Join the MDS community. Become a Professional Member of The MDS Foundation and connect with experts around the world who are committed to advancing research in MDS. Membership includes grant opportunities, resources, discounts, and more. Learn more: bit.ly/3DjefMB

Join us on October 19 at Boston Common for the Move for MDS walk! Come together for a day of support, and fun, including yard games, face painting, and more. This event is more than just a walk, it’s a movement of hope and progress. Register today: bit.ly/3ZAqnBj

We’re on a mission to raise $1 million this year to support those affected by MDS. Every donation helps provide free education, support, and resources. Your generosity keeps us at the forefront of patient care, advocacy, and hope. Donate today: bit.ly/donatespr25

Join us on December 5, 2025 in Orlando, FL for 𝗠𝗼𝗺𝗲𝗻𝘁𝘂𝗺 𝗶𝗻 𝗠𝗗𝗦: 𝗠𝗮𝗸𝗶𝗻𝗴 𝗣𝗿𝗼𝗴𝗿𝗲𝘀𝘀 𝗮𝗻𝗱 𝗦𝗵𝗮𝗽𝗶𝗻𝗴 𝗮 𝗕𝗲𝘁𝘁𝗲𝗿 𝗙𝘂𝘁𝘂𝗿𝗲. This event will highlight advances in biology, genetics, and pathogenesis of MDS. Learn more: bit.ly/45gQ398

Do you want to make a difference in the MDS community? We're looking for individuals to help expand our network of support groups. If you're interested in leading a group in your area, we can help with administrative and financial support. Learn more: bit.ly/4ilvahb

We’re excited to introduce MDS Exchange, the new and improved version of our MDS Message Board. Created with the MDS community in mind, this platform offers a more accessible and supportive space for patients, caregivers, and loved ones. Learn more: bit.ly/3Cf0Fdi

Join us as a Professional Member and connect with a worldwide network of experts dedicated to improving outcomes in MDS. Enjoy exclusive benefits, including access to research grants, expert-led resources, discounts, and more. For more information, visit: bit.ly/3DjefMB

Our upcoming Patient and Family Forums are almost here, and we hope you’ll join us. These events are designed to bring together MDS patients, caregivers, and families with leading experts. Learn about diagnosis, treatment, and options. Register today: bit.ly/4kv2WRS

The MDS Collective has introduced two new myMDS resources, created to help simplify important terms and concepts for those living with myelodysplastic syndromes (MDS). Materials available via digital download on our website here: bit.ly/45mP9YJ

MDS can lead to RBC transfusion-dependent anemia, risk of infection, and potential progression to AML. The ELEMENT-MDS Study is enrolling adults 18+ with MDS who are transfusion-independent and have not received prior ESA treatments. Learn more: BMSClinicalTrials.com/ELEMENT

Becoming an MDS Foundation Center of Excellence comes with the benefit of access to real-time updates on industry advancements. From drug approvals and foundation news to new resources and events, you'll stay connected to critical information. Learn more: bit.ly/417tC3S

We're in the running for #SXSW2026. Our proposed panel highlights how #AI + #patientadvocacy can transform care for rare diseases like #MDS. 🗳️ Vote to help us bring this conversation to the main stage: bit.ly/4m45zv3 #SXSWPanelPicker #PatientVoice #MDSAwareness

Join us on December 5, 2025 for Momentum in MDS: Making Progress and Shaping a Better Future. We will highlight advances in biology, genetics, and pathogenesis of MDS, while addressing topics such as morphology and more effective therapies. Learn more: bit.ly/45gQ398

Join us in Little Rock, AR on September 13 for our Patient & Family Forum. Designed to bring together MDS patients, caregivers, and families with leading experts. Gain insights into diagnosis, treatment options, and living well with MDS. Register today: bit.ly/458wtdU

We’re on a mission to raise $1 million to support those affected by MDS. For over 30 years, we have remained dedicated to providing education, support, and resources. Together, we can transform the future for everyone impacted by MDS. Donate today: bit.ly/3IMrWGR