I saw a new doctor this past Thursday who seems to know a lot more about RSD. He wants to do a nerve test and go from there. Mom said as of right nw things are loking good that I most likely don't have RSD, but she wants to see how the nerve test goes. Thanks everyone fr the advice and help, having somewhere to put things into words makes a big difference. Mom has also sat with me and read some posts. She thinks it's great that there is a place where people with RSD can talk and said this would have made her experience better when she was first diagnsed because she could have found someone who understood what she was going thrugh.

Hey Jessica! So happy to hear that you found a dr that knows about RSD, they are hard to find!! Good news that the neurontin is helping, hope it continues. I couldn't tolerate it, but I read on here that a lot of folks take it with successful results. I also hope the nerve test goes well for you. Please keep us posted!

All the best,
Nanc

I'm aware of no evidence it runs in families and this has been investigated.

Of course there are familial similarities that could cause onset in specific circumstances but it's unlikely in any given circumstance.