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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.
Join the Voices of MDS as we raise awareness, inspire others, and transform the future for all those impacted by MDS.
Join a powerful movement to amplify the voices of those impacted by MDS. By sharing your story, you can help support others, increase awareness of MDS, and drive change for a cancer too often overlooked.
Together, we're building a community and a collection of stories that honors real experiences and raises awareness. Your voice is a vital part of the story. Let it be heard.
Voices of MDS is a year-round initiative, that reflects key awareness moments and evolving community needs.

The MDS Exchange is a place where patients, caregivers, healthcare professionals, researchers, and advocates come together to engage in meaningful conversations and learn from one another.
Whether you're looking to ask a question, share your experience, follow discussions, or connect with people who understand the realities of MDS, you'll find a supportive, authentic community waiting for you.
Join a growing community where you can:
It's easy on the MDS Exchange - our online community.
Just follow these steps:
To get started, log in to the MDS Exchange. If you’re new, simply create an account—it only takes a minute.
Click on Settings in the top menu, then select Edit Profile to update your information.
Share your story in the space provided. You can also upload a photo if you’d like.
Decide whether you’d like your story to stay within the MDS Exchange community or also be featured on the MDS Foundation’s Story Wall web page.
Each report highlights the experiences, stories, and conversations shared by people living with MDS.
By sharing your story, you help others feel less alone, raise awareness of available support, and celebrate the resilience that defines our community. Sharing your story can also help the MDS Foundation understand the priorities and unmet needs of the MDS community - so that we can help make the future better for all those impacted by MDS.

Patient
After surviving APLm3 leukemia 2008-2010 and being pronounced ‘cured’ in 2014 I did my best to “het bsck into life”.
I, never feeling ‘myself’ and struggling with anemia(s) and all sorts of body pains…

Patient
Hello all, I’m gonna get down to the nitty-gritty first. Feb. 26, 2025 I was diagnosed with myelodysplastic syndrome MDS with SF3B1, SRSF2, CSF3R, and SETBP1 mutations identified. But unfortunately it…

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…
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.