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1,156 total results
Comments (1,069)
Small world! I lived in Los Angeles most of my life - I remember seeing fires...
https://connect.mayoclinic.org/comment/150675/
Before PV, I lived in Studio City, Sherman
Hello Pink Flamingo, I understand medical insurance companies are difficult to navigaye among other issues. If...
https://connect.mayoclinic.org/comment/836434/
their access centers if they have PV
I’m extremely late to this as I’m sure that by now you’ve been either diagnosed or...
https://connect.mayoclinic.org/comment/1192993/
offer some insight since I do have PV
I had a doctor in Houston that I really liked and who believed I have secondary...
https://connect.mayoclinic.org/comment/889376/
I have secondary or non cancerous PV
Did not know about sun impact, I always lather it on being fair with blue eyes...
https://connect.mayoclinic.org/comment/883029/
that point out the dangers of sun and PV
Thank so much for sharing It sounds like this is not easy fix for fatigue! I...
https://connect.mayoclinic.org/comment/1360256/
HCT AND RED BLOOD CELLS
I HAVE HAD PV
I have been seeing Dr. Palmer for PV and she is all that. And, she is...
https://connect.mayoclinic.org/comment/1315708/
Palmer for PV and she is all that.
Hi, I'm 69 and just ended up with serious lung embolism in the ER. Only indication...
https://connect.mayoclinic.org/comment/1401810/
Only indication on why I got them is PV ... have cancer but everything points to PV
Vent all you want here. Firstly, your getting it out and you have people with the...
https://connect.mayoclinic.org/comment/1324057/
appointment with a hematologist..He told me PV ... hemotologists that deal only with PV
@sanjb My story is not as extended as yours, but I was on HU for about...
https://connect.mayoclinic.org/comment/1420086/
I have found a friend with PV, we get
I find your post interesting because back in 2019 when I first discovered something was wrong...
https://connect.mayoclinic.org/comment/738066/
figure out why, until I read about PV ... I no longer believe I have PV but I
Hi @bohobruja Welcome to Mayo Connect. The National Institute of Health defines chronic myeloproliferative disorders as...
https://connect.mayoclinic.org/comment/786594/
with members who have either ET or PV ... Here are few discussions in the PV(
I went to my GP with other issues & checked with him re Sleep Apnea. He...
https://connect.mayoclinic.org/comment/1036484/
developed lung clot, blood test for PV ... treatment when it would seem that my PV
Hi Lori, long time no talk! Wishing you a very happy & healthy 2024. Wanted to...
https://connect.mayoclinic.org/comment/1004117/
give you an update, I DON'T have PV ... hunch that perhaps I don't have PV ... That definitely showed I do not have PV
Hi @mags17 I’m sorry if there was some confusion but my reply was written to @lostmonk...
https://connect.mayoclinic.org/comment/936391/
regarding their recent diagnosis of PV ... discussions where you mentioned that you had PV ... surgeon friend is right, people with PV
I can relate to the low adrenal function. I am 48, diagnosed with PV last year,...
https://connect.mayoclinic.org/comment/1126529/
I am 48, diagnosed with PV last year
Hello,how are you all ?❤️ Well ,my biopsy results:no evidence of granuloma or abnormal lymphoid cell...
https://connect.mayoclinic.org/comment/1049809/
biopsy ,he thinks it's secondary PV
Hello, I was diagnosed in Jan with PV. I too take a baby aspirin and Hydroxyurea....
https://connect.mayoclinic.org/comment/972640/
Hello, I was diagnosed in Jan with PV
Hi, Joining in to read up on PV while waiting for my Jak2 results.. I'm 43...
https://connect.mayoclinic.org/comment/840478/
Hi,
Joining in to read up on PV
Hi Steve, Becky has the JAK2 mutation which, from my understanding, makes primary ET more likely,...
https://connect.mayoclinic.org/comment/1154236/
myeloproliferative disorder, such as ET, PV
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