Is Chronic illness Live Art..?

A fairly recent, very light-hearted, conversation prompted a thought. And as my readers will know, that’s not unusual for me.Β 

The conversation…

I had been chatting with one of my children & reflecting on their recent visit to Tate Modern in London. (No, I still haven’t reached the dizzy heights of London.) We discussed our general feelings on modern art & how it is interpreted, and how I often struggle to interpret it. I mentioned a news piece I’d seen recently, which explored an installation of elevated vacuum cleaners.

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What’s in a shoe?… #MillionsMissing

Hi. I’m reblogging a post from last year, relating to the #millionsmissing campaign. Why? Today is International M.E. Awareness Day, and this part of my contribution to help raise awareness. I also have blue fairy lights ready…and will be wearing blue, well once changed from my pj’s! Thanks for reading and please share. Thank you so much. #millionsmissing

Hope found in M.E.

It’s unusual for me to attempt a second post in one week, but there is a landmark day approaching for the ME/cfs community…via those who are making incredible waves by their ingeniuity & grit..& who are extremely good at foghorns… September 27… when there will be a mass outpouring of shoes.Β I thought it only right and fair to post about it.

It’s known as #MillionsMissing.

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Peace in cloud spotting…

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Peace in the beautiful clouds…

I’ll admit to having a quite a weary on this week, struggling to write and am in need of energy (same old, lol!). Some very cheery sparklers at the weekend certainly helped, along with a few untoasted marshmallows… and this beautiful sky.

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