Who are we?
What is Mitochondrial Disease?
Mitochondrial disease, or ‘mito’ for short, refers to a group of disorders where dysfunctional mitochondria are present, resulting in a variety of developmental, muscular and brain abnormalities. Mitochondrial disease is a genetic, chronic condition that is sadly progressive and can affect anyone at any time in their life. Symptoms of the disease vary hugely between individuals, but the most common symptoms are fatigue, neurological problems, visual and/or hearing impairment, heart, liver or kidney dysfunction, muscle weakness and poor growth, to name but a few. There are very few treatments for mitochondrial diseases and there is currently no cure.
Did you know?
Every day a child in the UK will be born and go on to be diagnosed with a mitochondrial disorder.
Did you know?
1 in 2,000 people will face a diagnosis of mitochondrial disease.
Did you know?
1 in 10 people have a rare disease.
Did you know?
Mitochondrial disease can cause symptoms in any organ at any age.
Did you know?
Many diseases stem from mitochondria dysfunction, including Alzheimers, Parkinson’s, diabetes and autism.
Did you know?
1 in 3 of all children with a rare disease never live to celebrate their fifth birthday.
Did you know?
3.5 million people in the UK will be affected by a rare disease in their lifetime – 50% of them will be children.
Challenge 21
What will you do?
We have 21 amazing challenges that YOU can get involved with. Whether you like baking, running, crafting, gaming, horse riding, reading or dog walking – we have something for everyone!
Take on the challenge and raise funds for children and adults affected by mitochondrial disease and help us create a brighter mito future because mito matters.
Charlie's Law
Charlie’s tragic death on 28th July 2017 exposed the limitations of current processes available to parents, doctors and the NHS in efforts to ensure the best outcomes for seriously ill children. Charlie’s fight highlighted an urgent need for changes in the law, policy and legal and health practice to support families, as well as medical and legal professionals involved in what are deeply emotive, difficult and life-changing circumstances.
Charlie’s parents, Connie Yates and Chris Gard, have been working with NHS medical professionals, world-leading ethicists and legal experts to develop draft legislation that will prevent further long and painful conflicts between hospitals and families with sick children.
The bill provides three key changes to improve existing legislation. Charlie’s Law will:
Monkey Adventures!
Raise awareness and show everyone where your Monkey has been on their adventures with our Monkey Map. We’d love to know where in the world are our mito monkeys!
Would you like a Monkey of your own? Visit our shop today!
Our Latest News
5 Years since Charlie Gard passed away
Charlie's Law: Rosie Wright speaks to parents of Charlie Gard, Connie Yates and Chris...
Hope for Charlie’s Law
The parents of tragic 11-month-old Charlie Gard are set to address MPs on a proposed law...
Charlie Gard’s parents wouldn’t wish court battle to save child ‘on worst enemy’
Connie and Chris – Charlie's mum and dad – spoke to Louise Scott the...
Charlie’s Law Needs You!
Dear supporter, We need your support: Ask your MP to vote for Charlie’s Law...
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