Hello, I was diagnosed with Graves disease in June this year and had all the usual Hyper symptoms so was given 30 mg of Carbimazole from GP. Long story short, felt more or less better by Aug-Sept on 10 mg, then was asked by Specialist to reduce to 5 mg from Oct. This was because my levels were appearing within normal range, whatever that means. I don't have the levels details to hand, I am not organised, lol. Now, at the end of month, instead of being sleepy and achy on 10 mg of Carbimazole which I was coping with!, I now have subtle palpitations back, extreme agitation with everyone, a low mood, and loads of anxiety as well as an aching body and tiredness. WHY do the gps/specialists change what was making my life more liveable?!
I have two little daughters and they need a capable, coping Mummy.
Any thoughts please? I had bloods done two weeks ago still in 'normal' range. Thanks