On the 8th of April the most amazing baby girl was born, Molly Rose Wilmot, I wasn’t sure how I’d be as a Dad, I knew I’d love her, I already loved Bump, but when she arrived, game changer!! We found out in week 3 that Molly had rare Cystic Fibrosis. Shattering news, but indomitable human spirit kicks in, Mollys beautifully brilliant, and we’re campaigning for a life unlimited by CF. It can be life shortening. Our role as parents is to be life enriching. This is to raise money to be life normalising. If you can run, register, if you can walk, register, name a target distance and help our little girl and thousands others, if you can’t do that, perhaps you can sponsor me. Thank you.  The below spiel is generic, but relevant.

Right now, we need you more than ever. With hundreds of our events postponed this year due to COVID-19, weve seen a substantial drop in our fundraising income. The Team CF Running Festival this September will help us reach every person with CF and their family when they need us most.£150 could support an individual or family in financial difficulty with a grant for basic essentials.£200 could buy exercise equipment for someone with CF, ensuring they maintain their daily treatment regime and stay healthy.£250 could protect the health of someone with CF, paying for essential white goods like a fridge to store vital medication.