\ud83d\udcdd 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 | 24 | Founded | 3 years ago | Last Issue | 9 days ago |
| Active | |||||
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janeharrison.substack.comLatest Issues
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...
Here I Go Again
Photo by Artem Bryzgalov on Unsplash
It’s probably not the best idea I’ve ever had to write a comeback piece for this blog in the middle of an uncharacteristic May heatwave here in the UK. But the power of the sun has forced me inside, MS...
Can I handle the seasons of my life?
Photo by Andriy Nestruiev on Unsplash
“We receive and we lose, and we must try to achieve gratitude; and with that gratitude to embrace with whole hearts whatever of life that remains after the losses.”
Andre Dubus II, Broken Vessel...
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| Subscribers | Engagement | 70 | Monthly Web Visits | ||
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| Accepts Sponsors | Estimated Cost per Ad | ||||
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Authors
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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