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Saturday, 17 September 2011

So what's the point of this blog? It's not to rant and rave (although I probably will a little) or to get others to 'feel sorry for me', not atall. It's to educate others about EDS and for me to learn more about other invisible disabilities.

I'd like this blog to be a support network where those who suffer from invisible disabilities can share advice and tell their stories to others that may be in a similar situation or may just be interested in learning more...

Essentially, it's an easy access virtual area to gather helpful information about all kinds of invisible disabilities! So get in contact via the comment section if you want me to feature your ID story :) ...

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  1. Hi Abi :)

    Stumbled across your blog and thought I'd take a look. I also suffer from an 'invisible' disability - ME/CFS. I have been ill since I was 14 and never thought of it as a disability, I guess, because I look 'fine' on the outside. I'm so glad I have found your blog - it looks wonderful. Its hard coping with something people can't see and it's nice to find someone who is talking about invisible disabilities. I haven't looked at all of it yet but thought I'd leave you a comment to say hi :)

    Amy x

  2. Hi Amy!

    Glad to hear you find the blog useful, that's what it is for to offer support to all those with invisible conditions. Good to hear you have found us :)
    Have a look around and if you have any questions ask away!

    Abi x