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MISSION & VISION LEADERSHIP ANNUAL REPORT BY LAWS PRIVACY POLICY
 
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Pediatric to Adult Care
Transitioning Guide
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Fall/Winter 2011 Newsletter Now Available
CLICK HERE

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The Living with Cystinosis Survey Results
Now Available

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2011 CRN Family Conference is July 14-16 in San Francisco

 

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Cystinosis is a rare disease that primarily affects children. Without specific treatment, children with Cystinosis develop end stage kidney failure at approximately age nine.

The Cystinosis Research Network is an all-volunteer, non-profit organization dedicated to supporting and advocating research, providing family assistance and educating the public and medical communities about Cystinosis. We are a private, nonprofit 501(c)(3) corporation, Federal Tax ID 04-3323789.

The vision of the Cystinosis Research Network is the discovery of improved treatments and ultimately a cure for Cystinosis. Our commitment to our community lies in our tireless efforts to provide family assistance through facilitating several support groups as well as hosting an annual conference. At this conference we bring families and the medical community together in hopes to accelerate the accomplishment of our stated goals and objectives.

Our hope is that you find this website informative and compelling. A cure for Cystinosis can only be found through a highly cooperative approach that involves those afflicted by the disease, their families, and the medical community.

 

 
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