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Margaret Tuchman, co-Founder and President of The Parkinson Alliance, and Beacon in the Parkinson’s Community “Margaret leaves an extraordinary legacy of advocacy on behalf of her fellow patients. She gave endlessly of herself to usher countless individuals into Parkinson’s activism and engagement. I was one of them, and I will forever be grateful.” — Michael J. Fox Margaret Ujvary Tuchman, of Princeton, New Jersey, and co-Founder and President of The Parkinson Alliance, a nonprofit dedicated to funding research for Parkinson’s disease, died of pneumonia Sunday evening, December 16, 2018 at Robert Wood Johnson Hospital in New Brunswick. She was 77. Margaret was born on November 18, 1941 in Budapest, Hungary. She immigrated to the United States in 1956, married Martin (“Marty”) Tuchman, a businessman and entrepreneur, and had a BA in Psychology and an MA in Social Work. At age 38, Margaret was diagnosed with Parkinson’s. At that time disease treatment, information, and research was limited. Combining her thirst for knowledge and passion for helping others, she began a lifelong journey to shine a light on Parkinson’s. As she learned, she shared, using early online Internet bulletin board services to connect with people around the country. Margaret quickly became an expert—a beacon and vital go-to resource in the Parkinson’s community. Recognizing there was not enough research funding for Parkinson’s disease, both Margaret and Marty, along with The Tuchman Foundation, got involved. Marty joined the boards of the leading Parkinson’s organizations of the time; they both joined the cause of the Parkinson’s Unity Walk; they were early supporters of the then newly-formed Parkinson’s Action Network (which today is operating under The Michael J. Fox Foundation for Parkinson’s Research); and they were among the several key grassroots advocates who worked tirelessly to help pass the Morris K. Udall Parkinson’s Research Act of 1997. But the slow pace of the legislative process to release funds remained frustrating. That frustration motivated Marty to apply fundamental business practices to accelerate the flow of dollars into the hands of researchers. In 1999, they founded The Parkinson Alliance, dedicated to raising funds for the most promising research to find a cure and to share educational information to help improve the quality of life for those suffering with the disease. When NYC ABC News Anchor and Reporter, Michelle Charlesworth, learned the news of her passing, she was immediately saddened. “Margaret Tuchman left this world a better place. She took her diagnosis at such a young age and turned it into an incredible fight that has helped so many others. She truly lived a meaningful life with loving and lasting impact.” Pausing, she reflected and fondly shared that Margaret and her dear grandmother shared the same name. “So in addition to rooting for her always, when I read or heard her name, I would always remember that and smile.” In 2000, ever attentive to new therapies, Margaret became one of the first people in the United States to have Deep Brain Stimulation (DBS) surgery. Seeing the need to better inform the Parkinson’s community about the treatment, Margaret started DBS4PD.org, a website dedicated to DBS information, education, and, most importantly, surveys designed to give the patient a voice because she strongly believed that the voice of people with Parkinson’s and those who love and care for them must be heard. “I have known Margaret for over 15 years, and she had an unwavering determination to give a voice to individuals with PD,” said Jeffrey Wertheimer, Ph.D., ABPP-CN, Chief Research Consultant and Chief of Neuropsychology Services at Cedars-Sinai Medical Center, LA, California. “Although she had many vehicles for assisting the PD community, one of her many legacies is her patient-centered research, using surveys to obtain patient-reported outcomes. She addressed the very matters that were most relevant to PWP, and she had the credibility to give a voice to others. She was a woman with great knowledge and a psychological altitude that gave and still gives wings to the spirit. Her words and ideas soared, casting inspiration in far reaching ways, to others with Parkinson’s, their families, and professionals in the PD community.” With DBS now well-known, this ever-growing resource is today part of The Parkinson Alliance website under Patient-Centered Research. In the years since its inception, The Parkinson Alliance also took over the management of the Parkinson’s Unity Walk and Team Parkinson. It hosts regular events, such as the annual 5K & Fun Run at Carnegie Center and the Food, Wine, & Maybe Tuscany fundraiser. At this past November’s Food event, Margaret shared time with her good friend May May Ali, eldest child of Muhammad Ali, who was the inspiring keynote speaker. “I feel blessed to have known Margaret and call her a friend. She was a giving and courageous woman who defied her disease. As her physical movements became slower, her advocacy to help others was done with speed. As the volume of her speaking voice lowered, her voice to speak up for the advancement of Parkinson’s research increased. I will always admire this great woman who lived a life of service to others.” To date, the efforts of The Parkinson Alliance have raised over $30 million for Parkinson’s research. Margaret also enjoyed gardening and flowers, especially orchids, and was an avid reader on a wide variety of topics. But championing worthwhile missions was in her soul. She was an animal and nature lover and took pride in supporting many organizations that fought for the rights of protecting both. For over two decades she helped fund a ranch in Texas that works with abused horses. She quietly supported beneficial programs and projects too numerous to list. At her core, Margaret consistently delighted in helping those in need while always shunning attention for doing so. Her favorite musician Leonard Cohen wrote, “There is a crack in everything, that’s how the light gets in.” Parkinson’s may have been the crack, but Margaret simply allowed it to spread more of her extraordinary light into the world to positively affect a myriad of people. Ever optimistic, Margaret remained deeply involved in the work of The Parkinson Alliance. She continued to be passionate in finding ways to improve quality of life and in research that would ultimately find a cure for Parkinson’s disease. She was in regular communication with doctors and researchers throughout the country, including an over two decade relationship with Dr Brian Harris Kopell, who is now the Director of the Center for Neuromodulation at Mount Sinai Health System in NYC. “She has always been an inspiration through her own personal courage in the face of Parkinson’ disease. More impressively, she proved how one person’s unwavering dedication can leave a legacy of healing for others.” Margaret was predeceased by her parents, Josef and Margit Ann Ujvary. Margaret is survived by her husband and partner of 57 years, Marty, their Coton de Tulear, Mumbo, and African Gray, Lori. She is also survived by her cousins, Michael Erdely and George Airday, and many friends who deeply love her. In keeping with her wishes and generous spirit, Margaret’s body and brain were donated to the University of Pennsylvania for Parkinson’s research. There will be no funeral. We welcome you to honor Margaret and her passionate work. Memorial donations can be made to The Parkinson Alliance, Post Office Box 308, Kingston, NJ 08528 or online at parkinsonalliance.org in her memory. With a broken heart I say "So long Friend" helping the Parkinsn list from its beginning. John Cottingham ---------------------------------------------------------------------- To sign-off Parkinsn send a message to: mailto:[log in to unmask] In the body of the message put: signoff parkinsn