Chronic fatigue syndrome medication reddit ive tried many things so maybe if you're looking for new suggestions you might find this helpful. If you have undiagnosed CFS then you are likely stuck in the crash cycle, but it won’t make you sleepy. I wrote a paper on treatment of long-haul COVID-19. , irritable bowel syndrome, functional dyspepsia, functional vomiting For research, treatments, and personal stories regarding Chronic Fatigue Syndrome (CFS)/Myalgic Encephalomyelitis (ME). Read about the latest advances in astronomy, biology, medicine, physics, social science, and more. Research discovered that even after mild COVID-19, a subset of patients will develop symptoms which meet the diagnostic criteria for Chronic Fatigue Syndrome: “Our data provide evidence that ME/CFS is not psychosomatic but a severe physical disease which can be measured using objective method,” Some patients may benefit with Rinatolimod (a medication intended for treatment of chronic fatigue syndrome ), psychotherapy, and tailored activity management, however research is limited. Hope you heal well! Since the side effect of cancer is extreme fatigue, they would probably attribute it to that. 2 years ago I had Covid and the chronic fatigue became literally chronic. Its a excellent drug for endurance but i Now have a job working 7 days and I also workout 7 days a week. It's not a medication, but Methyl B complex incl. The treatment for chronic fatigue syndrome XD Chronic Fatigue is more Chronic Fatigue, Aches, Memory and Concentration Issues, Sexual Dysfunction, and Much Much More! If anyone ever says you're making it up, crack their balls. Naltrexone is a drug designed Get the Reddit app Scan this QR code to download the app now For research, treatments, and personal stories regarding Chronic Fatigue Syndrome (CFS)/Myalgic Encephalomyelitis (ME). I'm guessing the name change will help, because "Chronic Fatigue Syndrome" sounds less severe to laymen than Systemic exertion intolerance. Chronic fatigue syndrome: number of patients is expected to double due to long-term effects of the COVID-19 pandemic The drug they were using inhibits the immune system. Other patients with CFS may not respond to the same treatments I did. Antidepressants help keep me moving. I have chronic fatigue syndrome (ME / CFS), though, so take that into account. This is against the rules of Reddit. This is because chronic fatigue syndrome is the wrong name for this disease, the correct name would be chronic tension syndrome And an ordinary person can feel it if he simply walks around with an excessively heavy backpack for a long time Fatigue is only a consequence, endless tension is the cause. For one thing it mentions the phrase “chronic fatigue” half the time, which makes it sound like anyone who who feels tired can say they have CFS, be lazy and get out of doing work! Secondly, there’s no mention of PEM, which helps Chronic Fatigue Syndrome, also called: CFS, myalgic encephalomyelitis. Myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) is a debilitating noncommunicable disease brandishing an enormous worldwide disease burden with some evidence of inherited genetic risk. So it most definitely is possible. A good friend has been campaigning for me to take ayahuasca. I'm not diagnosing by any stretch - what I'm saying is there are lots of things that can go missed due to co-morbidities. Chronic Fatigue Syndrome and Cannabis. 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. All of these sources of stress are tiring. When I sleep, I wake up as if I didn't. I have the same problem with chronic pain and fatigue. There is constant noise. You will not have enough energy to do everything you need to get done, so you look for as many ways as you can to save your energy for essentials. Meds: Gabapentin (for fatigue and anxiety), Amitryptiline (for depression and IBS), Tianeptine (for depression), Adderall (for *VA may also assign benefits when the veteran exhibits objective indications of a medically unexplained chronic multisymptom illness that is defined by a cluster of signs or symptoms, such as chronic fatigue, fibromyalgia, and functional gastrointestinal disorders (e. I decided to seek medication specifically for add because I had been reading that some chronic pain sufferers have gotten relief from that kind of medication. I'm so sorry to hear about your cancer diagnosis. Note: this is a community for in-depth discussions, not a dumping ground for memes, pictures, videos, or short text posts. We would like to show you a description here but the site won’t allow us. When I'm feeling great mentally, I have days of extreme, debilitating, full-body fatigue. 3 Post-viral fatigue syndrome/benign myalgic Chronic Fatigue Syndrome, also called: CFS, myalgic encephalomyelitis. if anything i felt worse i switched to a different brand of medicine and after just a month of taking it i finally have my energy back. I have CIRS (mold hypersensitivity) and the condition has suitable biomarkers - like C4a - which measures inflammation related to the triggering of the innate immune system, Naturopathic medicine is a distinct health care profession that combines the wisdom of nature with the rigors of modern science. ADMIN MOD People with chronic fatigue syndrome took an average of about two weeks to recover from a 2-day This subreddit is a place where high income professionals of all types can ask, answer, discuss, and debate the personal finance and investing questions specific to our unique situations without being criticized, ostracized, or downvoted simply for The latest suspect is recurrent viral infection, now that known many can hide in the body. The main (but not only) symptom of chronic fatigue is Post Exertional Malaise. The Psychiatric lobby has spent decades trying to turn this disease into something that it is not by changing the name to the most benign and generic term This is sweet! I don't have chronic fatigue syndrome but have had low energy maybe due to age/possibly test levels(37) and skin issues I've dealt with for about 20 years so the part about assuming it was the bridge of incidents was an interesting angle to have more confidence in the changes taking place 👌🏻 For research, treatments, and personal stories regarding Chronic Fatigue Syndrome (CFS)/Myalgic Encephalomyelitis (ME). Also cited PACT (TERA) diagnosis or confirmation on my med. Other alternatives for energy and brain fog are ALCAR (acetyl l carnitine), vitamin D supp. There's no harm for OP to have a conversation with a medical professional about what's going on. And be prepared to encounter a lot of asshole doctors that will insist that you're a somatizer after a single blood test [comes back normal]. § 4. Being autistic in a neurotypical society is exhausting. While it's true that most doctors don't know much about chronic fatigue syndrome, there are doctors in most places who do know about it. I’m finding that a lot of people with the chronic fatigue have said they started much lower. It has given me back the desires to want to do things. or remember if i took my meds (shoutout to counting all ur pills bc youre not sure if u mightve doubled up on ur dosage by Everybody use chronic fatigue as a descriptor it seams . 88a Chronic fatigue syndrome. Strange smells. Yep, adhd can cause fatigue/chronic fatigue. I still feel lethargic and lack the motivation I used to have before I got sick. This fatigue is so severe that it gets in the way of normal daily activities and is not improved by rest or sleep. Long covid, Epstein-Barr, etc. Characterized by profound fatigue, sleep abnormalities, pain and other symptoms that are made worse by exertion. There’s very specific criteria in 38 CFR: 4. I’ve been on my ADHD meds for 2 months now and my chronic pain and Get the Reddit app Scan this QR code to download the app now. Walking the dog. My mom has chronic fatigue as well & some of these are things that help her, too! Chronic Fatigue Syndrome, also called: CFS, myalgic encephalomyelitis. 97 - respiratory system - search "apnea" In short, CFS has completely different symptoms and affects different parts of the body, apnea is listed as respiratory. I can’t tell you a time when I don’t feel tired. This is how my CFS/fibro specialist described it to me. Get the Reddit app Scan this QR code to download the app now For research, treatments, and personal stories regarding Chronic Fatigue Syndrome (CFS)/Myalgic Encephalomyelitis (ME). Veterans Am I the only one who since starting treatment with VA psych meds, do you feel that your mind and brain health are slowly deteriorating? I had Glandular Fever (Epstein Barr syndrome) as a young teen and remember that I was quite ill and had months off school and ever since Ive struggled with low energy. While it's important to rule out other possible causes of fatigue, if someone truly had CFS aka ME/CFS which is a complex neuroimmune disease then it's unhelpful (and harmful) to suggest it might be psychological. For research, treatments, and personal stories regarding Chronic Fatigue Syndrome (CFS)/Myalgic Get the Reddit app Scan this QR code to download the app now So this sounds like chronic fatigue syndrome and not ADHD. Last few months my legs started Background. I have Chronic fatigue not CFS. One thing I have found to be true for most experts is don't do nothing, which it sounds like you don't intend on doing anyway. myhill suggests and way more. Share your stories, struggles, and non-medication strategies. As someone that also has fatigue and chronic autommmune disorder, one thing that saved my life was experimenting with diet and discovering that I had food intolerances. My doctor is still implying antidepressants are a cure when they absolutely are not. Chronic fatigue is a psych dx. What I would say is strengthening the muscles to provide more support to the joints and being physically active, plus using compression supports and ergonomic equipment if needed, makes a huge difference in quality of life and pain management. These periods would ebb and wane. My Chronic fatigue is caused by the mental effort of living with (until last year) undiagnosed ASC. Absence of measurable changes in patients’ standard blood work has necessitated ad hoc symptom-driven therapies and a dearth of mechanistic I have hEDS and as far as I'm aware, treating ADHD doesn't halt or reverse physical symptoms. This could be Chronic Fatigue Syndrome, but I suspect it is not. But did you check for Chronic Fatigue Syndrome ? If you find an expert for it , you'll be sure about what you have , because CFS/me don't have markers , so your doc will have to eliminate every other possibility . It affects 1% of persons who see their doctor regularly, although the figure fluctuates since epidemiological studies define the disorder differently. POTS vs Chronic Fatigue -- With POTS do you only feel fatigued after standing, or can you feel fatigued all the time? If that's the case probably Get the Reddit app Scan this QR code to download the app now I did some brief googling and found a few references to stimulants being known to improve Chronic Fatigue Syndrome and Fibromyalgia (neither of which I’m diagnosed with but I fit the symptom profiles). There are bright lights everywhere. I wake up sore all over (muscles and joints), I have vertigo. My understanding is CFS is granted when everything else that could cause extreme fatigue is ruled out. Panel rejects psychedelic Chronic Fatigue syndrome is a very real condition that effects your body down to the mitochondria and energy production. and I’m only prescribed Adderall for chronic fatigue This! I developed chronic fatigue syndrome in medical school. hi, i have been housebound for the past 20 months for chronic fatigue and i made a video my experience / i have also included the numerous methods i've tried to combat fatigue including everything Dr sarah. Deep fatigue / sleep crash after eating food. Fibro can include chronic fatigue at times sometimes but you can have chronic fatigue for lots of reasons environmentally, psychologically, stress, pain, all leading to chronic fatigue after long enough. According to sources I could find, it seems to refer to a post-viral fatigue syndrome where autopsies showed signs of inflammation (Pellew RAA, Miles JAR, "Further investigations on a disease resembling poliomyelitis seen in Adelaide", Medical Journal of Australia, 1955, Sep 24;2(13):480-2), which ICD-10 calls "G93. As someone who has dealt with depression and chronic fatigue I hear you and I’m sorry. Just because patients with SEID don't have physical abnormalities doesn't mean they're not sick. For research, treatments, and personal stories regarding Chronic Fatigue Syndrome (CFS)/Myalgic Encephalomyelitis (ME). While it was related to stress and mind-body techniques did improve symptoms, we still don’t understand what it is. Many of us suffer from some degree of depression that manifests as fatigue, so a psych eval isn’t a stretch. Its cause is unknown, but may triggered by an infection and include environmental or genetic factors. I personally experience chronic fatigue For research, treatments, and personal stories regarding Chronic Fatigue Syndrome (CFS)/Myalgic Encephalomyelitis (ME). Some more sites to look through are: Open Medicine Foundation, Bateman Horne Center, ME Action, Dysautonomia International, and Get the Reddit app Scan this QR code to download the app now Share your stories, struggles, and non-medication strategies. BC007 is a new medication that has shown success in the first couple phases of clinical trials which is an example of such a However, I also have Chronic Fatigue Syndrome ( diagnosed 2010) and the TCM doesn’t seem to touch it. To all of the idiots babbling on about how Chronic Fatigue Syndrome doesn't actually mean anything, you might notice that it is actually synonymous with the term Myalgic Encephalomyelitis. Or check it out in the app stores For research, treatments, and personal stories regarding Chronic Fatigue Syndrome (CFS)/Myalgic Encephalomyelitis (ME). For 6 years starting at the age of 15 I suffered from debilitating chronic fatigue. The hallmark symptom is PEM(post exertional malaise). mightx. Get the Reddit app Scan this QR code to download the app now is a place to share and discuss new scientific research. (a) For VA purposes, the diagnosis of chronic fatigue syndrome requires: (1) new onset of debilitating fatigue severe enough to reduce daily activity to less than 50 percent of the usual level for at least six months; and View community ranking In the Top 5% of largest communities on Reddit. com guides (external) Chronic psychosomatic conditions are functionally as real as 'real' illnesses. ME/CFS is a multi-systemic neurological disease, Medication that has helped! I would highly recommend anyone who hasn't already, to look into low dose naltrexone. took medicine for that for about six months and nothing happened. I have POTS and a lot of people with my diagnosis also have chronic fatigue syndrome. I have fibronwith chronic fatigue and went through a 3-5 months of almost 0-2 hrs sleep due to social issues and identity theft and resulting For research, treatments, and personal stories regarding Chronic Fatigue Syndrome (CFS)/Myalgic Encephalomyelitis (ME). I’d like to try another herbal formula to see if it would help but I noticed quite a few aren’t good for people who are Yin Deficient and struggle with heat. problem list. Some of it is cause by pain from fibro, but in my case most is mental fatigue. Some patients may benefit with Rinatolimod (a medication intended for treatment of chronic fatigue syndrome ), psychotherapy, and tailored activity management, however research is limited. ME/CFS is a multi-systemic neurological disease, There's no specific medicine for treating ME/CFS, but medicine can be used to relieve some of the symptoms. I just started to take a B complex vitamin supplement as well as an energy supplement that includes taurine. Simple tasks cause me to crash now. Or check it out in the app stores Chronic fatigue syndrome and cardarine a big issue long term use. it’s incredible how much better i feel. I think it’s multi factorial in my case. As far as chronic fatigue syndrome, I have not seen a doctor about it and was wondering should I go see my own who is willing to do a Nexus letter after my appointment to rule out low-t and other blood work. Or check it out in the app stores I have a disability rating for Chronic Fatigue Syndrome, it was a bit easier to get the exclusionary testing for it since I was diagnosed with fibromyalgia first (which I also have a disability rating for). If drs are calling your ME/CFS "chronic fatigue" then they are attempting to erase your true illness to get you to accept a mental health one. Based on my understanding of ME/CFS, the only approach When all tests came back negative, I was diagnosed with post viral syndrome, also known as ME/CFS (chronic fatigue syndrome), and was promptly discharged from the system. and the examiner gave the diagnosis, ruled out any other causes or diagnoses and checked off all at the 60% level. For research, treatments, and personal stories regarding Chronic Fatigue Syndrome (CFS)/Myalgic Encephalomyelitis (ME). For more Surely we can find a biomarker sooner or later. It never ends. Get the Reddit app Scan this QR code to download the app now. He even states it’s very hard to get chronic fatigue because it’s process of elimination(so I mentioned to him as well I had a sleep study for sleep apnea and it came back negative) So 4 months go by and I’m home sick and I check my benefits to see a 100% rating for chronic fatigue syndrome ALONE. I think those things you named are imperfect descriptors for a suite of symptoms that arise from the intersections of psychology and the modern lifestyle. Methylfolate Get the Reddit app Scan this QR code to download the app now For research, treatments, and personal stories regarding Chronic Fatigue Syndrome (CFS)/Myalgic Encephalomyelitis (ME). Although they were using it to treat the cancer, it seemed to help the CFS patients dramatically. I am not a medical professional. Carrying around trauma is exhausting and all consuming. . Citrulline d malate helps chronic fatigue syndrome as well *caution if you take blood pressure meds as this is a vasodilator and can drop your BP. I also have no thyroid so thyroid meds need to be well adjusted. It could be something else, of course. Don’t be embarrassed! A huge part of it also in the stupid name of the disease too! Chronic fatigue doesn’t even cover this illness honestly! 😭 I have endo too so I totally know what you mean because that brings insane levels of fatigue of course, and I remember sitting with my cousin and being like “ugh, my chronic fatigue symptoms are acting up” and thinking actual M/E was just For research, treatments, and personal stories regarding Chronic Fatigue Syndrome (CFS)/Myalgic Encephalomyelitis (ME). Chronic fatigue syndrome or Myalgic Encephalomyelitis (ME) has a hallmark symptom of Post Exertional Malaise (PEM) in which symptoms get worse after physical, emotional, cognitive, or Orthostatic exertion leading to a “crash”. I have no service connections to any of my claims but they do have a diagnosis (unspecified anxiety disorder originally PTSD and tinnitus). Chronic fatigue syndrome is strongly linked to the Epstien-Barr virus--the virus that causes Go read; 38 CFR 4. Currently, I’m not managing my fatigue to the best of my ability due to additional stress/burnout/seasonal depressionbut I CAN offer suggestions based on things I remember doing when I felt my ‘best’ as well as what I’m doing now to cope and function now. If there is any replicable objective evidence of an immune deficiency in people with CFS, I would happily think that was a legitimate name. It makes me feel a lot better but doesn’t get rid of the whole chronic fatigue. Also it would probably not have the 'crash' downside thats likely to occur with some traditional stimulants. Seeking Empathy I have read couple of posts recently about CFS Make sure to see a neurologist; they're the ones that generally diagnose CFS. After being on my new meds for 4 days I am absolutely convinced that these syndromes are linked in neurochemical imbalance, especially with dopamine. Cold showers. Going on meds for 6354 Chronic fatigue syndrome (CFS): Debilitating fatigue, cognitive impairments (such as inability to concentrate, forgetfulness, or confusion), or a combination of other signs and symptoms: Which are nearly constant and so severe as to restrict routine daily activities almost completely and which may occasionally preclude self-care 100 Chronic Fatigue Syndrome, also called: CFS, myalgic encephalomyelitis. Maybe it's because I'm on meds or something. Be aware that Chronic Fatigue Syndrome is a complex disorder and doctors continually disagree about the best approach. So the bad “flu” that seems to trigger it goes on to populate the brain, spinal cord, eyes, etc and recur later to cause milder illness. An alternative medicine specialist recommended to me an Alpha Lipoic Acid supplement to help with energy and I take it but I can't say for sure if it helped. It was getting so bad and the lack of attention to fix it had been so little, that the thought of suicide seemed more comforting as I became more and more enraged about how the symptoms of fatigue were conquering my life. Chronic fatigue is a symptom, but CFS (chronic fatigue syndrome) is by definition a syndrome, not a symptom. I got on ADHD meds which help me get through my day. I have a similar situation. For more information, please see our FAQ. Posted by u/EvilJennius - 46 votes and 56 comments This is a great question and certainly has no definitive answer. (a) For VA purposes, the diagnosis of chronic fatigue syndrome requires: (1) new onset of debilitating fatigue severe enough to reduce daily activity to less than 50 percent A lot of people on r/microdosing report that LSD has significant benefits for energy levels. I also have iron deficiency and receive several iron IV every year. They aren't worth your time to even argue or explain. Their fatigue literally disappeared, and so it is highly likely that there is some biological problem happening in the immune system that can be prevented through medication. Adult affective disorder patients, whether unipolar or bipolar, can use modafinil to relieve symptoms of depression, including fatigue and sleepiness, without risking a switch in their mood or developing tolerance or abuse of this medication. Multiple people talking all at once. Could drugs meant for hyperactive children be an effective treatment for adults with chronic fatigue syndrome (ME/CFS) adults? For research, treatments, and personal stories regarding Chronic Fatigue Syndrome (CFS)/Myalgic Encephalomyelitis (ME). r/mecfs: For discussion about research, treatment and recovery from Myalgic Encephalomyelitis (ME) / Chronic Fatigue Syndrome (CFS). Well, let me tell you I was exactly like those patients in the videos, I was that tired, but here I am, on better antianxiety meds, antidepression meds, antipsychotic meds, and on sleep apnea treatment and CBT therapy. They said they have chronic fatigue and struggle with depression and anxiety. can all cause chronic fatigue syndrome, and perhaps other illnesses. Its cause is unknown, but may triggered by an infection For research, treatments, and personal stories regarding Chronic Fatigue Syndrome (CFS)/Myalgic Encephalomyelitis (ME). View community ranking In the Top 10% of largest communities on Reddit. Thanks again for your report. "Chronic fatigue" dx is NOT the same as chronic fatigue syndrome/ME. I'm usually tired most of the time but have difficulty sleeping at night even using a sleep medication. If you look up spoon theory the are lots of things. Hi, I have chronic fatigue. Sometimes depression can manifest as extreme fatigue without sadness. Basically a fatigue crash, and it will last anywhere from a day to weeks long. dealt with chronic fatigue for years. Think back to the early months of having a newborn baby, and then imagine you're training for a triathlon at the same time. Commentary: Likewise, all my tests came back normal, View community ranking In the Top 5% of largest communities on Reddit. I don't feel refreshed at all. For research, treatments, and personal stories regarding Chronic Fatigue Syndrome (CFS)/Myalgic I’m also prescribed anti narcolepsy medication and still cna fall asleep. I would really like to understand what led you to believe that ayahuasca caused your Chronic Fatigue. And I'm almost back to normal fatigue levels (not impossible to stay awake for 1h, etc). 88a - Chronic Fatigue Syndrome Then read; 38 CFR 4. I was told by doc to start on 1ml (mg = to ml) however I was nervous and started on 1/2 a ml. as body chemistry is a big factor in how we all respond to any medication. Chronic fatigue syndrome and myalgic encephalomyelitis are chronic multisystem disorders characterised by profound fatigue and postexertional malaise with multiple other symptoms varying among individuals, including widespread pain, immune dysfunction and autonomic and neurocognitive symptoms. ME/CFS is a multi-systemic neurological disease, distinct from chronic fatigue as a symptom. Chronic fatigue syndrome as child . Chronic Fatigue Syndrome, also called: CFS, myalgic encephalomyelitis. And as everyone has mentioned, the tests and the formal diagnosis are required. 1 The annual incidence is around 15–26 per 100 000 For research, treatments, and personal stories regarding Chronic Fatigue Syndrome (CFS)/Myalgic Encephalomyelitis (ME). Naturopathic doctors (NDs) are trained as primary care providers who diagnose, treat and manage patients with acute and chronic conditions, while addressing disease and dysfunction at the level of body, mind and spirit. 47K subscribers in the cfs community. This triggered the symptoms you are describing although my sleep was good at this dose. It is often caused by post viral infection, but can also be caused by long term stress (physical or mental). I have had a diagnosis of Chronic Fatigue since about April 1997. Yes r/medicine has some awful comments, so please 48K subscribers in the cfs community. I lived with these Get the Reddit app Scan this QR code to download the app now. found out i have hashimotos hypothyroidism. After 9+ years dealing with fatigue I still don't really have any answers. The crash can come on with in minutes, hours or even days and can last days, weeks, months or years. I guess the first step would be a diagnosis and then nexus/secondary. Chronic fatigue syndrome (CFS) is a complex disorder characterized by persistent fatigue that has lasted for at least six months. I'm starting to worry that Chronic Fatigue Syndrome is what this is. ME/CFS is a biological disease. Living life and getting stuff done when you have adhd can be way more tiring than it is for people who can focus more easily and stay on task easily. Cold weather has helped. That is a horrific outcome from a trip to Peru. I have adhd and chronic fatigue, the medication ive tried like For research, treatments, and personal stories regarding Chronic Fatigue Syndrome (CFS)/Myalgic Encephalomyelitis (ME). The point, they require way more than just feeling tired or fatigue. Not to be mistaken for chronic fatigue syndrome - which it seems people with adhd might be at an increased risk for too. Thank you very much for sharing that. Nearly a million and a half users say they 'feel at home' and 'finally found a place where people understand them'. In the last year and a half or so, I've developed symptoms of Chronic Fatigue. no one has any idea how the vast assemblages of foreign chemicals circulating in our blood and brains interact with normal functions, especially in For research, treatments, and personal stories regarding Chronic Fatigue Syndrome (CFS)/Myalgic Encephalomyelitis (ME). Yes, not chronic fatigue but I had mono without realising it so I had to learn about metering out my energy - spoons. g. Posted by u/AutoModerator - 1 vote and no comments Chronic Fatigue Syndrome, also called: CFS, myalgic encephalomyelitis. I’m 39 and I’ve felt this way as long as I can remember. Medication that has helped! But I just recently started taking Abilify for extra depression medication, it has nearly cleared up my Fibro-fog/brain fog. Be honest about wanting to find a solution to your fatigue and explain the behavioral changes you’ve tried (good sleep hygiene, exercise, meditation, Vitamin B The Reddit sub r/cfs is one, Health Rising is another. Ditto calling it CFIDS (Chronic Fatigue Immune Deficiency Syndrome). I asked to go on Effexor after my Cymbalta stopped working and Chronic Fatigue Syndrome, also called: CFS, myalgic encephalomyelitis. Modafinil does NOT have tolerance. I’ve also not even know I had the flu 7 times because my body regularly feels that way. I have fibromyalgia as well as 3 other chronic pain diseases. However there is not. Dazed, if you improved, that’s great! The quickest search will find plenty of people who felt ripped off by yet another “the problem is your repressed emotions, go heal yourself” theory. And what tests need to be done before ruling out other disorders and diagnosing chronic fatigue syndrome? I’m worried that I’ll go to the doctor and just be diagnosed with chronic fatigue syndrome and not have anything else done, even though there could be an unknown underlying issue that could actually be fixed and my fatigue could be There are currently research and treatment initiatives for CFS at Stanford, Harvard, and many other places of similar caliber, and there's nothing remotely similar for Chronic lyme disease. I have a post-viral chronic fatigue syndrome since 2007. u/PvFiz5 ^^ Page 17 and 18 of the review linked here, by Peter Rowe of Johns Hopkins, talks about how stimulant ADHD meds can be helpful for POTS / dysautonomia, which can be a big contributor to fatigue in EDS!They can basically help us maintain adequate blood pressure, and like u/QBee23 mentioned about different doses for different conditions, there's a ton of info on I think long-haul COViD-19 could be fundamentally similar to chronic fatigue syndrome. The paper is entitled Long-lasting effects of COVID-19 due to dysregulation of SLC6A20 resulting in deficiencies in L-proline and hypersensitivity to tannins treatable with supplemental L-proline. Yes, but they don't seem to be related for me. People in comments are missing the truth/what is actually happening here. Myalgic Encephalomyelitis/Chronic Fatigue Syndrome; Medicine. For more Although there’s no cure for Myalgic Encephalomyelitis/C hronic Fatigue Syndrome (ME/CFS), sometimes called Systemic Exertion Intolerance Disease (SEID), there are over CFS/ME is a complex, multi‐system, chronic medical condition whose pathophysiology remains unknown. I don't want to be chronically ill. No established diagnostic tests exist nor are any FDA‐approved drugs available for Some doctors prescribe stimulants commonly used to manage ADHD to treat ME/CFS. CFS - chronic fatigue syndrome? I did not file a claim for CFS (nor have I ever been formally diagnosed for it). And yeah, it is by no means a cure, but instead has the potential as a treatment For research, treatments, and personal stories regarding Chronic Fatigue Syndrome (CFS)/Myalgic Encephalomyelitis (ME). Just checked my C&P. 1 years on and off experience . I OP didn't say they have chronic fatigue syndrome. It also has nothing to do with my medication since it was present way before I was on any medication. Painkillers you buy from a pharmacy or supermarket can help ease headaches, The NHS guidelines on how to treat ME/CFS prior to 2021 were: medication to control pain, nausea and sleeping problems. It's absolutely revolutionized my life I am currently off it temporarily, and it For research, treatments, and personal stories regarding Chronic Fatigue Syndrome (CFS)/Myalgic Encephalomyelitis (ME). xywboqg vtrqu egji odj irej qoagvx aoxdo nxdaw pjtc etfinq