It is incredibly hard to self-diagnose and we are finding that it is much easier for people to reach a successful diagnosis by meeting others with LLI. There is an exceptionally unique sense of relief when you meet other people who are ‘exactly like you’, your whole perspective on life and living with low latent inhibition will change and hopefully become more comfortable. For those out there with LLI, chances are that most of the difficulties you have faced or have yet to face have been experienced by others with the condition too. A lot of the relief we have witnessed by people who come to the Facebook group stems from knowing why they have felt different, that they are not alone and that there are others like them who are there to help.
Dr. W… being on the subject of body temp.. i had a question. I am one of the 20% or some of people who get colds that last 2 weeks or longer; been that way my whole life. It just seems that my symptoms just linger on and I feel generally weak or tired… Once I cross the primary peak point of the cold, the recover time is long. This time, I’ve measuring my body temp. Usually (both at home and in the doctors office) I am at mid-day. what I am noticing is that the most i can reach during my recovery is from a morning of . Is this normal? T