Patients and professionals - The Lily Foundation
The Lily Foundation logo featuring a butterfly, hearts and an 'x' for a kiss

Fighting mito,
finding hope.

Mum crouched down smiling and  cuddling her child in a lily Tshirt, whilst another child in a pushchair is smiling Mum crouched down smiling and  cuddling her child in a lily Tshirt, whilst another child in a pushchair is smiling

Are you affected by mito?

If you’ve received a mitochondrial disease diagnosis, The Lily Foundation charity can offer emotional support and practical advice as you navigate your illness.

Have you or a loved one been diagnosed with mitochondrial disease?

If you or someone you know has recently received a mitochondrial disease diagnosis, The Lily Foundation are here to offer compassionate, ongoing support.

Receiving a diagnosis can feel overwhelming and isolating, especially when mitochondrial disease is unfamiliar. You may have questions, fears and uncertainties about what lies ahead, including:

  • Is mitochondrial disease curable?
  • Can I live a normal life with mitochondrial disease?
  • What causes mitochondrial disease?

We’re here to help you navigate these questions, offering resources, guidance and a caring community so you don’t have to face these challenges alone.

Our support for patients and families

Whether you’re a patient, a parent, a sibling or a friend, we’re here to provide comprehensive support. Our resources and services are designed to help you manage the emotional, physical and practical aspects of mitochondrial disease, with a focus on improving quality of life.

Support for medical professionals

We also work closely with healthcare providers, offering up-to-date information on mitochondrial disorders to assist in the diagnosis, treatment and care of patients. Our goal is to empower medical professionals with the knowledge they need to support patients and their families effectively.

Need someone to talk to?

We provide a free counselling service for patients affected by mitochondrial disease in conjunction with Rareminds. Find out more.

Our vision for the mitochondrial disease community

Our vision is for a world in which every mitochondrial disease patient has a voice and access to treatment, support to improve their life and, ultimately, a cure.

Together we’re navigating the complexities of mitochondrial disease:

  • today raising awareness of mito across the globe;
  • tomorrow unlocking the cure through pioneering research;
  • forever supporting the mito community and empowering everyone to make a difference.

Join our community – you’re not alone

We invite you to explore our website and learn more about our work, our mission and how you can connect with others who share your journey. Together we’re stronger, and together we’re making a difference.

Welcome to our community. You’re not alone x

Fighting mito, finding hope