Hi Melian

so sorry to hear about your experience with trying to access support

Have you tried community groups or anything else to help? It’s mad how it’s purely a diagnostic pathway.
I’m personally apprehensive about groups because the girl who put me on to diagnosis said the local ones were very male-oriented. I did a virtual NHS course (that was the only aftercare I had) and it was annoying more than anything. Just people I had nothing in common with going on and on. I got frustrated at the facilitators for not running it better and spent most of the time on mute like this
I enjoy your posts on here and it’s nice to hear of someone with the condition