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Who we are behind our CP?

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I have seen other support groups that opened up another message board

secondary to their support board that was designed to discuss personal

interests. These posts related to work discussions, hobbies,

activities, music and art interests, children, etc.

Something like that would be wonderful for this group, as I do agree

with Anyse, that it would be nice to know who we really are, behind

our CP. We have a group with so many varied interests and ideals, and

that really doesn't come out into discussion on our current forum. Or

when it does, some people object, saying they aren't interested in

hearing about so-and-so's personal business.

An example of this is when I was so enthused talking about the

preparations for my daughter's wedding last year. Several other

members kept asking for more details, they had daughter's themselves,

or weddings that they had participated in, or were just interested in

the discussions of decorations, fabrics, design, flowers, planning,

etc. A member wrote in and complained, saying that she had " no

interest " in hearing about any of that, that it was off topic, etc.

So from that point on, I refrained from any wedding discussion, even

though several other members said they loved hearing about it and

wanted to hear more. So we kept our discussions off the board.

The thing is, for those six + months, that wedding was a very

important part of my life and was in direct relation to my mental

health, and how I was coping with my CP. It would have been nice to

have shared the excitement, fear, worries and expectations with

someone else who was also interested.

Whether it's something like that, or the other things that make us

tick; computer programing, software design, gardening, sports, crafts,

medicine, art, music, cooking, etc, etc.....the list goes on and

on.....there's so much more to us than just this dreadful

disease....it would be mentally beneficial for us to be able to show

the other side of who we really are.

People may know that I have (had) my own business as an architectural

draftsman, but do they know that I've been painting landscapes in oil

for the past 40 years, have strong interests in horticulture, do

decorative sewing, taught alpine skiing for 6 years and like to fish?

These things are elemental to my well being, just as I know that each

of you has more behind you than CP.

I dunno, it might not be possible, but I know I'd be interested in

seeing if we could develop another way to learn more about each other

than just how many surgeries we've had, whether stinting worked, or

the latest tricks for treating nausea...

If anyone has any ideas, let's discuss it and figure out how we could

do it. I think it would be really healthy for us to have something

else, other than our health, to discuss and share....lol!

With love, hope and prayers,

Heidi

Heidi H. Griffeth

www.pancassociation.org/anthology#Heidi.html

Bluffton, SC

SC State & SE Regional Representative

Pancreatitis Association, International

www.health.groups.yahoo.com/group/pancreatitis/

Note: All comments or advice are personal opinion only, and should

not be substituted for professional medical consultation.

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I agree Heidi, I am here to learn more about my CP but I also want to

make " friends. " I want to be able to talk about my health but also

be

able to relate to others that know not everyday is good. Some are

very

bad and it's ok. Let's do something like this!

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Heidi I agree with you 100%. I think you should be able to post about your

wedding or any other thing you want to share with the group. There is this

really cool button called delete if people are not interested in reading

your post because they are to personal...It shouldn't be that big of a deal.

I hope this finds you and yours well

Mark

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Hi all, I totally agree with the idea of a database or bulletin board

so we can learn more about each other. I think this would be great

because in our own lives we are often seen by others as the person

with the pancreas problems. I think to have a place to escape that and

just chat would be a good thing. So far the patch is working on the

pain but the side effects are not lessening with time. The anxiousness

side effect has been the worst so far. I can't sleep and if I do, I

wake up every hour or so. I will need to see my doctor this week. Also

going to the endocrinologist on Wednesday. Hope you are all well...Jim

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,

I didn't know that you are a runner. I too am a runner. I am a

distance runner at Idaho State University. However, I have been

plagued by stress-fractures since Novemeber. I was cleared to start

running again just the past couple of weeks.

Crystal Galloway

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