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Phone within the US
1-(800)-637-0839Outside the US only
1-609-298-1035Address
The MDS Foundation
228 Park Ave S
PMB 118983
New York
NY 10003-1502
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.
© 2024 MDS Foundation. All rights reserved.
One Voice Inspires, Many Voices Transform
Patient
I was diagnosed with MDS ring sideroblasts in 2018. I was on Procrit for two
years and then Luspatercept for two years. my hemoglobin dropped to 7.8
and had my first transfusion on August 1, 2025. I will be starting Imeltestat
on August 20th. I have been dizzy, lightheaded and fatigued.
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.
Discover genuine accounts from individuals navigating MDS. These stories reflect the real challenges and strengths within our community.
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…

Patient
I wanted to rejoice in the Lord and testify to the power of prayer, healing, and deliverance - and God directing my Doctors and path.
In August of 2019, I was diagnosed with Myelodysplastic Syndrome (M…
Patient
I was diagnosed with MDS in November 2022. My immature white blood cell count was very high, 15.6% - (at 20% it is Leukemia; normal is less than 1%). My doctors brought that down with chemotherapy a…