🔥The 9th Round of Easy Loan, Earn $40 Reward is in progress❗️ ⏰ Promotion Period: January 15th - Feburary 15th, 2025 👉 Register now and check more details at gate.io/campaigns/358

#NedWeinshanker shared this while reading suleika jaouad book: “We were more than circumstantial friends. We were family.”  It’s what Bob Rosen set out to build — a community where patients are partners.  Join us: f.mtr.cool/lzvyigoolu   #FoundationForward #MPNResearch

Did you know? We assembled the Progression Research Network in 2020 to unite MPN experts & advocates around one goal: to collaboratively improve long-term outcomes for patients through research on MPN progression. This September, the 2025 PRN Summit continues that mission.

MPNs don’t appear overnight — mutations like JAK2 V617F can start decades before symptoms. Over time, mutant stem cells outcompete healthy ones, reshaping the bone marrow. Donate to research: goto.mpnresearchfoundation.org/4js24x1  #MPNResearch #FoundationForward #BloodHealth

This #ClinicalTrialsDay, we’re honoring Ned. Diagnosed with #MF. Transfusions every 3 weeks. Then he joined a clinical trial. 4 years later: no transfusions. Spleen reduced by 2/3.  Support clinical trials and stay informed: goto.mpnresearchfoundation.org/425ellc   #MPNResearch

MPNRF & Haymarket Medical Education launched a 2-part CME-accredited series on #PV diagnosis & treatment. Experts analyze survey data from 250 PV patients & 30+ clinicians to discuss evolving care strategies.  Earn CE credits: mycme.com/polycythemia #MPN #MedEd #BloodCancer

What’s a citation trail? It’s when one study sparks another — and another...  MPN Research Foundation has funded research with rich citation trails that stretch from years ago to today’s most promising advances.  Join us: goto.mpnresearchfoundation.org/425ellc #MPNResearch #CitationTrail

In 1997, Bob Rosen was diagnosed with PV — and found no roadmap. So, he built one.  25 years later, we’re moving #FoundationForward, empowering patients with research, resources, and support.  📥 Join our community: goto.mpnresearchfoundation.org/425ellc  #MPNResearch #RareDisease

627 voices. 31 countries. 1 shared mission.  From Bob Rosen’s vision to global momentum — the global response to our Unmet Needs Survey is shaping the future of MPN research.  👉 Reply with your country & join the movement.

72% of MPN patients haven’t heard of the MPN 10 — a tool for tracking symptoms & advocating in care.  We're moving #FoundationForward by raising awareness.  💬 Ever used it? Heard of it? Tell us below!  📥 Subscribe for updates: mpnresearchfoundation.org/subscribe-to-o… #MPNResearch #RareDisease

MPN patients + caregivers: Join us June 5 for FDA 101, a free webinar on how the FDA approves treatments — and how YOU can get involved. Recording included!  ⏰ 5–6PM CT 🔗 Register: us02web.zoom.us/webinar/regist…  #MPNVoices #FDA101 #MPNPathways

25 yrs ago, MPNs had no research roadmap. Then came Bob Rosen. His first grant helped lead to the discovery of JAK2 in 2005 — a breakthrough that changed everything. We're moving #FoundationForward. Join us: goto.mpnresearchfoundation.org/425ellc #MPNResearch #RareDisease #BobRosenLegacy

Thank you to everyone who donated to #FoundationForward — you're powering patient-driven research and honoring Bob Rosen’s legacy.  ⏳ Today’s the last day to give.  Let’s finish strong.  📥 Donate now: goto.mpnresearchfoundation.org/4js24x1  #MPNResearch #RareDisease #LastDayToGive

Meet Andrea Spica: MPN patient and 7-year post-transplant recipient turned advocate. From clinical trials to MPN Research Foundation Patient Impact Council, her journey fuels hope, research & support for others. 💪 Read her story: mpnresearchfoundation.org/patient_storie… #MPN #MPNAdvocate #PatientSupport

Join us today, 5–6 PM CST for FDA 101 — a crash course on how the FDA works and how MPN patients & caregivers can engage in the drug approval process. Featuring FDA expert Sarah Wicks.  🔗 Register: goto.mpnresearchfoundation.org/4knHgqZ  #MPN #FDA101 #PatientVoices #DrugDevelopment

Don’t leave your donation unmatched. Many employers will double your gift — turning $100 into $200 for MPN research. ✅ Check your match and donate: mpnresearchfoundation.org/donate-to-mpn-…  #EmployerMatch #DoubleYourDonation #MPNResearch #MakeItCount

Essential thrombocythemia (ET) affects about 39 in 100,000 in the U.S. Raised platelets means raised risk of clots, stroke & progression to myelofibrosis or leukemia. Know the signs. Support early MPN diagnosis. mpnresearchfoundation.org/newsletter-sig… #ETAwareness #BloodCancer #RareDisease

What do kidneys have to do with #MPNs? A clinical trial hold-up led Dr. Brandi Reeves to a new theory: MPNs may trigger silent kidney damage through clotting signals in neutrophils. She's testing it. 🔗 Read more: goto.mpnresearchfoundation.org/4kNfjsw  #MPNChallenge @UNC_Health #hematology

Young. Thriving. Overlooked.  Dana Turner is redefining what it means to live with a myeloproliferative neoplasm (MPN) — and why younger patients must be seen and heard.    Join our community and read her story: mpnresearchfoundation.org/subscribe-to-o…   #MPNAdvocate #RareButReal #PatientVoices

Why do some MPNs progress?  Scientist like Dr. Anandi Krishnan measure MPN mutant cell dysfunction to get answers: “Quality control is gone” — like “a factory where the pace has increased so much that the protein folding machinery is going awry.”  #MPNProgression #MPNs

We’re celebrating 25 years of MPN progress by honoring our founder, Bob Rosen. 💙  Join our webinar tomorrow to learn how you can support the next 25 years of life-changing blood cancer research.  5 PM CT  goto.mpnresearchfoundation.org/402Cjfd #MPNResearch #LegacyGiving