How do you know when your baseline is officially lower ?
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.
How to get rid of concussed or burning brain feeling ??
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.
Severe 18 months then mild for 6 months now I’ve been in a bad crash that’s been up and down for a month. Wake up feeling concussed, sometimes better at night. Sometimes have a decent day. Is this my new baseline? It’s been exactly a month since I crashed.
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 DXM make brain fog worse?
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.
How long does it take for DXM to work after ingesting??
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.
Have you traveled being moderate? Any advice? It’s a 6 hour flight.
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 liquid dextromethorphan like robitusin work for PEM?
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.
3 week crash waking up with brain inflammation and severe fatigue. Was mild before this, could leave the house everyday with no symptoms. Has anyone experienced a crash lasting this long then getting back to a mild baseline? I’m so worried. I used to be severe, I have some of those symptoms
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 causes fast breathing, anxiety and fast heart rate during sleep? Is this a pots flare? I’ve been sleeping all for two days straight which I never do.
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.
Was mild now in a 3 week crash not getting better. Does this mean my baseline is lowered now? I was functioning at 70% before and 10% now. I don’t know what caused the crash but has anyone mild experienced this and became mild again?
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.
Crash for the first time in 4 months on April 14th. I felt better this weekend and went to a wedding. Now in a crash again. Is it possible to return back to baseline after a 3 weeks rolling crash after not crashing for so long? I almost thought I was in a partial remission
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.
First crash in 3 months. Was mild and living 60-70% of a normal life. Now I’ve been in a pem crash for 10 days and getting worse. There have been moments in the first couple days where I felt better for a few hours. Ativan not really helping. Is this my permanent baseline now?
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 usually go back to baseline after the flu?
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.
Need Advice: Dealt with a boyfriend with BPD
"r/ BPD Loved Ones" is a support forum and safe space for people to discuss the challenges and abuse they have endured at the hands of someone who has Borderline Personality Disorder (BPD). This subreddit is an abuse support forum.
Worst crash can’t even eat. How long does a bad crash usually take for you to get over?
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 Nucca make you worse? Has anyone gotten much better from it?
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 have this symptom? When I talk it’s like my battery is running out. My chest gets weak and my voice starts sounding weaker.
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)
Severe onset and still severe at 18 months post covid. Suffering every minute. Any hope?
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.
When I walk my head feels weird, no oxygen feeling mixed with a headache and brain fog.
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.
Forhead burning?
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)
Brain stings when looking at screens. Has this improved for anyone?
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 feel the brain and spinal cord inflammation?
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 feel the brain and spinal cord inflammation?
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.
Still have a hard time talking because I’m so weak. Has this improved a lot for anyone?
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 anyone feel “concussed” if they’ve pushed themselves? I get really bad brain fog after doing tasks.
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)
