Question:
This is a support sub for those with Ehlers-Danlos syndrome (all types) and HSD—diagnosed or waiting to be diagnosed. This is a welcoming place for those affected (or those simply wanting to learn more) to ask questions, share successes and failures, feel less alone, and discuss everyday life. Before participating, please read our rules. This subreddit does not allow medical advice. Thank you! _._._._._ Feedback Forms: https://www.reddit.com/r/ehlersdanlos/s/fwQN2A4c2nHow to you guys go about getting your braces for Hypermobile EDS
This is a support sub for those with Ehlers-Danlos syndrome (all types) and HSD—diagnosed or waiting to be diagnosed. This is a welcoming place for those affected (or those simply wanting to learn more) to ask questions, share successes and failures, feel less alone, and discuss everyday life. Before participating, please read our rules. This subreddit does not allow medical advice. Thank you! _._._._._ Feedback Forms: https://www.reddit.com/r/ehlersdanlos/s/fwQN2A4c2nGot my first brace to protect my wrist only to find out I already have a sprain:
This is a support sub for those with Ehlers-Danlos syndrome (all types) and HSD—diagnosed or waiting to be diagnosed. This is a welcoming place for those affected (or those simply wanting to learn more) to ask questions, share successes and failures, feel less alone, and discuss everyday life. Before participating, please read our rules. This subreddit does not allow medical advice. Thank you! _._._._._ Feedback Forms: https://www.reddit.com/r/ehlersdanlos/s/fwQN2A4c2nCan you be hyper mobile in certain areas if you have EDS, but not others?
This is a support sub for those with Ehlers-Danlos syndrome (all types) and HSD—diagnosed or waiting to be diagnosed. This is a welcoming place for those affected (or those simply wanting to learn more) to ask questions, share successes and failures, feel less alone, and discuss everyday life. Before participating, please read our rules. This subreddit does not allow medical advice. Thank you! _._._._._ Feedback Forms: https://www.reddit.com/r/ehlersdanlos/s/fwQN2A4c2nHow To Navigate Working A Hot And Humid Craft Fair With Pots:
Postural Orthostatic Tachycardia Syndrome (POTS) is a form of dysautonomia that is estimated to impact between 1,000,000 and 3,000,000 Americans, and millions more around the world. POTS is a form of orthostatic intolerance that is associated with the presence of excessive tachycardia and many other symptoms upon standing.Not Sure What To Do:
Welcome to our supportive Peer-Support community, where we come together to share our experiences with Bipolar Disorder. We are a haven for people with Bipolar Disorder (including Cyclothymia and Schizoaffective Disorder) and those on their journey towards a diagnosis to discuss Bipolar-related issues; a community, not just a help page. Be a part of something that cares about who you are. Join us in our discussions, share your story, and let's support each other.How do I put up a party poster without damaging the restaurant’s wall?
A place to get help planning your upcoming party, share ideas and tips, post party photos, and more!Hurt my wrists and arm getting out of a pool. Still undiagnosed. pending a Dr’s apt. Does it get better? And how can I prevent this in the future?
This is a support sub for those with Ehlers-Danlos syndrome (all types) and HSD—diagnosed or waiting to be diagnosed. This is a welcoming place for those affected (or those simply wanting to learn more) to ask questions, share successes and failures, feel less alone, and discuss everyday life. Before participating, please read our rules. This subreddit does not allow medical advice. Thank you! _._._._._ Feedback Forms: https://www.reddit.com/r/ehlersdanlos/s/fwQN2A4c2nGoing To A Rheumatologist Next Month For a Hypermobile EDS diagnosis. What can I expect?
This is a support sub for those with Ehlers-Danlos syndrome (all types) and HSD—diagnosed or waiting to be diagnosed. This is a welcoming place for those affected (or those simply wanting to learn more) to ask questions, share successes and failures, feel less alone, and discuss everyday life. Before participating, please read our rules. This subreddit does not allow medical advice. Thank you! _._._._._ Feedback Forms: https://www.reddit.com/r/ehlersdanlos/s/fwQN2A4c2nIt’s been suggested I might have EDS. Just wondering what to do at this point:
This is a support sub for those with Ehlers-Danlos syndrome (all types) and HSD—diagnosed or waiting to be diagnosed. This is a welcoming place for those affected (or those simply wanting to learn more) to ask questions, share successes and failures, feel less alone, and discuss everyday life. Before participating, please read our rules. This subreddit does not allow medical advice. Thank you! _._._._._ Feedback Forms: https://www.reddit.com/r/ehlersdanlos/s/fwQN2A4c2nJust saw this ad for a Ren Faire in Carrolton, Tx and am wondering if it’s worth going to

Welcome! This is a subreddit to talk about Renaissance Faires and Festivals. Discuss upcoming events, ren faire-related news, costume ideas, acts, guilds or just ask questions. Actors, guilds, clubs, promoters and fans are all welcome. Huzzah!
Birthday Party Questions:
This subreddit is the place for anything related to the Dave & Buster's restaurant/arcade chain, with a focus on strategies for winning and profiting from their redemption games. All D&B-related posts are welcome!Need party theme ideas:
A place to get help planning your upcoming party, share ideas and tips, post party photos, and more!How much would you charge for these?

Get the low down on craft fairs, festivals and markets for you to participate in or shop at! Shop small, shop local, support handmade business!