PKS KIDS

A Forum For Those Touched By Pallister-Killian Syndrome



this is a link that you may either order a new subscription or renew an existing subscription and money will be donated to pks kids.

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Hello all,
Not only can you get great deals on magazines, music and COOKIE DOUGH at the link above, we've also decided to try something else to fundraise.

For all you pop and beer drinkers, would you mind setting a little cup in your kitchen and collecting the pop tops off the cans? Cam Haas will be glad to recycle these for cash as you mail them to her. Cam can be reached via email at cehaas1@hotmail.com for mailing instructions when you have a nice big batch to send her.

An online Tupperware campaign is about to start!!!

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Hi Camilla/Lauren, Just a thought how would we do fund raising for the group here in New Zealand as Kassicus is the only child here with PKS and talking to people here no one has heard of PKS. Fund raising would not be a problem. The only problem we would have is where do we send th funds that we raise. My aim is to get Kassicus to the next forum and because we are so far away we would need to have funds for air fares and accomadation when we get there. I am sure you would have a few answers for me . cheers for now Nana Ivy

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Ivy,

We are taking this idea to our next broad meeting in November to discuss this. We will let you and everyone else know how this can work for all the family members. Thanks for the great idea.

Ivy Ashby {Grandmother} said:
Hi Camilla/Lauren, Just a thought how would we do fund raising for the group here in New Zealand as Kassicus is the only child here with PKS and talking to people here no one has heard of PKS. Fund raising would not be a problem. The only problem we would have is where do we send th funds that we raise. My aim is to get Kassicus to the next forum and because we are so far away we would need to have funds for air fares and accomadation when we get there. I am sure you would have a few answers for me . cheers for now Nana Ivy

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