Wednesday, 3 May 2017
EDS Awareness Month
I have mentioned before on this blog, the sad fact that all my three children have genetic hereditary illnesses.
My eldest daughter is severely affected by Ehlers Danlos Syndrome.
She is now chronically disabled and mobility very limited.
A pain free day is never an option.
Her younger sister is also affected but in a much milder form..for now.
We all know that it can, and will progress.
May has been designated EDS Awareness Month
As a chronic pain sufferer myself, am fully aware that pain is invisible to those around you and hard for non sufferers to really understand how it limits life.
So, am just making you aware...
...please go and read about it, it is more common than you think.
Thank you for listening