Hello everyone. I was diagnosed with MS in August. I of course started reading and researching and looking for answers. It was a relief after 13 years of being in an after doctors offices an being told it was in my head, nothing was wrong with me, or being given a laundry list of other diagnoses with no relief. My best friend was diagnosed with MS a few years ago and my mother’s best friend has lived with it for as long as I can remember. I’ve struggled with how to explain to my husband how bad I feel sometimes. I feel like he doesn’t understand at all. I would have thought with some of his health issues and things he’s been through he’d be more supportive. And motivating myself to do all I need to do when sometimes I just want to stay in bed even though I know it’s worse for me to do that. Since this is all new to me I am looking for advice and information and such. I have been reading articles and looking through info. throughout the site. I am looking forward to getting to know you all.