Hi YogaLover,My night sweats began after nearly 20 years of taking hydroxyurea and aspirin. However, I have Myelofibrosis (post Polycythaemia) and it was ruxolitinib that took away that symptom. Sorry if that's no help to you, only my experience. The sweats are indeed the pits! 😞 Jeanette
Yes I think it's similar for all of us ,but I was much worse on hYdroxycarbamide .and clopitorol ... Then I had PV. Since iv moved on and have mpn I'm told ..I take ruxolitinib ,the night sweats are very much reduced ,,it's a combination of the illness and the drugs which we need to control it .. Don't eat late and drink lots of bottled water ...cut down tea x coffee ,,and never ever drink from a can !! Or that poison. Coca. Cola ....try a nutri bullet ..I think they are a god send ...get all the vitamins and minerals in one drink every day ..wonderful product !! Twinkly. Xxx
My night sweats worsened considerably after taking Hydroxy, but couple of years on, no longer on H, they have got worse yet again and only on aspirin. Worked out that if I eat v much earlier in the evening and also avoid alcohol, they seem much less. You really have my sympathy!! Tinkerbell13
Thanks for the strategies - sorry to hear that you too are having this unpleasant problem to deal with. Last couple of nights I've had bedroom window open and sleeping without pjs (!) which has given me some relief.
I think Twinkly is right and it is a combination of both the condition and the drug. I had the dreaded sweats before taking hydroxy and they got worse after starting to take it. They are worse than ever lately after the dose was increased.
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