MDS Foundation

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

[MDS Foundation @MDSFoundation]

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: https://t.co/1Zi4dOnUwW

#VoicesOfMDS #MDSWorldAwarenessDay

[MDS Foundation @MDSFoundation]

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: https://t.co/9myk8i8PXD

[MDS Foundation @MDSFoundation]

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: https://t.co/M5EppF2qtq

[MDS Foundation @MDSFoundation]

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 created with patients, caregivers, and loved ones in mind.

Register today: https://t.co/5PsXotsWGc

[MDS Foundation @MDSFoundation]

A huge thank you to everyone who joined us yesterday for the Move for MDS Walk in Los Angeles. 👟

Your energy, support, and dedication helped make the day so special.

Couldn’t join us in Los Angeles? Register for our Virtual Move for MDS Walk: https://t.co/gYYVGlbqsQ

[MDS Foundation @MDSFoundation]

Today, on World Cancer Research Day, we recognize the researchers, clinicians, patients, and advocates working to turn questions into discoveries.

For the MDS community, research is a pathway toward better treatments and a future where every MDS patient has more options.

[MDS Foundation @MDSFoundation]

Please join us in welcoming two new members to the MDS Foundation team!

We’re excited to welcome Victor Gonzalez, Vice President of Partnerships & Programs, and Stacia Anderson, Vice President of Finance & Operations, to our growing team.

[MDS Foundation @MDSFoundation]

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 help us move MDS care forward: https://t.co/YNAlRwFfC1

[MDS Foundation @MDSFoundation]

Voting closes Sept 30, the final day of Blood Cancer Awareness Month.

Help shape what MDS World Awareness Day shines a spotlight on - and put what matters most to our community at the center of the conversation on October 25.

Vote today → https://t.co/lSLyBhyHpk

[MDS Foundation @MDSFoundation]

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 https://t.co/1bwzos9fbR or contact:
Lisa Liskey
[email protected]
[phone] x.201

[MDS Foundation @MDSFoundation]

Every decision we make begins with a question: How will this help our patients?

That question guides the programs we create, partnerships we cultivate, and every dollar we invest.

With your support, we can continue to answer that question.

Donate Today! https://t.co/A2tBX5Ddhs

[MDS Foundation @MDSFoundation]

On October 18, 2026, the MDS community will come together for the Boston Move for MDS Walk, a meaningful day to honor loved ones, celebrate those affected by MDS, and show support.

Register today and join the movement: https://t.co/lyyrOMohey

[MDS Foundation @MDSFoundation]

Join us 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 AM-10:00 AM.

Register today: https://t.co/6Q29GPH2a5

#ASH26

[MDS Foundation @MDSFoundation]

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: https://t.co/CFC2LLsAOW

[MDS Foundation @MDSFoundation]

What should MDS World Awareness Day shine a spotlight on this year? Cast your vote by September 30, the final day of Blood Cancer Awareness Month, and help decide what the MDS community puts at the center of the conversation on October 25.

Vote today: https://t.co/lSLyBhyHpk

[MDS Foundation @MDSFoundation]

Join us on September 26 from 9:00 AM - 2:00 PM for a day dedicated to education, connection, and support for those affected by MDS.

This forum offers an opportunity to learn from experts about treatment options and emerging therapies.

Register today: https://t.co/qxjpTv7IhP

[MDS Foundation @MDSFoundation]

Get ready to Move for MDS in Los Angeles. 👟

Join us on September 27, 2026, for the Move for MDS 5K.

Together, patients, loved ones, friends, and MDS advocates can help raise awareness, support research, and show strength in numbers.

Register today: https://t.co/3ZY5bYFUJ9

[MDS Foundation @MDSFoundation]

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 https://t.co/Q5WK1eFmE8 or contact Lisa Liskey at [email protected]

[MDS Foundation @MDSFoundation]

Join us on September 12, 2026, at 12:00 PM ET for Caregiver Training 101.

Brittany McCoy, MPAS, PA-C, brings more than 10 years of experience in malignant hematology, cellular therapy, and bone marrow transplantation.

Register today: https://t.co/AeAD3PXjkG

[MDS Foundation @MDSFoundation]

This September, for Blood Cancer Awareness Month, we're putting the MDS community at the center of MDS World Awareness Day (Oct 25). We are asking YOU to help decide.

Vote by September 30 and help shape the focus of MDS World Awareness Day.

Vote now → https://t.co/lSLyBhyHpk