Collins Galloway

Collins Galloway was diagnosed with Cystinosis at 18 months old. Her daily routine consists of medicine and nutrition through her g-tube seven times a day. She gets routine blood work to test her levels and adjust her medicine dosage. Despite all she has been through and continues to go through, she is the most upbeat happy girl! Her strength inspires us daily!

Collins Cure Cup Tournament 
Thank you to the Galloway family for hosting their 2nd Annual Collins’ Cure Cup golf tournament on November 12. The event was a tremendous success thanks to the tournament sponsors, dedicated volunteers, and 114 enthusiastic golfers. Following the fun-filled day of golf, the Cumming community of family and friends joined the participants for dinner, live music, and fundraising festivities at the Windermere Country Club. By the end of the evening, the generous guests had contributed more than $52,701 in honor of Collins and cystinosis research!  We are grateful to the Windermere Country Club and its staff and especially the Cumming community for their contributions and support of the Galloway family and for making a difference in the lives of those with cystinosis. Donations are still coming in, so there is still time to donate in honor of Collins!

Thank you for supporting CRF and Collins’ Cure! We won’t stop until our sweet girl is healed!  
Thank you, the Galloway Family
Christina, Hunt, Rowyn, and Collins