Invisible illnesses: EDS:

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EDS, Hypermobility and hEDS/EDhS affect everyone differently—even when we share the same diagnosis.


Many of us experience similar symptoms and familial patterns, but our day-to-day realities can vary hugely.


This is just one version of how EDS can show up in someone’s life.

For example, I don’t have flat feet—but I’m affected by nearly everything else on this list, and more.


I'm proud to share this to raise awareness, because dynamic disabilities and invisible illnesses aren’t something you can see.

You can't diagnose us with your eyes.


So I ask you—look beyond the photo.

Think outside the frame.

See the whole picture.


Thank you for taking the time to read.

If you know someone with an invisible illness, why not share this with them?

Let’s remind them:

You are loved. You are seen. You are not alone.


With love,

Sarah Wingfield ❤️

Independent Disability Advocate


#DisabilityInclusion #StrongerTogether #DisabilityAwareness #DisabilitySupport #DisabilityRights #ChronicIllnessWarrior


Alt text:


An infographic titled "What my EDS doesn’t show" features a blue silhouette of a human body, highlighting various symptoms of Ehlers-Danlos Syndrome (EDS) with red marks on affected areas. Labels point to different issues, including:


Migraine


TMJ (jaw pain)


Neck pain


Popping shoulders


Damaged joints


Dislocating joints


Torn cartilage & ligaments


Pain everywhere


Flat feet


Arthritis


Sciatica


Organ ruptures


Stomach problems


Unstable joints



The illustration aims to raise awareness of the often invisible and widespread impact of EDS on the body.





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