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Less than 100 miles to go…

  • nicoleedwards254
  • Aug 14, 2021
  • 2 min read

I started my running challenge in January (1,083.8 miles!). The sole purpose was to raise money for @cftrustuk and also to share with our friends, family (and anyone who might be interested!) what we were going through as new parents to a CF baby. I wanted to raise awareness by sharing the good (and for the most part it’s been a glorious journey!), the bad and the ugly (although Arlo is frigging cute so there’s not much ugliness here peeps!😜).


I remember the first post that I put on my personal Instagram profile when I announced the start of the running challenge (swipe to see it!) and it felt like a monumental step to even write down that Arlo has cystic fibrosis.


And whilst from the outside this challenge may have looked like a fundraising project, it became so much more.


I have been able to connect with other people in the CF community. I’ve been able to share some moments from our CF journey - some things that I maybe would not otherwise have shared. And boy have I learned so much - about cystic fibrosis but also about myself - and I have so much still to learn.


I can’t thank you enough if you have supported us on this ‘big jog’ - Arlo and I thank you from the bottom of our hearts.


But I do have one last favour to ask - let’s see if we can get this last £372 so I can reach my target.


I know it was an obnoxious target - I started at £2,500, then £5,000 and then I got greedy and went for £7,500!


But it’s an obnoxious target that equals the complexity of the cause - CF is different for every single person who has it. There is no cutting corners. No quick fix. It consumes our every day. We cannot miss a treatment. And no one drug works for everyone - YET! But with more funding for research - and more awareness raised - we can make a difference. For everyone affected by cystic fibrosis.


So please, if you can share my donation page, or even donate yourself - it will be much appreciated.





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Post: Blog2_Post
Arlo’s Army: We Won’t Stop Until CF Does

There’s no cure for CF yet. Even with groundbreaking new treatments, daily life for people with CF remains a heavy burden and many aren't eligible for these new drugs. That's why we're raising money. To fund cutting-edge research. To support families like ours. To keep pushing until CF stands for Cured Forever.

CF affects over 11,000 people in the UK — and more than 100,000 globally. It impacts the lungs, pancreas, and other organs, turning mucus thick and sticky, and making everyday life a battle for breath.

 

The Cystic Fibrosis Trust is leading the charge to change this. They fund game-changing science, support families, and fight for better treatments, care, and — one day — a cure.


Join Arlo’s Army today.

 

Stand with us. Donate. Share. Fight for a future where no child has to grow up fighting CF.

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