Hi Suzieq,

Please forgive me for my error. In any event you read it and brought up some
rather interesting questions. As you mentioned, you are doing well on
Gleevec, and that is very good. A bone or stem cell transplant is like a
life preserver on a sinking ship. While the ship is going down there are
people trying to hang onto that life preserver, and no one really knows if
there is another ship nearby to pick them out of the water. This should be
the absolute last thing that someone wants to do especially if another
therapy is working well.

I am sorry to hear about your brother and he is probably still watching over
you. Think about it as your doing well on the Gleevec, and not needing a
transplant.

I still think about my donor who unfortunately has passed away, but not from
the marrow donation. The story would take me hours to explain, so I will
just leave it at that...


In the time I had my transplant the 6 out of 6 Human Leukocyte Antigen (HLA)
match was considered a "perfect" match. Now there is a 10 out of ten HLA.
Times have changed and so has the ways a transplant is given. How long ago
were you dx'ed?

Finally, as far as the immuno suppressive or anti rejection drugs, I had to
take huge doses for the first year, then it tapered to nothing after that
first year. So, in my case it was not a "for life" situation. However, since
my kidneys are failing I will require another transplant probably within a
year or so. Once this kidney transplant happens, I will then have to be on
immuno suppressive drugs for the rest of my life. So, who ever said that
life is fair, but I just roll with the punches.

I often get asked about all that I went through, and I always answer by
asking if every one put their troubles into a paper bag and left all of
those bags in a pile then which one would I choose... MINE!

GOD bless,

Marty


On Thu, Feb 25, 2010 at 2:17 PM, Suzieq <[email protected]> wrote:

> Marty:
>
> You've confused me with Russel who is the one who responded that he
> had the bone marrow transplant and was looking for ways to thank his
> donor.  I still have the CML and on 400mgs of Gleevec which is keeping
> the CML at a very low range & I've done fine on it since being dx'ed
> in Jan. '04.  As long as it is working, I have no thoughts of doing
> anything different.  He is also the one who spoke of "selling to the
> highest bidder",  not me.  I only wrote the article I read in the
> paper.  I have no qualms with the way they would like to pay.....I
> think it would be a commendable way of trying to generate more donors
> rather than just giving the donor money free and clear.  I think this
> brings up some very good issues with those of us who might one day
> face this possibility of having a BMT as some of you have already had.
>
> And, Marty, you are so right about the 1 in 4 percent range of a
> sibling match.  I have two older brothers...neither of which matched
> me. (smile)  I told my husband that I felt pretty sure that my perfect
> match lies in the grave yard back where I'm from.  He was an older
> brother who was hit by a car and killed at six years old (I wasn't
> quite 1 year old at that time).  The National Registry found twenty
> four 6 for 6 matches to me back when I was first dx'ed.  That was the
> best they could do........at that time, I didn't even know what that
> meant.  And after reading up on how they did BMT's,  I told my husband
> then that I would never want to put someone through that unless it was
> the last option I had.
>
> By the way, Marty,  do you still have to take the "anti-rejection"
> medication?   I was just wondering if that was a "for life" thing once
> it was done.
>
> Thanks,
> Suzieq
>
> --
> [CMLHope]
> A support group of http://cmlhope.com
> -------------------------------------------------
>
> You received this message because you are subscribed to the Google Groups
> "CMLHope" group.
> To post to this group, send email to [email protected]
> To unsubscribe from this group, send email to
> [email protected]
> For more options, visit this group at
> http://groups.google.com/group/CMLHope
>

-- 
[CMLHope]
A support group of http://cmlhope.com
-------------------------------------------------

You received this message because you are subscribed to the Google Groups 
"CMLHope" group.
To post to this group, send email to [email protected]
To unsubscribe from this group, send email to 
[email protected]
For more options, visit this group at http://groups.google.com/group/CMLHope

Reply via email to