|
Mark Popovsky
In 1993 I had a severe case of the flu. Two weeks later,
I noticed numbness and tingling in my feet, which over the
course of the next 18 hours progressed up my legs and arms.
My legs began to feel "heavy" and I had difficulty walking.
While this was happening, I was in denial of these symptoms
because I was "too busy" to be sick. During the second day
of these symptoms I noticed that I had trouble swallowing
food.
GBS is a rare illness similar to multiple sclerosis, but
unlike the latter, there are effective treatments. Without
these treatments, about 20% of patients die.
I was taken to the hospital where the physicians agreed
with my self-diagnosis. The irony of my predicament was
that over my career I had treated numerous patients with
GBS with therapeutic plasma exchange, and now I was going
to be the beneficiary of this treatment. It wasn't a moment
too soon! I could no longer walk or use my arms and my breathing
became labored as the disease progressed to my diaphragm.
I underwent an emergency plasma exchange, receiving plasma
and albumin. Over the next week, I received more than 80
blood products during a series of 6 exchanges. Thank goodness,
the blood was available.
The good news is that I was in that fortunate group of
patients who have a spectacular recovery. The disease stopped
advancing. Ten days later I left the hospital and went into
a rehabilitation hospital where I relearned how to walk
over the next 3 months. I made a complete recovery and 15
months later ran in a 10k race.
If it were not for the advances in transfusion medicine,
the availability of automated blood collection devices and
a safe, and sufficient blood supply, I might not be around
today. This is one of many stories about the importance
of blood therapy and the people who make it possible through
blood donation.
|