MS Experiences? Or Lyme?
We seek out similar disease experiences on the internet to obtain advice and to feel less alone, and was (and still is) a resource for those coping with MS. But while many of my tips and tricks for living with MS still carry over, I never had the disease. Who else doesn’t? Those who are dispensing guidance through social media or other blogs might not have the disease either without realizing it. Something to keep in mind when you are reading or watching online.