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Has anyone actually ever found a “root cause” to their 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. Learn more at [Dysautonomia International](http://www.dysautonomiainternational.org/page.php?ID=30)

Post shower weakness

Dysautonomia is an umbrella term for conditions in which the autonomic nervous system malfunctions.

Oxaloacetate benefits time

For research, treatments, and personal stories regarding Chronic Fatigue Syndrome (CFS)/Myalgic Encephalomyelitis (ME). ME/CFS is a multi-systemic neurological disease, distinct from chronic fatigue as a symptom. For more information, please see our FAQ.

Burning hot swollen hands

Dysautonomia is an umbrella term for conditions in which the autonomic nervous system malfunctions.

Burning hot swollen hands

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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.

Success stories in treating Mcas and pots

For research, treatments, and personal stories regarding Chronic Fatigue Syndrome (CFS)/Myalgic Encephalomyelitis (ME). ME/CFS is a multi-systemic neurological disease, distinct from chronic fatigue as a symptom. For more information, please see our FAQ.

Lost some faith in sleep accuracy

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A forum for discussion of all Fitbit-related products. Come ask questions, encourage/challenge others, and join a community making steps towards their goals.

Too high a dose on LDN experience

For research, treatments, and personal stories regarding Chronic Fatigue Syndrome (CFS)/Myalgic Encephalomyelitis (ME). ME/CFS is a multi-systemic neurological disease, distinct from chronic fatigue as a symptom. For more information, please see our FAQ.

BARD1

r/breastcancer is a support and information group for people who have been diagnosed with breast cancer.

No appetite + grass eating

Sick pet? r/vet. Welcome to your online veterinary information line. Office visits add up, and even consultations with veterinarians can cost you thousands annually. We all love our pets, but some people just don't have that continual access to care for their pets in order to guarantee them a safe, healthy life. We don't want to see you endure unnecessary heartache! This is a place you can consult professionals. Let's keep your animals healthy!

Flu symptoms

Low Dose Naltrexone has been shown to have amazing anti-inflammatory properties. It has helped people neutralize and cure everything from crohn's, MS, allergies, cancer and more... Lots of information can be found here: Low dose Naltrexone (LDN) for chronic illness & infections…. https://www.facebook.com/groups/108424385861883

Visible App x LDN

For research, treatments, and personal stories regarding Chronic Fatigue Syndrome (CFS)/Myalgic Encephalomyelitis (ME). ME/CFS is a multi-systemic neurological disease, distinct from chronic fatigue as a symptom. For more information, please see our FAQ.

What was your acceptance journey

For research, treatments, and personal stories regarding Chronic Fatigue Syndrome (CFS)/Myalgic Encephalomyelitis (ME). ME/CFS is a multi-systemic neurological disease, distinct from chronic fatigue as a symptom. For more information, please see our FAQ.

Does anyone live in New York/ Brooklyn?

For research, treatments, and personal stories regarding Chronic Fatigue Syndrome (CFS)/Myalgic Encephalomyelitis (ME). ME/CFS is a multi-systemic neurological disease, distinct from chronic fatigue as a symptom. For more information, please see our FAQ.

Can PEM come prior to 24hrs later

For research, treatments, and personal stories regarding Chronic Fatigue Syndrome (CFS)/Myalgic Encephalomyelitis (ME). ME/CFS is a multi-systemic neurological disease, distinct from chronic fatigue as a symptom. For more information, please see our FAQ.

Mild folks how do you prep before socializing?

For research, treatments, and personal stories regarding Chronic Fatigue Syndrome (CFS)/Myalgic Encephalomyelitis (ME). ME/CFS is a multi-systemic neurological disease, distinct from chronic fatigue as a symptom. For more information, please see our FAQ.

Got the harsh truth finally !

For research, treatments, and personal stories regarding Chronic Fatigue Syndrome (CFS)/Myalgic Encephalomyelitis (ME). ME/CFS is a multi-systemic neurological disease, distinct from chronic fatigue as a symptom. For more information, please see our FAQ.

Anyone found infectious disease helpful?

For research, treatments, and personal stories regarding Chronic Fatigue Syndrome (CFS)/Myalgic Encephalomyelitis (ME). ME/CFS is a multi-systemic neurological disease, distinct from chronic fatigue as a symptom. For more information, please see our FAQ.

Experience with stranger reactive / protective dog?

We are a community for people that own reactive dogs! We support the LIMA (Least Intrusive, Minimally Aversive) approach to dog training. The tips and advice here cannot replace a qualified certified trainer or veterinary behaviorist - if you are struggling please consider these resources for your dog. Everyone is welcome. A reactive dog is not required to join, but please keep discussions and posts focused on dog reactivity.

Anyone got positive ANA or rheumatoid factor?

For research, treatments, and personal stories regarding Chronic Fatigue Syndrome (CFS)/Myalgic Encephalomyelitis (ME). ME/CFS is a multi-systemic neurological disease, distinct from chronic fatigue as a symptom. For more information, please see our FAQ.

Anyone out there never the same after mono?

Discussion for everything related to the Epstein-Barr Virus

Vitamin c malabsorption

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3-oxoglutaric, succinic, phosphoric results

A subreddit dedicated to discussing Functional Medicine. This sub attempts mirror /r/Medicine in allowable content, while not being quite as highly moderated. Looking for a practitioner in your area? Try: https://www.ifm.org/find-a-practitioner/

Could use support

For research, treatments, and personal stories regarding Chronic Fatigue Syndrome (CFS)/Myalgic Encephalomyelitis (ME). ME/CFS is a multi-systemic neurological disease, distinct from chronic fatigue as a symptom. For more information, please see our FAQ.

Do high Mononucleosis antibody counts mean a worse case?

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