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About us and Arachnoid Cysts
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| FAQ |
Arachnoid Cyst Awareness is here to support all arachnoid cyst patients and their loved ones, in addition to helping the general public become more aware of how an arachnoid cyst can affect someone. ACA is helping to end the stigma of, "It's all in your head", which is commonly associated with this disorder, and through raising awareness hopes people will learn how badly arachnoid cysts affect lives.
Arachnoid Cyst Awareness was founded in June of 2003 when Dia DiCristino was suffering from bacterial meningitis. Over the years the awareness has been directed towards how the medical community often disregards arachnoid cysts and turns patients away with a psychosomatic diagnosis. ACA hopes in time patients will be able to find a doctor who is aware of the symptoms this disorder can cause. To help achieve this, ACA has started an Arachnoid Cyst Petition to show how many people are affected by arachnoid cysts and the common symptoms they share.
ACA has launched both a Motability Fund and Home2Hospital Fund to help those who may need wheelchairs, walkers, canes, etc and to defray the costs of traveling to an out of state doctor.
Just this year the new ACA Network was launched. It has many features including the ability to host blogs, user groups, forums, mp3 uploads, picture galleries and so much more. If you are newly diagnosed, feel free to check it out.
© Copyright 2003-2010 Arachnoid Cyst Awareness Arachnoid Cyst Awareness #4316 Arachnoid Cyst Awareness is proud to be a member of the Social Enterprise Coalition
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