Nancy Kotush
1.1K posts
Happy National Flag of Canada Day! Proudly Canadian today and every day! ❤️🇨🇦❤️
#nationalflagofcanadaday #canadaproud #truenorthstrongandfree
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Another successful Decant Gala raising awareness and funds in support of the important work of @CFCanada
From the inaugural gala in 2015 to the 10th gala this year, we have raised just over $3 million!
#decantgala2024 #cheersto10years #cysticfibrosiscanada
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Nancy Kotush retweetledi
🌟 Breaking News! 🌟 Dr. Michael Strong's team at Western University may have found a potential cure for ALS by targeting a specific protein. "After 30 years, we finally see a path to treatment," says Dr. Strong. New hope for millions affected!
#ALSResearch #EndALS #ALSCanada
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May is Cystic Fibrosis Awareness month! @TourCNTower looked fabulous on Saturday, May 11 lit up in the teal & blue colours of Cystic Fibrosis Canada. Thank you for helping to spread CF awareness.
#cysticfibrosisawareness #gofurtherforall #lightup4CF
@CFCanada
@torontoadultcf
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Thank you @cntower for raising awareness for the cystic fibrosis community! #furtherforall #cysticfibrosisawareness
@CFCanada
CN Tower / Tour CN@TourCNTower
Tonight the #CNTower will be lit blue and teal for Cystic Fibrosis Awareness Month / Ce soir, la #TourCN sera illuminée en bleu et bleu sarcelle pour le Mois de sensibilisation à la fibrose kystique
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Mila Mulroney, along with the support of Brian Mulroney, has been an incredible champion for Canadians with cystic fibrosis. Her efforts to raise awareness, encourage donations, and support critical research made a lasting impact.
#cfawareness #cysticfibrosiscanada
@CFCanada
The Hospital for Sick Children (SickKids)@SickKidsNews
Ahead of former Prime Minister Brian Mulroney’s state funeral tomorrow, we reflect on his dedication to children’s health care. In 1990, the Mulroneys visited SickKids to launch the Mila Mulroney Cystic Fibrosis Research Fund.
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Fantastic goal scorer and an incredibly kind person! What a weekend Auston Matthews! Thanks to you and your buddy Finn for sharing your friendship and for raising awareness for cystic fibrosis.
@AM34 @sickkids @CCMHockey @CFCanada
#kindness #cfawareness
Toronto Maple Leafs@MapleLeafs
“You’re my secret weapon” The Leaf: Blueprint Moment presented by @Rogers
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@bethdenniss Thank you Madi & Beth ~ very grateful for your committed advocacy efforts!
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Madi struggled mentally for a few years after a public battle for a drug that saved her life. She has been back in the battle hoping to promote change for all who suffer with a Rare Disease. Hopefully the much needed change will come. #RareDiseases #cysticfibrosis #healthpolicy
New Tecumseth, Ontario 🇨🇦 English
Wonderful collaboration and amazing experience for Finn! Thank you @CCMHockey @AM34 @sickkids for raising awareness of cystic fibrosis.
@CFCanada
#cfawareness #gofurtherfor #cysticfibrosis
CCM Hockey@CCMHockey
An All-Star collaboration between Finn and @AM34 Stay tuned for the skate’s debut this Saturday, February 3rd, as their drawings come to life!
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@bethdenniss Well done, Beth & Madi! Your continued efforts advocating for the rare disease community are commendable!
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#takeda_changemaker
Working together to promote change for people living with Rare Diseases in Canada.
#Iamnumber12 #RareDisease
toronto.citynews.ca/video/2023/11/…
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@bethdenniss @SimcoeNews You and Madi are such inspirations! Very grateful for your incredible advocacy efforts. What a difference you both have made for our CF community!
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Simcoe County mother and daughter share cystic fibrosis story, continue to help others simcoe.com/opinion/simcoe… via @SimcoeNews
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Proud of our committee and grateful for everyone who made a contribution to another incredibly successful Decant Gala & Fine Wine Auction!
#decantgala2023 #decantcf #furtherforall #cysticfibrosis
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Nancy Kotush retweetledi
CF is a progressive, genetic disease that affects the lungs, pancreas, & other organs. This disease will manifest in a number of ways & there are many different factors that will affect a person's health & the course of the disease, including age of diagnosis
#cfawarenessmonth
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@bethdenniss So interesting and eye-opening. I’m still amazed by all of the unique CF stories even after being a part of the community for 27 years. #cysticfibrosisawareness
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Another informative podcast! Cystic Fibrosis is not just a Caucasian disease.
#cysticfibrosis #cysticfibrosisawareness
The Bonnell Foundation@RoadmapToCF
Our newest Board member is featured in todays podcast. Rachel Alder was not diagnosed until she was 26 years old. The CF diagnosis came late because she’s a person of color. thebonnellfoundation.org/audio-podcasts/ Anyone can be born with this genetic disease.
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Nancy Kotush retweetledi
@kgroverto Exactly!🙌 So grateful for all of the meaningful impact accomplished by everyone at Cystic Fibrosis Canada
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Some have said we push too hard at #CFCanada or we are not aligned with the right side of debates. Without apology, we do push hard for the CF community and are on the side of debates that result in people with #cysticfibrosis living healthier lives. Take a look at our impact.
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