It comprised of a mixture of visual and written pieces. Each piece gave a moving insight into how this horrible illness effected each of their lives.
In this series of posts I am going to share with you some of the photos I took at the exhibit.
Say the word ‘ Disability, now what do you see?
Visual information plays a key role in our perception of reality. What we see is filtered through a lens of past experience. We can only become consciously aware of our misperceptions if we open to receiving new information that may challenge out existing understanding.
This photography exhibition asks you to re-imagine your concept of disability.
This is a portray of CFS/ME a chronic complex neurological illness.
We present to you seven individuals who have suffered, or are still suffering from the devastating effects of CFS/ME. Often this illness had no visual expression, instead it manifests itself by causing disarray to many of the body’s communication systems and can be extremely debilitating both physically and mentally. Symptoms can be so sever that sufferers may become wheelchair, house or even bed-bound.
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If you want to see more of the exhibits check out posts two (Link) & three (Link) – Coming Soon.
To find out more about my experience with CFS/ME check out my earlier posts:
- Diagnosis: GP and referral to specialist clinic
- The Rainbow in the Storm- Checking in with CFS/ME
- The Ugly Truth of Bad Day with CFS… But its ok!
- 30 Things About My Invisible Illness You May Not Know
Or for a full list of my CFS/ME related posts check out my CFS/Me Index