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CF Adventurers 9h
Wishing everyone in the community a great week ahead!
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🇨🇦Vish Black Lives Matter🇨🇦 Sep 16
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Anthony usher 10h
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Shane Howard Magill Sep 19
Who ever says laughter is the best medicine is absolutely right. That's the second day in a row my good mate has had me laughing so hard that my chest has shook the crap loose. Who needs chest physio with mates like these?
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Strawfie Challenge Sep 20
Trikafta could have saved Ryan Saulnier - aged 31 This young man didn't need to die His family want people to MAKE SOME NOISE for access to Pls RT everyone
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Jane Davies 44m
Great progress for with the advent of , but more drug trials urgently needed. Our team at & want to better understand what would influence your decision to take part. If you are 16+ & have CF please help  
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lisagrono 🇨🇦 9h
You should learn something from these compassionate a mom and an RN I am deeply disturbed by your lack of ability to triage what is life threatening and requires your immediate attention.
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Adrian Sep 19
Shame on every politician in Canada. This is your drug policy legacy. As patients deteriorate in hospital you sit on your hands instead of publicly covering drugs that are available in over 20 countries
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Cystic Fibrosis Canada BC/Yukon Sep 20
Sign up or join our Vancouver planning committee and help out Canada! We're looking for volunteers for our planning committee or on the day at our scavenger hunt. Message us for details. Proudly supported by Vancouver Mitsubishi.
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CF Trust Youth 14h
HEY!Taking part in clinical trials isn’t just for adults – teens, children and even babies can take part too. If you're a young person with and interested in taking part, check out our resources and info on how below! 👇👇
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Beth Finn 7h
So this happened today 💛 Tomorrow will be the first day of Isabelle’s new life on Feeling every emotion possible at the minute. Thank you will never be enough 🙏🏻💛
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Canadian Cystic Fibrosis Treatment Society Sep 18
To every politician & bureaucrat who makes false aspersions about our motives, let us be clear - we take NO funding from any pharmaceutical company. Never have. We fight hard for access to life-saving medications for patients. No One Left Behind is our motto. 1/2
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CFscience Sep 17
I will soon be honored in a special event recognizing outstanding young professionals. In accepting this distinction, I have committed to raise money to CFF! To donate and read my story as a CF patient and CF scientists go to:
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Dan Klaes Sep 19
Come on down to Madison Seminary today and meet me! Enter the raffle to stop and get a chance to win your 50 hours of footage from your next haunt at The Hinsdale House!
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jillian mc nulty Sep 20
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Cystic Fibrosis Foundation Sep 20
affects every individual with the disease and their family differently. Chad Lucci, and adult with CF, opens up about how CF's emotional effects reach far beyond the person living with the disease.
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✰ erin leigh ✰ Sep 20
It’s officially been ONE YEAR since my last hospital stay!!!! I haven’t gone this long without a hospital visit since before high school 🥳🥳🥳 I’m SO thankful
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Cystic Fibrosis Foundation 14h
After receiving a double-lung transplant in 2016, Kyle Cole, an adult with , wasn’t sure he and his wife would be able to have children of their own. He was wrong.
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Cystic Fibrosis Foundation Sep 19
Life with can come with mental and emotional stress. Make connections and relieve some of your stress through meditation, yoga, and art at , a free, two-day, virtual event for adults with CF. Register ➡️
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Emma Boniface 18h
Check out my latest about Week 1: "From The Purge To Almost Super Human" Thank you for these drugs!!
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