How do You Manage Side Effects Of Hydrea or Hydroxyurea for ET?
I was diagnosed with Essential Thrombocythemia last November and am on Hydroxyurea 1500mg daily in an effort to reduce my platelet count, still in 9000s. Developed peripheral neuropathy & pain left leg, hip to foot. Oncologist thinks due to arthritis back per X-ray, wondered if others have this also, maybe due to the disease or meds?. Dr. says rare disease so difficult to predict outcome/symptoms. Anyone know of support group in Seattle area for this? Have called the local hospitals, cancer lifeline, etc.; no positive results.
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hi @kathy5brothers, I moved your question about fluctuating bloodwork although you've been on hydroxyurea for 20 years to this existing discussion:
- How do You Manage Side Effects Of Hydrea or Hydroxyurea for ET? https://connect.mayoclinic.org/discussion/side-effects-of-hydroxyurea-et/
I did this so fellow members like @pearly @lzimmerman @betherelynda @claire39 @nohrt4me @huronshores @markdi @dwlowrance @wa34937 @stevehurlburt would see your post and you can connect with them more easily.
Kathy, has something else in your health changed recently? Did you doctor order another round of blood tests to see if this may have been an anomoly or lab error?
After 3 yrs on hydroxy, WBC 4.0 RBC 3.8. I'm taking 1,000 mg daily. When my platelets dropped below 500 my hema cut back on the dosage and it hit 760 after 6 weeks. My retest was delayed by Ian, hoping I'm near normal again.
They told me to stop the Hydrea, and made an appointment with my Oncologist in two days.
I see my oncologist in two days after stopping the Hydrea until then.
They ran that lab a couple of times.
Hello, I've just found out I have the Jak2 mutation and will go for a biopsy soon. I have an ET that has been rising slowly the past few years and is now at 520. Doc wants to start me on Hydrea and baby asprin. I noticed the last post was Feb 21. Is there a place to go that is more active? Thanks
Hello cowestwinds......I have been on Hydrea for 4 years for ET. My side effects were a bit of nausea. I also have itchiness, fatigue and headaches but I believe they are side effects of the ET. I do find that the Hydrea helps a lot with the fatigue and weakness which I have on different levels, depending on what I do in a given day. Also, I have blood work every month........Good luck
Hope you do well with your treatmant
I’ve seen many who get there numbers down in the 500’s and are ok with that. I just found out I have Jak2 any my platelets are at 521. Should I wait to see if my numbers keep going up before I start Hydrea? Thanks
I take hydrea 500 mg on MWF only. Started out taking 2 500 mg 7 days a week - which threw blood disorder 180 degree so had to balance things out. I have no symptoms tolerating hydrea.
I'm running into the same problem - an active site. I have the JAK2 mutation and have had a biopsy. My blood disorder is balanced with hydrea/500 mg MWF weekly and 81 mg baby aspirin daily.
If platelets have been monitored and risen over 3 to 4 months - i would see an oncologist - yes. Mine were in the 800 range before i started -