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.

from Blogger http://ift.tt/20c7htP

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About Hypermobility Syndrome India/Viv

I an an Indian woman with Ehlers Danlos Syndrome Hypermobility Type (EDS-HT), also known as joint hypermobility syndrome. Although I have "suffered" from this disease all my life, I was diagnosed at 38 years, 2 years after my child was born. My work mainly involves being a mom to my beautiful and compassionate child. I also write and work from home in the field of science. I aim to raise awareness about EDS-HT, chronic pain, invisible illnesses, mental illnesses and invisible disabilities through my blogs. Viv (Latin root, meaning Life/ Alive) is my blogging pseudonym and alludes to my continued endeavor to rediscover my life and its meaning.
This entry was posted in Awareness, Hypermobility Syndrome in Children, JHS/H-EDS and tagged , , , , . Bookmark the permalink.

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