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chocolateKitten
Polycythemia Vera Discussion • March 5
Introducing Myself: PV with Jak2
Not sure if anyone actually participates in this group since I see the last post was in July so I guess this is me attempting to connect. I'm a 49 year old woman who was diagnosed with the Jak2 mutation back in 2016 when routine labs came back with barely elevated platelets. Since then I have added a few more diagnoses to my list. Wondering if anyone else has experience balancing their treatments and care for a variety of chronic illnesses. Thanks
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DianaSoto • Admin
Chronic Myelomonocytic Leukemia Discussion • February 26
testing again :)
testing again :)
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Fight4us
Myelofibrosis Discussion • February 23
Managing Myelofibrosis Before Treatment?
I have myelofibrosis and am not currently taking any meds but if symptoms worsen my hematologist/oncologist has mentioned Ojjaara as an option. Is anyone currently taking this & any side effects?
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apsmile
Myelofibrosis Discussion • February 18
Northeast Ohio
Hello to all the warriors. I'm looking for people living with a MPN in northeast Ohio, specifically Cleveland and the surrounding areas. I'd like to start a support group, unless you know of one. Let me know.