Rare Disease Day 2018 Polycythemia Vera MPN's PV MF ET Blood Cancer

Rare Disease Day 2018 and the one-year anniversary of my being open and telling everyone I have Polycythemia Vera. MPN Research Foundation: http://www.mpnresearchfoundation.org/ NORD National Organization for Rare Disorders: https://rarediseases.org/ "In honor of Rare Disease Day I'd like you all to know I have a rare chronic cancer called Polycythemia Vera. You've probably seen some of my posts on my page about it. It has been a struggle for the past couple years although I push everyday to feel better. Because it is rare there is not a lot of funding for a cure, I am generally private about such things but at this time I'm comfortable enough to share and hope that with more knowledge of this disease, something can be done to find a cure. We all have our battles, this just happens to be mine. Wishing you all health, peace and love! ❤ Amazon Smile: https://smile.amazon.com/ Please Like the video and subscribe to my channel, Thank you. www.instagram.com/nine_and_vine/ www.pinterest.com/NineVine/ www.twitter.com/NineandVine @NineandVine #polycythemiaVera #myeloproliferativeneoplasm #bloodcancer #nineandvine #treatment #symptoms #ninenvinempn #essentialthrombocythemia #myelofibrosis #MPN #MPNs #myeloproliferativeneoplasms #cancer #bloodcancerawareness #bloodcancerawarenessmonth #bloodclots #chronicillness #spoonie #chronicillnessawareness #chronicillnessblogger #chronicillnesscommunity #vlogger #cancervlog #interferon #pegasys #depression #mpnhumor

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