According to a lot of sources, like the Amputee-Coalition as cited in this article that there are lots of support groups out there as well as peer councilors. The article states:
According to Susan Tipton, national peer network coordinator for the Amputee Coalition of America (ACA), there are about 260 support groups for amputees across the United States.
The article seems to state that it is very likely that a new amputee would have support set up by the hospital or some other group out there. I can tell you that for me this was not the case.
So far the only support was there has been from my prosthetist, He is a great guy with a ton of experience, but really has no first hand knowledge of how it feels to be an amputee. It is hard to explain to people that have both legs. Short of duct taping their legs together for a week, I don't think that anyone could really get the FINALITY of losing a limb. Yes, I put on a prosthesis to walk, but I have to put it on. I tend to leave mine on 99% of the time I am awake. I seldom remove it for anything other than to adjust the sock levels or straighten out a wrinkle.
The point of this post isn't to complain, but to possibly inspire amputees to become peer counselors and to pay forward the things we have not had. I suspect that there are quite a few amputees out there that have not had any peer counseling whatsoever. With almost 3 million amputees in America alone, we have the base to make a huge difference. With spokes-people like Josh Sundquist and Adrianne Haslet, the support of great publications like Amplitude Magazine and In Motion Magazine and our drive to make the amputee world a better place - We can make a big difference.