Kathy Bates to Kick Off 1st Annual CA Run/Walk to Fight Lymphedema & Lymphatic Diseases
(firmenpresse) - SANTA MONICA, CA -- (Marketwired) -- 06/26/15 -- The announced that Academy Award-winner and LE&RN will kick off the first annual in Santa Monica on June 28, 2015.
developed lymphedema in both arms following a double mastectomy. "Lymphedema is a chronic souvenir from my surgery and initially I felt alone and frightened," says Ms. Bates. "On my journey with lymphedema, I found that up to 10 million Americans suffer from this disease. This represents more sufferers than those Americans who have AIDS, Parkinson's disease, muscular dystrophy, multiple sclerosis and ALS combined! Yet, I also learned that lymphedema often goes undiagnosed and untreated. This affliction affects children, a high percentage of cancer victims and anyone who has suffered traumatic injuries damaging the lymph glands, including our military. Yet incredibly it is virtually unknown by most Americans as well as many physicians. I can afford help. Millions can't. This is why I joined the Lymphatic Education & Research Network (LE&RN) as a spokesperson spreading lymphedema awareness wherever I am able."
"Lymphatic disease and lymphedema will only become a national priority once those affected come forward and join this fight," says LE&RN Executive Director William Repicci. "Kathy Bates has become a lightening rod for the movement, and kicked-off and campaign this past year to usher in this change. Now, she's leading the charge to raise awareness and funding through our first Run/Walk in California."
Ms. Bates recently talked about her lymphedema on and in published news interviews. "I didn't know where to go for help when first diagnosed. Then the more I learned what I would have to do to manage my lymphedema each day, every day, I became angry," she states. "I'm in this fight for the long-haul."
Ms. Bates will also host a reception at a Santa Monica restaurant, followed by a dinner hosted by the night before the Run/Walk for the top ten fundraisers. The actress recently took to Twitter to encourage everyone to register for the , which takes place on her birthday.
To register, simply visit the event's .
Founded in 1998, the Lymphatic Education & Research Network (formerly LRF) is a 501(c)(3) not-for profit organization whose mission is to fight lymphatic disease and lymphedema through education, research and advocacy. LE&RN provides valuable education resources for the millions of people who suffer from lymphedema and lymphatic disease. LE&RN fosters and supports research that can deepen the medical community's understanding of the lymphatic system. For more information about lymphatic disease or the Lymphatic Education & Research Network, please visit or call (516) 625-9675.
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Amy Cook
925.552.7892
William Repicci
Lymphatic Education & Research Network
516-625-9675
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Datum: 26.06.2015 - 15:30 Uhr
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