Well, it’s official; I got my bone marrow biopsy results
today. My doctor states I’m still in
remission and I have 100% donor cells (which is a good thing)!!! My appointment began with the physician
assistant reviewing my results and explained more in depth what all the numbers
mean, etc. All I heard was this number
is on the lower side and this other number is higher than normal. The “higher than normal” part scared me
because that was the red flag that told us something was wrong three years
ago. But both the physician assistant
and the doctor stated that all is well and assured me that I’m still in
remission.
I am very happy about this don’t get me wrong. I’m not afraid to live and embrace life but
why do I not feel the need to celebrate.
I have experienced beating leukemia the first time and I celebrated that
remission. I was living and loving life,
than I relapsed. The relapse changed
me. Even though everything was looking
good, the relapse is preventing me now from fully celebrating this two-year
remission. That initial relapse has kept
things in perspective for me. It tells
me that just because everything is looking good and feeling good, it can all be
taken away in a second. I think it has
kept me more grounded and realistic.
During my first bout and treatment with leukemia , the
doctors were saying how well I was doing and how quickly my body was healing and
recovering my from chemo treatments.
They kept telling me how great everything was and when I made it to that
year mark of being in remission, I was told that my chances of relapse were
significantly low. Well, I was that
small percentage that relapsed. So here
I am today, being told the same things.
Being told how well I’m doing, how my body is going to take its time in
recovering. So, after hearing all the
same things that were stated to me before, yes, I’m a little hesitate to
celebrate.
I guess how I am looking at things now, I see myself as already
celebrating. I’m enjoying this 3rd
chance of life. I’m embracing life. I’m embracing me. And by embracing all that is being given to
me, now is my form of celebration. I don’t
want to label this “celebration” to just this day or to this biopsy or
appointment. I am already celebrating by
being able to live and breathe each day with my husband and children, family
and friends.
Great blog, your write REALLY well & its very informative. I will keep watch. Wishing you the best, may you stay cancer free FOREVER!
ReplyDeleteThank you, I am glad that you have found my blogs informative. One of the main reasons I began this blog was to educate others about what one person has experienced with stem-cell transplant and I hope that it helps others who have also experienced it or will be going through it someday.
DeleteIf you have anything to offer, please comment on this entry or the other entries. Thank you for your support!!!
Deanna, I just joined the mail site today although I have already had my SCT as of 4/26/12. I had an auto-immune disease called CIDP (cousin to MS) and went to Chicago for an SCT trial. I was the 30th person to have this for my disease. Dr Richard Burt does SCTs for over 20 different auto-immune diseases using our body's own stem cells! We liken it to "alt/control/delete" of resetting your body of disease like you would reboot your computer after you have cleaned out a virus! I will read more of your blog and if you would like to read mine, it is here: http://wendyssct.blogspot.com
ReplyDeleteYou will discover my faith is a very important part of my whole process and He worked a lot in my story! God bless you and I hope you continue to do well!
Wendy (wegrow4him@gmail.com)