First signs of GB
/r/guillainbarre is a small, welcoming community for those who have survived or are currently battling Guillain Barre Syndrome or Chronic Inflammatory Demyelinating Polyneuropathy, the family/friends of patients and survivors, and for those curious about the disease. We welcome anything related to GBS/CIDP: questions, insightful articles or news, stories about experiences or just general ranting (because, let's be honest, sometimes it sucks!). Feel free to grab a flair and share (or vent!) away.
No pain but “signal dropping out” in hands
Free-form non-commercial discussion of Carpal Tunnel Syndrome (CTS). Identifying and relieving the symptoms of CTS, and the types of Carpal Tunnel Release (CTR) surgeries available today. Post-op and non-op/mitigating experiences especially welcomed.
I treated one side with my arthroscopy. Now, for the first time, my left side is having major problems.
A place for TMJD sufferers to share their fears, worries, stories and successes. We are not Drs. We cannot diagnose you. If you are concerned please see a Dr rather than consult the internet! No advertising, fundraisers or pyramid scheme invites. No medical professionals. This isn’t a place to advertise your practise or sell your profession! Please be kind. We are all in this together and whilst you may not agree with what the other person says, they are still a fellow sufferer and person.
Bone on bone pain
A place for TMJD sufferers to share their fears, worries, stories and successes. We are not Drs. We cannot diagnose you. If you are concerned please see a Dr rather than consult the internet! No advertising, fundraisers or pyramid scheme invites. No medical professionals. This isn’t a place to advertise your practise or sell your profession! Please be kind. We are all in this together and whilst you may not agree with what the other person says, they are still a fellow sufferer and person.
What was the final sign you needed a TJR?
A place for TMJD sufferers to share their fears, worries, stories and successes. We are not Drs. We cannot diagnose you. If you are concerned please see a Dr rather than consult the internet! No advertising, fundraisers or pyramid scheme invites. No medical professionals. This isn’t a place to advertise your practise or sell your profession! Please be kind. We are all in this together and whilst you may not agree with what the other person says, they are still a fellow sufferer and person.
Everyone says to get out of mould. But where are we supposed to go.
This is a subreddit for the countless people suffering as a result of exposure to environmental toxins such as toxic mold.
I always take my mask off
I always take my mask off
We are a community that is centred around the most common treatment modality for sleep apnea, CPAP. We're here to support and help each other.
Crazy symptoms. Shaking vision, crunching jaw, vertigo, perforated eardrums, involuntary chin and cheek jerking, trigeminal neuralgia.
A place for TMJD sufferers to share their fears, worries, stories and successes. We are not Drs. We cannot diagnose you. If you are concerned please see a Dr rather than consult the internet! No advertising, fundraisers or pyramid scheme invites. No medical professionals. This isn’t a place to advertise your practise or sell your profession! Please be kind. We are all in this together and whilst you may not agree with what the other person says, they are still a fellow sufferer and person.
On high pain days, what do you do?
A place for TMJD sufferers to share their fears, worries, stories and successes. We are not Drs. We cannot diagnose you. If you are concerned please see a Dr rather than consult the internet! No advertising, fundraisers or pyramid scheme invites. No medical professionals. This isn’t a place to advertise your practise or sell your profession! Please be kind. We are all in this together and whilst you may not agree with what the other person says, they are still a fellow sufferer and person.
Where is safe?
This is a subreddit for the countless people suffering as a result of exposure to environmental toxins such as toxic mold.
Where is safe?
This group is for those afflicted with MCS and/or to raise awareness of environmental substances that have negative effects on people's health. This is YOUR community, feel free to post what you think is appropriate. I do not rule this subreddit with an iron fist, if a problem arises I will discuss it with that user. Please be kind and compassionate, we all have different levels of sensitivities and some have suffered greatly with this condition.
AHI halved. Still exhausted.
AHI is halved, still exhausted
Upper Airway Resistance Syndrome, or UARS is a form of Sleep Disordered Breathing characterized by a narrow airway and excessive respiratory effort. The primary symptoms include unrefreshing sleep, brain fog, fatigue, sleepiness, and sometimes chronic insomnia. Though many sleep studies do not differentiate between UARS and OSA, it is typically diagnosed via polysomnogram (PSG), and sometimes PES (esophageal pressure) which can detect abnormal negative pressure.
My disc is badly perforated. Does anyone else have experience with this. What did you do?
A place for TMJD sufferers to share their fears, worries, stories and successes. We are not Drs. We cannot diagnose you. If you are concerned please see a Dr rather than consult the internet! No advertising, fundraisers or pyramid scheme invites. No medical professionals. This isn’t a place to advertise your practise or sell your profession! Please be kind. We are all in this together and whilst you may not agree with what the other person says, they are still a fellow sufferer and person.
So there’s no way out apart from abandoning society?
This is a subreddit for the countless people suffering as a result of exposure to environmental toxins such as toxic mold.
So there’s no way out apart from abandoning society?
This group is for those afflicted with MCS and/or to raise awareness of environmental substances that have negative effects on people's health. This is YOUR community, feel free to post what you think is appropriate. I do not rule this subreddit with an iron fist, if a problem arises I will discuss it with that user. Please be kind and compassionate, we all have different levels of sensitivities and some have suffered greatly with this condition.
So, there’s no cure?
This is a subreddit for the countless people suffering as a result of exposure to environmental toxins such as toxic mold.
Can you take pregabalin and be on emgality?
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.
Started emgality for vestibular migraines. Anyone else had success?
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.
Anyone else have MCS and toxic mold syndrome?
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.
Is there any cure? This condition is making me want to unalive myself. I've moved six times this year already. I can't find a safe property or make my current property safe.
This is a subreddit for the countless people suffering as a result of exposure to environmental toxins such as toxic mold.
Is there any cure? This condition is making me want to unalive myself. I've moved six times this year already. I can't find a safe property or make my current property safe.
This group is for those afflicted with MCS and/or to raise awareness of environmental substances that have negative effects on people's health. This is YOUR community, feel free to post what you think is appropriate. I do not rule this subreddit with an iron fist, if a problem arises I will discuss it with that user. Please be kind and compassionate, we all have different levels of sensitivities and some have suffered greatly with this condition.
It’s not mould, but the chemicals are causing me so much pain
This is a subreddit for the countless people suffering as a result of exposure to environmental toxins such as toxic mold.
