AML 7 months post transplant chimerism - Leukaemia Support

Leukaemia Support

1,288 members807 posts

AML 7 months post transplant chimerism

3 Replies

I am 7 months post transplant with no MRD and blood work normal. 97% donor cells in BM. Platelets always slow to pick up, hovering around mid 60's but cause no issues. Overall health great full time back at work, driving etc. However at last check up advised need to bring the dreaded bone marrow biopsy forward to check T cells/chimerism as they have dropped from 90 to 30. May have to have extra top up T cells. This has started my head spinning again. Anybody else experienced similar?

Read more about...
3 Replies
2003UK profile image
2003UK

Hi I cannot help you with your medical question but I do know the head spinning all too well. I think ever since the shock of my diagnosis my emotions and thoughts are on this high alert rollercoaster and it just takes a medical person to say one word and they go into overdrive. I also get anxious before all medical tests and appointments to and if my results are all stable apart from one, it is only that one that I focus on. My head spins whilst I am waiting and don't we do some waiting, it seems never ending. Really look after and be kind to yourself and if you would like to talk to someone the Leukaemia Care support line is there for you

in reply to2003UK

Thank you 2003UK for taking the time to read my question. I am so glad you have high lighted exactly how I feel too before appointments and like you point out the focus and anxiety is always on that lower reading, or repeat tests. It certainly is a rollercoaster isn't it! I think people forget if you look well and are doing normal things then they think you are fine. On the inside though some days can be emotionally draining. Have a lovely weekend.

2003UK profile image
2003UK in reply to

Oh, my pet hate is someone saying 'oh, you do look well' went I am feeling so, so rough inside. Yes, I can feel drained emotionally, physically or practically. Beautiful weather here today and since diagnosis I have realised that the best things in life are free.

Not what you're looking for?

You may also like...

Update on my AML.

This an update on my AML. Recently had my fourth bone marrow biopsy and good results - still in...
snoopy101 profile image

MDS and AML

Despite feeling lethargic and tired for over two years and going to the doctors on a regular basis...
sportydad profile image

My dads AML at 81 years

My dad of 81 years old has been diagnosed with AML and given 6 months to live. He is a very fit man...
Meeawwww profile image

31 year old facing AML fight.

Evening everyone. In the last few days ive had to come to terms that i will be battling AML. But...
NathaN89 profile image

Post stem cell transplant vaccinations

Hi. I am 11 months post transplant (AML). I am due to have my childhood vaccines next week. Just...

Popular Posts

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.