I was diagnosed 11 years ago, and I have a pretty good handle on my MS. I haven't had a real flare in almost 5 years.
I recently switched from Copaxone to Aubagio, about 2 months ago.
Also, it's June and it's been hot, which is exhausting, but at least with the pandemic, I have a great reason to not go outside. My whole company is working from home, and my HR is not going to make me come back until my doctors approve it.
My question is, are my fatigue and depression related to a flare, or Aubagio, or is it just June with MS? I have a neurologists' appointment next month, and I will discuss all of this with her, but I just needed to get this out.
Like I said, I'm doing well with my MS. I'm not angry like I used to be, it's just part of me. I just have my moments when it's overwhelming, and need to get it out.
I recently switched from Copaxone to Aubagio, about 2 months ago.
Also, it's June and it's been hot, which is exhausting, but at least with the pandemic, I have a great reason to not go outside. My whole company is working from home, and my HR is not going to make me come back until my doctors approve it.
My question is, are my fatigue and depression related to a flare, or Aubagio, or is it just June with MS? I have a neurologists' appointment next month, and I will discuss all of this with her, but I just needed to get this out.
Like I said, I'm doing well with my MS. I'm not angry like I used to be, it's just part of me. I just have my moments when it's overwhelming, and need to get it out.
Comment