📝 Notes from an MS Lifer
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Can I handle the seasons of my life?
I hit a low and think about gratitude, resilience and overwhelm (and possibly use you as my therapist).
Sep 27, 2025
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Jane Harrison
18
24
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And I’m on my knees… looking for the answer
It really was that hard, digging deep on topics from superpowers, to relationships, to travel and gardening...
Aug 5, 2025
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Jane Harrison
16
25
3
Ask Me Anything
A post in which I invite you to ask me whatever you want.
Jul 14, 2025
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Jane Harrison
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4
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Ch-ch-changes, oh, look out you rock ’n’ rollers
A short announcement: my blog has changed its name
Jun 10, 2025
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Jane Harrison
13
12
1
Something to Talk About
Seven important conversations on my MS journey and how they matter.
May 22, 2025
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Jane Harrison
16
13
2
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Why ...
Jan 31, 2024
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Jane Harrison
33
20
4
The Great Pretender
Mar 16, 2024
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Jane Harrison
23
20
3
Dog Days Are Over?
Mar 3, 2025
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Jane Harrison
21
24
4
Here Comes the Sun
Aug 25, 2024
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Jane Harrison
21
18
1
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I am the passenger
As I surrender my driving licence, I reflect on why this journey was so long and hard, and think about what freedom and independence really mean.
Apr 17, 2025
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Jane Harrison
18
26
5
Dog Days Are Over?
What I’m discovering about accessibility as I navigate the world with wheels.
Mar 3, 2025
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Jane Harrison
21
24
4
January. Sick and tired you’ve been hanging on me.
But in your icy grasp, I get back on track with brain health.
Jan 31, 2025
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Jane Harrison
14
9
1
It’s Beginning to Look a Lot Like Christmas
A short piece about good news, coming late to the Christmas party, and feeling all the feelings.
Dec 23, 2024
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Jane Harrison
16
8
There is a light ...
A pause, and a poem for hard times.
Nov 29, 2024
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Jane Harrison
17
6
It's, oh, so quiet. Shh. Shh.
Have you been to my little library of MS related resources?
Sep 30, 2024
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Jane Harrison
10
8
Here Comes the Sun
And I say… I feel f..ked. MS and the heat intolerance beast
Aug 25, 2024
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Jane Harrison
21
18
1
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📝 Notes from an MS Lifer
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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📝 Notes from an MS Lifer
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