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Under-active Thyroid

After some initial blood tests (currently waiting another 10 days for a 2nd round of blood tests) it would appear an under-active thyroid gland has been responsible for my sciatic nerve pain and lower stiff back which I have been suffering with for over 6 months.

I have been prescribed some anti-inflammatories by my GP until the results of the 2nd round of blood tests are known. The anti-inflammatories have pretty much cleared up both back problems but has left me desperately lethargic on my runs.

It would seem likely that I am to be prescribed a daily dose of thyroxine for the rest of my life.
Does anyone else have any long term experiences of an under-active thyroid, thyroxine and running.

Many thanks.
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    Hi Sean
    Do a search using thyroid as the key word. There have been loads of threads on this, some very recent. There are lots of us around - I mean hypo runners, of course!

    I was diagnosed 3 years ago, take 275mcg thyroxine and 30mcg liothyronine daily. I train 6 days/week - running and gym and race 5k up to mara. There are lots like me.

    Post if you need any info or have specific questions. Good news about your back - the lethargy will decrease as you get your doseage of thyroxine going.
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    Thanks Shirl.

    Looks like I'm going to become a member of a-not-so-elite club!

    I would say I'm not showing many of the "typical" symptons. Definitely no recent weight gain - 6'3" and 11St2lb albeit 5 years ago I was 14st4lb. No hair loss. The only "real" recent sign has been muscle swelling that has manifested itself in my lower back. The reason I started to run (5 years ago) was to get fit to play Sunday League football at a decent level.

    Prior to the back troubles (pre June 04) I was running 35-40 miles a week and did the FLM last year too.
    Currently, stuggling to run 6 miles at a pace I would have considered a very slow recovery run 8 months ago.
    So far, I haven't been advised to stop running or excercising. My GP has advised me to keep running but nothing too stressful.

    How long can I expect to wait from seeing my GP (after to 2nd set of blood test results) to seeing a specalist and getting/taking medication?

    Many thanks.
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    you wont neccesarily be referred to a spacialist .im treated just by my gp - take 50mg thyroxine daily which is reviewed yearly -unless i go and ask for more regualr tests
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    Hi Sean
    Like Buney says, you probably won't see an endocrinologist unless you don't respond to standard thyroxine therapy. After confirming your dx with the blood test, the usual protocol is for your GP to prescribe 50mcg thyroxine. You will probably go back to your GP for a further blood test after a minimum of 6 weeks - it takes that long for the dose to be reflected in a blood test.

    Depending on the next test result, your GP might increase your dose and so it goes on until you (hopefully) get to a dose where you feel well.

    There's no reason to stop exercising - you're an athlete so just carry on listening to your body. Good luck and keep us posted on progress.
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    I would not assume your back problem is related to the thyroid problm
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    Don't worry Sean, I take 150mg a day, as long as you keep taking the tablets its no sweat.

    I have never heard of it effecting your sciatic nerve or giving you lower back trouble, sounds weird to me, but then I am not a doctor.
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    I haven't seen a specialist but have gradually moved up to 125mcg thyroxine. I eventually notice when it is too low when my hair drops out. The tiredness and lethargy you feel sound familiar but i wouldn't bet the back pain is throid related. Good luck
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    my 3 yr old daughter has no thyroid function at all and therefore takes thyroxin daily. She is developing completely normally.

    I'm no medical expert but I think I am right in saying that thyroxin is unique in being virtually identical to the naturally produced hormone.
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    All,

    Many thanks for your responses and replies.

    The way the initial (and I do stress initial) findings were explained to me was that my bodies anti-bodies are likely to be attacking my thyroid. The anti-bodies inturn has caused the muscles in my lower back to swell and stiffen up which has could have caused the sciatica (pinched by a stiff muscle) and lower back stiffness.

    I did find a posting on a forum (via google) with someone else saying the same thing. I will try and find the link and post it.

    The anti-inflammatories have done wonders.

    Once again, many thanks.
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    Hi Sean
    I'm a member of a number of patient support groups and peripheral neuropathy is often reported as a symptom. Your experience has similar characteristics to carpal tunnel syndrome which is also common with hypo. Bad CTS was what got me diagnosed.

    I'm currently working my way through a large list of research studies into muscular and neuromuscular function in hypothyroidism. It's fascinating stuff - I think the surface has only just been scratched as far as this disease is concerned.

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    Shirl whats the link with PN ..does it manifest as tingling, pins and needles etc (fingertips)

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    Shirl
    I hope you are writing a book
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    Hi Buney
    The CTS I had was pins and needles at night that woke me up constantly and then would take so long to subside that sleep was very disturbed. It was confirmed with nerve conduction tests and it went away with the thyroid treatment.

    I think what happens is that the myxoedema ('jelly swelling') caused by the TD interferes with nerves that pass through narrow structures like the carpal tunnel. I've heard of nerve pain associated with hypo all over though, not just CTS.
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    I wish Hippo..... But it would be out of date before it got published! 'Cos I've no medical training it can take me a very long time to understand some of the technical stuff and lots of it I never understand :)

    I'm on a really interesting paper at the mo - Human Mitochondrial Transcription Factor A Reduction and Mitochondrial Dysfunction in Hashimoto’s Hypothyroid Myopathy. Small sample size but very interesting for Hashi athletes.
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    well-no shirl
    there all that practical advice you have been posting on the forums
    especially about not relying on TSH, diet and lithyronine
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    mavamava ✭✭✭
    Hi all

    what a co-incidence. I went to my gp today with some odd swellings around my eyes which I thought was sinuses. She's given me antiobiotics for sinusitis but, she also took blood to check my thyroid. The only other things I mentioned were the fact that I've had swollen tonsils quite regularly over the last 3 months and the fact that I regularly suffer from depression. Does this all make sense to anyone?

    Cheers
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    Hi,

    I'm hypo. Depression is a common symptom. I have swollen glands, particularly on the right side of my neck which I've never linked to the hypothyroidism (and haven't gone away with treatment)but flare up when I'm tired or stressed.
    If you think you can or you think you can't you're probably right.
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    mavamava ✭✭✭
    Thanks LMH. The depression is a lifetime thing and I've always thought it was chemically related. I'm sure it's also inherited. And one of my last tonsil periods was after I did 2 10k races in 8 days so the tired/stressed thing would make sense! Plus the swellings round my eyes came up after a really tough 10 miler - I was practically on my hands and knees at the end of it.
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    Hi mava - taking a break from fundraising! The thing with thyroid disease is that the symptoms can be the same as dozens of other things.

    Puffiness around the eyes can be TD from the oedema but it won't go away with antibiotics and it's not connected with sinuses.

    Is it actually your tonsils that are swollen or is it a feeling of a lump or fullness in your throat? TD can cause the thyroid gland to become enlarged, sometimes temporarily, sometimes permanently but it's not associated with tonsils.

    Depression is certainly another TD symptom but again not everyone who has depression has TD.

    Other symptoms include inappropriate exhaustion, weight gain, constipation, heat/cold intolerance, loss of eyebrows, body hair and head hair, brittle, flaking, ridged and loose nails, brain fog, loss of libido, menstrual irregularity, low body temperature....... the list is large. Do any of these sound familiar?

    In any case, it sounds like your doc is on the ball as far as getting you tested is concerned. Results usually only take a couple of days so you should know soon. If you want any info, I can bore for England on TD! so just ask.
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    mavamava ✭✭✭
    Hey Shirl! Wow. It's not puffiness around the eyes so much as spots of swelling in the corners between the eyebrow and nose.

    It certainly looks like my tonsils but I might be wrong. I do feel exhausted a lot but I do get up very early and do fit in a fair bit of exercise. No weight gain - I've (intentionally) lost a great deal of weight in the past 13 months or so - around 15kg. My big surprise is that I gave up smoking 3 months ago and I haven't gained weight. My nails did go through a period of disintigrating a while back but they're fine now. Yes, low libido. not sure what you mean by brain fog but crap short term memory (have always put that down to a very, very mis-spent youth), very irregular periods, very cold hands and feet (lifelong problem).

    But, the GP didn't ask about any of this.

    Well, if there's anything in the blood test they'll call me.
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    Hi Mava
    Those sound more like the usual type of TD symptoms unfortunately. And the big red flag is stopping smoking. Anecdotally, hypothyroidism is often diagnosed soon after stopping smoking. The theory is that the nicotine creates an artificially high metabolism that masks the symptoms of TD.

    There are also a fair few studies that have shown that smoking damages thyroid function. "One component of tobacco smoke is cyanide, which is converted to thiocyanate, which acts as an anti-thyroid agent, directly inhibiting iodide uptake and hormone synthesis."

    However, this is all just speculation so best to wait for your results!
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    mavamava ✭✭✭
    Well there you go. I did mention to doc that I'd given up smoking. You're a mine of information. Thanks. I shall wait and see.
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    I'll keep my fingers crossed for you, mava. Let us know how you go. Good luck.
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    Shirl - you are an amazing source of knowledge on this subject. I've learnt more about hypothyroidism from you than from any of my doctors. I'm quietly convinced that I'm not on enough thyroxine (25mcg/day). This was enough to bring me into the 'normal' range but I never got my energy levels back to what they were before, also very intolerant of cold still. However I was subsequently diagnosed as having perniscious anaemia too (also supposedly now controlled) but I'm still TATT!
    If you think you can or you think you can't you're probably right.
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    mavamava ✭✭✭
    Hi again Shirl - one other question if I may. Hot flushes. Does that come in to it anywhere? I'm too young for the menopause! They're actually interfering with my sleep now because I'm either too hot (covers on) or too cold (covers off).
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    LMH - I was on 50mcg and then 75mcg for ages and still felt carp. went back to the GP numerous times until they increased the dose to 100mcg. Eventually the GP who agreed to the increase listened because he also did sport - the previous hadn't. He mentioned to me the concept that runners have a higher standard of what feels right and normal to them than the standard population as we are more used to listening to our bodies than a couch potato - I tend to agree with him.

    If your blood tests come back normal and you still feel under par - it is worth pushing to get it increased for a trial period and see if:
    1. you feel better
    2. your results are still normal
    If so stay on the higher dose.

    Now, a question for Shirl - do you know of any contraindications for thyroxine and glucosamine? I've had achy joints recently (I don't think it's thyroid related, no other symptoms and I usually have a myriad) so have been taking glucosamine, but now feeling a bit ropey. Bloated stomach, generally sluggish stomach action? Now I don't know if it's the thyroid acting up or a reaction with the glucosamine or just the glucosamine???
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    LMGTS - thanks for that, it seemed like a closed door, 'your levels are now normal thyroid isn't the problem' but my GP has increased my B12 jabs from 12 week intervals to 8 week ones.

    Mava - I think hot flushes are the thyroid or I'm in for the early menopause too!
    If you think you can or you think you can't you're probably right.
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    can glucosamine cause any digestive problems ? its a sort of 'sugar' isnt it - so may be that (or whatever its formulated with might be causing probs - try taking it at different times after food etc)


    Cod liver oil and tablets is very good for achey joints too
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    ditto probs with sweats - night sweats for me - but not all the time ..unfortunately stress can do all these things too
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    mavamava ✭✭✭
    evening all. the sweats aren't just at night. I've been getting them on and off during the day too - just brief flushes. Maybe I should have said I think I'm too young for the menopause....early 40s. I should stop trying to second guess the blood test although I'm so exhausted today that I'm almost wishing thyroid is the problem so something can be done to stop me feeling so tired. I was OK until I came back to work.
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