Virtual Roundtable on Myelofibrosis (MF): Ask Your Questions to an MPN Expert
- 7 days ago
- 1 min read
We invite you to join a virtual roundtable designed for patients and caregivers living with Myelofibrosis (MF)—one of the rarer but most impactful Myeloproliferative Neoplasms (MPNs) when it comes to quality of life.
🗓 Monday, May 12th, 2025
🕕 6:00 PM – 7:00 PM (CEST)
📍 Online via Zoom
Content guide
About the roundtable
This session will feature Dr. Natalia de las Heras (León, Spain), a leading hematologist in MPNs based in León, Spain. With her extensive clinical experience, Dr. de las Heras will share valuable insights on diagnosis, symptoms, progression, and treatment options for Myelofibrosis.
This is your space to ask questions
This roundtable is interactive and focused on real community concerns. You can submit your questions directly in the registration form, or send them in advance to events@gmpnsf.org with the subject line "Roundtable MF". We’ll do our best to address as many as possible during the live session.
Who should attend?
Patients diagnosed with Myelofibrosis
Caregivers and family members supporting someone with MF
Anyone seeking to better understand this rare MPN
The event will be conducted in Spanish, with simultaneous interpretation into English.
This roundtable is organized by the Global MPN Scientific Foundation, as part of our mission to empower the MPN community through education, connection, and patient-centered support.
We look forward to seeing you there—and hearing your questions.
Comments