• Cody Dieruf Benefit Foundation for Cystic Fibrosis
  • Cody Dieruf Benefit Foundation for Cystic Fibrosis
  • Cody Dieruf Benefit Foundation for Cystic Fibrosis
  • Cody Dieruf Benefit Foundation for Cystic Fibrosis
  • Cody Dieruf Benefit Foundation for Cystic Fibrosis
  • Cody Dieruf Benefit Foundation for Cystic Fibrosis
  • Cody Dieruf Benefit Foundation for Cystic Fibrosis
  • Cody Dieruf Benefit Foundation for Cystic Fibrosis
  • Cody Dieruf Benefit Foundation for Cystic Fibrosis
  • Cody Dieruf Benefit Foundation for Cystic Fibrosis
  • Cody Dieruf Benefit Foundation for Cystic Fibrosis
  • Cody Dieruf Benefit Foundation for Cystic Fibrosis

 

Mark your Calendars for the 8th Annual Live and Silent Auction

Feb. 16, 2013 at the Hilton Garden Inn

Purchase tickets now.

A Big Thank You

The Cody Dieruf Benefit Foundation wants to give thanks to the Greg and Cindy Kindschi family for their most kind donation in honor of there parents, Richard and Carmen Kindschi from Wisconsin. They both fell at their home 6 days apart in June, 2011 and passed away 26 days apart in August, 2011at 79 years of age.

Through life, Richard and Carmen have contributed to helping organizations and taking care of others, and through death, their family felt it fit that they contribute to CDBF. Richard passed away due to pulmonary fibrosis and was on supplemental oxygen for over 5 years. Carmen passed away due to pulmonary embolisms and other factors. Their kids and grandkids wanted to continue to help with pulmonary disorders by donating $5,000 to the CDBF cause, Breathin' is Believin'.

This contribution is a gateway to helping Montana children and young adults who live with Cystic Fibrosis. Because they understood what it is like to live with a lung disease, the family is reaching out to others.

Cystic Fibrosis is a progressive disease. There is a need in Montana for financial assistance. Richard and Carmen will be remembered by many. Their lives continue on through those who are living with Cystic Fibrosis.

Maman Jolie Maternity is excited to announce our collaboration with our favorite Bozeman, Montana-based charity, Cody Dieruf Benefit Foundation For Cystic Fibrosis to bring you the From Bump to Breathe campaign. From May through July you can show your support and help the foundation raise social awareness for Cystic Fibrosis by purchasing one of our special garments made just for this cause. All proceeds go to benefit the Cody Dieruf Benefit Foundation. Limited supply, get your shirt, or tunic dress now, and Get your Glow on!

The Gallatin Quilt Guild of Bozeman, MT has chosenThe Cody Dieruf Benefit Foundation as part of their gifting for the year of 2012. The Guild Assoc, has expressed an interest in the foundations efforts to further the foundations fund raising to help families of Montana who live with Cystic Fibrosis, The Quilt, named, "Wild Women Don't get the Blues", was presented to The Cody Foundation on May 8th, 2012. Countless hours were put into the creation of this queen sized quilt. The backing of this quilt has a rose design which signifies the story behind Cystic Fibrosis. All monies raised from the raffle sales will be earmarked for Montana kids and young adults who live with Cystic Fibrosis.

The Cody Foundation is honored to accept this quilt in tribute to our Cystic Fibrosis families.

Buy a single ticket for $10

Or, buy 3 tickets for $20

Help us help our own Montana kids and young adults with Cystic Fibrosis. The Cody Dieruf Benefit Foundation is now raising funds to help Montana CF kids who live with this disease. Purchase a bronze sculpture, designed by Pam Harrj of Bridger Bronze. This bronze signifies peace, hope, joy, love and is an extraordinary gift symbolic of strength.

Each sculpture sold will come with its own authenticity papers. Place this beautiful sculpture in your home or office and know that through your purchase your money will be earmarked for a Montana child in his/her fight with Cystic Fibrosis.

Additional details (PDF).


The Faces of Cystic Fibrosis


Thank you for your support of the Cody Dieruf Benefit Foundation for Cystic Fibrosis

George and Ginny Dieruf

Raising money for our Cystic Fibrosis families is hard work but so much fun to see the results. Our family finds it so fulfilling in helping families who live with Cystic Fibrosis. Just as our daughter, Cody, lived, we want our families to find comfort in knowing that they have financial help, along with emotional support, and educational and cultural opportunities. Cody would be so proud to know that families in our communities are living and finding hope with this disease.

This year, our Foundation formed the "grant a wish" program. This years recipient went to Eli, his wish, a 650 Kowasawki KLR Motorcycle.

A very rewarding moment in the presentation of this bike. We could not do this without the help of our community, our families, friends, volunteers, board members, business sponsors, and all who believe in our cause. A huge thank you to all.