RP Foundation newsletter

[Guest guest]

Hi all. The RP Foundation is about to get it's newsletter off. If any one

in this support group would like to contribute their story, we will keep it

on file for future editions. We can learn alot about RP by other peoples

experiences. This will also help to educate those who don't have RP.

If you wish to receive a copy of the newsletter, all you have to do is

contribute $15 yearly to the RP Foundation. Remember we do have angels that

will help anyone who can't donate at this time. Please visit the Foundations

new Web site at;

www.polychondritis.org

Anyone wishing to donate at anytime can. Please remind family members that

they don't have to feel helpless, that this is a way to help their loved one

afflicted with this disease. Donating to the Fondation is an excellent way

to get involved and help their loved one. The more members we have, the more

contributions we will have and that means we can contribute more to Dr.

Buckner for her research and also spread the awareness of RP. Remember, only

through research will we find a cure for RP.

Any donations can be made out to " RP Foundation " and mailed to

RP Foundation

c/o Colloran

775 Bounty Place

Manteca, CA 95337

We increased our members last year by 500% and I plan on doing the same this

year. Please take the time to remind friends and family what they can do to

help. Then they can ask their friends and family. We will grow so large

that pretty soon, RP awareness will spread really fast. Maybe even get your

drs. involved. (I know, I'm pushing here) LOL Well, mine are. I keep

reminding them. I think pretty soon they will contribute just to shut me up.

LOL We don't need to be shut up though, we need to become known. Thanks to

all of you who have donated already. Without you we wouldn't have come as

far as we did the first year.

Thanks to all. I'll be popping again soon to nag you all (or as Connie would

say, " nudge " )

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