Eva's Dilation |
Her conclusion was that her vision is currently 20/60 with a slight astigmatism. This is not something that is required to need aided correction.
Today we had a visit with the orthopedic. For background information, we have not seen her orthopedic since the scheduled follow up from the bilateral hip dysplacia in 2012. At this office, we were greeted by a completely overpopulated waiting room. This office holds all four of the pediatric orthopedic doctors that serve the metro area, and they have clinical visits for two days only a week. Busy was an understatement. We were told that Eva was going to get an updated x-ray of her hips before been seen. We watched as most of the waiting room dissipated into patient rooms and Eva was finally called. We had the x-ray done, without resistance, and was taken to the last empty room, a cast room. Ironically, it was the same room we were in when that retched frog cast taken off. Horrible, awful, disturbing memories.
He explained that the left ball on the hip is still lacking cartilage but is slowly regenerating. I had a few questions for him - one was her running ability. I notice that when she is running, her right leg swags outward. He said this is call genu valgum (knee knock). This is typical for children aged 3-6. Because of her age (4.5 yrs) I should not be concerned. If it continues after age six, there is a corrective surgery for this. I also asked about physical therapy. He stated that he can write a prescription that has nothing to do with her deletion whereby we can receive therapy through insurance again. Finally, I asked if he knew of any podiatrist or trades person that does shoe lifts without going through insurance. He only wished that he knew someone. We were scheduled for an appointment for 12 months out.
Information about genu valgum:
http://www.nlm.nih.gov/medlineplus/ency/article/001263.htm