Guest guest Posted April 19, 2000 Report Share Posted April 19, 2000 In a message dated 4/19/00 12:20:45 AM, lizabethreintjes@... writes: << Hello! I am a junior at the University of Notre Dame and I am studying in Washington DC this semester. I am actually working at Congressman Walter B. , Jr.'s office as an intern. I initially got interested in the topic of anthrax through his office and since have chosen to write two of my research papers for Notre Dame on this issue. I am also in Navy ROTC and so this issue will affect me in a year and half if these bills are not passed through Congress. My question is " Why hasn't anything been done with the bills? " Has anything happened with them since their introduction. Where are they on the agenda. This issue really scares me because I don't think after all the research I have done that I could possibly allow someone to give me these shots. What should I do? Any advice over what I can do? Or should I just hold out and hope something happens with these bills? >> These bills have not yet been brought to a vote because I believe there are not yet enough votes to pass them. That is why it is important for us all to contact our representatives in congress and inform them of the truth. Many have been swayed so far. Many more still to go... Blackburn Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 20, 2000 Report Share Posted April 20, 2000 In a message dated 4/19/00 4:20:38 AM !!!First Boot!!!, lizabethreintjes@... writes: << What should I do? Any advice over what I can do? Or should I just hold out and hope something happens with these bills? >> I personally wouldn't count on those bills being passed. The government moves very, very slowly, and I wouldn't expect them to move any faster on any of these bills, or other legislation, unless us, at the grass roots level, can generate enough huge popular support for the bills to pass as soon as Congress decides to vote on them. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 17, 2009 Report Share Posted March 17, 2009 Do you have any medical writing or database experience? Can you send me a resume. Several are interested. Clarence E. Grim, BS, MS, MD On Tuesday, March 17, 2009, at 09:19AM, " a Hall " <shahall@...> wrote: > >I'll gladly do anything I'm able to help with this. > >a > > > >Clarence Grim wrote: >> >> To all. I believe we now have enough folks with a similar story that >> we can think about publishing a paper on the anxiety symptoms and >> signs of primary aldosteronism. >> >> Any one interested in being a coauthor? >> >> On Mar 16, 2009, at 10:07 AM, callie.nelle wrote: >> >> > I am new to this group, and I am grateful that you are here. >> > >> > I was diagnosed with primary hyperaldosteronism on February 9 after >> > about six trips to the emergency room with heart attack-like >> > symptoms (sharp pain in the chest, irregular heart beat, high BP, >> > nausea, tingling in the hands). This happened over about 18 months >> > time during the highest period of stress of my lifetime. They never >> > found anything except low potassium and high BP. After the first >> > trip, they sent me to a cardiologist who put me on BP meds that >> > depleted potassium and gave me xanax for what he diagnosed as panic >> > attacks. The episodes just got worse. Finally, I got a primary care >> > physician who sent me to a nephrologist who diagnosed primary >> > aldosteronism. My aldosterone was 46.8 and my renin 0.57 (upright). >> > Then I was sent to an endo who did a CT scan and found nodules on >> > both adrenals. Since the first of December I have been on 40 meq K >> > and 25 mg amlodipine for BP. Some time I feel like myself, and >> > sometime I feel pretty bad. >> > >> > Today I am supposed to begin taking 25 mg spiro, reduce my K to >> > 10meq and continue the 25 mg amlodipine. To tell the truth, I am >> > pretty nervous about stopping the K. >> > >> > I have always been healthy before this--even had LOW BP for many >> > years and no primary care doctor. Now, sometimes I feel like I have >> > lost my life. The hardest part is the exhaustion and not being able >> > to do what I need to do and want to do. Also, the feeling that my >> > body is out of control is pretty scary. >> > >> > Thanks for listening. >> > >> > Callie >> > >> > >> > >> >> Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 17, 2009 Report Share Posted March 17, 2009 I too am happy to assist with this effort in any way I can. Regards From: hyperaldosteronism [mailto:hyperaldosteronism ] On Behalf Of a Hall Sent: Wednesday, 18 March 2009 1:20 AM hyperaldosteronism Subject: paper I'll gladly do anything I'm able to help with this. a Clarence Grim wrote: > > To all. I believe we now have enough folks with a similar story that > we can think about publishing a paper on the anxiety symptoms and > signs of primary aldosteronism. > > Any one interested in being a coauthor? > > On Mar 16, 2009, at 10:07 AM, callie.nelle wrote: > > > I am new to this group, and I am grateful that you are here. > > > > I was diagnosed with primary hyperaldosteronism on February 9 after > > about six trips to the emergency room with heart attack-like > > symptoms (sharp pain in the chest, irregular heart beat, high BP, > > nausea, tingling in the hands). This happened over about 18 months > > time during the highest period of stress of my lifetime. They never > > found anything except low potassium and high BP. After the first > > trip, they sent me to a cardiologist who put me on BP meds that > > depleted potassium and gave me xanax for what he diagnosed as panic > > attacks. The episodes just got worse. Finally, I got a primary care > > physician who sent me to a nephrologist who diagnosed primary > > aldosteronism. My aldosterone was 46.8 and my renin 0.57 (upright). > > Then I was sent to an endo who did a CT scan and found nodules on > > both adrenals. Since the first of December I have been on 40 meq K > > and 25 mg amlodipine for BP. Some time I feel like myself, and > > sometime I feel pretty bad. > > > > Today I am supposed to begin taking 25 mg spiro, reduce my K to > > 10meq and continue the 25 mg amlodipine. To tell the truth, I am > > pretty nervous about stopping the K. > > > > I have always been healthy before this--even had LOW BP for many > > years and no primary care doctor. Now, sometimes I feel like I have > > lost my life. The hardest part is the exhaustion and not being able > > to do what I need to do and want to do. Also, the feeling that my > > body is out of control is pretty scary. > > > > Thanks for listening. > > > > Callie > > > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 17, 2009 Report Share Posted March 17, 2009 thanks Do you have any experience doing mdoingscience writing or data base or data analysis? Can you send me your resume we have several who are interested and we may want to do another Group to work on the paper and data. CE Grim MD On Mar 17, 2009, at 7:44 PM, megra0409 wrote: > I too am happy to assist with this effort in any way I can. > > Regards > > > > From: hyperaldosteronism > [mailto:hyperaldosteronism ] On Behalf Of a Hall > Sent: Wednesday, 18 March 2009 1:20 AM > hyperaldosteronism > Subject: paper > > I'll gladly do anything I'm able to help with this. > > a > > Clarence Grim wrote: > > > > To all. I believe we now have enough folks with a similar story that > > we can think about publishing a paper on the anxiety symptoms and > > signs of primary aldosteronism. > > > > Any one interested in being a coauthor? > > > > On Mar 16, 2009, at 10:07 AM, callie.nelle wrote: > > > > > I am new to this group, and I am grateful that you are here. > > > > > > I was diagnosed with primary hyperaldosteronism on February 9 > after > > > about six trips to the emergency room with heart attack-like > > > symptoms (sharp pain in the chest, irregular heart beat, high BP, > > > nausea, tingling in the hands). This happened over about 18 months > > > time during the highest period of stress of my lifetime. They > never > > > found anything except low potassium and high BP. After the first > > > trip, they sent me to a cardiologist who put me on BP meds that > > > depleted potassium and gave me xanax for what he diagnosed as > panic > > > attacks. The episodes just got worse. Finally, I got a primary > care > > > physician who sent me to a nephrologist who diagnosed primary > > > aldosteronism. My aldosterone was 46.8 and my renin 0.57 > (upright). > > > Then I was sent to an endo who did a CT scan and found nodules on > > > both adrenals. Since the first of December I have been on 40 meq K > > > and 25 mg amlodipine for BP. Some time I feel like myself, and > > > sometime I feel pretty bad. > > > > > > Today I am supposed to begin taking 25 mg spiro, reduce my K to > > > 10meq and continue the 25 mg amlodipine. To tell the truth, I am > > > pretty nervous about stopping the K. > > > > > > I have always been healthy before this--even had LOW BP for many > > > years and no primary care doctor. Now, sometimes I feel like I > have > > > lost my life. The hardest part is the exhaustion and not being > able > > > to do what I need to do and want to do. Also, the feeling that my > > > body is out of control is pretty scary. > > > > > > Thanks for listening. > > > > > > Callie > > > > > > > > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 14, 2010 Report Share Posted May 14, 2010 This is best way to go , to use information from the Doctor's site . I will greatly appreciate it if somebody will come up with the link P L E A S E !!! viva Quote Link to comment Share on other sites More sharing options...
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