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RE: ME/CFS Hypothyroidism

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Oh Dee, welcome, you have opened Pandora’s Box with that question! Everyone

has an opinion and they are quite, well, divergent… By my reckoning and in

my researches and experience, my own particular opinion is that ME is an

infectious neurological disease that has been well documented since the

30’s, and CFS was the invention of the US. CDC in the 80’s to cover up the

multiple ME epidemics taking place. The diagnostic criteria for CFS is much

broader than for ME. Doubtless some will disagree and there have been

numbers of books written about it, and I’m not gonna write another right now

LOL!

As to the hypothyroid theory, it’s patently ridiculous. Let’s just say that

many folks with ME (CFS, CFIDS etc) do develop thyroid dysfunction, but

everyone with hypothyroid does NOT have ME (CFS etc.) It does not account

for many/most of the symptoms and process of this disease.

Good luck with your explorations, if you only follow this list for awhile

the great debate will present itself quite nicely! Take Care, Aylwin - a

Canadian with ME.

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I have been diagnosed with hypothyroidism in addition t cfs,

fibromyalgia & MCS. I also have intermittent high intracranial pressure

which affects my pituitary gland.

Any questions ask, I'm not shy. Take care of you.

Big gentle huggles,

Di in Feasterville-Trevose, PA :o)

dimntd on AIM, IRC, ICQ & Yahoo! Messenger

deb wrote:

> Hi, i'm quite new here but i do have some questions that you might be able to

help with?

>

> I was wondering why CFS and ME are still put together as the same thing when

ME has been discovered to be something very different. (from my research anyway

:)

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Hi, Dee.

With CFS/FM and related chronic illnesses/syndromes, the diagnosis of

hypothyroidism must be done clinically, not relying on blood tests.

(As someone said, lab tests lie, but patients don't.) My daughter

(sick for 9 years) is recently being treated as if she has

hypothyroidism by a doctor who, through his experience, has found

that folks with chronic fatigue (and related unidentified illnesses),

sometimes fit the clinical diagnosis for hypothyroidism - even though

their blood tests look normal. So, find a list of symptoms for

hypothyroidism and check to see if you fit most of the

characteristics. Then talk to your doc about treatment with thyroid

meds.

>

> Hi, i'm quite new here but i do have some questions that you might

be able to help with?

>

> I was wondering why CFS and ME are still put together as the same

thing when ME has been discovered to be something very different.

(from my research anyway :)

>

> I'm also wondering what others think of the 'CFS is undiagnosed

hypothyroidism' debate?

> I have hashimoto's so thats why i have an interest in this.

> I find it all so confusing as there are so many different ideas and

opinions on these subjects.

> Just wondering what everyone elses thoughts were?

>

> Thanks so much,

> Dee

>

>

>

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Hi Di,

Thanks so much for answering as i'm new to all this and am just starting to find

out things about these illnesses (as docs are mostly putting it all down to a

'depressive reaction'. They've never said what i'm 'reacting' to strangely

enough. lol

Anyway, i've been diagnosed with Hypo Hashimoto's disease. But even though i'm

taking my meds for that i'm not feeling much better, and i'm having strange

sypmtoms which don't seem to match up to the hashi, so i've been researching and

my symptoms led me to the cfs/me and fibro direction. My question though, is

that there seem to be a lot of people with hypothyroid disease are telling me

that cfs, fibro etc...doesn't exist. That is it just an undiagnosed form of

hypothyroidism, or something that the drug companies made just so they could

invent another medication. A case of, why just flog them thyroid medication when

we can say they are completely seperate conditions and sell double the amount of

medications.'

Is this true? I'm only asking as i'm trying to sort myself out, and being from

Australia we don't really have that huge 'drug companies' thing here. We just

kind of go along with what the US seems to do and say.

Any adice would be greatly appreciated.

Thanks so much

dee

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Hi Dee!

I've noticed on my RA and Lupus health board that many have thyroid issues and

hyperactive thyroid with their autoimmune disease. I do have an article that

was written in my local paper from a nurse practitioner. They found that

although most blood tests were normal, almost all patients had 's Disease

(thyroid disease). They did this by comparing symptoms. One of them being a

temperature always below 98.6. If I can locate the article in my files I will

post the information for you.

" J. Catchpole " wrote: Oh Dee, welcome, you have opened

Pandora’s Box with that question! Everyone

has an opinion and they are quite, well, divergent… By my reckoning and in

my researches and experience, my own particular opinion is that ME is an

infectious neurological disease that has been well documented since the

30’s, and CFS was the invention of the US.

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Dee,

My opinion on CFS & Fibromyalgia... I know CFS & Fibromyalgia are

assigned to people with certain sets of symptoms. Until there is a test

for either condition both terms can be used a diagnosis for anyone with

similar symptoms. There is no treatment for either condition, only

treatment of symptoms. The quality of the treatment varies with the

quality of the doctor prescribing the treatment. Some doctors refer to

CFS & Fibromyalgia as garbage can diagnoses, eliminate specific

conditions and dump everyone left in. Some doctors do not believe in

conditions which have specific tests, humans are funny critters.

My medical history is a bit complex, I have been diagnosed with

approximately 35 separate conditions. Several of these conditions can

be responsible for many of the symptoms of CFS & Fibromyalgia, I have

been diagnosed with both. I also have conditions which impair the flow

of cerebrospinal fluid in my head which puts pressure on my adrenal

glands. I do not know whether I truly have hypothyroidism or it is an

effect of the high intracranial pressure (ICP). I do know I had a

wonderful endocrinologist who treated me based upon both symptoms and

lab results. She took a full set of labs every 4-6 weeks. She would

raise the thyroid meds when i stopped losing weight. She would go over

the symptoms of overdose each visit, I was to go back to the lower dose

if I had a symptom of overdose. I have also been diagnosed with an

adrenal condition which is genetic, though I have no idea of the degree

the high ICP affects the hormone and related conditions. I keep track

of the symptoms, give the list to the doctors and let them worry about

whether a specific condition is involved.

Any questions ask, I'm not shy. Take care of you.

Big gentle huggles,

Di in Feasterville-Trevose, PA :o)

dimntd on AIM, IRC, ICQ & Yahoo! Messenger

My blog Dimntd Thoughts http://dimntd.livejournal.com/

deb wrote:

> Hi Di,

>

> Thanks so much for answering as i'm new to all this and am just starting to

find out things about these illnesses (as docs are mostly putting it all down to

a 'depressive reaction'. They've never said what i'm 'reacting' to strangely

enough. lol

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