Recently someone mentioned that Visual Snow Syndrome is common with people on the spectrum. I have had V.S.S. all my life but did not know others had it too. In fact, I've struggled to get doctors to even acknowledge I have a real problem.
Appearently this disease /syndrome has only been recognised by the medical community since 2014. Currently the syndrome is thought to be rare but researchers acknowledge that there are probably many undiagnosed cases.
I am curious about others experience with Visual Snow. How long have you had it? Do you have other symptoms identified by researchers as often being cocurrent with V.S. such as migraine or tinnitus?
How does V.S. affect your life? Do you see V.S. in your dreams?
Have you attempted to tell doctors or others about your V.S.? How did they react?
Please share your experiences! Add as much detail as you want, the more the better!
Last edited: