Cystic fibrosis (CF) is a life-limiting genetic condition affecting more than 10,600 people across the UK. It causes the body to produce thick sticky mucus, which can have a wide range of symptoms, but it mainly affects the lungs and digestive system. Everyone with CF will have a slightly different variety and severity of symptoms. 

As CF Mama’s we always find it incredible how one child’s journey can differ so much from another. One thing that’s exactly the same for all our babies, is how amazingly brave and inspiring they all are 💛

On a daily basis our little warriors battle through endless medications, physio, nebulisers and a very high fat diet to keep them healthy. As Mama’s we wanted to push ourselves out of our comfort zones doing this challenge, to really raise awareness of this extremely challenging and terrible genetic disease. A lot of CF parents struggle mentally on a day to day basis, we wanted to let you know you’re not alone, we’re in this fight together 🙏🏼

We’ll each be covering 100km in 6 weeks and finishing on the 18th June - CF Awareness Day. We’ve set ourselves a huge target of £14k... go big or go home right?!  💛 The Cystic Fibrosis Trust is fighting for a brighter future for people with CF and their families by funding cutting-edge research into life changing drugs. 

Let’s help CF now stand for ‘Cure Found’ for our gorgeous little miracles 💛

Max’s Mama - Pamela

Matilda’s Mama - Rose

Arlo’s Mama - Ellie

Lana’s Mama - Emma

Aria’s Mama - Sas

Nolah’s Mama - Lisa

Chester’s Mama - Laura

Billy’s Mama - Amber

Natalya’s Mama - Tasha

Archie’s Mama - Anna

George’s Mama - Georgia

Alfie’s Mama - Sophie

Harper’s Mama - Aimee

Yoel’s Mama - Beatriz

💕