Hello there @Motorman, welcome to the forum. Thank for joining and for sharing this, it’s really heartening to know you’ve been living with Essential thrombocythemia ('ET') for so long. Well done, I hope to do likewise with Polycythaemia vera ('PV')!
I was diagnosed in 2023 and take aspirin and hydroxyurea like you. I hope the change in medicines is treating you well, here’s to another 33 years or more, right?
Do please keep us posted about you get on @Motorman. If you haven’t already, perhaps look around the forum as you’ll find many others living well with Myeloproliferative neoplasms ('MPN') like Essential thrombocythemia ('ET'). Here’s a lovely group of folks who comment regularly: ET diagnosis finally sinking in