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RING20 RESEARCH AND SUPPORT UK CIO

✓ Registered charity · 1165651

About

We provide support and information to individuals, families and health professionals who are affected by, or come into contact with Ring Chromosome 20 Syndrome, or r(20) for short, an ultra-rare disease, the main symptom being difficult to treat epilepsy.We raise funds to help promote research into r(20) to try to improve overall quality of life for those living with the disease.

Where we work

Throughout England And Wales Scotland Northern Ireland

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Registered charity no. 1165651 · England & Wales