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A petition has been posted on the White House website, We the People, to require free access over the Internet to scientific journal articles arising from taxpayer-funded research. Expanding access would accelerate the research process and increase the return on our investment in scientific research. With FDA-approved treatments for only about 5% of the 7,000 rare disorders, this initiative is very relevant for the rare disorder patient community.
The first step towards instituting this policy is to secure 25,000 signatures on the petition by June 19, 2012. With that level of visible public support in place, the measure will be reviewed by White House staff, and considered for action