M (is) Living with Long Covid
I'm a Long Covid long-hauler living with M.E., POTS, dysautonomia, and hEDS. I write about living with chronic illness and disability through an airborne-aware and covid realist lens.
| Platform |  | Pricing | Only free issues | Publishes | Weekly |
|---|---|---|---|---|---|
| Issues | 105 | Founded | 2 years ago | Last Issue | 7 days ago |
| Active | |||||
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livingwithlongcovid.substack.comLatest Issues
All the souls stolen from us
Photo by David Tomaseti on Unsplash
[TW: suicide and death. Please proceed/read with care]
I recently read a story published in The Sun about a mother in the UK who ended her own life after dealing with Long Covid. The mother was first ho...
How are we supposed to juggle it all?
Photo by atelierbyvineeth ... on Unsplash
[For the record, this is not a cry for help…just a much needed rant]
Living with a complex web of chronic illnesses often feels like trying to hold the ocean in your hands. The water will slip thr...
The young, voiceless victims of Covid
Photo by Sean Nufer on Unsplash
If you ask me, one of the biggest catastrophes of the (ongoing) Covid-19 pandemic is the fact that we have let children bear the brunt of repeated and unmitigated infections, without their consent and withou...
First Kathleen, now Poppy...
I’m a little late to the game with this one, but I still have thoughts so here we go:
It feels like only a few weeks ago, we (the disability community) were collectively poo-pooing Kathleen Stock’s awful piece about young women “faking” th...
What's it to you if I mask?
Photo by Dennis Rochel on Unsplash
CW: anti-mask harassment, abuse, sanism, ableism, Covid minimization
I want to talk about a recent experience I had while wearing a mask and what it meant to me, and perhaps what it signifies as well for...
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\ud83c\udf49\ud83d\udd3b\ud83d\ude37\ud83c\udff3️\ud83c\udf08(she/her) Chronicling life with Long Covid, ME/CFS, POTS, hEDS, MCTD, MCAS, endo, and a whole host of other fun stuff. An N95 might save your life and someone else's!
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