Rare Masquerade Ball

Excitement is building for the inaugural Rare Masquerade Ball hosted by Evans Syndrome Foundation! This signature fundraiser will take place on October 21, 2017 at the Oslunds’ residence in Orlando from 7:30pm-
11:30pm. Our goal is to unmask Evans Syndrome.
About the Ball
The Rare Masquerade Ball will bring together more than 100 distinguished members, benefactors and leaders of the city of Orlando for a lovely evening of music, hors d’oeruvres, dessert, libations, an auction and surprise entertainment. It’s the perfect mix of networking to help the Foundation get off the ground.
About Evans Syndrome
Evans Syndrome is a very rare, autoimmune, chronic blood disorder where the body creates antibodies that kill the red blood cells, white blood cells and platelets. One in a million people are diagnosed with Evans Syndrome. There are around 500, known, cases worldwide.
Funding Research
By becoming a sponsor, you will support research specific to Evans Syndrome conducted by Dr. David T.
Teachey, MD at the Children’s Hospital of Philadelphia.
Also, by supporting the Evans Syndrome Foundation, you will be part of an amazing group of Lake Nona area residents who have dedicated precious resources and countless hours to unmask Evans Syndrome.
To learn more about Evans Syndrome Foundation, please visit www.evanssyndromefoundation.org.