Garrett's House is dedicated to the support, advice, and education of a genetic skin condition called Epidermolysis Bullosa or EB for short. Currently there is no cure or effective treatment for EB. Please take a moment to learn about EB, and how you can support others who struggle with EB everyday. Garrett's House also honors the memory of those who lost their brave fight against EB. Please check out the Garden of Angel to learn more about the precious butterfly angels.

May 23, 2011

A.J. Highfield - Spaghetti Dinner

 Chartiers Valley High School
50 Thoms Run Road
Bridgeville, Pennsylvania
Saturday, June 11 · 4:00pm - 7:00pm
Additional Info:
Dinner includes Beverage, Salad, Bread, Pasta & Dessert
Adults: $8 per ticket
Children ages 5-12: $5
Children under 5: $Free
Checks payable to: ACHIEVA Family Trust - Benefit of A.J. Highfield
Also available at the dinner:
Raffle Tickets for Chinese Auction Baskets
“Lottery” Raffle Tickets

All proceeds benefit A.J. Highfield Butterfly Kid.
A.J. Highfield was born on March 20, 2011 with Epidermolysis Bullosa (EB). With skin as fragile as a butterfly wing, EB patients are dubbed “Butterfly Children”.

EB is a rare skin disease that causes the skin to be so fragile that the slightest friction can cause severe blistering. Severe forms of EB cause patients to live with constant pain and scarring.

The only treatment for EB is daily wound care and bandaging.
Today there is no cure.

Can't attend? You can send a donation of any amount directly to ACHIEVA Family Trust - Benefit of A.J. Highfield
Attn: Amy Dolan Strano, Esq.
711 Bingham Street
Pittsburgh, PA 15203

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