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1,156 total results
Comments (1,069)
I have both PV and ET I have had issues with my right hand. I will...
https://connect.mayoclinic.org/comment/1067652/
I have both PV and ET I have had issues
After having terrible side effects while taking HU my doctor had me switch to Jakafi. Three...
https://connect.mayoclinic.org/comment/994946/
It has really helped with PV side effects
I also am taking Jakafi. It helps immensely with PV side effects however I still need...
https://connect.mayoclinic.org/comment/887767/
It helps immensely with PV side effects
According to the Hematologist, even a high EPO of 61 is still lower than what she...
https://connect.mayoclinic.org/comment/231791/
Continuing to treat me as if PV with
Have you thought about a second opinion? In my opinion, for what it's worth, a PV...
https://connect.mayoclinic.org/comment/1194839/
opinion, for what it's worth, a PV
Please do not be scared. Improvements in care and medications are happening. Important to know that...
https://connect.mayoclinic.org/comment/1469996/
I am over 50 with PV/JAK2 and it has
Welcome @toriaflo. I hope you saw @loribmt's post with some info related to your question about...
https://connect.mayoclinic.org/comment/737415/
about altitude and Polycythemia vera (PV ... may also wish to connect with fellow PV
Hi @martine0224, welcome. PV stands for Polycythemia Vera, a type of blood cancer that causes the...
https://connect.mayoclinic.org/comment/1100471/
PV stands for Polycythemia Vera, a type
Usually they are checking an for enlarged spleen and if any of your other organs appear...
https://connect.mayoclinic.org/comment/889536/
first diagnosed to determine if the PV
@irishnanny3 Hello. Based on what I have read about PV, it appears to me that there...
https://connect.mayoclinic.org/comment/1455104/
Based on what I have read about PV, ... clot and it’s determined you’ve got PV
Weclome @lwengel, as you likely already know, the most common treatment for polychythemia vera (PV) is...
https://connect.mayoclinic.org/comment/738023/
treatment for polychythemia vera (PV ... Fellow PV members like @jerrlin @tlsantin ... have you recently been diagnosed with PV
I agree. I have had PV for 14 years. I take Hydrea 1000 mg daily. I...
https://connect.mayoclinic.org/comment/994856/
I have had PV for 14 years.
sounds so familiar! Can iron supplementation lead to a low epo value? seems hematocrit went up...
https://connect.mayoclinic.org/comment/602492/
Now epo is low and attributed to PV
Katrink, welcome to the Mayo Polycythemia Vera (PV) page. I was diagnosed with PV in 2018...
https://connect.mayoclinic.org/comment/1400143/
welcome to the Mayo Polycythemia Vera (PV ... I was diagnosed with PV in 2018 with ... is a great comfort with this pesky PV
Hello , I have been treated for PV/ JAK2 for four years . I was on...
https://connect.mayoclinic.org/comment/773685/
Hello , I have been treated for PV/
I was officially diagnosed with PV in Dec22 after developing high BP when I attempted to...
https://connect.mayoclinic.org/comment/890803/
I was officially diagnosed with PV in ... #39;thick blood,' which led to PV
Hello, I do not have ET but I do have PV which is the ugly sister...
https://connect.mayoclinic.org/comment/976216/
Hello, I do not have ET but I do have PV ... PV is one of the MPNs. ... I became a member of the PV club in
@chorusgirl500 Just keep at doing what you’re doing. I’m 72, and I’m still a full-time architecture...
https://connect.mayoclinic.org/comment/1466758/
The PV is now more of a nuisance that
@kate3 hi Kate ! I am sorry you have MF ! I also have confirmed MF...
https://connect.mayoclinic.org/comment/1469568/
It’s secondary to PV , I had for over
And good luck to you, AngieP. Three days on from Acupuncture and I’m still doing well....
https://connect.mayoclinic.org/comment/855070/
Jakafi is the medication I am on for PV
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