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.
Do you have water drip/bubbles sensation in your head?
Myalgic Encephalomyelitis sufferers unite. This is a place to find new friends , have a laugh as well as sharing information about how we feel. This is a safe place to talk freely about all aspects of this awful illness and what it does to us every day of our lives. This is a safe place 😊
Do you have water drip/bubbles sensation in your head?
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 have water drip/bubbles sensation in your head?
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 water drip/bubbles sensation in your head?
Brainfog is a form of cognitive impairment which itself is a symptom of one or more conditions, ranging from a mild, to debilitating severity. This subreddit exists to serve as a community support group to keep eachother strong on the journey through discovery (of cause) to recovery, as well as to serve as a congregation of community brainstorming & useful resources. We welcome brainfog of any kind and severity here. Feel free to come and introduce yourself!
Do you have water drip/bubbles sensation in your head?
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.
Do you have water drip/bubbles sensation in your head?
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.
Did your anhedonia ever go away?
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.
Anyone familiar with this?
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.
Anyone familiar with this?
CIRS (Chronic Inflammatory Response Syndrome) is a multi-system, multi-symptom illness characterized by exposure to biotoxins. Patients with CIRS are often misdiagnosed as having depression, anxiety, PTSD, Alzheimer’s, fibromyalgia, or CFS/ME, among other conditions. Effective diagnosis and treatment for CIRS exists via the Shoemaker Protocol. The purpose of this community is to share new information, personal experiences, and help answer CIRS-related questions.
