I just got done with the doctors appointment and they want to increase my treatment. Since I was diagnosed seven years ago with MS. I have been on Glatopa. Unfortunately, may last two MRIs showed new lesions and my doctor says it’s best to try a different treatment. I am very nervous about side eff...

I was recently diagnosed with MS, last year November (the day before my birthday) 😩 and I still haven’t completely accepted the fact that I have it. At times I’m embarrassed, don’t want to talk to anyone or be seen. I’ve been slowly becoming more comfortable with having MS though just not the way I...

So I've been feeling nauseous 🤢 and moody 😡/emotional 😭 and I just had a feeling something was going on. I had my husband go get me a few different pregnancy tests and took two last night and sure enough, got my answer. I found out that I am pregnant again already.

Living with MS has taught me to face the unknown with courage — and today I’m stepping into a new chapter. I just found out I’m pregnant 🤍 This journey may look different for me, but it is filled with hope, strength, and faith. MS is part of my story, not the end of it.

Is it just me or has anyone else been getting treated differently since being diagnosed. And when I say differently I mean like treating like your not capable of doing things you normally would. Because I have and I don’t like it, it makes me feel incapable or disabled.

So supposed to be on August 1st but no one knows I have a mess then I rather not share it because it's my business up theirs also it's a California and I live in Texas so I cut that as I got saved

What are you all taking for pain to help you sleep at night?