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Breathe Their Name Tribute Wall
Breathe Their Name Tribute Wall
You are invited to submit a tribute in memory of a loved one. To submit your tribute please fill out the form below.
Register here for Unite65
Register here for Unite65
This CF Month we're standing out to make the invisible, visible! Choose your way to stand out this May and help raise life-saving funds for people living with cystic fibrosis (CF)!
CFRD – What’s age got to do with it?
CFRD – What’s age got to do with it?
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The CF Together Podcast
The CF Together Podcast
We know the importance of sharing stories and creating community for people living with CF, that's why we are excited to welcome you to our first season of the CF Together Podcast. Subscribe to this Podcast to keep updated with the latest research as well as stories of lived experience from our community to help you feel more connected and supported, whether you're living with CF, or loving someone with CF.
Finding Some Peace Through Travel - Sams Story
Finding Some Peace Through Travel - Sams Story
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2026 Marathons for CF Together.
2026 Marathons for CF Together.
CF Together: Advancing progress for people living with cystic fibrosis.
Hospital Packs
Hospital Packs
CF Together: Advancing progress for people living with cystic fibrosis.
Mandy’s Play-Based Tips: Helping Her Son Feel Confident for Clinic Visits
Mandy’s Play-Based Tips: Helping Her Son Feel Confident for Clinic Visits
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Educator Series 2026
Educator Series 2026
At CF Together we offer dedicated education support, working with school children and their families to ensure all young people with CF have the best learning opportunities and experiences while managing their CF.
REGISTER HERE | Newly Diagnosed Peer Support Group
REGISTER HERE | Newly Diagnosed Peer Support Group
Events and peer support that help the CF community to live a well-informed, supported and connected life.
Get your tickets HERE! Caulfield Charity Family Day
Get your tickets HERE! Caulfield Charity Family Day
CF Together is delighted to be a chosen charity partner of the Melbourne Racing Club (MRC) Foundation for their 2026 Family Charity Race Day.
BREAKING NEWS | Alyftrek listed on PBS!
BREAKING NEWS | Alyftrek listed on PBS!
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Back to School Resources
Back to School Resources
At CF Together we offer dedicated education support, working with school children and their families to ensure all young people with CF have the best learning opportunities and experiences while managing their CF.
Lyndall Grace - A Late Diagnosis of ADHD
Lyndall Grace - A Late Diagnosis of ADHD
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Break a Sweat 2025 Images
Break a Sweat 2025 Images
Sydney | Melbourne | Virtual
Key Dates 2026
Key Dates 2026
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Impact Report 2025
Impact Report 2025
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Limited Edition Christmas Rose Pins
Limited Edition Christmas Rose Pins
How to submit comments to the PBAC
How to submit comments to the PBAC
The Pharmaceutical Benefits Advisory Committee (PBAC) meet approximately six times per year, to discuss listing new medications as well as the expansion of medications that are already listed. Prior to each meeting the CF community can submit comments in support of each medication. The PBAC welcomes input from patients, carers, health professionals, consumer groups or organisations and members of the public.
Advocacy Update July - December 2025
Advocacy Update July - December 2025
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Make a donation
Make a donation
Alyftrek approved by TGA
Alyftrek approved by TGA
Pledge for Giving Day
Pledge for Giving Day
Access CF support
Access CF support
Dreamnight 2025 at Taronga Zoo
Dreamnight 2025 at Taronga Zoo
Break a Sweat 2025 - Register to walk virtually
Break a Sweat 2025 - Register to walk virtually
CFRD Update - MSAC defers CGM decision
CFRD Update - MSAC defers CGM decision
Volunteer for Giving Day 2025
Volunteer for Giving Day 2025
Mummy's lungs are different: Catherine Maguire
Mummy's lungs are different: Catherine Maguire
Nardia- Living longer with CF
Nardia- Living longer with CF
Breaking News | Alyftrek approved by PBAC
Breaking News | Alyftrek approved by PBAC
CF Together CEO Announcement
CF Together CEO Announcement
Savannah's story | new mum living with cystic fibrosis
Savannah's story | new mum living with cystic fibrosis
Catherine's story | Listable, but not listed
Catherine's story | Listable, but not listed
Meet Jade - Living Longer with CF
Meet Jade - Living Longer with CF
Meet John - Diagnosed with CF at 62
Meet John - Diagnosed with CF at 62
Cystic Fibrosis Centre for Research Excellence (CF CRE)
Cystic Fibrosis Centre for Research Excellence (CF CRE)
Become a Regular Giver
Become a Regular Giver
Become a CF Together member
Become a CF Together member
Share Your Story
Share Your Story
Peer Support Groups | REGISTER
Peer Support Groups | REGISTER
CF Together CFRD Position Statement | Equitable Access for All
CF Together CFRD Position Statement | Equitable Access for All
Fundraise with us
Fundraise with us
Staying Hydrated with CF - Sodii Partnership
Staying Hydrated with CF - Sodii Partnership
CFRD Factsheet
CFRD Factsheet
Research - Register to be kept up to date
Research - Register to be kept up to date
National CF Support Line - 1300 CF HELP
National CF Support Line - 1300 CF HELP
Fundraise with us
Fundraise with us
CF Together - Strategic Plan 2024-2027
CF Together - Strategic Plan 2024-2027
Share your Story
Share your Story
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