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The Bonnell Foundation: Living with Cystic Fibrosis and Rock CF organized the CF Task Force in January of 2017 to make certain that we were raising awareness as a CF community. Our hope since then has been that lawmakers will use us as a resource when making decisions that will impact people with CF and even people with other chronic illnesses. We meet periodically to discuss our concerns (healthcare, awareness, preexisting conditions and more). We encourage you to get involved. Please shoot us an email at: thebonnellfoundation@gmail.com.

“I am glad to be part of the CF Task Force because we have to stick together as a CF community and raise awareness to local legislators and anyone who will listen.” — Laura Hartson