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.

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