Older women on the forum? Your early years?

Older women on the forum? Your early years? Mine are in my profile. Share?

Parents
  • Hello Uhane

    It's good to know that there are other older ladies out there. Since I began researching the symptoms of autism (about 2-3 years ago) I've not noticed many of us 60+ year olds out there with a big voice. The "late diagnosed" content creators I follow on YouTube are mostly in their 30s and 40s. I wish I could find some 60+ year olds on there. I was diagnosed less than a year ago so still processing.

    Your comment that you've been Maskmasking so long that you don't know who you are really struck a cord with me. I'm still masking heavily and don't know who I really am.  I had a fairly good childhood. I usually had one friend who I could tag along with and that one friend sometimes enabled me to join a wider group but I've never been happy in groups. My happiest times were spent playing alone. 

    As I got into my teenage years I tried really hard to fit in, often going places where I felt very uncomfortable. My favourite thing to do as a teen was to go for a walk in the countryside - usually on my own but occasionally with my one special friend but I forced myself to go to social events even though I hated them. I was often overlooked or ignored and with hindsight I wonder if neurotypical folks could see that there was something different about me. (I believe there are studies that show that this does happen even to high masking autistics)  Knowing you're different but not knowing why is very painful and difficult. 

    I met my husband at school. We were 16. He joined the armed forces a few months later so we only saw each other at weekends and when he was on leave so that gave me lots of alone time which I needed. We married at 20 and I was a mum a year later. I found it hard to make friends and even when I had friends I felt disconnected from them but I didn't know why. We went to lots of social occasions and I would always drink too much as a way to cope 

    My husband died almost 9 years ago now. Knowing I'm a masked autistic makes me feel sad and a bit of a fraud. My husband really didn't know me. Looking back I can see that he enabled me to lead a relatively normal life. Now he's gone I find myself retreating from life. I'm mostly very happy to be safe in my own home with my dog for company. Sometimes I do feel  lonely though.

    I've been a video gamer for many years and my current hyperfocus is Minecraft. I think if I could put as much focus and energy into something useful I could have done amazing things with my life! 

    I hope this isn't too much of an essay for you to get through. 

    Inula

Reply
  • Hello Uhane

    It's good to know that there are other older ladies out there. Since I began researching the symptoms of autism (about 2-3 years ago) I've not noticed many of us 60+ year olds out there with a big voice. The "late diagnosed" content creators I follow on YouTube are mostly in their 30s and 40s. I wish I could find some 60+ year olds on there. I was diagnosed less than a year ago so still processing.

    Your comment that you've been Maskmasking so long that you don't know who you are really struck a cord with me. I'm still masking heavily and don't know who I really am.  I had a fairly good childhood. I usually had one friend who I could tag along with and that one friend sometimes enabled me to join a wider group but I've never been happy in groups. My happiest times were spent playing alone. 

    As I got into my teenage years I tried really hard to fit in, often going places where I felt very uncomfortable. My favourite thing to do as a teen was to go for a walk in the countryside - usually on my own but occasionally with my one special friend but I forced myself to go to social events even though I hated them. I was often overlooked or ignored and with hindsight I wonder if neurotypical folks could see that there was something different about me. (I believe there are studies that show that this does happen even to high masking autistics)  Knowing you're different but not knowing why is very painful and difficult. 

    I met my husband at school. We were 16. He joined the armed forces a few months later so we only saw each other at weekends and when he was on leave so that gave me lots of alone time which I needed. We married at 20 and I was a mum a year later. I found it hard to make friends and even when I had friends I felt disconnected from them but I didn't know why. We went to lots of social occasions and I would always drink too much as a way to cope 

    My husband died almost 9 years ago now. Knowing I'm a masked autistic makes me feel sad and a bit of a fraud. My husband really didn't know me. Looking back I can see that he enabled me to lead a relatively normal life. Now he's gone I find myself retreating from life. I'm mostly very happy to be safe in my own home with my dog for company. Sometimes I do feel  lonely though.

    I've been a video gamer for many years and my current hyperfocus is Minecraft. I think if I could put as much focus and energy into something useful I could have done amazing things with my life! 

    I hope this isn't too much of an essay for you to get through. 

    Inula

Children
  • I like 3D Mahjong, myself, and Go and Gomoku.

  • Hi Inula

    I'm 60+ and also enjoy playing video games. My favourites are Sims 4, Fallout 4, Assassins creed Valhalla, Origins & Odyssey, and Hogwarts Legacy. 

  • thsi is a fine essay. thank you. I see myself there and that is a balm.

  • Hi   there  Inula. 

    Welcome to the club,   I am also,  a 60+  Autistic lady, who also has been widowed, and so. I  can empathise 

    with what you are saying.

    I was bullied right up to the time that I met my future husband, I always thought that  I was the worst person in the world, and so (when I met my late fiance`e,) I  was able to get my Autism diagnosis, I felt that a great boulder had been taken off my shoulders!   

    My late fianc`e helped me to gain my diagnosis,for he was reputed to have Autism, but he did not want to be Diagnosed.

    When I was diagnosed,   I made up my mind to devote my time to help other Neurodiverse people, so that they would not have to go through what I had been through,and so,. I helped to set up a Group  for other Autistic people.

    I was to be wed to him, but he was terminally with brain cancer and other things as well.

    I hope Inula,that you can empathise,from a fellow widows point of view,that I did not go out of my way to meet someone else,it just happened!

      My fianc`e, was the icing on the cake.

    My soulmate was,is,and always will be my late husband.