were run. He did not order a CT scan >>> of>>> >> > >>>> my adrenals. After being hospitalized, my family physician>>> >> > >>>> (after I>>> >> > >>>> pushed for it) ordered a CT scan of my kidneys and renal >>> arteries>>> >> > >>>> and stated that they looked fine. That was prior to seeing the>>> >> > >>>> internist. After reading postings in this group, I requested on >>> May>>> >> > >>>> 5th to have a CT scan performed to look at my adrenal glands. He>>> >> > >>>> stated that he was not going to do it now, but might in about 2 >>> >> > >>>> months.>>> >> > >>>> I told the internist that I am still extremely fatigued, that I>>> >> > >>>> have>>> >> > >>>> headaches, my mind is cloudy, having a problem with >>> concentration>>> >> > >>>> and memory and that I am concerned because it was affecting my>>> work>>> >> > >>>> (I have been off work for about a month). Internist told me that >>> he>>> >> > >>>> believed that I was just depressed and prescribed lexapro. He>>> >> > >>>> stated>>> >> > >>>> that I should be excited because my blood pressure was coming >>> down.>>> >> > >>>> I told him that I was excited but that I did not think that I>>> was>>> >> > >>>> depressed to the point of needing medication. I am thinking of >>> >> > >>>> either going to the University of Birmingham to see a>>> nephrologist>>> >> > >>>> and/or endo. Is this a good idea? Is UAB a good place to go for >>> >> > >>>> hyperaldosterinism? If not, can you refer a place near MS? I>>> need>>> >> > >>>> to>>> >> > >>>> make sure that I have this condition ( I have all the symptoms >>> and>>> >> > >>>> the spiro-75mg- is helping my bp) and if so, how I can cure or>>> best>>> >> > >>>> treat it. The internist stated that he did not know what caused >>> it>>> >> > >>>> and that he did not believe that I had a tumor. I am grateful>>> that>>> >> > >>>> he looked into hyperaldosteronism but I think the internist is >>> more>>> >> > >>>> concentrated on the bp, since that is his specialty. I am>>> concerned>>> >> > >>>> not only about the bp, but also the mental aspects of this >>> >> > >>>> condition>>> >> > >>>> because it emy livelihood. Please respond.>>> >> > >>>>>>> >> > >>>> --- >>> >> > >>>> --->>> >> > >>>> ---------------------------------------------------------->>> >> > >>>> *From:* Clarence Grim <lowerbp2mac (DOT) com> >>> >> > >>>> *To:* hyperaldosteronism>>> >> > >>>> *Sent:* Thursday, May 7, 2009 1:32:35 AM>>> >> > >>>> *Subject:* Re: [hyperaldosteronism ] Renewing Conn's journey >>> >> > >>>>>>> >> > >>>> Dont recall your previous story. Do we need to update your>>> story?>>> >> > >>>> >>> >> > >>>>>>> >> > >>>> CE Grim MD>>> >> > >>>> On May 6, 2009, at 6:05 PM, hdrewe wrote:>>> >> > >>>> >>> >> > >>>>> I have not been in contact with this site for a few weeks,>>> >> > >>>>> however,>>> >> > >>>>> am now back on track. I visited Dr Nikwan at Greenslopes >>> Hospital,>>> >> > >>>>> and am going ahead with the workups prior to maybe having>>> surgery.>>> >> > >>>>> He was certainly surprised to see me after 9 years. >>> >> > >>>>>>>> >> > >>>>> My Aldosterone/ Renin assays wer e:->>> >> > >>>>> Aldosterone (upright) 1923 (pmol/L) (100 - 950) >>> >> > >>>>> Renin (upright) 14 (mU/L) (3.3 - 41)>>> >> > >>>>> Aldosterone/ Renin Ratio 137>>> >> > >>>>>>>> >> > >>>>> These results were while on 25mg Spironolactone. >>> >> > >>>>>>>> >> > >>>>> I have been taken off Spiro and put on Verapamil SR 240mg/day,>>> >> > >>>>> which I began this morning. >>> >> > >>>>> I am to have CT scan of adrenal gland to see what has happened>>> >> > >>>>> after all this time.>>> >> > >>>>> Will revisit Dr Nikwan in 8 weeks. >>> >> > >>>>> Helen D>>> >> > >>>>>>> >> > >>>>>>> >> > >>>>>>> >> > >>> >>> >> > >>>>>> >> > >>>>>> >> > >>>>> >> > >>>>> >> > >>>>> >> > > >>> >> > >>>> >> > >>>> >> > > ------------------------------------>>> >> > >>>> >> > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 12, 2009 Report Share Posted May 12, 2009 Thank you Clarence. Good reminder to me re Hans Selye's book. My BP is stable, and K only being tested because I am off Spiro. On Wed, May 13, 2009 at 4:06 AM, lowerbp2 <lowerbp2@...> wrote: Yes but stress does its damage by biochemical mechanisms.You might want to read Hans Selye's book old but still good. Clarence E. Grim, BS, MS, MD On Tuesday, May 12, 2009, at 06:46AM, " Helen Drewe " <hdrewe@...> wrote:>Am due for k blood test again Friday. Will keep a chart re brain fog and low >K. Still think stress changes all my biochemistry. 2 deaths in my family in>last 2 months.>>On Tue, May 12, 2009 at 11:22 AM, Clarence Grim <lowerbp2@...> wrote: >>>>>>> Can you correlate with your K? CE Grim MD>>>> On May 11, 2009, at 4:47 PM, Helen Drew wrote:>>>>>>>> I agree Carol. I was working in Case Management 9 years ago when first >> diagnosed, and had to resign that position, because the brain fog was so>> severe. I had been working in Dementia care, and thought I was getting>> dementia. I have had episodes of brain fog over the years. I also times when >> I am very clear. Its an up and down thing. At present it is down.>>>> On Tue, May 12, 2009 at 9:22 AM, Carol Christie <carolch@...> >> wrote:>>>>>>>>>>> I have been taking clonazepam for only a few months. The mental>>> fogginess/confusion has been with me for about 5 years. My assessment is >>> that there is some correlation with the PA condition itself.>>> Carol>>>>>>>>> Clarence Grim wrote:>>> >>>> >>>> > I would discuss this with your sleep Dr and try being off clonazepam >>> > to assess its role in this. Were you on it before the problems emerged>>> > or after?>>> >>>> >>>> > CE Grim MD>>> > On May 10, 2009, at 10:03 PM, Carol Christie wrote: >>> >>>> >>>>> >>>>> >> Hello again Dr Grim. My current medications are>>> >> verapamil 240mg/day>>> >> spiro 50mg/day >>> >> clonazepam .5mg(as required)>>> >> vitamin D 2000iu/day>>> >> Carol>>> >>>>> >>>>> >> Clarence Grim wrote: >>> >> >>>> >> >>>> >> > Tell us all meds u>>> >> > Are taking.>>> >> >>>> >> > Tiped sad Send form mi >>> >> > iPhone ;-)>>> >> >>>> >> > May your pressure be low!>>> >> >>>> >> > CE Grim MD>>> >> > Specializing in Difficult >>> >> > Hypertension>>> >> >>>> >> > On May 10, 2009, at 10:48 PM, Carol Christie <carolch@...<carolch%40gil.com.au> >>>>>> >> <mailto:carolch%40gil.com.au <carolch%2540gil.com.au>> >>> >> > <mailto:carolch%40gil.com.au <carolch%2540gil.com.au>>> wrote: >>> >> >>>> >> > > I, too identify strongly with dealing with mental changes.>>> >> > > I thought my personal papers filing was only a few months behind. I >>> >> > > started sorting yesterday and found it had been a year since I had>>> >> > > filed/sorted things out.>>> >> > > I used to be meticulous in recording payments due/made etc. My >>> >> > > organisational skills have deteriorated badly.>>> >> > > Carol>>> >> > >>>> >> > >>>> >> > > Isa Hackett wrote: >>> >> > >>>>> >> > >>>>> >> > >> ->>> >> > >>>>> >> > >> I can identify with your challenges RE mental sharpness. It seems, >>> >> > >> especially within the past six or so months, that my language>>> >> > >> (vocabulary) is suffering. I also find myself making silly>>> mistakes. >>> >> > >> It makes things very hard with work. I often have to be " on " - and>>> I>>> >> > >> am very aware that I am not.>>> >> > >> >>> >> > >> I've also recently been diagnosed - actually, I still have the>>> >> > >> salt-loading test yet to confirm. I believe my father had PA and>>> will >>> >> > >> likely be tested for GRA. From what I have read, there is an>>> >> > >> increased>>> >> > >> risk of early stroke. My father began having small strokes in his >>> >> > >> 40's>>> >> > >> and died of a massive stroke in his early 5o's.>>> >> > >>>>> >> > >> Anyway, I encourage you to read as much as possible about GRA. >>> >> > >>>>> >> > >> DR Grim -are you aware of any differences in symptoms or treatment>>> ->>> >> > >> or>>> >> > >> follow-up for those with GRA? >>> >> > >>>>> >> > >> , you should know that there are lots of understanding, helpf>>> ul>>> >> > >> and experienced people on this board -welcome. >>> >> > >>>>> >> > >> Wishing you better health!>>> >> > >>>>> >> > >> >>> >> > >> >>> >> > >> Sent via BlackBerry from T-Mobile>>> >> > >>>>> >> > >> --->>> >> > >> ---------------------------------------------------------- >>> >> > >> *From*: Echols>>> >> > >> *Date*: Sun, 10 May 2009 19:17:24 -0700 (PDT)>>> >> > >> *To*: <hyperaldosteronism <hyperaldosteronism%40> >>>>>> >> <mailto:hyperaldosteronism%40<hyperaldosteronism%2540> >>> >>>> >> > <mailto:hyperaldosteronism%40<hyperaldosteronism%2540> >>> >>>>> >> > >> *Subject*: Re: Renewing Conn's journey>>> >> > >> I plan to check my history and talk with my dad (it may take me a >>> >> > >> little time though). I think I posted my story but I'll check my>>> past>>> >> > >> posts.>>> >> > >>>>> >> > >> --- >>> >> > >> ---------------------------------------------------------->>> >> > >> *From:* Clarence Grim <lowerbp2@... <lowerbp2%40mac.com> >>> >> <mailto:lowerbp2%40mac.com <lowerbp2%2540mac.com>> <mailto:>>> lowerbp2%40mac.com <lowerbp2%2540mac.com>>> >>>>>> >> > >> *To:* hyperaldosteronism <hyperaldosteronism%40> >>>>>> >> <mailto:hyperaldosteronism%40<hyperaldosteronism%2540> >>> >>>> >> > <mailto:hyperaldosteronism%40<hyperaldosteronism%2540> >>> >>>> >> > >> *Sent:* Sunday, May 10, 2009 1:34:25 AM>>> >> > >> *Subject:* Re: Renewing Conn's journey >>> >> > >>>>> >> > >> If you father had PA can you give us his story as well (check with>>> >> > >> him>>> >> > >> first of course). >>> >> > >>>>> >> > >>>>> >> > >> If he has clearly been diagnosed then it is likely that you and he>>> >> > >> have the same thing (assuming your have a Dx of PA that is clear >>> as>>> >> > >> well). You likely have GRA which is an autosomal dominate genetic>>> >> > >> cause of PA in which 1/2 of all your first degree relatives will >>> have>>> >> > >> it as well (on the average).>>> >> > >>>>> >> > >> Recommend you find out as much as you can about your FH of HTN, >>> low>>> >> > >> K,>>> >> > >> causes and age of death as far back as you can go.>>> >> > >>>>> >> > >> I am looking for the Dr. in ville and should get back with >>> you>>> >> > >> soon.>>> >> > >>>>> >> > >> Have you given us you complete story yet. I may have missed it as>>> >> > >> have been at the Am Soc of HTN meeting for last week. Lots of >>> things>>> >> > >> to report to the group.>>> >> > >>>>> >> > >>>>> >> > >> On May 9, 2009, at 10:18 PM, Echols wrote: >>> >> > >>>>> >> > >>>>>> >> > >>>>>> >> > >>>>>> >> > >>> D oc, I am closer to than I am Birmingham. To answer the >>> >> > >>> family history question, my father was diagnosed with PA in 2007>>> but>>> >> > >>> he stated that no CT was ran. It appears that the spiro is >>> lowering>>> >> > >>> my bp.>>> >> > >>> As far as my CT scan, would a scan of my renal arteries and>>> kidneys>>> >> > >>> reveal a bump? I am still suffering extreme fatigue and muscle >>> >> > >>> weakness and tingling in my extremities, headaches, mental>>> confusion>>> >> > >>> and cloudiness (harde to concentrate) , memory loss, language >>> >> > >>> difficulty. I also have intermittent pain in the region of my>>> coccyx>>> >> > >>> bone. Further, when I am surprised, or see something that causes >>> me>>> >> > >>> to cringe, I feel a tingling sensation in my lower back that>>> flows>>> >> > >>> down toward my rear pelvic region. >>> >> > >>> Doc, I agree with your comment as to other physicians do not>>> appear>>> >> > >>> to want to work with others to assist in the care of their >>> patients.>>> >> > >>> I don't know if it is pride or the fact that the concern of>>> >> > >>> keeping a>>> >> > >>> patient overrides the overall health of the & nbsp;patient. I have >>> >> > >>> the>>> >> > >>> same concerns in the legal profession. I have heard attorneys say>>> >> > >>> that " you can't help people " . The statement broke my heart. Last >>> I>>> >> > >>> checked, there were three (3) noble professions: Doctors, lawyers>>> >> > >>> and>>> >> > >>> ministers. We provide a service. Don't misunderstand me, doc, >>> this>>> >> > >>> is my livelihood and I am not apologizing for the salaries in our>>> >> > >>> respective professions. I pprovide a service and plan to receive >>> >> > >>> compensation for those services. My concerned is that we need to>>> >> > >>> keep>>> >> > >>> in my that we are providing " people " with those services. >>> >> > >>> I am not a complainer. I have been told that I am kind of stoic>>> in>>> >> > >>> nature. However, in my profession, I cannot afford to lose my >>> mental>>> >> > >>> edge or acuity. My job depends on it and I am on a quest to feel>>> >> > >>> better. Thanks for responding.>>> >> > >>> If the best doctors are in Birmingham, I will go there but if you >>> >> > >>> know someone in , that is closer. Thanks, Doc.>>> >> > >>>>>> >> > >>> --->>> >> > >>> --- >>> >> > >>> ---------------------------------------------------------->>> >> > >>> *From:* Clarence Grim <lowerbp2mac (DOT) com>>>> >> > >>> *To:* hyperaldosteronism >>> >> > >>> *Sent:* Friday, May 8, 2009 10:39:57 AM>>> >> > >>> *Subject:* Re: [hyperaldosteronism ] Renewing Conn's journey>>> >> > >>> >>> >> > >>> As you can see from our group's stories we need to increase the>>> >> > >>> knowledge base or every one who sees pts with high blood>>> pressure. >>> >> > >>> HTN + low K = PA.>>> >> > >>>>>> >> > >>> At some point we would like to have your complete story as well>>> if >>> >> > >>> you have time.>>> >> > >>>>>> >> > >>>>>> >> > >>>>>> >> > >>> Your aldo and renin confirm this Dx. >>> >> > >>>>>> >> > >>> If you have not read my article on the evolution of PA please do>>> >> > >>> so-and take to your Dr. I would be happy to work with him in your >>> >> > >>> care but most Drs don't seem to be interested. Which blows my>>> mind.>>> >> > >>>>>> >> > >>> Any family Hx of HTN and/or low K? >>> >> > >>>>>> >> > >>> If spiro works for BP and K and your are DASHing to the max that>>> >> > >>> essentially confirms the Dx. >>> >> > >>> If the first CT did not show a bump on the adrenal then others>>> will>>> >> > >>> not likely show anything.>>> >> > >>> >>> >> > >>>>>> >> > >>> Our basic approach here(based on 45 years of experience) is to>>> treat>>> >> > >>> with medications and DASH and if BP and K are controlled and >>> other>>> >> > >>> Sx>>> >> > >>> go away not to do any further D x tests at this stage.>>> >> > >>> If there is a single bump and Rx fails to get to feeling normal >>> >> > >>> then>>> >> > >>> would do AVS to see if the problem is unilateral or bilateral.>>> >> > >>>>>> >> > >>> I know folks in MS, in New Orleans and in Birmingham who >>> are>>> >> > >>> experts in PA. I would recommend you go to someone who has a lot>>> >> > >>> of>>> >> > >>> experience in this and has been doing it for some time. >>> >> > >>>>>> >> > >>>>>> >> > >>>>>> >> > >>>>>> >> > >>> Clarence Grim BS, MS, MD >>> >> > >>>>>> >> > >>> Clinical Professor of Medicine>>> >> > >>> Medical College of Wisconsin>>> >> > >>> Senior Consultant to Shared Care Research and Education >>> >> > >>> Consulting, Inc.>>> >> > >>>>>> >> > >>> Specializing in Difficult to control high blood pre ssure.>>> >> > >>> >>> >> > >>>>>> >> > >>>>>> >> > >>>>>> >> > >>>>>> >> > >>> On May 7, 2009, at 1:49 PM, Echols wrote: >>> >> > >>>>>> >> > >>>>>>> >> > >>>>>>> >> > >>>>>>> >> > >>>> Dr. Grim, I am an attorney in Mississippi and have just recently >>> >> > >>>> been diagnosed with PA. My family physician was attempting to>>> treat>>> >> > >>>> my extremely high bp to no avail and after nearly 3 years fina >>> lly>>> >> > >>>> told me that he did not have a clue as to what was going on and>>> >> > >>>> referred me to an internist. The internist specializes in >>> >> > >>>> hypertension. I really don't know how much the internist>>> >> > >>>> understands>>> >> > >>>> about PA but I am glad that he has at least heard of it after >>> I've>>> >> > >>>> suffered for about 15 or more years with nearly all the symptoms>>> >> > >>>> listed by others here. The internist ordered a blood workup and >>> my>>> >> > >>>> aldosterone levels were 3 times the normal amount and my renin>>> was>>> >> > >>>> undetected. No other tests were run. He did not order a CT scan >>> of>>> >> > >>>> my adrenals. After being hospitalized, my family physician>>> >> > >>>> (after I>>> >> > >>>> pushed for it) ordered a CT scan of my kidneys and renal >>> arteries>>> >> > >>>> and stated that they looked fine. That was prior to seeing the>>> >> > >>>> internist. After reading postings in this group, I requested on >>> May>>> >> > >>>> 5th to have a CT scan performed to look at my adrenal glands. He>>> >> > >>>> stated that he was not going to do it now, but might in about 2 >>> >> > >>>> months.>>> >> > >>>> I told the internist that I am still extremely fatigued, that I>>> >> > >>>> have>>> >> > >>>> headaches, my mind is cloudy, having a problem with >>> concentration>>> >> > >>>> and memory and that I am concerned because it was affecting my>>> work>>> >> > >>>> (I have been off work for about a month). Internist told me that >>> he>>> >> > >>>> believed that I was just depressed and prescribed lexapro. He>>> >> > >>>> stated>>> >> > >>>> that I should be excited because my blood pressure was coming >>> down.>>> >> > >>>> I told him that I was excited but that I did not think that I>>> was>>> >> > >>>> depressed to the point of needing medication. I am thinking of >>> >> > >>>> either going to the University of Birmingham to see a>>> nephrologist>>> >> > >>>> and/or endo. Is this a good idea? Is UAB a good place to go for >>> >> > >>>> hyperaldosterinism? If not, can you refer a place near MS? I>>> need>>> >> > >>>> to>>> >> > >>>> make sure that I have this condition ( I have all the symptoms >>> and>>> >> > >>>> the spiro-75mg- is helping my bp) and if so, how I can cure or>>> best>>> >> > >>>> treat it. The internist stated that he did not know what caused >>> it>>> >> > >>>> and that he did not believe that I had a tumor. I am grateful>>> that>>> >> > >>>> he looked into hyperaldosteronism but I think the internist is >>> more>>> >> > >>>> concentrated on the bp, since that is his specialty. I am>>> concerned>>> >> > >>>> not only about the bp, but also the mental aspects of this >>> >> > >>>> condition>>> >> > >>>> because it emy livelihood. Please respond.>>> >> > >>>>>>> >> > >>>> --- >>> >> > >>>> --->>> >> > >>>> ---------------------------------------------------------->>> >> > >>>> *From:* Clarence Grim <lowerbp2mac (DOT) com> >>> >> > >>>> *To:* hyperaldosteronism>>> >> > >>>> *Sent:* Thursday, May 7, 2009 1:32:35 AM>>> >> > >>>> *Subject:* Re: [hyperaldosteronism ] Renewing Conn's journey >>> >> > >>>>>>> >> > >>>> Dont recall your previous story. Do we need to update your>>> story?>>> >> > >>>> >>> >> > >>>>>>> >> > >>>> CE Grim MD>>> >> > >>>> On May 6, 2009, at 6:05 PM, hdrewe wrote:>>> >> > >>>> >>> >> > >>>>> I have not been in contact with this site for a few weeks,>>> >> > >>>>> however,>>> >> > >>>>> am now back on track. I visited Dr Nikwan at Greenslopes >>> Hospital,>>> >> > >>>>> and am going ahead with the workups prior to maybe having>>> surgery.>>> >> > >>>>> He was certainly surprised to see me after 9 years. >>> >> > >>>>>>>> >> > >>>>> My Aldosterone/ Renin assays wer e:->>> >> > >>>>> Aldosterone (upright) 1923 (pmol/L) (100 - 950) >>> >> > >>>>> Renin (upright) 14 (mU/L) (3.3 - 41)>>> >> > >>>>> Aldosterone/ Renin Ratio 137>>> >> > >>>>>>>> >> > >>>>> These results were while on 25mg Spironolactone. >>> >> > >>>>>>>> >> > >>>>> I have been taken off Spiro and put on Verapamil SR 240mg/day,>>> >> > >>>>> which I began this morning. >>> >> > >>>>> I am to have CT scan of adrenal gland to see what has happened>>> >> > >>>>> after all this time.>>> >> > >>>>> Will revisit Dr Nikwan in 8 weeks. >>> >> > >>>>> Helen D>>> >> > >>>>>>> >> > >>>>>>> >> > >>>>>>> >> > >>> >>> >> > >>>>>> >> > >>>>>> >> > >>>>> >> > >>>>> >> > >>>>> >> > > >>> >> > >>>> >> > >>>> >> > > ------------------------------------>>> >> > >>>> >> > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 13, 2009 Report Share Posted May 13, 2009 Recall that cow milk contains nearly 10 the sodium concentration of human milk.  This is the reason that cow milk based infant feeding vs human milk sodium content increase BP in infants and this high blood pressure persists at least until the teens. CE Grim MDOn May 12, 2009, at 4:40 AM, Helen Drewe wrote:Val, I absolutely avoid sodium like the plague. The only sodium I have is naturally occurring sodium in meat, milk and Yoghurt,etc. I eat lots of high K veges and fruit. Take my own foods wherever I go. Dont trust restaurants etc. Have had too many headaches in early days of diagnosis. I dont eat any breads etc. eat oats, millet etc for carbs. Have been eating this way for nearly 9 years. Since starting Dash, have increased dairy (milk and yoghurt) and making sure I eat enough protein. I could quite happily just live on fruit. I have wondered for a while whether eating such a low sodium diet creates the very thing I am trying to avoid as the body tries even harder to retain sodium, thereby pushing out even more aldosterone.On Tue, May 12, 2009 at 3:00 PM, Valarie  <val@...> wrote:Helen, the only way I made it through six weeks off spiro was to absolutely avoid sodium.  We traveled to Mayo Clinic so I could take my own food along.  When I got a urinary sodium test there, the sodium was too low to measure.  Very low sodium diet will increase your renin and make the ARR invalid. Val From: hyperaldosteronism  [mailto:hyperaldosteronism ] On Behalf Of Helen DreweIf I Dash to max, I put on weight because I am small build. I eat natural high K foods as nature intended. When I put on weight and begin to feel bloated, it affects my breathing and I get more chest pain. So I dash at 1200- 1600 calories, sticking to the guidelines in the the books - "The Dash Diet for Hypertension", "The Dash Diet Action Plan", and "Eat to Beat High Blood Pressure" which features the Dash-Plus Plan.On Mon, May 11, 2009 at 10:49 PM, Clarence Grim <lowerbp2mac> wrote: DASH to the max. CE GrimMD On May 10, 2009, at 10:36 PM, Helen Drewe wrote:  I understand Carol, I have only been off spiro since Friday, and feel dreadful. Headaches, flushing, bloating, slight tremors, brain fog.......Dont know if it may be reaction from Verapamil. My sister told me she cant take calcium channel blockers, as she also had headaches and flushing. What do you do? I dont want to back out of having the AVS this time.HelenOn Mon, May 11, 2009 at 3:08 PM, Carol Christie <carolchgil.au> wrote: I should add that I was going to have a second AVS done at Greenslopes. However, after about 3 weeks without spiro I felt so terrible I decided to take it again. Dr Stowasser still recommends a dose of only 25mg, but I feel better on 50mg.CarolClarence Grim wrote:>>> Tell us all meds u> Are taking.>> Tiped sad Send form mi> iPhone ;-)>> May your pressure be low!>> CE Grim MD> Specializing in Difficult> Hypertension>> On May 10, 2009, at 10:48 PM, Carol Christie <carolchgil.au > <mailto:carolch%40gil.com.au>> wrote:>> > I, too identify strongly with dealing with mental changes.> > I thought my personal papers filing was only a few months behind. I> > started sorting yesterday and found it had been a year since I had> > filed/sorted things out.> > I used to be meticulous in recording payments due/made etc. My> > organisational skills have deteriorated badly.> > Carol> >> >> > Isa Hackett wrote:> >>> >>> >> -> >>> >> I can identify with your challenges RE mental sharpness. It seems,> >> especially within the past six or so months, that my language> >> (vocabulary) is suffering. I also find myself making silly mistakes.> >> It makes things very hard with work. I often have to be "on" - and I> >> am very aware that I am not.> >>> >> I've also recently been diagnosed - actually, I still have the> >> salt-loading test yet to confirm. I believe my father had PA and will> >> likely be tested for GRA. From what I have read, there is an> >> increased> >> risk of early stroke. My father began having small strokes in his> >> 40's> >> and died of a massive stroke in his early 5o's.> >>> >> Anyway, I encourage you to read as much as possible about GRA.> >>> >> DR Grim -are you aware of any differences in symptoms or treatment -> >> or> >> follow-up for those with GRA?> >>> >> , you should know that there are lots of understanding, helpf ul> >> and experienced people on this board -welcome.> >>> >> Wishing you better health!> >>> >> > >>> >> Sent via BlackBerry from T-Mobile> >>> >> ---> >> ----------------------------------------------------------> >> *From*: Echols> >> *Date*: Sun, 10 May 2009 19:17:24 -0700 (PDT)> >> *To*: <hyperaldosteronism  > <mailto:hyperaldosteronism%40>>> >> *Subject*: Re: Renewing Conn's journey> >> I plan to check my history and talk with my dad (it may take me a> >> little time though). I think I posted my story but I'll check my past> >> posts.> >>> >> ---> >> ----------------------------------------------------------> >> *From:* Clarence Grim <lowerbp2mac <mailto:lowerbp2%40mac.com>>> >> *To:* hyperaldosteronism  > <mailto:hyperaldosteronism%40>> >> *Sent:* Sunday, May 10, 2009 1:34:25 AM> >> *Subject:* Re: Renewing Conn's journey> >>> >> If you father had PA can you give us his story as well (check with> >> him> >> first of course).> >>> >>> >> If he has clearly been diagnosed then it is likely that you and he> >> have the same thing (assuming your have a Dx of PA that is clear as> >> well). You likely have GRA which is an autosomal dominate genetic> >> cause of PA in which 1/2 of all your first degree relatives will have> >> it as well (on the average).> >>> >> Recommend you find out as much as you can about your FH of HTN, low> >> K,> >> causes and age of death as far back as you can go.> >>> >> I am looking for the Dr. in ville and should get back with you> >> soon.> >>> >> Have you given us you complete story yet. I may have missed it as> >> have been at the Am Soc of HTN meeting for last week. Lots of things> >> to report to the group.> >>> >>> >> On May 9, 2009, at 10:18 PM, Echols wrote:> >>> >>>> >>>> >>>> >>> D oc, I am closer to than I am Birmingham. To answer the> >>> family history question, my father was diagnosed with PA in 2007 but> >>> he stated that no CT was ran. It appears that the spiro is lowering> >>> my bp.> >>> As far as my CT scan, would a scan of my renal arteries and kidneys> >>> reveal a bump? I am still suffering extreme fatigue and muscle> >>> weakness and tingling in my extremities, headaches, mental confusion> >>> and cloudiness (harde to concentrate) , memory loss, language> >>> difficulty. I also have intermittent pain in the region of my coccyx> >>> bone. Further, when I am surprised, or see something that causes me> >>> to cringe, I feel a tingling sensation in my lower back that flows> >>> down toward my rear pelvic region.> >>> Doc, I agree with your comment as to other physicians do not appear> >>> to want to work with others to assist in the care of their patients.> >>> I don't know if it is pride or the fact that the concern of> >>> keeping a> >>> patient overrides the overall health of the & nbsp;patient. I have> >>> the> >>> same concerns in the legal profession. I have heard attorneys say> >>> that "you can't help people". The statement broke my heart. Last I> >>> checked, there were three (3) noble professions: Doctors, lawyers> >>> and> >>> ministers. We provide a service. Don't misunderstand me, doc, this> >>> is my livelihood and I am not apologizing for the salaries in our> >>> respective professions. I pprovide a service and plan to receive> >>> compensation for those services. My concerned is that we need to> >>> keep> >>> in my that we are providing "people" with those services.> >>> I am not a complainer. I have been told that I am kind of stoic in> >>> nature. However, in my profession, I cannot afford to lose my mental> >>> edge or acuity. My job depends on it and I am on a quest to feel> >>> better. Thanks for responding.> >>> If the best doctors are in Birmingham, I will go there but if you> >>> know someone in , that is closer. Thanks, Doc.> >>>> >>> ---> >>> ---> >>> ----------------------------------------------------------> >>> *From:* Clarence Grim <lowerbp2mac (DOT) com>> >>> *To:* hyperaldosteronism> >>> *Sent:* Friday, May 8, 2009 10:39:57 AM> >>> *Subject:* Re: [hyperaldosteronism ] Renewing Conn's journey> >>>> >>> As you can see from our group's stories we need to increase the> >>> knowledge base or every one who sees pts with high blood pressure.> >>> HTN + low K = PA.> >>>> >>> At some point we would like to have your complete story as well if> >>> you have time.> >>>> >>>> >>>> >>> Your aldo and renin confirm this Dx.> >>>> >>> If you have not read my article on the evolution of PA please do> >>> so-and take to your Dr. I would be happy to work with him in your> >>> care but most Drs don't seem to be interested. Which blows my mind.> >>>> >>> Any family Hx of HTN and/or low K?> >>>> >>> If spiro works for BP and K and your are DASHing to the max that> >>> essentially confirms the Dx.> >>> If the first CT did not show a bump on the adrenal then others will> >>> not likely show anything.> >>>> >>>> >>> Our basic approach here(based on 45 years of experience) is to treat> >>> with medications and DASH and if BP and K are controlled and other> >>> Sx> >>> go away not to do any further D x tests at this stage.> >>> If there is a single bump and Rx fails to get to feeling normal> >>> then> >>> would do AVS to see if the problem is unilateral or bilateral.> >>>> >>> I know folks in MS, in New Orleans and in Birmingham who are> >>> experts in PA. I would recommend you go to someone who has a lot> >>> of> >>> experience in this and has been doing it for some time.> >>>> >>>> >>>> >>>> >>> Clarence Grim BS, MS, MD> >>>> >>> Clinical Professor of Medicine> >>> Medical College of Wisconsin> >>> Senior Consultant to Shared Care Research and Education> >>> Consulting, Inc.> >>>> >>> Specializing in Difficult to control high blood pre ssure.> >>>> >>>> >>>> >>>> >>>> >>> On May 7, 2009, at 1:49 PM, Echols wrote:> >>>> >>>>> >>>>> >>>>> >>>> Dr. Grim, I am an attorney in Mississippi and have just recently> >>>> been diagnosed with PA. My family physician was attempting to treat> >>>> my extremely high bp to no avail and after nearly 3 years fina lly> >>>> told me that he did not have a clue as to what was going on and> >>>> referred me to an internist. The internist specializes in> >>>> hypertension. I really don't know how much the internist> >>>> understands> >>>> about PA but I am glad that he has at least heard of it after I've> >>>> suffered for about 15 or more years with nearly all the symptoms> >>>> listed by others here. The internist ordered a blood workup and my> >>>> aldosterone levels were 3 times the normal amount and my renin was> >>>> undetected. No other tests were run. He did not order a CT scan of> >>>> my adrenals. After being hospitalized, my family physician> >>>> (after I> >>>> pushed for it) ordered a CT scan of my kidneys and renal arteries> >>>> and stated that they looked fine. That was prior to seeing the> >>>> internist. After reading postings in this group, I requested on May> >>>> 5th to have a CT scan performed to look at my adrenal glands. He> >>>> stated that he was not going to do it now, but might in about 2> >>>> months.> >>>> I told the internist that I am still extremely fatigued, that I> >>>> have> >>>> headaches, my mind is cloudy, having a problem with concentration> >>>> and memory and that I am concerned because it was affecting my work> >>>> (I have been off work for about a month). Internist told me that he> >>>> believed that I was just depressed and prescribed lexapro. He> >>>> stated> >>>> that I should be excited because my blood pressure was coming down.> >>>> I told him that I was excited but that I did not think that I was> >>>> depressed to the point of needing medication. I am thinking of> >>>> either going to the University of Birmingham to see a nephrologist> >>>> and/or endo. Is this a good idea? Is UAB a good place to go for> >>>> hyperaldosterinism? If not, can you refer a place near MS? I need> >>>> to> >>>> make sure that I have this condition ( I have all the symptoms and> >>>> the spiro-75mg- is helping my bp) and if so, how I can cure or best> >>>> treat it. The internist stated that he did not know what caused it> >>>> and that he did not believe that I had a tumor. I am grateful that> >>>> he looked into hyperaldosteronism but I think the internist is more> >>>> concentrated on the bp, since that is his specialty. I am concerned> >>>> not only about the bp, but also the mental aspects of this> >>>> condition> >>>> because it emy livelihood. Please respond.> >>>>> >>>> ---> >>>> ---> >>>> ----------------------------------------------------------> >>>> *From:* Clarence Grim <lowerbp2mac (DOT) com>> >>>> *To:* hyperaldosteronism> >>>> *Sent:* Thursday, May 7, 2009 1:32:35 AM> >>>> *Subject:* Re: [hyperaldosteronism ] Renewing Conn's journey> >>>>> >>>> Dont recall your previous story. Do we need to update your story?> >>>>> >>>>> >>>> CE Grim MD> >>>> On May 6, 2009, at 6:05 PM, hdrewe wrote:> >>>>> >>>>> I have not been in contact with this site for a few weeks,> >>>>> however,> >>>>> am now back on track. I visited Dr Nikwan at Greenslopes Hospital,> >>>>> and am going ahead with the workups prior to maybe having surgery.> >>>>> He was certainly surprised to see me after 9 years.> >>>>>> >>>>> My Aldosterone/ Renin assays wer e:-> >>>>> Aldosterone (upright) 1923 (pmol/L) (100 - 950)> >>>>> Renin (upright) 14 (mU/L) (3.3 - 41)> >>>>> Aldosterone/ Renin Ratio 137> >>>>>> >>>>> These results were while on 25mg Spironolactone.> >>>>>> >>>>> I have been taken off Spiro and put on Verapamil SR 240mg/day,> >>>>> which I began this morning.> >>>>> I am to have CT scan of adrenal gland to see what has happened> >>>>> after all this time.> >>>>> Will revisit Dr Nikwan in 8 weeks.> >>>>> Helen D> >>>>> >>>>> >>>>> >>>> >>>> >>>> >>> >>> >>> >> >> >> > ------------------------------------> >> > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 13, 2009 Report Share Posted May 13, 2009 If you enjoy breads, this cookbook has some excellent low sodium bread recipes. They tend to be a thicker bread, but I love making them with some orange rind and cinnamon to use for French Toast. I enjoyed this cookbook so much I even invested in a new bread machine! http://www.amazon.com/No-Salt-Lowest-Sodium-Baking-Book/dp/0312335245 From: hyperaldosteronism [mailto:hyperaldosteronism ] On Behalf Of Clarence Grim Sent: Wednesday, May 13, 2009 9:28 PM hyperaldosteronism Subject: Re: Renewing Conn's journey Recall that cow milk contains nearly 10 the sodium concentration of human milk. This is the reason that cow milk based infant feeding vs human milk sodium content increase BP in infants and this high blood pressure persists at least until the teens. CE Grim MD On May 12, 2009, at 4:40 AM, Helen Drewe wrote: Val, I absolutely avoid sodium like the plague. The only sodium I have is naturally occurring sodium in meat, milk and Yoghurt,etc. I eat lots of high K veges and fruit. Take my own foods wherever I go. Dont trust restaurants etc. Have had too many headaches in early days of diagnosis. I dont eat any breads etc. eat oats, millet etc for carbs. Have been eating this way for nearly 9 years. Since starting Dash, have increased dairy (milk and yoghurt) and making sure I eat enough protein. I could quite happily just live on fruit. I have wondered for a while whether eating such a low sodium diet creates the very thing I am trying to avoid as the body tries even harder to retain sodium, thereby pushing out even more aldosterone. On Tue, May 12, 2009 at 3:00 PM, Valarie <val@...> wrote: Helen, the only way I made it through six weeks off spiro was to absolutely avoid sodium. We traveled to Mayo Clinic so I could take my own food along. When I got a urinary sodium test there, the sodium was too low to measure. Very low sodium diet will increase your renin and make the ARR invalid. Val From: hyperaldosteronism [mailto:hyperaldosteronism ] On Behalf Of Helen Drewe If I Dash to max, I put on weight because I am small build. I eat natural high K foods as nature intended. When I put on weight and begin to feel bloated, it affects my breathing and I get more chest pain. So I dash at 1200- 1600 calories, sticking to the guidelines in the the books - " The Dash Diet for Hypertension " , " The Dash Diet Action Plan " , and " Eat to Beat High Blood Pressure " which features the Dash-Plus Plan. On Mon, May 11, 2009 at 10:49 PM, Clarence Grim <lowerbp2@...> wrote: DASH to the max. CE GrimMD On May 10, 2009, at 10:36 PM, Helen Drewe wrote: I understand Carol, I have only been off spiro since Friday, and feel dreadful. Headaches, flushing, bloating, slight tremors, brain fog.......Dont know if it may be reaction from Verapamil. My sister told me she cant take calcium channel blockers, as she also had headaches and flushing. What do you do? I dont want to back out of having the AVS this time. Helen On Mon, May 11, 2009 at 3:08 PM, Carol Christie <carolch@...> wrote: I should add that I was going to have a second AVS done at Greenslopes. However, after about 3 weeks without spiro I felt so terrible I decided to take it again. Dr Stowasser still recommends a dose of only 25mg, but I feel better on 50mg. Carol Clarence Grim wrote: > > > Tell us all meds u > Are taking. > > Tiped sad Send form mi > iPhone ;-) > > May your pressure be low! > > CE Grim MD > Specializing in Difficult > Hypertension > > On May 10, 2009, at 10:48 PM, Carol Christie <carolch@... > <mailto:carolch%40gil.com.au>> wrote: > > > I, too identify strongly with dealing with mental changes. > > I thought my personal papers filing was only a few months behind. I > > started sorting yesterday and found it had been a year since I had > > filed/sorted things out. > > I used to be meticulous in recording payments due/made etc. My > > organisational skills have deteriorated badly. > > Carol > > > > > > Isa Hackett wrote: > >> > >> > >> - > >> > >> I can identify with your challenges RE mental sharpness. It seems, > >> especially within the past six or so months, that my language > >> (vocabulary) is suffering. I also find myself making silly mistakes. > >> It makes things very hard with work. I often have to be " on " - and I > >> am very aware that I am not. > >> > >> I've also recently been diagnosed - actually, I still have the > >> salt-loading test yet to confirm. I believe my father had PA and will > >> likely be tested for GRA. From what I have read, there is an > >> increased > >> risk of early stroke. My father began having small strokes in his > >> 40's > >> and died of a massive stroke in his early 5o's. > >> > >> Anyway, I encourage you to read as much as possible about GRA. > >> > >> DR Grim -are you aware of any differences in symptoms or treatment - > >> or > >> follow-up for those with GRA? > >> > >> , you should know that there are lots of understanding, helpf ul > >> and experienced people on this board -welcome. > >> > >> Wishing you better health! > >> > >> > >> > >> Sent via BlackBerry from T-Mobile > >> > >> --- > >> ---------------------------------------------------------- > >> *From*: Echols > >> *Date*: Sun, 10 May 2009 19:17:24 -0700 (PDT) > >> *To*: <hyperaldosteronism > <mailto:hyperaldosteronism%40>> > >> *Subject*: Re: Renewing Conn's journey > >> I plan to check my history and talk with my dad (it may take me a > >> little time though). I think I posted my story but I'll check my past > >> posts. > >> > >> --- > >> ---------------------------------------------------------- > >> *From:* Clarence Grim <lowerbp2@... <mailto:lowerbp2%40mac.com>> > >> *To:* hyperaldosteronism > <mailto:hyperaldosteronism%40> > >> *Sent:* Sunday, May 10, 2009 1:34:25 AM > >> *Subject:* Re: Renewing Conn's journey > >> > >> If you father had PA can you give us his story as well (check with > >> him > >> first of course). > >> > >> > >> If he has clearly been diagnosed then it is likely that you and he > >> have the same thing (assuming your have a Dx of PA that is clear as > >> well). You likely have GRA which is an autosomal dominate genetic > >> cause of PA in which 1/2 of all your first degree relatives will have > >> it as well (on the average). > >> > >> Recommend you find out as much as you can about your FH of HTN, low > >> K, > >> causes and age of death as far back as you can go. > >> > >> I am looking for the Dr. in ville and should get back with you > >> soon. > >> > >> Have you given us you complete story yet. I may have missed it as > >> have been at the Am Soc of HTN meeting for last week. Lots of things > >> to report to the group. > >> > >> > >> On May 9, 2009, at 10:18 PM, Echols wrote: > >> > >>> > >>> > >>> > >>> D oc, I am closer to than I am Birmingham. To answer the > >>> family history question, my father was diagnosed with PA in 2007 but > >>> he stated that no CT was ran. It appears that the spiro is lowering > >>> my bp. > >>> As far as my CT scan, would a scan of my renal arteries and kidneys > >>> reveal a bump? I am still suffering extreme fatigue and muscle > >>> weakness and tingling in my extremities, headaches, mental confusion > >>> and cloudiness (harde to concentrate) , memory loss, language > >>> difficulty. I also have intermittent pain in the region of my coccyx > >>> bone. Further, when I am surprised, or see something that causes me > >>> to cringe, I feel a tingling sensation in my lower back that flows > >>> down toward my rear pelvic region. > >>> Doc, I agree with your comment as to other physicians do not appear > >>> to want to work with others to assist in the care of their patients. > >>> I don't know if it is pride or the fact that the concern of > >>> keeping a > >>> patient overrides the overall health of the & nbsp;patient. I have > >>> the > >>> same concerns in the legal profession. I have heard attorneys say > >>> that " you can't help people " . The statement broke my heart. Last I > >>> checked, there were three (3) noble professions: Doctors, lawyers > >>> and > >>> ministers. We provide a service. Don't misunderstand me, doc, this > >>> is my livelihood and I am not apologizing for the salaries in our > >>> respective professions. I pprovide a service and plan to receive > >>> compensation for those services. My concerned is that we need to > >>> keep > >>> in my that we are providing " people " with those services. > >>> I am not a complainer. I have been told that I am kind of stoic in > >>> nature. However, in my profession, I cannot afford to lose my mental > >>> edge or acuity. My job depends on it and I am on a quest to feel > >>> better. Thanks for responding. > >>> If the best doctors are in Birmingham, I will go there but if you > >>> know someone in , that is closer. Thanks, Doc. > >>> > >>> --- > >>> --- > >>> ---------------------------------------------------------- > >>> *From:* Clarence Grim <lowerbp2mac (DOT) com> > >>> *To:* hyperaldosteronism > >>> *Sent:* Friday, May 8, 2009 10:39:57 AM > >>> *Subject:* Re: [hyperaldosteronism ] Renewing Conn's journey > >>> > >>> As you can see from our group's stories we need to increase the > >>> knowledge base or every one who sees pts with high blood pressure. > >>> HTN + low K = PA. > >>> > >>> At some point we would like to have your complete story as well if > >>> you have time. > >>> > >>> > >>> > >>> Your aldo and renin confirm this Dx. > >>> > >>> If you have not read my article on the evolution of PA please do > >>> so-and take to your Dr. I would be happy to work with him in your > >>> care but most Drs don't seem to be interested. Which blows my mind. > >>> > >>> Any family Hx of HTN and/or low K? > >>> > >>> If spiro works for BP and K and your are DASHing to the max that > >>> essentially confirms the Dx. > >>> If the first CT did not show a bump on the adrenal then others will > >>> not likely show anything. > >>> > >>> > >>> Our basic approach here(based on 45 years of experience) is to treat > >>> with medications and DASH and if BP and K are controlled and other > >>> Sx > >>> go away not to do any further D x tests at this stage. > >>> If there is a single bump and Rx fails to get to feeling normal > >>> then > >>> would do AVS to see if the problem is unilateral or bilateral. > >>> > >>> I know folks in MS, in New Orleans and in Birmingham who are > >>> experts in PA. I would recommend you go to someone who has a lot > >>> of > >>> experience in this and has been doing it for some time. > >>> > >>> > >>> > >>> > >>> Clarence Grim BS, MS, MD > >>> > >>> Clinical Professor of Medicine > >>> Medical College of Wisconsin > >>> Senior Consultant to Shared Care Research and Education > >>> Consulting, Inc. > >>> > >>> Specializing in Difficult to control high blood pre ssure. > >>> > >>> > >>> > >>> > >>> > >>> On May 7, 2009, at 1:49 PM, Echols wrote: > >>> > >>>> > >>>> > >>>> > >>>> Dr. Grim, I am an attorney in Mississippi and have just recently > >>>> been diagnosed with PA. My family physician was attempting to treat > >>>> my extremely high bp to no avail and after nearly 3 years fina lly > >>>> told me that he did not have a clue as to what was going on and > >>>> referred me to an internist. The internist specializes in > >>>> hypertension. I really don't know how much the internist > >>>> understands > >>>> about PA but I am glad that he has at least heard of it after I've > >>>> suffered for about 15 or more years with nearly all the symptoms > >>>> listed by others here. The internist ordered a blood workup and my > >>>> aldosterone levels were 3 times the normal amount and my renin was > >>>> undetected. No other tests were run. He did not order a CT scan of > >>>> my adrenals. After being hospitalized, my family physician > >>>> (after I > >>>> pushed for it) ordered a CT scan of my kidneys and renal arteries > >>>> and stated that they looked fine. That was prior to seeing the > >>>> internist. After reading postings in this group, I requested on May > >>>> 5th to have a CT scan performed to look at my adrenal glands. He > >>>> stated that he was not going to do it now, but might in about 2 > >>>> months. > >>>> I told the internist that I am still extremely fatigued, that I > >>>> have > >>>> headaches, my mind is cloudy, having a problem with concentration > >>>> and memory and that I am concerned because it was affecting my work > >>>> (I have been off work for about a month). Internist told me that he > >>>> believed that I was just depressed and prescribed lexapro. He > >>>> stated > >>>> that I should be excited because my blood pressure was coming down. > >>>> I told him that I was excited but that I did not think that I was > >>>> depressed to the point of needing medication. I am thinking of > >>>> either going to the University of Birmingham to see a nephrologist > >>>> and/or endo. Is this a good idea? Is UAB a good place to go for > >>>> hyperaldosterinism? If not, can you refer a place near MS? I need > >>>> to > >>>> make sure that I have this condition ( I have all the symptoms and > >>>> the spiro-75mg- is helping my bp) and if so, how I can cure or best > >>>> treat it. The internist stated that he did not know what caused it > >>>> and that he did not believe that I had a tumor. I am grateful that > >>>> he looked into hyperaldosteronism but I think the internist is more > >>>> concentrated on the bp, since that is his specialty. I am concerned > >>>> not only about the bp, but also the mental aspects of this > >>>> condition > >>>> because it emy livelihood. Please respond. > >>>> > >>>> --- > >>>> --- > >>>> ---------------------------------------------------------- > >>>> *From:* Clarence Grim <lowerbp2mac (DOT) com> > >>>> *To:* hyperaldosteronism > >>>> *Sent:* Thursday, May 7, 2009 1:32:35 AM > >>>> *Subject:* Re: [hyperaldosteronism ] Renewing Conn's journey > >>>> > >>>> Dont recall your previous story. Do we need to update your story? > >>>> > >>>> > >>>> CE Grim MD > >>>> On May 6, 2009, at 6:05 PM, hdrewe wrote: > >>>> > >>>>> I have not been in contact with this site for a few weeks, > >>>>> however, > >>>>> am now back on track. I visited Dr Nikwan at Greenslopes Hospital, > >>>>> and am going ahead with the workups prior to maybe having surgery. > >>>>> He was certainly surprised to see me after 9 years. > >>>>> > >>>>> My Aldosterone/ Renin assays wer e:- > >>>>> Aldosterone (upright) 1923 (pmol/L) (100 - 950) > >>>>> Renin (upright) 14 (mU/L) (3.3 - 41) > >>>>> Aldosterone/ Renin Ratio 137 > >>>>> > >>>>> These results were while on 25mg Spironolactone. > >>>>> > >>>>> I have been taken off Spiro and put on Verapamil SR 240mg/day, > >>>>> which I began this morning. > >>>>> I am to have CT scan of adrenal gland to see what has happened > >>>>> after all this time. > >>>>> Will revisit Dr Nikwan in 8 weeks. > >>>>> Helen D > >>>> > >>>> > >>>> > >>> > >>> > >>> > >> > >> > >> > > > > > > > > ------------------------------------ > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 14, 2009 Report Share Posted May 14, 2009 Human milk has per cup 125mg K and 41.8 mg sodium. ( Nutrition Data) Cows milk has per cup 349 K and 97.6 Sodium. (Nutrition Data)I can see the reasoning why cows milk is too concentrated for the human system.  After both my surgeries, all I lived on was warm milk as I could not tolerate anything else. Same as when I am feeling unwell. Maybe this ties in with craving for sodium? The very thing I shouldnt have with PA  On Thu, May 14, 2009 at 12:28 PM, Clarence Grim <lowerbp2@...> wrote: Recall that cow milk contains nearly 10 the sodium concentration of human milk.  This is the reason that cow milk based infant feeding vs human milk sodium content increase BP in infants and this high blood pressure persists at least until the teens. CE Grim MD On May 12, 2009, at 4:40 AM, Helen Drewe wrote: Val, I absolutely avoid sodium like the plague. The only sodium I have is naturally occurring sodium in meat, milk and Yoghurt,etc. I eat lots of high K veges and fruit. Take my own foods wherever I go. Dont trust restaurants etc. Have had too many headaches in early days of diagnosis. I dont eat any breads etc. eat oats, millet etc for carbs. Have been eating this way for nearly 9 years. Since starting Dash, have increased dairy (milk and yoghurt) and making sure I eat enough protein. I could quite happily just live on fruit.  I have wondered for a while whether eating such a low sodium diet creates the very thing I am trying to avoid as the body tries even harder to retain sodium, thereby pushing out even more aldosterone. On Tue, May 12, 2009 at 3:00 PM, Valarie  <val@...> wrote: Helen, the only way I made it through six weeks off spiro was to absolutely avoid sodium.  We traveled to Mayo Clinic so I could take my own food along.  When I got a urinary sodium test there, the sodium was too low to measure.  Very low sodium diet will increase your renin and make the ARR invalid.  Val  From: hyperaldosteronism  [mailto:hyperaldosteronism ] On Behalf Of Helen Drewe If I Dash to max, I put on weight because I am small build. I eat natural high K foods as nature intended. When I put on weight and begin to feel bloated, it affects my breathing and I get more chest pain. So I dash at 1200- 1600 calories, sticking to the guidelines in the the books - " The Dash Diet for Hypertension " , " The Dash Diet Action Plan " , and " Eat to Beat High Blood Pressure " which features the Dash-Plus Plan. On Mon, May 11, 2009 at 10:49 PM, Clarence Grim <lowerbp2@...> wrote:  DASH to the max.  CE GrimMD  On May 10, 2009, at 10:36 PM, Helen Drewe wrote:   I understand Carol, I have only been off spiro since Friday, and feel dreadful. Headaches, flushing, bloating, slight tremors, brain fog.......Dont know if it may be reaction from Verapamil. My sister told me she cant take calcium channel blockers, as she also had headaches and flushing. What do you do? I dont want to back out of having the AVS this time. Helen On Mon, May 11, 2009 at 3:08 PM, Carol Christie <carolch@...> wrote:  I should add that I was going to have a second AVS done at Greenslopes. However, after about 3 weeks without spiro I felt so terrible I decided to take it again. Dr Stowasser still recommends a dose of only 25mg, but I feel better on 50mg. CarolClarence Grim wrote:>>> Tell us all meds u> Are taking.> > Tiped sad Send form mi> iPhone ;-)>> May your pressure be low!>> CE Grim MD> Specializing in Difficult> Hypertension>> On May 10, 2009, at 10:48 PM, Carol Christie <carolch@... > <mailto:carolch%40gil.com.au>> wrote: >> > I, too identify strongly with dealing with mental changes.> > I thought my personal papers filing was only a few months behind. I> > started sorting yesterday and found it had been a year since I had > > filed/sorted things out.> > I used to be meticulous in recording payments due/made etc. My> > organisational skills have deteriorated badly.> > Carol> >> >> > Isa Hackett wrote: > >>> >>> >> -> >>> >> I can identify with your challenges RE mental sharpness. It seems,> >> especially within the past six or so months, that my language > >> (vocabulary) is suffering. I also find myself making silly mistakes.> >> It makes things very hard with work. I often have to be " on " - and I> >> am very aware that I am not. > >>> >> I've also recently been diagnosed - actually, I still have the> >> salt-loading test yet to confirm. I believe my father had PA and will> >> likely be tested for GRA. From what I have read, there is an > >> increased> >> risk of early stroke. My father began having small strokes in his> >> 40's> >> and died of a massive stroke in his early 5o's.> >> > >> Anyway, I encourage you to read as much as possible about GRA.> >>> >> DR Grim -are you aware of any differences in symptoms or treatment -> >> or> >> follow-up for those with GRA? > >>> >> , you should know that there are lots of understanding, helpf ul> >> and experienced people on this board -welcome.> >>> >> Wishing you better health! > >>> >> > >>> >> Sent via BlackBerry from T-Mobile> >>> >> ---> >> ---------------------------------------------------------- > >> *From*: Echols> >> *Date*: Sun, 10 May 2009 19:17:24 -0700 (PDT)> >> *To*: <hyperaldosteronism  > <mailto:hyperaldosteronism%40>> > >> *Subject*: Re: Renewing Conn's journey> >> I plan to check my history and talk with my dad (it may take me a> >> little time though). I think I posted my story but I'll check my past > >> posts.> >>> >> ---> >> ----------------------------------------------------------> >> *From:* Clarence Grim <lowerbp2@... <mailto:lowerbp2%40mac.com>> > >> *To:* hyperaldosteronism  > <mailto:hyperaldosteronism%40> > >> *Sent:* Sunday, May 10, 2009 1:34:25 AM> >> *Subject:* Re: Renewing Conn's journey> >>> >> If you father had PA can you give us his story as well (check with > >> him> >> first of course).> >>> >>> >> If he has clearly been diagnosed then it is likely that you and he> >> have the same thing (assuming your have a Dx of PA that is clear as > >> well). You likely have GRA which is an autosomal dominate genetic> >> cause of PA in which 1/2 of all your first degree relatives will have> >> it as well (on the average).> >> > >> Recommend you find out as much as you can about your FH of HTN, low> >> K,> >> causes and age of death as far back as you can go.> >>> >> I am looking for the Dr. in ville and should get back with you > >> soon.> >>> >> Have you given us you complete story yet. I may have missed it as> >> have been at the Am Soc of HTN meeting for last week. Lots of things> >> to report to the group. > >>> >>> >> On May 9, 2009, at 10:18 PM, Echols wrote:> >>> >>>> >>>> >>>> >>> D oc, I am closer to than I am Birmingham. To answer the > >>> family history question, my father was diagnosed with PA in 2007 but> >>> he stated that no CT was ran. It appears that the spiro is lowering> >>> my bp.> >>> As far as my CT scan, would a scan of my renal arteries and kidneys > >>> reveal a bump? I am still suffering extreme fatigue and muscle> >>> weakness and tingling in my extremities, headaches, mental confusion> >>> and cloudiness (harde to concentrate) , memory loss, language > >>> difficulty. I also have intermittent pain in the region of my coccyx> >>> bone. Further, when I am surprised, or see something that causes me> >>> to cringe, I feel a tingling sensation in my lower back that flows > >>> down toward my rear pelvic region.> >>> Doc, I agree with your comment as to other physicians do not appear> >>> to want to work with others to assist in the care of their patients. > >>> I don't know if it is pride or the fact that the concern of> >>> keeping a> >>> patient overrides the overall health of the & nbsp;patient. I have> >>> the > >>> same concerns in the legal profession. I have heard attorneys say> >>> that " you can't help people " . The statement broke my heart. Last I> >>> checked, there were three (3) noble professions: Doctors, lawyers > >>> and> >>> ministers. We provide a service. Don't misunderstand me, doc, this> >>> is my livelihood and I am not apologizing for the salaries in our> >>> respective professions. I pprovide a service and plan to receive > >>> compensation for those services. My concerned is that we need to> >>> keep> >>> in my that we are providing " people " with those services.> >>> I am not a complainer. I have been told that I am kind of stoic in > >>> nature. However, in my profession, I cannot afford to lose my mental> >>> edge or acuity. My job depends on it and I am on a quest to feel> >>> better. Thanks for responding. > >>> If the best doctors are in Birmingham, I will go there but if you> >>> know someone in , that is closer. Thanks, Doc.> >>>> >>> ---> >>> --- > >>> ----------------------------------------------------------> >>> *From:* Clarence Grim <lowerbp2mac (DOT) com>> >>> *To:* hyperaldosteronism> >>> *Sent:* Friday, May 8, 2009 10:39:57 AM > >>> *Subject:* Re: [hyperaldosteronism ] Renewing Conn's journey> >>>> >>> As you can see from our group's stories we need to increase the> >>> knowledge base or every one who sees pts with high blood pressure. > >>> HTN + low K = PA.> >>>> >>> At some point we would like to have your complete story as well if> >>> you have time.> >>>> >>> > >>>> >>> Your aldo and renin confirm this Dx.> >>>> >>> If you have not read my article on the evolution of PA please do> >>> so-and take to your Dr. I would be happy to work with him in your > >>> care but most Drs don't seem to be interested. Which blows my mind.> >>>> >>> Any family Hx of HTN and/or low K?> >>>> >>> If spiro works for BP and K and your are DASHing to the max that > >>> essentially confirms the Dx.> >>> If the first CT did not show a bump on the adrenal then others will> >>> not likely show anything.> >>>> >>> > >>> Our basic approach here(based on 45 years of experience) is to treat> >>> with medications and DASH and if BP and K are controlled and other> >>> Sx> >>> go away not to do any further D x tests at this stage. > >>> If there is a single bump and Rx fails to get to feeling normal> >>> then> >>> would do AVS to see if the problem is unilateral or bilateral.> >>>> >>> I know folks in MS, in New Orleans and in Birmingham who are > >>> experts in PA. I would recommend you go to someone who has a lot> >>> of> >>> experience in this and has been doing it for some time.> >>>> >>> > >>>> >>>> >>> Clarence Grim BS, MS, MD> >>>> >>> Clinical Professor of Medicine> >>> Medical College of Wisconsin> >>> Senior Consultant to Shared Care Research and Education > >>> Consulting, Inc.> >>>> >>> Specializing in Difficult to control high blood pre ssure.> >>>> >>>> >>>> >>> > >>>> >>> On May 7, 2009, at 1:49 PM, Echols wrote:> >>>> >>>>> >>>>> >>>>> >>>> Dr. Grim, I am an attorney in Mississippi and have just recently > >>>> been diagnosed with PA. My family physician was attempting to treat> >>>> my extremely high bp to no avail and after nearly 3 years fina lly> >>>> told me that he did not have a clue as to what was going on and > >>>> referred me to an internist. The internist specializes in> >>>> hypertension. I really don't know how much the internist> >>>> understands> >>>> about PA but I am glad that he has at least heard of it after I've > >>>> suffered for about 15 or more years with nearly all the symptoms> >>>> listed by others here. The internist ordered a blood workup and my> >>>> aldosterone levels were 3 times the normal amount and my renin was > >>>> undetected. No other tests were run. He did not order a CT scan of> >>>> my adrenals. After being hospitalized, my family physician> >>>> (after I> >>>> pushed for it) ordered a CT scan of my kidneys and renal arteries > >>>> and stated that they looked fine. That was prior to seeing the> >>>> internist. After reading postings in this group, I requested on May> >>>> 5th to have a CT scan performed to look at my adrenal glands. He > >>>> stated that he was not going to do it now, but might in about 2> >>>> months.> >>>> I told the internist that I am still extremely fatigued, that I> >>>> have > >>>> headaches, my mind is cloudy, having a problem with concentration> >>>> and memory and that I am concerned because it was affecting my work> >>>> (I have been off work for about a month). Internist told me that he > >>>> believed that I was just depressed and prescribed lexapro. He> >>>> stated> >>>> that I should be excited because my blood pressure was coming down.> >>>> I told him that I was excited but that I did not think that I was > >>>> depressed to the point of needing medication. I am thinking of> >>>> either going to the University of Birmingham to see a nephrologist> >>>> and/or endo. Is this a good idea? Is UAB a good place to go for > >>>> hyperaldosterinism? If not, can you refer a place near MS? I need> >>>> to> >>>> make sure that I have this condition ( I have all the symptoms and> >>>> the spiro-75mg- is helping my bp) and if so, how I can cure or best > >>>> treat it. The internist stated that he did not know what caused it> >>>> and that he did not believe that I had a tumor. I am grateful that> >>>> he looked into hyperaldosteronism but I think the internist is more > >>>> concentrated on the bp, since that is his specialty. I am concerned> >>>> not only about the bp, but also the mental aspects of this> >>>> condition> >>>> because it emy livelihood. Please respond. > >>>>> >>>> ---> >>>> ---> >>>> ----------------------------------------------------------> >>>> *From:* Clarence Grim <lowerbp2mac (DOT) com> > >>>> *To:* hyperaldosteronism> >>>> *Sent:* Thursday, May 7, 2009 1:32:35 AM> >>>> *Subject:* Re: [hyperaldosteronism ] Renewing Conn's journey > >>>>> >>>> Dont recall your previous story. Do we need to update your story?> >>>>> >>>>> >>>> CE Grim MD> >>>> On May 6, 2009, at 6:05 PM, hdrewe wrote: > >>>>> >>>>> I have not been in contact with this site for a few weeks,> >>>>> however,> >>>>> am now back on track. I visited Dr Nikwan at Greenslopes Hospital, > >>>>> and am going ahead with the workups prior to maybe having surgery.> >>>>> He was certainly surprised to see me after 9 years.> >>>>>> >>>>> My Aldosterone/ Renin assays wer e:- > >>>>> Aldosterone (upright) 1923 (pmol/L) (100 - 950)> >>>>> Renin (upright) 14 (mU/L) (3.3 - 41)> >>>>> Aldosterone/ Renin Ratio 137> >>>>> > >>>>> These results were while on 25mg Spironolactone.> >>>>>> >>>>> I have been taken off Spiro and put on Verapamil SR 240mg/day,> >>>>> which I began this morning. > >>>>> I am to have CT scan of adrenal gland to see what has happened> >>>>> after all this time.> >>>>> Will revisit Dr Nikwan in 8 weeks.> >>>>> Helen D > >>>>> >>>>> >>>>> >>>> >>>> >>>> >>> >>> >>> >> >> > > > ------------------------------------> >> > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 14, 2009 Report Share Posted May 14, 2009 Thanks for recommendation . I love bread, but only have a couple of recipes with no salt. Actually looked at this book on the MegaHeart site. Think I will now geT it! On Thu, May 14, 2009 at 2:35 PM, Malotky <leslie@...> wrote: If you enjoy breads, this cookbook has some excellent low sodium bread recipes. They tend to be a thicker bread, but I love making them with some orange rind and cinnamon to use for French Toast.   I enjoyed this cookbook so much I even invested in a new bread machine!  http://www.amazon.com/No-Salt-Lowest-Sodium-Baking-Book/dp/0312335245  From: hyperaldosteronism [mailto:hyperaldosteronism ] On Behalf Of Clarence Grim Sent: Wednesday, May 13, 2009 9:28 PMhyperaldosteronism Subject: Re: Renewing Conn's journey  Recall that cow milk contains nearly 10 the sodium concentration of human milk.  This is the reason that cow milk based infant feeding vs human milk sodium content increase BP in infants and this high blood pressure persists at least until the teens.   CE Grim MD On May 12, 2009, at 4:40 AM, Helen Drewe wrote:   Val, I absolutely avoid sodium like the plague. The only sodium I have is naturally occurring sodium in meat, milk and Yoghurt,etc. I eat lots of high K veges and fruit. Take my own foods wherever I go. Dont trust restaurants etc. Have had too many headaches in early days of diagnosis. I dont eat any breads etc. eat oats, millet etc for carbs. Have been eating this way for nearly 9 years. Since starting Dash, have increased dairy (milk and yoghurt) and making sure I eat enough protein. I could quite happily just live on fruit.  I have wondered for a while whether eating such a low sodium diet creates the very thing I am trying to avoid as the body tries even harder to retain sodium, thereby pushing out even more aldosterone. On Tue, May 12, 2009 at 3:00 PM, Valarie  <val@...> wrote:   Helen, the only way I made it through six weeks off spiro was to absolutely avoid sodium.  We traveled to Mayo Clinic so I could take my own food along.  When I got a urinary sodium test there, the sodium was too low to measure.  Very low sodium diet will increase your renin and make the ARR invalid.  Val  From: hyperaldosteronism  [mailto:hyperaldosteronism ] On Behalf Of Helen Drewe If I Dash to max, I put on weight because I am small build. I eat natural high K foods as nature intended. When I put on weight and begin to feel bloated, it affects my breathing and I get more chest pain. So I dash at 1200- 1600 calories, sticking to the guidelines in the the books - " The Dash Diet for Hypertension " , " The Dash Diet Action Plan " , and " Eat to Beat High Blood Pressure " which features the Dash-Plus Plan. On Mon, May 11, 2009 at 10:49 PM, Clarence Grim <lowerbp2@...> wrote:  DASH to the max.  CE GrimMD  On May 10, 2009, at 10:36 PM, Helen Drewe wrote:    I understand Carol, I have only been off spiro since Friday, and feel dreadful. Headaches, flushing, bloating, slight tremors, brain fog.......Dont know if it may be reaction from Verapamil. My sister told me she cant take calcium channel blockers, as she also had headaches and flushing. What do you do? I dont want to back out of having the AVS this time. Helen On Mon, May 11, 2009 at 3:08 PM, Carol Christie <carolch@...> wrote:  I should add that I was going to have a second AVS done at Greenslopes. However, after about 3 weeks without spiro I felt so terrible I decided to take it again. Dr Stowasser still recommends a dose of only 25mg, but I feel better on 50mg. Carol Clarence Grim wrote:>>> Tell us all meds u> Are taking.>> Tiped sad Send form mi> iPhone ;-)>> May your pressure be low!>> CE Grim MD> Specializing in Difficult > Hypertension>> On May 10, 2009, at 10:48 PM, Carol Christie <carolch@... > <mailto:carolch%40gil.com.au>> wrote: >> > I, too identify strongly with dealing with mental changes.> > I thought my personal papers filing was only a few months behind. I> > started sorting yesterday and found it had been a year since I had > > filed/sorted things out.> > I used to be meticulous in recording payments due/made etc. My> > organisational skills have deteriorated badly.> > Carol> >> >> > Isa Hackett wrote: > >>> >>> >> -> >>> >> I can identify with your challenges RE mental sharpness. It seems,> >> especially within the past six or so months, that my language > >> (vocabulary) is suffering. I also find myself making silly mistakes.> >> It makes things very hard with work. I often have to be " on " - and I> >> am very aware that I am not. > >>> >> I've also recently been diagnosed - actually, I still have the> >> salt-loading test yet to confirm. I believe my father had PA and will> >> likely be tested for GRA. From what I have read, there is an > >> increased> >> risk of early stroke. My father began having small strokes in his> >> 40's> >> and died of a massive stroke in his early 5o's.> >> > >> Anyway, I encourage you to read as much as possible about GRA.> >>> >> DR Grim -are you aware of any differences in symptoms or treatment -> >> or> >> follow-up for those with GRA? > >>> >> , you should know that there are lots of understanding, helpf ul> >> and experienced people on this board -welcome.> >>> >> Wishing you better health! > >>> >> > >>> >> Sent via BlackBerry from T-Mobile> >>> >> ---> >> ---------------------------------------------------------- > >> *From*: Echols> >> *Date*: Sun, 10 May 2009 19:17:24 -0700 (PDT)> >> *To*: <hyperaldosteronism  > <mailto:hyperaldosteronism%40>>> >> *Subject*: Re: Renewing Conn's journey > >> I plan to check my history and talk with my dad (it may take me a> >> little time though). I think I posted my story but I'll check my past> >> posts.> >>> >> --- > >> ----------------------------------------------------------> >> *From:* Clarence Grim <lowerbp2@... <mailto:lowerbp2%40mac.com>> > >> *To:* hyperaldosteronism  > <mailto:hyperaldosteronism%40> > >> *Sent:* Sunday, May 10, 2009 1:34:25 AM> >> *Subject:* Re: Renewing Conn's journey> >>> >> If you father had PA can you give us his story as well (check with > >> him> >> first of course).> >>> >>> >> If he has clearly been diagnosed then it is likely that you and he> >> have the same thing (assuming your have a Dx of PA that is clear as > >> well). You likely have GRA which is an autosomal dominate genetic> >> cause of PA in which 1/2 of all your first degree relatives will have> >> it as well (on the average).> >> > >> Recommend you find out as much as you can about your FH of HTN, low> >> K,> >> causes and age of death as far back as you can go.> >>> >> I am looking for the Dr. in ville and should get back with you > >> soon.> >>> >> Have you given us you complete story yet. I may have missed it as> >> have been at the Am Soc of HTN meeting for last week. Lots of things> >> to report to the group. > >>> >>> >> On May 9, 2009, at 10:18 PM, Echols wrote:> >>> >>>> >>>> >>>> >>> D oc, I am closer to than I am Birmingham. To answer the > >>> family history question, my father was diagnosed with PA in 2007 but> >>> he stated that no CT was ran. It appears that the spiro is lowering> >>> my bp.> >>> As far as my CT scan, would a scan of my renal arteries and kidneys > >>> reveal a bump? I am still suffering extreme fatigue and muscle> >>> weakness and tingling in my extremities, headaches, mental confusion> >>> and cloudiness (harde to concentrate) , memory loss, language > >>> difficulty. I also have intermittent pain in the region of my coccyx> >>> bone. Further, when I am surprised, or see something that causes me> >>> to cringe, I feel a tingling sensation in my lower back that flows > >>> down toward my rear pelvic region.> >>> Doc, I agree with your comment as to other physicians do not appear> >>> to want to work with others to assist in the care of their patients. > >>> I don't know if it is pride or the fact that the concern of> >>> keeping a> >>> patient overrides the overall health of the & nbsp;patient. I have> >>> the > >>> same concerns in the legal profession. I have heard attorneys say> >>> that " you can't help people " . The statement broke my heart. Last I> >>> checked, there were three (3) noble professions: Doctors, lawyers > >>> and> >>> ministers. We provide a service. Don't misunderstand me, doc, this> >>> is my livelihood and I am not apologizing for the salaries in our> >>> respective professions. I pprovide a service and plan to receive > >>> compensation for those services. My concerned is that we need to> >>> keep> >>> in my that we are providing " people " with those services.> >>> I am not a complainer. I have been told that I am kind of stoic in > >>> nature. However, in my profession, I cannot afford to lose my mental> >>> edge or acuity. My job depends on it and I am on a quest to feel> >>> better. Thanks for responding. > >>> If the best doctors are in Birmingham, I will go there but if you> >>> know someone in , that is closer. Thanks, Doc.> >>>> >>> ---> >>> --- > >>> ----------------------------------------------------------> >>> *From:* Clarence Grim <lowerbp2mac (DOT) com>> >>> *To:* hyperaldosteronism> >>> *Sent:* Friday, May 8, 2009 10:39:57 AM > >>> *Subject:* Re: [hyperaldosteronism ] Renewing Conn's journey> >>>> >>> As you can see from our group's stories we need to increase the> >>> knowledge base or every one who sees pts with high blood pressure. > >>> HTN + low K = PA.> >>>> >>> At some point we would like to have your complete story as well if> >>> you have time.> >>>> >>> > >>>> >>> Your aldo and renin confirm this Dx.> >>>> >>> If you have not read my article on the evolution of PA please do> >>> so-and take to your Dr. I would be happy to work with him in your > >>> care but most Drs don't seem to be interested. Which blows my mind.> >>>> >>> Any family Hx of HTN and/or low K?> >>>> >>> If spiro works for BP and K and your are DASHing to the max that > >>> essentially confirms the Dx.> >>> If the first CT did not show a bump on the adrenal then others will> >>> not likely show anything.> >>>> >>> > >>> Our basic approach here(based on 45 years of experience) is to treat> >>> with medications and DASH and if BP and K are controlled and other> >>> Sx> >>> go away not to do any further D x tests at this stage. > >>> If there is a single bump and Rx fails to get to feeling normal> >>> then> >>> would do AVS to see if the problem is unilateral or bilateral.> >>>> >>> I know folks in MS, in New Orleans and in Birmingham who are > >>> experts in PA. I would recommend you go to someone who has a lot> >>> of> >>> experience in this and has been doing it for some time.> >>>> >>> > >>>> >>>> >>> Clarence Grim BS, MS, MD> >>>> >>> Clinical Professor of Medicine> >>> Medical College of Wisconsin> >>> Senior Consultant to Shared Care Research and Education > >>> Consulting, Inc.> >>>> >>> Specializing in Difficult to control high blood pre ssure.> >>>> >>>> >>>> >>> > >>>> >>> On May 7, 2009, at 1:49 PM, Echols wrote:> >>>> >>>>> >>>>> >>>>> >>>> Dr. Grim, I am an attorney in Mississippi and have just recently > >>>> been diagnosed with PA. My family physician was attempting to treat> >>>> my extremely high bp to no avail and after nearly 3 years fina lly> >>>> told me that he did not have a clue as to what was going on and > >>>> referred me to an internist. The internist specializes in> >>>> hypertension. I really don't know how much the internist> >>>> understands> >>>> about PA but I am glad that he has at least heard of it after I've > >>>> suffered for about 15 or more years with nearly all the symptoms> >>>> listed by others here. The internist ordered a blood workup and my> >>>> aldosterone levels were 3 times the normal amount and my renin was > >>>> undetected. No other tests were run. He did not order a CT scan of> >>>> my adrenals. After being hospitalized, my family physician> >>>> (after I> >>>> pushed for it) ordered a CT scan of my kidneys and renal arteries > >>>> and stated that they looked fine. That was prior to seeing the> >>>> internist. After reading postings in this group, I requested on May> >>>> 5th to have a CT scan performed to look at my adrenal glands. He > >>>> stated that he was not going to do it now, but might in about 2> >>>> months.> >>>> I told the internist that I am still extremely fatigued, that I> >>>> have > >>>> headaches, my mind is cloudy, having a problem with concentration> >>>> and memory and that I am concerned because it was affecting my work> >>>> (I have been off work for about a month). Internist told me that he > >>>> believed that I was just depressed and prescribed lexapro. He> >>>> stated> >>>> that I should be excited because my blood pressure was coming down.> >>>> I told him that I was excited but that I did not think that I was > >>>> depressed to the point of needing medication. I am thinking of> >>>> either going to the University of Birmingham to see a nephrologist> >>>> and/or endo. Is this a good idea? Is UAB a good place to go for > >>>> hyperaldosterinism? If not, can you refer a place near MS? I need> >>>> to> >>>> make sure that I have this condition ( I have all the symptoms and> >>>> the spiro-75mg- is helping my bp) and if so, how I can cure or best > >>>> treat it. The internist stated that he did not know what caused it> >>>> and that he did not believe that I had a tumor. I am grateful that> >>>> he looked into hyperaldosteronism but I think the internist is more > >>>> concentrated on the bp, since that is his specialty. I am concerned> >>>> not only about the bp, but also the mental aspects of this> >>>> condition> >>>> because it emy livelihood. Please respond. > >>>>> >>>> ---> >>>> ---> >>>> ----------------------------------------------------------> >>>> *From:* Clarence Grim <lowerbp2mac (DOT) com> > >>>> *To:* hyperaldosteronism> >>>> *Sent:* Thursday, May 7, 2009 1:32:35 AM> >>>> *Subject:* Re: [hyperaldosteronism ] Renewing Conn's journey > >>>>> >>>> Dont recall your previous story. Do we need to update your story?> >>>>> >>>>> >>>> CE Grim MD> >>>> On May 6, 2009, at 6:05 PM, hdrewe wrote: > >>>>> >>>>> I have not been in contact with this site for a few weeks,> >>>>> however,> >>>>> am now back on track. I visited Dr Nikwan at Greenslopes Hospital, > >>>>> and am going ahead with the workups prior to maybe having surgery.> >>>>> He was certainly surprised to see me after 9 years.> >>>>>> >>>>> My Aldosterone/ Renin assays wer e:- > >>>>> Aldosterone (upright) 1923 (pmol/L) (100 - 950)> >>>>> Renin (upright) 14 (mU/L) (3.3 - 41)> >>>>> Aldosterone/ Renin Ratio 137> >>>>> > >>>>> These results were while on 25mg Spironolactone.> >>>>>> >>>>> I have been taken off Spiro and put on Verapamil SR 240mg/day,> >>>>> which I began this morning. > >>>>> I am to have CT scan of adrenal gland to see what has happened> >>>>> after all this time.> >>>>> Will revisit Dr Nikwan in 8 weeks.> >>>>> Helen D > >>>>> >>>>> >>>>> >>>> >>>> >>>> >>> >>> >>> >> >> > > > ------------------------------------> >> > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 14, 2009 Report Share Posted May 14, 2009 Hi All, After reading Carol’s email on Monday I decided to increase my Spiro to 50mg too (my Dr here in Australia also does not want me on anymore than 25mg), and I have to say that I am definitely feeling improved. In fact, this is the best I have felt in a while. I am back to see the Dr on Wednesday so unless there is some dire reason as to why I can’t stay on this dosage, I will be advocating maintaining this dosage from this point on. I have recorded some elevated pulse increases, but other than that, everything seems OK. From: hyperaldosteronism [mailto:hyperaldosteronism ] On Behalf Of Carol Christie Sent: Monday, 11 May 2009 3:08 PM hyperaldosteronism Subject: Re: Renewing Conn's journey I should add that I was going to have a second AVS done at Greenslopes. However, after about 3 weeks without spiro I felt so terrible I decided to take it again. Dr Stowasser still recommends a dose of only 25mg, but I feel better on 50mg. Carol Clarence Grim wrote: > > > Tell us all meds u > Are taking. > > Tiped sad Send form mi > iPhone ;-) > > May your pressure be low! > > CE Grim MD > Specializing in Difficult > Hypertension > > On May 10, 2009, at 10:48 PM, Carol Christie <carolch@... > <mailto:carolch%40gil.com.au>> wrote: > > > I, too identify strongly with dealing with mental changes. > > I thought my personal papers filing was only a few months behind. I > > started sorting yesterday and found it had been a year since I had > > filed/sorted things out. > > I used to be meticulous in recording payments due/made etc. My > > organisational skills have deteriorated badly. > > Carol > > > > > > Isa Hackett wrote: > >> > >> > >> - > >> > >> I can identify with your challenges RE mental sharpness. It seems, > >> especially within the past six or so months, that my language > >> (vocabulary) is suffering. I also find myself making silly mistakes. > >> It makes things very hard with work. I often have to be " on " - and I > >> am very aware that I am not. > >> > >> I've also recently been diagnosed - actually, I still have the > >> salt-loading test yet to confirm. I believe my father had PA and will > >> likely be tested for GRA. From what I have read, there is an > >> increased > >> risk of early stroke. My father began having small strokes in his > >> 40's > >> and died of a massive stroke in his early 5o's. > >> > >> Anyway, I encourage you to read as much as possible about GRA. > >> > >> DR Grim -are you aware of any differences in symptoms or treatment - > >> or > >> follow-up for those with GRA? > >> > >> , you should know that there are lots of understanding, helpf ul > >> and experienced people on this board -welcome. > >> > >> Wishing you better health! > >> > >> > >> > >> Sent via BlackBerry from T-Mobile > >> > >> --- > >> ---------------------------------------------------------- > >> *From*: Echols > >> *Date*: Sun, 10 May 2009 19:17:24 -0700 (PDT) > >> *To*: <hyperaldosteronism > <mailto:hyperaldosteronism%40>> > >> *Subject*: Re: Renewing Conn's journey > >> I plan to check my history and talk with my dad (it may take me a > >> little time though). I think I posted my story but I'll check my past > >> posts. > >> > >> --- > >> ---------------------------------------------------------- > >> *From:* Clarence Grim <lowerbp2@... <mailto:lowerbp2%40mac.com>> > >> *To:* hyperaldosteronism > <mailto:hyperaldosteronism%40> > >> *Sent:* Sunday, May 10, 2009 1:34:25 AM > >> *Subject:* Re: Renewing Conn's journey > >> > >> If you father had PA can you give us his story as well (check with > >> him > >> first of course). > >> > >> > >> If he has clearly been diagnosed then it is likely that you and he > >> have the same thing (assuming your have a Dx of PA that is clear as > >> well). You likely have GRA which is an autosomal dominate genetic > >> cause of PA in which 1/2 of all your first degree relatives will have > >> it as well (on the average). > >> > >> Recommend you find out as much as you can about your FH of HTN, low > >> K, > >> causes and age of death as far back as you can go. > >> > >> I am looking for the Dr. in ville and should get back with you > >> soon. > >> > >> Have you given us you complete story yet. I may have missed it as > >> have been at the Am Soc of HTN meeting for last week. Lots of things > >> to report to the group. > >> > >> > >> On May 9, 2009, at 10:18 PM, Echols wrote: > >> > >>> > >>> > >>> > >>> D oc, I am closer to than I am Birmingham. To answer the > >>> family history question, my father was diagnosed with PA in 2007 but > >>> he stated that no CT was ran. It appears that the spiro is lowering > >>> my bp. > >>> As far as my CT scan, would a scan of my renal arteries and kidneys > >>> reveal a bump? I am still suffering extreme fatigue and muscle > >>> weakness and tingling in my extremities, headaches, mental confusion > >>> and cloudiness (harde to concentrate) , memory loss, language > >>> difficulty. I also have intermittent pain in the region of my coccyx > >>> bone. Further, when I am surprised, or see something that causes me > >>> to cringe, I feel a tingling sensation in my lower back that flows > >>> down toward my rear pelvic region. > >>> Doc, I agree with your comment as to other physicians do not appear > >>> to want to work with others to assist in the care of their patients. > >>> I don't know if it is pride or the fact that the concern of > >>> keeping a > >>> patient overrides the overall health of the & nbsp;patient. I have > >>> the > >>> same concerns in the legal profession. I have heard attorneys say > >>> that " you can't help people " . The statement broke my heart. Last I > >>> checked, there were three (3) noble professions: Doctors, lawyers > >>> and > >>> ministers. We provide a service. Don't misunderstand me, doc, this > >>> is my livelihood and I am not apologizing for the salaries in our > >>> respective professions. I pprovide a service and plan to receive > >>> compensation for those services. My concerned is that we need to > >>> keep > >>> in my that we are providing " people " with those services. > >>> I am not a complainer. I have been told that I am kind of stoic in > >>> nature. However, in my profession, I cannot afford to lose my mental > >>> edge or acuity. My job depends on it and I am on a quest to feel > >>> better. Thanks for responding. > >>> If the best doctors are in Birmingham, I will go there but if you > >>> know someone in , that is closer. Thanks, Doc. > >>> > >>> --- > >>> --- > >>> ---------------------------------------------------------- > >>> *From:* Clarence Grim <lowerbp2mac (DOT) com> > >>> *To:* hyperaldosteronism > >>> *Sent:* Friday, May 8, 2009 10:39:57 AM > >>> *Subject:* Re: [hyperaldosteronism ] Renewing Conn's journey > >>> > >>> As you can see from our group's stories we need to increase the > >>> knowledge base or every one who sees pts with high blood pressure. > >>> HTN + low K = PA. > >>> > >>> At some point we would like to have your complete story as well if > >>> you have time. > >>> > >>> > >>> > >>> Your aldo and renin confirm this Dx. > >>> > >>> If you have not read my article on the evolution of PA please do > >>> so-and take to your Dr. I would be happy to work with him in your > >>> care but most Drs don't seem to be interested. Which blows my mind. > >>> > >>> Any family Hx of HTN and/or low K? > >>> > >>> If spiro works for BP and K and your are DASHing to the max that > >>> essentially confirms the Dx. > >>> If the first CT did not show a bump on the adrenal then others will > >>> not likely show anything. > >>> > >>> > >>> Our basic approach here(based on 45 years of experience) is to treat > >>> with medications and DASH and if BP and K are controlled and other > >>> Sx > >>> go away not to do any further D x tests at this stage. > >>> If there is a single bump and Rx fails to get to feeling normal > >>> then > >>> would do AVS to see if the problem is unilateral or bilateral. > >>> > >>> I know folks in MS, in New Orleans and in Birmingham who are > >>> experts in PA. I would recommend you go to someone who has a lot > >>> of > >>> experience in this and has been doing it for some time. > >>> > >>> > >>> > >>> > >>> Clarence Grim BS, MS, MD > >>> > >>> Clinical Professor of Medicine > >>> Medical College of Wisconsin > >>> Senior Consultant to Shared Care Research and Education > >>> Consulting, Inc. > >>> > >>> Specializing in Difficult to control high blood pre ssure. > >>> > >>> > >>> > >>> > >>> > >>> On May 7, 2009, at 1:49 PM, Echols wrote: > >>> > >>>> > >>>> > >>>> > >>>> Dr. Grim, I am an attorney in Mississippi and have just recently > >>>> been diagnosed with PA. My family physician was attempting to treat > >>>> my extremely high bp to no avail and after nearly 3 years fina lly > >>>> told me that he did not have a clue as to what was going on and > >>>> referred me to an internist. The internist specializes in > >>>> hypertension. I really don't know how much the internist > >>>> understands > >>>> about PA but I am glad that he has at least heard of it after I've > >>>> suffered for about 15 or more years with nearly all the symptoms > >>>> listed by others here. The internist ordered a blood workup and my > >>>> aldosterone levels were 3 times the normal amount and my renin was > >>>> undetected. No other tests were run. He did not order a CT scan of > >>>> my adrenals. After being hospitalized, my family physician > >>>> (after I > >>>> pushed for it) ordered a CT scan of my kidneys and renal arteries > >>>> and stated that they looked fine. That was prior to seeing the > >>>> internist. After reading postings in this group, I requested on May > >>>> 5th to have a CT scan performed to look at my adrenal glands. He > >>>> stated that he was not going to do it now, but might in about 2 > >>>> months. > >>>> I told the internist that I am still extremely fatigued, that I > >>>> have > >>>> headaches, my mind is cloudy, having a problem with concentration > >>>> and memory and that I am concerned because it was affecting my work > >>>> (I have been off work for about a month). Internist told me that he > >>>> believed that I was just depressed and prescribed lexapro. He > >>>> stated > >>>> that I should be excited because my blood pressure was coming down. > >>>> I told him that I was excited but that I did not think that I was > >>>> depressed to the point of needing medication. I am thinking of > >>>> either going to the University of Birmingham to see a nephrologist > >>>> and/or endo. Is this a good idea? Is UAB a good place to go for > >>>> hyperaldosterinism? If not, can you refer a place near MS? I need > >>>> to > >>>> make sure that I have this condition ( I have all the symptoms and > >>>> the spiro-75mg- is helping my bp) and if so, how I can cure or best > >>>> treat it. The internist stated that he did not know what caused it > >>>> and that he did not believe that I had a tumor. I am grateful that > >>>> he looked into hyperaldosteronism but I think the internist is more > >>>> concentrated on the bp, since that is his specialty. I am concerned > >>>> not only about the bp, but also the mental aspects of this > >>>> condition > >>>> because it emy livelihood. Please respond. > >>>> > >>>> --- > >>>> --- > >>>> ---------------------------------------------------------- > >>>> *From:* Clarence Grim <lowerbp2mac (DOT) com> > >>>> *To:* hyperaldosteronism > >>>> *Sent:* Thursday, May 7, 2009 1:32:35 AM > >>>> *Subject:* Re: [hyperaldosteronism ] Renewing Conn's journey > >>>> > >>>> Dont recall your previous story. Do we need to update your story? > >>>> > >>>> > >>>> CE Grim MD > >>>> On May 6, 2009, at 6:05 PM, hdrewe wrote: > >>>> > >>>>> I have not been in contact with this site for a few weeks, > >>>>> however, > >>>>> am now back on track. I visited Dr Nikwan at Greenslopes Hospital, > >>>>> and am going ahead with the workups prior to maybe having surgery. > >>>>> He was certainly surprised to see me after 9 years. > >>>>> > >>>>> My Aldosterone/ Renin assays wer e:- > >>>>> Aldosterone (upright) 1923 (pmol/L) (100 - 950) > >>>>> Renin (upright) 14 (mU/L) (3.3 - 41) > >>>>> Aldosterone/ Renin Ratio 137 > >>>>> > >>>>> These results were while on 25mg Spironolactone. > >>>>> > >>>>> I have been taken off Spiro and put on Verapamil SR 240mg/day, > >>>>> which I began this morning. > >>>>> I am to have CT scan of adrenal gland to see what has happened > >>>>> after all this time. > >>>>> Will revisit Dr Nikwan in 8 weeks. > >>>>> Helen D > >>>> > >>>> > >>>> > >>> > >>> > >>> > >> > >> > >> > > > > > > > > ------------------------------------ > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 14, 2009 Report Share Posted May 14, 2009 I have also had similar experiences with Spiro - both good and bad. It most certainly reduced my blood pressure to normal levels at 50mg 2x daily, but had side effects as well as do all medications. For instance, Spiro not only blocks aldosterone in males, but it blocks testosterone as well. For example, I believe that if Sigmund Freud were to have been on Spiro he would have never reached acclaim over his theories on libido! My Endo switched me to Inspra yesterday and is going to start taking me off of the other medications that he believes are useless - based on the confirmed findings of bi-lateral hyperaldosteronism. Unfortunately, this should be treated with medications rather than removal of an adrenal gland as primary hyperaldosteronism would be. Incidentally, if anyone is curious I received an invoice for my AVS yesterday, which fortunately is being paid by Blue Cross. The total for the performance of this procedure at the University of Michigan was $13,222! > >>>>> >>>>> I have not been in contact with this site for a few weeks,> >>>>> however,> >>>>> am now back on track. I visited Dr Nikwan at Greenslopes Hospital,> >>>>> and am going ahead with the workups prior to maybe having surgery.> >>>>> He was certainly surprised to see me after 9 years.> >>>>>> >>>>> My Aldosterone/ Renin assays wer e:-> >>>>> Aldosterone (upright) 1923 (pmol/L) (100 - 950)> >>>>> Renin (upright) 14 (mU/L) (3.3 - 41)> >>>>> Aldosterone/ Renin Ratio 137> >>>>>> >>>>> These results were while on 25mg Spironolactone.> >>>>>> >>>>> I have been taken off Spiro and put on Verapamil SR 240mg/day,> >>>>> which I began this morning.> >>>>> I am to have CT scan of adrenal gland to see what has happened> >>>>> after all this time.> >>>>> Will revisit Dr Nikwan in 8 weeks.> >>>>> Helen D> >>>>> >>>>> >>>>> >>>> >>>> >>>> >>> >>> >>> >> >> >> > ------------ --------- --------- ------> >> > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 14, 2009 Report Share Posted May 14, 2009 This depends on the sodium intake of the mother as well as I recall.CE Grim MDOn May 14, 2009, at 1:55 AM, Helen Drewe wrote:Human milk has per cup 125mg K and 41.8 mg sodium. ( Nutrition Data)Cows milk has per cup 349 K and 97.6 Sodium. (Nutrition Data)I can see the reasoning why cows milk is too concentrated for the human system. After both my surgeries, all I lived on was warm milk as I could not tolerate anything else. Same as when I am feeling unwell. Maybe this ties in with craving for sodium? The very thing I shouldnt have with PA On Thu, May 14, 2009 at 12:28 PM, Clarence Grim <lowerbp2mac> wrote:Recall that cow milk contains nearly 10 the sodium concentration of human milk.  This is the reason that cow milk based infant feeding vs human milk sodium content increase BP in infants and this high blood pressure persists at least until the teens. CE Grim MDOn May 12, 2009, at 4:40 AM, Helen Drewe wrote:Val, I absolutely avoid sodium like the plague. The only sodium I have is naturally occurring sodium in meat, milk and Yoghurt,etc. I eat lots of high K veges and fruit. Take my own foods wherever I go. Dont trust restaurants etc. Have had too many headaches in early days of diagnosis. I dont eat any breads etc. eat oats, millet etc for carbs. Have been eating this way for nearly 9 years. Since starting Dash, have increased dairy (milk and yoghurt) and making sure I eat enough protein. I could quite happily just live on fruit. I have wondered for a while whether eating such a low sodium diet creates the very thing I am trying to avoid as the body tries even harder to retain sodium, thereby pushing out even more aldosterone.On Tue, May 12, 2009 at 3:00 PM, Valarie  <val@...> wrote:Helen, the only way I made it through six weeks off spiro was to absolutely avoid sodium.  We traveled to Mayo Clinic so I could take my own food along.  When I got a urinary sodium test there, the sodium was too low to measure.  Very low sodium diet will increase your renin and make the ARR invalid. Val From: hyperaldosteronism  [mailto:hyperaldosteronism ] On Behalf Of Helen DreweIf I Dash to max, I put on weight because I am small build. I eat natural high K foods as nature intended. When I put on weight and begin to feel bloated, it affects my breathing and I get more chest pain. So I dash at 1200- 1600 calories, sticking to the guidelines in the the books - "The Dash Diet for Hypertension", "The Dash Diet Action Plan", and "Eat to Beat High Blood Pressure" which features the Dash-Plus Plan.On Mon, May 11, 2009 at 10:49 PM, Clarence Grim <lowerbp2mac> wrote: DASH to the max. CE GrimMD On May 10, 2009, at 10:36 PM, Helen Drewe wrote:  I understand Carol, I have only been off spiro since Friday, and feel dreadful. Headaches, flushing, bloating, slight tremors, brain fog.......Dont know if it may be reaction from Verapamil. My sister told me she cant take calcium channel blockers, as she also had headaches and flushing. What do you do? I dont want to back out of having the AVS this time.HelenOn Mon, May 11, 2009 at 3:08 PM, Carol Christie <carolchgil.au> wrote: I should add that I was going to have a second AVS done at Greenslopes. However, after about 3 weeks without spiro I felt so terrible I decided to take it again. Dr Stowasser still recommends a dose of only 25mg, but I feel better on 50mg.CarolClarence Grim wrote:>>> Tell us all meds u> Are taking.>> Tiped sad Send form mi> iPhone ;-)>> May your pressure be low!>> CE Grim MD> Specializing in Difficult> Hypertension>> On May 10, 2009, at 10:48 PM, Carol Christie <carolchgil.au > <mailto:carolch%40gil.com.au>> wrote:>> > I, too identify strongly with dealing with mental changes.> > I thought my personal papers filing was only a few months behind. I> > started sorting yesterday and found it had been a year since I had> > filed/sorted things out.> > I used to be meticulous in recording payments due/made etc. My> > organisational skills have deteriorated badly.> > Carol> >> >> > Isa Hackett wrote:> >>> >>> >> -> >>> >> I can identify with your challenges RE mental sharpness. It seems,> >> especially within the past six or so months, that my language> >> (vocabulary) is suffering. I also find myself making silly mistakes.> >> It makes things very hard with work. I often have to be "on" - and I> >> am very aware that I am not.> >>> >> I've also recently been diagnosed - actually, I still have the> >> salt-loading test yet to confirm. I believe my father had PA and will> >> likely be tested for GRA. From what I have read, there is an> >> increased> >> risk of early stroke. My father began having small strokes in his> >> 40's> >> and died of a massive stroke in his early 5o's.> >>> >> Anyway, I encourage you to read as much as possible about GRA.> >>> >> DR Grim -are you aware of any differences in symptoms or treatment -> >> or> >> follow-up for those with GRA?> >>> >> , you should know that there are lots of understanding, helpf ul> >> and experienced people on this board -welcome.> >>> >> Wishing you better health!> >>> >> > >>> >> Sent via BlackBerry from T-Mobile> >>> >> ---> >> ----------------------------------------------------------> >> *From*: Echols> >> *Date*: Sun, 10 May 2009 19:17:24 -0700 (PDT)> >> *To*: <hyperaldosteronism  > <mailto:hyperaldosteronism%40>>> >> *Subject*: Re: Renewing Conn's journey> >> I plan to check my history and talk with my dad (it may take me a> >> little time though). I think I posted my story but I'll check my past> >> posts.> >>> >> ---> >> ----------------------------------------------------------> >> *From:* Clarence Grim <lowerbp2mac <mailto:lowerbp2%40mac.com>>> >> *To:* hyperaldosteronism  > <mailto:hyperaldosteronism%40>> >> *Sent:* Sunday, May 10, 2009 1:34:25 AM> >> *Subject:* Re: Renewing Conn's journey> >>> >> If you father had PA can you give us his story as well (check with> >> him> >> first of course).> >>> >>> >> If he has clearly been diagnosed then it is likely that you and he> >> have the same thing (assuming your have a Dx of PA that is clear as> >> well). You likely have GRA which is an autosomal dominate genetic> >> cause of PA in which 1/2 of all your first degree relatives will have> >> it as well (on the average).> >>> >> Recommend you find out as much as you can about your FH of HTN, low> >> K,> >> causes and age of death as far back as you can go.> >>> >> I am looking for the Dr. in ville and should get back with you> >> soon.> >>> >> Have you given us you complete story yet. I may have missed it as> >> have been at the Am Soc of HTN meeting for last week. Lots of things> >> to report to the group.> >>> >>> >> On May 9, 2009, at 10:18 PM, Echols wrote:> >>> >>>> >>>> >>>> >>> D oc, I am closer to than I am Birmingham. To answer the> >>> family history question, my father was diagnosed with PA in 2007 but> >>> he stated that no CT was ran. It appears that the spiro is lowering> >>> my bp.> >>> As far as my CT scan, would a scan of my renal arteries and kidneys> >>> reveal a bump? I am still suffering extreme fatigue and muscle> >>> weakness and tingling in my extremities, headaches, mental confusion> >>> and cloudiness (harde to concentrate) , memory loss, language> >>> difficulty. I also have intermittent pain in the region of my coccyx> >>> bone. Further, when I am surprised, or see something that causes me> >>> to cringe, I feel a tingling sensation in my lower back that flows> >>> down toward my rear pelvic region.> >>> Doc, I agree with your comment as to other physicians do not appear> >>> to want to work with others to assist in the care of their patients.> >>> I don't know if it is pride or the fact that the concern of> >>> keeping a> >>> patient overrides the overall health of the & nbsp;patient. I have> >>> the> >>> same concerns in the legal profession. I have heard attorneys say> >>> that "you can't help people". The statement broke my heart. Last I> >>> checked, there were three (3) noble professions: Doctors, lawyers> >>> and> >>> ministers. We provide a service. Don't misunderstand me, doc, this> >>> is my livelihood and I am not apologizing for the salaries in our> >>> respective professions. I pprovide a service and plan to receive> >>> compensation for those services. My concerned is that we need to> >>> keep> >>> in my that we are providing "people" with those services.> >>> I am not a complainer. I have been told that I am kind of stoic in> >>> nature. However, in my profession, I cannot afford to lose my mental> >>> edge or acuity. My job depends on it and I am on a quest to feel> >>> better. Thanks for responding.> >>> If the best doctors are in Birmingham, I will go there but if you> >>> know someone in , that is closer. Thanks, Doc.> >>>> >>> ---> >>> ---> >>> ----------------------------------------------------------> >>> *From:* Clarence Grim <lowerbp2mac (DOT) com>> >>> *To:* hyperaldosteronism> >>> *Sent:* Friday, May 8, 2009 10:39:57 AM> >>> *Subject:* Re: [hyperaldosteronism ] Renewing Conn's journey> >>>> >>> As you can see from our group's stories we need to increase the> >>> knowledge base or every one who sees pts with high blood pressure.> >>> HTN + low K = PA.> >>>> >>> At some point we would like to have your complete story as well if> >>> you have time.> >>>> >>>> >>>> >>> Your aldo and renin confirm this Dx.> >>>> >>> If you have not read my article on the evolution of PA please do> >>> so-and take to your Dr. I would be happy to work with him in your> >>> care but most Drs don't seem to be interested. Which blows my mind.> >>>> >>> Any family Hx of HTN and/or low K?> >>>> >>> If spiro works for BP and K and your are DASHing to the max that> >>> essentially confirms the Dx.> >>> If the first CT did not show a bump on the adrenal then others will> >>> not likely show anything.> >>>> >>>> >>> Our basic approach here(based on 45 years of experience) is to treat> >>> with medications and DASH and if BP and K are controlled and other> >>> Sx> >>> go away not to do any further D x tests at this stage.> >>> If there is a single bump and Rx fails to get to feeling normal> >>> then> >>> would do AVS to see if the problem is unilateral or bilateral.> >>>> >>> I know folks in MS, in New Orleans and in Birmingham who are> >>> experts in PA. I would recommend you go to someone who has a lot> >>> of> >>> experience in this and has been doing it for some time.> >>>> >>>> >>>> >>>> >>> Clarence Grim BS, MS, MD> >>>> >>> Clinical Professor of Medicine> >>> Medical College of Wisconsin> >>> Senior Consultant to Shared Care Research and Education> >>> Consulting, Inc.> >>>> >>> Specializing in Difficult to control high blood pre ssure.> >>>> >>>> >>>> >>>> >>>> >>> On May 7, 2009, at 1:49 PM, Echols wrote:> >>>> >>>>> >>>>> >>>>> >>>> Dr. Grim, I am an attorney in Mississippi and have just recently> >>>> been diagnosed with PA. My family physician was attempting to treat> >>>> my extremely high bp to no avail and after nearly 3 years fina lly> >>>> told me that he did not have a clue as to what was going on and> >>>> referred me to an internist. The internist specializes in> >>>> hypertension. I really don't know how much the internist> >>>> understands> >>>> about PA but I am glad that he has at least heard of it after I've> >>>> suffered for about 15 or more years with nearly all the symptoms> >>>> listed by others here. The internist ordered a blood workup and my> >>>> aldosterone levels were 3 times the normal amount and my renin was> >>>> undetected. No other tests were run. He did not order a CT scan of> >>>> my adrenals. After being hospitalized, my family physician> >>>> (after I> >>>> pushed for it) ordered a CT scan of my kidneys and renal arteries> >>>> and stated that they looked fine. That was prior to seeing the> >>>> internist. After reading postings in this group, I requested on May> >>>> 5th to have a CT scan performed to look at my adrenal glands. He> >>>> stated that he was not going to do it now, but might in about 2> >>>> months.> >>>> I told the internist that I am still extremely fatigued, that I> >>>> have> >>>> headaches, my mind is cloudy, having a problem with concentration> >>>> and memory and that I am concerned because it was affecting my work> >>>> (I have been off work for about a month). Internist told me that he> >>>> believed that I was just depressed and prescribed lexapro. He> >>>> stated> >>>> that I should be excited because my blood pressure was coming down.> >>>> I told him that I was excited but that I did not think that I was> >>>> depressed to the point of needing medication. I am thinking of> >>>> either going to the University of Birmingham to see a nephrologist> >>>> and/or endo. Is this a good idea? Is UAB a good place to go for> >>>> hyperaldosterinism? If not, can you refer a place near MS? I need> >>>> to> >>>> make sure that I have this condition ( I have all the symptoms and> >>>> the spiro-75mg- is helping my bp) and if so, how I can cure or best> >>>> treat it. The internist stated that he did not know what caused it> >>>> and that he did not believe that I had a tumor. I am grateful that> >>>> he looked into hyperaldosteronism but I think the internist is more> >>>> concentrated on the bp, since that is his specialty. I am concerned> >>>> not only about the bp, but also the mental aspects of this> >>>> condition> >>>> because it emy livelihood. Please respond.> >>>>> >>>> ---> >>>> ---> >>>> ----------------------------------------------------------> >>>> *From:* Clarence Grim <lowerbp2mac (DOT) com>> >>>> *To:* hyperaldosteronism> >>>> *Sent:* Thursday, May 7, 2009 1:32:35 AM> >>>> *Subject:* Re: [hyperaldosteronism ] Renewing Conn's journey> >>>>> >>>> Dont recall your previous story. Do we need to update your story?> >>>>> >>>>> >>>> CE Grim MD> >>>> On May 6, 2009, at 6:05 PM, hdrewe wrote:> >>>>> >>>>> I have not been in contact with this site for a few weeks,> >>>>> however,> >>>>> am now back on track. I visited Dr Nikwan at Greenslopes Hospital,> >>>>> and am going ahead with the workups prior to maybe having surgery.> >>>>> He was certainly surprised to see me after 9 years.> >>>>>> >>>>> My Aldosterone/ Renin assays wer e:-> >>>>> Aldosterone (upright) 1923 (pmol/L) (100 - 950)> >>>>> Renin (upright) 14 (mU/L) (3.3 - 41)> >>>>> Aldosterone/ Renin Ratio 137> >>>>>> >>>>> These results were while on 25mg Spironolactone.> >>>>>> >>>>> I have been taken off Spiro and put on Verapamil SR 240mg/day,> >>>>> which I began this morning.> >>>>> I am to have CT scan of adrenal gland to see what has happened> >>>>> after all this time.> >>>>> Will revisit Dr Nikwan in 8 weeks.> >>>>> Helen D> >>>>> >>>>> >>>>> >>>> >>>> >>>> >>> >>> >>> >> >> >> > ------------------------------------> >> > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 14, 2009 Report Share Posted May 14, 2009 Thanks for the note. As you will note in my article I discuss why most meds dont work in PA. Most MDs have not read this article. DASHing will clearly improve your BP and lower you need for meds. Excess aldo no salt = no high blood pressure. Excess aldo excess salt = high blood pressure. Do you have any 24 hr urine Na, K and aldo results? Lets see now $13,000 would pay for lots of eplerenone. Good thing you did not have to pay. Was this just the radiology bill or did it also include the aldo and cortisol testing of the blood drawn? Another reason we recommend vigorous attempt at BP control with it before going to AVS. Clarence E. Grim, BS, MS, MD On Thursday, May 14, 2009, at 07:12AM, " Debartolo " <pdebartolo@...> wrote: >I have also had similar experiences with Spiro - both good and bad. It most certainly reduced my blood pressure to normal levels at 50mg 2x daily, but had side effects as well as do all medications. For instance, Spiro not only blocks aldosterone in males, but it blocks testosterone as well. For example, I believe that if Sigmund Freud were to have been on Spiro he would have never reached acclaim over his theories on libido! My Endo switched me to Inspra yesterday and is going to start taking me off of the other medications that he believes are useless - based on the confirmed findings of bi-lateral hyperaldosteronism. Unfortunately, this should be treated with medications rather than removal of an adrenal gland as primary hyperaldosteronism would be. Incidentally, if anyone is curious I received an invoice for my AVS yesterday, which fortunately is being paid by Blue Cross. The total for the performance of this procedure at the University of Michigan > was $13,222! > > >> >>>> >> >>>>> I have not been in contact with this site for a few weeks, >> >>>>> however, >> >>>>> am now back on track. I visited Dr Nikwan at Greenslopes Hospital, >> >>>>> and am going ahead with the workups prior to maybe having surgery. >> >>>>> He was certainly surprised to see me after 9 years. >> >>>>> >> >>>>> My Aldosterone/ Renin assays wer e:- >> >>>>> Aldosterone (upright) 1923 (pmol/L) (100 - 950) >> >>>>> Renin (upright) 14 (mU/L) (3.3 - 41) >> >>>>> Aldosterone/ Renin Ratio 137 >> >>>>> >> >>>>> These results were while on 25mg Spironolactone. >> >>>>> >> >>>>> I have been taken off Spiro and put on Verapamil SR 240mg/day, >> >>>>> which I began this morning. >> >>>>> I am to have CT scan of adrenal gland to see what has happened >> >>>>> after all this time. >> >>>>> Will revisit Dr Nikwan in 8 weeks. >> >>>>> Helen D >> >>>> >> >>>> >> >>>> >> >>> >> >>> >> >>> >> >> >> >> >> >> >> > >> > >> > >> > ------------ --------- --------- ------ >> > >> > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 14, 2009 Report Share Posted May 14, 2009 Dash is next...Invoice included what appears to be everything. Twelve charges each for Lab-Cortisol Serum and Lab-Aldosterone Serum! I have not read your article, but would be most interested. Is it on the site? > >> >>>> > >> >>>>> I have not been in contact > with this site for a few weeks, > >> >>>>> however, > >> >>>>> am now back on track. I > visited Dr Nikwan at Greenslopes Hospital, > >> >>>>> and am going ahead with the > workups prior to maybe having surgery. > >> >>>>> He was certainly surprised to > see me after 9 years. > >> >>>>> > >> >>>>> My Aldosterone/ Renin assays > wer e:- > >> >>>>> Aldosterone (upright) 1923 > (pmol/L) (100 - 950) > >> >>>>> Renin (upright) 14 (mU/L) > (3.3 - 41) > >> >>>>> Aldosterone/ Renin Ratio 137 > >> >>>>> > >> >>>>> These results were while on > 25mg Spironolactone. > >> >>>>> > >> >>>>> I have been taken off Spiro > and put on Verapamil SR 240mg/day, > >> >>>>> which I began this morning. > >> >>>>> I am to have CT scan of > adrenal gland to see what has happened > >> >>>>> after all this time. > >> >>>>> Will revisit Dr Nikwan in 8 > weeks. > >> >>>>> Helen D > >> >>>> > >> >>>> > >> >>>> > >> >>> > >> >>> > >> >>> > >> >> > >> >> > >> >> > >> > > >> > > >> > > >> > ------------ --------- --------- ------ > >> > > >> > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 14, 2009 Report Share Posted May 14, 2009 Yes Evolution of PA in our files. Clarence E. Grim, BS, MS, MD On Thursday, May 14, 2009, at 12:32PM, " Debartolo " <pdebartolo@...> wrote: > >Dash is next...Invoice included what appears to be everything. Twelve charges each for Lab-Cortisol Serum and Lab-Aldosterone Serum! I have not read your article, but would be most interested. Is it on the site? > > >> >> >>>> >> >> >>>>> I have not been in contact >> with this site for a few weeks, >> >> >>>>> however, >> >> >>>>> am now back on track. I >> visited Dr Nikwan at Greenslopes Hospital, >> >> >>>>> and am going ahead with the >> workups prior to maybe having surgery. >> >> >>>>> He was certainly surprised to >> see me after 9 years. >> >> >>>>> >> >> >>>>> My Aldosterone/ Renin assays >> wer e:- >> >> >>>>> Aldosterone (upright) 1923 >> (pmol/L) (100 - 950) >> >> >>>>> Renin (upright) 14 (mU/L) >> (3.3 - 41) >> >> >>>>> Aldosterone/ Renin Ratio 137 >> >> >>>>> >> >> >>>>> These results were while on >> 25mg Spironolactone. >> >> >>>>> >> >> >>>>> I have been taken off Spiro >> and put on Verapamil SR 240mg/day, >> >> >>>>> which I began this morning. >> >> >>>>> I am to have CT scan of >> adrenal gland to see what has happened >> >> >>>>> after all this time. >> >> >>>>> Will revisit Dr Nikwan in 8 >> weeks. >> >> >>>>> Helen D >> >> >>>> >> >> >>>> >> >> >>>> >> >> >>> >> >> >>> >> >> >>> >> >> >> >> >> >> >> >> >> >> >> > >> >> > >> >> > >> >> > ------------ --------- --------- ------ >> >> > >> >> > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 14, 2009 Report Share Posted May 14, 2009 I am on 100 mg and used to be on 150 mg. Val From: hyperaldosteronism [mailto:hyperaldosteronism ] On Behalf Of megra0409 Hi All, After reading Carol’s email on Monday I decided to increase my Spiro to 50mg too (my Dr here in Australia also does not want me on anymore than 25mg), and I have to say that I am definitely feeling improved. In fact, this is the best I have felt in a while. I am back to see the Dr on Wednesday so unless there is some dire reason as to why I can’t stay on this dosage, I will be advocating maintaining this dosage from this point on. I have recorded some elevated pulse increases, but other than that, everything seems OK. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 14, 2009 Report Share Posted May 14, 2009 I take 100 mg twice per day, total of 200 mg per day. In the US it's acceptible to go up to 400 mg daily for PA. a Hi All, After reading Carol’s email on Monday I decided to increase my Spiro to 50mg too (my Dr here in Australia also does not want me on anymore than 25mg), and I have to say that I am definitely feeling  improved. In fact, this is the best I have felt in a while. I am back to see the Dr on Wednesday so unless there is some dire reason as to why I can’t stay on this dosage, I will be advocating maintaining this dosage from this point on. I have recorded some elevated pulse increases, but other than that, everything seems OK.  Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 15, 2009 Report Share Posted May 15, 2009 Please take him your BPs and pulses and ask for you Ks so you can plot them as well.  You might want to rint ou the endocrine societies guidelines and ask him to look up recent articles on drug resistant HTN by Dr. Calhoun.  I trust you have already taken him my evolution article.CEOn May 14, 2009, at 6:05 AM, megra0409 wrote:Hi All,After reading Carol’s email on Monday I decided to increase my Spiro to 50mg too (my Dr here in Australia also does not want me on anymore than 25mg), and I have to say that I am definitely feeling  improved. In fact, this is the best I have felt in a while. I am back to see the Dr on Wednesday so unless there is some dire reason as to why I can’t stay on this dosage, I will be advocating maintaining this dosage from this point on.I have recorded some elevated pulse increases, but other than that, everything seems OK. From: hyperaldosteronism [mailto:hyperaldosteronism ] On Behalf Of Carol ChristieSent: Monday, 11 May 2009 3:08 PMTo: hyperaldosteronism Subject: Re: Renewing Conn's journey I should add that I was going to have a second AVS done at Greenslopes. However, after about 3 weeks without spiro I felt so terrible I decided to take it again. Dr Stowasser still recommends a dose of only 25mg, but I feel better on 50mg.CarolClarence Grim wrote:>>> Tell us all meds u> Are taking.>> Tiped sad Send form mi> iPhone ;-)>> May your pressure be low!>> CE Grim MD> Specializing in Difficult> Hypertension>> On May 10, 2009, at 10:48 PM, Carol Christie <carolchgil.au > <mailto:carolch%40gil.com.au>> wrote:>> > I, too identify strongly with dealing with mental changes.> > I thought my personal papers filing was only a few months behind. I> > started sorting yesterday and found it had been a year since I had> > filed/sorted things out.> > I used to be meticulous in recording payments due/made etc. My> > organisational skills have deteriorated badly.> > Carol> >> >> > Isa Hackett wrote:> >>> >>> >> -> >>> >> I can identify with your challenges RE mental sharpness. It seems,> >> especially within the past six or so months, that my language> >> (vocabulary) is suffering. I also find myself making silly mistakes.> >> It makes things very hard with work. I often have to be "on" - and I> >> am very aware that I am not.> >>> >> I've also recently been diagnosed - actually, I still have the> >> salt-loading test yet to confirm. I believe my father had PA and will> >> likely be tested for GRA. From what I have read, there is an> >> increased> >> risk of early stroke. My father began having small strokes in his> >> 40's> >> and died of a massive stroke in his early 5o's.> >>> >> Anyway, I encourage you to read as much as possible about GRA.> >>> >> DR Grim -are you aware of any differences in symptoms or treatment -> >> or> >> follow-up for those with GRA?> >>> >> , you should know that there are lots of understanding, helpf ul> >> and experienced people on this board -welcome.> >>> >> Wishing you better health!> >>> >> > >>> >> Sent via BlackBerry from T-Mobile> >>> >> ---> >> ----------------------------------------------------------> >> *From*: Echols> >> *Date*: Sun, 10 May 2009 19:17:24 -0700 (PDT)> >> *To*: <hyperaldosteronism  > <mailto:hyperaldosteronism%40>>> >> *Subject*: Re: Renewing Conn's journey> >> I plan to check my history and talk with my dad (it may take me a> >> little time though). I think I posted my story but I'll check my past> >> posts.> >>> >> ---> >> ----------------------------------------------------------> >> *From:* Clarence Grim <lowerbp2mac <mailto:lowerbp2%40mac.com>>> >> *To:* hyperaldosteronism  > <mailto:hyperaldosteronism%40>> >> *Sent:* Sunday, May 10, 2009 1:34:25 AM> >> *Subject:* Re: Renewing Conn's journey> >>> >> If you father had PA can you give us his story as well (check with> >> him> >> first of course).> >>> >>> >> If he has clearly been diagnosed then it is likely that you and he> >> have the same thing (assuming your have a Dx of PA that is clear as> >> well). You likely have GRA which is an autosomal dominate genetic> >> cause of PA in which 1/2 of all your first degree relatives will have> >> it as well (on the average).> >>> >> Recommend you find out as much as you can about your FH of HTN, low> >> K,> >> causes and age of death as far back as you can go.> >>> >> I am looking for the Dr. in ville and should get back with you> >> soon.> >>> >> Have you given us you complete story yet. I may have missed it as> >> have been at the Am Soc of HTN meeting for last week. Lots of things> >> to report to the group.> >>> >>> >> On May 9, 2009, at 10:18 PM, Echols wrote:> >>> >>>> >>>> >>>> >>> D oc, I am closer to than I am Birmingham. To answer the> >>> family history question, my father was diagnosed with PA in 2007 but> >>> he stated that no CT was ran. It appears that the spiro is lowering> >>> my bp.> >>> As far as my CT scan, would a scan of my renal arteries and kidneys> >>> reveal a bump? I am still suffering extreme fatigue and muscle> >>> weakness and tingling in my extremities, headaches, mental confusion> >>> and cloudiness (harde to concentrate) , memory loss, language> >>> difficulty. I also have intermittent pain in the region of my coccyx> >>> bone. Further, when I am surprised, or see something that causes me> >>> to cringe, I feel a tingling sensation in my lower back that flows> >>> down toward my rear pelvic region.> >>> Doc, I agree with your comment as to other physicians do not appear> >>> to want to work with others to assist in the care of their patients.> >>> I don't know if it is pride or the fact that the concern of> >>> keeping a> >>> patient overrides the overall health of the & nbsp;patient. I have> >>> the> >>> same concerns in the legal profession. I have heard attorneys say> >>> that "you can't help people". The statement broke my heart. Last I> >>> checked, there were three (3) noble professions: Doctors, lawyers> >>> and> >>> ministers. We provide a service. Don't misunderstand me, doc, this> >>> is my livelihood and I am not apologizing for the salaries in our> >>> respective professions. I pprovide a service and plan to receive> >>> compensation for those services. My concerned is that we need to> >>> keep> >>> in my that we are providing "people" with those services.> >>> I am not a complainer. I have been told that I am kind of stoic in> >>> nature. However, in my profession, I cannot afford to lose my mental> >>> edge or acuity. My job depends on it and I am on a quest to feel> >>> better. Thanks for responding.> >>> If the best doctors are in Birmingham, I will go there but if you> >>> know someone in , that is closer. Thanks, Doc.> >>>> >>> ---> >>> ---> >>> ----------------------------------------------------------> >>> *From:* Clarence Grim <lowerbp2mac (DOT) com>> >>> *To:* hyperaldosteronism> >>> *Sent:* Friday, May 8, 2009 10:39:57 AM> >>> *Subject:* Re: [hyperaldosteronism ] Renewing Conn's journey> >>>> >>> As you can see from our group's stories we need to increase the> >>> knowledge base or every one who sees pts with high blood pressure.> >>> HTN + low K = PA.> >>>> >>> At some point we would like to have your complete story as well if> >>> you have time.> >>>> >>>> >>>> >>> Your aldo and renin confirm this Dx.> >>>> >>> If you have not read my article on the evolution of PA please do> >>> so-and take to your Dr. I would be happy to work with him in your> >>> care but most Drs don't seem to be interested. Which blows my mind.> >>>> >>> Any family Hx of HTN and/or low K?> >>>> >>> If spiro works for BP and K and your are DASHing to the max that> >>> essentially confirms the Dx.> >>> If the first CT did not show a bump on the adrenal then others will> >>> not likely show anything.> >>>> >>>> >>> Our basic approach here(based on 45 years of experience) is to treat> >>> with medications and DASH and if BP and K are controlled and other> >>> Sx> >>> go away not to do any further D x tests at this stage.> >>> If there is a single bump and Rx fails to get to feeling normal> >>> then> >>> would do AVS to see if the problem is unilateral or bilateral.> >>>> >>> I know folks in MS, in New Orleans and in Birmingham who are> >>> experts in PA. I would recommend you go to someone who has a lot> >>> of> >>> experience in this and has been doing it for some time.> >>>> >>>> >>>> >>>> >>> Clarence Grim BS, MS, MD> >>>> >>> Clinical Professor of Medicine> >>> Medical College of Wisconsin> >>> Senior Consultant to Shared Care Research and Education> >>> Consulting, Inc.> >>>> >>> Specializing in Difficult to control high blood pre ssure.> >>>> >>>> >>>> >>>> >>>> >>> On May 7, 2009, at 1:49 PM, Echols wrote:> >>>> >>>>> >>>>> >>>>> >>>> Dr. Grim, I am an attorney in Mississippi and have just recently> >>>> been diagnosed with PA. My family physician was attempting to treat> >>>> my extremely high bp to no avail and after nearly 3 years fina lly> >>>> told me that he did not have a clue as to what was going on and> >>>> referred me to an internist. The internist specializes in> >>>> hypertension. I really don't know how much the internist> >>>> understands> >>>> about PA but I am glad that he has at least heard of it after I've> >>>> suffered for about 15 or more years with nearly all the symptoms> >>>> listed by others here. The internist ordered a blood workup and my> >>>> aldosterone levels were 3 times the normal amount and my renin was> >>>> undetected. No other tests were run. He did not order a CT scan of> >>>> my adrenals. After being hospitalized, my family physician> >>>> (after I> >>>> pushed for it) ordered a CT scan of my kidneys and renal arteries> >>>> and stated that they looked fine. That was prior to seeing the> >>>> internist. After reading postings in this group, I requested on May> >>>> 5th to have a CT scan performed to look at my adrenal glands. He> >>>> stated that he was not going to do it now, but might in about 2> >>>> months.> >>>> I told the internist that I am still extremely fatigued, that I> >>>> have> >>>> headaches, my mind is cloudy, having a problem with concentration> >>>> and memory and that I am concerned because it was affecting my work> >>>> (I have been off work for about a month). Internist told me that he> >>>> believed that I was just depressed and prescribed lexapro. He> >>>> stated> >>>> that I should be excited because my blood pressure was coming down.> >>>> I told him that I was excited but that I did not think that I was> >>>> depressed to the point of needing medication. I am thinking of> >>>> either going to the University of Birmingham to see a nephrologist> >>>> and/or endo. Is this a good idea? Is UAB a good place to go for> >>>> hyperaldosterinism? If not, can you refer a place near MS? I need> >>>> to> >>>> make sure that I have this condition ( I have all the symptoms and> >>>> the spiro-75mg- is helping my bp) and if so, how I can cure or best> >>>> treat it. The internist stated that he did not know what caused it> >>>> and that he did not believe that I had a tumor. I am grateful that> >>>> he looked into hyperaldosteronism but I think the internist is more> >>>> concentrated on the bp, since that is his specialty. I am concerned> >>>> not only about the bp, but also the mental aspects of this> >>>> condition> >>>> because it emy livelihood. Please respond.> >>>>> >>>> ---> >>>> ---> >>>> ----------------------------------------------------------> >>>> *From:* Clarence Grim <lowerbp2mac (DOT) com>> >>>> *To:* hyperaldosteronism> >>>> *Sent:* Thursday, May 7, 2009 1:32:35 AM> >>>> *Subject:* Re: [hyperaldosteronism ] Renewing Conn's journey> >>>>> >>>> Dont recall your previous story. Do we need to update your story?> >>>>> >>>>> >>>> CE Grim MD> >>>> On May 6, 2009, at 6:05 PM, hdrewe wrote:> >>>>> >>>>> I have not been in contact with this site for a few weeks,> >>>>> however,> >>>>> am now back on track. I visited Dr Nikwan at Greenslopes Hospital,> >>>>> and am going ahead with the workups prior to maybe having surgery.> >>>>> He was certainly surprised to see me after 9 years.> >>>>>> >>>>> My Aldosterone/ Renin assays wer e:-> >>>>> Aldosterone (upright) 1923 (pmol/L) (100 - 950)> >>>>> Renin (upright) 14 (mU/L) (3.3 - 41)> >>>>> Aldosterone/ Renin Ratio 137> >>>>>> >>>>> These results were while on 25mg Spironolactone.> >>>>>> >>>>> I have been taken off Spiro and put on Verapamil SR 240mg/day,> >>>>> which I began this morning.> >>>>> I am to have CT scan of adrenal gland to see what has happened> >>>>> after all this time.> >>>>> Will revisit Dr Nikwan in 8 weeks.> >>>>> Helen D> >>>>> >>>>> >>>>> >>>> >>>> >>>> >>> >>> >>> >> >> >> > ------------------------------------> >> > Quote Link to comment Share on other sites More sharing options...
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