New Member
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Join Date: Oct 2012
Posts: 2
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New Member
Join Date: Oct 2012
Posts: 2
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Thank you all
Thank you everyone! We decided to NOT continue with the aggressive PT approach.
It's so difficult watching your child in tremendous pain and not be able to help.
We have a fabulous Orthopaedic Surgeon in Annandale (for the Fairfax member) who has experience with CRPS/RSD/RND - she has worked with many service members who develop the disease. Unfortunately still having trouble finding therapists who have experience in the pediatric form.
Regarding the ultrasound - that's interesting because my daughter's OS mentioned ultrasound at her appt on Fri. I asked about Calmare and she said there are a lot of studies being done on electrical stimulation and u/s in veterans. I'll look into that more.
I appreciate all of the advice and support. Many days as parents we just feel lost.
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