This Is What EDS Looks Like…

May is Ehlers Danlos Syndrome (EDS) Awareness Month.

This is what EDS looks like…

Petrina and Anita (mum)


Maddi EDS


Kitty EDS


Mary EDS




Stryder EDS


Kathy EDS


Lucy EDS


Nicky EDS


Quinn EDS


Linda EDS



All images and clips have been used with permission.  If there is any reason you feel that someone has been fraudulent in their giving permission, please feel free to email me at  I take children safety very seriously!!!

Disability consumer and activist. Pissed off since 1995... Mad as a hatter since way before that.

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Posted in Disability, Ehlers Danlos Syndrome
One comment on “This Is What EDS Looks Like…
  1. Elizabeth Lovett says:

    I give permission for you to use my Daughter Madison’s picture for EDS Awareness 🙂

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Pissed off since 1995. Mad as a hatter since way before that.

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We are raising money to cover the boys medical and disability expenses. ALL funds raised go into their own account, to pay for these expenses. Things such as speech therapy, occuptational therapy, psychology, chaperoned sport and social activities, and special equipment etc. I hate having to do this, but hey, if you don't like it, then give me a job ;-). Please click on the photo to go to their GoFundMe page, and thank you for your time (and I do hope, your generous donation *cheeky grin*)!!!

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