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Ramsays Disease

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Bottle garden

Thank you for interest and instructions on how pictures go into a post only hope finally put what was asked for with help of other members messages.

Thank you for interest and instructions on how pictures go into a post only hope...

•9 years ago

Distraction

Finding some distraction from pain or the limits imposed on activity which gives some purpose or pleasure that was probably taken as granted in the life...

Finding some distraction from pain or the limits imposed on activity which gives...

•9 years ago

What does that mean

Defining words can change with illness severity - fatigue can be anything from tired onto mental and physical paralysis, what we mean by a word will often need...

Defining words can change with illness severity - fatigue can be anything from t...

•9 years ago

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This article is so clear and poignant. I recommend sharing it.

Written by Jeannette Burmeister's husband about the contrast between attitudes of people toward his hip replacement surgery and towards her severe ME...

Written by Jeannette Burmeister's husband about the contrast between attitudes o...

•9 years ago

The thorny realities of 'pacing' for those who live alone

I understand the concept of pacing. I think it is the best thing we can do to keep from constant flareups and boom and bust cycles. But it requires certain...

I understand the concept of pacing. I think it is the best thing we can do to ke...

•9 years ago

Spoon Theory

Sharing this with all that understand http://www.butyoudontlooksick.com/articles/written-by-christine/the-spoon-theory/

Sharing this with all that understand http://www.butyoudontlooksick.com/articles...

•9 years ago

Info from the ME Association about the New Social Care Act

http://www.meassociation.org.uk/2015/04/new-social-care-act-comes-into-force-today-and-we-have-a-leaflet-to-explain-how-it-might-affect-people-with-mecfs-1-apri

http://www.meassociation.org.uk/2015/04/new-social-care-act-comes-into-force-tod...

•9 years ago

Can we have a poll or info gathering on how we are treated as Fibro/ME patients in the UK?

I am wondering if there is a way we can get some information gathering as to how our GPs are treating us after they start to think we may have Fibromyalgia or...

I am wondering if there is a way we can get some information gathering as to how...

•9 years ago

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