Is there too much information on developmental hip dysplasia online, or not enough? Parents will often feel confused or misinformed when it comes to their baby's treatment and head online to look for answers.
There are lots of wonderful online resources with general information and supportive Facebook groups where families affected by hip dysplasia can trade tips and stories. These resources can often be a great help but they can also be a hindrance when advice is conflicted. As the type, length and circumstances of each treatment varies, it is impossible to have specific advice that is "one size fits all".
If you are unsure or confused about something specific related to your own baby, don't be afraid to ask the medical professional who is managing your baby's treatment. They should be able to provide you with advice that is specific to you and your family's circumstances.
For those who are looking for online resources and support, here are some goodies:
Official Hip Dysplasia Organisations:
Facebook Support Groups (type these names into your Facebook search bar):
- Hip Dysplasia Australia Group
- Hip Dysplasia in babies (clicky hips or chd, ddh)
Hip Dysplasia Awareness Groups:
For more posts about life with a baby receiving treatment for developmental dysplasia of the hip, browse our blog here: https://www.hipsleepers.com.au/blog/
To view our range of specialty hip dysplasia baby clothes and accessories, click here: https://www.hipsleepers.com.au/view-everything/