Hello
Before we begin if you notice any spelling errors please tell me or correct me. Would be very appreciated secondly: I know everyone on this site is very respectful to others but I still always feel the need to say this.
This is a very personal thing to me. People used to make fun of me for it or would stop speaking to me after knowing about my pdd-nos. This got to the point where I started to get a depression. Because of this I just wanna ask you to still respect me and not view me as any different as that your used to. I’m really not that different and really not a danger to anyone.
I thought that it would be nice to start a topic about pdd nos.
Your probably wondering: pdd-nos? What is that?
Well pdd-nos ( stands for Pervasive Development Disorder Not Otherwise Specified) it means on the autism spectrum but it does not fall within any of the other existing categories.
This short video explains it perfectly:
My life with pdd-nos:
Pdd-nos has a big impact on my life and still does till this day. When I was diagnosed with pdd-nos a lot changed in my life. I had to change schools because my old school couldn’t give me the care that I needed. I had to go to a special primary school. In those school there were children who had dyslexcia, adhd and more. Because I was diagnosed with pdd-nos a lot of people like to either make fun of me or treath me like someone who can’t do anything or won’t make it far in life. I used to have a lot of anger issues and had to use medication to calm myself down. I have trouble with unexpected new things. For example if we went on a school trip instead of just normal school I would feel very scared and could get very angry. Things like that are still very hard for me. I just can’t handle unexpected changes in my day to day schedules. I did manage to control my anger issues a lot more. my head is also always busy so I get tired pretty easily. I have trouble interacting with other people. I sometimes am unable to control myself so I will not be able to control my hands or feet but this is really rare. It only happens if I haven’t been able to walk around or move all day.
I have one more link with more information about pdd-nos that can explain things way better then I do:
https://www.autismspeaks.org/pervasive-developmental-disorder-pdd-nos
If you would like to know more about any of this you can always ask me any questions.
But now I have a question for you: is there anyone else with pdd-nos here?