|
The House Committee on Energy and Commerce
Subcommittee on Oversight and Investigations
June 3, 2003
10:00 AM
2322 Rayburn House Office Building
Hello, my name is Reginald Augustus and I am here today to tell you about how
my life been dealing with kidney failure while waiting for a kidney transplant.
In May of 1999, during a routine physical, my doctor told me my kidney's were
not functioning properly.On that day my life changed forever. As time went on I
began to not feel well. My bloodpressure began to elevate, I felt shortness of
breath, and I would feel nauseous often. By the time I went back to the doctor
in March of 2001, I needed to be put on emergency dialysis, given 2 blood
transfusions, and I had to spend 5 days in the hospital.
Since March of 2001, I've been on kidney dialysis. I had to change a lot of
things such as my diet. I now have to watch certain foods and fluids that are
high in potassium which couldcause a heart attack, high phosphorous foods which
could eventually thin my bones and make them brittle. I also have to watch my
fluid intake, since my body no longer gets ridof this fluid which can cause
problems by getting into my lungs which has happened and around my heart which
can lead to other problems. I also have to go 3 times a week forkidney dialysis
where I get stuck with 2 large needles into my arm where a surgery was performed
called a fistula where an artery and a vein are connected to make the vein
largeenough to handle your blood being sucked out and pumped through a filter (dialyzer)
thatcleans my blood and take's out excess fluid. Not only is this process
inconvenient, lasting about 4 hours per treatment, but it leaves me feeling worn
out afterwards. Manydialysis patients such as myself, cramp badly from the
fluids being taken off. We also have to deal with our blood pressure dropping
and the stripping out of our bodies not justtoxins, but minerals and vitamins
are bodies need. The process of dialysis effects one's body in a negative way.
Long periods of time on dialysis will shorten a person's life. Other than
dialysis, going about my day to day activities, I don't feel the same as I use
to.
I get tired faster as the toxins in my body don't have anywhere to go. They
build up and kill red blood cells. At the dialysis center, I get epogen
medication to help produce red red blood cells which my kidney's once did for
me. I also get a medication called Zemplar, to help control my phosphorous and
calcium levels and my parathyroid. I've met many people at the dialysis center.
Some who have been on dialysis a short time andsome a very long time. The ones
who have been on for several years look different than the newer ones. Years of
dialysis and kidney failure have darkened there skin and made them weak and
sickly looking. My uncle spent 20 plus years on dialysis before dying in his
early 40's. I watched his body deteriorate, his bones become brittle, and was
basically a hunched over shell of a man at the end. For many, work is not an
option. Many work part time or not at all because of dialysis. Everyday more and
more people go on dialysis and the need is greater than ever for organ donation.
Currently, I believethe national average wait is over 3 ½ years and it's even
longer for African-Americans.I've been on the waiting list for 2 years but many
I know have been waiting more than twice as long as me. The need for organs is
great and we need to increase there availability. Thank you for your time.
Sincerely, Reginald A. Augustus
Printer
Friendly |