← Return to Essential Thrombocythemia: Looking for information and support

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@loribmt

Welcome to Mayo Connect @docoltun. Thank you for sharing your experience with ET and what’s been working for you to keep your platelet level managed with Anagrelide. It’s always encouraging for others with essential thrombocythemia to hear a positive story from someone who’s had this blood condition for many years and doing well!
How long were your taking Hydroxyurea before it was switched to the Anagrelide? What were your side effects?

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Replies to "Welcome to Mayo Connect @docoltun. Thank you for sharing your experience with ET and what’s been..."

OMG, my medical plan changed so I lost my hematologist after 10 years on Anagrelide. New guy was SHOCKED, said I should definitely be switched to hydroxyurea and attempted a very lengthy, painful bone marrow biopsy which ultimately provided nothing unusual. Biopsy had never been done since the Agrylin (pre-generic anagrelide, may have been brand new) did the trick lowering platelets from 1800+ to below 400 quickly. So after five pokes (I remember asking if he'd ever done this procedure on a live person) my medication was switched awaiting results. A nightmarish 6 weeks of weekly out of control blood draw results. Took me that long to get approval for a DIFFERENT provider who basically said, if it works, why change it? So...I'm probably heading to 25+ years without symptoms from ET. I may have been an anomaly with the hydroxyurea, impatient since there hadn't been any symptoms or might have been an over enthusiastic new doctor. Thanks for asking.