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The Bonnell Foundation: Living with cystic fibrosis

@bonnellfoundation.bsky.social
45 followers 6 following 31 posts

We support cystic fibrosis families with financial assistance,transplant grants and education scholarships. We host the Living with Cystic Fibrosis podcast. To view our programs visit: thebonnellfoundation.org

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The Bonnell Foundation: Living with cystic fibrosis @bonnellfoundation.bsky.social · 02/04/2026
You can see our short documentary at the end of the month! Watch the trailer today on YouTube! youtu.be/RYjlB25Cr9Y
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The Bonnell Foundation: Living with cystic fibrosis @bonnellfoundation.bsky.social · 10/12/2025
End of the year donations for The Bonnell Foundation are appreciated! We help families Living with cystic fibrosis!
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Boogie Underground @alhanda.bsky.social · 07/11/2025
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The Bonnell Foundation: Living with cystic fibrosis @bonnellfoundation.bsky.social · 13/09/2025
Showing off our new golf shirts!
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The Bonnell Foundation: Living with cystic fibrosis @bonnellfoundation.bsky.social · 18/08/2025
The aharvet of Hope event is September 20 th!
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The Bonnell Foundation: Living with cystic fibrosis @bonnellfoundation.bsky.social · 19/06/2025
A documentary: coming later this year!
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The Bonnell Foundation: Living with cystic fibrosis @bonnellfoundation.bsky.social · 14/05/2025
Yard Signs are raising awareness!
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The Bonnell Foundation: Living with cystic fibrosis @bonnellfoundation.bsky.social · 02/05/2025
Beautiful colors.
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The Bonnell Foundation: Living with cystic fibrosis @bonnellfoundation.bsky.social · 28/04/2025
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! Thebonnellfoundation@gmail.com
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The Bonnell Foundation: Living with cystic fibrosis @bonnellfoundation.bsky.social · 07/04/2025
Family night with Children’s Hospital of Michigan.
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The Bonnell Foundation: Living with cystic fibrosis @bonnellfoundation.bsky.social · 04/04/2025
It’s Opening Day! Go Tigers! #DetroitTigers
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The Bonnell Foundation: Living with cystic fibrosis @bonnellfoundation.bsky.social · 26/03/2025
New podcast out April 7 th! A CF Life: The Inspirational Voices of cystic fibrosis. @siriVaeth shares her stories.
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The Bonnell Foundation: Living with cystic fibrosis @bonnellfoundation.bsky.social · 23/03/2025
Colores Mexicano! Beautiful! #art #CF #cysticfibrosis
Colores Mexicano.
Peacock at Colores Mexicano
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Reposted by The Bonnell Foundation: Living with cystic fibrosis
The Bonnell Foundation: Living with cystic fibrosis @bonnellfoundation.bsky.social · 14/03/2025
St. Patrick’s Day is fast approaching! Have a little fun with us and donate $17!
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The Bonnell Foundation: Living with cystic fibrosis @bonnellfoundation.bsky.social · 14/03/2025
St. Patrick’s Day is fast approaching! Have a little fun with us and donate $17!
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The Bonnell Foundation: Living with cystic fibrosis @bonnellfoundation.bsky.social · 13/03/2025
Dr. Frances Collins recently retired. His is an incredible human. substack.com/@lstb/note/c...
substack.com
Laura Bonnell on Substack
Dr. Frances Collins recently retired from the NIH. This is a huge loss for not only the cystic fibrosis community, but for the world. While at the University of Michigan Dr. Collins was part of the t...
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The Bonnell Foundation: Living with cystic fibrosis @bonnellfoundation.bsky.social · 10/03/2025
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
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The Bonnell Foundation: Living with cystic fibrosis @bonnellfoundation.bsky.social · 03/03/2025
Please consider donating in honor of St. Patrick’s Day! Thebonnellfoundation.org/donate
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The Bonnell Foundation: Living with cystic fibrosis @bonnellfoundation.bsky.social · 01/03/2025
💜💜💜Advocating in DC! A good few days!
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The Bonnell Foundation: Living with cystic fibrosis @bonnellfoundation.bsky.social · 23/02/2025
Great to speak at Rare Disease day! #RareDisease @grandrapidsnews.mastodon.social.ap.brid.gy
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The Bonnell Foundation: Living with cystic fibrosis @bonnellfoundation.bsky.social · 16/02/2025
From snow…. To Florida sunshine….snd back to @puremichigan1.bsky.social #weather #sunshine
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The Bonnell Foundation: Living with cystic fibrosis @bonnellfoundation.bsky.social · 06/02/2025
Our bookkeeper! Welcome to the team Olga!
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The Bonnell Foundation: Living with cystic fibrosis @bonnellfoundation.bsky.social · 04/02/2025
Be part of the CF cheer team!! Donate: link in bio! Spread the sunshine!
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The Bonnell Foundation: Living with cystic fibrosis @bonnellfoundation.bsky.social · 22/01/2025
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!
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The Bonnell Foundation: Living with cystic fibrosis @bonnellfoundation.bsky.social · 02/01/2025
Join us in 2025!
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The Bonnell Foundation: Living with cystic fibrosis @bonnellfoundation.bsky.social · 23/12/2024
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!
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The Bonnell Foundation: Living with cystic fibrosis @bonnellfoundation.bsky.social · 13/12/2024
Heading home from DC!
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The Bonnell Foundation: Living with cystic fibrosis @bonnellfoundation.bsky.social · 12/12/2024
Bye bye DC for now!
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The Bonnell Foundation: Living with cystic fibrosis @bonnellfoundation.bsky.social · 12/12/2024
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!
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The Bonnell Foundation: Living with cystic fibrosis @bonnellfoundation.bsky.social · 05/12/2024
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!
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The Bonnell Foundation: Living with cystic fibrosis @bonnellfoundation.bsky.social · 03/12/2024
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 SenWBrinks@senate.michigan.gov
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The Bonnell Foundation: Living with cystic fibrosis @bonnellfoundation.bsky.social · 03/12/2024
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 SenWBrinks@senate.michigan.gov thebonnellfoundation.org/time-to-pass...
thebonnellfoundation.org
Time to pass HB 4167: The Bonnell Foundations Laura Bonnell talks with Greg Bowman on WWJ. | Roadmap to CF: The Bonnell FoundationTime to pass HB 4167: The Bonnell Foundations Laura Bonnell talks with...
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The Bonnell Foundation: Living with cystic fibrosis @bonnellfoundation.bsky.social · 03/12/2024
Hello! The Bonnell Foundation has arrived on Bluesky Social! We’re all about cystic fibrosis! Ask us anything! Send us a hello at Thebonnellfoundation@gmail.com
Laura Bonnell, CEOPam and Jack! Great volunteers!Future medical doctors who attended our gala
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