Hi. My name is Charlie. I’m 53 and was diagnosed with RRMS in May 2003. Over that time I’ve only had one serious attack.
Although I have a constellation of symtoms, most are invisible to most except my family. By this I mean that most people wouldn’t know that I have MS.
For most of my MS life, I have been on Copaxone with few side effects. That said, I often think about stopping for no reason other than I’m tired of MS meds. I’m also worried about potential long-term side effects. I have an upcoming doctor’s appt during which I will discuss this.
Until next time. Take care.