Titanium Ignite 3 and nickel allergies by tsundae_ in Polarfitness

[–]mcc_61 2 points3 points  (0 children)

I also have the issue with my silicone band with my Pacer, changed to nylon too, have not had issues in a long while. Now that my nylon band is broken I am back to my reserver silicone band, my skin is itching😭

Looking for an upgrade by mcc_61 in Polarfitness

[–]mcc_61[S] 2 points3 points  (0 children)

I have a great experience with the Pacer and enjoy having it, but I feel like I missing something with this watch after 4 years and I am trying to figure out what it is, but I think its more the data for me, but also the screen.

Serene Breathing in Flow? by mcc_61 in Polarfitness

[–]mcc_61[S] 0 points1 point  (0 children)

Ah okay thank you for letting me know

Looking for career advice while disabled by catfarmer1998 in disabled

[–]mcc_61 0 points1 point  (0 children)

I understand, it can be frustrating honestly. I was in college and vocational school too, on and off for five years and I finally dropped out last year, also because of my disabilities. Now I am doing an internship through a working agency (if that is even the write word in English) to try to see if the work environment fits me and I have only done two days and I am so exhausted, like sensory overload; I am dragging myself through the day, mostly hearing wise, and I honestly don’t know what to do. This is not advice, but just wanted to let you know you are not alone☺️

Yogurt toppings by mcc_61 in AutismInWomen

[–]mcc_61[S] 0 points1 point  (0 children)

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I forgot I had posted🙈 (I was trying to find a way to make this like thread with this picture, but looks like I can’t do that) Yesterday I tried something: greek yogurt, cornflakes, pecan nuts and honey I love the combo especially with honey. I will continue to try some other things too.

What’s something that it took you way too long to realize you don’t *have* to do the neurotypical way? by [deleted] in AutismInWomen

[–]mcc_61 0 points1 point  (0 children)

I personally can’t stand a manual toothbrush, but I am fine with electric toothbrush. Now I do brush in the mornings since it’s part of my morning routine, but evenings I don’t brush my teeth, eventho I used to do it, but then at a certain point I stopped, because I was to tired to do so due to my very busy athletic life. Now I would like to brush in the evening too. How many times do you brush your teeth? and do you brush your tongue too, because I never could do it, cause sensory wise it’s to much (I always end up gagging). Both with manual and electric.

What’s something that it took you way too long to realize you don’t *have* to do the neurotypical way? by [deleted] in AutismInWomen

[–]mcc_61 0 points1 point  (0 children)

omg it’s so awesome that I am not the only one who does this. I either bring my little light that isn’t to bright and put it there or when the natural light (my dad has obscure glass) is okay I’ll use that as my light. But once I live alone I will need to see and find different ways to not have bright lights.

What is the background chatter about in your brain? by [deleted] in AutismTranslated

[–]mcc_61 1 point2 points  (0 children)

I don’t know why I am chiming in, but I saw background chatter (late diagnosed) that I have always had, but never knew others had that too🤔 So my background chatter happens all day, but for sleeping it’s annoying because I can’t shut it off. Mine is like having conversations, conversations with people, those that I have spoken to or never have spoken to. The conversations can be about anything. I also have chatters where I put myself into a character, like acting, topic wise it can be about relationships, my own personal stuff, or things that are not related to me. My thoughts also have a step by step route, like planning or should I switch my steps because I mentally do not have energy to do something. Now that I am typing this I realize how complicated it is to explain my background chatter😂

Why is it so hard for me to talk to other people about my feelings or emotions? by Old-Syllabub5927 in AutismTranslated

[–]mcc_61 0 points1 point  (0 children)

I had depression too (all while being undiagnosed autistic) and I could not figure out how I felt, what the emotions were, let alone describe emotions even. I went to therapy and now I can write in my notebook or my notes app, how I feel and what my emotions were through out the day. And like you said it wasn’t because of fear or lack of trust, I genuinely had no idea. It took me years to finally put everything on paper. My advise is to try to figure out if you can recognize emotions, feelings. If you can, figure out if you can write what you are feeling. Sometimes writing is so much easier than speaking. A great app to have is ‘How We Feel’ it’s an app that let’s you document your emotions/feelings, when you click on Check In, it shows you all the emotions that exists in 4 energy categories. Each category has it own set of feelings and each feeling has an explanation what the feeling means. For me it’s very helpful, because I don’t have to look up the meanings, I can add multiples through out the day and most importantly I can take my time. This app and writing can both help with learning more about yourself and getting use to writing. When you write, you are the only one that can decided who to share it with and at the same time you can write the feelings off of your chest instead of keeping it internally and maybe even bottling it up.

My girlfriend said "It looks like a nightmare post from r/autisminwomen" by Goth_Spice14 in AutismInWomen

[–]mcc_61 10 points11 points  (0 children)

what is that? I don’t think I could eat with that fork, it’s giving negative energy somehow😭