One girl's view of disease as a gift, not a burden.
My recovery from Covid is making me very emotional. To be fair, people have always told me that I am overly sensitive. And I do cry a lot. Not over personal things or big things or real life things, but all of the little things that ultimately have nothing to do with me. That swell […]
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Myth: People with MS shouldn’t have children. I personally don’t want to have children at this point in my life and I am really, really good with that decision. There were several years in my 30s where I dreamed of kids and felt it was something I needed to experience. Now, in my 40s, single […]
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My dad has never been a dog person and he is falling in love with mine. I am in my hometown, exploring the breathtaking marshes and soft, white sandy beaches. Meditating on bittersweet memories and mulling through ideas as I always do when I visit the home of my beloved and missed mother. I took […]
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Myth: Exercise is bad for you if you have MS. The day I was diagnosed with Multiple Sclerosis my neurologist went over a huge list of things I should know about my disease. Thank goodness I had a friend with me to be my advocate, because in that moment about 9 out of 10 of […]
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In my 20s I convinced myself I had drowned in a past life. We all have fears, yet some run deeper than others. Just like the mystery of MS, extra special phobias can seemingly come out of nowhere but feel like they are a part of our very core. Impenetrable and immovable, random but ever […]
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The word “okay” is incredibly underrated. Whenever I get a call or an email from someone newly diagnosed, I feel so privileged they have chosen to speak with me. To connect, to vent, to cry, to express anger, or to simply ask a few of the hundred questions we all have at the very beginning. […]
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I have never been so worried about a person I’ve never met. A few months ago I commented on Elan Gale’s IG post “you are my favorite person I have never met.” I don’t know Elan personally, but I have always found him to be funny and wise and kind of wonderful. I waved at […]
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Tracy's Life with MS 