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Citizenship by descent

The official English language subreddit for Poland and Polish news. Questions get answered, recommendations get recommended, and - you know - things get done.

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AITAH if I leave my partner for being so negative

This is a community like r/AmITheAsshole, except unlike that subreddit, you can post interpersonal conflicts. Anything that's AITA, including relationships, hypotheticals, and would I be the asshole (wibta) posts are allowed. AI scenarios/posts are not welcome or tolerated. An elaboration on our rules can be found here: https://www.reddit.com/r/AITAH/wiki/index

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IV rehydration options

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/fwQN2A4c2n

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Incident report written about me

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Buying my first Vespa

/r/moped, or mopeddit, is for discussion and celebration of vintage mopeds on Reddit. We ride mostly 1970s pedal-equipped two-stroke models, such as those manufactured by Puch, Motobécane, Peugeot, Tomos, Garelli, Sachs, Kreidler, etc. Post pictures, ask questions, find your local gang, and share knowledge.

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Endoscopy RN

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School nursing

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What interview questions should you expect for an intake RN position?

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Where do you experience myotonia and what does it feel like?

This is a home for all Myotonic Redditors off all types.

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You know that moment when you’re smoking 🍃 and you take a hit and realize “this was one hit too many”. What happens to you after that?

r/AskReddit is the place to ask and answer thought-provoking questions.

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What’s your experience

This is a home for all Myotonic Redditors off all types.

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Stiff neck

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/fwQN2A4c2n

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Accommodations

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/fwQN2A4c2n

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Accommodations

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So frustrated

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/fwQN2A4c2n

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So frustrated

A sub all about chairs on wheels. Here you can discuss your wheelchair, experiences, anecdotes and sob stories, purchase tips, wheelchair sports, accessibility concerns, pitfalls, tips, pictures, wheelchair concepts, travel advice, etc.

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Wheelchair assessment referral

A sub all about chairs on wheels. Here you can discuss your wheelchair, experiences, anecdotes and sob stories, purchase tips, wheelchair sports, accessibility concerns, pitfalls, tips, pictures, wheelchair concepts, travel advice, etc.

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Overwhelmed and need advice

Ehlers Danlos Syndrome (EDS) is a underdiagnosed connective tissue disorder characterized by a genetic fault in collagen. It manifests as hypermobile joints and affects every organ system because we’re all made of connective tissue! We welcome all EDS subtypes, hypermobility spectrum disorder, Loeys Dietz, unnamed genetic disorders that present like EDS, self-diagnosed & suspected zebras. || || || Crowdsourced medical care saves lives. We welcome medical advice!

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Disabled nurse requesting advice

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Facebook & zoom group for NYC zebras

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/fwQN2A4c2n