Hi,
We've had concerns about our (nearly) two year old male twin for sometime now. Recently, we got our excellent HV to have a look at him and within no time, we had appts. with a speech therapist, who immediately refered us to a consultant paediatrician at Harrogate CDC.
Everyone appears to be looking at autism. And certainly that's what we think is at the root of this. There's stacks of ticked boxes next to the symptoms in each of the three key areas.
After an initial burst of activity, I think we feel a little at sea, and we're hearing bits and pieces about the consultant, that contradict what we understand to be the best way forward.
In short, DS is nearly two, and we've heard that early diagnosis and intervention leads to significantly better outcomes - we obviously want access to the resources and services available - and are unsure whether diagnosis is necessary for this.
We've also heard that diagnosis can take a "significant amount of time" (years?), and that the consultant we are seeing won't diagnose until the age of seven.
Is this usual - or are just hearing a touch of gossip. Has anyone any advice generally about the first appt. or about Harrogate CDC specifically...
Sorry to rant - help!
J+E