We asked for one AGES ago but it never happened. I think its a good idea because we do give advice on meds, dx, legal stuff (statementing etc). AND people need to understand that we are all parents of kids with SN/disability and therefore need support ourselves as well as giving it. Also, the nature of our kids means that we can't always be as responsive/supportive as we might like to be. Mind you, I was at home all Saturday morning with just DS and I had total freedom to catch up on emails, MN etc while he stimmed [guilt]