ine l Life Care Walk 2012
Transcription
ine l Life Care Walk 2012
Life l ine January 2012 Non-Profit Org. U.S. Postage Paid New York, NY 330 Seventh Avenue, #200 New York, NY 10001 Permit No. 4814 Address service requested Cooley’s Anemia Foundation Leading Get out your calendars – open up your eCalendars – and mark Sunday, May 6 for CAF’s Care Walk 2012! CAF’s Care Walk is planned as a way to bring together the thalassemia community and its supporters around the country. Rather than hold one huge walk in one location, which many people would have a difficult time reaching, we ask our friends and supporters to plan their own Walk. It can be as simple as one person walking around his neighborhood or a hundred people walking through a nearby park. * Centers marked with an have been selected to receive funding from the Centers for Disease Control and Prevention for a specific thalassemia initiative. Thalassemia Treatment Centers Children’s Hospital & Research Center at Oakland Dir: Elliott Vichinsky, MD Contact: Dru Foote, (510) 428-3342 * Weill College of Cornell University Hospital, Chicago * Children’s Memorial Dir: Alexis Thompson, MD Contact: Janice Beatty, (773) 880-4618 Children’s Hospital Los Angeles * Dir: Thomas Coates, MD Contact: Susan Carson, (323) 361-4132 of Philadelphia * Children’s Hospital Dir: Alan Cohen, MD Contact: Vanessa Nixon (215) 590-2197 Children’s Medical Center Dallas Hospital Boston * Children’s Dir: Ellis Neufeld, MD Contact: Jennifer Braunstein, (617) 355-2457 New Patients: Michelle Burnett, (617) 355-8246 Dir: Zora R. Rogers, MD Contact: Deborah Boger, (214) 456-6102 These Thalassemia Treatment Centers are equipped to address the multiple concerns of thalassemia patients, including annual comprehensive care evaluations. They are also happy to work with your current hematologist to help coordinate your care. Texas Children’s Hospital (Houston) Dir: Donald Mahoney, MD Contact: (832) 822-4213 Call today to set up your appointment! * Dir: Patricia Giardina, MD Contact: Dorothy Kleinert, (212) 746-3404 Healthcare of Atlanta * Children’s Dir: Jeanne Boudreaux MD Contact: Laurie Thomas, (404) 785-3529 In addition, there are a number of thalassemia treatment centers which are associated with the centers listed above. Contact CAF at (800) 522-7222 for a list of these Centers. Last year, our first Care Walk was a huge success, raising almost $200,000 for CAF’s programs while creating a sense of excitement in the thalassemia community. (This year’s goal: $350,000!) More than 2,000 people across the country participated as a way of saying “No one with thalassemia is alone!” “Children’s Hospital Los Angeles (CHLA) organized a Care Walk to connect patients and families and spread awareness of thalassemia to the public,” says Liz Morasso, Social Worker at CHLA, of last year’s event. “With such a geographically diverse population, we found that many of our patients had never met. We also found that many people in the community, even members of patient’s family, were unfamiliar with thalassemia and how it affects those they love every day.” “The Care Walk was so fun and touching at the same time,” says Liz. “I was overwhelmed by the support of this cause from patients, families, friends, and the community. I loved the enthusiasm each team shared in their signs, cheers and high fives. Patients and families alike connected at the resource and snack tables and provided each other with support they may the Fight Against Thalassemia Care Walk 2012 is Coming on May 6 not have been able to easily access before this experience. “We left Care Walk motivated to continue working towards a cure, provide psychosocial support, and assist our families in becoming advocates for themselves and the thal community. These creative methods also lent a voice to all those affected by thalassemia, both directly and indirectly, living and deceased. The Care Walk provided people that space.” For Tara Maziarz, organizing a Care Walk near her college was a way to honor her fiancée, Ian Wiles, who had recently passed away from complications related to thalassemia. “I absolutely loved the Care Walk experience,” she says. “I couldn't think of a more uplifting and helpful way to remember Ian. It got me through a lot of hard times, and I am thankful to my entire Public Relations class for helping out. There was a real sense of unity between everyone and a positive attitudes towards helping a great cause.” Ro Malik, whose sister has thalassemia, helped organize a Chicago area Care Walk to become more involved with CAF and because “there seems to be a larger support network on the east and west coasts but not as much in the midwest. My sister is such an inspiration to me. I wanted to raise awareness of thalassemia in Chicago and bring other people and families together who are affected by this rare blood disorder. “I thought the Care Walk Experience was wonderful. One of the fathers reached out to the local NBC station and secured us a spot on the morning news to promote the Care Walk.” Ro especially liked the fact that the Care Walk brought family and friends together to provide a sense of community. “One of the nurses from Children's Memorial Hospital commented, ‘I have been to a number of events in Chicago over the years that support thalassemia but this is by far the best turn out we have ever seen.’ I cannot tell you how happy I was to hear that.” Whether walking alone or with 100 other people, participating in a Care Walk is an unforgettable experience. Make sure you are part of that experience this year. For more details, go to www.tinyurl.com/CareWalk2012 or contact NathaliaPerozo, n.perozo@cooleysanemia. org or (212) 279-8090. DISCLAIMER:The information in this publication is for educational purposes only and is not intended to substitute for informed medical advice. You should not use this information to diagnose or treat a health problem or disease without consulting a qualified health care provider. The Cooley's Anemia Foundation strongly encourages you to consult your health care provider with any questions or concerns you may have regarding your condition. Cooley’s Anemia Foundation 1