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TLC - My Story |
Lynchburg's
Organ Transplant Support Group |
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Ken Hudson
Forest,
VA
I am the Father Chris Hudson. Chris was 17 years old and a Junior at
Lynchburg Christian Academy. On April 27, 1999, Chris fell out of the back
of a pick-up truck. The truck was not going fast but Chris landed on the
back of his head. He never regained conciousness and five days later he died
from swelling of the brain. As the realization of his death sank in, his
Mother and I felt that if we could just keep one other family from going
through this, it would help add meaning to our loss. Six people and thier
families have been helped by Chris. Half of those were life-saving and three
children got their Moms back. So far we have heard from two of the families
and thier stories have been a huge help to us. Organ donation has brought so
much love to us that it proves what the Bible says, "Whatsoever a man
soweth, that shall he also reap." So much love has come our way that it has
really helped us get through our grief. The reciepient of Chris' lungs sent
us a wonderful poem. It is written as from an organ recipient to thier
donor. If you would like to get this, e-mail me and I will be glad to
forward it to you. Thank-you and may God bless.
Click here to read these poems
Alin Chitanu
Romania (now
Long Beach CA)
I'm originary from Romania and with the help of my sister which is an US
resident I'll get as charity the posibility to have a kidney transplant here
in the US. The donor was my mother, the operation was succesfuly and me and
my mom are recovering and doing well. The problems seems to be the
medication which I can't find in my country Romania and so far I can't go
back and the hospital who perform the surgery agree to give me medication
only for 6 weeks after transplant and after this I supose to go back in my
country but I didn't react to the Ciclosporine wich is the only medicine to
find in Romania from this category!! and that for they'll put me on Prograf
and so I'll get in this situation with only one exit, to stay in the US. Now
I'l try to get me transfered with the job in the US (Iwork in Romania for a
big German Company with many subsidiary in the US) but will take a lot of
time till i'll get employed and in 2 weeks I'm out of Prograf and Celcept
and Zovirax 800. Please be so kind and try to help me geting this medicine.
This is a desparate situation. Alin Chitanu , paulmg99@gte.net
Billie Sue Cornett
Eastern
Kentucky
Jacob was born on July 22, 1997, a repeat C-section. We had no ideal any
thing was wrong. Jacob was in respiratory distress at birth and was
transferred to a bigger hospital in Lexington, Ky. He was soon put on a
ventilator, he was diagnosed quickly thanks to God and some wonderful
doctors. He has a genetic disorder called Surfactant Protein B deficeincey,
which there is no treatment except a lung transplant. We left for St. Louis
Childrens Hospital on August 12, 1997, jacob was three weeks old. Jacob was
put on the waiting list for lungs in just a few days after we arrived in St.
Louis. We waited for lungs one hundred and twenty-one days the longest any
baby had waited for lungs. So on dec. 13, 1997 we received an early
Christmas present, a new set of lungs for Jacob. He came off the ventilator
in five days and oxygen on the eighth day and out of the hospital on the
18th day after his double lung transplant, Jacob set records one after the
other, thanks to God above, who we give all the honor and glory. We had to
stay in St. Louis for two more months for tests and monitoring of
medications, etc. We came home on March 11, 1998 to our beautiful mountain
home in Kentucky. Jacob is doing wonderful, he has never rejected his new
lungs which is unheard of almost every transplant will reject at first or
sometimes in the early months, but this is one more of Gods blessings. We
practice good handwashing and keep Jacob away fromsick people and dangerous
situations and say lots and lots of prayers. We have had little virus and
colds but nothing that a perfectly healthy child wouldn't have.
Greg Partch
Whitman County,
Wash. USA
I belong to a local grassroots organization named "Whitman County Transplant
Organization". Started 5 years ago we are a non-profit 50C3. After raising
over a $165,000 for a local resident to secure a liver transplant we tied up
with a national non-profit to administer our project. The person needing the
transplant recovered miraculously recovered but the national would not give
us back our money. We decided that from here on out we would form our own
group and 99% of all monies would go directly to the person in need. We help
defray upfront costs with grants in varing amounts up to $10,000. We screen
carefully with an anonomyous committee who decide the need and amount. After
that we give the money without any strings or obligations attached. We have
been fortunate to offset the immediate needs of local people as well as a
strong support group as many of our members are former transplant survivors,
relatives or currently waiting. Anyone interested in our group please
contact me. I hope to one day have a web site set up when I get the time.
Thanks for allowing me the use of your site. Our motto is "From the heart of
the Palouse". The Palouse area we live in is a famous agricultural area in
eastern Washington State. Best Regards, Greg
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