I am a 41 year old living in Southern California. In 2000 my wife was
diagnosed with a brain tumor and over the past 5 years we have been
through 2 surgeries and 18 months of Chemotherapy. She is high
functioning, holds a part time job, but was left with several
"deficiencies" (that is what the doctors call them). Doctors have told
us that what she experiences and what she has to learn and re-learn is
very similar to someone who had an injury to the brain. The hardest
thing is having an injury that you can't see - not like a limp or
something that you can see and have other accomodate more easily. A
brain injury can affect personality, patience, emotions, judgement ---
all things that can't be seen.
I look forward to learning more about all of you.
Gregory
On Oct 9, 10:40 am, "michael fluharty" <fluharty.mich...@gmail.com>
wrote:
All-new Yahoo! Mail - Fire up a more powerful email and get things done faster.
Date: Mon, 16 Oct 2006 18:19:14 -0700
From: rjsch...@yahoo.com
Subject: [brain-injury-support:84] Re: what do you think?
To: brain-inju...@googlegroups.com
I'm a 54 year-old recovering alcoholic, sober for 31 years, living in
Cleveland, Ohio.
Prior to my 1994 accident, I had suffered 3 concussions (fell drunk
down a staircase, with a hairline fracture to my skull in 1970, was
assaulted by drug associates who grabbed me by my hair and knocked my
head against the wall in 1974, and I knocked my head hard on a low
overhanging arch while cleaning a foundry in 1986. I did not seek
medical help after that one, but I know I did some damage beacuse I
suffered a week or so of mild aphasia afterwards.) Also I know a 1971
aerosol sniffing binge caused some brain damage because I suffered
aphasia after that as well. I continued self-destructive drinking and
drugging for four and a half more years, but never sniffed fumes again
after that experience.
Then early in 1994, after 12 years of being ill with a bowel disease
that forced me to rise several times a night, I was weak, exhausted and
in the habit of simply diving back onto my flophouse-style mattress
after my trips to the loo. Well, one night I took one step too many
and
dove head-first into the wall. My head rang like a bell, and I knew I'd
knocked something loose, but I did not immediately lose consciousness.
I was too tired, too weak and too fed up with years of sitting around
in hospital emergency rooms after bloody flare-ups of my bowel disease
to even care any more, so I simply went back to sleep and got up in the
morning feeling woozey and confused. Over the course of several hours
things got worse till I was stumbling around delerious and falling down
repeatedly, probably having seizures. At some point I left the water
running and flooded the apartment downstairs, and my apartment
building's live-in custodian found me comatose when he came in to turn
it off. The apartment was not cold, but for some reason I was
suffering from hypothermia, and had a body temp of 90F.
I was only unconscious for about 24 hours. The ICU residents came
running when the nurse told them I'd spoken, and administered a
cognitive test that they repeated countless times for the next ten
days: Name? Address? Social Security number? What year is
it? Who is the president of the USA? Who is the VICE PRESIDENT?
After the first couple times I got them all right except for the last
one. No matter how many times they told me the answer (Al Gore) I
could not for the life of me remember it the next time they came in to
grill me. I mean, I'd VOTED for him along with Bill Clinton less than
18 months earlier, but to me in that hospital room, the vice president
of the United States was, and remained for my entire stay, a complete
blank.
And they kept giving me arithmetic tests that I did not do well on. The
guy who I think was the head of the neurology dept seemed particularly
annoyed at that and I overheard him saying something about "long term
care," which scared the bejeezus out of me.
They told me I had two subcranial hemotomas (blood clots underneath the
skull) One was on my left frontal lobe, the other on my left temporal
lobe. There was some discussion about cutting into my skull to remove
them, but they dissolved quickly and brain surgery was not necessary.
Thank God.
Elliott came to see me. I immediately recognized her, but didn't know
her name. But unlike the case with Al Gore, as soon as she told me I
remembered it. Apparently some idiot at the hospital had told her I was
brain dead and she drove from Cincinnati expecting to find a vegetable.
If she hadn't been there, I don't know what might have hapened to me.
Elliott, you truly saved my life!
The tv in my room was on most of the time I was there and since I was a
little too rattled to read, I watched a lot of it. The local stations
were covering the construction of Cleveland's Rock & Roll hall of fame
and Museum, which was scheduled to open the following year. Not
thinking too clearly, I hit on an idea to make a collection of
rock&roll sculptures for them. I did that upon release, and the
results can be seen here:
http://www.dreamwater.org/art/johnarndt/rock2.html
I was able to speak, but it was a real struggle. It was hard enough to
put three coherent words together, let alone a full sentence. I was
being given a lot of medications, some of which I'd been taking for
years for the intestinal thing, but didn't recognize any of the pills
that a male nurse brought me one day, so with a certain amount of
stammering, I asked what they were. He wouldn't say. So I told him I
wasn't taking them till he did. Then he accuses me of being
"uncooperative," and I just about went postal on him. Somehow my anger
gave me the ability to speak clearly and I told him he had a lot of
nerve to call me uncooperative when I was just trying to be a
responsible patient. I don't think he was
expecting that. I even called in the head nurse and complained to her
about him. That was a very empowering experience and gave me strength
for the struggle to come. (That nurse lives in my neighborhood and I
still make sure to give him a dirty look every time I see him, 12 years
afterwards. It turns out those drugs were generics of the same
medication I'd been taking, plus some antibiotics.)
They kept giving me that same damned cognitive test seemingingly every
hour, and that neurologist who'd been talking about sending me off for
long term care seemed even more concerned about my inability to
remember Al Gore's name than about my poor arithmetic skills, so I knew
I'd better do something about it. I'm a writer and I remembered that
if you called the Reference Department of a library, they could look up
the answers to questions for you. I even rememered the phone numbers
for a two suburban libraries I'd called often in the years prior to the
accident. So I called each of them a couple times to ask in my very
drunk-sounding voice: "Thish might thound like a thupid questhion, but
who is tttthhe Vish preshidunt of ttthhheee United Shtates?"
"Al Gore," they'd say. Heck, they didn't even have to put me on hold to
look
it up. So after the fourth or fifth time, I was able to write it on the
palm of my hand before I forgot it again. A resident neurologist who'd
administered that test numerous times (and who all along seemed to have
a rosier assessment of my chances of being released than that other
guy...) laughed out loud when he saw me sneaking a peek at 'ol Al's
name on my hand, and said: "Buddy, if you're well enough to cheat on
this test, you're well enough to go home!"
They released me the very next day. In the exit briefing they gave me,
I was told I faced a 50/50 chance of developing epilepsy within 5
years. If I made it 5 years without seizures, it probably wouldn't
happen. Also, a nurse told me she'd heard I might be written up in a
neurological journal as being a case of an exceptionally quick recovery
from the type of injury I had. I don't know if my pal Al Gore had
anything to do with that. I keep telling myself I should go across the
street to the medical library at Case Western Reserve University and
see if I can find it, but part of me is afraid of what it might say.
I was confused and disoriented for weeks after I was released, but
somehow I was able to take care of myself and not stumble out into
traffic. I met with a speech therapist a couple times, but since his
treatment was just to have me read aloud, I told him I could do that
myself, as I was working on a novel at the time. (It didn't help me
find a publisher, but I haven't quite given up on it.) A few months
later I had to have surgery for that bowel condition. It greatly
improved my physical health and I became an avid bicyclist, but I never
ride ANYWHERE without a helmet. And I'm always nagging other cyclists
to wear theirs. "You only get one brain in this life, and they haven't
started doing transplants yet," I'll tell them.
Then late in 1995, I started having the seizures they warned me
about. Violent, grand mal seizures. I had to go on a drug called
dilantin, which worked well for several years with a minimum of
problems, but suddenly early in 2001, I started having very severe side
effects to it and had to shift over to a drug called carbamazepine
(generic of Tegretol.) The fact that it is also used on people who are
branded as being "bipolar" pisses me off to no end, because the way it
works is to suppress the emotional centers of the brain. The idea that
my feelings have to be kept locked in a chemical cage to prevent
life-threatening physical symptoms eats at me every waking hour. A
recent experiment with a different medication that is known to have a
less-lobotomizing effect was a failure. I take a very dim view of the
"mental health" racket and this experience has not brightened that at
all. I'll spare you all the angry political rants except to say anybody
considering going to a shrink should visit Dr. Peter Breggin's web site
at:
before they do. His site is a wealth of information on psychiatirc
drugs that the pharmaceutical industry has fought to suppress.
There are some fascinating articles I'm trying to dig up about recovery
from brain injuries in case anybody here is interested, and I would be
especially interested in sharing notes with anybody who has had to deal
with epilepsy as a result of a brain injury.
Well, I think I've rambled on much too long, so I'll end off here.
John W. Arndt
johnwa...@yahoo.com
On Apr 5, 2009, at 10:52 AM, delami...@googlemail.com wrote:
> Hi group, I'm michael, from UK, i'm 23 and i was born with a cycst
> blockage at 4 weeks old, and had a shunt inserted, then when i was 9 i
> had to have it replaced, but by that time the cycst was getting bigger
> and it caused minor damage.
>