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SarahCJR's avatar

Another compassionate and highly practical article. Thank you so much for the energy you put into this work. I always feel more grounded and positive after reading one of your posts.💜

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Amy - The Tonic's avatar

This is excellent, thanks doc. I don’t much have these symptoms anymore five years in, but I remember being frustrated at how friends and family didn’t understand this particular set of symptoms. It’s like I was just being told I was too sensitive (and YES, I was actually!). But like touchy or emotionally sensitive. I’m going to share this post in my next roundup. Thanks again.

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Nancy E. Holroyd, RN's avatar

Thank you for this article. I can think of several people (not on Substack) that might benefit from reading this article!💙💛💙

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kelly's avatar

Thank you so much for doing this pod cast. You share very helpful information in a way that's easy for my covid brain to absorb. You are a fabulous resource.

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LittleElf's avatar

Is there something that could help with brain fog?

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Kira Stoops's avatar

Such an underrated hell! I have a hard time at a party if someone pops on music on top of the already hard time I'm having tracking cross-talk. Woof.

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M (is) Living with Long Covid's avatar

This resonates SO much!

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Suze's avatar

I have AuADHD and long covid. I already had sensory issues before but the LC has exacerbated them. As Amy said, trying to explain it to people who have never suffered with misophonia and misokinesia is so hard. I have some cards from soQuiet.com which I can hand out to people which has come in handy. Thank you so much for raising this subject. I have often felt very alone with this.

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