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Question:
Hello, I understand your need to know as much as possible about your disease. That is very important in your ability to cope. I had never heard of SD when I was diagnosed. I must admit when I dove into investigating it I just ended up more frightened than before. Don’t stop because the more you seek the more you’ll find that there are a lot of hope out there for us. Don’t let stories scare you because this disease affects everyone differently and on different severity levels. There is a lot of information on the net in regards to the disease. Visit the websites devoted to Scleroderma, here are the links. Surviving Scleroderma…http://ps.superb.net/smessick/survive Kate’s "I have Scleroderma Page"…http://www.epix.net/~knance Always check in here at the newsgroup for information that can be helpful. If you have any questions in particular than please email me personally or post a message and I will try to find the info for you or find someone that could help you. I hope to hear from you soon. Sherry, Messick, Cheltenham Maryland SURVIVING SCLERODERMA: http://ps.superb.net/smessick/survive ********************************************* When fear holds me captive, I will turn outside myself to find a helping hand. Together we can beat the odds.
Response:
I’m new with this bueatiful situation in my life. If you could assist me in my quest, I’s like to learn more, please? how soes this new direction in my life effect my brain waves? When my liver,kidney’s, etc… are effected, how does this effect my mental capacity in the long term expectancy of my duration. Honest facts will result in reward, if need be,please respond send E-mail to: aqu…@aol.com
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