Does your ME/CFS come with balance issues?
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.
Montelukast helps with joint inflammation?
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.
Ivabradine not working during MCAS flare-ups?
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.
What is it? Opened the airco for the first time
This sub is dedicated to all types of air conditioning systems. If you have any questions regarding your air conditioning system, feel free to post here.
Cholinergic crisis: something you need to know about if you take Mestinon / Pyridostigmine
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.
Cholinergic crisis: something you need to know about if you take Mestinon / Pyridostigmine
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.
Singulair/Montelukast: did you titrate up? What dose does work for you?
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.
Does sugar trigger flare-ups for you?
A place to learn more about PsA and relate to others that are going through the same thing
How long after stopping did your excessive sleepiness go away?
A community for those prescribed Lexapro or Cipralex, also known as Escitalopram. Please be positive and supportive. [> If you are feeling suicidal call 1-800-273-8255. If you need emergency medical attention call 911. [> Read all the rules before posting the first time, and please do not ask for medical advice, contact your doctor or psychiatrist.
Flare-up pattern: Weeks of daily pain followed by days with no pain at all?
A place to learn more about PsA and relate to others that are going through the same thing
Ivabradine improving Heart Rate Variability (HRV) and "Stress score" (on Garmin)?
Dysautonomia is an umbrella term for conditions in which the autonomic nervous system malfunctions.
For the ones with enthesitis only, do you have visible swelling?
A place to learn more about PsA and relate to others that are going through the same thing
Has anyone diagnosed with an autoimmune illness (like PsA or spondyloarthritis) found that treating it improved their ME/CFS 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.
Finally got to see a (new) rheumatologist after years of pain and fatigue… His number one theory is that I might have PsA (surprise surprise!)
A place to learn more about PsA and relate to others that are going through the same thing
Does anyone have physical fatigue from PsA so bad that walking feels as exhausting as running through mud? Anyone bedbound?
A place to learn more about PsA and relate to others that are going through the same thing
Ivabradine?
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.
Ivabradine?
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's your immune system?
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.
Rupatadine vs Ebastine vs Bilastine?
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.
Advice for dental procedures with MCAS?
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.
Anyone who's had MCAS for years before developing ME/CFS?
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.
Loratadine makes me drowsy, Fexofenadine doesn't do much, Ketotifen overstimulates me. What next?
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 what medication Dr. Scheibenbogen (Charité Berlin) usually prescribes?
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 what medication Dr. Scheibenbogen (Charité Berlin) usually prescribes?
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.
Ketotifen causing word retrieval 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.
