Snowdon/Yr Wyddfa Climb for Cavernoma 2026

Cavernoma Alliance UK is raising money for Cavernoma Alliance UK

Team: Snowdon Climb for Cavernoma 2026

Snowdon Climb for Cavernoma 2026 · 6 June 2026

Cavernoma Alliance UK (CAUK) supports people affected by cavernoma. A cavernoma is a common but often unheard of condition caused by a cluster of abnormal blood vessels in the brain or spine. Our mission is to improve the quality of life for those affected through education, support and research.

Story

On 6 June 2026, the cavernoma community will come together to take on the incredible challenge of climbing Snowdon, also known as Yr Wyddfa - the highest mountain in England and Wales 🏔️. This special event launches Cavernoma Awareness Month and raises vital funds for Cavernoma Alliance UK (CAUK) 🫶

Now in its fourth year, the Annual Snowdon Climb for Cavernoma has become a powerful symbol of strength, solidarity and hope. In 2025, 87 amazing people took part, raising awareness and over £27,000 for CAUK 🌟

This year, we’re aiming even higher. Our goal is for 100 people to take part, either climbing Snowdon in person or completing the challenge virtually throughout the month of June. That might mean walking, hiking or climbing the equivalent height or distance of Snowdon (1,085 metres or around 4,610 steps) from wherever they are 🏡🪜🏃‍♀️

Why Your Support Matters

By donating to the Snowdon Climb, you’ll help to:

📢 Raise awareness of cavernoma

🧪 Fund research into better treatments and a cure

💬 Provide life-changing support to people affected by the condition

Every donation takes us one step closer to change. Whether you’re sponsoring a loved one, sharing our story or giving what you can, thank you for being part of it ❤️

Donate now and help us make a difference 🙌

What is a Cavernoma?

A cavernoma is a cluster of abnormal blood vessels in the brain or spinal cord, often described as looking like a raspberry 🍓. Their thin, leaky walls can bleed without warning, at any age.

Around 1 in 625 people have a cavernoma, and 1 in 2,700 experience symptoms such as:

🩸 Brain haemorrhages

⚡ Seizures

🧍‍♀️ Neurological problems

There’s currently no cure. Treatment options are limited to monitoring, neurosurgery or stereotactic radiosurgery. That’s why your support matters so much.

About Cavernoma Alliance UK (CAUK)

CAUK was founded by Dr Ian Stuart after a sudden cavernoma bleed changed his life. What began as a small helpline in Ian’s bedroom is now a national charity supporting over 4,000 people across the UK.

Our mission is to:

🔬 Fund research to find a cure

📚 Provide trusted, accessible information

🤝 Offer connection, understanding and support when it’s needed most

To find out more, visit www.cavernoma.org.uk

Cavernoma Alliance UK is a registered charity in England and Wales, number 1197257

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