Speaking Up About My Mpn Diagnosis: Journey To Acceptance

Speaking Up About My MPN Diagnosis: Journey to Acceptance

Speaking Up as an MPN Caregiver: Our Side of the Story

Speaking Up About Symptoms of Myeloproliferative Neoplasms (MPNs): Taking an Active Role

Laurie’s MPN journey: from an ET diagnosis to MF

Fine Is Not Enough: Asha’s MPN Story

Fine Is Not Enough: Mickey’s MPN Story

My MPN Journey, Getting the Best Care After ET and MF Diagnoses

Patient Empowerment Network

Fine Is Not Enough: Christine’s MPN Story

Owning her quest for disease education: Louise's myelofibrosis (MF) story

Why Fine Is Not Enough for Louise’s MPN Journey

Guiding My MPN Journey with the NCCN Guidelines for Patients®: MPNs

Speaking Up With Your Healthcare Team: Advocating for Better Care

Important Questions About Symptoms and Living With Your MPN

My Journey of Living With a Myeloproliferative Neoplasm for 30 Years

Patient Empowerment Network

The Unknown: Nick’s MPN Story

A Care Partner’s Journey: How Life Goes on After an MPN Diagnosis

Patient Empowerment Network

Marilyn’s MPN Story: The Importance of Finding Trust and Building Support

A Conversation with an MPN Specialist: From Diagnosis to Current Treatment Options

MPN Advocacy & Education International

Diagnosed Early in Life With Polycythemia Vera: Todd’s MPN Story