Firstly, I am aware of PND being a sensative issue, I had it for a long time,and to do this, I need some answers through a qustionnaire(attempting to get some funding).
I'm thinking of setting up a PND Support group in the local area, and would be able to get a grant.
I know that most of you are not in my area, but just need to know the general feel for something like it.
There are quite a few questions, and everything is confidential.
If you are interested, please email me on
jopowell1 at yahoo dot co dot uk , or leave your email address here.
Thanks