I’m new and so pleased that this organisation ex... - MPN Voice

MPN Voice

10,443 members14,394 posts

I’m new and so pleased that this organisation exists.

trotty100 profile image
10 Replies

I had my diagnosis of thrombocytaemia on 1 Aug 2018 following high white (platelet) count on a routine blood test

I was prescribed hydroxycarbamide 100 mugs and after 4 weeks my levels had reduced From ? 7,500 or is it 750 to 4,500 /450 I was told this was a good response to treatment.

My next months treatment was interrupted due to surgery and I had to stop treatment for 14 days. My white celllevels went up again to around the original high levels.

I have just seen the haematologist following a further 12 weeks of treatment and have been told my levels are high and unstable. I am having a bone marrow biopsy in 1 days time and an abdominal scan in6 days time.This has led to various questions without answers at the moment It was a great help to make contact with MPN at this stage and to learn there is a wealth of information and support

I am 81 years old and know my time is becoming more limited but I am optimistic by nature At my initial diagnosis I was told that this illness is not life limiting.

I look forward to being part of this community

Written by
trotty100 profile image
trotty100
To view profiles and participate in discussions please or .
Read more about...
10 Replies
mhos61 profile image
mhos61

Hi trotty100,

Welcome to our friendly forum. You will find plenty of support with likewise people here. I can remember the relief I felt when I came across this forum after my ET diagnosis.

I hope your BMB goes well. It maybe that you just need an increase in your medication to reduce your platelets further. Your haematologist will know what’s required.

Take care

Mary x

trotty100 profile image
trotty100 in reply to mhos61

Thanks,lovely to have had such a speedy response,I feel part of the community .

Margaretx

Lemon123 profile image
Lemon123

Hi trotty100, and welcome

Like mhos61, I was really pleased to find this friendly, supportive forum. I was diagnosed with ET JAK2 positive in May last year, I'm in my mid 60s. As MPNs are rare, it's been really important to me to know there's a reliable source of information, and a place where I can ask questions alongside others travelling a similar journey. I hope your BMB goes well, and send every good wish to you.

trotty100 profile image
trotty100 in reply to Lemon123

Thank you it is so good to have the support ,means a lot

Mazcd profile image
MazcdPartnerMPNVoice

Hello Trotty and welcome to our forum, I am glad you have found us. I would suggest that you read information on our website mpnvoice.org.uk as well as the posts on here. I hope all goes well with your bone marrow biopsy and that it isn't too uncomfortable for you. It will take a few weeks for the result to come back, but once you have the result your consultant will be able to discuss ongoing treatment with you. Just remember though that your platelet count will go up and down, even when you are on medication, and the dose may have to be changed a few times to get the optimum dose to keep the platelets at a steady count, they go up and down for many reasons and it happens to all of us, so try not to panic when you get your results if they have gone up. Anyway, let us know how you get on with the bone marrow biopsy. Best wishes, Maz

trotty100 profile image
trotty100 in reply to Mazcd

Thank you I will keep in touch

MiltonBradley profile image
MiltonBradley

Welcome! I was diagnosed last February after a heart attack at age 58. This site has been a God send; so much helpful information!

trotty100 profile image
trotty100 in reply to MiltonBradley

Thank you I hope you are recovering well .I am so pleased to be part of this “family”

isimmy profile image
isimmy

Hi Trotty100 and welcome to our group.

I have learned and understood far more about my condition, ET Jak2+, since joining this forum just over 12 months ago than in the previous 13 years since I was diagnosed.

It is a great place to raise your questions and concerns because the replies that you will get are from people who understand and have been through the same.

People outside our community do not understand our issues because, in most cases, we look perfectly well on the outside.

Good luck going forwards.

trotty100 profile image
trotty100 in reply to isimmy

Thanks a lot,I’ve just had my bone marrow biopsy and am about to write.again in the hope of some further light on my experience.

You may also like...

BMB question - I’m new, so bear with me!

results in 2015, as I trusted I would have been told if anything was abnormal. I had a complete...

I’m still new to this forum

Here I go again! Nine weeks and four days into treatment with Jakavi for MF I am experiencing some...

So scared and new to this board

and legs. Slight elevated HCT (44.7) and RBC are high normal. Been referred to hematology and...

So... this is new. Question on shortness of breath

Hi all -- I have ET (about 2 years since diagnosis) and up to a month ago, the most challenging...

Hydroxycarbamide and platelet count: is my experience so far typical?

started chemotherapy treatment for ET and raised platelets. Following the diagnosis of ET about a...