I’m back to talk more about anger and my difficulty in controlling it since my medical crisis. I do have to consider that some of it is purely biological. As I’ve mentioned, I’ve found out that it’s a common side effect of having as stroke. And the war I had in my brain and body the last time I was arguing with my mother felt almost physically impossible to stop. I wrote about it at length in my last post, but I want to talk more about it in this one.
When you’re a weirdo as I am (neurodivergent), it’s difficult to know what is a flaw and what is just partof my personality and does not need to be changed.
For example. When I was younger, I had a really hard time going anywhere because I felt like all my senses were being assaulted all the time. Smells, sounds, and sights that I couldn’t just mute. If someone had told me that I wasn’t being oversensitive or too fussy, but that my brain was just wired differently, that would have helped a great deal. I got scolded often by my mother when I would protest about my environment.
She told me a story about how when I was two or three and my brother was five or six and upwards, she would take us to the State Fair every year. She told me I would be crying and screaming, and I asked why she continued to do it. She said because my brother loved it, and she could not afford a babysitter.
That was my standing in the family in a nutshell. My brother was always more important than I was for several reasons. The first and biggest reason is beacuse he’s the son. Boys were much better than girls. girls were less than useless, and their only worth was to be married off to procreate. Oh, and in my case, to be my mother’s therapist. That’s it. I had no use as a person in and of myself, and I was treated accordingly.
Two. My brother was/is on the spectrum. He was never diagnosed with it (hell, it was barely acknowledged back in the eighties), but he has the classic symptoms. I was the one who clued him into the fact that he was on the spectrum, and this was a few months before I had my medical crisis. He said it changed his life, and it made so many things make sense. My only regret was that I didn’t tell him earlier because I knew decades earlier. It’s just that he displayed such stereotypical behavior for an autistic person, and he knew his son was autistic that I assumed he knew it about himself.
One of the most strenuous arguments K and I have ever (and it was really mild, but we don’t argue0 was about how talking about mental health was so much more open now than when we were younger. Neither of us was saying we should go back to the old days of not talking about it at all, but she was concerned that there was too heavy a reliance on medication. But, also, was there a need to label everything? Both she and her husband deal/have dealt with mental health issues. She pointed out that they got through it with some therapy, yes (on her part), but that was it.