MDS Foundation, Inc.

There are many benefits to becoming an MDS Foundation Center of Excellence, one including gaining real-time awareness of industry advancements. From timely communications on foundation updates, drug approvals, and community awareness events to new resource development, you’ll stay informed and connected to critical updates that support patient care. Partner with us to drive progress and make a difference in the MDS community. Learn more about becoming a Center of Excellence: https://bit.ly/40oGSBw #MDS #MDSTreatment #TreatmentOptions #ClinicalResearch #HopeForMDS

If you were not able to attend one of our Move for MDS walks, you can still make an impact by joining our Move for MDS Virtual 5K Walk anytime, anywhere. 🌍 Whether you choose to walk solo, with loved ones, or alongside your regular walking group, you decide the time and place—day or night. Walk to show your support for those affected by MDS and be part of this inspiring movement. 💙 Register today: https://bit.ly/4dooHz1 #MDS #MDSJourney #MDSSupport #HopeForMDS

Did you have the support you needed during your cancer journey? The Cancer Experience Registry (CER) survey from the Cancer Support Community (CSC) is designed to explore the emotional, physical, practical, and financial effects of cancer. It helps ensure patients and caregivers receive the support they need. By participating in the CER survey, you can add your voice to this vital research. For every 100 participants from the Myelodysplastic Syndromes community, The MDS Foundation will receive $25,000 to fund programs and research for MDS patients, caregivers, and their families. Share your opinion today: https://bit.ly/3UvGbTr #CancerResearch #MDSTreatment #ClinicalTrials #MDSSupport #ClinicalResearch

This year's symposium, MDS 2024: Let’s Overcome the Challenges, promises lively discussions and debates led by some of the most notable research and treatment experts in the field of MDS. Gain the latest insights and developments that can enhance your clinical practice and improve patient care. Don’t miss this opportunity to connect, learn, and elevate your understanding of MDS. Register now (virtual or in-person): https://bit.ly/4fHJGhD This symposium is jointly provided by The Myelodysplastic Syndromes Foundation, Inc., and AKH Inc. #MDS #MDSTreatment #ClinicalResearch #Innovation #MedicalAdvancement

MDS Patient Study Opportunity. 📢 If you’re an MDS patient with anemia who hasn’t received treatment yet, you may be eligible to participate in a clinical study with Akesobio. To see if you qualify and to find a participating center near you, visit www.sparkcures.com and search for AK117-205. For more information or assistance, reach out to Ashley Moncrief, RN, BS at The MDS Foundation at 1-800-637-0839 ext. 210. Don’t wait—enroll today and be part of advancing MDS research. #CancerResearch #MDSTreatment #TreatmentOptions #ClinicalTrials #ClinicalResearch

The MDS Foundation’s Patient Message Board is a quick and easy way to connect with others in the MDS community. Whether you’re seeking answers to basic questions or looking to share your journey, this space is here for you. Engage with patients, caregivers, and experts in a supportive environment. You're never alone in your fight against MDS – we’re here together. Learn more about our MDS Patient Message Board: https://bit.ly/2HV0Nzn #MDS #MDSJourney #MDSTreatment #MDSSupport #HopeForMDS

At The MDS Foundation, we deeply appreciate the dedication and love that family caregivers provide to those living with Myelodysplastic Syndromes (MDS). You are the unsung heroes, offering unwavering support, compassion, and strength every step of the way. We recognize the challenges you face and are here to support you with valuable resources, education, and a community that understands. Thank you for all you do—you make a world of difference. #MDS #MDSJourney #MDSSupport #HopeForMDS

Join us for a new Myelodysplastic Syndromes (MDS) Support Group on Zoom, led by Junia Papas, PhD, CA—a dedicated MDS patient committed to making a difference. Whether you’re a patient, caregiver, or loved one, this group is here to offer support, strength, and shared understanding in facing the challenges of MDS together. 📅 Schedule: The 1st Tuesday of each month at 1pm ET 📍 Venue: Zoom ✉️ For more information or to register, please reach out to Junia at [email protected] To learn more about the facilitator, visit: https://bit.ly/4feckqP Let’s build resilience, find hope, and support one another through this journey. #MDS #MDSJourney #MDSTreatment #MDSSupport

November is National Marrow Awareness Month. 🩸 Join The MDS Foundation in celebrating this vital month as we honor the incredible achievements of physicians dedicated to transplant research. We also extend our heartfelt gratitude to the selfless individuals who have donated stem cells and bone marrow to save lives. Your generosity makes a profound difference in the fight against MDS and other blood cancers. Together, let's raise awareness and highlight the importance of marrow donation. 💙 #MDS #ClinicalTrials #BloodDisorders #TreatmentOptions #ClinicalResearch

Rare Patient Voices proudly welcomes MDS patients and family caregivers to participate in a compensated survey, offering a chance to contribute to impactful research. This is your opportunity to make a meaningful difference. Learn more: https://bit.ly/3PF51Np #MDS #MDSJourney #MDSTreatment #TreatmentOptions #ClinicalResearch