Understanding Aspies: The Cost of Masking

As of the moment, we are currently in the third week of the #TakeTheMaskOff Challenge, and the experience of writing about masking and stimming has been quite liberating for me, and it is also interesting to see how far I’ve come from when I myself didn’t understand my own diagnosis and myself, and I hope that these posts, which talk about masking from my own personal point of view, will allow the readers to understand what we go through, and at the same time, I hope that others like me are encouraged to speak out and make their own voices heard. So far we have talked about masking and stimming. So, for the third week of the challenge, let’s take a look at the physical and mental cost that masking has on individuals with autism, my own personal experience of how exhausting it can be, and what coping strategies I use now in order to lessen the physical and mental exhaustion and stress.

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Understanding Aspies: Stimming & Masking

This week’s blog posts are a little bit different, as I posted twice for this week. However, that was only because I had a little “social report” that went hand in hand with a very recent event, and you might see “social reports” like that every once in a while, but, as a rule, I’m sticking to  the current schedule of having one blog post per week.

Last time, I kicked off the #TakeTheMaskOff Challenge here on my blog, and talked a little bit about masking and my own experience of masking. This week (Week 2 of the challenge), we’ll be talking about stimming, how it’s related to masking, and my own experience of stimming.

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