When you're not a fan of nasal wash 😅😁 #LivingLifeWithCysticFibrosis #NasalWashStruggles #CfMom #VihaansLifeWithCysticfibrosis #TilluSquare

#CysticFibrosis #VihaansLifeWithCysticFibrosis #MileStoneCelebration #HappyMoments #CFMom

Kelly, #CFmom and graphic designer hit the nail on the head this year! For a few reasons, this year we are #pheonixrisingfromtheashes #IYKYK #CFYukon

May is Cystic Fibrosis Awareness month! My first born has Cystic Fibrosis so, let's wear purple,donate to the Cystic Fibrosis Foundation and bring Awareness. 💜💜 #cysticfibrosisawareness #cfmom #cysticfibrosis

V approved 😋 #OatsChocolateaCake #cfmom #happybirthdaytome

Cake cheskovadam asala easy task kadu naa lanti vallaki😅 fat calculation must vihaan kosam😇 #cfmom #cysticfibrosislife #pancreaticinsufficiency #chocolatecake #airfryerrecipes

JOIN #CFRI's #MothersDay CELEBRATION! We provide you with beautiful cards to send to friends and family, inviting them to help improve the lives of those with #CysticFibrosis. Artwork by #CFmom Wanda Olson. Email [email protected] to order. #CFcommunity #65Roses #BreatheEasy

#CFRI'S EMBRACE RETREAT FOR MOTHERS OF CHILDREN/ADULTS WITH #CysticFibrosis When: May 5-7 Where: Vallombrosa Retreat Center, Menlo Park, CA Enjoy art, yoga, writing, #CFresources, advocacy, support, and respite time with women who share the #CFmom path. cfri.tiny.us/Embrace2023

Doctor appointment 9:40 memu inkaa on the way, ivala half day inka hospital lone ayipotadi 🥲 #cfmom #cflife

Sharon is a #CFmom to Valentino, 17. She makes sure he gets the care he needs while advocating for change in an industry that impacts his life. Watch her video in our #CFMasterClass series at cfmasterclass.org! This series made possible w/ support from the Cystic Fibrosis Foundation.

The #CFMasterClass series is out now! In her video, #CFMom Heather Trammell speaks on the decision to only have 1 child after learning of the gene she & her husband carried. Hear her story at cfmasterclass.org! This series made possible with support from Cystic Fibrosis Foundation.

The #CFMasterClass series will be available to subscribe to for FREE on our website next month! Heather Trammell is another wonderful #CFMom you'll meet. Heather's only child, Charlie, is 4 years old and has #cysticfibrosis. #cfcommunity #cfawareness

Another amazing #CFMom you'll hear from in our upcoming #CFMasterClass series is Julie McCaffrey! Julie is the mother of Jenna, 17, who has #cysticfibrosis. Julie talks about the importance of keeping one's mental health in check. #cfcommunity #cfawareness

The #CFMasterClass is coming soon! Kati Pannecouck is another #CFMom you'll hear from in our new series. Kati's son Ben, 14, has #cysticfibrosis. She speaks on raising a teen with #CF as well as exercise and sports in relation to the disease. #cfcommunity #cfawareness

Another amazing #CFMom you'll meet in our new #CFMasterClass series is Kim Bowman. Kim's son, Blake, died from complications of #cysticfibrosis at 14. Her other son, Brett, had a double-lung transplant; he's thriving, though he lost his vision after the transplant. #cfcommunity

The #CFMasterclass series is coming soon! You'll hear from Samantha Fuller whose middle child, Ethan, has #cysticfibrosis. Among other great advice, she reminds us how essential it is for every #CFmom to take time for themselves. #cfcommunity #cfawareness #cf

Dena Johnson is another incredible #CFMom you'll meet in our #CFMasterClass series! Dena is a mom of 2 kids, and her 9-year-old son Zachary has #cysticfibrosis. You'll hear about what she's learned during her journey so far as a #CFparent. CF Master Class is coming next month!