New here... : Diagnosed in July 201... - Non Hodgkin's Lym...

Non Hodgkin's Lymphoma Friends

1,799 members805 posts

New here...

Mrjackwagon profile image
6 Replies

Diagnosed in July 2014- RCHOP treated in Pittsburgh at the Mario Lemieux Center for Blood Cancers. Relapsed in November of 2015, received RICE then BEAM before April 2016 auto stem cell transplant.

Written by
Mrjackwagon profile image
Mrjackwagon
To view profiles and participate in discussions please or .
Read more about...
6 Replies
Glenmeadow profile image
Glenmeadow

Me jackwagon tell us how you found that stem cell transplant. I think there is one in my future as well so I want to learn all I can

Mrjackwagon profile image
Mrjackwagon in reply toGlenmeadow

It is a standard treatment at Shadyside Hospital, Pittsburgh. They have a specialty unit there and 20 days in the hospital--I was taken good care of. My wife stayed with me everyday. They have a family house across the street and it was very convenient. The Hillman Cancer Center is next to the hospital. That is where the Mario Lemimex Center for Blood Cancers is (where my doctors are and a wonderful treatment center).

Tinkerbellcgy profile image
Tinkerbellcgy

Mrjackwagon, I also underwent an autologous stem cell transplant during the summer of 2012. As well, I have been treated with R-CHOP in 2008 and the R-MICE and R-BEAM in 2012 in conjunction with the transplant. The transplant was successful and that the of lymphoma remains in remission.

Wishing you future health.

Jennchap1 profile image
Jennchap1

I am 3 months post auto stem cell transplant after my NHL relapsed into my CNS.( after more chemo of course and the immune system wipeout chemo). Doing well. Tough road, but if you have strong support (my husband stayed in hospital with me the whole,month!:) you will be ok. I wish you well!

Cjjn3 profile image
Cjjn3

Thankyou for sharing, I'm going through stages for transplant.just waiting for siblings to have donor tests. It's a bit nerve wracking waiting for everything to get into place. I'm told because of my age (67 almost) that only siblings will be considered. Good to hear feedback from patients who have had experience cause most people can't relate to the anxiety that goes with the treatments as well as disease!

Tinkerbellcgy profile image
Tinkerbellcgy in reply toCjjn3

I am sorry that you are experiencing anxiety. I tended to view my transplant as an adventure and, for the most part, looked forward to what each new day would bring. By changing my focus on how I viewed the procedure along with my wicked sense of humour, it got me through even the most trying of days.

May your transplant experience be a smooth one for you.

Not what you're looking for?

You may also like...

I am New here

I was diagnosed with waldenstroms macroglobulinemia in June. Have had treatment and now waiting for...
Anne946 profile image

Relapsed Mantle Cell Lymphoma--I'm new here!

My name is Gail and I am 66 years old. I was diagnosed with MCL in February, 2008 when I was 58...
Gail2050 profile image

Hi! I'm new.

Hello-I have been fighting Non-Hodgkins Lymphoma since I was 35, and for almost 12 years. I had...
MsMindy profile image

New member....new to NHL...new to chemo...so many questions ???

Hello everything, I'm excited to have a community of people to talk to. I need support and am...
Ralbright89 profile image

New member here my name is Alan and I've just been diagnosed with FNHL

Hi guys i,m still trying to get my head around whats happening to me, Some doctors are saying its...
GeordieAl profile image

Moderation team

krayburn profile image
krayburnPartner

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.