I was recently diagnosed with limited systemic sclerosis with secondary Raynauds. Honestly, the Raynauds and hand swelling has been the worst ongoing symptoms that I've had. Getting muscle and joint pain, fatigue under control with Celebrex, Plaquenil, and low dose naltrexone. I also take a lot of vitamins and natural supplements. I tried taking a calcium channel blocker for my Raynauds, but it didn't help, and caused pretty significant edema in my feet and legs. My Rheumy just prescribed fluoxetine, starting at 10mg with room to increase. Has anyone else had any success with this, and at what dosage? Also, how long does it take to see results? I don't have a follow up until July. Even though we're going into the warmer months, my office is always cranking up the air conditioning! I'm afraid of getting ulcers..I've been lucky so far.
I also wanted to say Hi from Idaho, USA! I'm so happy to have found this site, and to hear a different perspective from the UK. Wishing everyone good health!