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Hi

For those lucky enough to have a properly functioning adrenal system

and who don't need either steroids or thyroid hormones and likely

don't have depressive symptoms ...... and don't have a megalomaniac

government wanting to invade your household at the drop of a

hat.....to jam 'drugs' down your throat ~ it must be really pleasant.

In the meantime, I've requested a tertiary referral for someone who

isn't getting better fast, after dropping the citalopram and

quetiapine, preceeded by a whole 'Armada' of prescription psychiatric

meds over an unacceptably protracted number of years.

The paper I posted shows to whom it is approriate to refer....in the

first instance.

best wishes

Bob

> What point are you making there Bob? Sorry didnt really get it!

>

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I do agree you need to be on SSRI's for a while, 6/8 weeks just to see if it works, but I dont believe in stopping and starting and then trying something else too quick, I always give them a good chance, a lot of people stop after the first pill if they get back effects, some docs fail to tell them they need time work. I am lucky enough to know how this works but have found it out myself, although I now see a very good doctor, who is so easy to talk to and we actually have a laugh

Hi ,Age about 40y male.The diagnosis is in doubt.The quetiapine was a bolt on goody that was supposed to compensate for the poor response to citalopram (SSRIs). Polypharmacy ~ if you drop one of the drugs, all the withdrawal symptoms then confound the issue as to whether you had anything wrong in the first place so they then say, ah, a relapse..... ..I accompanied someone to an appointment where citalopram was prescribed and that was the exact line that was taken by another doctor ... you need to be on this for a longer time.... like as not, the words ~ straight from the mouth of the very pretty dolly bird that gave him all this guff.best wishesBob--- In thyroidpatientadvoc acygroups (DOT) com, sarah s <xxsarahxx_40@ ...> wrote> Just out of interest Bob I see the

other drug you mentioned is an antiphycotic (sp?) is this person you refer to young or old?>

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  • 1 year later...

, I have had the same symptoms as your father - waking up and while

mowing the lawn. Saw a respiratory specialist and they did complete diagnostics

and found nothing that would cause it.

A few months later after being diagnosed with achalasia, i had the Heller

Myotomy surgery and that seemed to help with the waking up out of breath or

choking. Of course now I sleep with the head of my bed elevated too.

I think mine is related to neck injuries and not hereditary.

Marco

>

> Interesting . I have a full blooded cousin who has the " A " and also

his

> mother my full blooded aunt has " A " . There was some genetic research done in

our

> local General Hospital but i don't know if the results are out yet. As I said

> interesting.

> from the UK

>

>

>

>

> ________________________________

> From: zlmmom1 <mcnairmichelle@...>

> achalasia

> Sent: Mon, October 18, 2010 5:55:54 PM

> Subject: something interesting

>

>  

> something that's making me think...

> my biological father has had some moderate gerd for several years now. He's

been

> taking PPI's and sleeping elevated for some time. He has told me before about

> waking up feeling like he can't breathe but it has never sounded like

aspiration

> and he's had it looked at and no real answers from any of his doctors.

> Anyway, about 6 weeks ago, he was cutting the grass and said he felt a big

load

> of pressure in his chest and starting feeling short of breath. He went inside

> and after about 30 min. with no improvement, he went to the hospital. Had the

> full cardiac workup and they said - no heart attack and referred him to his

> normal cardiologist for follow up. Had stress tests and some kind of nuclear

> testing done and now his cardiologist has diagnosed him with 'esophageal

> spasms'. He said there's no pain with them, only shortness of breath but I

still

> thought it very strange, given my medical history - that my father has spasms.

> While we don't have reason to believe that A is hereditary - this leads me to

> believe that there is SOMETHING genetic to it. Maybe some kind of genetic

quirk

> that has just manifested more fully in me or some kind of recessive trait that

I

> inherited. I have 1/2 blooded siblings but none that are full blooded.

> Hmmmm.

> Any thoughts?

>

> ~ in NC

>

>

>

>

>

>

>

>

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