I was diagnosed with Hashimoto's back in July and have had my medication increased to 100mcg in August. My symptoms definitely resided somewhat and I was feeling a lot better. Unfortunately this last week I've been feeling tired again and the pain in my feet has worsened again, I also have a new symptom of really sore wrists to add to that. I wondered if this could just be another symptom of Hashimoto's or if it could be Rheumatoid Arthritis? I've had on and off joint pain over the last few years too. Any help or advice would be greatly appreciated!
Hashimoto's or RA?: I was diagnosed with... - Thyroid UK
Hashimoto's or RA?
Have you not had a blood test since your increase in July? You should be retested six weeks after an increase and another increase of 25 mcg. 100 mcg is little more than a starter dose. And, by the sound of it, you need another increase of 25 mcg. Go back to your doctor as soon as possible, and get retested. Then you will see if this new symptoms goes or stays.
Thanks for replying. I only had an increase last month to 100mcg from 50mcg and my GP said I should wait till mid Nov for my next blood tests. Is that too long do you think?
Hi Polly2501,
Have you had your Vitamin B12, Folate, Ferritin and Vit D tested?
These are very important and should be tested to check if your levels are at a good level.
Post you results on here and PAS ( within HU) for members to comment . Include ranges ( the numbers in brackets)
J 🍀
Regarding your question about RA - I have Hashis and was diagnosed with and treated for RA five years ago. It turns out that I have primary Sjogrens instead with features of RA. Almost everyone with primary Sjogrens will have thyroid disease and arthritis.
Apart from thyroid levels and high protein, inflammation levels in my blood - all the B12, folate and ferritin levels have always been fine with me. Vitamin D was deficient for a while but I have corrected this now and can tell which is causing which sensation now too. When my thyroid is undermedicated I feel terrible - sluggish, lose concentration and can only think about my bed all the time. When it's overmedicated I suffer palpitations and have awful sweats.
When my vitamin D levels slump I feel miserable, achy and even clinically depressed. When the Sjogrens is very active my nerves all tingle (pins and needles) and I feel dizzy with vertigo and fatigued in a way that is almost like narcolepsy and my eyes hurt and feel extra tight and dry. The dryness also causes chronic constipation and thrush and trouble swallowing, hoarseness, reflux plus dry cough and nose bleeds from dry nose.
My joint pain is often bilateral and affects the areas you mention. It would be a good idea to get your autoantibodies checked for Rheumatoid Factor and ANA and if these come back raised then the doctor should refer you straight away to a rheumatologist. If not then it doesn't mean you haven't got RA or a connective tissue disease unfortunately - it would just make it less likely and harder to diagnose. Also they should check your ESR/PV and CRP ask well as a full blood count. There are important measures of inflammation/ protein levels in your blood. With RA or connective tissue diseases they are often very elevated. Hope this helps.