JAK2 Mutation - Effects and Questions
Have JAK2 mutation verified twice; one year apart and from different labs. As I understand, it may cause polycythemia vera, essential thrombocytosis, or leukemia. My hematologist has not provided any real info on this mutation so I've been researching via internet. I knew leukemia is cancer but was disappointed to find out today that the other 2 are blood cancers as well. I have been seeing a hematologist every 3 mos. about this since my 2nd blood clotting event in 09/2016. To date, all my blood factors have been in the normal range. Here are some of my questions: 1. Is it typical to verify this mutation well before it triggers one of these diseases? 2. I know early detection of cancer can be a real plus, but is there any research or experience that supports proactive steps that can be taken to deter the onset of any of these possibilities? 3. With polycythemia vera and essential thrombocytosis, is blood letting the primary treatment? If so, can the blood be donated? 4. Since none of my blood factors have ever been out of the normal range to date, no specific result of the JAK2 mutation has raised its ugly head. Is this normal? I'm not typically a worrier. In fact, I do really well with things like this once I know what I am dealing with. Information becomes my sword which allows me to take worry and nip it in the bud.
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I take HU and ibuprofen fairly frequently. I will switch to Tylenol and ask the pharmacist next time I am in there. Thanks for the heads up.
I have Polycythemia Vera Jak2. I all of a sudden have my platelets go up and down like a roller coaster with my red blood and hemocrit staying stable. I was taken off of hydroxyurea but it hasn’t made a difference. Is anyone else dealing with situation.?
No blood cannot be donated they discard it. continue to see your hematologist. Keep a list of your symptoms and talk to your dr.
I have pv and when first diagnosed was oh HU every day developed anemia and was taken off and put on iron . now take HU 3x week with baby asprin and count is in control. Pv is a rare blood cancer was told no cure just take meds . You can live for a long time with this just enjoy your life.
I have polycythemia vera also a jak 2. If this is your diagnosis there is no cure for it just take you med to control the red blood count. Get a second opnion
before worrying
I have been on HX 500mg for last 2 weeks now plus 100mg Aspirin. I have been on Aspirin since Nov. 23 when my platelets were 840. Early this month when Hematologist started me on HX, she insisted i continue taking the Aspirin as well as they both work differently, the aspirin is watching on the clothing part of the equation but HX is reducing the excess production of platelets. My 2 cents!
i wonder why? do you know? did dr say?
Yes, my doctor told me no ibuprofen. Acetomenophen (Tylenol) is okay, but only if really needed.
Any one else told ....not to take ibuprofen......not at same time as HU & baby aspirin.......but never heard this warning
Thank you, yes I get screened frequently.