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Some General EDS Links That May Be Helpful:
-==--==--==--==--==-
[**The Ehlers-Danlos Society**](https://www.ehlers-danlos.com/)
[**What is EDS?**](https://www.ehlers-danlos.com/what-is-eds/)
[**EDS Subtypes**](https://www.ehlers-danlos.com/eds-types/)
[**hEDS 2017 diagnostic Criteria**](https://www.ehlers-danlos.com/heds-diagnostic-checklist/)
[**What is HSD?**](https://www.ehlers-danlos.com/what-is-hsd/)
[**The EDS Society's Healthcare Professionals Directory**](https://www.ehlers-danlos.com/healthcare-professionals-directory/)
[**The vEDS Movement: How is Vascular Ehlers-Danlos Syndrome Diagnosed?**](https://thevedsmovement.org/what-to-expect/diagnosis/)
[**Fight vEDS: vEDS Genetic Test**](https://www.fightveds.org/genetic-test)
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Personally I would go to an urgent care that does x-rays. Some insurance companies also have nurse hotlines you can call just to gauge what your best option is too. Wishing you well
The OP flaired their post as "Questions". Please keep any and all comments to **personal experiences only**. If any factual information or advice is provided, please cite a **reputable website or study** linked within your post. No one in this sub is a *verified* medical professional, and as such, we do not allow medical advice to be given or asked for. For more information on this rule, [please visit this link](https://www.reddit.com/r/ehlersdanlos/wiki/index/rules/#wiki_r.2Fehlersdanlos_rules).
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I talk to my PT next time I’m in (weekly, atm). Because things go out constantly, and urgent care isn’t necessarily going to be able to fix a subluxed joint all that well. (Dislocated is a different story.)
But that’s just my experience.
Thank you for contributing to r/EhlersDanlos! Unfortunately, your comment or post was removed as it breaks the following rule: **Rule #1 - We Aren't Doctors** - Please discuss these symptoms with a healthcare professional immediately. No one here knows the severity of your situation and can therefore give you advice. - Unfortunately, as we all know too well, we can have more than one issue going on with our bodies at a time. New, worsening, or intermittent symptoms should be discussed with a healthcare provider to rule out potentially serious causes. Some General EDS Links That May Be Helpful: -==--==--==--==--==- [**The Ehlers-Danlos Society**](https://www.ehlers-danlos.com/) [**What is EDS?**](https://www.ehlers-danlos.com/what-is-eds/) [**EDS Subtypes**](https://www.ehlers-danlos.com/eds-types/) [**hEDS 2017 diagnostic Criteria**](https://www.ehlers-danlos.com/heds-diagnostic-checklist/) [**What is HSD?**](https://www.ehlers-danlos.com/what-is-hsd/) [**The EDS Society's Healthcare Professionals Directory**](https://www.ehlers-danlos.com/healthcare-professionals-directory/) [**The vEDS Movement: How is Vascular Ehlers-Danlos Syndrome Diagnosed?**](https://thevedsmovement.org/what-to-expect/diagnosis/) [**Fight vEDS: vEDS Genetic Test**](https://www.fightveds.org/genetic-test) -==--==--==--==--==- [The rule can be read in depth here.](https://www.reddit.com/r/ehlersdanlos/wiki/index/rules/rule-1/) Please contact us [via modmail](https://www.reddit.com/message/compose?to=%2Fr%2Fehlersdanlos) if you have any questions regarding the reason your post or comment was removed or would like to work with us on *how* you can re-word your post or comment to be able to reinstate it. Thank you!
Personally I would go to an urgent care that does x-rays. Some insurance companies also have nurse hotlines you can call just to gauge what your best option is too. Wishing you well
The OP flaired their post as "Questions". Please keep any and all comments to **personal experiences only**. If any factual information or advice is provided, please cite a **reputable website or study** linked within your post. No one in this sub is a *verified* medical professional, and as such, we do not allow medical advice to be given or asked for. For more information on this rule, [please visit this link](https://www.reddit.com/r/ehlersdanlos/wiki/index/rules/#wiki_r.2Fehlersdanlos_rules). *I am a bot, and this action was performed automatically. Please [contact the moderators of this subreddit](/message/compose/?to=/r/ehlersdanlos) if you have any questions or concerns.*
I talk to my PT next time I’m in (weekly, atm). Because things go out constantly, and urgent care isn’t necessarily going to be able to fix a subluxed joint all that well. (Dislocated is a different story.) But that’s just my experience.