Neck symptom
Q and A with Dr. Centeno, the creator of the PICL procedure which is non-surgical treatment for craniocervical instability (CCI). Ask questions about PICL, posterior injections, or anything CCI related.
Improve your vagal tone
Anhedonia is the lack of interest, enjoyment or pleasure. It can be caused by drugs, trauma, depression, etc. In the process of dealing with anhedonia, individuals often have several questions as they navigate their emotional numbness and seek understanding and support. Welcome to r/anhedonia. Please be sure to read the rules.
Could I have CCI? Need input based on symptoms and reports
Subreddit about cervical instability/craniocervical instability/atlantoaxial instability, aka CCI. I have been through the journey, and have a lot to say. I've done PRP and the PICL procedure 2x each. Hope this helps ☺ none of this is medical advice, if you have symptoms, please talk to your doctor. Lastly, open discussion is encouraged, we're not affiliated with or endorsing any single clinic.
Could I have CCI? Need input based on symptoms and reports
Welcome! Share your experience. Cranial Instability is a condition in which the ligament structure of the neck becomes “loose” or broken down in which makes it difficult to stabilize the neck and head. As a result, causes symptoms such as dizziness, POTS, floaters, and in severe causes passing out.
Could I have CCI? Need input based on symptoms and reports
Q and A with Dr. Centeno, the creator of the PICL procedure which is non-surgical treatment for craniocervical instability (CCI). Ask questions about PICL, posterior injections, or anything CCI related.
Are you able to work?
Welcome! Share your experience. Cranial Instability is a condition in which the ligament structure of the neck becomes “loose” or broken down in which makes it difficult to stabilize the neck and head. As a result, causes symptoms such as dizziness, POTS, floaters, and in severe causes passing out.
A must read for all anhedonics
Anhedonia is the lack of interest, enjoyment or pleasure. It can be caused by drugs, trauma, depression, etc. In the process of dealing with anhedonia, individuals often have several questions as they navigate their emotional numbness and seek understanding and support. Welcome to r/anhedonia. Please be sure to read the rules.
A must read for all anhedonics
A community for individuals suffering from the effects of COVID-19 longer than the estimated 4 weeks, also known as PACS, PASC, and Long Covid.
Can you have mcas without itching and gastro issues?
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.
Do you know anyone who recovered from mecfs+anhedonia?
This Long COVID support group is sponsored by COVID Care Group, LLC, connecting the dots of long COVID through education, research, & resources for recovery and symptom management. Our clinical team provides FREE educational information to help you help yourself and seeks out valid recovery tools to help with symptom management. Visit us at https://www.covidcaregroup.org for more information. All sales proceeds support our community outreach programs. Keep moving - Keep Breathing!
Do you know anyone who recovered from mecfs+ anhedonia?
A place of support for those living with, or affected by, chronic illness. Open and welcoming to all. This subreddit is for social and community support, not medical advice.
Do you know anyone who recovered from mecfs+ anhedonia?
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 you know anyone who recovered from mecfs+ anhedonia?
A community for individuals suffering from the effects of COVID-19 longer than the estimated 4 weeks, also known as PACS, PASC, and Long Covid.
Do you know anyone who recovered from mecfs+anhedonia?
Anhedonia is the lack of interest, enjoyment or pleasure. It can be caused by drugs, trauma, depression, etc. In the process of dealing with anhedonia, individuals often have several questions as they navigate their emotional numbness and seek understanding and support. Welcome to r/anhedonia. Please be sure to read the rules.
People with anhedonia,are you able to work?
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.
People with anhedonia,are you able to work?
A community for individuals suffering from the effects of COVID-19 longer than the estimated 4 weeks, also known as PACS, PASC, and Long Covid.
Is your top back of head always hot and burning?
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.
Is your top back of head always hot and burning?
A community for individuals suffering from the effects of COVID-19 longer than the estimated 4 weeks, also known as PACS, PASC, and Long Covid.
How many of you have permanent dry nose with no mucus?
A community for individuals suffering from the effects of COVID-19 longer than the estimated 4 weeks, also known as PACS, PASC, and Long Covid.
Doesnt h1 alone help ?
A community for individuals suffering from the effects of COVID-19 longer than the estimated 4 weeks, also known as PACS, PASC, and Long Covid.
Does Lyme causes severe shortness of breath?
Support community for those struggling with Lyme Disease and other Tick Borne infections
Do you have EBV Reactivation?
A community for individuals suffering from the effects of COVID-19 longer than the estimated 4 weeks, also known as PACS, PASC, and Long Covid.
Do you have EBV Reactivation?
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.
Should I take aspirin ?
A community for individuals suffering from the effects of COVID-19 longer than the estimated 4 weeks, also known as PACS, PASC, and Long Covid.
Are you from india?
A community for individuals suffering from the effects of COVID-19 longer than the estimated 4 weeks, also known as PACS, PASC, and Long Covid.
