February 2002 |
| Update: CJ: Fibromyalgia, UCTD, and Systemic Sclerosis My brother has been diagnosed with Stiff Man Syndrome,which we've been told is a form of neuoropathy, akin to scleroderma... |
| Sherry: Fibromyalgia and Hypothyroidism He said Fibromyalgia is just pain, and if I could not handle my job, I should quit... |
| Nan: Mixed Connective Tissue Disease and Fibromyalgia Finally after several years of struggle, one wonderful doctor at OSU got gutsy and gave me the MCTD diagnosis... |
| (Italiano) Roberta: Morphea Sono una ragazza di 25 anni e due giorni fa mi è stata diagnosticata una macchia di morphea sull'avambraccio destro... |
| (Update) Buggzy: Autoimmune Hepatitis, Fibromyalgia, Undiagnosed Since my first letter in 1999 I have had many unnamed illnesses... |
| (Update) Phyllis: Morphea Scleroderma After a year of taking the Vitamin E and rubbing it on three times a day, the lesions disappeared and have not returned... |
| A.M. Keyes: Surviving Daughter My father died on February 9, 2002 from pulmonary fibrosis, a complication of scleroderma... |
| Shirley Wright: Limited Scleroderma I have had this disease for over twenty years now and I plan on being around a lot longer... |
| (Update) Linda: Morphea Scleroderma I have gotten four new spots the last months... |
| (Update) Mo: Mother of Undiagnosed Girl Alexa passed the "eat the radioactive sandwich test" with flying colors... |
| Cindy: Undifferentiated Connective Tissue Disease (UCTD) He seems to think that I have Systemic Lupus Erythematosus, but until my symptoms show more criteria for it, he can't call it that... |
| Star: Widow of Scleroderma Patient I am 43 and I lost my husband on October 7, 2001... |
| Kathi: Scleroderma/Lupus I am 43 years old and have not been feeling well for 10 years... |
| (Update) Deborah Peck: Diffuse Systemic Sclerosis My doctor contacted Dr. White in Maryland who thought that I have not received enough cytoxan... |
| (Update) Dienne: Morphea plus Possible CREST I am now Chair of the Scleroderma Awareness Committee as well as the Graphic Designer for the International Scleroderma Network... |
| CJ: Fibromyalgia, UCTD, and Systemic Sclerosis I have been going to doctors for over five years now and have just recently been diagnosed... |
| Soose: Limited Scleroderma I may have had scleroderma for the last year and a half or two years and did not know it... |
| Joy: Mom of Cassi, Who Has Morphea I carefully checked the bruises; Cassi (age 6) said that they did not hurt and she did not have anyone hit her... |
| Teresa: Scleroderma I was just diagnosed a few hours ago. Tears are streaming down my face... |
| (Update) Deborah Peck: Diffuse Systemic Sclerosis I try to live one day at a time and trust God to heal me. I know He may use cytoxan to do it and/or a combination of other treatments... /td> |
| Takeya: Morphea Scleroderma "I thank God that it's not harmful to me or the baby..." |
| (Update) Dawn: Confirmed Early Scleroderma During the past year I have made a remarkable turnaround both symptomatically and emotionally... |
| (Italiano) Arianna: Early LcSSc con interessamento polmonare (DLCOc=44%), recente alveolite polmonare, esofagite di II grado con ernia iatale Mi chiamo Arianna e sono una ragazza di 26 anni... |
