We lost our husbands to motor neurone disease (MND) also known as ALS or Lou Gehrig's disease. This disease has NO cure and is always fatal. The nerves that make your muscles work die and so the muscles waste away and die also. People with this disease become paralysed, cannot eat or speak and eventually can no longer breathe. MND NSW gave us the equipment we needed to care for our husbands with dignity at home until the end. This is an invaluable service. MND NSW also provide large amounts of funding to research to fine a cure. EVERY AUGUST UNTIL THERE IS A CURE! Please help by supporting our ice bucket challenge and donating to MND NSW.
MND NSW provides information, support and education about motor neurone disease for people living with motor neurone disease, their families, friends and carers.
KJ
About Fundraiser
Katrina Jeffery
Tuckurimba, NSW
Sat, 15 Aug 2015
Wendy Stapleton
$ 100
Sat, 15 Aug 2015
Debbie Ridd
$ 50
Remembering our brother/brother in law Andy Ridd.
Sat, 15 Aug 2015
Anonymous
$ 20
Sat, 15 Aug 2015
Ellie Day
$ 20
Fri, 14 Aug 2015
Sheelagh Hearn
$ 20
Stay strong ladies. You are all a great inspiration.
Fri, 14 Aug 2015
Nikki Waters
$ 20
Fri, 14 Aug 2015
Helen Newton
$ 50
In Memory of Andy.
Fri, 14 Aug 2015
George Woods
$ 50
Thu, 13 Aug 2015
Deborah Woods
$ 20
This cause is worth way more than I can afford. But far better to donate something than nothing. I hope others follow my lead.
MND NSW provides information, support and education about motor neurone disease for people living with motor neurone disease, their families, friends and carers.
Remembering our brother/brother in law Andy Ridd.