Please help. . . I live in Oregon and suffered/suffer from horrible horrific symptoms for three years. No doctor has been able to figure it out. Recently I learned about Kleine Levin Syndrome and those symptoms are identical to my last 3 years. It is surreal but now, I can not find a doctor or specialist in Oregon who specializes in KLS nor even aware of it. I am at a loss and desperate for help.
I will go anywhere needed just to finally get answers.
Can anyone please give me any information possible.