Top Tweets for #CFMasterClass
In our #CFMasterClass series, CF Dad Joel Hersh speaks on his family's journey and how he was able to raise three kids on his own after the loss of his ex-wife.
Hear his story by subscribing for FREE at https://t.co/cixTsWBG4X!
Made possible w/ support from the @cf_foundation.
In our #CFMasterClass series, Cesar & Nora Hernandez speak on the challenge of finding info about CF in their native language of #Spanish.
Learn more about their family's story by subscribing for FREE at https://t.co/cixTsWBG4X!
Made possible w/ support from @CF_Foundation.
In our #CFMasterClass series, Tom Armstrong speaks on the role that prayer has played in his life. Tom's life completely changed as he became the main caregiver to son Michael, 23.
Subscribe for FREE at https://t.co/cixTsWBG4X!
Made possible w/ support from the @CF_Foundation.
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 https://t.co/cixTsWBG4X!
This series made possible w/ support from the @CF_Foundation.
Have you seen our NEW #CFMasterClass series yet? It's full of hope, laughter, tears and inspiration! Delve into each story and finish at your own pace.
Check it out for FREE at https://t.co/cixTsWBG4X.
This series was made possible by support from the @CF_Foundation!
The #CFMasterClass is out now!
Having multiple kids with #cysticfibrosis is tough; losing one to the disease is unbearable. Kim Bowman talks about living life after losing Blake at age 14. Hear her story at https://t.co/cixTsWBG4X.
Made possible w/ support from @CF_Foundation.
Our #CFMasterClass series is out NOW! #CFparents tell emotional stories of raising children with #CF.
@PeteOdland's 26-year-old son, Dylan, was adopted and lives with #cysticfibrosis.
Hear his story at https://t.co/cixTsWBG4X!
Made possible w/ support from @CF_Foundation.
#CFMasterClass is about parents sharing the challenges & joys of raising a child with CF. It's also important to share the story of what life is like for a CF spouse.
Hear Heather Carmona's story at https://t.co/cixTsWBG4X!
Made possible w/ support from @CF_Foundation.
Like many ppl living w/ a chronic illness, Julie McCaffrey's daughter Jenna struggles with her mental health. In her #CFMasterClass video, Julie talks about day-to-day realities of CF.
Hear her story at https://t.co/cixTsWBG4X!
Made possible w/ support from @CF_Foundation.
What's been your favorite part of #CFMasterClass?
@LauraTbonnell has 2 adult daughters with CF; after their diagnoses, she found that parents needed more all-around support.
Hear her story at https://t.co/cixTsWBG4X!
This series made possible w/ support from @CF_Foundation.
#CFMasterClass is here!
@sgreen8's son Ethan, 9, hopes to be the first football player with CF to play at the National level. Samantha speaks on embracing your kids’ goals.
Hear her story at https://t.co/cixTsWBG4X!
This series made possible w/ support from @CF_Foundation.
#CFMasterClass is NOW AVAILABLE!
One #CFparent you'll hear from is Sharon Tischio, an expert in getting things done in the form of advocacy.
Hear her story by subscribing for FREE at https://t.co/cixTsWBG4X!
This series was made possible with support from the @CF_Foundation.
Please consider making an end of the year donation to The Bonnell Foundation! https://t.co/n7DJ4ei6RE
And check out our #CFMasterClass series that showcases 12 CF parents and a spouse of someone with CF. They share their journey so far. https://t.co/ySrS2D7QvO
The #CFMasterClass series is NOW AVAILABLE to watch!
These videos center around 12 CF parents sharing the challenges and joys of raising children with #cysticfibrosis.
Watch for FREE at https://t.co/k5IaC20kK8! This series was made possible with support from @CF_Foundation.
Heather Carmona's 56-year-old husband, Scott, has #cysticfibrosis. Although born with the disease, he wasn’t diagnosed until later in life after they were married.
Hear Heather tell the story of her family's journey in her #CFMasterClass, coming soon!
#cfcommunity #cfawareness
.@lauratbonnell, Founder of The Bonnell Foundation, has 2 adult daughters w/ #cysticfibrosis. Laura knew as soon as Molly was diagnosed that parents needed more help, both emotionally and financially.
In her #CFMasterClass Laura talks about how her foundation is helping parents.
.@sgreen8's son is the middle child. Ethan is 9 years old and loves football. He hopes to be the first football player with #cysticfibrosis to play at the National level.
Samantha shares the importance of embracing your kids’ goals in our #CFMasterClass.
#cfcommunity
Bringing a child into the world with #cysticfibrosis can cause a lot of guilt amongst parents.
This is one thing @peteodland couldn’t relate to; son Dylan, 26, was adopted. But both agree that the father/son duo was meant to be as he explains in his #CFMasterClass.
#cfcommunity
Having multiple children with #cysticfibrosis is tough. Losing one of your two kids to the disease is unbearable.
In her #CFMasterClass, Kim Bowman talks about living life after son Blake died at age 14. Kim moves forward alongside son Brett, 26.
#cfcommunity #cfawareness
#CysticFibrosis, the invisible disease. If you saw 14-year-old Ben swim, you probably wouldn’t think he had any health issues.
In her #CFMasterClass, CF Mom Kati Pannecouck talks about how her son perseveres regardless of his CF challenges and scars.
#cfcommunity #cfawareness
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