May You Never Take One Single Breath For Granted.

May you never take one single breath for granted.

To be grateful for each breath, is something we should practice every day. Not everyone has the ability to fill their lungs with ease. I’ve grown up knowing that. It is because of Cystic Fibrosis, that I feel so vastly that my lungs should never be taken for granted. Every breath, every inhale and every exhale. The way my respiratory system is so intricately and beautifully made. My body, for being healthy and carrying me throughout my journey of life. I refuse to not practice gratitude. To be grateful, every second, for another breath, every day for another day to experience life. I am grateful.

We should not take moments for granted. We should not take our time here, on this earth, for granted. We should not take our bodies for granted. We should embrace every second. We should inhale the goodness and the grace we have of another day of life.

Today, I will bask in the goodness of another day. I will be grateful. I will not take a single breath for granted. I will take my body as high and low as it can go. These moments, this life and my body- are not forever. I will make every second as beautiful as I possibly can- however I choose to.

Today, I am grateful for each breath.

on

https://barefootbabysite.wordpress.com

18 year old Madison Ivey never got to grow up with her cousin Cody, who passed away from Cystic Fibrosis, but she holds her close to her heart. From a very young age, Madison would see a butterfly or hear a song and would know that it was Cody making herself known.  She says that, “I feel that Cody is always giving me a sign, leading me to believe that I am on the right path”. ” Madison says that “Cody is her angel on this earth, always dancing to her own beat of the drum”.

Team Cody

It takes a team and The Office of Gallatin County in Bozeman, MT. formed a softball team and played with hearts full of love in hopes to draw awareness of Cystic Fibrosis.  Being strong supporters of The Cody Dieruf Benefit Foundation, Gallatin County Softball Team would like to stike out Cystic Fibrosis.

Whether you make a donation, spread awareness, become an organ donor, or just simply believe in hope for a cure, CDBF hopes that the kindness of others, will inspire you to always try and help people in need and to truly make a difference in the life of those with this disease called cystic fibrosis.

2017 Mothers’ Retreat

CF affects the entire family. There are doctor appointments, travel, scheduling family activities around treatments and hospitalizations that dominate the lives of these families. Beyond a restful weekend, mothers of children with CF from throughout Montana will have the opportunity to connect and support each other. We hope each mother may find new approaches to care for herself and return home, renewed, with new insight to meet the constant needs of CF in her family. All expenses of the retreat will be fully covered for each mother that attends.  Registration is now closed for this event.

A big shout out to the 320 Ranch –

A big shout out to the 320 Ranch – www.320ranch.com. We are holding our WE WALK TOGETHER retreat on Sept. 29 through Oct 2 and they have been such great supporters. We are so very thankful to be able to have our retreat at 320 ranch. A great get a way for moms of CF. We are looking forward to this event and meeting all of your fantastic mothers.