Resources that bring the MS community closer together to address the body, mind and brain as a unit are important.
I now understand I have not failed as a parent. I have a chronic illness, and that is okay.
My mom was diagnosed with MS almost 10 years ago, so I have a very personal connection to the National MS Society.
This is the intersection of autism and MS where my worry resides.
Here are 5 tips to keep in mind when speaking about or to those in the MS community living with a disability.