Leah's skydive

Leah Taylor is raising money for Mitochondrial Disease, The Abel Foundation
Donations cannot currently be made to this page

skydive · 27 June 2020

The Abel Foundation was created to aid the sufferers of Mitochondrial Disease and help their families deal with the Darkness of this life limiting illness, we want to create help and support across the uk, Mitochondrial Disease is heart breaking and confusing. We want to be there to help

Story

Thanks for taking the time to visit my JustGiving page.

The Abel Foundation was set up in 2015 to help provide support for sufferers and the families of Mitochondrial Disease due to the lack of support when we needed it.  Our son Abel now four has got Leighs Mitochondrial Disease with Narp Mutation. There is no cure – Being life limited it’s a matter of just keeping Abel safe from viruses as they can lead to further illnesses, which to Abel can be life threatening. As well as other Mito sufferers. We run a support phone line and support group for families and sufferers, and our main goal is to build a hospice for Mito sufferers.

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.

I would appreciate all your support and help, Kind regards. 

Donation summary

Total
£145.00
+ £31.25 Gift Aid
Online
£145.00
Offline
£0.00

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