Every
May, people throughout the world unite to support those with Ehlers-Danlos
syndrome (EDS). We come together to celebrate our global community, share
stories, and raise awareness.
Ehlers-Danlos
Syndrome (EDS) is a genetic condition that affects a person’s connective
tissues, like joints, skin, or tendons. Ehlers-Danlos Syndrome is a disability.
There are 14 different types of EDS, but the most common form of this condition
is hypermobile Ehlers-Danlos Syndrome (hEDS). hEDS can make a person’s joints
move beyond the normal range of motion, a symptom called hypermobility.
Hypermobility can result in unstable joints going out of place causing pain.
Other parts of the body can be affected by hEDS too. It can cause skin
stretchiness, poor balance, stomach issues, fatigue, spinal instability, nerve
pain, and other symptoms. Managing hEDS can be difficult, and a lot of
management is about decreasing the severity of symptoms. Many healthcare workers
may not know about EDS or how to treat it, so it can be hard for people with EDS
to get help or have their pain taken seriously. The main therapy for EDS is
physical therapy to strengthen muscles, improve posture and balance, and prevent
future joint damage.
Need
help or want more information on Ehlers-Danlos Syndrome? Explore the resources
listed:
The Ehlers-Danlos Society
EDS Awareness
Ehlers-Danlos News
Sources:
https://www.mayoclinic.org/diseases-conditions/ehlers-danlos-syndrome/symptoms-causes/syc-20362125
https://www.ehlers-danlos.com/what-is-eds/
https://www.nhs.uk/conditions/ehlers-danlos-syndromes/
Additional
Resources:
@Cortdoesscience
on Instagram
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