Cystic Fibrosis Trust

They are really small molecules rather than anything else.

And so interestingly, the CF Foundation in the US and the CF Trust here in the UK are focusing on that remaining 10%.

And actually the therapeutic strategies designed against that 10% relate to gene editing and relate to kind of that ATMP manufacturing rather than the small molecules.

So it's been transformed, I think, from a drug perspective, but I wouldn't say that those

And thanks so much to all the adventurers from the cystic fibrosis community for joining us today.

If you would like more information on cystic fibrosis, please visit the Cystic Fibrosis Trust website at www.cysticfibrosis.org.uk. See you next time!

Imaginations fly.

Armchair Adventures is a Made by Mortals production.

This episode was co-created with the Trailfinder CF Innovation Hub and is supported by Cystic Fibrosis Trust.

Funded by Alder Hay Children's Charity, the University of Liverpool Faculty of Health and Life Sciences Public Engagement Grant Scheme, the University of Liverpool Microbiology Society and the Trailfinder CF Innovation Hub.

part of the Translational Innovation Hub Network for CF Lung Health and Infection, which is funded by LifeArc and Cystic Fibrosis Trust.

With special thanks to Liv, Josie, Arabella, Elena, Paige, Natalia, Summer and Drs.

Armchair Adventures is a Made by Mortals production.

This episode was co-created with the Trailfinders CF Innovation Hub, and is supported by Cystic Fibrosis Trust.

Funded by Alder Hey Children's Charity, the University of Liverpool Faculty of Health and Life Sciences Public Engagement Grant Scheme, the University of Liverpool Microbiology Society, and the Trailfinders CF Innovation Hub, part of the Translational Innovation Hub Network for CF Lung Health and Infection, which is funded by Life Arc and Cystic Fibrosis Trust.

With special thanks to Liv, Josie, Elena, Paige, Natalia, Summer, and Doctors Sharn and Christian.

Hey, adventurers.

I mean, it's only been the last, what, 20 years or even... 30 maybe, where people with cystic fibrosis actually live into adulthood.

So the Cystic Fibrosis Trust and the community have had to follow that.

And it's going to be the same with Dravet's in terms of the fact that a lot of young people with Dravet's now, there's more understanding and people are living longer.

And so it's only going to be it's going to be the same pathway to actually develop that sort of process in order for it to be a whole.