Hypothyroidism?
Posted , 9 users are following.
I could do with some help if anyone is willing to read this very long post!
I'm a 22 year old woman. The last year or so I've had fairly manageable fatigue which I never thought a lot of, but in the last few months it's become awful to the point that I can barely get out of bed in the morning, take at least one day off from work a week (despite loving my job) and tell myself I'll work at home but end up in bed all day. The days I do go in I'm often in well after 9, and generally have to head home around 3 or 4 beacuse I'm so exhausted. It's like I have a fog in my brain which makes it hard to concentrate on anything from work to conversations to films, and my short term memory is poor. I only recently found out this can be a symptom of an underactive thyroid, and I wouldn't be convinced they were linked... except that my nan, mum, both maternal aunts and my younger sister all suffer from it.
I haven't had any weight gain which I know is another common symptom but my sister has quite severe hypothyroidism and has never suffered from weight gain. I do have bad muscle/joint pain and stiffness, various mental and emotional issues to do with anxiety and depression, cold extremities, breathlessness, poor coordination, hoarse voice, swollen tongue, post-nasal drip, and dry patches of skin. I am very prone to UTIs, thrush, sore throats, headaches, and constipation. I know that these are symptoms "normal" people get all the time, but hypothyroidism is the only thing I've found that links everything I've ever thought was abnormal about me. My diet is very good and I walk fast enough to build up a sweat for an hour a day to get to and from work.
My doctor is reluctant to diagnose me with this beacuse my hormone levels are within normal range, which I understand, but she's also unwilling to discuss my symptoms and keeps sending me for more blood tests. This week I'm getting my white blood cell count checked as she thinks it could be viral because my CRP level was high - it seems unlikely to me that it would have been going on for so long if it was, but I'm no doctor. I'm also getting my Vitamin D done again as the lab forgot it last time. I'm completely open to the possibility of it not being hypothyroid, but it's the only thing I've found while researching that fits, and with every woman on my mum's side having it it does seem likely.
So my questions are: do I sound like I fit the bill? If so, how can I convince my doctor? If not, any ideas - literally anything - as to what it could be? Thank you so much to anyone who took the time to read all that, absolutely any information would be so helpful.
Blood test results for the last month, and how they were "graded":
Serum TSH: 2.2miu/L (normal)
Serum FT3: 5.8pmo/L (satisfactory)
Serum FT4: 19.2pmol/L (satisfactory)
Glucose: 2.7mmol/L (low, but I hadn't eaten before this test)
Coeliac: Negative
Liver function: Normal (can give breakdown)
Full blood count: Normal (can give breakdown)
Ferritin: 17ug/L (satisfactory)
C reactive protein: 9mg/L (high)
B12: 216ng/L (normal)
Urea and electrolytes: Normal (can give breakdown)
1 like, 33 replies
alice79312
Posted
shellyC19 alice79312
Posted
I have had Hashimoto's since I was 27. It is not the end of the world. I am now 54 and you can live a good long life as long as you take the replacement hormone.
It will help keep your body working well, and once you build a level, which can take 6 to 8 weeks, the bad symptoms will subside.
If I can be of any help, just ask.
Shelly
alice79312 shellyC19
Posted
cindy72112 shellyC19
Posted
I wondered if you knew if NDT is prescribed in the US? It is not routinely prescribed in the UK apparently.
Cindy
shellyC19 cindy72112
Posted
NDT, called Armour Thyroid in USA and a few others are prescribed for people who need it. I was on it for years, before my doctor discovered my converting T4 problem. It is a fine medication and can be bought online via Amazon and other websites I hear. I also hear you can get it without a prescription online, and a few women on the forum do that.
In the USA we pay for insurance and are not on socilaized medicine like UK is. We have to pay a percentage of the cost of the medication depending on our insurance plan and it was under $10.00 dollars when I was on it.
I am now on T3 alone Liothyronine (Cytomel) since I can't convert T4 LEVO.
NHS is bound by certain rules and reg's because of the socialized medicine set-up. USA operates on private insurance plans. Also this medication is a natural mediciation made from a pig and you can't patent a pig and claim it as your own.
Regards,
Shelly
cindy72112 shellyC19
Posted
Thank you for the information.
I was reading a medical book on thyroid disorders and it has left me feeling puzzled in some respects because it states that carbimazole may be dangerous..
I also read that nodular goitre and sub clinical hyperthyroidism can lead to osteoporosis and cardiac disease and should be treated with rai but a few days ago I also read that there is no evidence to support this.
I wondered if you knew anything to back up the original claims.
Cindy
LAHs cindy72112
Posted
You have just read an article on hyperthyroidism while you are at the other end of the scale with hypothyroidism. Hyper is an overactive thyroid while hypo is an underactive thyroid. Yes, Carbimazole can be dangerour, it slows things down and an overdose can slow you down too much and put you in a coma. Levo can also be dangerous, too much can speed you up into hyperthyroidism - which could put a strain on your heart.
That is the gist of our problems, it takes a great deal of patience on the patients part as well as the doctor to fiddle around with the dose in order to get you just right. Very often your doctor gets fed up with the process and doesn't see it through. My doctor took 2-3 years (yes, years!) to get me to the right dose, it takes tenacity on the part of both parties.
Regarding the other comment, I have hypo and when my TSH is suppressed (it has been for 8 years) they say this is a hyper condition (it is not) and it will cause osteoporosis - it did not, in fact my bone density got even better. I can understand why it may affect the heart, but it hasn't caused me any harm so far - however - all thyroid meds can raise your blood pressure, you have to watch this one, another factor to be careful trying to get to your critical levels.
cindy72112 LAHs
Posted
I was diagnosd with hyperthyroidism as the TSH was low being 0.14. Are yu saying that i have been incorrectly diagnosed!!
I was sweating excessively , very agitated, anxious, depressed, throbbing sensation in one eye.
I would be grateful for your thoughts on this.
barbara98940 cindy72112
Posted
If you are getting these symptoms after taking thyroxine treatment for an underactive thyroid (hypoactive) then you are being over medicated with thyroxine and need to reduce the dose. It is the second of these to which LAHs is referring. It all depends whether you are taking thyroxine or not when you had the blood test results of TSH = 0.14.
LAHs barbara98940
Posted
My apologies Cindy I thought because you were asking about NDT that you were hypo and obviously your symptoms and TSH point to hyper. And yes, Barbara sorted it all out, I agree with everything she says, thanks for that input Barbara.
Cindy, you might want to go down to the pharmacy (chemist?) and measure your blood pressure, throbbing in any part of the head whilst hyper might suggest seriously high blood pressure.
cindy72112 barbara98940
Posted
The T4 and thyroid peroxidase antibodies were within normal reference ranges.T3 was not done.
I have never been on any thyroid medication. I am very worried about all this.
I see on another forum that a lot of people are dissatisfied with the care of thyroid patients in the UK.
I feel destrauht at being left without treatment.
I was enquiring about NDT because I am having signs and symptoms of both hypo and hyper at different times of course. I do not know what to do anymore.In the US these symptoms would have been treated by now.
I read a book iwritten by a dr n which it stated that people with a nodular goitre should have RAI and it is safe because it will not knock the thyroid gland out and therefore will not lead to being on thyroxine for the rest of my life.
In the same book ,bought from a chemists, it says that Carbimazole is safe. Yet I read conflicting views on a forum elsewhere.
Thanks again for replying.
cindy72112 LAHs
Posted
I am already taking an anti hypertensive drug. I monitor my BP myself at home then advise the GP accordingly. the headaches started over one year ago .
I was investigated tehn told they are due to tense neck muscles.
I am still awaiting treatment so that is why I was inquiring aboutNDT because my thyroid appears to fluctuate between hypo and hyper.
Thanks for your concern anyway.
Cindy.
barbara98940 cindy72112
Posted
barbara98940 cindy72112
Posted
Are you in the UK? I am. In my area, we can 'self refer' to a physiotherapist. Ask your GP and if your area does self referral they will give you the physio's phone mumber and you just ring them. Pilates is good for posture and hypertension.