Joni's Journal
Vibrant and motivated, Joni isn't going to let relapsing MS get in the way of her goals. Follow her story as she balances her life with her relapsing MS.

The most important thing that I’ve learned since being diagnosed with multiple sclerosis is that my life didn’t end when the doctor said, “You have relapsing MS.” After diagnosis, I went through the stages of grief, denial, anger, bargaining and acceptance. But after acceptance, I still thought that life as I knew it was over.
Of course, I’ve had to make some modifications in my life as a result of my diagnosis, but it’s far from over. For a couple of years after diagnosis, I scaled back the amount of activities I took part in. Most of this was due to the fear of not being able to complete what I started. However, as time progressed, I realized that I could do more than what I was limiting myself to.
Now, I’m as active as I was before diagnosis, just in a different way. I know my limits and listen to my body to make sure I don’t over do it. Had I known how to adjust my activities and not just quit them, I would have been able to do so much more for those first couple of years after I was diagnosed. The good news is that now I know, and I can tell all of you not to make the same mistakes I did.
Check back on February 9th for Joni’s next journal entry.