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A patient from Cuba transformed complex #MPN biology into a powerful human story.
Living with polycythemia vera is challenging anywhere.
Support global patient education:
• Donate
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• Join MPN World

#PolycythemiaVera #MPNCommunity #GlobalHealth #PatientAdvocacy

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20 years after her ET diagnosis, MJ Tooey’s journey is one of research, resilience & trust. From treatment setbacks to advocacy wins, her care team partnership made all the difference.  

Read her story here: https://mpnresearchfoundation.org/patient_stories/mj/

#MPNs #PatientVoice #MPNCommunity

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👏 We’re proud to support the #MPNHeroes Recognition Program by @VoicesofMPN.

This year, MPN Research Foundation’s Director of Patient Engagement, Sara Douglas, was honored to serve as a judge — helping recognize the inspiring contributions of this year’s heroes.

#MPNCommunity #PatientAdvocacy

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#BloodDisorderSupport #RareDiseaseAwareness #MPNCommunity #HealthcareInnovation #MPNEducation #SurvivorStories #BloodDisorderResearch

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