Team Kirsteen

The Ben Nevis Challenge for Cystic Fibrosis in Aid of Kirsteen Lambe

Fundraising for Cystic Fibrosis Trust
£4,920
raised of £4,500 target
by 53 supporters
Donations cannot currently be made to this page
Event: Cystic Fibrosis Trust - Ben Nevis Weekend Challenge, on 10 September 2010
Participants: Pauline Lambe, Scott lambe, Walter Brown, Rab Pearson, Joanne Brown, Kenny McDonald, Ricky Thomson, Martin Rae & Graham Barrie.
Cystic Fibrosis Trust

Verified by JustGiving

RCN 1079049 (England and Wales) & SC040196 (Scotland)
We fund vital research to ensure effective treatments for all.

Story

Family & Friend's of Kirsteen Lambe aged 13 who suffers from Cystic Fibrosis (CF) one of the UK's most common life-threatening inherited diseases Is taking part in The Ben Nevis Challenge on the 10-12 Sep 2010. Each one of us has to have a minium pledge of £450, we're asking all our friends & family to help with this with donating, so please dig deep and donate to this great cause. We're also holding a dance on the 18th Sep 2010 looking for raffles and will be in touch about tickets.

Kirsteen was diagnosed with Cf at the Age of 8 1/2 months old. It has been a struggle for Kirsteen through out her life, she has had her up's and down's but still mangages to stay strong, she takes a varitey of medication and also has 2 sessions of physiotheraphy each day to keep her well. Kirsteen had a Porto-caf inserted in her chest when she was 6  to make life easier for her drugs to be given while in Hospital.

Kirsteen leads an active life and can keep up with her friends, also her school particapes with her physiotherapy and takes an interest in her well being.

On the outside people with Cystic Fibrosis can look perfectly normal but on the inside peolpe are more likely to suffer from a number of distressin conditions including lung damage, malnutrition, diabetes,liver diseases and gallstones, Nasal Polyps in witch Kirsteen has had surgery 5 times and is booked in for her 6th time to have removed. These disorders seriously affect quality of life as well as LIFE EXPECTANCY

1 in 25 ..... the odds are that someone you know carries the CF gene.

Cystic Fibrosis (CF) is the UK's most common life-threatening inherited diease.

1 in 25 of us carries the faulty gene that causes Cystic Fibrosis.

If two carriers start a family, each baby has a 1 in 4 chance of having Cystic Fibrosis.

WITH YOU SUPPORT WE CAN FIND A CURE

NO DONATION IS TOO SMALL , PLEASE DONATE TODAY

 

Thanks for taking the time to visit my JustGiving page.

Donating through JustGiving is simple, fast and totally secure. Your details are safe with JustGiving – they’ll never sell them on or send unwanted emails. Once you donate, they’ll send your money directly to the charity and make sure Gift Aid is reclaimed on every eligible donation by a UK taxpayer. So it’s the most efficient way to donate - I raise more, whilst saving time and cutting costs for the charity.

So please dig deep and donate now.

About the charity

Cystic Fibrosis Trust

Verified by JustGiving

RCN 1079049 (England and Wales) & SC040196 (Scotland)
Cystic fibrosis (CF) is a life-shortening genetic condition that slowly destroys the lungs and digestive system. The Cystic Fibrosis Trust is the only UK-wide charity fighting for a life unlimited, when everyone living with CF can look forward to a long, healthy life. www.cysticfibrosis.org.uk

Donation summary

Total raised
£4,920.00
+ £139.61 Gift Aid
Online donations
£920.00
Offline donations
£4,000.00

* Charities pay a small fee for our service. Find out how much it is and what we do for it.