Essential Thrombocytosis symptoms
Having had high platelets since 2017 and doctors could not find a cause I paid to see a haematologist and I was diagnosed with ET in 2019. With a platelet level of 723 I was put on baby Asprin but unfortunately it did not suit me. I was then put on Clopidogrel but had an allergic reaction to it. I have refused to have a biopsy so far but said I will if levels go over 800. The haematologist made it quite clear that I am at a high risk of having a stroke. So I am taking Arnica homeopathy twice a day to thin the blood which helps the headaches which I have suffered with for years and take 2 paracetamol a day, usually when I wake-up as that’s when I get most headaches and sometimes it is like having a massive hangover. I also get tired and lightheaded and since January I am suffering with constant tingling hands and feet which according to the internet is another side affect. But as of two weeks ago I have tingling lips and tongue which is not listed as a side affect and I am wondering if anyone else also has these symptoms tingling symptoms. Having tried to see a doctor the surgery have said I can have a routine appointment which is weeks away. My doctor has agreed that I have a blood test every 3 months to monitor, at the moment it ranges from 750 to 800. Any advice gratefully received.
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This is one of the best articles I have read related to ETA. Thank you so much.
I can tell you from experience that in the U.S. you CAN get life insurance with ET, however, it will come at a premium.
Agree, it is just unfortunate for those of us allergic to it
It may. Again, it varies, and I have not added on more life insurance since my diagnosis. However, given that life insurance companies basically want to get as much money as they can before you "cash out," I am guessing most will use an ET diagnosis to charge higher premiums. Could they also use an undisclosed diagnosis to deny payment? Again, don't know, but prudent to talk to an agent.
Hi, are you still taking Arnica? If so, is it still helping? My doc has suggested 30c, but I’ve read others are taking 9c. A baby aspirin is keeping my platelets around 600, but I’d try anything else that might work short of the “real drugs”.
So, I am male and thus my condition is quite rare?
Very interesting article
Thank you
Check with your doc, but my understanding is that aspirin does not lower platelet counts, it just makes them "slippery" so that they are less likely to clot. There's some research being done on clotting factors of platelets of MPN patients, specifically on why super high platelet levels cause bleeding, which seems counter-intuitive. That research is WAY beyond my grasp, but it does suggest that there are things about our blood cells, and blood cells generally, still to be understood.
How important is the aspirin if you are being treated and the treatment has brought blood lab numbers into the normal zone?
Yes I am, my homeopath said I can take 200 3 times a day and yes I find it helps, it thins the blood and no side affects, but it does not reduce platelets. Always best to seek advice on what to take.