The world is teeming with people having problems with th

The world is teeming with people having problems with this illness, although treated with thyroxine and within the 'normal range'of the blood test. I was diagnosed 20 years ago and have had constant problems with variable health since. I have had many disheartening interviews with medics who look at a blood-test result and insist that I am euthyroid (normal), so any symptoms must be due to something else. Their usual off-the-cuff diagnosis is 'depression'in spite of having conducted no relevant investigation. I am one of the least depressive people ever and yet I have been offered anti-depressents several times, rather than more/less thyroxine.

I recently discovered 2 important things about thyroxine.

(1) One is that the same dosage is not 'bio-equivalent' from one brand to another. This means that 100mcgs thyroxine from one manufacturer will act differently from 100mcgs thyroxine from another. (I found this info through an internet search).

(2) Secondly, thyroxine is regarded as a 'narrow therapeutic range' medicine. In other words it has to be JUST RIGHT (like Goldilocks' porridge). Too much is as bad as too little.

If you put these two facts together it is easy to see why people have on-going problems. A blood-test showing on a physician's screen could be weeks/months old and taken when on a brand different to the one in current use.

I am presently staying on one brand constantly in order to test this. I have had to go to a private doctor who will prescribe a brand name.

If this makes no difference after perhaps a year, my next step is to try Armour Thyroid, derived from animal thyroid-glands (the original treatment) which contains 5 thyroid-hormones instead of just one. I don't recall hearing any adverse comments about this treatment.

Dr. Joan Gomez' book 'Coping With Thyroid Problems' points out that symptoms can be mis-leading and I have experienced, in the past, symptoms which I attributed to being under-active actually being due to slightly too much thyroxine.(There-fore, in effect, over-active). The person who reported lowering dosage for 2 days because of tiredness and breathing-problems demonstrates the effect of tiny but important 'fine-tuning' and possibly would benefit from a small over-all drop in dosage. I have found breathlessness & tiredness together to be symptomatic of too much thyroxine.

With regard to weight-gain,it is a primary symptom and an on-going problem - and how is one to lose it with no energy to crawl to work, let alone get to the gym?

I will be interested to hear how people get on with Armour (natural) thyroid medication.

This message was automatically imported from the original Patient Experience

MY THYROID WAS RADIATED WITH RADIOVACTIVE IODINE IN

1992.It was destroyed. Since then I have been on different strengths of Synthroid. I now take 125mcg.

I MOST CERTAINLY DO NOT FEEL WELL ! I DEVELOPED

Fibromyalgia in 1993. Sometimes the best place for me

is in bed, asleep, but that is no way to live.

I am now 64 year old: my mind says "BE ACTIVE "

MY BODY SAYS " I AM SO TIRED. STAY IN BED ". I

WAS A TEACHER AND VERY ACTIVE IN COMMUNITY AND SPORTS.

MARRIED 44 YEARS--3 CHILDREN--3 GRANDCHILDREN AND NOT ENOUGH

ENERGY TO ENJOY ! B.P.

This message was automatically imported from the original Patient Experience

hi i am glad to hear from someone who has experienced the same as me and loads of others by sound of it. i was diagnosed with underactive thyroid as my doctor tested for it routinely five to six years ago. i too am frustrated by the attitude of drs where your test results are fine but my life is non existent. i saw a specialist some years ago as my doctor kept hearing about my feeling ill and wouldnt contribute any of the symptoms to thyroxine. the specialist told me my reading meant that i was a borderline case really i wasnt bad enough to be treated and should have been checked again to see if it had got any worse later on. this cheered me up no end as you can imagine! since then i have been really upset about the fact i cant get my health back to where i was before i was diagnosed. i questioned the drs decision to put me on them at the start as i felt really well. but i thought well if i dont i willl have a weak heart and die early so i had better. the doctor became quite annoyed that i had questioned her judgement at the time . then at the specialists years later i found out that i really didnt need to be.

i am now making the best of it at times i feel like crying at the life i cant get back. i too feel like not wanting to exercise. i joined a gym last year as i felt i needed to help myself a bit . like you say everything is an effort. i really think doctors need to think twice before dishing these pills out. its hard to see the benefits of it. there are so many people on the web sites who are all feeling the same. my biggest battle is convincing the doctor that my symptoms are related to thyroxine. it wont even be considered. leaving me feeling i have nowhere to turn for help .i knowhow you feel but we arent alone. i think something needs top be done about this.

so many people with ruined lives. i dont know the answer i afraid . at leaast we are not alone hope you find a solution .

If you are lacking in T3, but T4 is ok, then by taking more Thyroxine (T4), your body will go hyper because it may not be the T4 that is needed.

The body needs to be able to convert T4 to T3 (the active hormone), if it can't do this then the Thyroxine will make you feel overactive.

There is plenty on the internet re thyroid resistance and problems with conversion.