MDS Foundation (@MDSFoundation) header
MDS Foundation (@MDSFoundation) profile picture

The MDS Foundation is a global nonprofit raising awareness of myelodysplastic syndromes (MDS), a rare and often undetected blood cancer. 🔬🩸

Global
Joined April 2009
Photo by MDS Foundation (@MDSFoundation)Photo by MDS Foundation (@MDSFoundation)Photo by MDS Foundation (@MDSFoundation)Photo by MDS Foundation (@MDSFoundation)Photo by MDS Foundation (@MDSFoundation)Photo by MDS Foundation (@MDSFoundation)Photo by MDS Foundation (@MDSFoundation)Photo by MDS Foundation (@MDSFoundation)Photo by MDS Foundation (@MDSFoundation)Photo by MDS Foundation (@MDSFoundation)
You’re invited to connect with your MDS community in Phoenix, AZ. Our Patient & Family Forum is taking place November 14 from 8:00 AM–2:00 PM, bringing patients, caregivers, and loved ones together for a day of education, and support. Register today: bit.ly/4rQj0lY
112
We invite healthcare professionals to participate in our MDS Healthcare Professionals Survey. The insights you share will guide our programs, educational efforts, and initiatives. Take a few minutes to share your voice and help us move MDS care forward: bit.ly/4qLRgyz
93
Faron Pharmaceuticals is conducting a placebo-controlled trial of bexmarilimab (BEXERA) combined with standard of care azacitidine. Newly diagnosed patients 18 or older with higher-risk MDS may qualify. Learn more at bit.ly/bexera or email [email protected].
112
Today is MDS World Awareness Day. This year, YOU told us that Understanding Your Treatment Options is what our community wanted to see in the spotlight. Today, we are sharing this resource, created in response to what you told us matters most to you. bit.ly/4zwkKnh
2
1
2
222
Make the most of your ASH weekend by joining the MDS Foundation for our Friday Satellite Symposium, MDS In Practice: Navigating Complex Decisions Across the Disease Spectrum, on Friday, December 11, 2026, from 7:00–10:00 AM. Register today: bit.ly/4iQcw4l
123
At the MDS Foundation, we’re proud to stand alongside patients and families at every step, providing trusted education, meaningful support, and connections to a community that understands. Because no one should have to face MDS alone. 💙
2
131
More options are needed for MDS A clinical research study is now enrolling for MDS and MDS-related anemia To learn more and find out if you qualify visit bit.ly/ELRiSETakeda or contact: Lisa Liskey [email protected] (609) 298-1600 x.201
1
121
Thank you to everyone who came yesterday for the Boston Move for MDS Walk. Your enthusiasm, compassion, and commitment made the day truly unforgettable. Couldn’t join us in Boston? Register for our Virtual Move for MDS Walk and walk wherever you are: bit.ly/4dL9DhV
126
An early look at our new MDS resource, made possible by you! Hundreds of you voted to shine a spotlight on ‘Understanding Your Treatment Options’ as the focus of #MDSWorldAwarenessDay Live first on the MDS Exchange, ahead of its release on October 25: bit.ly/4zwkKnh
116
Join us April 14-16, 2027, for the 19th International Congress on Myelodysplastic Syndromes (MDS 2027). Connect with leading experts, discover the latest research and advances, and explore what’s next for MDS care. Register today: mds.kenes.com/ #MDSCommunity
1
98
The Boston Move for MDS Walk is happening THIS SUNDAY, October 18. Join us for a meaningful day of coming together to honor  those affected by MDS. Gather your family and friends, lace up your shoes, and get ready to #MoveForMDS Register today: bit.ly/4eCYlfe
1
1
113
Living with MDS and MDS-related anemia means constant blood transfusions, unpredictable fatigue, and shortness of breath. Consider participating in clinical research exploring potential options for adults with MDS and MDS-related anemia. Learn more: bit.ly/RENEWTakeda
88
One of the benefits of our Center of Excellence partnerships is the opportunity to connect more patients with specialized MDS care. We can connect patients with Centers of Excellence for second opinions, clinical trials, and specialized care. Learn more: bit.ly/3thyQMA
1
108
Join the MDS Foundation during your ASH weekend for our Friday Satellite Symposium, MDS In Practice: Navigating Complex Decisions Across the Disease Spectrum, taking place Friday, December 11, 2026, from 7:00–10:00 AM. Register today: bit.ly/4iQcw4l
3
209
Only 10 days to go. ⏰ Join us on October 18 as we come together with patients, caregivers, families, friends, and supporters to walk for the MDS community. Register today and join the movement: bit.ly/4eCYlfe
108
Connect, learn, and find support at our Patient & Family Forum in Kansas City, MO. Join us on October 24 from 9:00 AM–2:00 PM for a day dedicated to patients, caregivers, and loved ones in the MDS community. Register today: bit.ly/4xq33ox
113
Rigel Pharmaceuticals, Inc. Is conducting a study with R289 on patients who are relapsed/refractory/resistant to prior LR-MDS therapies. Every participant will receive R289. Determine eligibility at bit.ly/IRAKRigel or contact Lisa Liskey at [email protected]
1
140
You voted. We listened. 💙 This MDS World Awareness Day (Oct 25), we’re putting Understanding Your Treatment Options in the spotlight, the #1 topic chosen by our community. Join the conversation on the MDS Exchange: mds-foundation.org/support/v… #VoicesOfMDS #MDSWorldAwarenessDay
116
Join us on November 7 from 12:00–3:00 PM EDT for a global virtual event created for the MDS community. You’ll also have the opportunity to ask questions and find support. A Zoom link will be sent to your email after registration. Register today: bit.ly/4hRHhES
140
This Health Literacy Month, the MDS Foundation is highlighting the educational resources available to help people impacted by MDS better understand and make informed decisions about their care. Explore the MDS Foundation’s educational resources: mds-foundation.org/
115