The inaugural Chair’s Christmas Challenge is for the purposes of benefiting ME/CFS Australia Ltd, the national body which represents the affiliated state bodies and their membership, and the interests of up to 250,000 Australians impacted by this complex neuroimmunological condition.
This challenge is for patients with ME/CFS, by reaching out to their families, friends, team mates, work colleagues and all those others that know of, or support someone with ME/CFS. The challenge is to raise their awareness and support.
For those unfamiliar - we recommend you watch “Unrest” on netflix - see: https://www.netflix.com/au/title/80168300
A preview can be seen here: https://youtu.be/JvK5s9BNLzA
As Chair of ME/CFS Australia - I challenge you to ask the rest of Australia to make a tax deductible donations to support you, the patients with the condition, and your organisation.
Whether it’s $2, $20 or $2,000 - every little bit helps.
So please share this as far and as wide as possible. Use your Facebook, your Instagram, or your twitter - do what you can to encourage your circle, and their circle, to show support.
ME/CFS Australia Ltd is working to improve the lives of up to 250,000 people with Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS), a complex and very debilitating illness which affects the neurological, endocrine and immune systems.
About Fundraiser
Geoffrey Hallmann
Goonellabah, NSW
Mon, 24 Dec 2018
Jennifer Tosolini
$ 100
Having had ME/CFS for 40 years I am hoping that eventually a cure will be available so that no-one has to deal with the long-term consequences of this devestating illness.
Sun, 23 Dec 2018
Penelope DF
$ 30
Sun, 23 Dec 2018
Penelope McMillan
$ 20
Tue, 11 Dec 2018
Annette Cordeiro
$ 10
Sat, 8 Dec 2018
Anonymous
$ 10
Thu, 6 Dec 2018
Anonymous
$ 250
Thu, 6 Dec 2018
Anonymous
$ 30
Wed, 5 Dec 2018
Gab Cooper
$ 20
Hi Geoff, Hoping for more research, assistance to relieve symptoms and provide relief for all people and families associated with Me/Cfs. Xx all health to you and everyone associated.
Wed, 5 Dec 2018
Anonymous
$ 20
Wed, 5 Dec 2018
Fiona Hayes
$ 10
Wish i could donate more. Huge need for great advocacy for CFS/ME/FM SUFFERERS. This organisation and Chairman us the voice we need!
ME/CFS Australia Ltd is working to improve the lives of up to 250,000 people with Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS), a complex and very debilitating illness which affects the neurological, endocrine and immune systems.
Having had ME/CFS for 40 years I am hoping that eventually a cure will be available so that no-one has to deal with the long-term consequences of this devestating illness.