Essential Thrombocythemia: Looking for information and support
I was recently diagnosed with Essential Thrombocythemia, a rare incurable blood cancer. Platelet count aside, I am asymptotic. This current condition morphed from (constitutional) thrombcytosis, something I’ve lived with for 25+ years. While the new diagnosis was the result of a bone marrow aspiration and biopsy, my age was an additional factor, which was completely disarming, having been walking around unwittingly for the past 8 years! While at the low end of risk for clots, heart-attacks and stroke, nothing has truly changed - except the “C” word. No chemo yet, but active discussion about hydroxyurea. Uncertainty about ET is anxiety provoking and swoethatl, but I’m feeling betrayed by my blood. I’m looking for all information about ET, the chemo and support.
Thanks!
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Lots of us on this forum take HU.
Many of us have no problems with it.
Unfortunately fatigue, headaches and dry skin are "gifts" of ET itself.
They're indicators that getting our platelets under control is essential.
We are so fortunate there are options to treat our cancer. Work with your own doctor, and you will find the treatment option that's best for you.
This is exactly what I heard from my two ET doctors. According to them it could be real trend. Or it is just because more and more tests are being done to disclose this ET medical condition. Most of the time ET is symptom free.
It will be interesting to follow this .
just want to share what I came across on internet regarding ET and treatment options. This seems to me to be very good discussions among doctors specialized in the ET disease area. The ET case discussion is in Ep 14 to EP 19. I found it very informational. https://www.targetedonc.com/expert-perspective-tumor-board/myeloproliferative-neoplasms
Thank you so much for proving this link, sdduan.
It's really interesting to hear high-level MPN specialists talking about ET. In just a few minutes, I learned a lot.
My favorite line: The progression of ET to myelofibrosis [MF] or acute myeloid leukemia [AML] is not seen very often.
Cheers!
Thanks for sharing this information. It was very very interesting.
These discussions are very interesting. Thank you for sharing. I will watch them again. So much to learn when you’re new to this experience.
It is actually way more complicated than I was originally led to believe.