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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Thanks so much for your reply. This is very helpful and I will have my GP check my blood test for these items. Wishing you the best in your journey with a ET
Thank you so much for the feedback. I will check this out at our local health food store. Hope everything is good with you…..Claire
I take hydrea 2000 mg a day for 20 years know getting skin cancer. I don't know what else to take since this has been keeping me alive but know side affect is this. Hematologist has no answers ..
Don't know where to turn any suggestions
@bchampagne62
2000 mg daily of Hydroxyurea seems like an extremely high dose. My suggestion to you is to get a second opinion from an MPN specialist even if you have to travel.
Agree . . . 2000 mg a day for 20 years?
I have read that HU can lose its efficacy with prolonged use, so maybe your oncologist has been increasing your dosage over time?
But to me it seems a better strategy would be considering alternative treatments for your ET.
As Eileen says, find an MPN specialist for a second opinion.
Do you have a good dermatologist keeping a close eye on your skin? Many lesions can be fairly easily removed, if caught at an early stage.
Let this be a reminder to all of us. HU makes us more vulnerable to skin cancer. Use a mineral-based sun cream, wear a sun hat, cover as much of your skin as possible when you have to be in the sun.
bchampagne, let us know how it goes.
You might ask your doc about anagrelide, Jakafi, or Pegasys if you are maxing out on HU. If he draws a blank on these suggestions, I agree it's time for a second opinion. These side effects can become more discouraging than the disease. It's hard to get doctors to address quality of life sometimes.
https://www.nccn.org/patients/guidelines/content/PDF/mpn-patient.pdf
I think you will find this helpful. It will take a couple of readings before it all becomes more clear.
I suggest a second opinion with someone who specializes in Blood Cancers. I have had this since 2003, so going on 22 years now. Baby aspirin is a key in preventing blood clots (stroke, blindness, heart attack) and microvascular ischemia (headaches, tingling, burning, itching, visual disturbances). Hydrea or other meds such as pegasys, anagrelide, or Jakafi will decrease the number of platelets. Review the article and then decide. Facts and research are important and correct resources and medical expertise can improve our lives.
Hope this helps.
I have had 7 surgeries to remove it since June and a number of freezing sessions.when I say they don't know what to do it is true. 2000mg is down from 4000 I used to take...what does MPN stand for?
"MPN" = myeloproliferative neoplasm!
How's that for a tongue twister?
MPNs are blood cancers, including ET.
I hope your intensive skin cancer treatment phase will end soon.
Even more, I hope you find an MPN specialist to review your treatment options. You have been taking a LOT of HU.