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Has anyone with HSD or EDS gotten dry needling? Could you tell me about your experience? I’m really scared of both the pain and the risk of my muscles relaxing /too/ much.
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Anonymous 5d

i wouldn’t risk anyone putting needles into me unnecessarily

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Anonymous 5d

I have, and it helped for a bit, but it would only give me a couple hours of relief before the pain was back

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Anonymous 3d

a pt actually told me not to bc the muscles in my neck are so screwed up that if we were to do dry needling/acupuncture it might just push the tension higher and make my migraines worse 😃

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Anonymous 4d

To #3 dry needling does actually have scientific basis :) Chiropracty does not

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Anonymous replying to -> #1 5d

I’m assuming you don’t have EDS or HSD

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Anonymous replying to -> #1 5d

Would you say someone with an illness who needs IV treatment is getting needles put into them “unnecessarily”

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Anonymous replying to -> #2 5d

Thank you! How bad did it hurt to get done?

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Anonymous 5d

Yeah you clearly don’t have EDS or HSD so kindly screw off ☺️ And no it is exactly the same babes. Do you think people with POTS who get saline treatments are sticking needles into themselves “unnecessarily”?

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Anonymous 4d

Adding onto this about risk of injection. To me it doesn’t sound any more legit than chiropractics, and I do have EDS, along with other chronic pain conditions

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Anonymous replying to -> OP 4d

Not really, honestly. It just felt like small pinches. A few pinches hurt a tiny bit more than others, but nothing really bad Granted, I have a pretty high pain tolerance, so I would take my words with some salt

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Anonymous replying to -> #4 3d

Oh no! My PTs have all suggested I do it but I’m scared lol

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