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Heidi,

That was absolutely the best laugh I have had in awhile!!! I can

totally relate!! I was caught laughing out loud at the computer so I

read your post to my mother, who proceeded to laugh also because she

has witnessed this same exact thing with me. (rolling veins, etc...)

Thanks for the chuckle.

Take care

Kris in TN

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Yeah I ran into some doc's and nurses that hated trying to access the

port when I had it. I was in the hospital for a thyorid storm and on

demoral for pain. When an RN brought a student nurse in. I told the

RN that it would be fine for her to try and see if the port would

work. Next thing I know the student nurse has the crooked needle in

her hand and she pokes the cath and pops it.

It took me almost three yrs to find a doc that would be willing to

take it out cause the doc that had put it in was up on charges of

malpractice. It was really awful but I was happy to have it out. Now

I get the phantom pains from where it had been in for so long.

I just got back from the doc's office. Things didn't go very well.

Since I have had pancreatitis for so long my kidney's are starting to

fail, my heart is beating so fast I have to be on bed rest for the

next week so maybe it will slow down. I am trying lunesta for the

first time tonite...does anyone else have problems sleeping and what

kind of meds has the doc's tried you on?? Well I am going to try to

eat and watch a movie...hope that everyone has a pain free nite...take

care all..

KebaJ.

>

> Kebaj, I have a port, have had one for over 2 years, and a central

> line before that and a PICC line before that. I have found the port

to

> be a lifesaver, but there are still hospitals/doctors who refuse to

> use it. I have 2 hospitals converted just for me at the moment, but

> still come up against those who want to stick me rather than access

my

> port...

>

>

>

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Keba,Heidi and Mark, I was in the ER last Sunday and they stuck me 7

or 8 times. I warned them it was gonna be tuff and the male nurse

tried the back of my hand, twice and it killed each time! I was

squirming around, I know how you feel....Jim

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Oh my gosh! I am so sorry.

I didn't know this could happen. Is it common for the kidneys to fail

with CP?

This disease gets more frightening the more I learn about it.

What will they do for you?

Eileen

>

> I just got back from the doc's office. Things didn't go very well.

> Since I have had pancreatitis for so long my kidney's are starting

to

> fail, my heart is beating so fast I have to be on bed rest for the

> next week so maybe it will slow down. I am trying lunesta for the

> first time tonite...does anyone else have problems sleeping and what

> kind of meds has the doc's tried you on?? Well I am going to try to

> eat and watch a movie...hope that everyone has a pain free

nite...take

> care all..

>

> KebaJ.

>

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Yeah think I am the only one that has had CP for so long. I got

sick when I was 10. So I was written up in JAMA and was a vandebilt

test subject for a very long time. I was lucky though I had a nurse

for a mom...so when the doc's wanted to do anything to me my mom

would tell me everything they were going to do. I have a lot of

things wrong with me....I have been sick for 19 yrs now. The doc's

always said I should have died when I was 15....made it to 15 and

they said 21...when I made it to 21 they told me 30...and now I am

29. Not to scare you but I am going to try and list everything that

I have developed over the last 19 yrs...

1. In 1986, I had two and a half liters of fluid drained off my

pancreas.

2. I had my gallbladder taken out.

3. I had to have sweat glands taken out from under both arms and

breasts. I was on robinaul to help control the fluid around

pancreas and it ended up clogging sweat glands. I still have them

between my legs....cause you can't walk for a few weeks when those

are taken out.

4. I was raped while in college and since the child was pressing

against my pancreas my body was shutting down. So I had to make the

choice of me dying in child birth or the baby living. I ended up

having an abortion.

5. I have severe hypothyroidism. I have had a round of radation

once at vandy and about to go back to have another round.

6. I have severe depression and bi-polar. I think cause of all the

stress of knowing that I am going to be sick and more then likely

die very young.

7. I have been in the hospital three times now for having mega

colon's. Which are when you are on so many pain pills that you

don't have bowl movements at all. So I have had to cut out most of

my pain pills so I can try to be regular.

8. I have severe Type 1 diabetes. When I first was diganosed with

this...it was about 4-5 yrs ago. The doc's were surprsied that my

pancreas was working that well. Now it only works 20-30% of the

time.

9. I have had two thyroid storms which are like mini heart attacks

and I was in the hospital a month each time.

10. I have also developoed extreme insomnia because of how long I

have had to be on narc's for pain.

11. My latest problem wrong with me is I have developed a case of

severe sleep apathnia. Not sure how this is going to turn out

though. Will keep ya posted.

12. My eye sight is going down a little every few yrs which

surprises some ppl since I always have a blood suger over 300-400

normally.

With all these things wrong with me. I was very lucky to get

disablity with the diagonis of Chronic Pancreatitis. I know that

this is very hard to do cause I was turned down three times before I

went befor a judge. If anyone is trying to get on disablity please

let me know and I will try to put my decision onto the group page so

maybe that can help ppl see how the judge decided in favour and

maybe it will help with your case. If you have any questions post

here or feel free to email me at kebajackson@...

Hope everyone has a pain free nite

KebaJ.

> >

> > I just got back from the doc's office. Things didn't go very

well.

> > Since I have had pancreatitis for so long my kidney's are

starting

> to

> > fail, my heart is beating so fast I have to be on bed rest for

the

> > next week so maybe it will slow down. I am trying lunesta for

the

> > first time tonite...does anyone else have problems sleeping and

what

> > kind of meds has the doc's tried you on?? Well I am going to

try to

> > eat and watch a movie...hope that everyone has a pain free

> nite...take

> > care all..

> >

> > KebaJ.

> >

>

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Yeah I know...I don't tell everyone how truly sick I am. I talk about

it here cause there are other ppl just as sick...and I want to be able

to help everyone here if I can and give as much advice as I can. I

think the only thing that has stopped me from ending it all is my

fiancee/bf Jay....he has lived with me for the last 8 yrs. My mom is

happy that I found someone that is so willing to take care of me as

much as he has too. I have had times where I just couldn't take it

anymore and thought it would be better for everyone if I took my

life. Jay was there at that lowest point in my life and told me that

I was here on this earth still for a purpose and I think helping as

many ppl as I can is why I still live and breath.

I also am a part of the eastern band of cherokee indians. We get a

check every six months...which helps me pay for the medicine's that

tenncare won't cover anymore. If anyone has any questions at all

email me.....

>

> Keba, I am overwhelmed at your courage. Really, all that you have

been

> through, just reading it made me speechless.

>

> Eileen

>

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Jim,

I'm squirming just as I read that.....yuck!! The back of the hand is

the worst place for me, that's where the anesthesiologist tried an

hour for a triple lumen access, and never could get it. It hurts

just to think about it, he said it was like trying to get a square

peg into a round hole....

Sorry that you had to go to the hospital. Where did they finally

get access?

With love, hope and prayers,

Heidi

Heidi H. Griffeth

SC & SE Regional Rep.

PAI

Note: All comments or advice is based on personal experience or

opinion only, and should not be substituted for professional medical

consultation.

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Hi Heidi, my computer is down so I'm on my roomates, thats why this

reply took so long...the head phlebotomist came in and got a vein on

my left forearm. I'm still black and blue a week later...Jim

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Heidi,

That is awful about what they did to you with those needles. I am blessed

with great veins. In fact the nurses always say I have rope veins. Very large

and easy to get to. My mom is like you though and it is hard to watch that. In

our house, we say, " it makes your coochie draw up just looking at it! " LOL!

Angie in SC

" The happiest of people don't necessarily have the

best of everything; they just make the best of everything that comes along

their way. "

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