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Profile picture for bluegrasspv2018 @bluegrasspv2018

@hipsu5, I am also a member of the myeloproliferative neoplasm (MPN) club. My condition is called Polycythemia vera (PV). PV is an ugly sister of your ET and in the MPN family. In May of 2018 I was diagnosed with PV after a routine blood test with platelets in the 685,000 range. Fast forward to 2026. I take one 500 Hydroxyurea (HU) every morning. I call this "Chemo in a pill." I have little or no symptoms. I am determined not to let this condition rule my life. I thought my diagnose was the end, it turned out to be a new beginning for me. I go to my gym 3 times a week, I stay active with my veteran's organizations and am on my American Legion Honor Guard detail. I am a volunteer for Hosparus where I visit veterans on hospice. I have fatigue every evening. Is that from PV or just being an old timer? Who knows? Today is my 67th birthday. Everyday is a new adventure. Long live the fighters!

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@bluegrasspv2018

I'm in awe. RESPECT.

@bluegrasspv2018 Great Attitude!.. Almost my story.. was dx in 1992 with ET been on "chemo pill" (my name for it too) since then, and now at 68, have converted to PV and waiting to see at next blood draw if something else pops up! I still work full time as a Nursing Director at a home health agency and lately have been battling long covid : ( . This just means MORE fatigue. I find the immune system does not work well enough to kick things out quickly once you get sick). Been fighting for a long time, and taking it all in stride.. still walk the beaches, and hang out with friends, every day is a gift - keep your loved ones close and try not to isolate huggs