Please refer to previous post- last week I was experiencing tingling/numb/ swollen fingers and lost my sense of touch along with a few other symptoms. I was prescribed steroids for suspected rheumatoid arthritis by my GP (without being seen.) I decided to not start taking the steroids and to get a blood test instead. Here are the results below…..
I guess they are the results of a flare up??
I still haven’t started the steroids and am waiting to speak to my GP again over the phone on Friday this week. Symptoms have now calmed a little.
Endocrinology appointment rescheduled for September.
(Not yet diagnosed or on any medication)
Written by
sunshineisbetter
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I don't know that there is such a thing as a Hashi's 'flare-up'. But, a Hashi's flare is when the immune system attacks the thyroid, and the dying cells dump their stock of hormone into the blood, causing levels of FT4/3 to shoot up suddenly, and the TSH to drop.
Those results are not saying Hashi's flare - aka Hashi's 'hyper' swing. They are showing hypothyroidism due to Hashi's. Which would, of course, cause all sorts of bad symptoms. Your TSH is over-range, your FT4 only 32.5% through the range (euthyroid is at least 50%) and your antibodies are very high, so your doctor should now start treating you with thyroid hormone replacement.
A euthyroid person is a person that has no thyroid problems - in other words: normal. However, when a doctor says 'normal', all s/he means is 'in-range', which isn't always good. As you can see, yours is in-range, but too low. A truly 'normal' FT4 would be about 50% through the range. Yours is only 32.5%, so that indicates that your thyroid is struggling and can only manage to make that small amount of hormone when the TSH is over-range.
I don't know how much you know about this, and don't want to tell you things you already know, but TSH - Thyroid Stimulating Hormone - is a pituitary hormone that stimulates the thyroid to make more thyroid hormone. In a euthyroid person, it would be around 1 - never over 2 - so you can see that yours is quite high. The problem is that doctors know very little about thyroid and believe that the TSH has to be over 10 before they can diagnose. That is not true if there are high antibodies. Because the antibodies indicate that things are going to get worse, not better.
I have researched into TSH and antibody levels so have a better understanding of those and yes I assumed things were not going to improve without some help!
T4 is a thyroid hormone which is basically a storage hormone. It has to be converted to T3, the active thyroid hormone, before it does very much.
When you're diagnosed as hypo, the doctor puts you onto levo, which is T4. You should start on 50 mcg unless you're very young, very old, or have a heart condition. But not all doctors understand that, and some of them think you should start on 25 mcg, which is wrong. So, watch out for that.
I’m so glad you tested privately and didn’t go on your GPs telephone diagnosis. I hope you receive prompt treatment for your Hashimotos & you start to feel better soon.
Update: Spoke to a different GP today who has recommended that I take the steroids and wait to see an endo before trialling any thyroxine as it might make me feel worse. She openly admitted that they don’t know enough about it all as it’s a specialist area so would prefer to wait for advice from the endocrinologist! Frustrating 😬
Don't understand how Thyroxine might make you feel worse, if your body isn't producing enough of it. Worsening hypo symptoms from untreated disease will definitely make you feel worse. This site says that patients with R.A. are more likely to develop hypothyroidism. creakyjoints.org/comorbid-c...
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