About the Foundation
The Editor's Desk
Funding the Foundation
Patient Information
MDS Centers of Excellence
International Patient Registry
International Research Updates
Contacting the Foundation
Clinician Resources
Employment Opportunities
Links and Archive Articles
Currrent Newsletter

US Patient Liaison: Audrey Hassan • Patientliaison@mds-foundation.org • P.O. Box 353, Crosswicks, NJ 08515
Phone: 1-800-MDS-0839, outside the US only: 609-298-6746 • Fax: 1-609-298-0590
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EU Patient Liaison: Sophie WintrichSwintrich@mds-foundation.org
The Rayne Institute, Denmark Hill Campus, 123 Coldharbour Lane London SE5 9NU, UK Tel: +44 20 7733 7558

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Forums
Forums

 

Overview of the Foundation

The Myelodysplastic Syndromes Foundation was established by an international group of physicians and researchers to provide an ongoing exchange of information relating to MDS.

Until the Foundation was set up, no formal working group had been devoted to MDS. During the past decade we have conducted eight international symposia —in Austria, England, the United States, Spain, Czech Republic, Sweden, France, and Japan. The Ninth International Symposium is being held in May 2007 in Florence, Italy.

A major Foundation effort is our international information network. This network provides patients with referrals to Centers of Excellence, contact names for available clinical trials, sharing of new research and treatment options between physicians, and extension of educational support to both physicians and patients.

In response to the needs expressed by patients, families, and physicians, we have established patient advocacy groups, research funding, and physician education.

The MDS Foundation is a publicly supported organization, exempt from federal income tax under section 501(C)(3) of the IRS code.

 

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Frequently Asked Questions About MDS
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The MDS Foundation is supported by unrestricted educational grants from the sponsors shown on the left.