Books influencing the “voice” of your inner monologue
The sister sub of r/CasualConversation. The serious side of Reddit. r/SeriousConversation is a subreddit for in-depth discussion. Offer a theory, share an opinion, or pose a question about (almost) any serious or heavier topics you can think of. This subreddit **is not** for venting about yourself.
Taking on the narrator/author’s voice?
This is a moderated subreddit. It is our intent and purpose to foster and encourage in-depth discussion about all things related to books, authors, genres, or publishing in a safe, supportive environment. If you're looking for help with a personal book recommendation, consult our Weekly Recommendation Thread, Suggested Reading page, or ask in r/suggestmeabook.
Ate a trigger food, feeling awful. What can I do to mitigate things at this point?
A science-focused sub for Mast Cell Activation Disorders. Please note: The content on this subreddit is not intended as, and is not a substitute for, medical advice or diagnosis. It must not be interpreted as such. You are strongly advised to consult your own qualified healthcare professionals for any medical questions or concerns.
Another POTs/heart rate question: spike is like 20 bpm, but stays up?
Dysautonomia is an umbrella term for conditions in which the autonomic nervous system malfunctions.
80s early chapter book, boy and girl build a model castle then shrink/time travel
Can't remember the title of the book you've enjoyed reading? Crowdsource it to readers on Reddit!
Today I ate food and still don’t feel like crap! Please applaud 👏
A science-focused sub for Mast Cell Activation Disorders. Please note: The content on this subreddit is not intended as, and is not a substitute for, medical advice or diagnosis. It must not be interpreted as such. You are strongly advised to consult your own qualified healthcare professionals for any medical questions or concerns.
Cystoscopy looks great! Umm, now what?
A place for sufferers of the chronic bladder disease interstitial cystitis (IC; also known as painful bladder syndrome or PBS) to share advice, give support, ask questions, and give answers.
Migraine/IC/MCAS relationship?
A science-focused sub for Mast Cell Activation Disorders. Please note: The content on this subreddit is not intended as, and is not a substitute for, medical advice or diagnosis. It must not be interpreted as such. You are strongly advised to consult your own qualified healthcare professionals for any medical questions or concerns.
Triggers: does quantity over time matter?
A place for sufferers of the chronic bladder disease interstitial cystitis (IC; also known as painful bladder syndrome or PBS) to share advice, give support, ask questions, and give answers.
Quercetin not ok for hypothyroidism apparently?
A place for sufferers of the chronic bladder disease interstitial cystitis (IC; also known as painful bladder syndrome or PBS) to share advice, give support, ask questions, and give answers.
Advice for a newbie on getting some relief while sorting out official diagnosis?
A place for sufferers of the chronic bladder disease interstitial cystitis (IC; also known as painful bladder syndrome or PBS) to share advice, give support, ask questions, and give answers.
Ocular migraine without pain/nausea/etc?
A community of headache disease sufferers. Whether migraines, cluster headaches, or whatever head pain you experience. We support each other, and spread knowledge about our various conditions.
Delayed poop - what is this called/what is the mechanism?
A science-focused sub for Mast Cell Activation Disorders. Please note: The content on this subreddit is not intended as, and is not a substitute for, medical advice or diagnosis. It must not be interpreted as such. You are strongly advised to consult your own qualified healthcare professionals for any medical questions or concerns.
Post cath procedure pain, praying it’s not becoming another CRPS pain site
Official subreddit for Complex Regional Pain Syndrome. Nothing in this forum should be taken as professional medical advice. If you are seeking personalized care, please contact your physician. If you are a medical professional and would like to be verified by the mod team, we will provide you with a specialized user flair for your profession in the near future.
I thought this was normal before MCAS
A science-focused sub for Mast Cell Activation Disorders. Please note: The content on this subreddit is not intended as, and is not a substitute for, medical advice or diagnosis. It must not be interpreted as such. You are strongly advised to consult your own qualified healthcare professionals for any medical questions or concerns.
Curious: changing triggers over the years?
A science-focused sub for Mast Cell Activation Disorders. Please note: The content on this subreddit is not intended as, and is not a substitute for, medical advice or diagnosis. It must not be interpreted as such. You are strongly advised to consult your own qualified healthcare professionals for any medical questions or concerns.
Skin reaction to something I’ve used a million times before!
A science-focused sub for Mast Cell Activation Disorders. Please note: The content on this subreddit is not intended as, and is not a substitute for, medical advice or diagnosis. It must not be interpreted as such. You are strongly advised to consult your own qualified healthcare professionals for any medical questions or concerns.
OTC trial - one day off triggers symptoms?
A science-focused sub for Mast Cell Activation Disorders. Please note: The content on this subreddit is not intended as, and is not a substitute for, medical advice or diagnosis. It must not be interpreted as such. You are strongly advised to consult your own qualified healthcare professionals for any medical questions or concerns.
EDS and congenital heart defects?
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
What’s the best type of dr for MCAS?
A science-focused sub for Mast Cell Activation Disorders. Please note: The content on this subreddit is not intended as, and is not a substitute for, medical advice or diagnosis. It must not be interpreted as such. You are strongly advised to consult your own qualified healthcare professionals for any medical questions or concerns.
Help Reading for 6th grader
We're an inclusive, disability-oriented peer support group for people with ADHD with an emphasis on science-backed information. Share your stories, struggles, and non-medication strategies. Nearly two million users say they 'feel at home' and 'finally found a place where people understand them'.
The jaw bone’s connected to the…rib bone?
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
Episodic pain - meloxicam?
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
Horseshoe of raised patches?
**Welcome to /r/DermatologyQuestions!** Got a rash, bump, or skin concern? Ask here. Get support and insights from the community. Please remember, this is not a substitute for professional medical advice.
Eczema + droopy face + migraine and period
A community of headache disease sufferers. Whether migraines, cluster headaches, or whatever head pain you experience. We support each other, and spread knowledge about our various conditions.
