My ds was diagnosed very young with autism. We had to fight to get the official dx due to a change in funding in our area (officially dx just after 2nd birthday), we then had to fight for a statement at 3 for nursery, then had to fight for therapies (do this regularly), then had to fight for the therapies to be put in the plan properly, social care package, dla, people judging when out and the comments that go with it, provision, needs..... now we're fighting for the right secondary placement all whilst being exhausted from lack of sleep, juggling interventions, social stories, sensory needs, adaptations, dla renewals, independent reports, tribunal application, millions of emails. It is absolutely soul destroying. All the time, energy and cost could be spent on so many other things including quality family.
I guess I'm just having a bit of a moan. I know there must be other parents fed up like this, does anyone want to join me for a bit of a moan?