Hello. I need a ask a long question. I am really at the end of coping. The question centres around PDA autism. I have spoken to a lot of people, including the autism helpline and assessment centres, but if I don't access some pathway of support soon I don't think I can be responsible for what I do next.
My son is 24. He has a a 20 year old sister. My husband and I gave them a beautiful full life; not materially, but in terms of gentle, consistent love and support for everything they were and everything they did. I could see my son was dramatically different to his peers and I thought he was highly evolved and I just loved him. The 20 year old is an outcome of this upbringing; hugely happy, confident and successful. However, she won't come home because of her brother. My husband left 9 years ago and professes to hate our son. We divorced. I felt I had to choose our son, but I get where my ex-husband is coming from. The rest of my family don't even say his name. There is no christmas or birthdays because my son is disengaged and gets upset around ideas of the passage of time.
Why? Because our son displays all of the traits of PDA autism, minus any aggressive meltdowns. He does diversion and shutdown. He is the gentlest, most passive and frustrating person. He has no shame (i never actually wanted him to but ... ), he has no concept of authority. he is kind of fearless but will not attempt any action or see anything through. He talks like the most confident well spoken person you ever met - which sure as hell does not help his case. He is sitting in the garden at the moment, in the rain, **** and listening to white noise. He has advised me that he needs to rip all of the carpets up because of the heat. I said 'feel free'; like how the hell do i have the energy to give a damn about carpets? Since he started smoking cannabis there has been a huge improvement in his sleep and the terrible night terrors have stopped. Prior to that there was no day or night pattern and the only thing that calmed him was rainstorms. He has poor executive function except for when he is hungry. Then he goes to a large supermarket and efficiently steals as much food as he needs, choosing it with great attention to its nutritional content and not batting an eyelid as he pretends to pay for it. Occasionally I crack and ask him to leave. He goes for a few days; steals food to live and then returns. the atmosphere at home is horrible. I can't work full time because he is a danger in the house. I can hardly express how desperate and isolated I feel. This week I phoned CRISIS and, true to form, they could offer nothing, just like MIND, SAMARITANS and all the others; suggested I want to my GP .......
I can't afford to look after him properly. He hasn't been to a dentist for 10 years. He has no phone. His clothes are just a heap of random stuff he has found. I make beautiful healthy food for him but that's really all i can afford. My son has never engaged in formal sport, cannot swim, drive, access benefits etc. If you praise him he goes into shut down. He is hugely manipulative and 'bends' reality until you don't know what the original request even was. He was excluded from school at 16 following his stunningly good GCSE results. The school said he was too 'malign' to be allowed to stay.
Sorry. Will now get to the point. We (now I) have been to the GP countless times since he was aged 8 and hallucinating - possibly I now wonder due to years of no sleep. We repeatedly asked for referrals but I didn't know to what. Now I need to get my act together (and this time I mean it

. I have requested his medical records so that I can at least understand why we received no medical response. Then I will make an appointment with the GP, ignoring the looks. Then I was thinking of taking a small group of people with me to the appointment who don't look like they occupy hell. I am afraid I am looking dreadful - beyond burnt out, with eyes like slits.
I need some companions to assertively and politely access help on my son's behalf.
So what do we say? I think he has PDA autism based on my 24 years of living with him. I am not a psychologist or a psychiatrist so my credentials in this area are poor. If I say this (again) the GP will stare extra hard at the computer screen. Last time we went to ask for a PDA autism referral the GP at last turned to my son and said "oh. so do you have delusions of grandeur?". I sighed deeply and said something pithy - never rude, but so exasperated. The GP turned to me and said there was no such thing as assessment for anyone aged over 18. The GP added that, as he was stealing from supermarkets, the prison system would soon pick him up and that would be good because prisoners get help. This is the sort of advice I am given. I am so shattered.
In truth, I think he needs 2 referrals: one to a well trained mental health professional and one to a PDA autism assessment centre - the problem is the autism questionnaire doesn't really pull out the issues around his behaviours. Maybe something else? How can I articulate this in a way that a GP will respond to? I have taken NICE advice etc. but I think they think I am trying to be clever. I am waiting for the medical records to be sent through then want to make a GP appointment. I need to hold my ground. I need to get him some help whilst I have a fragment of resilience left.
So you people who have walked a similar path, please advise me - what should the advocates I take with me to my son's GP appointment request?
Thank you for taking the time to read this
Emmu