Guest guest Posted May 22, 2011 Report Share Posted May 22, 2011 With summer soon approaching we decided to try a waterproof cast. We are casted at Strong Memorial in Rochester and Dr. R and I discussed bracing for the summer but I wanted to stick with casting so we went with this one. Amaya is able to take baths, go in swimming pools and water parks. She can not go in lakes, rivers, or oceans. I like the cast as it is lighter then the other however, when she takes a bath or shower she is wet for hours, she drips from the bottom of the cast. I guess this is something I can deal with to enable her to enjoy summer. Seeing as I don't want to keep this type of cast on again I was doing research and found what is called a Hickman Drysuit, this is available through Hammond Drysuits. My husband and I have decided to order one for Amaya to be able to take swimming lessons this fall. They are quite pricey but I feel it will be money well spent in the long run. Amaya is in her 5th cast and we have seen minimum improvement however I feel this is the best treatment to hold off what might be surgery. We have also decided to not x-ray her at every casting and cast removal. This will limit her exposure to radiation and possible side effects of that. She seems to have adjusted well to her cast and life with it. I remember when she was diagnosed with progressive infantile scoliosis in June of 2010, how scared and alone I felt. Then I found this group and without all of you I don't know what I would have done. I would love to be able to raise awareness of infantile scoliosis and hopefully Amaya and I will be in a local magazine to let others out there know they are not alone and that resources are available, as well as treatment options. Tammy Mullins, mom to Amaya almost 3 diagnosed by mom in April 2010 and finally by pediatrician in June casting at Strong Memorial, Rochester, NY Quote Link to comment Share on other sites More sharing options...
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