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Artwork for \ud83d\udcdd Notes from an MS Lifer

\ud83d\udcdd Notes from an MS Lifer

Jane Harrison

Hard 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.

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Substack
PricingOnly free issuesPublishesMonthly
Issues25Founded3 years agoLast Issue14 days ago
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Artwork for \ud83d\udcdd Notes from an MS Lifer

Latest Issues

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...

14 days ago
18
14

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...

a month ago
17
12

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....

3 months ago
21
16

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...

4 months ago
21
10

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...

5 months ago
16
22

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  • Jane Harrison

    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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