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Brooklyn Bridge walk aims to bring attention to rarely recognized diseases

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CONTACT:
Laura Farrell
917.751.7379
lfarrell@lymphaticnetwork.org

Brooklyn Bridge walk aims to bring attention to rarely recognized diseases
2015 Walk to Fight Lymphedema & Lymphatic Diseases to be held September 19

New York, NY – September 1, 2015 – Hundreds of people will gather to walk across the Brooklyn Bridge to Manhattan on Saturday, September 19 in hopes of building community, raising funds, and garnering more attention for lymphedema and lymphatic diseases.

The Lymphatic Education & Research Network (LE&RN) will host the 2015 5k Walk to Fight Lymphedema & Lymphatic Diseases, which will begin at 9:30 a.m. with registration at Cadman Plaza Park, Brooklyn and commence at 11:00 a.m. with a ribbon cutting and speeches. Registration is easy and teams are forming now.

The event will provide an opportunity for families and individuals to spend a day out for a good cause. For those who cannot attend there are other ways to help. Donations can be made online at www.LymphWalk.org, and there’s even a chance to become a virtual walker. 

Lymphedema and lymphatic diseases remain unknown to most people despite affecting up to 10 million Americans — that's more than AIDS, Parkinson’s disease, multiple sclerosis, muscular dystrophy, and ALS combined. People affected by lymphedema and lymphatic diseases can be of all ages and backgrounds.

The current fundraising leader for this year’s event is 7-year-old Emma Detlefsen, who started a lemonade stand to help raise money for the disease that has affected her first-hand. At the Walk Emma will be awarded the LE&RN Youth Ambassador Award, which will be presented to her by New York State Senator Martin J. Golden (R-C-I, Brooklyn) and Assemblymember Linda B. Rosenthal (D-WF, Manhattan).

Emma says her efforts have been partially inspired by Academy Award-winning actress Kathy Bates who has spoken out about her own battle with lymphedema. Bates helped kick off last year’s Walk, and this year organizers and participants are hoping to make her proud again.

"At last year's Walk, Kathy Bates inaugurated the Face of Lymphedema Challenge™,” said William Repicci, LE&RN’s Executive Director. “This year, we’ll show her she isn't alone with New Yorkers coming forward and standing tall for lymphedema and lymphatic disease awareness."

This event is brought to you by LE&RN and presenting sponsor BSN medical, and sponsored by ImpediMed, L-Dex, Bio Compression Systems, Eiger Pharmaceuticals, Mikimoto, Luna Medical, The Norton School, Printology, Lohmann & Rauscher, Solaris, ShechterCare, Tactile Medical, Lympha Press, Bio Horizon Medical, and Mount Sinai.


About LE&RN
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 www.LymphaticNetwork.org or call (516) 625-9675.

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