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Tag: how is EDS diagnosed

Ehlers Danlos: Self Management

Ehlers Danlos Syndrome / Hypermobility Spectrum Disorder, how to self manage

Published 7 Jun 2022
Categorised as Ehlers Danlos Awareness Month Tagged connective tissue disorder, ehlers danlos, ehlers danlos syndrome, how is EDS diagnosed, hypermobility, hypermobility pilates specialist, hypermobility spectrum disorder, pilates, pilates hypermobility specialist, pilates specialist, what is EDS, What is Ehlers Danlos

Ehlers Danlos: how would I recognise it

Ehlers Danlos Syndrome / Hypermobility Spectrum Disorder, how is it diagnosed

Published 6 May 2022
Categorised as Ehlers Danlos Awareness Month Tagged connective tissue disorder, ehlers danlos, ehlers danlos syndrome, how is EDS diagnosed, hypermobility, hypermobility pilates specialist, hypermobility spectrum disorder, pilates, pilates hypermobility specialist, pilates specialist, what is EDS, What is Ehlers Danlos
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One person’s experience of symptoms and issues with Ehlers Danlos Syndrome (EDS) or Hypermobility Spectrum Disorder (HSD) may not be the same as another person with the same condition. Remember that we are all unique and beautiful ❤.

 

EDS and HSD have varying characteristics in their presented issues, therefore you may not experience all or any of the issues highlighted on this page. Also, the severity experienced may be different to that of another person with the same issue. It’s good to listen to the experiences of others, to help us increase our understanding, and awareness, and ultimately help support those with EDS/HSD accordingly.

 

Not all issues/symptoms appear at once – they may manifest at different times during your life, some in childhood, many begin during puberty, but many as we get older too.

 

This page of information is not meant to replace the many amazing resources of information out there, but simply to provide another source of awareness of EDS/HSD. If you have more questions, contact Tanya for further support to see if she can either help you or direct you to someone who can help you further.

 

This page is in no way means of a complete source of information / awareness about EDS/HSD, but more as a quick reference. Check out our other posts for more info,

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