Maybe a little good news

[Guest guest]

Ya'll know that I have been on this tangent to get word out about

our wonderful support group that we have here. I have asked all

ya'll to share the web site with your docs so they can inturn share

it with their other panc patients. As we all know, not all docs are

so receptive to " online " activites.

I had asked the surgeon at MUSC who had done all my sugeries and

referred me to Cincy to do just that and got no response. I was

beginning to think I would be sharing 's unfortunate

experience. I had even planned on making my own fliers and taking

them to the ERCP unit when/if I went to MUSC to check on Kim.

Tonight I received an email from the surgeon at MUSC with the name

of the gentleman, whom I am guessing is the webmaster for the DDC at

MUSC, asking if I could send him the link. I sent it immediately.

Hopefully, I sent it correctly and it will be added to the support

group section of the pancreatitis part of the DDC web page soon.

Boy thats a mouthful. That is an excellent site that provides tons

of valuable info and now maybe more people who have cp will find the

support, comfort, knowledge and love just like I and the rest of us

have been so fortunate to find. Sure do hope I sent it right.

Warmly,

[Guest guest]

,

I think that it is great that the DDC at MUSC site is willing to put

the link to this board on their homepage.

I agree that having this board is about the best thing there is

about CP and all the stuff that is associated with it. I also think

that the more people that join in on our discussions the more we

can learn and maybe start to understand why certain things

happen in certain circumstances. It always is helpful to get many

opinions with various viewpoints. The bigger we grow, the

stronger we get as an organization.

We should get magnates made and we can place them in

strategic locations when we visit gastroenterologists. We can

join the array that is up there that the drug reps give to clinics!

Laurie