Join the Fight Against MDS

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Voices of MDS

Share Your MDS Story

One Voice Inspires, Many Voices Transform

Janice's Story

Patient

I was sent to a hemotologist because of routine blood tests showing low WBC and low platelets.  Since then I have had a bone marrow biopsy and diagnosed with low risk MDS, bilineage cyopenia and blast cells of 2.9%. Also, 3 acquired mutationed genes.  I was told that we would monitor my blood.  I wanted to look for others that have also been diagnosed with this and hopefully learn more about MDS.

Share Your MDS Story

Your story matters. If you'd like to contribute your experience with MDS and inspire others in our community, we invite you to share. Your voice can make a meaningful impact and offer support to those on a similar journey.

The MDS Foundation proudly partners with the following organizations

MDS AllianceKnow AMLALANThe NHLBI Blood Health Network

Get in touch

Email

support@mds-foundation.org
hcp@mds-foundation.org

Phone within the US

1-(800)-637-0839

Outside the US only

1-(609)-298-1035

Address

The MDS Foundation
228 Park Ave S
PMB 118983
New York
NY 10003-1502

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The MDS Foundation is a global nonprofit 501(c)(3) advocacy organization (EIN 22-3283911), supporting patients, families, and healthcare providers in the fields of MDS and related diseases for over 30 years.

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