Diagnosed polycythemia vera at 26: Any young PV patients out there?
Hi everyone,
I am in the process of being diagnosed with PV. I am 26 years old and I am going to be honest , I am terrified. I have insurance, but I am a teacher, I cant afford thousands of dollars in phlebotomys and blood work. However I also know if I dont do my treatments I I will not survive. I dont know how to tell my mom and husband I need to make a will and that I may not outlive them. I have always been terrified of needles, and have become a human pin cushion. I am scared and angry and confused and it feels like everything I read is for people 50+. I have researched and know everything about PV , but it isnt relieving any of the stress or anxiety of knowing i have to live with this for the rest of my life. I know i need to repriortize and put my health before anything , work and family included, but thats never who I have been, I always put everyone first. Any young PV patients out there to offer some advice?
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@eloise999 thank you again for all your advice. Same to you. 🙂
@chorusgirl500 Thank you for providing more information! No wonder you’re starting to feel like a pin cushion…a feeling I know all too well. But it’s important to get to the bottom of your uptrending RBC.
That’s where the bone marrow biopsy can be of great value. It’s one of those tests that sounds worse than the reality of the procedure. While I did have 13, three were completed with local anesthetic…the other 10 were done while I was blissfully sleeping. The 3 biopsies with anesthetic injection were a little uncomfortable with more of a pressure than pain? Not sure how to describe it. The local anesthetic was effective and quick. I think the anticipation was worse than the event. Anyway, it didn’t take any arm twisting to jump into the sedation when offered for the others.
Considering your reluctance, I hope you are at a larger clinic where sedation is offered.
Like I mentioned earlier, most doctors will also give you a one-time dose of lorazepam which you’d need to take an hour or so before the procedure. So if you want that, ask ahead of time so your doctor can get that prescription in before the procedure date.
The biopsy is actually taken in small of the back, right above or near the large dimples above the butt cheeks. The area may remain tender for a day or so and feel a little bruised.
Wish getting insurance to pay up wasn’t always such a circus act of jumping through hoops to get approval and I hope you have answers soon! I’m sure this is frustrating and troubling for you. Our bodies are complex with no service manual which can make for some challenging puzzles sometimes. But it sounds like you have a great team working with you!
Wishing you and your family a happy holiday season.
@chorusgirl500 LOL. Let’s just say the biopsies weren’t ever on the top of my list of fun things to do…but they were vital to my diagnosis and follow-up to treatments!
I really will admit I prefer sedation but would do it with just the local anesthetic if I had to. However, with sedation I got to wake up to Lorna Doone cookies and juice! Like dangling a carrot in front of my nose!! Yes please. LOL.
Good luck with that insurance…I just wrote in another reply to you about wishing we didn’t have to jump through hoops like a circus act to get approval for some of our vital tests!
@loribmt I have never heard of a Lorna Doone cookie but now that I've googled it I have to try them! I already told my husband he is buying me my favorite Chinese food after my biopsy and putting up with watching my favorite shows he hates haha thank you for your kindness and good attitude. 🙂
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1 Reaction@chorusgirl500 My 18 year old son just went through several rounds of CBCs until one came out normal . This started two years ago. The Jak2 test was negative. Because he has had a normal CBC and negative Jak2 , the hematologist said he did not have PV. He blamed it on the lab. I sure hope he is correct. He also said probably sleep apnea that lowers O2 and causes the body to make too many red blood cells is also a possibility. From what we were told, if he was positive, he could live a normal life.
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2 ReactionsHi! I hope your sons labs remain normal and he is healthy. That is a blessing. I am in a situation now where my Dr. has ruled out less serious causes , like sleep apnea, and now we have to see if i have rare primary ( part of the 2% with no mutation) or if i have secondary with a more serious cause ( kidney disease , tumor , etc). People here have attested to being able to live a normal life with PV, which is comforting to hear. It seems, with time, the tests will end and it will become routine maintenence, but right now as we search for the cause ( as im sure you and your son went through too) it just feels like constant pocking and proding and testing.
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1 Reaction@joycelen I cant imagine having to go through all this at 16-18. I struggled with other illnesses in my youth, but nothing that required this much testing and support. You raised a strong kid. Thanks for being a good mother and getting him the resources he needs.
@chorusgirl500 Hi me again lol, Is your Hematocrit and hemoglobin high? I didn’t see you mention that. Also if your platelets are normal that’s great news because only some of us get high platelets like myself. I hope you can forget for a few days and enjoy the holidays!
@nypara66 Yes it is. Sorry, he actually stopped mentioning it after the initial testing to focus on all the other things I mentioned, but its in the labs. They were 18 and 48, and they've been going down after each blood draw and then back up by the next appointment. Thank you and happy Holidays!
New question:
How long after taking HU, did you see your hematocrit numbers drop and by how much?
I’ve only done one blood test since diagnosis and that was only after almost a week of Aspirin and hydrating and my platelet numbers went from 409 to 381.
Now taking HU and will test again Monday after a week on HU (taking it 4x per week) and one more week of Aspirin and hydrating.
Curious about your experiences and how fast or slow it went.
Thank you!
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