MDS Foundation, Inc.

🩸 Today marks the start of Blood Cancer Awareness Month 2024! This September, we are encouraging everyone to stay United for MDS as we work together to raise awareness of myelodysplastic syndromes (MDS), an often unrecognised and underdiagnosed type of blood cancer. MDS is a journey no one should face alone. #MDS patient organisations offer vital support and resources, with healthcare professionals providing essential care. Throughout this month, we will share informative content and insights from patients, caregivers and healthcare professionals to spark meaningful discussions about MDS. Don’t just #ThinkMDS—let’s stay #United4MDS to make a real difference. Stay tuned and join the conversation! For more information go to: https://lnkd.in/dJWk7Bbt

The MDS Foundation’s Spring/Summer 2024 Newsletter is now available online and in print. 📰 Packed with valuable educational resources, this issue is designed to support you and your loved ones on your journey with Myelodysplastic Syndromes (MDS). Dive into the latest insights, updates, and tips to help navigate the challenges of MDS. Explore our newsletter today and empower yourself with the knowledge you need. You can find the Spring/Summer 2024 Newsletter on our website at: https://bit.ly/3X7fG70 #MDS #MDSJourney #MDSTreatment #MDSSupport #ClinicalResearch

Join us on Tuesday, September 10th, 2024, at 12pm ET for an enlightening webinar on the MDS Foundation: Who We Are and What We Do!. Hear from our Executive Director, Tracey Iraca, on what The MDS Foundation has to offer. We will dive into all of our resources (printed, mobile apps, e-learning tools, events, and online community platforms). This webinar will also be hosted by our Director of Patient Care, and MDS nurse, Ashley Moncrief. Hear from Ashley on how she can help you - from priority referrals to our Centers of Excellence (COEs) to patient education. Don't miss this opportunity to gain a deeper understanding of The MDS Foundation and have all of your questions answered. Register today: https://bit.ly/3ZnaEGD #MDS #MDSJourney #MDSTreatment #MDSSupport #HopeForMDS

TODAY IS THE DAY! #WLD24 #BELEUKEMIAAWARE #BeLeukemiaAware #WLD24 #WorldLeukemiaDay #BloodCancerAwarenessMonth #yourenotalone #WorldLeukemiaDay #Leukemia #PatientAdvocacy #Alan Acute Leukemia Advocates Network CLL Advocates Network CML Advocates Network

On World Leukemia Day, The MDS Foundation stands in solidarity with everyone affected by leukemia and related blood cancers. Today, we honor the courage of patients, caregivers, and families navigating this challenging journey. As we continue to advance research, provide support, and raise awareness, we remain committed to empowering those impacted by Myelodysplastic Syndromes (MDS) and other blood cancers. Together, we can make a difference and bring hope to those who need it most. Donate today: https://bit.ly/3z57RH2 #CancerResearch #MDS #ClinicalTrials #MDSSupport #BloodDisorders

Mark your calendars. 📅 Join us for the MDS Patient and Family Forum in Houston on Saturday, September 7th, at 9:00 AM CDT. This free, in-person event will take place at the Marriott Medical Center Museum District in Houston, TX. This is your chance to connect with fellow patients and caregivers, while gaining valuable knowledge about MDS, the latest treatments, and emerging therapies from top experts. Don’t miss this opportunity to find support, answers, and hope, and to learn essential tips and strategies for living with MDS. Secure your spot today for this unique opportunity: https://bit.ly/4cTELsI #CancerResearch #MDS #MDSJourney #MDSTreatment #ClinicalTrials

The MDS Foundation is proudly celebrating 30 years of dedicated advocacy. 💙 The MDS Foundation was established three decades ago as the first non-profit organization entirely devoted to supporting those impacted by Myelodysplastic Syndromes (MDS). For 30 years, we've been a pillar of hope, providing resources, education, and support to MDS patients, caregivers, and healthcare professionals. Thank you for being a part of our journey. Together, we will continue to make a difference. We are the people who make hope work. #MDS #MDSF #MDSJourney #MDSTreatment #ClinicalResearch

September is World Blood Cancer Awareness Month, a time to shine a light on the struggles and triumphs of those impacted by blood cancers like Myelodysplastic Syndromes (MDS). As a rare and complex form of blood cancer, MDS presents unique challenges for patients, caregivers, and healthcare providers alike. For 30 years, The MDS Foundation has been at the forefront of providing support, education, and advocacy for the MDS community. We are dedicated to connecting patients with specialized care through our global network of Centers of Excellence, advancing research, and ensuring that no one faces this journey alone. This month, join us in raising awareness for MDS and honoring the resilience of those living with this rare disease. Together, we can make a difference in the lives of those affected by MDS and continue the fight against blood cancers. 💙 Donate today: https://mdsdonate.org #BloodCancer #BCAM #CancerResearch

Join us on Tuesday, September 10th, 2024, at 12pm ET for an enlightening webinar on the MDS Foundation: Who We Are and What We Do!. Hear from our Executive Director, Tracey Iraca, on what The MDS Foundation has to offer. We will dive into all of our resources (printed, mobile apps, e-learning tools, events, and online community platforms). This webinar will also be hosted by our Director of Patient Care, and MDS nurse, Ashley Moncrief. Hear from Ashley on how she can help you - from priority referrals to our Centers of Excellence (COEs) to patient education. Don't miss this opportunity to gain a deeper understanding of The MDS Foundation and have all of your questions answered. Register today: https://bit.ly/3ZnaEGD #MDS #MDSJourney #MDSTreatment #MDSSupport #HopeForMDS

Thirty years ago, only three pharmaceutical companies were pursuing cures and treatments for Myelodysplastic Syndromes (MDS). Thanks to the relentless efforts of The MDS Foundation, that number has grown to over 30 companies worldwide. Together with health care professionals, pharma partners, and dedicated donors, we're transforming the landscape of MDS research and care. Here's to three decades of progress and the promise of even more breakthroughs ahead. #MDS #MDSTreatment #MDSSupport #MedicalAdvancement #HopeForMDS