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.
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. 💖❇️
Meet Joseph, our #WarriorOfTheWeek! Learn how #VisualSnowSyndrome symptoms affect Joseph’s life yet how optimistic he is for a cure. 🌟
Introducing our #WarriorOfTheWeek! Hear Patrick’s unique story of how he deals with #VisualSnow and how he uses spiritual teachings and learning to expand his mind and perceptions. 💛🧠📖
Meet our next awesome #WarriorOfTheWeek! Hear about Gabriella’s obstacles she faces in school and what she found that helps alleviate her afterimages. 💪📓💕👓
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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.