Angel Kirsty’s CF Wishes
Donation protected
Kirsty’s wish is to grant your wish
Hello, my name is Jayne. I hope you are all safe and well.
Covid-19, our indiscriminate and invisible enemy, is certainly working to bring out the best in us isn’t it?
So many amazing people coming together with one ultimate purpose - to shield the vulnerable and help those in need. It is truly empowering.
I’ve been thinking what on earth can I do to help in this global pandemic?
After many hours of considered thought, and inspired by my late daughter Kirsty, the beginnings of an idea popped into my head.
I would like to grant wishes to people who suffer from Cystic Fibrosis.
On 6 August 2019, just ten short months ago, my beautiful 25-year-old daughter sadly passed away from this incurable life-shortening inherited disease.
CF is caused by a faulty gene, and one in 25 of us carries that gene.
At any one time, there are almost 10,000 people living with CF in the UK. The disease causes the lungs and digestive system to become clogged with mucous, making it difficult for sufferers to breathe and digest food.
We take breathing for granted don’t we? Kirsty struggled to breathe every day.
My goodness we miss her so much. Her love and her laughter inspired us all. Her bucket list demands drove us crazy and she was at her happiest when she was meeting celebrities or simply out in our locality having a coffee and a chat with her family and friends.
We all know the saying ‘laughter is the best medicine’ - so let’s prescribe some laughter and joy for someone who suffers from the effects of Cystic Fibrosis every single day.
Let’s give them something to look forward to.
Together we can make this happen.
On behalf of Angel Kirsty, please help me grant a wish for someone with CF.
Hello, my name is Jayne. I hope you are all safe and well.
Covid-19, our indiscriminate and invisible enemy, is certainly working to bring out the best in us isn’t it?
So many amazing people coming together with one ultimate purpose - to shield the vulnerable and help those in need. It is truly empowering.
I’ve been thinking what on earth can I do to help in this global pandemic?
After many hours of considered thought, and inspired by my late daughter Kirsty, the beginnings of an idea popped into my head.
I would like to grant wishes to people who suffer from Cystic Fibrosis.
On 6 August 2019, just ten short months ago, my beautiful 25-year-old daughter sadly passed away from this incurable life-shortening inherited disease.
CF is caused by a faulty gene, and one in 25 of us carries that gene.
At any one time, there are almost 10,000 people living with CF in the UK. The disease causes the lungs and digestive system to become clogged with mucous, making it difficult for sufferers to breathe and digest food.
We take breathing for granted don’t we? Kirsty struggled to breathe every day.
My goodness we miss her so much. Her love and her laughter inspired us all. Her bucket list demands drove us crazy and she was at her happiest when she was meeting celebrities or simply out in our locality having a coffee and a chat with her family and friends.
We all know the saying ‘laughter is the best medicine’ - so let’s prescribe some laughter and joy for someone who suffers from the effects of Cystic Fibrosis every single day.
Let’s give them something to look forward to.
Together we can make this happen.
On behalf of Angel Kirsty, please help me grant a wish for someone with CF.
Organizer
Jayne Jones
Organizer