Welcome to the forum. You bet, you're in the most perfect place you can be! There are LOTS of us here with UCTD or MCTD. I think it's great your doctor wants you to get a second opinion too! Is it your rheumy who wants you to get a second opinion? UCTD is simply a lable for "we don't know which connective tissue diseases you have, but you do have something." The "U" standing for "Undifferenciated". It's still just as serious as a Lupus diagnosis and you'll be medicated the same.
I also have Fibromyalgia. It's very difficult living with both Lupus and Fibro. I sure hope you can attain a remission with your UCTD. It's hard to do. But not impossible. Keep up the positive thinking!
You should probably be keeping a diary of all your symptoms and taking pictures of any rashes you get. It will all help your future doctors.
I can do anything through Jesus Christ who strengthens me. I have learned in whatever state I am in,to be content. Phillipians 4:11-13
35 years old. Diagnosed with Lupus in 2000. Fibromyalgia, Anti-phospholipid syndrome(APS)(stroke, 2002), Sjogren's, Raynaud's, Libman Sach's Endocarditis, vasculitis, sacroiliitis, arthritis (neck), anxiety, Chinook migraines. Prednisone, Imuran, Coumadin, Clobazam, Amitriptyline, Didrocal, Cozaar, Zoloft, Neurontin, calcium, multi-vitamin, vitamin D, Magnesium, vitamin B6, Acidophilus
Co-Moderator for the Lupus and Fibromyalgia forums