Hello all! As we attempt to return to gathering events, Kate and Drew Smith’s Cystic Fibrosis walk will be done in person at Wickham Park, Manchester on Saturday, May 21st, 10 am. Outdoors is quite safe and we hope to have you join us.
Our granddaughter Sarah was born 12 years ago with Cystic Fibrosis and is doing quite well. All within one week last July, she started taking the new drug Trikafta and received her second vaccine. She has grown several inches and almost surpasses her mom at 5 feet.
Team Strolling for Sarah does their annual walk, about 3 miles or one hour, to support the Great Strides program which raises research dollars for this genetic lung disease. The new drug Trikafta treats some of the causes for her illness and not just the symptoms.
Please join us to support Cystic Fibrosis research. Donate online above or Make your check payable to:
CFF (Cystic Fibrosis Foundation)
Memo: Strolling for Sarah CT
Mail to me Kate Smith at: 106 Vista Way, Bloomfield, CT 06002 anytime!