📝 Notes from an MS Lifer
Jane HarrisonHard truths, good vibes, and lame jokes in monthly-ish essays about life with Multiple Sclerosis. For folks with MS, those who love them, and anyone with an interest in disability, chronic illness and dealing with change.
| Platform |  | Pricing | Only free issues | Publishes | Monthly |
|---|---|---|---|---|---|
| Issues | 26 | Founded | 3 years ago | Last Issue | 8 days ago |
| Active | |||||
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Girl, you have no faith in medicine
Photo by Nik on Unsplash
*In Part 1 I wrote about how I became eligible for siponimod, an MS medication known as a disease modifying therapy (DMT), after seven years of not having any treatment available to me. I outlined what the research...
I got some pills, I'm gonna give you some
So pretty. Photo by Towfiqu barbhuiya on Unsplash
So it’s finally here, the one where I explore a decision about whether I should take siponimod, or not. I've been hinting at the arrival of this piece of writing for a while. Have I been pu...
I know the sound of your wheels
Abstract wheel. Photo by bennett tobias on Unsplash
Adapting to disability has meant dealing with my failing body and learning to use mobility aids. My troubles played out as I attempted to make sense of it all through writing. Three of m...
One Potato, Two Potato
Photo by Hai Nguyen on Unsplash
*A new series of occasional posts in which I recount a desperate attempt to do something (usually culinary), that I can no longer really do because of the impact of my MS. With often disastrous consequences....
You had a bad day.
Plural. Photo by Kevin Grieve on Unsplash
I am feeling very happy to be back writing after last month’s comeback. This month I dusted down a piece I originally wrote back in November, but didn’t manage to finish at the time.
As aut...
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| Subscribers | Engagement | 71 | Monthly Web Visits | ||
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The writers behind this newsletter.
Trying to make sense of life with this wrecking ball condition. “This is the best blog out there about living with Multiple Sclerosis” - Jane’s mum.
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