Hello, I’m John, from Cumbernauld, North Lanarkshire. My story tells of how mitochondrial disease has affected lots of generations in my family, as our particular variation is maternally inherited.
Hi, I’m John from Cumbernauld. Everyone in my family unfortunately has mitochondrial disease, on my mum’s side as our gene (A3243G) is maternally inherited. My older sister sadly died of mito in 2014.
Sadly, she died around 20 years ago. I have another older sister and an older brother who both have mito too, and a younger brother who lives in Switzerland.
I also have three nephews and a niece, but many of my family understandably aren’t sure about getting tested for mito.
I also get swollen limbs, especially my feet which has been treated with injections.
I also have restless legs, proximal myopathy and Wolff-Parkinson-White (WPW) syndrome, which causes episodes of fast heart rates (tachyarrhythmia).
I had a stroke on my left side, and a cyst was found in the left side of my brain. This means I go for an MRI every two years. I have lactic acidosis, chronic fatigue and I have to use a CPAP machine at night.
I live with my wife Pauline, who has mild cerebral palsy and rheumatoid arthritis, and I enjoy going out on Saturday nights to socialise and visiting my dad when I can.
and was excited to attend their Mito Community Day in Glasgow where I met other people impacted by mitochondrial disease.
Any funds raised by John’s mission goes to My Mito Mission’s
central funds to be granted towards research and support projects
to benefit everyone affected by mito.
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