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Dystonia Awareness Fundraiser
Story
Dystonia is a rare neurological movement disorder which cause severe involuntary muscle contractions. This forces certain parts of the body into repetitive, twisting movements or painful postures.
THERE IS NO CURE
It took me 15 years to get diagnosed, others up to 40 years. This is why it is so important for me raise awareness and much needed funds for the brain foundation in further research for dystonia.
November 30th we are having a Dystonia Awareness Fundraiser. All are welcome, but for those who can’t make it, please feel free to donate to this great cause.
HELP US MAKE DYSTONIA KNOWN AND RECEIVE THE RESEARCH IT DESERVES.
Activity
Brain Foundation
The Brain Foundation is a national registered charity dedicated to funding world-class research Australia wide into neurological disorders, brain disease and brain injuries.
Established in 1970 by neurologists and neurosurgeons, the Brain Foundation funds ground breaking research projects that aim to advance diagnoses, treatment and patient outcomes. The Brain Foundation annually provides research grants nation-wide to candidates who are selected by eminent neurological practitioners.
Receiving no government funding, the Brain Foundation relies on the generosity of individuals, corporate donors and bequests.
Your support will make a difference - now and for generations to come.
Headache Australia is a division of the Brain Foundation and can be accessed by www.headacheaustralia.org.au