My smallest child has the ability to emotionally destroy me, she can break my heart with a simple action.
Today she wandered away from my side in a cinema aisle after the act of watching a full feature-length movie became all too much for her. To amuse herself and me she would wobble five steps away and then turn and run, as best one can with a dislocated hip, and throw herself into my arms, finishing the act with a high-pitched giggle of joy. I am not sure the rest of the movie theatre appreciated it but every time she collapsed into my arms with a whoop of happiness my face lit up and tears threatened to cascade down my cheeks.
BB can’t walk more than a few steps without wobbling and then hitting the ground, her hip throws her off-balance and she spends most of the day hugging the carpet. She has become so accustomed to falling that she rarely cries, instead she merely picks herself up, brushes herself down and wobbles on.
BB’s unique way of walking is testament to her strength, she shouldn’t be able to walk, she should have been diagnosed before she even tried to learn; but she wasnt and so she taught herself against the odds to get those legs moving. Emma, a fellow blogger, new friend and mother of a child with ddh captured her child, Erin, doing her wobbling walk as to not forget how it was before the spica cast and so I have done the same.
I cant wait to say goodbye to the falls, but part of me will miss the wobble.
(Concerned readers: please note I don’t often play fetch with my daughter, we normally embark in educational games, because playing fetch with your toddler would be wrong *coughs*)
http://www.youtube.com/watch?v=XKSPBNtFdvE&feature=youtu.be
Blimey, she’s gorgeous!!
Thanks, I think so but I am bias!
Oh my goodness. My daughter’s DDH was discovered at 15 mos. She’s set to come out of her cast a week from Monday. Finally. We also took a video of her wobble walking before surgery. It’s a terrible video – but the similarities between your cutie and ours are so striking. Here’s our video:
http://www.simplifylivelove.com/2011/09/walking-with-hip-dysplasia.html
It is the exact same walk isnt it, scary, I imagine I could recongnise a child with hip dysplasia from 50 yards away now – hope all is well with your little one x
She is such a beautiful girl. I have been thinking of you all. Can you send me your address.
are you coming to visit? should I wash the china?
Kids are very resilient aren’t they? I know of a mum who’s little girl wasn’t diagnosed until she was walking too.Thinking of you 🙂
Thanks lovely
Jane, you know you are all constantly in my thoughts at the moment. I am very intrigued and can’t imagine when Erin does find her feet again that the wobble will be gone. I have also been thinking about how tall she will look when she comes out of cast as it has been a long time since seeing her vertical! Sending lots of virtual hugs.
right back at ya x
I don’t have video of my wobbly walk but in 1964 my mother noted in my baby book that I, aged two, “was still walking on tippy toes”. (I had started walking at 11 months). I also, according to the book “walked like a drunkard” till I was nearly three! My mother, sadly no longer around, never did know that her second born, soon to become ballet dancer (starting ballet aged 2 1/2), gymnast, and later on in life mother of 3 (all natrual births) and multiple marathon runner had severe bi-lateral Hip Dysplasia. I have only recently found these quotes in my baby book and realised the poingnancy of them. It was there staring at us full in the face and we never knew! BB has done what comes naturally – adapted to cope with the situation, but luckily she lives in an age where these things tend to get noticed (albeit in her case, a little late – better than 46 years late) and dealt with. Lovely to have a record of that wobbly walk – a very special memory.
Do you have, or have you had any pain? My daughter has severe hip dysplasia and I wonder how she would be if we hadn’t done the surgery. She was diagnosed at the age of 5
How is she now vivian?
Hello Vivian,
That was the funniest thing about all of this – I had no pain really. All through my life I just ‘went and did’ without thinking that there was anything abnormal going on. I now know, from having joined the ‘Hip Women Yahoo Group’, that there are others out there that have suffered severe disabling pain throughout their lives, wrongly diagnosed for years etc., as well as being told it was all in the mind, but for some reason, I was smiled upon. I look back and can pick out ‘hip pain’ which at the time was I presumed was from some gymnastic move, or whatever, but I now realise it was my dysplasia, but I had never, ever dreamt then that it was something so serious. It was a real shock when I was diagnosed as I thought I had pulled a hip flexor.
Jacq posted that a 20 year old has it uncorrected – she will, if she doesn’t get it sorted, be looking at full hip replacements in her twenties or thirties, which is, obviously, not great. That worries me, and it is something that I am trying to help in raising the awareness of Adult Hip Dysplasia. So little is known about it.
How is your little girl doing now? Such a hard thing for you to have to go through. At least for me, it was me that was going through it, I wasn’t having to explain to a child what was going on. Having said that I probably acted just like a child post-op, not doing as I was told, and being bloody minded about being independent!
Hope all goes well Vivian
you are amazing!
out of interest what would be the danger if you hadnt had the surgery?
Hi Jane,
The danger was that osteoarthritis was setting into my left hip (from the marathon running!) and my right hip would have done the same, which would have meant that I would have been looking at having a full hip replacement to both hips within the next couple of years, dependent on how quickly the hips deteriorated. The op that I had (PAO) uses your own hip socket, so extends the life of your hip by probably 10 to 15 years. I will undoubtedly need a FHR on my left, but hopefully, because the surgery was done before damage had set into my right, I might get away without one on that side. Keep fingers crossed. From the looks of the video, BB seems to wobbly on just one side – am I right, or is it both hips? She is such a bonny lass, despite all that is being thrown at her.
It is just her left hip, other is formed normally.
and yes – she is a dream – when she is not yelling atr me!
still cant believe you ran marathons on it!
Thanks for all your support x
What a cutie, even with the wobble in her walk. And what on earth is wrong with playing fetch with your toddler? It’s quite normal isn’t it? Maybe I’ve just been a dog owner for too long?
There is a girl in her 20’s at DS’s nursery who has uncorrected congenital HD and she walks pretty much exactly like you DD does. It ust be very limiting for such a pretty young girl. Her mother didn’t get it sorted when she was a baby because she was worried about the GA, and from what I gather she still exerts the same sort of influence. It’s pretty sad really 🙁
BB is getting old hat at GA!
(And she loves playing fetch)
She so cute and she’s just getting on with her life, complete with wobble: lesson for all of us adults perhaps who complain so much?
I could learn from her, I spent most of yesterday dying from a headache…
What a wonderful wee pet- full of determination and personality. She’ll be fine
Ta mrs
omg she is totally gorgeous! Is her op scheduled now?
Yes she goes in again on the 13th – prepare for lots of emotional weepy tweets
My, what a beautiful, determined little girl she is. And although once you know about her HD you can see her walk is a bit too wobbly, I can quite see how it wouldn’t have been picked up at first – let’s face it all early toddler walks are pretty wobbly.
Thanks she is a bit of a stunner x
She’s stunning!!
She is isnt she – I love the way she waves hello!
Awww Jane, BB is beautiful, and so grown up! I have been thinking of you all as well. xxxxx
Doesn’t she look like you?! I’m not normally good and seeing who kids look like but she’s yours alright! I love the way that you write about her, I read this this morning on the way to work and have been thinking about it all day – such lovely words, you have an easy honest style that comes right from the heart.
Thanks caroline 🙂
so very cute!
i found you through the love all blogs special needs showcase.
watching your daughter’s wee clip brings tears to my eyes – watching a little one stumble and trip (ddh or not!) will always make me cry as i will never see my little one walk…
enjoy those steps of her – every one is precious
Thanks x sending hugs
thanks for sending this and other posts in for the carnival of differences. post is up now. I hope all is going well.
Thanks jax