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My mom is so confident she can judge how I feel, and how to fix things, that I rarely see a doctor. I haven't been diagnosed with anything other than temporary things like the flu. If I tell her I think something is wrong, she either doesn't take me seriously or blames it on small diet changes or recent activity. What is my family's explanation on why I act the way I do? They have to at least be confused. I'm afraid my constant effort to be normal is actually bad- because people might not believe me.
I think I have: Asperger's, had depression, general anxiety, and the worst- IBS. IBS really ruins things. I probably have other things that I don't understand yet.
I struggle to comprehend a page of words, and since elementary school have no math skills. I'm confused as to why no-one's helped me with ANY problem described above.... I feel so screwed.... This is the true source of all my problems, I'm realizing. I'm scared to say anything for some reason. Not sure what to do.
Oh and I am also in the midst of being tested for celiac diesie which my gastro Doctor and my dietician think I have since my blood test are positive and exhibit symptoms of a form of it (apparently not the typical one, go figure).The usual such as dyspraxia, dyslexia, ADHD and anxiety. (When I seee usual I mean the conditions lot of people with autism also have).
I have also have ehlers danlos, ataxia,hypertonic, vasa vagual issues, POTS and eplilsy although that might be changed to a non epileptic seizure disorder.
So is mine and it can't seem to make it any higher.I was told last week that my blood pressure is too low.
What are your special clothes like I have to wear special boots and multi braces to stop my constant dislocations.Well, aside from the usual anxiety-depression combo, I have Ehlers-Danlos syndrom as well, like ZebraAspie. There seems to be a correlation between ASD and EDS, but because EDS is not very well-known, the cause for the correlation hasn't been found yet. It is a genetic disorder.
Anyways, it comes with the same sensory issues than autism, especially regarding touch, light and sounds --definitely doesn't help with my misophonia.
As an added bonus, EDS brings muscle hypotonia, chronic pain, frequent sprains and tendinitis, very dry eyes, cysts that keep on forming everywhere, migraines and irritable bowel syndrom, along with low blood pressure and POTS, which is basically a mix of tachycardia and lower blood pressure that makes you dizzy every time you change posture.
But: I get to wear special clothes to keep my joints in place, it's like the superhero suit for "SuperSensory Girl".
Hey ZebraAspie,What are your special clothes like I have to wear special boots and multi braces to stop my constant dislocations.
Thats super cool thanks for the picture. I'm not sure how i'd feel abou wearing one tightness upsets my EDS skin.Hey ZebraAspie,
I'm not sure what is the exact term they would be called in English, because I got them in France, but it's contention clothing, as is used for people who suffered severe burns. They help with proprioception and with muscle contractions, so on top of not dislocating my joints all the time, I don't bump into doors, walls and furniture quite as often. They are not manufactured in series, but made to my exact measurements. I have hypermobile-type EDS.
A possible downside to consider is that the clothes are very tight (think head-to-toe Spanx), and I don't know how you feel about tight clothing. Personally, the pressure it exerts helps even with AS, but sometimes even I can't stand being covered in rigid spandex. Overall, I still think they're a good thing to use.
For some reason, the picture I found via Google will not upload, so I'll try again later. Is it OK if I send it to you?
I know the bottom part of the "suit" can go until mid-thigh only for those with better knees. I got pants that stop at the ankle, though. As for the top, mine stops below the shoulder, and then I have sleeves I can add for my elbows. I didn't want socks made, though, that I couldn't stand wearing.
I do have braces to wear at night instead of the suit, but they're bulky and hurt a little.