One year ago, I did my last Copaxone shot. From July 2015 until May 2019, I gave myself shots, three times a week, like clockwork to control my MS. I was first suggested to switch my therapy to a new and much more effective treatment in January 2019. I considered it for a while, and … Continue reading My Next Ocrevus Infusion-thoughts
I’m frustrated right now. I feel bad every single day. It’s been about three months of whatever this is. I feel nauseous. Exhausted. My ears are ringing. My head hurts more often than not. Sometimes it hurts to breathe. My numbness is not worse, but more regular. So mostly, nothing significant, but all together-ahhhh! Maybe … Continue reading My Check Engine Light is On
Last Thursday was my first infusion with Ocrevus, and the truth is, I am so thankful I made the change in switching to this drug. It wasn’t flawless, but much better than I expected, and I haven’t given myself a shot for 9 days….that is the longest I have gone without injecting myself in 4 … Continue reading Ocrevus Part 1
Days with Andrea 