May is Ehlers-Danlos Awareness Month and today in honor of it, I’m linking to my daughter’s blog. She has written an incredible post about what it’s like to live with EDS/Hypermobility, a disease we both share. Life isn’t easy when you have a disease and her post is a great read for anyone that lives with a disease, especially an invisible disease. Her post is all about how friends, family and even strangers see her disease first before seeing her. As a mom, it breaks my heart. Please take time and read her post, it is gut-wrenchingly honest.
This link will take you to her blog and the post. Emily Bare: See Me
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