Just diagnosed with prv jak2 confirmed - MPN Voice

MPN Voice

10,886 members15,201 posts

Just diagnosed with prv jak2 confirmed

john0084 profile image
10 Replies

Hi everyone, I live in the UK and male aged 54. Confirmed with primary polycythamia Vera I have the jak2 gene . I take 1 hydroxy. Tablet every other day with a blood thiner. What starting to worry me is weight loss, I've lost about 10ibls in the last month. Anyone with any help.

Written by
john0084 profile image
john0084
To view profiles and participate in discussions please or .
10 Replies
Susana7 profile image
Susana7

Hi John, I also have PV, since 2014, and am on Pegasys interferon and low dose aspirin. My bloods have now been normal for 2 years. I lost weight initially but that was because I changed diet (very little meat or alcohol now)! Is your spleen enlarged? That could cause loss of apetite as you feel fuller. If so, some people have had success with Ruxolitinib/Jakafi in reducing the spleen. I suggest discussing further with your haematologist. Good luck! Susana

john0084 profile image
john0084 in reply toSusana7

thanks for your reply susana , im seeing my haematologist on Wednesday so shall ask him his opinion of my spleen. I too have cut out red meat and alcohol but I do eat normally. thanks for wishing me luck.

Inca profile image
Inca in reply tojohn0084

I also lost weight,prior to P V diagnosis and the first few months when I was quite ill,once blood improved ,Hydrea and other Meds to thin blood,I soon got back to my life long 50kilos,in 8 yrs stayed exactly that,tho up and down with Hydrea dose,depending on blood results monthly. So worry not you I'll get back to normal!!Some people say Hydrea makes them put on weight.....As you mention a sensible diet is essential,and lots of water daily.Best to you .

Poppy112 profile image
Poppy112

Hi I also lost weight just prior to pv diagnosis some was intended but lost more than ever set out to do. I found the 1st 5months when I had lots of side effects on the standard interferon I just couldn't put any weight on, but now on pegasys Interferon and have no side effects and weight increased slightly. Talk to your doctor for reassurance and to check your spleen size otherwise try not to worry. All the best.

MCW22 profile image
MCW22 in reply toPoppy112

I too lost weight at first. Probably due to the worry of the diagnosis then the nausea caused by the hydroxy. However the nausea wore off after a couple of months and now I've put on the lost weight and more besides.

Carol

Peter18 profile image
Peter18

Dear John,

I was diagnosed with PV in February this year. Since Summer 2017, I have lost about a stone. I have attributed this to a conscious change in diet this Spring in terms of content and quantity. My weight is now stable. I hope things settle down for you in this respect. Best wishes, Peter

john0084 profile image
john0084 in reply toPeter18

Thanks Peter for getting in touch, the replies on here are keeping me positive, I guess it's early in my diagnosis to be that worried.

john0084 profile image
john0084 in reply toPeter18

I was wondering what a clinical haematolgy appt. might entail as it is I have weekly apptts at just the haematologyy dept. Many thanks in advance

Mazcd profile image
MazcdPartnerMPNVoice

Hi John, hope you get some reassurance tomorrow when you see your haemtologist, it is a worrying time when you are first diagnosed, it can take a while to come to terms with it all and to learn about it, I would urge you to read as much as you can on our website mpnvoice.org.uk and when you see your haematologist write down the questions you want to ask, it helps to keep you and him/her focused, and if all your questions are not answered perhaps you could leave them with the haematologist or the nurse specialist and they can email the answers to you. It also is a good idea to take someone with you as another person hears different things and maybe thinks of different things to ask. Hope all goes well tomorrow. Maz

john0084 profile image
john0084 in reply toMazcd

Thanks I will take your advice. Regards

Not what you're looking for?

You may also like...

Newly diagnosed with ET Jak2+

Hi, I’m newly diagnosed. My platelets are around 700 so not massively high. For the past couple of...

Newly diagnosed with PV JAK2 positive

Hi, I am new to this as recently found out have PV, started by mentioning to GP about terrible...
Cityreach profile image

Newly diagnosed – ET Jak2+ with added drama!

Hi everyone! I've been wanting to post here for some time, but it's taken me a couple of months to...
Timjonze profile image

Has anyone been diagnosed with jak2

I have recently found out I have jak2 mutation and want to speak to anyone that has the same...

Newly diagnosed. ET jak2+

Hi all, I'm a 43 year old male, and only got my diagnosis on 21/3/2016. I must say that I went...
RobPV profile image

Moderation team

Debinha profile image
DebinhaAdministrator
Mazcd profile image
MazcdPartner

Content on HealthUnlocked does not replace the relationship between you and doctors or other healthcare professionals nor the advice you receive from them.

Never delay seeking advice or dialling emergency services because of something that you have read on HealthUnlocked.