My platelet count has increased after a year on Hydroxyurea (HU)
I have been taking HU (1000mg per day) for one year for essential Thrombocytosis . I have experienced little side effects and my platelet count have steadily gone down.
My latest blood tests showed an increase for the first time since I started HU. It went from 360 to 420.
Has anyone experienced fluctuations in their platelet count. Is it normal?
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ET was formerly referred to as a blood disorder. Our bodies make too many platelets. Doing the right thing, but just too much of it. I don’t know when or why it started getting referred to as ‘cancer’ and I can see on this thread that it really freaks people out. So yes, I do NOT call what I have cancer.
I was diagnosed 27 years ago and am as healthy as anybody else. I am on Anagrelide now, formerly on HU.
My hem is happy if my numbers are under 600.
27 years is a long time. I am glad you are feeling
well. You must have good medical care in your area.
I live in North East Georgia. Unfortunately in the
more rural areas your care is hit or miss. I was referred
to a great Dr. in Gainesville, Ga. So I do feel lucky.
Why did your Dr. change your medication?
It is a numbers game. I was diagnosed with ET in 2018 - high platelets. It did well for awhile at lower doses of HU, it did sometimes have large fluctuations and counts steadily increased eventually was at 2 g/ d. Then in less than 30 days all my counts, rbc, wbc, and platelets were way under normal (and I lost 30 lbs and really felt bad). My body no longer liked HU 😞. Have been on Jakafi 10 mg 2x/d for 2 years now, platelets run in the 600 to 800 range. Also should note have been on ld aspirin the whole time. Other typical symptoms are there and slowly progressing. Fortunately do not have history of clotting so still considered lower risk.
My biggest help is finding things that motivate me to be physically active; for me it is long walks with the dogs year round and skiing in the winter.
After 15 years on HU I developed locally advanced Basel cell carcinoma on my scalp and long term use ofHU apparently can do that though nobody told me that so -beware.
I see my hem thru telemed so find a good cancer center and get onboard with a doctor there and you just need to have blood work done locally. Do your homework and read up on all you can about what you have. We have to be our own advocate.
Thank you for your advice.
I see my hem every 4 months.
Get blood work done and a full exam. I was told to cover up in the sun, sunscreen, long sleeve, hat. I am not a beach person, so I do not have to worry about that. I do cover up walking the dog. I do keep myself informed. Hope having a good
Diet and exercise is helping.
Just FYI, about 15 years ago, the World Health Organization reclassified ET as cancer. Clinicians and researchers around the world advised this change because more was understood about how mutations caused platelet cells to proliferate in the bone marrow. ET is actually a bone marrow cancer.
Fine by me if folks don't want to call ET cancer. The designation did cause some controversy with a few researchers and doctors.
Maybe a minor point, but do be aware that your insurance company may think differently. Those who want to increase life insurance, for instance, will be asked if they have been treated for cancer in the past 6 months. I would be wary of answering "no" for fear of jeopardizing the policy.
Hi:
Fluctuations can be quite normal and 420 is perfectly fine insofar as HGB. You needn't worry about the spike. It happens from time to time and you learn to roll with it. Please do not be alarmed and have a great day.
Ann
Mikemp:
Sorry, I meant to say the 420 fluctuation is perfectly normal for your PLATELET count, not your HGB. My bad.
Ann