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Marie B: Progressive Systemic Sclerosis

I do not know how much tighter my skin can get.

Cat by Sherrill Knaggs, ISN Artist I am almost three years into this disease, without seeing any change for the better. The doctors say they have never seen such skin tightening, but I am lucky to not have had any organ involvement yet.

The pain in my arms is so bad that I have to take large doses of pain killers, and this barely helps. I do not know how much tighter my skin can get. It is crushing the blood vessels and my arms and hands are just about frozen. I am still able to write and use the computer, but I am slowly losing that ability.

I have tried chemo, cytoxan, and cellcept. Nothing has helped. I have been to pain clinics and therapy, but nothing has worked. I have a lot of bowel trouble (bleeding, nausea, vomiting, stomach pain and diarrhea). I also have trouble with swallowing and have lost a total of seventy pounds in two years. I am all bent over at the waist and have to use a walker or a wheelchair to get around. All the bones in my face are very painful to the touch, and my mouth is very sensitive to spicy or carbonated beverages.

To say I live in misery is putting it mildly. If the weather is lousy, it is a good bet that I will have to stay in bed for the day. I would love to hear from someone that is as sick as I am. Just to know that I am not alone would help. This disease has many faces, so I hope to hear from others who are going through the same thing.

To Contact the Author
Marie
New email address needed 08-06-09 SLE
Old Email Prefix: mak3812
Story edited 12-09-05 JTD
Story posted 01-10-06 SLE
Email address added 01-26-06 SLE

ISN Senior Artist: Sherrill Knaggs
Story Editor: Judith Devlin
LINKS
Bowel Involvement
Dysphagia (Difficulty Swallowing)
Progressive Systemic Sclerosis
Skin Tightening
Types of Scleroderma
What is Scleroderma?
ISN Artist: Sherrill Knaggs (In Loving Memory)
Sherrill Knaggs Sherrill 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
Maria T: Daughter of Deceased Scleroderma Patient (Italy) He, upon looking at my mom's face and hands diagnosed her with sclerodermia, in fact he took care of her until the end...
(Italiano) Maria T: Figlia di una Paziente Defunta di Sclerodemia (Italia) Lui, come vide a mia madre disse "tu hai la sclerodermia", guardandole le mani e la faccia...
(Update) Dee B: Limited Scleroderma/CREST Syndrome (South Africa) There is so much I want to add to my original letter after reading more of other peoples stories. I am certainly not getting better but wish I was...
Tessa: Morphea The nurse just told me that I have morphea and knew nothing about it and she told me to look online for information...
More New Stories: August-November 2009
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