The International Hip Dysplasia Institute- This is the central hub for hip dysplasia and was established by The Git-R-Done Foundation. Here you will learn the most up-to-date information on hip dysplasia, including awareness campaigns, research projects and more.
The International Hip Dysplasia Institute-SPANISH- The IHDI has made it possible to have their website translated into SPANISH! This is the central hub for hip dysplasia and was established by The Git-R-Done Foundation. Here you will learn the most up-to-date information on hip dysplasia, including awareness campaigns, research projects and more.
The International Hip Dysplasia Institute– This is a great place to find information supported by International Hip Dysplasia Institute
Developmental Dysplasia of The Hip, Babies, Kids, Adults- Another great community support group. This one tends to be more for adults with hip dysplasia.
DDH- Hip Dysplasia- Children Facing Surgery or Spica Casts Facebook Page– This is a great community of supportive families going through the tough road of childhood hip dysplasia. This community tends to be geared more towards childhood hip dysplasia.
The Parents’ Guide to Hip Dysplasia This book covers hip dysplasia in babies and children from diagnosis through treatment. Written in everyday language, this book explains what hip dysplasia is and how doctors diagnose it, and discusses treatments for mild to severe cases. Practical advice includes instructions for diapering, ways to make a child more comfortable, clothing tips, recommended car seats and more.
Link to purchase your copy of The Parents’ Guide to Hip Dysplasia
Hope the Hip Hippo -a story about Hip Dysplasia in Children by Gina Jay & Julie Beattie To all the children who have embarked on a journey with hip dysplasia, we hope that you will be able to spread your wings far and wide, and soar farther then you ever imagined.
GINA JAY & JULIE BEATTIE
We are two mothers, from two different countries with two beautiful children both diagnosed with Bilateral Hip Dysplasia. When our children were first diagnosed we both independently searched for a story to help explain and understand ourselves, a little of what was going to happen to them. Nothing being found we have embarked on this journey to create a book for you; in hopes it takes a little of the “scary” out of what they and you may endure.
From a mothers heart; to your baby.
Baby Center– This is a great place where parents have gotten together to discuss their children’s conditions and experiences.
One Hip World– Started by a hip dysplasia mom, Gina Jay has created a blog spot for all things HD related including the One Hip World fund raising event on June 30th of each year.