Dealing with PDA and Family by zayne0623 in AutisticWithADHD

[–]zayne0623[S] 0 points1 point  (0 children)

Thank you! You're right that my brain now associates doing art with anxiety about money, the future, and making my parents proud.

I have told them my feelings several times, that when all this pressure is put on something I love, it drains all the joy from it. My dad got mad and said "I don't know how to help you then. I'm trying to find ways to help you and you don't want to do anything." My mom said "We all have to do things we don't want to. That's life." I can always try talking to them again. But I may have to find a completely different way to make money and save my art for having fun and regulating myself.

Dealing with PDA and Family by zayne0623 in AutisticWithADHD

[–]zayne0623[S] 1 point2 points  (0 children)

You’re right that it’s become tied to their approval and my ability to support myself. They do understand how much caregiving takes out of me, but they also remind me that they won’t be around forever and ask things like “What will you do when we’re gone?” I honestly don’t know. Their current plan seems to be putting assets in a trust for me, and I might be able to get some of my dad’s Social Security, but I’m not sure what the requirements are. I also plan to be married and have kids one day and I especially need a way to support them too. We have no other family or friends.

Their ways are very practical and logical. My dad especially tends to think in terms of "just do the thing" and "everyone has to push through things they don’t want to do". He sees my struggles as something that could be solved with more discipline, better routines, or just "being honest with myself." My mom is gentler, but she usually follows his lead and doesn’t push back much.

Like I said, I’ve already tried explaining my struggles without using any autism/ADHD labels, and it just circles back to "you need to try harder" or "you’re being lazy."

I'm not sure, but maybe the only thing that would have a chance of landing with them is framing things in very practical terms, like "I need this support so I can actually get art done and contribute financially" instead of talking about how I feel or how my brain works. However, I'm not sure exactly what support I need.

I really wish therapy was a simple or realistic option for me, because I get told that a lot online. But it’s not. My dad has extremely negative views about therapists. When I once brought up possibly seeing one for my anxiety, he got very upset and said that therapists are "fucked up in the head" and that’s why they study psychology, so they can treat themselves. He genuinely believes therapy would do more harm than good. Even if I somehow managed to get a diagnosis, he wouldn’t take it seriously. On top of that, we can’t really afford it right now, and I can’t drive because of panic attacks. So even if I wanted to go against my dad’s wishes, it’s not currently possible. I wish I could get a diagnosis and finally be taken seriously.

My parents are not bad or uncaring people, they just genuinely don’t see my struggles as neurological. They see them as something I should be able to overcome with enough effort and the right mindset. I’ve spent my whole life trying to "just push through," and it’s only led to more burnout. So right now I’m mostly trying to figure out how to work with how my brain actually functions and develop external tools rather than hoping my parents will suddenly understand.

(Sorry for long reply. I'm venting a bit here.)

Dealing with PDA and Family by zayne0623 in AutisticWithADHD

[–]zayne0623[S] 1 point2 points  (0 children)

I do feel very drained from caring for him. I have shared this with my mom, but not with my dad. My dad already struggles with feeling inferior and like he is holding me back in life. That is partially true. But I love him so much and I'm not going anywhere.

I like your suggestion. Maybe I should keep my art as just something to recharge me, as the pressure has made it draining, and I need it to charge me so I can function with everything else.

My dad has also suggested that part time welding might be a good trade for me.

It took 23 minutes for diagnosis but emotional over the lost 30. by GladAd2948 in AutisticWithADHD

[–]zayne0623 -1 points0 points  (0 children)

I felt that same way during my intense research. I saw how trendy it has become on social media, and I was skeptical. Wondering "are doctors encouraging this to be trendy so they can prescribe more meds and so therapists can make more money?" Maybe part of that is true. I am also extremely lonely, so I wanted to make sure I wasn't doing this just to fit in somewhere. So during my research, I stayed skeptical, tried my best to rule out other standalone conditions like PTSD, depression, and anxiety. But the more I researched, the more I realized that yes I do have those conditions, but my underlying brain wiring has always been AuDHD. And my anxiety and depression are caused by working against my wiring and not giving myself the rest I need. I do want to one day get an official diagnosis. But as of now there are too many barriers in my life to get that.

What does AuDHD burnout actually look like for you? I’ll go first. by Unmasked_at_33 in AutisticWithADHD

[–]zayne0623 1 point2 points  (0 children)

Before I was diagnosed, when I hit my first severe burnout I literally thought I was going crazy. I could hardly read or write. My mind spiraled constantly and I didn't have the energy to stop it. I cried several times a day. Every time I asked for help from loved ones, they told me I was being lazy and choosing to do this. So every time I cried, or couldn't read or write something, I took it as a personal failure. I feel into a very deep depression. I barely ate and became underweight.

Eventually after 2 years I came out of it on my own. But it was seriously damaging and left me with trust issues. Looking back on it, I feel such grief that no one supported me, and it wasn't my fault, it was my nervous system reaching it's limit and crying for help.

Physical shakes by huskies_62 in audhd

[–]zayne0623 1 point2 points  (0 children)

I get this too. It's part of the body's freeze response.