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Don't MS with Jenny

Blog Summary

Sometimes life throws you unexpected curveballs that unknowingly turn out to be priceless life lessons. A silver lining is how I think of my MS and what I often tell people when they ask about my diagnosis.

Back in 2016, I woke up and the left side of my face was numb. I did not feel like Jenny. I felt like a completely different person with a numb face and a throbbing head. I trusted my gut and went to the emergency room after a few days of sitting on these symptoms. After a quick workup, they dismissed me quickly and said I needed to rest, take a day off work, drink plenty of fluids, and that these symptoms would subside quickly. I did as I was told, but still did not feel like me...

Getting My Infusion

Blog Summary

When I realized that my Ocrevus infusion was scheduled shortly after the COVID-19 outbreak and initial uproar (scheduled for mid-April), I began to panic. Since I work in a hospital and am around germs constantly, I was not so much worried about being in the hospital to receive my medicine… I was mainly worried about not being able to get it at all. With almost all elective procedures being put on hold, I was terrified that they would stop outpatient infusions completely. Therefore, I decided to call my neurologist and propose that we move up my infusion a few weeks to get it in and over with before things get worse from a virus standpoint. He agreed with that proposal and helped speed up my prior-authorization approval, and I was able to get my infusion about two weeks early...