My Nonprofit Reviews

I lost my sister to Cystic Fibrosis back in 2016.. she was only 23, I have a pendant with her ashes I take with me and it makes every event I go to that much more special. This event though I will always hold very close to my heart. Though I never got to meet Molly or Matt, they have treated me like family. Talking with Molly has been such a pleasure and what they do for people with Cystic Fibrosis can never be repaid. She made our night and I cannot praise her or the Take a Breather foundation enough!! They came into my life in a time I was feeling down and depressed and totally turned that around. I cannot thank Molly enough and Matt. Granting these Breathers is something amazing and I hope people keep donating so they can continue to help brighten the lives of CFers who really could use a Breather!