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COVID-19 AND ME/CFS

The ME Association has kept a close eye on the Covid situation ever since the pandemic began in March 2020. They continue to produce guidance and a series of free leaflets that are updated as the situation has changed. To find out more please visit their website listed below

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ANIMATED DOCUMENTARY ON ME/CFS – click to view video

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WHAT HAPPENS WHEN YOU HAVE A DISEASE DOCTORS CAN’T DIAGNOSE? – click to view video

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THE FATIGUE CONFERANCE 2021

In May 2021 Tanya attended the Fatigue Conferance and reported back: I did not have the strength to watch all of the seminar as each video was around 45 minutes or less and there were 6 a day for 7 days. Day one was on how the gut affects CFS.  Inflammation in the gut has […]

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NEW NICE GUIDENCE

It’s looking postitve and a step in the right direction https://www.nice.org.uk/guidance/ng206/documents/draft-guideline

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COMING OUT OF LOCKDOWN

As we start the process of hopefully gaining some form of normality out in the big wide world.   However, for some it will mean less freedom, less availability and less of being part of a community. Lockdown has allowed disabled people the freedom to attend concerts, theatre shows and museums from the comfort of […]

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‘DIALOGUES FOR A NEGLECTED ILLNESS’ A WELLCOME PROJECT

This exciting new project – Dialogues for a neglected illness – is a series of films created by Natalie Boulton and Josh Biggs. It has been financed by a grant from the Wellcome Public Engagement Fund. 

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KEY POINTS ON EMPLOYMENT WITH ME/CFS AND THE CORONAVIRUS

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Our Chairman Chris Spencer wants to share this great news with you.

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Hello!

Welcome to our new website. Over the next coming days we will be transfering posts over from our previous website that are still of great value to us all. Please bare with us whilst we do this. This new site is designed so that Tanya can work off of her mobile and upload on the […]