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Since my EDS has started getting worse, I had to quit my last job because of the pain and physical requirements. I see a lot of people on here recommending working from home but idk any computer jobs I'd actually enjoyđ working at a desk has never been for me, I love doing physical work. But now that I can't, I just feel depressed and I don't know what I can do for work anymore. Does anyone else have a similar problem?
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Ehlers-Danlos Syndrome (EDS)
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One person mentioned working as a home health worker, which doesn't involve much moving around. Another person found success working at the front desk of an urgent care center, which mostly involves sitting. Some people have managed to work part-time or full-time remotely, even with conditions like EDS and POTS. However, it's important to note that everyone's situation is different, and what works for one person might not work for another.
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