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Thread: Well-known people (celebrities) who have a personal interest in spinal cord injury

  1. #1

    Well-known people (celebrities) who have a personal interest in spinal cord injury

    Many people who are famous have a strong personal connection with spinal cord injury. I thought that I would start this topic for people to post about celebrities who have a personal connection or have expressed a strong personal interest in issues related to spinal cord injury.

  2. #2
    Judy Woodruff is a star anchor of CNN and host of "inside Politics". According to an AARP article, Judy's son has spina bifida:

    "Family really is the most important thing to her," says NBC News correspondent Andrea Mitchell (who is married to Alan Greenspan), a friend for 25 years and godmother to Judy's daughter. This maternal devotion was sorely tested after their eldest son, Jeff, was diagnosed with spina bifida, a defect of the spinal cord. Six years ago, an injury during surgery left Jeff, who was then 16, paralyzed on one side, with limited sight and speech and loss of short-term memory. This, I'm told more than once, is the most defining event of Judy's personal life.

    [This message was edited by Wise Young on 10-05-04 at 08:07 AM.]

  3. #3
    Charlize Theron recently did a black flip somersault while wearing platform shoes when she slipped and hurt her neck. She had a slipped C6/7 disc that injured her spinal cord.,00.html

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  5. #5
    There is of course Christopher Reeve that everybody here knows. However, many people may not know that he received the prestigious Lasker Award in 2003 and here is the Press release associated with that award:

    Mary Woodard Lasker Award for Public Service, 2003
    Press release
    Christopher Reeve

    This year's Lasker Public Service Award honors an actor who has transformed personal tragedy into public service. With bravery and perseverance, Christopher Reeve has worked tirelessly to bolster support for medical research in general and victims of disability in particular. His knowledge of the science and personal heroism have allowed him to wield tremendous influence as an advocate. Instead of bowing to a sudden, life-altering injury, he mustered his internal resources and exploited his connections to advance research that targets spinal cord repair. Through his dogged quest for funding from both the private and public sectors, he has improved the prospects that scientists will devise innovative treatments not only for this condition, but for a wide range of disabling illnesses such as Parkinson's disease, Alzheimer's disease, multiple sclerosis, amyotrophic lateral sclerosis (Lou Gehrig's disease), and the consequences of stroke. Reeve has informed himself about the scientific as well as political aspects of his mission; this approach, along with his role as a public figure, have earned him unique status with researchers, lawmakers, and private citizens alike. Although he must endure the physical and emotional hardships of living in a body that is largely immobile, he is far from paralyzed.

    In 1995, an equestrian accident paralyzed Reeve from the shoulders down. Unable to breathe without the help of a machine, Reeve confronted a new life. While grappling with his own situation and the grueling demands of an uncertain recovery process, he began to reach beyond his own self-interest. Even before he went home from the rehabilitation facility where he spent many months after the accident, he started plotting how he might make a difference for people with spinal cord injuries. He educated himself about the promise of various research strategies and mastered this material at a sophisticated level. His newfound knowledge nurtured the conviction that overcoming his seemingly hopeless medical situation is within reach, which has fueled his resolve to do everything within his power to convert that vision into a reality.

    Within months of his injury, Reeve joined the Board of Directors of the American Paralysis Association (APA), and less than a year later became its chair. Earlier, spinal cord research had been a backwater because conventional wisdom deemed the condition incurable. However, by the early 1990s, scientists were challenging that dogma, accomplishing feats such as nerve regeneration in rat spinal cords. Reeve reasoned that the more time researchers were at the lab bench and the less time they were writing grant proposals, the quicker they'd develop treatments. The APA was already funding research aimed at finding a cure for paralysis. Reeve's association with the organization made it much easier to raise money and put a face on spinal cord injury, thereby attracting proposals from investigators who weren't previously interested in the problem. In 1996, Reeve and his wife Dana established the Christopher Reeve Foundation; in its first year of operation, it raised $750,000 for the APA as well as groups dedicated to quality of life issues that affect disabled people. In 1999, this foundation merged with APA, the name was changed to the Christopher Reeve Paralysis foundation (CRPF), and Reeve continued to serve as chairman of the board. CRPF funds research that paves the way toward treatments and cures for paralysis caused by spinal cord injury and other central nervous system disorders; the organization also allocates a portion of its resources to grants that improve the quality of life for people with disabilities. In 2003, the foundation expects to award almost $7.4 million in grants for neuroscience research and more than $620,000 in Quality of Life awards.

    The combination of his personal commitment, star power, and desire and capacity to fully comprehend the complex political and scientific realities of medical research have collaborated to make Reeve a forceful advocate for scientific research. He has engaged scientists in frequent discussions so that he can understand the mechanisms that underlie potential cutting-edge treatments for problems that range from neurodegenerative disorders to diabetes to spinal cord injuries. As a result, Reeve has become conversant at a high level about, for example, stem cell technology, therapeutic cloning, and the molecular biology of nerve growth. His insistence on understanding the science reinforces his credibility with researchers and renders his arguments particularly compelling.

    Reeve prods and persuades lawmakers and the public with novel and forceful arguments that rouse people to action. Comparing the quest for finding a way to repair the spinal cord with the previously daunting task of landing a man on the moon, he maintains that we have conquered formidable challenges before. At the 1996 Democratic National Convention, he said "So many of our dreams at first seem impossible, then they seem improbable, and then, when we summon the will, they soon become inevitable. If we can conquer outer space, we should be able to conquer inner space too -- the frontier of the brain, the central nervous system, and all the afflictions of the body that destroy so many lives and rob our country of so much potential." Furthermore, he pointed out that investing in research is cost effective: The government spends billions of dollars to maintain Americans with spinal cord injuries, and only a fraction of that on research that would improve the quality of their lives, get them off public assistance, and possibly cure them. In 1998, Reeve lobbied congress to double the National Institutes of Health budget in five years, contributing to the growth of the agency's budget from $12 billion in 1998 to more than $27 billion in 2003.

    As a testament to Reeve's dedication to improving the lives of people with all types of paralysis, the House and Senate introduced the Christopher Reeve Paralysis Act to honor his 50th birthday on September 25, 2002. Congress is currently considering the legislation, which aims to promote research that could lead to spinal cord regeneration and to build programs nationwide that will advance self-sufficiency and opportunities for individuals with paralysis and other physical disabilities.

    Reeve has also worked at the state level, providing crucial support, for example, for the passage of the New York State Spinal Cord Injury Research Bill, landmark legislation that funnels funds collected from violations of motor vehicle laws to research facilities in New York. He helped lobby for similar bills in New Jersey, Kentucky, Virginia, and California. The fact that Reeve never blamed his horse for the accident inspired a philanthropist and horsewoman, Joan Irvine Smith, to create a research center in his name at the University of California, Irvine, dedicated to finding a cure for paralysis. The center raised matching funds from individuals and foundations to triple Smith's $1 million donation. It is already conducting research, supported by state, federal, and private funds, and has developed a state-of-the-art core facility in which any scientist with a novel idea can immediately undertake experiments in well-developed animal models.

    Reeve has tackled some of the most emotionally charged issues with graceful and moving arguments. In an essay for Time and in testimony before a Senate Subcommittee in 2000, he wrote about human embryonic stem cells: "In fertility clinics, women are given a choice of what to do with unused fertilized embryos: they can be discarded, donated to research, or frozen for future use ? Is it more ethical for a woman to donate unused embryos that will never become human beings, or to let them be tossed away as so much garbage when they could help save thousands of lives?" While the Senate was debating whether to lift the ban on NIH funding of research on human embryonic stem cells, Reeve wrote to all of the senators: "If your young child or grandchild became paralyzed because of a spinal cord injury, or brain damaged in an accident, would you be able to look him or her in the eye and say that research on the best hope for recovery is, in the words of Senator Brownback, 'illegal, immoral, and unnecessary?'"

    Knowing that even the most promising research endeavors will take time to gel into therapies, he is also toiling to help disabled individuals lead more fulfilling, productive, and independent lives. In addition to setting up the CRPF quality-of-life grants program, for example, he and Dana helped establish a national information clearinghouse for all issues related to paralysis.

    Reeve has mobilized movie stars as well as politicians to advance the cause. He has recruited celebrity friends such as Robin Williams and Paul Newman to engage in fundraising efforts and other projects aimed at educating the public about spinal cord injuries, and has called upon numerous Hollywood stars to help make the PBS Series "Freedom: A History of Us," in which the actors contributed their fees to CRPF. Corporate and foundation sponsors matched these donations, and the enterprise raised $100,000 for the organization.

    Reeve has juggled these advocacy activities with the rest of his life, pursuing a rigorous rehabilitation regimen, taking part in family life, continuing to act, and embarking on new adventures. In early 2001, he began combining his directing career (which began a year after his accident) with his activism when he directed four commercials featuring Ray Romano, Randy Newman, Toni Morrison and himself for Johnson & Johnson that attempted to help parents communicate with their children: "Tell your kids not to be discouraged in the face of adversity," he said. "Tell them that ? their bad days are just good days in disguise." Reeve has invited the public into his heart and mind through his two books about his experiences, Still Me and Nothing Is Impossible, and by participating in a television special that chronicles his personal struggles as well as his public ones. After the accident, he had sensation in 12% of his body; he has since regained feeling in an additional 58%, an achievement that doctors deem remarkable. Furthermore, Reeve is exploiting neural activity very far below the level of his injury. For example, he can now push off from a pool wall like a swimmer starting the backstroke. Until recently, he could breathe without the ventilator for only 90 minutes at most. Earlier this year, he underwent surgery intended eventually to wean him from the machine completely. He can now survive off of it for six or seven hours at a time.

    Under profoundly compromising circumstances, Christopher Reeve fashioned a new role for himself by grabbing opportunity and spearheading an entire movement. He has demonstrated great courage in a truly bleak situation, finding a way to exert tremendous power even though his body has lost much of its vigor. No longer able to leap tall buildings in a single bound, he continues to vault seemingly insurmountable obstacles from physical rehabilitation centers to congressional chambers -- and has transformed himself from one type of Superman into another.

    Citation text by Evelyn Strauss, Ph.D.

  6. #6
    Kent Waldrep was in college in 1975 when he was injured on the football field. He was a celebrity of sorts in Texas where playing college football is probably as important as being in the movies but he became a real star in the 30 years. Here is a nice story about Kent:
    A Family's Journey

    Kent Waldrep
    by Nancy Farrar


    If it is true that each man creates his own destiny, then this is a man who has done more than his fair share. Kent Waldrep, his wife Lynn, sons Trey and Charlie, and parents Al and Denise Waldrep, have together dedicated their lives, hopes, and dreams to create a brighter future for hundreds of thousands around the globe who are affected by paralysis from spinal cord injury.

    That he has a family at all is a testament to Kent's determination. Following his paralyzing injury on the football field during a 1975 game between Texas Christian and Alabama, Kent was sure he would never realize this dream. But technological advances allowed him to do what he never thought possible - have a family. Today, through his family and countless friends, the Kent Waldrep National Paralysis Foundation has worked for more than 27 years to raise more than $40 million to make another dream possible...a cure for paralysis.

    For Kent, it has always been about a cure. Anyone who has ever met Kent knows that he is driven by the goal of walking with his son when he graduates from high school. He knows there is a cure out there, and he wants it to be in his lifetime. Kent says that his plan is to "put himself out of business." Kent is surrounded by people who share his belief that finding a cure is possible, and by people who also know that it takes funds to support the research that will find that cure. The quest requires exposure, contacts, time, and connections with important, notable people to make it work. Kent has done all of that, and more.

    He has been an advisor to Presidents Ronald Reagan, George Bush Sr., and George W. Bush on the topic of disabilities in America. He co-authored the Americans with Disabilities Act. He has traveled the globe to bring together great minds dedicated to research in the field of paralysis so that valuable time won't be wasted. He has created a Research Think Tank for the sharing of important research models. He has befriended celebrities who rally around his cause. He has created a world-class research center in Dallas which bears his name. And he has assisted families like his own who need support when they are faced with the devastation that a paralyzing injury brings.

    The body of worldwide research and advances in paralysis are astounding and promising. Researchers have made paralyzed rats walk; they have made implantable devices that reduce the spasms that plague paraplegics and quadriplegics; they have found the gene that may regenerate nerve tissue and unlock the door to a cure. They are now working to apply this knowledge to those afflicted with spinal cord injuries, stroke, and diseases that demand central nervous system regeneration - more than a million and a half people in the United States and tens of millions worldwide.

    Kent did not choose his destiny, but he has created from it a hopeful future for many others. "When I walk out of this wheelchair," he declares, "I plan to take a lot of other people with me."
    Last edited by Wise Young; 10-27-2009 at 04:53 PM. Reason: I am sorry but the URL was abandoned. While I left the URL there, the image was porn. Wise.

  7. #7
    Nick Buoniconti is known to many as the host of "Inside the NFL" on HBO cable network and as an all-American linebacker at Notre Dame, an All-Pro with the Boston Patriots, and member of the Miami Dolphin's famous No-name defese. But his greatest work was probably as the founder of the Miami Project with his son Marc Buonocanti.

    [This message was edited by Wise Young on 10-03-04 at 08:15 PM.]

  8. #8
    Doug Heir was hardly a household name when he became a C6/7 quadriplegic when he dived into a swimming pool to rescue a drowning child in 1978. However, in the 25 years since, he became an attorney, an author, a corporate executives, a motivational speaker, and celebrated on the Wheaties box as "America's greatest wheelchair Athlete" who has won more modals and titles that any other Paralympic athlete in history. He lives in Cherry Hill, NJ.

    Here is his story:

    [This message was edited by Wise Young on 10-03-04 at 08:17 PM.]

  9. #9
    Gloria Estafan is of course best known as a singer. But she had spinal cord injury from which she recovered almost completely from and has been one of Miami Projects most enthusiastic and effective fundraiser.

  10. #10
    Willie Shoemaker is the most successful jockey in the history of thoroughbred horse racing. He retired from the racing world having ridden in over 40,350 races with a record-setting 8,833 victories. Shortly after his retirement in 1991, he was in a car accident that resulted in quadriplegia. His rehabilitation occurred at Craig Hospital. He took on the cause of spinal cord injury with a passion and served on the boards of many spinal cord injury organizations, created the Shoemaker Foundation to help those in the horse-racing industry who have suffered catastrophic accident or illness, and greatly contributed towards finding a cure for spinal cord injury. I heard him talk about spinal cord injury two years ago and he mentioned that he personally knew 20 jockeys who had spinal cord injury. He died October 2003. The House of Representatives unanimously voted to honor "The Shoe".

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