The Lymphangiomatosis & Gorham’s Disease Alliance (LGDA) is a founding member of the newly created Rare Bone Disease Advocacy Alliance, a coalition of rare bone disease organizations committed to advancing research of rare bone diseases by working directly with Congress and the Executive Branch. On September 18, 2013, advocates from ...
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Thank You for Your Support The first ever Central Florida LGDA Golf Tournament at Stoneybrook West Golf Club was a complete success! The hot weather didn’t seem to dampen the golfers’ enthusiasm and spirit. The Golf Tournament started early with our energetic volunteers setting up and organizing the details of ...
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In early April 2013 the Lymphangiomatosis & Gorham's Disease Alliance (LGDA) was contacted by Dr. Mishy Lesser, a Boston-based educator, seeking assistance for a child in the Amazon jungle region of Ecuador. Dr. Lesser had just received an urgent plea for help from a former student, Ladio Dominguez, who resides in ...
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The American Thoracic Society International Conference - Meet the Experts session in Philadelphia on Saturday, May 18, 2013, was a great success for the lymphangiomatosis and Gorham’s disease community. In attendance were 3 patients, 4 parents of patients, 2 spouses of patients, 1 friend of a patient, and 3 physicians ...
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200 people Run Balmoral to raise money for The Alfie Milne Lymphangiomatosis Trust   On April 27, 2013, Mum Tracy, Dad Mark and Big Brother Lewis put their trainers back on to run for Alfie’s Trust.  ...
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As a member of the American Thoracic Society Public Advisory Roundtable, the Lymphangiomatosis & Gorham's Disease Alliance (LGDA) is pleased to invite you to participate in the Patient-and-Family Forum, Saturday, May 18, 2013, during the International Conference of the American Thoracic Society at the Loews Philadelphia Hotel in Pennsylvania. For the ...
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