I've been seeing an endo for the past 8 months and just feel frustrated.
I was on 175mg of levo, thyroid feels fine but I am still having major trouble sleeping, ache all over and feel so tired all the time. I am convinced I have Fibromyalgia and have been asking my endo to refer me for tests. She upped my Levo on my last visit and told me to see how I was after that kicked in. I went back to see her yesterday and told her the pain and sleep were no better. She then asked me what I would like to do as she thinks that this is just normal for my condition and I may just have to accept it.! I asked her to keep to her word and refer me to the rheumatology dept but she then decided to put my Levo down to 100mg and see me in 6 weeks! Do these people not know how hard it is living with hashimotos never mind all the lack of sleep and pain. I'm dreading the next 6 weeks, 1 day taking the reduced meds and I can already feel myself going downhill 😭
Rant over x