Hi Everyone - I too have been recently diagnosed with UCTD. I am feeling a little bit frustrated because of its name, I feel like people don't think it is a real disease. In fact my husband, who is a very caring man, made a comment of this is getting in your head. As if my pains are made up.
As everyone has said there is not much information out there but I appreciate the articles that have been posted on the website. However I am curious on a few things: Does anyone have any of these symptoms:
- burning sensation in ankle. At night when I get into bed, the touch of the sheets can send an electric shock to my ankle.
- numb lips
-fuzzy head
The reason I ask is that I don't know if these are part of my flare up or other issues.
Also because I am new to this, during flare ups, do you exercise? I am runner but the other day I knew I shouldn't run because of my ankle were too tender so I went on a power walk. I was fine during the walk but once I got home, my whole body ached. I need to continue to exercise but would love suggestions on what are recommended exercises.
Hello @maryalicep, Welcome to Mayo Clinic Connect. I don't have UCTD but I do have degenerative arthritis and osteopenia along with a few other autoimmune conditions. I know that exercise helps a lot of us with different conditions but I try not to overdo the exercise if I'm having pain. Here is a link that discusses exercise and also has links to other articles that may be helpful.
- Exercise in patients with inflammatory arthritis and connective tissue disease: https://pubmed.ncbi.nlm.nih.gov/2087581/
Also the Genetic and Rare Diseases Information Center (GARD) has some information on UCTD that might be helpful: https://rarediseases.info.nih.gov/diseases/12342/undifferentiated-connective-tissue-disease
I think even just regular walking would be beneficial. Do you have any home exercise equipment or enjoy Yoga?