Hubby and I visited my dialysis center last Friday. We were overdue for a visit, but we just received the go-ahead at my last check-up from my lead transplant nephrologist.
We timed our
visit so that some of the techs would be on their dinner break and, hopefully not
too busy. I had mixed feelings about the visit. On the one hand, the
technicians and nurses have become my friends, and I do miss them. On the other,
the center had some really stressful and frustrating memories for me.
We were so warmly
welcomed. The technicians missed us. Unfortunately, my favorite ‘sergeant-at-arms,’
err … charge nurse was not there at the time. I guess we just have to visit again, some other day.
They commented
about how good I looked and how my complexion has improved (I remember having
really dry skin when I was in dialysis, and I probably looked tired a
lot). Most of them have been wondering
when or if I would come and visit. Most
folks don’t come back after getting their transplant. Some of the patients even
commented that we’re a good walking advertisement for a kidney transplant. I
look both very healthy and happy!
In spite of
the happy reunion, the place did look a bit sad and quiet that day. Maybe it
was because the techs were on dinner break. Normally, when I showed up for treatment,
I was in a fairly bright mood; the technicians and I would exchange jokes.
Don’t get me wrong, there were days when I did dread coming to dialysis,
especially when I was sick or had an awful day at work. Most of the time, I
tried to make the best it, usually by escaping in my fashion magazines, watching
my favorite TV shows, getting lost in playing games on my iPod, and of course,
enjoying a conversation with Hubby.
Looking around
that day, the patients looked very, very quiet. There was certainly sadness
in the air - perhaps a quiet acceptance of their situation. I talked to some of my old
friends, acquaintances (as did Hubby, who chatted with a fellow Pittsburg
Steelers fan, friend of his). I’ve learned that some of them have been waiting
for a transplant for even longer than I; one of them was recently refused a transplant
because he was deemed too old (and too ill). Many of these patients even had to
delay any travel, because of the ongoing dialysis treatments.
After this
visit, I appreciate the gift of a receiving a second chance in my life even
more!
I no longer
have to go to dialysis three times a week and have the ability to enjoy travel
without worrying where and when to dialyze. I am so sad that there are so many
others who are still waiting, wanting, and perhaps, running out of hope – can
you imagine! I so wish that they will not give up, because that gift can come
in the middle of the morning, on any given day, seemingly out of nowhere – as
it did for me and for us.
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