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Earn $150 on July 30th in Boston Marketing Research Study if you have scleroderma or CTD and have been screened for pulmonary hypertension!
Frog jumping for joy by Shelley EnszPDF Flyer: Boston Marketing Research Study. Schlesinger Associates-Boston, a national marketing research company, is currently looking for patients who have been diagnosed with Scleroderma or other Connective Tissue Disease, who either have pulmonary hypertension or who are regularly screened for it, to participate in a July 30th paid marketing research study in Boston. Read PDF Flyer: Boston Marketing Research Study or call Katherine at 617-542-5500 x310. Schlesinger Associates-Boston. Posted 07/26/10.
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Stacy M: Scleroderma and Lupus

I am only a thirty-three-year-old male and I feel like I am eighty years old.

Tools for Stacy by Sherrill Knaggs, ISN Artist I was diagnosed with lupus on October 28, 2004, and put on prednisone four days later, which cleared up my facial rash. They took a blood test to see what kind of lupus I had and on Sunday, November 7, 2004, they said I have scleroderma and lupus.

Finally I have something to go with all the problems I have had over the past ten years. I have had joint pain and swelling for ten years with a skin rash on my face and chest and on my scalp for six years. I also have been having migraines for three years.

Three years ago they told me I had degenerative disks in my neck from a car accident. I have carpal tunnel syndrome that was diagnosed in 1997 but I haven't had surgery for it. I have muscle weakness all the time. I also have bi-polar disorder and am not working because of that.

I am only a thirty-three-year-old male and I feel like I am eighty years old. I cannot get out of the house and go for walks like I used to. I am constantly sleeping all the time due to major fatigue. I have sores all over my legs and so many scars that I cannot even wear shorts in public anymore. I got the sores from scratching at night uncontrollably. My feet are very scarred, too, from athlete's foot. I put cream on my feet to cure that but it keeps coming back. I have facial cellulitis which has not gone away after taking antibiotics for it. I see a specialist this week for my disease.

I am a mess I need some advice. Please help me.

To Contact the Author
Stacy M.
New email address needed 09-26-06 SLE
Old Email Prefix: Mudrnner666
Story edited11-08-04
Story posted 11-23-04 SLE

ISN Senior Artist: Sherrill Knaggs
Story Editor: Judith Devlin
LINKS
Bipolar Disorder
Carpal Tunnel Syndrome
Joint Pain
Lupus
Scleroderma

PDF Brochure: What is Scleroderma?
ISN Artist: Sherrill Knaggs (In Loving Memory)
Sherrill KnaggsSherrill Knaggs, ISN Artist, created the digital photo to illustrate the story on this page. Sherrill lived in New Zealand. Her story was featured in ISN's book, Voices of Scleroderma Volume 2.
ISN Story Editor: Judith Thompson Devlin
Judith Rose ThompsonJudith Thompson Devlin is the ISN Story Editor for this story. She is also lead editor of the ISN's wonderful Voices of Scleroderma book series!
New Personal Stories
Mars: Scleroderma with Full Gastrointestinal Involvement I finally started total parenteral nutrition (TPN, or tubal feeding) in May 2010 and it was an absolute success...
Sonya D: Surviving Daughter of Systemic Scleroderma Patient (Portugal) She had difficulty eating, drinking and digesting her food, but yet doctors had no clue...
Hazel: Morphea Scleroderma In 1962 when I was just twelve years old, my mother took me to our family doctor with what looked like a blister under my right eye...
Angela R: Linear Morphea Scleroderma I am twenty-five now and only have the two spots that I deal with pretty easily. I just hope it doesn't get worse...
Heather A: Scleroderma (South Africa) My fingers started to curl up and I could not wear any rings on my fingers anymore as they were so swollen...
More New Stories: May-July 2010
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