Parkinson’s Action Network (PAN) Meets in DC
Next Monday, hundreds of the United States’ most dynamic and involved advocates for the rights and issues affecting people with Parkinson’s Disease will convene in our Nation’s capital. The goal is to be heard and represented but mostly to be understood that we, as a collective force need better funding and services.
Neurological disorders are rising as is the aging population. Even more importantly, younger and younger people are receiving neurological related diagnoses that one might find in an older patient. Whether the cause is our growing toxic world and/or a genetic component that gets triggered or some cocktail of switches, a desperate portion of our population seeks a solution to a real problem that plagues them everyday, all-day.
In less than a century our country replaced vacuum tubes for Silica chips, went from the horse-drawn carriage to the space shuttle, put a man on the moon, and mapped the human genome. Where is the push to eradicate or even slow neurological illnesses? Great strides have been made in other diseases. New therapies and drugs, while slow to come, only slow or mask symptoms. It is time for a push and a unification of voices to be heard in DC and across the nation that more must be done.
The PAN advocates are coming to DC to speak for the countless victims, both directly and indirectly, touched or shaken by Parkinson’s Disease. They are speaking for those who are unable to speak for themselves.
To learn more about PAN and to view an online webcast of our symposium, go to www.parkinsonsaction.org.
Posted on February 24, 2011, in Education & Support, Health, Parkinson's Disease, Politics and tagged 2011, advocacy, advocates, blog, cure, DC, doctor, government, Health, media, medicine, NIH, PAN, Parkinson's Action Network, Parkinson's Disease, patient, PDPatient, Robb, support, wellness. Bookmark the permalink. Leave a comment.
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