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.
Every gift helps patients, caregivers, and healthcare professionals access life-saving resources, support, and education. Together, we can make a difference. Even a small contribution can create a big impact. Thank you for your generosity.
One Voice Inspires, Many Voices Transform
Patient Advocate
From a young age, my parents instilled in me the importance of easing the burdens of others and leaving the world better than I found it. That early lesson shaped who I am and why I have always been driven by purpose. For me, purpose has never been found in strategy decks or reports – it’s found in the lives you touch. That is why my work has always been about people, impact, and the change we can spark together. That’s what led me to the MDS Foundation, and why blood cancer has become such a deeply meaningful cause in my life.
As CEO of the Foundation, I am reminded every day that MDS is more than a diagnosis – it’s a life suddenly turned upside down. Patients and families face fear, uncertainty, and overwhelming complexity. To stand with them, to offer education, support, and community in the middle of that storm, is both humbling and a privilege. Knowing that our work can make even just one person feel less alone and more hopeful today is what inspires me every day.
At the same time, I am equally committed to the long view. It is not enough to help people navigate the present – we must also simultaneously accelerate research, invest in science, and work relentlessly toward a future where patients have better treatments and, ultimately, cures. That balance of urgent support and future solutions is what makes this work so powerful and personally meaningful.
At the MDS Foundation, we are dedicated to improving the lives of everyone affected by MDS. We connect patients, caregivers, and healthcare professionals with the knowledge, resources, and community they need to face this disease with strength, understanding, and hope.
And so, this Blood Cancer Awareness Month, I invite you to share your story – because your story matters. One voice inspires, but many voices have the power to transform the future beyond what we ever thought possible.
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
Two years ago in September (2023) I became very ill. I went to Urgent Care with a bad cough and just feeling bad. They diagnosed me with Bronchitis and gave me a prescription and sent me on my way. …
Patient
I was initially diagnosed with MDS in 2014 after a bone marrow biopsy, although prior blood tests indicate that the start predated this date. Two follow-up BMBs confirmed the diagnosis. My classificat…
Patient
Hi, my name is Christina, and my journey with MDS began in 2021. With no previous medical history, my diagnosis came as a complete shock. My family and I quickly searched for a care team so I could be…