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| April 2006 |
| (Update) Leeben: Limited Scleroderma and CREST Since writing the first time, my disease has become progressively worse. I have increasing kidney damage which limits the kind of medications I can take... |
| Andi P: UCTD and Possible Scleroderma It is believed that I do have an autoimmune disease they are not sure if it is systemic or not, but I know what I live through on a daily basis... |
| R.G.: Raynaud's and Chillblains Within just a few minutes of vigorous swimming all of the chillblains had disappeared... |
| Nancy H: Raynaud's I also have the beginning stages of Crohn's, panniculitis, rheumatoid arthritis, and now Raynaud's... |
| Kathy M: CREST (Limited Systemic Scleroderma) If you do not have the right doctor, do not get furious, move on... |
| (Update) Donna C: Undifferentiated Connective Tissue Disase (UCTD) It has been three years since I was diagnosed with UCTD. Last year I finally realized I had a disease. It was so hard to understand that I was really sick because I kept getting symptoms but no real concrete disease... |
| (Update) Trish: Spouse of a Diffuse Scleroderma Patient My husband had the second surgery on his other hand but it was not as successful as the first... |
| Merrie: Mother of Daughter with Raynaud's and Fibromyalgia? They said it might mean something or not and referred her to a rheumatologist, but he just blew it off as nothing... |
| (Update) Jackie S: Overlap Syndrome I had about four months of tolerable pain. Then we moved up to Washington and the story begins... |