Fun for the whole family, children welcome, no experience necessary, plenty of safety instructors, prizes, 50/50 Draw Entry Fee - $20 per person (payable at the door) All proceeds go to the
Cystinosis Research Foundation For more information and to register go to
www.whoozin.com/shootforabbi ABBI MONAGHAN is an 11 year old from St. Catharines, living with Cystinosis, a incurable disease that slowly destroys the organs in the body. Because Cystinosis is such a rare disease affecting such a small population, and Abbi is the only known case in the Niagara Region, research money is scarce to nonexistent. All money for research comes directly from donations and fundraisers. Cystinosis has affected Abbi’s growth; she’s usually one of the smallest in her grade, but makes up for it with her big personality. She also has ongoing issues with photo sensitivity and wears sunglasses at all times when outside and sometimes inside when under the fluorescent lights of the school. Abbi is on a strict routine taking medication around the clock every 6 hours, upwards of 35 doses of medications per day, plus eye drops hourly and a growth hormone injection nightly.