Hi I have a 4yr old son who has an incomplete T12 since an RTA in Feb 06. I have heard alot about FES and electrical stimulators as ways of increasing movement, strenght and feeling. At the moment I am have being waiting 4 months for my son's wheelchair and stander and so the only way I will have access to other equipment is to fund it privately. I want to find out as much as I can before I part with my money.

I have read about Electrical stimulators in the US which claim a spinal cord injury breakthrough http://www.neurocare.com/cs5-1.html. It cost €2,000 but want to know if anyone has used this equipment or something similar.

Can anyone advise me.