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Mary L. continues to share her story in this 2nd video about getting diagnosed with myelofibrosis. In this segment, Mary goes in depth about how she was led to her first MF treatment (Pegasys) and the impact of a real lack of shared decision making between her and her oncologist. She also describes getting tested for gene mutations and how that affected treatment decisions, as well. In the end, she underwent Pegasys and then hydroxyurea. Mary describes both treatments and how she got through side effects. Mary spends a good amount of time also talking about switching not just doctors, but hospitals/healthcare providers, and the shift that happened following her decision to advocate for herself. Thank you for sharing your story, Mary! In this Series: Our 3-part series with Mary covers everything from getting diagnosed with a rare cancer (this video), the ups and downs of going through myelofibrosis treatment, including Pegasys and hydroxyurea, and the impact of living with a rare cancer. Videos: 1) Getting diagnosed with a rare cancer: • Getting Diagnosed with a Rare Cancer: Myel... 2) Myelofibrosis Treatment & Side Effects (Pegasys, Hydroxyurea): (this video) 3) Living with a rare cancer (myelofibrosis): • Living with a Rare Cancer (Myelofibrosis) ... Full story & transcript → Updated Soon at www.ThePatientStory.com Join Our Community: Website : https://www.thepatientstory.com/ Facebook: @ThePatientStory Instagram: @ThePatientStory Twitter: @patient_story ______________________________ The interview has only been edited for clarity. Contents of this video: 00:00 - Intro 08:00 - The struggle to get heard as a patient 09:20 - Primary Vs Secondary Myelofibrosis 12:25 - Seeing the right specialists 14:35 - Starting Hydroxyurea 17:15 - Hydroxyurea Side Effects 20:26 - Finding the right care for you ______________________________ #thepatientstory #myelofibrosis #rarecancers #patientstories #cancerstories #cancerpatient #cancersurvivor #MPN #myeloproliferativeneoplasms #MF #ET #PV #bloodcancer