You can see our short documentary at the end of the month! Watch the trailer today on YouTube! Https://youtu.be/RYjlB25Cr9Y

End of the year donations for The Bonnell Foundation are appreciated! We help families Living with cystic fibrosis!

Showing off our new golf shirts!

The aharvet of Hope event is September 20 th!

A documentary: coming later this year!

Yard Signs are raising awareness!

Beautiful colors.

Support The Bonnell Foundation with a yard sign! Want a simple, powerful way to make a difference? Here it is! Email us for your sign! [email protected]

Family night with Children’s Hospital of Michigan.

It’s Opening Day! Go Tigers! #DetroitTigers

New podcast out April 7 th! A CF Life: The Inspirational Voices of cystic fibrosis. @siriVaeth shares her stories.

Colores Mexicano! Beautiful! #art #CF #cysticfibrosis

St. Patrick’s Day is fast approaching! Have a little fun with us and donate $17!

St. Patrick’s Day is fast approaching! Have a little fun with us and donate $17!

Dr. Frances Collins recently retired. His is an incredible human. substack.com/@lstb/note/c...

Today’s podcast will inspire caregivers and have you bursting with hope! Why? Podcast host Laura Bonnell and guest @BobCoughlin (his son has CF) talk about advancements in treatment, a cure on the way, and the importance of advocacy. Bobs energy is infectious! #CFSTRONG #CFpower

Please consider donating in honor of St. Patrick’s Day! Thebonnellfoundation.org/donate

💜💜💜Advocating in DC! A good few days!

Great to speak at Rare Disease day! #RareDisease @grandrapidsnews.mastodon.social.ap.brid.gy

From snow…. To Florida sunshine….snd back to @puremichigan1.bsky.social #weather #sunshine

Our bookkeeper! Welcome to the team Olga!

Be part of the CF cheer team!! Donate: link in bio! Spread the sunshine!

Baby it’s cold out! So let’s think Spring! Register today for Education Day on May 3 rd! Thebonnellfoundation.org and click on events. It’s $5 per family. There is an outdoor space and we will gift you with family photos taken that day!

Join us in 2025!

The Rare Disease Advisory Council didn’t pass but were grate it got to the senate for a full vote. Thanks to everyone who gave their support. We will get it done in 2025!

Heading home from DC!

Bye bye DC for now!

More to come, but on my way home from Community Congress end of the year mtg! So much hope for the Rare Community. So many amazing advocates!

The one and only Emily Schaller is on Mondays Living with cystic fibrosis podcast! We laugh a lot! A joyful podcast. Listen wherever u get your podcasts. #RockCF She talks about her foundation, living with CF and the future!

Urgent Call to pass HB 4167. The Rare Disease Advisory Council (RDAC). Please call or email Senate Majority Leader Winnie Brinks office Tuesday or Wednesday December 4th to ask her to put HB 4167 for a vote to the full Senate. Call or email: 517-373-1801 or [email protected]

It's time to pass the Rare Disease Advisory Council (RDAC). Please contact Senator Winnie Brinks office on December 3rd and 4th. Call the Senator 517-373-1801 or email her [email protected] thebonnellfoundation.org/time-to-pass...

Hello! The Bonnell Foundation has arrived on Bluesky Social! We’re all about cystic fibrosis! Ask us anything! Send us a hello at [email protected]