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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:

Visual Snow Warrior of the Week – Jessee Sue Lively

Spotlight on: Jessee Sue Lively ???? @jesseesue

“I was in university for three years, and during this time, I developed static vision, tinnitus, palinopsia, and poor night vision. I had these symptoms 24/7 and thought I had a brain tumor and would go blind. My anxiety levels were very high. Which resulted in me experiencing depersonalization and derealization. I would feel numb and disconnected very often. When I saw my eye specialist; she was aware of the condition and diagnosed me with visual snow syndrome.

I did not give up on school and life even though I wanted to. Many days, I left class to cry because I could not see the board or my teacher’s face due to thick static. I knew there had to be helpful and that life was still worth living, and I had hope for improving my condition and ways to cope and lower symptoms. I sought support from an online visual snow support group. This helped tremendously. 

Today, I have my good and bad days with this condition. I am thankful for my vision and hearing, although they are both often impaired by constant noise. I can still see and hear. I take peace in the stillness and beauty of nature despite all the noise around me. Things that help me cope and often lower my symptoms are:

  • Making sure I get proper sleep.
  • Exercise.
  • Having a clean diet with no processed foods.
  • Grounding myself in nature.
  • Listening to peaceful music.
  • Surrounding myself with people who I love and who love me.

I am still in the support group because I want others to feel supported and that they aren’t alone. I have hope and faith for a cure/official treatment. ✨ ️ thank you for everyone researching and being involved.”

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