Cathy Chester
Cathy Chester was diagnosed with Multiple Sclerosis in 1987, but has lived with MS symptoms since 1981. Now in her fifties, her philosophy is life is precious and should be lived to the fullest each and every day. She views her MS as merely a small part of who she is as a person. Some days are better than others, but each day is a gift and one she cherishes dearly.
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I’ve been indoors for two weeks and counting, binge-watching British shows on BritBox, listening to music, and napping. A lot …
I used to think people who were superstitious either believed in the supernatural or were a bit nutty. Despite Stevie …
I’ve lived with symptoms of multiple sclerosis since 1981, was diagnosed in 1986 and thereafter settled into a steady life …
My infant son looked up at me from his crib, smiling and cooing after a satisfying nap. I picked him …
I can barely remember a time when I didn’t have MS, when I didn’t feel exhausted after waking in the …
When I learned I had Multiple Sclerosis, I shed some tears and then rearranged my life. There were no FDA …
After taking myself off Copaxone – because after 25 years I grew weary of injecting sharp needles into my body …
I recently went to see a Broadway show in New York City about the life and music of Carole King. …
I recently attended a red carpet gala for an award ceremony being held by my new women’s group. The group …
Dear Body, Why do you continue to disobey me? I don’t understand. Have I mistreated you so badly over the …
When December rolls around I find myself feeling joyful, anxious, happy and nervous. There’s so much to do that I’m …
The holidays can be a time of great stress for many in the Multiple Sclerosis community. Difficult symptoms make us …
The older I get the more confused I become about my health. That sounds odd coming from this midlife woman …
When I was a little girl I remember my mom driving me and my grandmother to visit my great-aunt in …
Sometimes it’d be easier to give into that black cloud of depression when our lives feel out of control. When …
I have never been invisible. Not before my diagnosis or since. I have a voice and opinions. I want to …
There’s strength in numbers when it comes to community. Shared stories and new ideas envelop us in love, hope, and …
A few years ago I went back to school to earn a certificate in patient advocacy. I wanted to marry …
There’s been a lot of buzz about a small clinical trial about diet and MS. Dr. Ilana Katz Sand, a …
There comes a time in everyone’s life when they face the difficult task of watching a loved one suffer with …
