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Tanya's
Story

I have been suffering all my life with pancreatitis, but just
recently got diagnosed with chronic pancreatitis. When I was little,
I remember having really bad stomach pains, and I would ask my
mother and sisters to rub my belly, the pain was always in my upper
belly and I would throw up a lot. My mother brought me to the
doctors all the time, I wasn't growing right either and was very
short for my age, the doctors always thought that I wasn't eating
correctly and would give my mother medications for my stomach, but
they never helped, and they never looked into it further.
For a few years the pains wouldn’t come that often, probably
once every few years, when I was a teenager I just kind of ignored
the pains and vomiting and blew them off as just being something I
ate, I went down to 79 pounds and doctors thought I had
anorexia/bulimia because I said I threw up after eating. When I was
about 20, I went to the doctors because I was getting the pains a
lot, he told me I had acid reflux and gave me a prescription for it,
but I stopped taking it after a few weeks thinking I was all better.
I was okay for a few years, and during this time I had
problems with alcohol, I would get the pains on and off, but nothing
too bad. Then when I was 22, in 1996, one night I awoke in serious
pain. I woke my mother up and asked her what ulcer pain felt like
because that's what I thought it was. She jumped up and told me she
was bringing me to the ER. By the time we got there I couldn't
breathe because the pain was so bad, they brought me into a room and
pressed on my belly, it was hard as a rock and I told them to stop
because it hurt so much. They took blood, hooked me up to IV's and
gave me a shot of Demerol.
I had ultrasound after ultrasound. They asked me if I was
drinking a lot, and at the time I wasn't. I hadn't drunk for months.
They told me I had pancreatitis and I may have a gallstone lodged in
my bile duct because they saw "something" wrong with my bile duct. I
then went for a cat scan and more ultrasounds, which showed no
gallstones, but something was seen. I was admitted for 5 days in the
pediatric unit because all beds where full. A surgeon came in to see
me and explained that my bile duct looked to be dilated, but I had
no idea what he was talking about. He said if I continued to have
pains I would have to see a specialist.
I was released on a Friday and went back to work that Monday.
I was still weak and tired, but I needed the money for my car. For a
while after this I only had pains occasionally, and when I did I
never thought it was my pancreas again. I just thought maybe it was
the vitamins I took, or something else. The pains started coming
more frequently when I was about 26. I would be at work and have to
rush to the bathroom to have diarrhea or vomit. Once I almost passed
out running a machine from the pains and my boss sent me home. It
seemed like everything I ate went right through me and caused me
pain from then on.
In March of 2001, I went on a trip to Mexico with my fiancee
and his sister and her husband. We had a great time, did a lot of
snorkeling and of course a lot of eating and drinking. I got sick
one day at the beach and had to go back to the hotel room to vomit,
but I thought it might've been the water there or the food. My
stomach bloated out pretty bad too. When we got home from the trip
that Thursday, I was feeling better, just tired, and I went back to
work that Monday. All day Monday I felt the pains growing worse and
worse. By the time it was time to go home I couldn't even talk or
laugh without holding my stomach. I went home and told my mother I
had to go to the doctors. I went into the shower and had trouble
even washing my hair or standing up. My mother decided on the ER
when she saw me come out of the shower. I didn't even dry my hair I
was in so much pain.
When I got there, they shot me up with Demerol, took some
ultrasounds and blood work, then I was admitted. I was told that it
was pancreatitis again. I remember thinking what is it with this
pancreatitis crap! I had my gallbladder removed 2 days after being
in the hospital, just for precaution even though no gallstones where
seen. The same surgeon came in that I had last time and told me I
had a choledochal cyst and would need to go to Boston to a
specialist because this was very rare. I was released 2 days after
my surgery and was set up for an ERCP in May.
I went for the ERCP may 7th and was very scared. They told me
that they had to test for cancer and they where going to do a
sphincterotomy to de-roof the cyst. I thought okay whatever that
means! I didn't remember anything about the ERCP thank God, and they
came in after and said I had a type 3 choledochal cyst or a
choledochocele and only very few people are born with this. I also
had a narrowing in my pancreatic duct and since there where no
tumors, that the scarring was due to chronic pancreatitis. He gave
me a prescription for enzymes to take after every meal and Ultram
for pain. I was kept overnight there and had a small attack that
required Demerol, but the next day I was feeling better so they let
me go home.
I thought after this I would be okay. I didn't know anything
about chronic pancreatitis or what it meant, but I kept getting the
pains after that and now they where constant. I went back to my
specialist and they took blood work. My amylase was still elevated,
it was elevated at my primary care doctors twice before this, and my
LFT's where elevated too. They did a tumor marker test, which came
back negative. He called and wanted another ERCP, but I scheduled it
for December because I had just found out I had graves disease and
little did I know ERCP's could be dangerous with hyperthyroidism.
So, I went back on December 13 of 2001 and had another ERCP,
had to take beta-blockers for my heart because of the graves. This
one I remembered a little more and I found it very unpleasant, they
gave me broth to drink before I could go home and I thought I would
die with pain after drinking it! But the pains finally subsided and
I was allowed home.
Ever since I have had nothing but pain, constant diarrhea,
fevers, exhaustion and weakness. I never did return to work and am
now on SSDI. I have also been diagnosed with other health problems
and have had 2 surgeries for other things since April. I am having
another on my thyroid and possibly another for big kidney stones.
They just keep finding more and more stuff wrong with me. I have
good days and bad days, but unfortunately the bad days rule.
Hope you liked my long story and hopefully I didn't bore
anyone!


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