Chromosome 18 research society!
Donation protected
Every cent counts!!! This year I have been asked to take part in the Thomas Bros Wagga takes 2 Charity event to sing along side Rebecca Hennesy on behalf of Ben Morgan. I've known Ben since moving to Wagga many years ago and I have decided to help him in his quest to raise money for the Chromosome 18 research society!
Chromosome 18 disorders are not uncommon, but very few babies survive birth. Those that do, usually experience mild to severe intellectual disability, chronic health conditions and other complications. However another common feature is a LOVE of life, singing, people and fun. So Wagga Takes Two is the perfect stage for fundraising!!
Well known local man, Ben Morgan, is the local "face" of chromosome 18 disorders. Having successfully raised almost $20,000 for research since 2014, Ben is now hoping that people will get behind him and myself and dig deep for this important research.
Please like and share our Go Fund me page! And please remember that every cent counts! Let's make a difference and show some support for such a great cause. I know how much of a smile it puts on Bens face!
Chromosome 18 disorders are not uncommon, but very few babies survive birth. Those that do, usually experience mild to severe intellectual disability, chronic health conditions and other complications. However another common feature is a LOVE of life, singing, people and fun. So Wagga Takes Two is the perfect stage for fundraising!!
Well known local man, Ben Morgan, is the local "face" of chromosome 18 disorders. Having successfully raised almost $20,000 for research since 2014, Ben is now hoping that people will get behind him and myself and dig deep for this important research.
Please like and share our Go Fund me page! And please remember that every cent counts! Let's make a difference and show some support for such a great cause. I know how much of a smile it puts on Bens face!
Organizer
Jonathan Punch
Organizer
New South Wales
