Tag Archives: CFS/ME

Work and how to decide when enough is enough

Employment and chronic fatigue syndrome aren’t two easy friends. They don’t like each other. The pain and fog make work hard to do, the fatigue makes it hard to be there. Friday night is here, the end of the week … Continue reading

Posted in Life with myalgic encephalomyelitis | Tagged , , , , , , , , | 9 Comments

Fogginess and frustration

I haven’t blogged for a while because I forgot the email address I used to log into wordpress. Today I called the dog my name, instead of his. Forgetting things, mixing up words, being unable to concentrate on anything…all major … Continue reading

Posted in Life with myalgic encephalomyelitis | Tagged , , , , , , | 5 Comments

Hypnotherapy

Along with my diagnosis of post-viral chronic fatigue syndrome, the specialist said I’d be better in 18 months. ¬†When that timeframe had ticked by, with only a moderate improvement, I was getting pretty panicked. Earlier, I had seen a psychologist … Continue reading

Posted in Life with myalgic encephalomyelitis | Tagged , , , , , , , , , , | 4 Comments