I will shave my head on 29 May 2020 on Go Orange for PWS day to raise the money and would love to reach $1,000!!!
My beautiful niece and god daughter Aiyana was born with PWS. There were many weeks initially spent in hospital and early diagnosis by the hospital assisted Aiyana's progress and connection to treatments and the PWS family. The strength of Aiyana is inspiring and of my brothers whole family, you have all supported Aiyana and made her be the beautiful young lady she is today. PWS can be crippling, the constant fight with hungar, not understanding what is going on or why you need more. The constant battle drives frustration and anger, a struggle for parents to consistently manage. Locks and alarms on doors, fridges and bins, so you know when food is being taken. Growth hormones, leg braces and other assistance to develop muscles and eventually walk unassisted, when strong and capable to run. Please visit this site for further information about PWS: http://www.pws.org.au/prader-willi-syndrome/ Please show support in donating money and I'll shave my head 29 May 2020. Please also wear orange on PWS Awareness day, show support and love
We are dedicated to improving clinical outcomes and delivering better treatments for people living with Prader-Willi Syndrome
We do this by funding cutting-edge research that will help people with Prader-Willi Syndrome live independent lives, free from the most debilitating aspects of the condition.
MP
About Fundraiser
Melanie Peterson
WITTITRIN, NSW
Fri, 5 Jun 2020
Chontelle Shore
$ 25
Great Job
Fri, 5 Jun 2020
Melanie Peterson
$ 30
making it the $2000 mark
Fri, 5 Jun 2020
Melanie Peterson
$ 50
Paul and Di - thanks for your support
Sat, 30 May 2020
KERRIE SCOBIE
$ 50
THANK YOU MELANIE. I LIVE IN KEMSPEY AND HAVE A GRANDSON WHO HAS PWS. KEEP SPREADING THE WORD
Fri, 29 May 2020
Kim Peterson
$ 50
Fri, 29 May 2020
Michael Woods
$ 20
Fri, 29 May 2020
Melanie Peterson
$ 355
From my awesome collegues at Kempsey Shire Council Thank you so much for your support
We are dedicated to improving clinical outcomes and delivering better treatments for people living with Prader-Willi Syndrome
We do this by funding cutting-edge research that will help people with Prader-Willi Syndrome live independent lives, free from the most debilitating aspects of the condition.
Great Job