I’m Cat. I have MS and I want to tell you about it.
I started this blog to help facilitate conversation about MS between myself and my friends. The internet can be a scary place, particularly during the diagnosis process and in the months following. There’s so much unknown and, at the same time, too much information out there.
This is real talk from a real person who was diagnosed with MS at a young age and I’m happy to share real experiences, real advice, and real positivity with the newly (and long-time) diagnosed, as well as friends, family, curious types, and anyone who loves someone with MS.
Social media and contact info:
You can also read articles I’ve written for the National Multiple Sclerosis Society here!
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Questions, comments, or love letters you don’t feel comfortable posting in the comments? Email me at firstname.lastname@example.org.