Guest guest Posted December 30, 2006 Report Share Posted December 30, 2006 Jeff, I had my adrenalectomy on November 3rd and I am noticing a lot of changes as well. I have tons of energy, no more naps, very calm, no brain fog, memory is better, pains are less, hair is growing faster and is healthier, no more late day eye blurriness, hands do not shake anymore, and I could probably list a few other positive notes. I actually have excitement about life where prior to surgery, I was planning on my death because I felt so horrible. I had made all my funeral arrangements, got a living will and power of attorney because I knew I would not live much longer. I feel so blessed. I also am not sure how much of the bad I felt before was due to 11 pills a day for BP alone (and still didn't phase my HT). My lipids are better, my catechols are normal now, and at last check, even my elevated 5-HIAAs were normal (not sure about that one but I'll have it rechecked later). All my blood levels are normal now (CBC, K, liver and kidney functions.....all normal). So yes, I tend to agree with you that a whole lot of my problems were due to the elevated aldo and I also believe taking a lot of meds doesn't help with our chemistry. I am looking forward to losing some weight and getting active again. peace out, Debi in Knoxville Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 30, 2006 Report Share Posted December 30, 2006 In a message dated 12/30/06 1:36:48 PM, moonium@... writes: So yes, I tend to agree with you that a whole lot of my problems were due to the elevated aldo and I also believe taking a lot of meds doesn't help with our chemistry. I am looking forward to losing some weight and getting active again. peace out, Debi in Knoxville Your story is one classical for PA and a good response. One reason I have spent my life looking for this is pts with difficult HTN. May your pressure be low! Clarence E. Grim, B.S., M.S., M.D. Specializing in Difficult to Control High Blood Pressure and the Physiology and History of Survival During Hard Times and Heart Disease today. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 30, 2006 Report Share Posted December 30, 2006 In a message dated 12/30/06 12:21:57 PM, datawrhsdoc@... writes: 1) Symptoms of Metabolic Syndrome / Insulin Cycle - No longer have periods of hypoglycemia. Fasting blood sugar is no longer pre-diabetic. Also, my lipid profile is much improved but needs some work. Low K impairs insulin release 2) Sleep apnea - I no longer appear to have it. Without CPAP, according to my wife, I no longer have sleep-disordered breathing. I'll be getting a sleep study to confirm, but I'm pretty sure this is fully resolved. This would be a great report. Suggest a repeat sleep study after 6 months or so. Keep good records and we will write it up. 3) Anxiety/rages - The intense anxiety and rages from nowhere have disappeared. I have been able to discontinue psychiatric medications prescribed to deal with this. Few have reported this but the data has never been gathered systematically in this area. 4) Lethargy - Tons of energy. I'm actually interested in working out at the gym. All the other above items resolved before I went back to the gym. Classical problem in low K and correction by ADX. Anybody else have a similar experience or have something to add? -Jeff May your pressure be low! Clarence E. Grim, B.S., M.S., M.D. Specializing in Difficult to Control High Blood Pressure and the Physiology and History of Survival During Hard Times and Heart Disease today. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 30, 2006 Report Share Posted December 30, 2006 Debi, Yep, brain fog gone for me as well. Also, I'm not sure if this is temporary, but the chronic cystic acne on my chest and back has cleared up post-surgery. I suspect it's related to change in lipid chemistry. I was commenting to my daughter today that I've been feeling grand (even with a sinus infection -- LOL) since coming home from the hospital on 12/12. Prior to the surgery, I can't remember feeling this good for maybe a day or two at a time. It's rather nice to look forward to the future with excitement rather than dread what's going to go wrong with my body next! I bet you feel the same. Happiest of New Years, Jeff > > Jeff, I had my adrenalectomy on November 3rd and I am noticing a lot of > changes as well. > .... > Debi in Knoxville > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 30, 2006 Report Share Posted December 30, 2006 Your recovery sounds like a miracle to me. I have alot of similar problems, and I am taking 75mg Inspra twice a day to control my blood pressure, but no relief from the other symptoms. 1) I still have Metabolic Syndrome / Insulin Resistance for which I am loosing weight. I am 5'6" and was 196 pounds and am now 173 pounds, but I want to get to 145 pounds to get to my ideal weight. Loosing weight for me is a struggle with lots of hunger feelings, and an up and down process - loose a few pounds, gain a few back, loose a few more pounds etc. 2) I have Sleep Apnea, and I thought loosing weight is the only possible solution. I did not know it had anything to do with hyperaldosteronism. 3) I definitely have anxiety, rage, depression and more. I am taking a psychiatric mediation called Cymbalta 30 mg (duloxetine) but it does not help., and I cannot get off of it. 4) Lethargy - I am always tired and have to take multiple naps each day. I have a hard time getting things done, because I am so tired that I just put them off. I definitely have NO ENERGY at all, and I have to force myself to take walks to exercise. How did you reverse your hyperaldosteronism problem? Did you get a tumor removed? Are you taking any medication? Did you loose weight? Did you use a CPAP machine for sleep apnea? Please explain your situation in more detail. ________________________________________________ Hyperaldosteronism and Secondary Health Impacts Seems to me that there are many more symptoms of hyperaldosteronismthan appear to be documented clearly in the literature. While curingthe aldo problem is not a cure all (I'm haven't instantly gainedathletic conditioning), in addition to the hypertension I've noticedseveral other major health issues rapidly disappear:1) Symptoms of Metabolic Syndrome / Insulin Cycle - No longer haveperiods of hypoglycemia. Fasting blood sugar is no longerpre-diabetic. Also, my lipid profile is much improved but needs somework.2) Sleep apnea - I no longer appear to have it. Without CPAP,according to my wife, I no longer have sleep-disordered breathing.I'll be getting a sleep study to confirm, but I'm pretty sure this isfully resolved.3) Anxiety/rages - The intense anxiety and rages from nowhere havedisappeared. I have been able to discontinue psychiatric medicationsprescribed to deal with this.4) Lethargy - Tons of energy. I'm actually interested in working outat the gym. All the other above items resolved before I went back tothe gym.Anybody else have a similar experience or have something to add?-Jeff Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 31, 2006 Report Share Posted December 31, 2006 I would like someone to collect these sleep apnea stories in a file and update it as they come in. I think we are on to something here. May your pressure be low! Clarence E. Grim, B.S., M.S., M.D. Specializing in Difficult to Control High Blood Pressure and the Physiology and History of Survival During Hard Times and Heart Disease today. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 31, 2006 Report Share Posted December 31, 2006 Again another thread we need to be gathering data on with an anxiety stories file. May your pressure be low! Clarence E. Grim, B.S., M.S., M.D. Specializing in Difficult to Control High Blood Pressure and the Physiology and History of Survival During Hard Times and Heart Disease today. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 31, 2006 Report Share Posted December 31, 2006 In a message dated 12/31/06 11:02:18 AM, shotzie@... writes: > > . He commented that my airway was > clear except for continued tissue swelling that was probably edema from > the PA. Interestingly, I've haven't been able to breath through my > right nostril for years...at least until after the adrenalectomy. > > WOW!! For years I had swelling of the soft palate and around the back of my throat, also frequent swelling of my left nostril without any cold or allergy symptoms. Haven't had that since surgery either. Very interesting. We need a detailed Shotzie before and after story. I lost an extra chin without weight loss, I regained cheekbones I haven't seen in years, I have a jawline again. And the frequent headaches that were attributed to my menstrual cycle haven't occured since the Oct 25th surgery either. In my experience this is a classic response to ADX when all things work well. Headaches stop in most cases. Again we need to build a database to document this today. You also mentioned the acne..I had acne like bumps occuring sporatically on my shoulders, chest , buttocks and thighs. Never developed into pustules, didn't respond to any topical therapy offered. Would remain for a month or more than slowly fade away only to develop in a different area. Also all gone with the surgery, old spots fading out, no new ones developed. It is just amazing how many symptoms are fading away post op and how many we all seem to have shared. May your pressure be low! Clarence E. Grim, B.S., M.S., M.D. Specializing in Difficult to Control High Blood Pressure and the Physiology and History of Survival During Hard Times and Heart Disease today. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 31, 2006 Report Share Posted December 31, 2006 > > 3) Anxiety/rages - The intense anxiety and rages from nowhere have > > disappeared. I have been able to discontinue psychiatric medications > > prescribed to deal with this. > > > Few have reported this but the data has never been gathered systematically in > this area. > There seems to be a common theme on the discussion group in this area. While controlled data is rather sparse, below are a couple of recent citations that suggest a link between aldosterone and anxiety: 1. Psychother Psychosom. 2006;75(5):327-30 Psychological aspects of primary aldosteronism. ....Seven patients (2 with aldosterone-producing adenoma and 5 with idiopathic hyperaldosteronism) received both DSM-IV and DCPR diagnoses, while 3 had neither. As to DSM-IV, generalized anxiety disorder was detected in 6 cases (in 1 it was associated with panic disorder and in 1 with major depression) and obsessive-compulsive disorder in 1. The most frequent DCPR cluster was demoralization (5 cases), while persistent somatization occurred in 2 cases (associated with demoralization in 1) and irritable mood in 1. ... http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve & db=PubMed & list_uids=1\ 6899970 & dopt=Abstract 2. Neuroendocrinology. 2001 Apr;73(4):261-71 Glucocorticoid and mineralocorticoid receptors are involved in the facilitation of anxiety-like response induced by restraint. Calvo N, Volosin M. Departamento de Farmacologia, Facultad de Ciencias Quimicas, Universidad Nacional de Cordoba, Ciudad Universitaria, Cordoba, Argentina. In previous studies, we have shown that male Wistar rats exposed to a single inescapable stressor session (15 min restraint) exhibited 24 h later an anxiogenic-like behavior in the elevated plus-maze (EPM), which was reversed by inhibition of corticosterone (CS) synthesis with metyrapone (75 mg/kg i.p.) 3 h before stress. Since CS binds to two central corticosteroid receptors, the mineralocorticoid (MR) and the glucocorticoid (GR) receptors, involvement of MR and GR in the modulation of anxiogenic responses was assessed in the EPM. Administration of the GR agonist dexamethasone (Dex, 1.25 microg/kg s.c.) to metyrapone-pretreated rats 1 h before restraint restored the anxiogenic-like response induced by the stressor. Removal of the adrenals also inhibited the anxiogenic-like effect, which was restored by either Dex (1.25 microg/kg s.c.), the MR agonist deoxycorticosterone (0.8 mg/kg s.c.) or CS, the common endogenous agonist of MR and GR (5 mg/kg s.c.) administered 1 h before stress. ... [To clarify this - a MR agonist means it is like aldosterone. " Anxiogenic-like effect " means anxiety inducing. So, part of the abstract is saying, in effect, aldosterone induces anxiety when we are in stressful situations involving being trapped.] http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve & db=PubMed & list_uids=1\ 1340340 & dopt=Abstract -Jeff Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 31, 2006 Report Share Posted December 31, 2006 >> Your recovery sounds like a miracle to me. I have alot of similar> problems, and I am taking 75mg Inspra twice a day to control my blood> pressure, but no relief from the other symptoms. It feels like a miracle to me as well. I am wondering if it not a miracle at all but rather under-reported. These changes, other than the HTN, are all post-surgical. I had a 1.2 cm APA on my left adrenal which was removed laporoscopically on 12/11/06. Prior to the adrenalectomy, I was taking Spirinolactone. > Loosing weight for me is a struggle with lots of hunger feelings, and an up and down > process - loose a few pounds, gain a few back, loose a few more pounds etc. The lethargy, brain fog and hypoglycemia made weight loss very difficult for me. In fact, my pattern was lose a few pounds and gain back a few more. After a while, I stopped trying as the end result was weight gain rather than weight loss. I don't believe that I'm in that pattern any longer.> I have Sleep Apnea, and I thought loosing weight is the only possible> solution. Several comments on this. I was diagnosed with HTN and sleep apnea within a couple of months of each other. Prior to the PA diagnosis, the theory was that the sleep apnea was causing the HTN since there was a small reduction in HTN and lethargy after I started CPAP therapy.Since being diagnosed with sleep apnea about 4 years ago, I have used CPAP nightly. In fact, my breathing was so disrupted that I would have difficulty falling asleep without CPAP. Using the CPAP was like a lullaby. I went from 210 to 190 about 3 years ago, but there was no let up in the apnea. About 1 year ago, I had sinus and soft palate surgery to eliminate or reduce the apnea. Not only was the surgery ineffective (actually, my pressure had to be increased), the recovery was hellishly painful. I began the spiro about 1 month before my adrenalectomy. The apnea continued but may have reduced somewhat while I was on spiro as I began to find the CPAP a bit uncomfortable. The day after returning home from adrenalectomy, I could no longer tolerate the CPAP and my sleep breathing no longer appears disordered. I'm not even snoring. > I definitely have anxiety, rage, depression and more. I am taking a> psychiatric mediation called Cymbalta 30 mg (duloxetine) but it does> not help., and I cannot get off of it. My drug of choice for anxiety, rage, and depression was also Cymbalta, but at 60mg. I tried to reduce to 30mg before, but the anxiety and rages came back. Last week, I reduced to 30mg, and am no longer taking the Cymbalta. I feel fine and am behaving no differently than when I was on the Cymbalta...perhaps a bit less zombiefied is all.As an aside, I've heard that getting off Cymbalta is a living hell for some. I'm sorry you are having such trouble with it.> Lethargy - I am always> tired and have to take multiple naps each day. I have a hard time> getting things done, because I am so tired that I just put them off. I> definitely have NO ENERGY at all, and I have to force myself to take> walks to exercise. Been there for sure and continued to feel like this on Spiro...perhaps a bit worse, but I had GI side effects which were probably making the lethargy worse. The lethargy is no longer an issue, even before I adjusted my Cymbalta. That said, when I was initially taking the Cymbalta, the lethargy and tiredness became MUCH worse.> Are you taking any medication? Yes, I'm taking an antibiotic for the sinus infection which I think I picked up from the AutoPAP at the hospital. I have ceased taking all HTN meds and Cymbalta.> Did you loose weight? I'm 5'9" and went from 219lb to 209 without even trying. This was probably the extra fluid from the PA. I will lose addtl weight and am targeting 185.> Did you use a CPAP machine for sleep apnea? Yep. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 31, 2006 Report Share Posted December 31, 2006 I forgot to mention one thing. My ENT was of the belief that my sleep apnea might go away post-adrenalectomy. He commented that my airway was clear except for continued tissue swelling that was probably edema from the PA. Interestingly, I've haven't been able to breath through my right nostril for years...at least until after the adrenalectomy.> > I have Sleep Apnea, and I thought loosing weight is the only possible> > solution.> > Several comments on this. I was diagnosed with HTN and sleep apnea> within a couple of months of each other. Prior to the PA diagnosis, the> theory was that the sleep apnea was causing the HTN since there was a> small reduction in HTN and lethargy after I started CPAP therapy.> > Since being diagnosed with sleep apnea about 4 years ago, I have used> CPAP nightly. In fact, my breathing was so disrupted that I would have> difficulty falling asleep without CPAP. Using the CPAP was like a> lullaby. I went from 210 to 190 about 3 years ago, but there was no let> up in the apnea.> > About 1 year ago, I had sinus and soft palate surgery to eliminate or> reduce the apnea. Not only was the surgery ineffective (actually, my> pressure had to be increased), the recovery was hellishly painful.> > I began the spiro about 1 month before my adrenalectomy. The apnea> continued but may have reduced somewhat while I was on spiro as I began> to find the CPAP a bit uncomfortable. The day after returning home from> adrenalectomy, I could no longer tolerate the CPAP and my sleep> breathing no longer appears disordered. I'm not even snoring.> Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 31, 2006 Report Share Posted December 31, 2006 > > . He commented that my airway was > clear except for continued tissue swelling that was probably edema from > the PA. Interestingly, I've haven't been able to breath through my > right nostril for years...at least until after the adrenalectomy. > > WOW!! For years I had swelling of the soft palate and around the back of my throat, also frequent swelling of my left nostril without any cold or allergy symptoms. Haven't had that since surgery either. I lost an extra chin without weight loss, I regained cheekbones I haven't seen in years, I have a jawline again. And the frequent headaches that were attributed to my menstrual cycle haven't occured since the Oct 25th surgery either. You also mentioned the acne..I had acne like bumps occuring sporatically on my shoulders, chest , buttocks and thighs. Never developed into pustules, didn't respond to any topical therapy offered. Would remain for a month or more than slowly fade away only to develop in a different area. Also all gone with the surgery, old spots fading out, no new ones developed. It is just amazing how many symptoms are fading away post op and how many we all seem to have shared. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 2, 2007 Report Share Posted January 2, 2007 > > > > > > . He commented that my airway was > > > clear except for continued tissue swelling that was probably edema > > from > > > the PA. Interestingly, I've haven't been able to breath through my > > > right nostril for years...at least until after the adrenalectomy. > > > > > > > > > > WOW!! For years I had swelling of the soft palate and around the > > back of my throat, also frequent swelling of my left nostril without > > any cold or allergy symptoms. Haven't had that since surgery either. > Very interesting. We need a detailed Shotzie before and after story. I had so many puzzling multi-system symptoms the past few years it is difficult to write a comprehensive story. So many misdiagnoses were made to explain away what was happening to me. I had over 50 doctor appointments between my PCP and specialist referrals in both 2005 and 2006. Not one of them ever suspected PA, I found the nephrologist who finally obtained the correct testing and diagnosis. It took him only 4 weeks to do so with proper testing, then he made sure the endo he referred me to was familiar with Conn's. I went from working 4 per diem jobs that I enjoyed to not being able to work at all over three year period. I loved to travel and I loved to drive. It was nothing to take a 12 hour trip, I transported both my kids to and from colleges, hauling and helping move in and out of dorms and apartments. Gradually I couldn't tolerate any trip at all, the 1 hour trip to Syracuse to see my doctors was torture. I kept adding new symptoms, my allergic response kept increasing, I had headaches almost daily which became debilitating around menstuation. Overwhelming fatigue, menstrual difficulties,sleep difficulties, brain fog, blurred vision, hypoglycemic spells, nausea, crippling muscle pain and spasms, dry eyes, dry mouth, increased dental decay. I had always looked many years younger than my age but suddenly I aged before my own eyes, my skin looked puffy and pasty, my eyes dull. The worse part was that the docs kept telling me " you look Great! " Fortunately a few of my close friends were more truthful and supported me in my effort to obtain proper treatment. Slowly symptoms are diminishing or disappearing. I was like Debi on this board, before surgery I was ready to die and knew I wouldn't make it much longer without some totally disabling event like a heart attack or stroke. I have read in several articles that it can take 3-6 months post op for the body to totally adjust. I do keep a daily record of BP readings and any symptoms occuring that day. So far little is noted for symptoms whereas pre op I didn't have room in the space for the day to write all the symptoms I was experiencing that day. I find it interesting that others who have had the surgery seem to have experienced many of the same symptoms which are now disappearing post op. I did ask my endo about the swelling and the breakouts but he had never heard of it. He said little is written about what happens post op. The main thing is the potassium normalizes and the BP falls, that's all he is concerned about. I did see an integrative physician many years ago who said a body out of balance cannot function. I believe the excess aldosterone for a prolonged period threw my body off so much that every system was affected. I am in the process of rebalancing, rebuilding and recovery now. It is a developing story. > May your pressure be low! > > Clarence E. Grim, B.S., M.S., M.D. > Specializing in Difficult to Control High Blood Pressure > and the Physiology and History of Survival During > Hard Times and Heart Disease today. > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 2, 2007 Report Share Posted January 2, 2007 In a message dated 1/2/07 11:14:49 AM, shotzie@... writes: I did see an integrative physician many years ago who said a body out of balance cannot function. yeo aldo upsets the balance-how did he miss it? May your pressure be low! Clarence E. Grim, B.S., M.S., M.D. Specializing in Difficult to Control High Blood Pressure and the Physiology and History of Survival During Hard Times and Heart Disease today. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 3, 2007 Report Share Posted January 3, 2007 In a message dated 1/2/07 11:14:49 AM, shotzie@... writes: I had so many puzzling multi-system symptoms the past few years it is difficult to write a comprehensive story. So many misdiagnoses were made to explain away what was happening to me. I had over 50 doctor appointments between my PCP and specialist referrals in both 2005 and 2006. Not one of them ever suspected PA, I found the nephrologist who finally obtained the correct testing and diagnosis. The history of misdiagnosis if common and adds to the story. When you have time you can detail the gaunlet you have run to get to PA. Very common. Good lets educate your PCP and team so he wont miss anymore. Please take my article to him on both PA and difficult HTN. You could even ask him to visit our site. May your pressure be low! Clarence E. Grim, B.S., M.S., M.D. Specializing in Difficult to Control High Blood Pressure and the Physiology and History of Survival During Hard Times and Heart Disease today. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 3, 2007 Report Share Posted January 3, 2007 In a message dated 1/3/07 3:03:34 PM, shotzie@... writes: Posted by: "lowerbp2@..." lowerbp2@... lowerbp2 Tue Jan 2, 2007 9:28 pm (PST) In a message dated 1/2/07 11:14:49 AM, shotzie (DOT) com writes: > I did see an integrative physician many years ago who said a body out > of balance cannot function. > >yeo aldo upsets the balance-how did he miss it? >May your pressure be low! He missed it just like all the others missed it, putting me into a category and refusing to consider anything else, I was labeled as chronic fatigue syndrome but still the physician, again like all the others, refused to test any hormone levels except Thyroid and FSH. Surely K was measured with all this other stuff. Nothing better to cause chronic fatigue than low K. Adrenals seem to be a forgotten organ in this area of the country. I did get vitamin, mineral and heavy metal levels done and was switched on to the benefits of Omega 3s. Bet they make a lot measureing heavy metals. Integrative medicine wasn't even called that when I saw this physician, but he did help me the most in teaching me to listen to my body, not block symptoms with meds, eat correctly, use supplements wisely. For many years I was able to clear symptoms by eating a clean diet, avoiding allegy triggers, resting more, doing yoga or whatever to get back to feeling "balanced" but the past few years that all stopped working and this physician also wrote me off as "nuts". Prob needed more nuts as in the DASH diet. Did anyone ever tell you about this diet? The other problem is that the specialists and PCPs refused to communicate with each other, sent little info to each other and refused to look at the entire patient as a whole. When things weren't working they then blamed the patient, either I was non-compliant or depressed or stressed. I have copies of some of my records. What is written and what was really said and done are totally different. I had stated before, my medical records read like a "fairy tale" doing little to convey my actual complaints , condition and treatment. good reason to keep your copies of all your records. Remind them to listen to you listening to your body. I have come in contact with many patients, in both the hospital and in office practice, who have legitimate symptoms but the docs refuse to do anything because they don't know what to do. It is much easier to write the patient off as too time consuming or having a mental problem than to try to think out of the box, do some research and really try to find out what is going on. PA should never be out of the box. They all learned about it in med school. And if they can give you a diagnosis code that allows frequent office visits without question by the HMO (in my case HTN), you are a gravy train for them, guaranteed income, why would you want to stop that? Maybe we need a few lawsuits??? Fortunately I did find a physician more interested in me than the diagnosis codes, I only had one office visit with him yet he was able to obtain the diagnosis and refer for proper treatment. The drive has to be there and unfortunately few docs around here have any left. And my guess is the experience to listen to the patient. Clarence E. Grim, B.S., M.S., M.D. Specializing in Difficult to Control High Blood Pressure and the Physiology and History of Survival During Hard Times and Heart Disease today. ____________ ________ ________ ________ ________ _ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 3, 2007 Report Share Posted January 3, 2007 Posted by: " lowerbp2@... " lowerbp2@... lowerbp2 Tue Jan 2, 2007 9:28 pm (PST) In a message dated 1/2/07 11:14:49 AM, shotzie (DOT) com writes: > I did see an integrative physician many years ago who said a body out > of balance cannot function. > >yeo aldo upsets the balance-how did he miss it? >May your pressure be low! He missed it just like all the others missed it, putting me into a category and refusing to consider anything else, I was labeled as chronic fatigue syndrome but still the physician, again like all the others, refused to test any hormone levels except Thyroid and FSH. Adrenals seem to be a forgotten organ in this area of the country. I did get vitamin, mineral and heavy metal levels done and was switched on to the benefits of Omega 3s. Integrative medicine wasn't even called that when I saw this physician, but he did help me the most in teaching me to listen to my body, not block symptoms with meds, eat correctly, use supplements wisely. For many years I was able to clear symptoms by eating a clean diet, avoiding allegy triggers, resting more, doing yoga or whatever to get back to feeling " balanced " but the past few years that all stopped working and this physician also wrote me off as " nuts " . The other problem is that the specialists and PCPs refused to communicate with each other, sent little info to each other and refused to look at the entire patient as a whole. When things weren't working they then blamed the patient, either I was non-compliant or depressed or stressed. I have copies of some of my records. What is written and what was really said and done are totally different. I had stated before, my medical records read like a " fairy tale " doing little to convey my actual complaints , condition and treatment. I have come in contact with many patients, in both the hospital and in office practice, who have legitimate symptoms but the docs refuse to do anything because they don't know what to do. It is much easier to write the patient off as too time consuming or having a mental problem than to try to think out of the box, do some research and really try to find out what is going on. And if they can give you a diagnosis code that allows frequent office visits without question by the HMO (in my case HTN), you are a gravy train for them, guaranteed income, why would you want to stop that? Fortunately I did find a physician more interested in me than the diagnosis codes, I only had one office visit with him yet he was able to obtain the diagnosis and refer for proper treatment. The drive has to be there and unfortunately few docs around here have any left. Clarence E. Grim, B.S., M.S., M.D. Specializing in Difficult to Control High Blood Pressure and the Physiology and History of Survival During Hard Times and Heart Disease today. __________________________________________________ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 3, 2007 Report Share Posted January 3, 2007 In my case, my -former- internist did listen. Unfortunatley, he didn't know what he was doing and apparently didn't bother to look up testing protocols. For example, about 4 years ago, he " tested " for PA by ordering an aldo and low specifity renin. Of course, there was no way to do an ARR because the renin came back as '<2'. He didn't bother to pursue. Since I 'clearly' didn't have PA, he treated each problem indepently. The result was run-away HTN, numerous ER visits, hospital stays, and specialist of the month. The best part of this was the white matter lesions in my brain (aka brain damage) from silent ischemic attacks and vascular damage...the gift that keeps on giving. The last straw was when I spent a week in the hospital with wires hooked up to my head. Although I liked him personally, the best healthcare decision i've ever made was to fire him. > The drive has to be there and > unfortunately few docs around here have any left. > > > > > Clarence E. Grim, B.S., M.S., M.D. > Specializing in Difficult to Control High Blood > Pressure > and the Physiology and History of Survival During > Hard Times and Heart Disease today. > > > > __________________________________________________ > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 8, 2007 Report Share Posted January 8, 2007 , after almost seven years struggling to get a correct Dx and Tx, I learned along the way that isolated nutrients (vitamins, and especially minerals) stimulate the adrenals in ways decidedly unhelpful to PA pts. In fact, people with too much aldo may create or exacerbate alkalosis when using most supplements. This can include terrible kidney stone problems - as if all the other ones weren't enough. This finally culminated in adoption of the DASH diet per 's little paperback, and lowering sodium to minimize my need for aldactone (which for men can cause hormone problems). I lowered my need for meds by 2/3 (to keep BP below 120.80) with DASH, and got WAY more nutrients from simply limiting myself to whole foods. Exercise and sleep rounded out the approach, and I feel amazingly well these days. Sigh, Dave On Jan 3, 2007, at 12:51 PM, shotzie wrote: > Posted by: " lowerbp2@... " lowerbp2@... > lowerbp2 > Tue Jan 2, 2007 9:28 pm (PST) > > In a message dated 1/2/07 11:14:49 AM, shotzie (DOT) > com writes: > > > I did see an integrative physician many years ago > who said a body out > > of balance cannot function. > > > > >yeo aldo upsets the balance-how did he miss it? > > >May your pressure be low! > > He missed it just like all the others missed it, > putting me into a category and refusing to consider > anything else, I was labeled as chronic fatigue > syndrome but still the physician, again like all the > others, refused to test any hormone levels except > Thyroid and FSH. > Adrenals seem to be a forgotten organ in this area of > the country. I did get vitamin, mineral and heavy > metal levels done and was switched on to the benefits > of Omega 3s. > > Integrative medicine wasn't even called that when I > saw this physician, but he did help me the most in > teaching me to listen to my body, not block symptoms > with meds, eat correctly, use supplements wisely. > For many years I was able to clear symptoms by eating > a clean diet, avoiding allegy triggers, resting more, > doing yoga or whatever to get back to feeling > " balanced " but the past few years that all stopped > working and this physician also wrote me off as > " nuts " . > > The other problem is that the specialists and PCPs > refused to communicate with each other, sent little > info to each other and refused to look at the entire > patient as a whole. When things weren't working they > then blamed the patient, either I was non-compliant or > depressed or stressed. I have copies of some of my > records. What is written and what was really said and > done are totally different. I had stated before, my > medical records read like a " fairy tale " doing little > to convey my actual complaints , condition and > treatment. > > I have come in contact with many patients, in both > the hospital and in office practice, who have > legitimate symptoms but the docs refuse to do anything > because they don't know what to do. It is much easier > to write the patient off as too time consuming or > having a mental problem than to try to think out of > the box, do some research and really try to find out > what is going on. And if they can give you a > diagnosis code that allows frequent office visits > without question by the HMO (in my case HTN), you are > a gravy train for them, guaranteed income, why would > you want to stop that? Fortunately I did find a > physician more interested in me than the diagnosis > codes, I only had one office visit with him yet he was > able to obtain the diagnosis and refer for proper > treatment. The drive has to be there and > unfortunately few docs around here have any left. > > > > Clarence E. Grim, B.S., M.S., M.D. > Specializing in Difficult to Control High Blood > Pressure > and the Physiology and History of Survival During > Hard Times and Heart Disease today. > > __________________________________________________ > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 9, 2007 Report Share Posted January 9, 2007 In a message dated 1/9/07 8:14:49 AM, erich_brueschke@... writes: Dave: Dave wrote: > I learned along the way that isolated nutrients (vitamins, and > especially minerals) stimulate the adrenals in ways decidedly unhelpful > to PA pts. In fact, people with too much aldo may create or exacerbate > alkalosis when using most supplements. Do you have a list of these vitamins, and especially minerals? What about the ones that cause alkalosis? Thanks, h Brueschke DASH dammit. May your pressure be low! Clarence E. Grim, B.S., M.S., M.D. Specializing in Difficult to Control High Blood Pressure and the Physiology and History of Survival During Hard Times and Heart Disease today. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 9, 2007 Report Share Posted January 9, 2007 Dave: Dave wrote: > I learned along the way that isolated nutrients (vitamins, and > especially minerals) stimulate the adrenals in ways decidedly unhelpful > to PA pts. In fact, people with too much aldo may create or exacerbate > alkalosis when using most supplements. Do you have a list of these vitamins, and especially minerals? What about the ones that cause alkalosis? Thanks, h Brueschke > > > Posted by: " lowerbp2@... " lowerbp2@... > > lowerbp2 > > Tue Jan 2, 2007 9:28 pm (PST) > > > > In a message dated 1/2/07 11:14:49 AM, shotzie (DOT) > > com writes: > > > > > I did see an integrative physician many years ago > > who said a body out > > > of balance cannot function. > > > > > > > >yeo aldo upsets the balance-how did he miss it? > > > > >May your pressure be low! > > > > He missed it just like all the others missed it, > > putting me into a category and refusing to consider > > anything else, I was labeled as chronic fatigue > > syndrome but still the physician, again like all the > > others, refused to test any hormone levels except > > Thyroid and FSH. > > Adrenals seem to be a forgotten organ in this area of > > the country. I did get vitamin, mineral and heavy > > metal levels done and was switched on to the benefits > > of Omega 3s. > > > > Integrative medicine wasn't even called that when I > > saw this physician, but he did help me the most in > > teaching me to listen to my body, not block symptoms > > with meds, eat correctly, use supplements wisely. > > For many years I was able to clear symptoms by eating > > a clean diet, avoiding allegy triggers, resting more, > > doing yoga or whatever to get back to feeling > > " balanced " but the past few years that all stopped > > working and this physician also wrote me off as > > " nuts " . > > > > The other problem is that the specialists and PCPs > > refused to communicate with each other, sent little > > info to each other and refused to look at the entire > > patient as a whole. When things weren't working they > > then blamed the patient, either I was non-compliant or > > depressed or stressed. I have copies of some of my > > records. What is written and what was really said and > > done are totally different. I had stated before, my > > medical records read like a " fairy tale " doing little > > to convey my actual complaints , condition and > > treatment. > > > > I have come in contact with many patients, in both > > the hospital and in office practice, who have > > legitimate symptoms but the docs refuse to do anything > > because they don't know what to do. It is much easier > > to write the patient off as too time consuming or > > having a mental problem than to try to think out of > > the box, do some research and really try to find out > > what is going on. And if they can give you a > > diagnosis code that allows frequent office visits > > without question by the HMO (in my case HTN), you are > > a gravy train for them, guaranteed income, why would > > you want to stop that? Fortunately I did find a > > physician more interested in me than the diagnosis > > codes, I only had one office visit with him yet he was > > able to obtain the diagnosis and refer for proper > > treatment. The drive has to be there and > > unfortunately few docs around here have any left. > > > > > > > > Clarence E. Grim, B.S., M.S., M.D. > > Specializing in Difficult to Control High Blood > > Pressure > > and the Physiology and History of Survival During > > Hard Times and Heart Disease today. > > > > __________________________________________________ > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 9, 2007 Report Share Posted January 9, 2007 It seems to vary with individuals, but the calcium forms usual in supplements turn to salt in serum, as do the ascorbic acids. The ascorbate forms of vitamin C are minerals when ingested, but turn into ascorbic acid in serum. Backward-fashion. Alkalosis occurs if the angiotensin system is troubled. As with hyperaldo or Cushings. Or with kidney or liver disease. Reduced ability to eliminate salts or electrolytes. Then, salts can build up and the sweat glands in the skin can take over, in a slower elimination attempt. White powder residue from dried perspiration. Since the skin is part of the embryonic nervous system, those researchers looking at BBNS or calcium metabolism are interested in this with respect to nervous disorders like Parkinsons or panic disorder. Or, if your diet is rich in things like black pepper or rhubarb (oxylate-forming), kidney stones can tend to form with more frequency and severity. I had many of these symptoms prior to DASHing. And aldactone. That's what perked up my interest. I had used supplements. No more. I DASH. There are a few aggregations of study on this at University of AZ, Tucson, and I am going to have to go back and find them again. DR Grim, I am sure is aware of this work. It is an interesting question. Dave On Jan 9, 2007, at 11:04 AM, lowerbp2@... wrote: > > In a message dated 1/9/07 8:14:49 AM, erich_brueschke@... > writes: > > > > Dave: > > Dave wrote: > > I learned along the way that isolated nutrients (vitamins, and > > especially minerals) stimulate the adrenals in ways decidedly > unhelpful > > to PA pts. In fact, people with too much aldo may create or > exacerbate > > alkalosis when using most supplements. > > Do you have a list of these vitamins, and especially minerals? > > What about the ones that cause alkalosis? > > Thanks, > h Brueschke > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 9, 2007 Report Share Posted January 9, 2007 Once again DASH dammit. At least till the other supplements etc prove they are as good as or better than DASH. In a message dated 1/9/07 1:50:37 PM, riothamus20@... writes: It seems to vary with individuals, but the calcium forms usual in supplements turn to salt in serum, as do the ascorbic acids. The ascorbate forms of vitamin C are minerals when ingested, but turn into ascorbic acid in serum. Backward-fashion. Alkalosis occurs if the angiotensin system is troubled. As with hyperaldo or Cushings. Or with kidney or liver disease. Reduced ability to eliminate salts or electrolytes. Then, salts can build up and the sweat glands in the skin can take over, in a slower elimination attempt. White powder residue from dried perspiration. Since the skin is part of the embryonic nervous system, those researchers looking at BBNS or calcium metabolism are interested in this with respect to nervous disorders like Parkinsons or panic disorder. Or, if your diet is rich in things like black pepper or rhubarb (oxylate-forming), kidney stones can tend to form with more frequency and severity. I had many of these symptoms prior to DASHing. And aldactone. That's what perked up my interest. I had used supplements. No more. I DASH. There are a few aggregations of study on this at University of AZ, Tucson, and I am going to have to go back and find them again. DR Grim, I am sure is aware of this work. It is an interesting question. Dave On Jan 9, 2007, at 11:04 AM, lowerbp2@... wrote: > > In a message dated 1/9/07 8:14:49 AM, erich_brueschke@... > writes: > > > > Dave: > > Dave wrote: > > I learned along the way that isolated nutrients (vitamins, and > > especially minerals) stimulate the adrenals in ways decidedly > unhelpful > > to PA pts. In fact, people with too much aldo may create or > exacerbate > > alkalosis when using most supplements. > > Do you have a list of these vitamins, and especially minerals? > > What about the ones that cause alkalosis? > > Thanks, > h Brueschke > May your pressure be low! Clarence E. Grim, B.S., M.S., M.D. Specializing in Difficult to Control High Blood Pressure and the Physiology and History of Survival During Hard Times and Heart Disease today. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 10, 2007 Report Share Posted January 10, 2007 Again did you read this? Exactly my point too. You seem to be seeing the opposites of what I say. Goji juice too. I found nothing but troubles. (I had many of these symptoms prior to DASHing. And aldactone. That's > what perked up my interest. I had used supplements. No more. I > DASH.) Dave On Jan 9, 2007, at 8:28 PM, lowerbp2@... wrote: > Once again DASH dammit. At least till the other supplements etc prove > they are as good as or better than DASH. > > In a message dated 1/9/07 1:50:37 PM, riothamus20@... writes: > > > It seems to vary with individuals, but the calcium forms usual in > supplements turn to salt in serum, as do the ascorbic acids. The > ascorbate forms of vitamin C are minerals when ingested, but turn into > ascorbic acid in serum. Backward-fashion. Alkalosis occurs if the > angiotensin system is troubled. As with hyperaldo or Cushings. Or > with kidney or liver disease. Reduced ability to eliminate salts or > electrolytes. Then, salts can build up and the sweat glands in the > skin can take over, in a slower elimination attempt. White powder > residue from dried perspiration. Since the skin is part of the > embryonic nervous system, those researchers looking at BBNS or calcium > metabolism are interested in this with respect to nervous disorders > like Parkinsons or panic disorder. Or, if your diet is rich in things > like black pepper or rhubarb (oxylate-forming), kidney stones can tend > to form with more frequency and severity. > > I had many of these symptoms prior to DASHing. And aldactone. That's > what perked up my interest. I had used supplements. No more. I > DASH. > > There are a few aggregations of study on this at University of AZ, > Tucson, and I am going to have to go back and find them again. DR > Grim, I am sure is aware of this work. It is an interesting question. > > Dave > > > On Jan 9, 2007, at 11:04 AM, lowerbp2@... wrote: > > > > > In a message dated 1/9/07 8:14:49 AM, erich_brueschke@... > > writes: > > > > > > > > Dave: > > > > Dave wrote: > > > I learned along the way that isolated nutrients (vitamins, and > > > especially minerals) stimulate the adrenals in ways decidedly > > unhelpful > > > to PA pts. In fact, people with too much aldo may create or > > exacerbate > > > alkalosis when using most supplements. > > > > Do you have a list of these vitamins, and especially minerals? > > > > What about the ones that cause alkalosis? > > > > Thanks, > > h Brueschke > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 10, 2007 Report Share Posted January 10, 2007 In a message dated 1/10/07 7:50:59 AM, erich_brueschke@... writes: Dr Grim and Uncle Dave: I am DASHing. But I also take some supplements/ I am DASHing. Bu extending purposes, ie not for BP lowering effects. The best and only good data on life extension (mostly in animals) is by calorie restriction and I have suggested that this works by lowering BP and lipids. Where is the data you have on your supplements? Dave made a vague statement concerning vitamins/supplement Dave m alkalosis producing via the angiotensin system (but which Dr Grim stated is not involved in PA in a previous post) and now Dave states again in a vague way that most calcium forms of these vitamins/supplement vitamins/supplement What I am trying to determine is which of the supplements I take might be doing these things that Dave talks about. I am familiar with the chemistry involved here and I don't see how what Dave states can be true. Even if they form up salt in the serum, if the Na is not from an exogenous source, then I don't see what the problems would be. Suggest all on our site get and read the Black and Elliott Book Hypertension: A companion for Braunwald's Heart Disease. Not cheap but the best I have seen in several years. That was all i was trying to determine. I just thought Dave might have a list. h > > > > I learned along the way that isolated nutrients (vitamins, and > > > > especially minerals) stimulate the adrenals in ways decidedly > > > unhelpful > > > > to PA pts. In fact, people with too much aldo may create or > > > exacerbate > > > > alkalosis when using most supplements. > > > > > > Do you have a list of these vitamins, and especially minerals? > > > > > > What about the ones that cause alkalosis? > > > > > > Thanks, > > > h Brueschke > > > > > > > > > > > > > > > > > May your pressure be low! > > Clarence E. Grim, B.S., M.S., M.D. > Specializing in Difficult to Control High Blood Pressure > and the Physiology and History of Survival During > Hard Times and Heart Disease today. > Messages in this topic (29) Reply (via web post) | Start a new topic Messages | Files | Photos | Links | Database | Polls | Members | Calendar Change settings via the Web ( ID required) Change settings via email: Switch delivery to Daily Digest | Switch format to Traditional Visit Your Group | Terms of Use | Unsubscribe Recent Activity •  1 New Members Visit Your Group Quote Link to comment Share on other sites More sharing options...
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