Thanks Joan, 

I really enjoyed reading your post, stay strong and God Bless!  Silas 

 

From: Joan Anglin [mailto:[EMAIL PROTECTED] 
Sent: Wednesday, January 09, 2008 3:58 PM
To: [email protected]
Subject: [QUAD-L] Ramblings on health

 

Over the years I have been amazed at the differences between levels of
spinal cord injury. As is so often noted, we vary tremendously. We each have
our own demons to deal with, and we each deal with them in often ingenious
ways. I have often felt frustrated that it was so difficult to find the
answers for seemingly small problems.

Until I came up on this list a couple of years ago, I had been relatively
isolated from other quads. Reno had no physiatrist, so I just used a family
practitioner and she and I dealt with problems as they came up. Lucky for
me, I hardly had any problems. The biggest whammy was being bitten by a
brown recluse spider, and not having it diagnosed until a lot of damage was
done. Luckily, that was during the time I had insurance. The people on this
list have so much experience, and are so willing to share it with the rest
of us, that many of the small problems can be resolved rather simply.

At Santa Clara Rehabilitation, they emphasized keeping everything simple.
Since I had very little access to information about quads, I kept it simple.
The first 14 years bowel care consisted of digital simulation every third
day, but after realizing that I was major lactose intolerant we changed it
to four times a week-Monday, Wednesday, Friday, Saturday-and I've stayed on
that routine since then.

I did not even have a urologist that was familiar with quads, so I just
stayed with intermittent catheterization, not knowing the options. I do use
an overnight bag with a 14 F red rubber catheter overnight as I do not have
anybody to cath me. I've been very fortunate and do not have many UTIs, and
have never had a serious one. I must admit that having to stop activities in
order to be cathed is somewhat of a nuisance, but if it means that I will
not have to deal with UTI's I will continue to live with the scheduling
problem. Of course, I cannot be sure that that is why I do not have UTI
problems, but if it ain't broke, why fix it? My new urologist told me that
one of the advantages of using intermittent catheterization is that my
bladder has stayed a normal size, and I am able to hold around 500 CC's
before my body lets me know it is time. If I watch what I eat and drink that
is usually around 6 to 7 hours.

Except for pressure sores I have enjoyed remarkable health, and thanks to
the clinitron bed my pressure sores have been cured, and I hope that I can
remain free of pressure sores.

Because I cannot feed myself, it has been relatively easy for me not to gain
weight because I hate being fed by other people. One would think after 17
years that I would be comfortable with it, but the only time it works well
is when I share a plate and realize I am not keeping somebody from eating
their food. JIt's also very difficult to snack when I have to ask somebody
else to fix it for me.

This summer I had many tests done, because my physiatrist was appalled that
I have not had scans done regularly. Everything was just OK, and luckily for
me everything was in its right place J. They noted I had a couple of
gallstones, and wanted to watch them.

But over the holidays everything changed. My years of being healthy made me
unaware of how sick I was.  When my daughter said that I was yellow, and I
had several days of burning pain in my stomach, I went to the ER. Except for
being yellow, everything appeared to be OK-blood pressure, no fever, pulse
rate OK, and my urine was rather dark, but not really worrisome.

They were extremely busy in the ER, but we let them know I would need to be
cathed in a couple of hours. They were very understanding, and came out a
couple of times to let us know they had not forgotten us, and were able to
get me into a room as quickly as possible. Everything changed however when
they found out I was passing a gallstone and had pancreatitis, and they
moved into high gear. I was admitted, and they explained my options, and we
all agreed that I would have to have my gallbladder removed as soon as the
pancreatitis subsided. My body was ready two days later-not my mind J-and I
went to surgery, only to wake up with a tracheotomy! Certainly not what I
was hoping for, as the anesthesiologist had said there was a 5% chance that
I would have to have a tracheotomy. Unfortunately the scar tissue from my
first tracheotomy prevented a simple intubation, and my daughter had to
agree to a tracheotomy.

Now I was facing a much longer stay in the hospital. I was in ICU for nine
days because I had a major bleed-rapid response and all the rest-and really
came face to face with my mortality. My care there was absolutely great, but
then I had to move to a more long-term facility. WOW what a difference. Got
there on Tuesday and, and by Thursday I wanted to leave. I went for hours
without anyone checking in, no call button that I could use, and no way to
call for anybody. Convinced my Dr. to take out the tracheotomy on Friday,
and after a night from hell on Friday night, convinced him I would be much
safer at home with people who would be there for me. Saturday night was
rough, but certainly not as bad as Friday night in the hospital had been,
and from there on things improved daily. I now empathize with those of you
who have multiple hospital stays, and I really hope that I will not have to
return to a hospital anytime soon. My trach has healed, and my energy has
returned.

I know as I get older that my health issues may become more of a problem,
but hopefully I will be wise enough to catch them at the beginning and not
let them progress to the hospital state! At Santa Clara they emphasized that
we should be in control of our bodies, and not let our bodies be in control
of us. I continue to think that God has a purpose and a plan for us, and
that our job is to focus on the positive aspects of our lives, educate as
many people as possible that wheelchairs are only the way that we walk, and
try to improve things for those who will follow.

Forgive my ramblings, but thanks for listening. From snowy Reno Joan

 

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