The Bonnell Foundation: Living with cystic fibrosis
@bonnellfoundation.bsky.social
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
End of the year donations for The Bonnell Foundation are appreciated! We help families Living with cystic fibrosis!
December 10, 2025 at 3:55 PM
End of the year donations for The Bonnell Foundation are appreciated! We help families Living with cystic fibrosis!
Reposted by The Bonnell Foundation: Living with cystic fibrosis
"Falls the Breath is extraordinary in how it bridges the spiritual and emotional with elegance. Pain and resilience are portrayed with poetic subtlety. The relationship between the living and dead becomes about healing, and that resonates with anyone who has loved and lost." #booksky
rb.gy/uiupva
rb.gy/uiupva
November 7, 2025 at 2:35 PM
Showing off our new golf shirts!
September 13, 2025 at 5:56 PM
Showing off our new golf shirts!
The aharvet of Hope event is September 20 th!
August 18, 2025 at 2:48 AM
The aharvet of Hope event is September 20 th!
A documentary: coming later this year!
June 19, 2025 at 1:24 AM
A documentary: coming later this year!
Yard Signs are raising awareness!
May 14, 2025 at 12:46 PM
Yard Signs are raising awareness!
Beautiful colors.
May 2, 2025 at 10:27 PM
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]
Want a simple, powerful way to make a difference?
Here it is! Email us for your sign!
[email protected]
April 28, 2025 at 7:43 PM
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]
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.
April 7, 2025 at 1:48 AM
Family night with Children’s Hospital of Michigan.
It’s Opening Day! Go Tigers! #DetroitTigers
April 4, 2025 at 11:31 AM
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.
March 26, 2025 at 10:13 PM
New podcast out April 7 th! A CF Life: The Inspirational Voices of cystic fibrosis. @siriVaeth shares her stories.
March 23, 2025 at 3:20 AM
Reposted by The Bonnell Foundation: Living with cystic fibrosis
St. Patrick’s Day is fast approaching! Have a little fun with us and donate $17!
March 14, 2025 at 12:56 AM
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!
March 14, 2025 at 12:56 AM
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...
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...
substack.com
March 13, 2025 at 2:03 PM
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
March 10, 2025 at 7:02 PM
Please consider donating in honor of St. Patrick’s Day! Thebonnellfoundation.org/donate
March 3, 2025 at 4:08 PM
Please consider donating in honor of St. Patrick’s Day! Thebonnellfoundation.org/donate
💜💜💜Advocating in DC! A good few days!
March 1, 2025 at 3:25 PM
💜💜💜Advocating in DC! A good few days!
Great to speak at Rare Disease day! #RareDisease @grandrapidsnews.mastodon.social.ap.brid.gy
February 23, 2025 at 11:27 PM
Great to speak at Rare Disease day! #RareDisease @grandrapidsnews.mastodon.social.ap.brid.gy
February 16, 2025 at 4:52 PM
Our bookkeeper! Welcome to the team Olga!
February 6, 2025 at 8:04 PM
Our bookkeeper! Welcome to the team Olga!
Be part of the CF cheer team!! Donate: link in bio! Spread the sunshine!
February 4, 2025 at 8:08 PM
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!
January 22, 2025 at 8:15 PM
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!
January 2, 2025 at 11:30 PM
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!
December 23, 2024 at 6:35 PM
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!