Katie Ryan

Katie Ryan's Fundraiser

Giving hope to all those living with the Ehlers-Danlos syndromes and hypermobility spectrum disorders. image

Giving hope to all those living with the Ehlers-Danlos syndromes and hypermobility spectrum disorders.

Join me and help make a difference, please give today.

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$200 towards $200

Join me in supporting the Ehlers-Danlos Society and all the amazing work they do for the EDS and HSD community!

Learning to live with EDS hypermobility type has been a tough journey. Getting the actual diagnosis at 25, after years of chasing joint and muscle pain and weird injuries, was such a relief. And the EDS Society was there to support me every step of the way. The conferences that they hold have also helped me with disease management, plus they also provided education credits for my doctors and physical therapists.

The Zebra community is full of lovely people who understand what you are dealing with. <3

Another big why for participating in EDS Awareness Month is that after being vocal and visible, 3 of my friends has since been diagnosed with hypermobility and EDS.

Please give what you can so the EDS Society can continue to do this great work.

-Katie