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Carmen Rijos: Systemic Scleroderma
This is a request for donations for the
Carmen Rijos Private Foundation

Mary's Fruitbowl by Shelley Ensz March 1, 2000

Dear Friend,

In October, 1998, my 21 year old niece, Carmen Rijos, was diagnosed as having Scleroderma, a disease that causes a persistent hardening of the body's own tissue - skin, lungs, digestive tract, heart, kidneys, muscles, and nerves.

The disease predominantly affects women in their 30's and 40's; however, cases have been diagnosed in very young children and in older adults. Although doctors and researchers find many aspects of the disease a mystery, those at Virginia Mason Research Center in Seattle, Washington have been very successful in performing on patients with Scleroderma an experimental treatment called Stem Cell Transplant.

Although the Virginia Mason Research Center believes that Carmen is an excellent candidate for this treatment, her family's insurance does not cover the expense of the procedure which costs approximately $250,000. Without the procedure, Carmen has a maximum life expectancy of five years and will become paralyzed during this short period of time.

The Carmen Rijos Private Foundation was established not only to raise the necessary funds for Carmen's Stem Cell Transplant but also to help other victims of this devastating illness. For this reason, we hope that you and other members of the community will join together in this cooperative philanthropic effort.

With your tax deductible contribution to the Carmen Rijos Private Foundation you will be making a personal commitment toward improving Carmen's chance at life, and you will be participating in making her recovery a reality. In addition, you will be helping other victims who will benefit from the results of this research.

Your generosity and support is greatly appreciated by Carmen, her family, and the outstanding staff of doctors and researchers at Virginia Mason Research Center.

Sincerely,

Piedad Nicolas

To Contact the Author
Piedad Nicolas, Director
Carmen Rijos Private Foundation
335 Locust Avenue
Port Chester NY 10573

(Story posted 3-1-00)
New email address needed 09-06-06 SLE
Carmen's Old Email Prefix: CLRIJOS

Story Artist: Shelley Ensz
LINKS
About Scleroderma
Stem Cell Transplants for Scleroderma
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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