Cody Dieruf Benefit Foundation | Life with Cystic Fibrosis
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The Cody Dieruf Benefit Foundation was formed in March of 2006 in honor of Cody Dieruf who passed away from Cystic Fibrosis at 23 years old. Uniting communities and families living with Cystic Fibrosis by raising awareness, providing emotional and financial assistance, encouraging health management, and inspiring life experiences.
Cody Dieruf Benefit Foundation | Life with Cystic Fibrosis
1M ago
The We Walk Together Mothers' Retreat, for mothers of children and adults living with Cystic Fibrosis (CF), will be held from Thursday, October 24th, to Sunday, October 27th. The registration deadline is Monday, September 23rd. REGISTER HERE The retreat is free for moms to attend. Registration is limited to 20. This year's topic is secondary ..read more
Cody Dieruf Benefit Foundation | Life with Cystic Fibrosis
4M ago
The Night of Hope Benefit Auction will feature heartwarming stories from our community, illustrious silent and live auction items for you to bid on, and support and hope for those affected by cystic fibrosis (CF). It will be a night you won’t soon forget, filled with inspirational stories about overcoming adversity on the CF journey.
You can purchase tickets to the Night of Hope auction online at Night of Hope Auction – Campaign (classy.org)
We understand that not everyone will be able to join us in person. Even if your schedule or location does not permit your attendance, you can still suppo ..read more
Cody Dieruf Benefit Foundation | Life with Cystic Fibrosis
6M ago
? Exciting News! ?
Mark your calendars for May 2nd and 3rd because Give Big is back! Join us for a 24-hour celebration of giving where we have the opportunity to make a difference in the lives of those living with Cystic Fibrosis.
Our goal for this year is to raise $20,000 to support individuals and families affected by CF. Together, we can make a meaningful impact and bring hope to those in need.
Donate Here
Stay tuned for an exciting announcement next week about matching funds that will amplify the impact of your generosity. Remember, every donation counts, no matter how big or small.
Let’s ..read more
Cody Dieruf Benefit Foundation | Life with Cystic Fibrosis
6M ago
“Dine to Donate” for Montana families living with Cystic Fibrosis on Monday, May 6th from 4:00 PM to 8:00 PM at Texas Roadhouse. Mention the Cody Dieruf Foundation (CDF) when you pay and 10% of your bill will go to support CDF programs!
We hope to see you all there ..read more
Cody Dieruf Benefit Foundation | Life with Cystic Fibrosis
6M ago
This year we are raffling off the choice of three vacation packages. The winner of this raffle will pick from either of our three trips.
⛷️ Trip 1 – Jackson Hole 3-night stay with lift tickets
?️ Trip 2 – Lodging & tickets to your choice of select regular season sporting event.
? Trip 3 – 3-night stay at Key West Marriott.
The winner will be drawn on Dec. 13, 2024. Make sure to buy your tickets online at:
https://live.classy.org/register/vacationraffle/551fc158-7416-4759-8a19-831111141940
Once you have registered you can proceed to enter the raffle by selecting which of the ticket values ..read more
Cody Dieruf Benefit Foundation | Life with Cystic Fibrosis
9M ago
If we were to sum up 2023 in one word it would be GROWTH! Through our partnership with the Billings Clinic and the help of our generous donors, we are able to serve a growing number of those who are living with Cystic Fibrosis.
Because of the generous support of our Cody Team in 2023, we were able to:
Purchase a swing set for 5-year-old Alaina to help keep her active and lungs clear.
Purchase an exercise bike for Marjean who is 52 and works hard at staying physically active.
Purchase an in-ground trampoline for 5-year-old Ivy. Ivy’s mom had this to say about her scholarship, “Cystic Fi ..read more
Cody Dieruf Benefit Foundation | Life with Cystic Fibrosis
1y ago
This year’s We Walk Together Mothers’ Retreat for mothers of children and adults living with cystic fibrosis will be held on Friday, November 17th, through Sunday, November 19th, at Chico Hot Springs in Pray, Montana.
At the We Walk Together mothers’ retreat, we will create a nurturing and encouraging environment where you can unwind and temporarily step away from daily responsibilities. The retreat will feature various activities, including sessions led by guest presenters, workshops, and activities designed with the special needs of caretakers in mind.
Lodging: All rooms are shared occupanc ..read more
Cody Dieruf Benefit Foundation | Life with Cystic Fibrosis
1y ago
Join us for this year’s Night of Hope Benefit Auction on Saturday, August 26 at the Grantree Inn of Bozeman. Doors open at 5:00 PM.
Proceeds from this event go to support Montanans who are living with Cystic Fibrosis (CF).
Special guest speakers include Lieutenant Governor Kristen Juras and local CDF father David Martinez. You will be inspired when you hear their stories about life with CF and all they strive to overcome.
Our Silent auction will be held online with items on display at the in-person event & online. You do not need to be present in person to bid on silent auction items. The ..read more
Cody Dieruf Benefit Foundation | Life with Cystic Fibrosis
1y ago
We are EXCITED to join with 250 nonprofits in the Gallatin Valley for this year’s Give Big hosted by the One Valley Community Foundation.
Give Big is a 24-hour celebration of giving. It connects generous community members with causes they care about in order to raise important funding for local nonprofits.
Because of the generous support of our Cody Team we have secured just over $13,000 in matching gifts for this year’s Give Big! That means when you donate on May 4th or 5th, your gift will be doubled!
A gift of $50 becomes $100
A gift of $100 becomes $200
We invite you to join ..read more
Cody Dieruf Benefit Foundation | Life with Cystic Fibrosis
2y ago
When you give to the Cody Dieruf Foundation (CDF), you give HOPE to someone living with cystic fibrosis (CF).
Thanks to the financial generosity of our Cody Team, CDF has been able to offer emotional and financial assistance to more individuals touched by CF in Montana in 2022.
There are many needs within the CF community and until a cure is found, we will be here to help. With your partnership, we will continue to offer much-needed support to Montanans living with cystic fibrosis in 2023.
Give a year-end gift today at www.breathinisbelievin.org/donate
  ..read more