A look at the true importance of gaming for people with chronic pain.

  • stopthatgirl7@kbin.socialOP
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    1 year ago

    Yeah, I’ve got EDS, and gaming is one of the few things I can do and not risk being too much in pain (I do have to watch out for my fingers spraining and dislocating, though). Days when I can’t walk very well, I can still sit down and play a game.

    • GONADS125@lemmy.world
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      1 year ago

      EDS is what my last provider mentioned might be a better diagnosis. The joint symptoms fit, but I definitely don’t have the skin or blood cell issues that can present in EDS. Which I’m definitely grateful of.

      • stopthatgirl7@kbin.socialOP
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        1 year ago

        Well, there are thirteen different types of EDS (most of them are REALLY rare, though), based on which connective tissue they impact the most. The most common are hypermobile, classical, and vascular. I have the hypermobile type, which mostly impacts joints. Classical EDS can have skin issues, and vascular is the type where it can cause your blood vessels to rip open inside of you. hEDS is the least likely to kill you, but most likely to negative impact your quality of life.

        https://www.nhs.uk/conditions/ehlers-danlos-syndromes/

    • BD1sHappyFeet@lemm.ee
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      1 year ago

      I never thought about it like that, but that explains why I played through Borderlands 2 over and over again while doing chemo. Everything hurt but I could still mow down some baddies.