EDS Awareness Month: Information booklet for JHS/HEDS in kids

May is EDS awareness month.

I have been mulling over what sort of a post would contribute to raising awareness about EDS. I think people who read EDS related blogs are already aware of it because of some sort of personal or professional connection to this disease.
Finally I decided to make a series of information brochures for JHS/HEDS, that could be easily downloaded and shared by people. And the brochures hopefully, would eventually reach some people who are not already deeply familiar with this disease.
This is the first one of the series. This brochure aims to provide information on how JHS/HEDS affects children, which should be of interest to parents and teachers.
EDS info
Click to view and download full-size image
The pdf file can be downloaded here.

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About Hypermobility Syndrome India

I am an Indian woman with Ehlers Danlos Syndrome Hypermobility Type (EDS-HT or hEDS). I have been living with this disease all my life, and fighting the manifestations blindly without knowing why my body was a living demo of textbooks of different branches of medicine. Getting a diagnosis at 38 years of age opened up the path for my emotional healing. I aim to raise awareness about hEDS, chronic pain, invisible illnesses, mental illnesses and invisible disabilities, and share my experiences through my blogs.
This entry was posted in Awareness, Hypermobility Syndrome in Children, JHS/H-EDS and tagged , , , , . Bookmark the permalink.

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