8 Comments

This is a vital resource for 'us' who are afflicted with a version of LC. Almost a year in for me and symptoms getting worse in certain areas. Your work gives an element of things happening. The forgotten millions of ME/CFS sufferers for many decades demonstrate sadly, what happens when another funding priority emerges, or simply, governments turn off research funding. Again, thank you for your commitment to 'us'. I am very grateful. Paul, Sydney Australia

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May 15, 2023Liked by Brandon

Thanks for your newsletters.

It’s great to be able to just read the summary of the main points - rather than spend all that energy reading through and processing the article in its entirety.

At least there is research happening but it’s such a worry there isn’t enough funding being invested.

Without suitable treatments, people are at risk of trialling dangerous treatments/drugs themselves, wasting money and energy on alternate treatments which may not help and peoples mental health declining.

I desperately hope there will be some answers on day.

I’m also from Australia 🇦🇺

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May 15, 2023Liked by Brandon

I really appreciate the work you are putting in. Please keep going!!

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May 17, 2023Liked by Brandon

Thank you so much for putting this newsletter together, really appreciate it! Hoping for a cure…..

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