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sarah's page

Sarah McIntosh is raising money for The Leanne Fund
In memory of Wendy
Donations cannot currently be made to this page
Each week 5 babies are born with Cystic Fibrosis (CF) and two young lives are lost. CF is a life-long, chronic condition and there is currently no cure. The Leanne Fund helps sufferers of CF and their families by providing a range of services to make life a little easier - making a difference today.

Story

I first found out about Cystic Fibrosis in 1994 when I met Wendy in the shop where I worked. She was always smiling and laughing and I couldn't believe it when Neil told me she had CF and explained what CF was.

From that day back in 1994 we formed a concrete friendship with highs and lows. We texted everyday, spoke as often as we could and went out as often as she could. She welcomed me into her family and we formed the greatest friendship.

Sadly our friendship was cut short when CF took her away from me on the 27th May 2010, a day I will never forget, one of the hardest days of my life.

 I would like to thank the following people for their help and support over the last 9 months, Lee for always being there for me, Donnie for being there always and going to the cemetary for me, Lynz for being at the other end of the phone, Linda for letting me moan the face off her in the office and of course Jan, Bobby, Neil and Louis, my Godson. My extended family.

I am running the 10k on the 8th May 2011 in her memory and hope to run many more for her. If you could find it in your hearts to donate anything I would be so grateful, doesn't matter how little it is, every penny counts. Thank you in advance, Wee Sarah.x

Donation summary

Total
£385.00
+ £94.01 Gift Aid
Online
£385.00
Offline
£0.00

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