A Public Account of Adult Hip Dysplasia and Peri-Acetabular Osteotomy.
How I Spent My Saturday
Get link
Facebook
X
Pinterest
Email
Other Apps
Sure, I almost gave myself heat stroke, but I am glad to report that my hip didn't hurt a bit. I just hope they all take. I'd hate to have to replant 30 mums.
So, you're been diagnosed with hip dysplasia and they send you off to get a "Hip Arthrogram MRI". This recently happened to me. No one told me what to expect. Here's the deal. I was sent to a hospital for this procedure. The arthrogram comes first, the MRI second. If you're claustrophobic, you might want to consider a sedative for the MRI portion of this event. First, the arthrogram. Basically, in a hip arthrogram, they will stick a needle in your hip and inject dye. First, I was stripped and put in a hospital gown. Then I had to lie down on a big table with an x-ray machine lookin' thing above it. Then, my joint was marked with a marker and the whole area was liberally painted with betadine. Your knickers will be destroyed ladies, betadine stains. Then, an anesthetic was injected into my hip area. This just pinches a little. While the anesthetic takes effect, they will mix up a little dye/lidocaine cocktail to inject into the hip joint. This injec...
Holy Crap - I'm Hyper Mobile! So, I have had increasing joint pain and joint stiffness in the last few years, as many of you hip folks know. What's been odd is that its not just in my hips anymore. Its my knees, my shoulders and elbows, even my fingers. Its also been coupled with fatigue, difficulty sleeping, headaches and muscle pain. So I was finally sent to a rheumotologist. She took one look at me and had me do a couple of my neat double jointed tricks (I can basically tie my fingers in knots, my knees practically bend backwards, as do my elbows, my feet can twist almost backwards, etc. etc.) and said that I was hypermobile. Hypermobility Syndrome to be specific. Now she didn't act like that could be the cause of any of my troubles and told me to avoid yoga at all costs (too late) and that she'd keep testing me for the real cause of my problems (like RA or Lupus, both of which I test negative for). But here's the deal....I started looking up Hypermobility...
Well, it's been 6 months since my RPAO. Here's the update: I can now walk MILES at a time. My right side is still sore and feels kind of bruised. I have partial numbness over the entire front and side of my right hip, but this is way better than immediately post-op when I had total numbness in a large percentage of the area. My left side is still giving me trouble, but only very sporadically. In the last few weeks, my right side has also given me a bit of trouble, but not very often and not for very long. I STILL can't sleep on my right side with making the bruised feeling more intense. BTW, I have 5 screws in the right hip and my surgeon gives me funny looks when I ask about screw removal. I feel fairly certain that I will have to do the left side as well, but hopefully its not for at least a few years. That's about it. There's really nothing else to say. I absolutely advocate the surgery. I have no regrets about it. you can e-mail me with ...