Please support 'Team Fuller' to walk/run a marathon to help raise money for PWS research. J-man might even take a few steps :)
Auckland
Our gorgeous son, Jasper or J-man as some of us call him, has a rare genetic condition - Prader-Willi syndrome, (PWS). So life is a wee bit harder for him...born with low muscle tone and delayed development. Later on in life there will be daily challenges with food and the fact he will never feel full after a meal. We don't want constant hunger to impact on Jasper's life in the future. The good news is several new drugs show great promise! Clinical trials are underway with money being the major factor in the length of time it will take to get them approved for our children. Thank you for your support - together we're creating a better future for people with PWS.
Participating in the Virtual Marathon for PWS Research 2016
Link to their fundraising page here: https://www.givealittle.co.nz/event/virtualmarathonforpws2016
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