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On Monday August 16 from 6-9 pm, please be sure and stop by Bruster’s in Tega Cay for a cool treat and raise money for a great cause.
A portion of the proceeds during that time frame will benefit the upcoming Dravet Syndrome Foundation Steps for a Cure fun walk on September 25 at Charlotte Knight’s Stadium. For more information on the walk, please visit http://www.dravetfoundation.org/walk_for_a_cure.html
Download the Foundation Fundraiser Flyer for the scoop night at Bruster’s. Stop by on Monday, August 16 from 6-9 pm and give to a great cause and learn more about the walk. Please pass this along to your family, friends and co-workers.
Dravet syndrome, also known as Severe Myoclonic Epilepsy of Infancy, is a rare and catastrophic form of epilepsy for which there is currently no cure. Seizures begin in the first year of life in an otherwise typically developing infant. All seizure types are remarkably resistant to medical therapy. Developmental delays often appear during the second year of life, although the course of severity varies among affected children. Children with Dravet syndrome do not outgrow this condition and it affects every aspect of their daily lives.
