Rare Masquerade Ball
Unmask Evans Syndrome
Excitement is building for the inaugural Rare Masquerade Ball hosted by Evans Syndrome Foundation! This community fundraiser will take place from 7:30pm to 11:30pm on October 21, 2017 at the home of Dr. and Mrs. Michael Oslund. Our goal is to unmask Evans Syndrome.
About the Ball
The Rare Masquerade Ball will bring together community members, benefactors and leaders for a lovely evening of music, hors d’oeruvres, dessert, libations, an auction and surprise entertainment. Food and drinks will be catered by Vital Flair Catering. It’s the perfect mix of community networking to help the Foundation.
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.
By participating in this event, you will be directly helping to fund research being currently conducted by Dr. David T. Teachey at the Children’s Hospital of Philadelphia. You will be part of an amazing group of individuals who have dedicated precious resources to unmask Evans Syndrome.
Thank you for your consideration.
Signature Lake Nona Area Event
This signature event is an ideal night to spend out with friends and neighbors, as well as networking with substantial, sophisticated Lake Nona area audience who appreciate your commitment to our community.
Download the Sponsor Packet here.
- Prominent sponsor recognition on all event-related marketing and promotional collateral: save the date, invitations, flyers, posters, and e-mails
- Sponsor listing on all at-event signage and in the event program
- Sponsor recognition and link from the event page on the Evans Syndrome website
- Company name mentioned in all media advertising: print and online
Individual Ticket $60 each