CForYourself: Youth Advisory Group takeover
CForYourself: A podcast from Cystic Fibrosis Trust04/22/24 • 41 min
In episode seven, Lucy has a virtual catch-up with Tilly, Rosie and Tehya from the Trust’s Youth Advisory group, otherwise known as YAG. They talk about growing up with CF, managing friendships, transitioning from primary to secondary school, navigating high school with CF and so much more.
We also hear from Ellie Mindel, Lead for Children and Young People at the Trust, to find out a little bit more about the YAG programme and how people can get involved.
Read the full episode transcript.
- For more information and support on any of the issues we've talked about in this podcast, you can call our Helpline on 0300 373 1000, or email [email protected], or message us on WhatsApp.
- CF Forum - Join the conversation on our Forum and connect with other people with CF.
- CF and transition - Find out about the move from paediatric to adult care and what it could mean for you and your family.
- Secondary school and CF - Whether you're a parent, young person or teacher, here you can find out more about the issues surrounding CF and secondary school education.
- Work Forwards - Find out about our programme of employment support for people with CF and their loved ones.
- Financial support - Cystic fibrosis can bring its own financial burden. We provide a range of grants for people with cystic fibrosis and their families, support for those applying for benefits and information about prescription charges.
- Join YAG - We're always looking for new people to join us, so if you're 14-25 years old and have CF or are close to someone who does (like a brother or sister) and would like to get involved, drop us an email at [email protected].
The podcast is also available on Spotify and Apple Podcasts.
04/22/24 • 41 min
CForYourself: A podcast from Cystic Fibrosis Trust - CForYourself: Youth Advisory Group takeover
Transcript
CForYourself: Youth Advisory Group takeover
Lucy (host): Hello and welcome to season two of CForYourself, a podcast brought to you by UK charity Cystic Fibrosis Trust. I'm your host, Lucy Baxter, and I myself have cystic fibrosis. I'm one of over 10,900 people in the UK living with the cystic fibrosis.
Now, CF is a genetic disease that causes a build-up of sticky mucus in the lungs. So that means I can experience a range of different symptoms, like s
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