Now that I have been on T3 Liothyronine for a few weeks some symptoms are improving. I was feeling much less stiff, and muscle pain had improved. Unfortunately I have now developed what I think is an elbow bursitis. When I read about it most articles say you are at higher risk with Thyroid disease. Currently taking Levo 100mcg, Liothyronine 10 mcg, Vit D, Vit B complex. Due to have private bloods done in 3 weeks. My worst symptoms throughout has been muscular skeletal pain and stiffness, constipation, skin problems and bladder retention, with frequent UTI’s. My skin and bladder are much better on the Liothyronine. Just feel this week that my symptoms have got a little worse. My private endo did reduce my levo from 125mcg to 100mcg when I started the Liothyronine so my GP didn’t have a panic as my TSH is very low. So my levo may be able to go back up to 125mcg?
Does anyone else suffer with bursitis? Frustratingly I have only just recovered from a frozen shoulder that appeared just before I was diagnosed.