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Re: NIH/POTS

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hi. I am glad I read ur letter. I was initially diag. with SDS. however

it was changed to POTS and parkinsonism. I am 42 and I jsut set blood to

NIH because they are doing research of some protein with the cells(?) on

patients diag with POTS. SEE NDRF.org or neurocardiogenic syncope. I

spoke to a nurse named Rita Mincemore at NIH. What doctor are u seeing

at NIH?

nancy

Txbriteyes@... wrote:

>

> Harriet,

>

> I have some news you will interesting. I had some autonomic tests

> at the

> National Institute of Health in Bethesda land. The doctor I was

> seen by

> is a very knowledgeable about the autonomic system. He told me in the

>

> beginning of the testing that he would be able to tell what I dont

> have, and

> maybe a little of what I do. Well, to make a long story short.

>

> I dont have Shy-drager syndrome, but one thing he knows for sure I

> have is

> POTS. Postural Orthostatic tachyacardia Syndrome. He asked me if

> anyone told

> me I had Parkinson's, I told him no. I guess he is curious to findout

> if I

> have that. Also he is testing me for another condition that on of the

> symptoms is POTS. I did read where POTS can turn into SHY-DRAGER, but

> I hope

> it doesn't. But I did tell the doctor about you and Anne. He said it

> is

> very rare for anyone to live with SHY-Drager for 11 years. He also

> said they

> sound like they have had a stroke. Thats when I told him about Bills

> wife.

> Wouldn't it be great if you did not have shy-drager but something

> similar

> like I do. He said the reason I was dx'ed with shy-drager was because

> POTs

> was not DX'ed until 2 years ago. It is inherited. and that could be

> what is

> happening to my son . I sure hope not.

>

> This condition mimics shy-drager, it has the same symptoms pretty much

> except

> the slurred speech, more tacycardia and the autonomic system is more

> affected. I am still hanging int here, I can walk or stand that much

> because

> of the fast heart rate and dizziness. They wont get back my blood

> test for 2

> weeks, and I guess they might want to perform some more test. They

> said they

> would call in a few weeks with some type of treatment plan until I get

>

> scheduled for the rest of the tests. I hope you feel better.

>

>

> If you do not wish to belong to shydrager, you may

> unsubscribe by sending a blank email to

>

> shydrager-unsubscribe

>

>

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Guest guest

HI ,

I am seeing Dr. Goldstein. He is a wonderful doctor. I am 43. I was dx'ed with shy-drager 11years ago.. The dx'ed was changed 1 week ago to Pots and possibly Parkinsons. Are you going to be included in the studies.. I will know next week if they want to do more testing. I get my blood work back next week. Where do you live? I live in Fairfax Va , so I am not far from the NIH. What are your symptoms?

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i don't know what pots is.

i'm in potomac

dx p+

i had petscan....sympathetic nerve endings in heart " missing " . i have oh,

but no one will say shy/dr. but i have serious temp control problem, and big

bp ups/downs.

i'm only on sinemet because every drug i try makes me " weak " (nearly pass

out).

nancy spires

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Guest guest

i don't know what pots is.

i'm in potomac

dx p+

i had petscan....sympathetic nerve endings in heart " missing " . i have oh,

but no one will say shy/dr. but i have serious temp control problem, and big

bp ups/downs.

i'm only on sinemet because every drug i try makes me " weak " (nearly pass

out).

nancy spires

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