Cystic Fibrosis Trust

Laurens page

Lauren butler

Lauren butler

My Story

My story, my why. - please share. πŸ«πŸ’›

I've never been a runner I mean all through school I absolutely loved sports, rugby & football and 100m sprint on sports day but I started to get into bodybuilding and that was my life from competing on stage winning my first show coming 4th in my second and two British invites but doing this marathon next year is personal. 

 My little girl coming into this world was the best, finding out at 3 weeks old from the heel prick test she has cystic fibrosis my newborn bubble was instantly popped. Where people would be seeing family and friends showing their baby off we were going to hospital appointments, physio learning what her life will now look like. The unknowing was hard & is hard. 

Seeing how far Billiee-Mae has come in her 10months is amazing from being so poorly with rsv at just 1month old and being so poorly and not getting any better after endless physio and antibiotics having a dreaded hospital stay for 10 days & watching her get put to sleep was heartbreaking. But she's now such a feral girl she's a true warrior! So if she can get through the hard days of cystic fibrosis and still be so happy I can do this marathon. This girl gives me all the motivation I need. πŸ’ͺπŸ»πŸƒπŸ» 

If you can donate just anything to help me reach my target I would be FOREVER GRATEFUL πŸ’•

I'm so grateful for how far research has come for Cystic fibrosis 🫁 hopefully one day CF will stand for CURE FOUND πŸ€žπŸ»πŸ«πŸ’› 

I'm doing a sky dive in spring to also raise money for CF & a half marathon in February for training for the marathon 

Cystic Fibrosis Trust is the charity uniting people to stop cystic fibrosis (CF). We fund vital research, improve care, speak out and race towards effective treatments for all. We won't stop until everyone with cystic fibrosis can live without limits.

Cystic Fibrosis Trust is the UK's leading charity supporting people with cystic fibrosis (CF). 

Cystic fibrosis (CF) is a genetic condition which causes sticky mucus to build up in the lungs and digestive system. It affects more than 10,800 people in the UK. One in 25 of us carries the faulty gene that causes it, usually without knowing.

Since 1964, we've supported people with cystic fibrosis to live longer, healthier lives - and we won’t stop until everyone can live without limits imposed by CF.

Cystic Fibrosis Trust

Raising for:

Cystic Fibrosis Trust
7%

Funded

  • Target
    Β£2,500
  • Raised so far
    Β£175
  • Number of donors
    7

My Story

My story, my why. - please share. πŸ«πŸ’›

I've never been a runner I mean all through school I absolutely loved sports, rugby & football and 100m sprint on sports day but I started to get into bodybuilding and that was my life from competing on stage winning my first show coming 4th in my second and two British invites but doing this marathon next year is personal. 

 My little girl coming into this world was the best, finding out at 3 weeks old from the heel prick test she has cystic fibrosis my newborn bubble was instantly popped. Where people would be seeing family and friends showing their baby off we were going to hospital appointments, physio learning what her life will now look like. The unknowing was hard & is hard. 

Seeing how far Billiee-Mae has come in her 10months is amazing from being so poorly with rsv at just 1month old and being so poorly and not getting any better after endless physio and antibiotics having a dreaded hospital stay for 10 days & watching her get put to sleep was heartbreaking. But she's now such a feral girl she's a true warrior! So if she can get through the hard days of cystic fibrosis and still be so happy I can do this marathon. This girl gives me all the motivation I need. πŸ’ͺπŸ»πŸƒπŸ» 

If you can donate just anything to help me reach my target I would be FOREVER GRATEFUL πŸ’•

I'm so grateful for how far research has come for Cystic fibrosis 🫁 hopefully one day CF will stand for CURE FOUND πŸ€žπŸ»πŸ«πŸ’› 

I'm doing a sky dive in spring to also raise money for CF & a half marathon in February for training for the marathon 

Cystic Fibrosis Trust is the charity uniting people to stop cystic fibrosis (CF). We fund vital research, improve care, speak out and race towards effective treatments for all. We won't stop until everyone with cystic fibrosis can live without limits.

Cystic Fibrosis Trust is the UK's leading charity supporting people with cystic fibrosis (CF). 

Cystic fibrosis (CF) is a genetic condition which causes sticky mucus to build up in the lungs and digestive system. It affects more than 10,800 people in the UK. One in 25 of us carries the faulty gene that causes it, usually without knowing.

Since 1964, we've supported people with cystic fibrosis to live longer, healthier lives - and we won’t stop until everyone can live without limits imposed by CF.