😁 Hey, I'm Mario! I'm 29 years old and the full time caregiver to William who's 27. To give some info first, he has Level 3 Autism, is nonverbal (only being able to say about 5 basic words), has an intellectual impairment, is legally blind and has spastic cerebral palsy. So I do have my hands full, but I take pride in caring for him and I love him dearly.
I've been feeling quite alone these past few years and feeling as if I have nobody to turn to or relate to on my situation. I'm desperate for support, someone to chat with and I'd even love to offer someone else support as well.
I have a couple of friends who take Will off my hands some weekends so I can get things done and relax, however it's all they can offer as they're busy people, neither can they help me much emotionally/mentally, so it might not be enough. I don't feel like my situation is bad enough to pay somebody to help me take care of Will, it's just I feel that I'm lacking in emotional support and someone to relate to, I'd even appreciate some advice for a few things.
One of those things is managing Will's meltdowns and mild aggression, he has them pretty frequently and it makes me wonder If I'm doing something wrong. He reacts strongly to being stopped from doing what he wants to, which are dangerous or destructive things such as trying to eat things he's not supposed to (such as plastic spoons & rocks) which I believe is PICA, and damaging my furniture. I have a ton of sensory toys for him, I've tried to redirect, I've tried to be firm when letting him know it's not okay to damage my furniture or eat dangerous things, but… It persists and I'd like to learn what else I could try. He's a sweetheart otherwise, it's just these are one of the things I'm a bit clueless about , I may need to be educated on this haha. Anyway thats all, I look forward to hearing from you guys. : ) Peace! 💚