When I first developed Myalgic Encephalomyelitis/Chronic Fatigue Syndrome, (ME/CFS) I was particu...

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If you suffer from ME/CFS or long covid, read on!

Why WE should fundraise for ME/CFS research

I’ve been living with ME/CFS now for over 9 years.  There are times when I operate at what appear...

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Why WE should fundraise for ME/CFS research

How songstresses inspired a ME/CFS jewellery brand

I love strong, powerful, lyrics that tell a story, speak to my soul and originate from lives live...

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How songstresses inspired a ME/CFS jewellery brand

Sally Cox, Founder Coppered

I'm not afraid to admit that when the two strips lit up on my RAT test, I felt a little wave of p...

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Long covid got me good! Here's what I'm doing about it.

9 Things you should know if you're living with ME/CFS

Myalgic Encephalomyelitis (pronounced mai·al·juhk en·seh·fuh·low·mai·uh·lai·tuhs) and Chronic Fat...

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9 Things you should know if you're living with ME/CFS

The Number 1 Reason why I'm fundraising to help cure ME/CFS

9 years ago I was struck by what I now know to be Myalgic Encephalomyelitis or Chronic Fatigue Sy...

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The Number 1 Reason why I'm fundraising to help cure ME/CFS

It's not about me, it's about M.E.

Myalgic encephalomyelitis M.E. otherwise known as Chronic Fatigue Syndrome - way easier to say, '...

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It's not about me, it's about M.E.

Why I want to help ME/CFS medical researchers 'fail-fast'

I've been involved in the business world now for some 30-plus years. In recent times, there's bee...

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Why I want to help ME/CFS medical researchers 'fail-fast'

Do you feel broken at a cellular level? Because I do.

Like many of you, my first ME/CFS crash was a doozy! I had been holidaying with friends in beauti...

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Do you feel broken at a cellular level? Because I do.

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