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PAI Pamphlet?

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I agree with when she said that we should share this

website with our physicians so they can share it with other CP

patients. I would like to know if there are any informational

pamphlets or flyers that could be posted or set out in offices to

invite and inform others of this wonderful support group.

If there was something that we could download or be mailed, each

member could take this information to their physicians resource

areas so others would know that there is support out there!! I

actually stumbled across this message board while searching for

support groups, and I thank God daily for a wonderful variety of

people who are willing to share in my laughter,tears,and answer my

hundreds of questions.

I will going to MUSC Feb.23 and would be happy to ask if I could

leave some information there for others to read. I think leaving

this in the waiting areas would be a huge boost for this site since

there is always a wait involved in all doctors offices.

As far as me staying over night at MUSC...I've had 2 other ERCP's

preformed in the past in which stenting was done both times and a

sphincterotomy the last. Each time I have had this procedure done,

I've ended up staying 2-3 nights due to aggrivation of my pancreas,

so if y'all want to call or come by, I'd love to hear or see ya! I

have no idea of what the phone number where I can be reached will

be, but I'll try to find a general one and you could ask for Kim

Stalcup's room from there.

Please let me know about the brochures...if they don't exist, maybe

we should get one made up. Take care all! :0)---Kim S.

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