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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I've been on HU for 3 years. The first year was the worst, hair loss, bone pain, diarrhea, multiple BM daily. After a year my gut got used to HU, my hair is back to normal, still have some bone pain.....and of course fatigue, which I just soldier thru. for leg cramps I make sure I eat fruit & veggies high in potassium???? works for me......This year my skin is very flakey, don't know what's causing it.....
My hematologist told me yesterday that CBD would not lower my platelets. So I will not be getting anymore. My BMB came back with mild fibrosis. I’m guessing from what he said that’s a good thing. Told me to continue with HU MWF. Go back in four weeks for a blood draw. As bad as it is it could always be worse.
Have you also been given Allopurinol to prevent gout and cramps - stops the build up of crystals. Im on Hydrea 500mg M-S Sun 1000mg 75mg Aspirin - 300mg Allopurinol daily on top of all the other meds - I'm between ET Jak2 - chronic prefibrotic myelofibrosis diagnosed May this year - feel fatigued and have some good days.
Thank you for your comment, it has given me hope!
My hair smells great even if I have less of it.
Chelated Magnesium Complex (capsules) works for my restless leg problem and it even helps me relax to sleep. I've tried ALL kinds of magnesium pills that did nothing! Believe me, it has to be chelated to be absorbed, and the complex of m.glycinate, m.malate, m.citrate and m.taurate does a lot of good in many areas of muscular tension and neurologic disorders. I get my Magnesium Complex capsules on Amazon if that helps. Good luck.
I take Magnesium Citrate and Co Q10 to help prevent my going into AFib. So maybe it is helping with the Hydroxyurea problems. I am also only taking HU on M/W/F.
I will look for the complex. Avoid magnesium oxide as it can cause loose bowels.
Eileen
Respecto a la fatiga, intento descansar cuando puedo y realizar algo de actividad física (me cuesta pero al finalizar me siento con más energía).
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Wish I could understand why more doctors don't recommend Anagrelide for ET....when a new physician switched me to Hydrea it caused SO MANY side effects and never did stablize the platelet count. Grateful when I was able to find a physican who said if it worked (for 10 years) why switch?
I'm 72, diagnosed over twenty years ago.
Get on the email list for the MPN Foundation and watch their excellent programs and videos. https://www.mpnresearchfoundation.org/
I was just diagnosed in Feb 2023, take iron and baby aspirin daily, HU 2x week at 500 mg each, and just try to live my life. Yes, I do get fatigue from the HU, plus dry skin, and dry eyes, but I need to take the HU to remain stable and prevent thrombotic events. I'm a high-risk with ET, Jak2, and over 60. Have never had a symptom; just high platelets on a regular CBC at my physical in Jan. 2023. Keep active and busy. We can manage this for a long time with this illness. Take care!
I was just diagnosed with ET. I am researching, reading, learning, processing what exactly this means for my life and my loved ones.