Meet Our

Warrior of the Week

These inspiring individuals with Visual Snow Syndrome are sharing their experiences living with this condition and how they try their best to overcome its symptoms everyday.

Spotlight on:

Sheila Lalani & Family

Meet our #Warrioroftheweek, Sheila Lalani & her Family💙

Spotlight on: Sheila and her family

Weʼre raising £2,500 to support the Visual Snow Initiative (VSI) by participating in the Tough Mudder on September 24, 2023.

We had never encountered the neurological condition known as Visual Snow Syndrome (VSS) before earlier this year, yet it affects 2% of the population. It was only given its own diagnosis less than 10 years ago. There is no known cure.

Due to the fantastic work of the VSI in the US, there exists just one researched and active therapy in the USA today. This therapy has yet to reach the UK.

Please support us and help us raise funds for all the people suffering from what is a life-changing and oftentimes debilitating condition so that more research and proven medicine can be put in place for all sufferers of VSS.

100% of the funds collected will be sent to the VSI donation page.

Donate Here

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Your generous tax-deductible donation ensures we can continue to generate awareness, education, resources, patient advocacy, treatments, and research to help people affected by Visual Snow Syndrome worldwide.