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Please honor Christopher Reeve's legacy by making a tax-deductible donation today.
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Make a donation in honor or in memory of someone with the option of sending a card.
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The Reeve Foundation Quality of Life program awards grants to non-profit organizations that provide services to individuals with paralysis.
International Research Consortium on Spinal Cord Injury The mission of the Reeve Foundation International Research Consortium on Spinal Cord Injury is to promote structural repair and functional recovery in the acutely and chronically injured spinal cord. The Consortium pursues this mission through collaborative research that focuses on how to optimize the intrinsic capacity of the adult nervous system to repair and remodel itself as well as how to elicit robust regenerative responses after injury.
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The North American Clinical Trials Network (NACTN) is one more way that the Reeve Foundation is moving promising therapies from the lab to spinal cord injured patients. NACTN is working hard to insure that any clinical trial will be done in a way that maximizes both patient safety and our ability to gather valid, meaningful data.
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Rob Summers, who is living with paralysis, stands, steps with assistance and moves his legs voluntarily after a regimen of epidural spinal cord stimulation plus extensive Locomotor Training.
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NeuroRecovery Network is developing and expanding access to activity-based therapies, resulting in improved health, quality of life, and function.
Hope in Motion: Christopher Reeve’s son, Matthew, has created a poignant and sincere portrait about the man known to the world as Superman, as he relentlessly fought to overcome paralysis after a horse-back riding accident in 1995.
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All proceeds from the sale of the Superman Dog Tags go to support the Christopher Reeve Foundation's ongoing research efforts leading to treatments and cures for spinal cord injury.
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The Reeve Foundation is dedicated to curing spinal cord injury by funding innovative research, and improving the quality of life for people living with paralysis through grants, information and advocacy.
One man, who for the last decade of his life was a ventilator-dependent quadriplegic, led an international movement to help those living with paralysis. He epitomized the words "nothing is impossible."
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