We’re a team of 7 taking on the 3 Peaks Challenge to raise money for the Cystic Fibrosis Trust — but this isn’t just a challenge for us… it’s personal to Jess.

Jess lives with cystic fibrosis.

Cystic fibrosis is a daily, lifelong battle. It’s waking up already exhausted. It’s constant treatments, medications, and the reality that your lungs and body are always working against you. It’s spending weeks — sometimes months — in hospital, hooked up to IVs, watching life carry on without you while you’re just trying to get through each day.

It’s missing out. It’s uncertainty. It’s having to stay strong even when you don’t feel it.

And something a lot of people don’t realise is that not everyone with cystic fibrosis has access to the life-changing drugs you might hear about. Jess is one of around 1,000 people in the UK who aren’t eligible for modulators — treatments that have transformed so many lives.

So while some people are getting a second chance at life…

people like Jess are still waiting.

Still fighting.

Still spending time in hospital.

Still facing the full weight of this condition every single day.

That’s why this challenge means so much.

Every step we take up those mountains represents the uphill battle that people with cystic fibrosis face daily. The breathlessness we’ll feel climbing is temporary — but for people like Jess, breathlessness is a constant.

We’re doing this to raise money for vital research, better treatments, and hope — hope that one day, everyone with cystic fibrosis will have access to the care and medication they deserve.

If you can donate, no matter how small, it truly means the world.

And if you can’t, sharing this could still make a difference.

Because this isn’t just about climbing mountains…

it’s about fighting for a future where people like Jess can finally breathe easier.

Thank you for supporting us

More information about Cystic Fibrosis Trust: The Cystic Fibrosis Trust is the only UK-wide charity dedicated to fighting for a life unlimited by cystic fibrosis (CF) for everyone affected by the condition. Since they started in 1964 they have dedicated themselves to promoting excellence in research and clinical care, as well as providing practical support and advice to people with CF and their families. Their mission is to create a world where being born with CF no longer means a life-long struggle.