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Event Details
“If I had a world of my own, everything would be nonsense.” –Alice
Join in the magic and nonsense at Great Lakes Hemophilia Foundation’s Mad Hatter’s Reception.
Step through our looking glass on Friday, March 30th at Pier Wisconsin.
Enjoy a pasta bar, drinks, desserts, live & silent auction and raffles while we raise funds and awareness for Wisconsin's bleeding disorder community.
We look forward to seeing you there. In the meantime, start looking for a crazy hat!
For more information visit glhf.org
I am unable to attend but would like to make a donation, click here.
When & Where
Pier Wisconsin
500 North Harbor Drive
Milwaukee,
WI 53202
Friday, March 30, 2012 from 5:30 PM to 9:30 PM (CT)
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Hosted By
Great Lakes Hemophilia Foundation
Great Lakes Hemophilia Foundation is dedicated to advancing the quality of life of individuals and families affected by hemophilia or other blood disorders by providing a broad range of services and programs while supporting research to improve care and find a cure.
In 1974, a group of family members and dedicated individuals came together to create a support network specifically for people diagnosed with and affected by hemophilia.
Now, Great Lakes Hemophilia Foundation (GLHF) is a statewide organization, serving individuals and families with hemophilia, von Willebrand disease and other lesser known bleeding disorders.
GLHF programs are designed to educate and support individuals and families with bleeding disorders by increasing public awareness, ensuring access to needed medical services, providing relevant information and resources, building a supportive community among individuals and families, and promoting choices that lead to optimal health and living life without limitations.
Here to Help
“We were able to meet many other families with children with bleeding disorders through foundation sponsored events. Knowing we were not alone and sharing stories, treatment tips and ideas helped our entire family cope with the problems of hemophilia. The foundation helped train us to become more independent.”
-Ed B., father of a son living with hemophilia
