And the actual reason I came here to this thread (now that I finished the rest of it), is that my aunt just told me she was diagnosed with systemic scleroderma in Oct 05. Unfortunately she has up to 4 more years . . . so I'm researching the heck out of the condition, research done, and clinical trials that she can go for. Luckily all the MDs working on CTs are pretty nice so far. If anyone has any information I would definitely appreciate it.
There may not be a lot I can do in the end, but I was hoping to find out a little more about symptoms and how to make her feel most comfortable if I visit her or vice versa. I will at least keep the fatigue in the back of my mind.
Procrastinators of the World UNITE!!! . . . . tomorrow.