Mito Mission

Based in Airdrie, N. Lanarkshire

Hello. I’m Bethany, 26. I hope that you’ll take the time to read about my journey so far with mitochondrial disease.


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Bethany with mum

My health was okay in early childhood but when I was around six, I became so ill with stomach upsets, vomiting and dehydration I needed to be hospitalised. Because my mum was diagnosed with a mitochondrial disorder called ‘MELAS’, I was investigated for the condition. Blood tests revealed a fault with the 3243A>G gene which meant the same diagnosis for me.

MELAS is short for ‘Mitochondrial Encephalomyopathy, Lactic Acidosis and Stroke-like episodes’

and it affects many of the body's systems

… but particularly the brain, nervous system and muscles.

Bethany with spaniels

My mum’s diagnosis has since been changed to MIDD (Maternally Inherited Diabetes & Deafness) and is caused by the same gene fault. As the name suggests, her main symptoms are diabetes and deafness. This form of mito is maternally inherited so it’s thought my older brother has it too – but mildly, as he’s asymptomatic. Unfortunately for me, mine’s not so mild and I spent a lot of time in and out of hospital as a child.

Since becoming an adult, I still have gastric problems and now also debilitating headaches, muscle pain

and really awful fatigue.

Fegie the Cat

Working has proved difficult for me because of my health issues, but luckily I have a very supportive husband, Ryan, who is really understanding.

My big passion is music – specifically, Queen. I heard ‘Don’t Stop Me Now’ as a teenager and loved it, got into all their songs and haven’t stopped listening! I’m an animal lover too and we have a gorgeous cat called Fegie who completes our little household.

Thanks for reading my story.

August 2022

Bethany and Ryan

I'd love for more people

to be aware of mito.

My mission is to help others
understand the condition better.

So many people still haven’t heard of mitochondrial disease, let alone know what it is.

Bethany with Oscar

It’s hard being ill, but it makes it even harder to have

something little known and not well understood

Mito is invisible a lot of the time, which doesn’t help. It would be so much easier if more people were aware of mito and understanding about its effects.

I’d like to play even a small part
in helping to make that happen.

Bethany's Mito Mission

Get involved and

support Bethany’s cause.

Whether you support Bethany’s mission, any other single mission or My Mito Mission as a whole – it’s all the same great cause.

Spreading the word, following, sharing, as well as donating and raising funds are all really helpful and valued. From running a race to hosting a bake sale, homing a collecting can to giving out Bethany’s Mito Mission leaflets – there are so many ways in which you can get involved.

If you’d simply like to donate to Bethany’s mission, choose a way that suits you below.

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Fundraise for Bethany’s Mito Mission

We’d love your support with our fundraising… and we can provide supporting materials. Just ask!

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Set up a fundraising page above (Use the orange ‘Fundraise For Us’ button)
Set up a fundraising event on Facebook using the image above
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Download a sponsor form to print off by clicking the image above
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Ask us for support materials such as buckets, cans, leaflets and more

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Support us at 100s of stores. Click green, ‘Find Your charity’ button
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Set us as your favourite charity (under our name to the right)

Other ways you can support us

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Collect stuff we can sell, raffle prizes, tombola prizes
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Donate your time. Let's chat about what you might do

Visit our Support Us page for more inspiration!

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    Let’s put energy into
    Mitochondrial Disease Research