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DDH UK

Because Hips Matter

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DDH UK INFORMATION

Developmental dysplasia of the hip (DDH) occurs when the hip joint fails to develop correctly. It is estimated 1 in 6 newborns will have an element of hip instability and 2 to 3 in every 1,000 infants will require treatment. Early detection and treatment is vital and having access to the reliable information and resources can make navigating this journey so much easier.

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'DDH UK has been an absolute life line for me. It has been amazing having round the clock knowledgable support covering every aspect of spica life, everything from hospital bags, nappies and sleeping positions, not forgetting the moral support. I would have really struggled without their help and support.'
Amie

'Without the DDH UK community and its non judgemental, always available support, we would have found this journey so difficult. They've provided us support, a shoulder to cry on, handy tips and a feeling of normalcy that cannot be underestimated.'

Anon
'With a DDH diagnosis for my daughter I had no idea who I could talk to or anyone who truly understands. DDH has been there and without the support I would feel lost and with no one with experience to talk to. They prepared me for the pre op with my daughter's surgeon which I wouldn't have had half the questions or knowledge I have without it.'
Stacey
'Although we aren't new to the experience, with this being the second time my little one has been in a hip spica, having support from DDH UK has made it so much more bearable. Knowing there is someone there for help, advice and support makes a massive difference. Thank you.'

Anon

DDH UK AWARENESS RAISING

DDH UK is dedicated to ensuring hip dysplasia is on the radar of health professionals. We work with midwives, health visitors and GPs all of whom play a vital role in the care and management of hip dysplasia. We also work with influencers and the media to put this life changing condition in the spotlight.

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DDH UK SUPPORT

When a child is diagnosed with DDH parents experience a range of emotions, often having an overwhelming need to understand everything about the condition and what the future holds. We offer a many services from cards being sent out to children in hospital to one-to-one buddies and regional coffee mornings, to ensure families feel supported and informed on their journey to healthy hips.

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Natalie Trice is a UK based mother of two sons and the founder of DDH UK, the UK’s only DDH charity. Natalie’s sister and two cousins were born with DDH and her second son, Lucas was diagnosed at nearly five months.

Natalie was amazed at the little support that was available for her and her family and set up DDH UK.
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