Hope for the future
Hope for the future
Life after a diagnosis and treatment can look different for everyone. This Ocular Melanoma October, we want to share our hope for the future and explore what life can look like after diagnosis. Whether you listen to Matt talk about our services or you want to learn more about future advancements, we hope this page on our online hub can provide hope for the future!
Our Advocacy Work
In 2026 so far, we have:
- hosted a parliamentary reception – “Securing Timely Treatment for Ocular Melanoma and Other Rare Cancers” – in partnership with Dr. Scott Arthur MP, the sponsor of the Rare Cancers Bill.
- watched the Rare Cancer Bill reach Royal Ascent and become law, now known as the Rare Cancer Act.
- welcomed the National Cancer Plan for England which was published by the Department of Health and Social Care, working with NHS England.
- marked Rare Disease Day by talking to a range of radio stations about ocular melanoma, reaching 45,845,500 listeners.
- celebrated our incredible community and fundraisers!
Our Head of Support
Hear from Matt, our Head of Support, as he shares more about his role, what support Ocular Melanoma UK offers, how to access that support and what hope we have for the future as we continue to bring Ocular Melanoma into focus.
Patient Stories
Hear from our members and their loved ones about their experience with this rare cancer.
What is Ocular Melanoma?
Learn about ocular melanoma, its signs and symptoms, diagnosis and treatment.
Our Corporate Page
Find out how your organisation can get involved this October and explore our resources.
Contact us for support
The Ocular Melanoma UK helpline offers confidential support to people living with Ocular Melanoma and their loved ones.
Call us on 0300 790 0512
Lines open between 10am – 7pm Monday – Friday
Email us
Email us on helpline@omuk.org