Here, our team will share all the latest news, research, and updates regarding the Visual Snow Initiative, including its global efforts to understand and cure Visual Snow Syndrome.
Hear Sasha’s inspiring #VSS story of being diagnosed with #VSS but continuing to push through to receive her postgraduate certification this year. 💛💪📓
Meet our awesome #WarriorOfTheWeek! Hear Ben’s inspiring #VSS story. 🌟
Meet Lucy, our #WarriorOfTheWeek! Hear her story about dealing with her condition, what helps alleviate symptoms, and her hope for the future. ❤️🙏
Hi everyone! VSI values transparency with our supporters. After years of agony and mounting unknowns, VSI’s Founder, Sierra, finally got a diagnosis: she had Visual Snow Syndrome. But when Sierra was told there was no available treatment for her condition, she set...
Q: Where is it? The team at VSI is working around the clock to optimize the VIP experience. Q: What exactly is the VIP? It is a visual experience program designed to reduce VSS symptoms. It will be accessible via a desktop computer through our website. It will require...
Introducing our next #WarriorOfTheWeek, Adriane! Hear how #VisualSnowSyndrome has affected her and learn her secret in how she copes with it. 💖❇️
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Support Research for a Cure!
Let’s work together to raise awareness and education for Visual Snow Syndrome within the medical community and amongst the public! Once both of these are firmly established, then we can get closer to solutions and importantly, a cure for those who need it most.