Chronic Fatigue - Cutting Through the B.S.

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Chronic Fatigue - Cutting Through the B.S.
In this episode of Cutting Through the B.S. series we tackle Chronic Fatigue Syndrome. We discuss the different causes of this very confusing conditions as well as the many different treatment options that are out there and why many of them fail. We will then further delve into what is causing the condition in many patients, and treatment options we have found to work in our clinic.
#DrMartinRutherford
#PowerHealthReno
#FunctionalMedicineReno
#ChiropracticNeurologyReno

[@townsendliving9750]

My childhood was quite crazy, had pneumonia about 5 differnt times, was subscribed antibiotics each time, I got streptococcus about a dozen times, like an idiot I kept taking antibiotics and I didnt know better I was a teenager that trusted doctors. Eventually started shaking when I had lack of sleep, my brain couldn't keep track of anything I was doing, acted just like Alzheimer's. I had a very high stress high pace job. I finally got fired after 7 years for being worthless, got fired from several jobs within a week cause they thought I was a drug addict from being so messed up physically and mentally. I finally went home and relaxed for about 6 months, opened up my own business and sleep 12 hours a day. I manage it through sleep and diet, it's still there, I am easily brought back to zero energy but now I have the option to go home, relax and sleep for however long as necessary. I'd like to get healed and go back to how I was before. I'm 29 years old. And it basically controlled my 20s. It's a very difficult disease. I have my reasons to say. Chronic fatigue is worse then cancer. It's a terrible thing to live with

[@sneakypress]

The lesson here, people, is that antibiotic use (and especially OVER-USE) leads to the development of chronic FATIGUE syndrome(s) , and, that doctors CANNOT BE TRUSTED to preserve your health.

[@cindyrella24673]

If you had metronidazole/ Flagyl or any fluoroquinolones like Cipro or Levaquin, these antibiotics cause mitochondrial dysfunction and can bring on so much of what these doctors are talking about. If you research fluoroquinolone toxicity or metronidazole toxicity you will see how those antibiotics injure people and curse so much of what Dr. Gates and Dr. Rutherford talk about, especially if you have a chronic virus on top of it. I don't have childhood trauma, but I do have metronidazole and fluoroquinolone toxicity which caused all of what they talked about to me.

[@susanvaughan-schiele210]

I feel for you. Sincerely. You've been treated badly. I wish you a full recovery and to find some understanding from people.

[@deeaustin6479]

This video has given me more information than anything else I have managed to learn since I became ill in 2004 at the age of 48. At 65 years old I have missed many milestone moments which can never be recaptured. If only the doctors who still believe this illness is a form of malingering were made to watch this things might actually change for the better. Thank you so much for making this invaluable video.

[@deannaavila4839]

i love this guy. this is a great doctor we need more like him.

[@michaelfortune9997]

My second comment on this video. It genuinely is so great to see people like yourself WITH ACTUAL REAL UNDERSTANDING of CFS and related illnesses. Its so amazing because there are thousands of people who think they cant get better.. they just arent educated. Keep up the good work.

[@the_dark_forest]

Sensational. It would be wonderful if we had medical professionals like yourselves here in Australia. Wondering do you still do evaluations? It's 5 years since you made and posted this video and a lot has changed in the world. Thank you so so SO much for the time and effort putting this together and publishing it on youtube. I would say that you have no idea how fantastic it is to find something like this but I suspect you most certainly do understand. All too well. Thank you gentleman. Greatly appreciated :-)

[@DrMartinRutherford]

Thank you for the kind words. We do still do evaluations. If you are interested in a consultation to see if you would be a good candidate for our program please visit powerhealthconsult.com

[@lilmisspeace]

You have made my health (or lack of) make so much sense!! I have had so many traumatic events over my 36yrs of life, some far worse than others, & many other factors and a bunch of increasing symptoms that have snowballed and now I'm so sick! Dr's have nothing to offer and have only made things worse with PTSD, depression, contraceptive and other meds and no explanation of why- just telling me to take a pill. Thank you for sharing your work.

[@michaelfortune9997]

I know a lot about CFS (I'm currently on my healing journey), I'm only 13 minutes in to this video and its great to see that you ACTUALLY KNOW WHAT YOU'RE TALKING ABOUT. Great content!

[@donnacline6618]

OMG! I went thru the same thing with all the DOCTORS/naturalists.

[@juliebella1221]

Same.

[@neetzyblog8269]

I appreciate your channel so much. With your help, I figured out I likely have PPPD after having treatment for BPPV last year. I was left in the lurch by my specialist and physiotherapist with no explanation of my new "vertigo" symptoms. I had to figure it out myself, with your help. So, thank you.

[@najibcasa2745]

Thanks for the Video! Apologies for butting in, I am interested in your initial thoughts. Have you heard the talk about - Dinanlinson Rebooting Health Approach (do a google search)? It is a smashing exclusive product for getting rid of chronic fatigue syndrome without the hard work. Ive heard some decent things about it and my cousin after many years got great success with it.

[@sealily6015]

Thank you so much gentleman for sharing this information. I may be able to heal now!. I am housebound with CFS and suffered severe abuse from childhood onwards. I am also a hyper-vigilant perfectionist! Maybe I can get my whole body/brain to calm down.

[@Truerealism747]

How are you nowadays

[@Josh-pe5pl]

SO very helpful! If my husband and I had only heard u and so much more cfs info that is readily available now, compared to 2010, we might still be happily married!

[@cindyrella24673]

Metronidazole is what pushed me over the edge to fight or flight. I have much of what you're talking about, but the third day of taking metronidazole after having it many times from diverticulitis, the metronidazole messed up my brain, so I think metronidazole can push people over the edge to fight or flight. Fluoroquinolones also messed me up. I literally felt it happening in my brain on that third day. I pray to God that medical insurance covers wonderful doctors like the two of you because you both understand what is really happening to people. After being in fight or flight for two years, one good dose of psilocybin helped my fight or flight, then I microdosed when I felt it was needed, which isn't very often. I have so much of the symptoms you talk about. Thank you for all you do and actually trying to help patients.

[@39skitfinland59]

Had to take a nap! My chronic fatigue is awful today.

[@poohbeared40]

I wish I lived closer to your practice. It's so frustrating to find doctors that understand. I don't know if I have CFS but I do have fibromyalgia and it is so frustrating. I use to have energy, never hurt and now I am totally opposite. I am in pain always, I have days that are better then others but because I can't do everything I use to, I get so frustrated. I feel like I am being lazy, I am overwhelmed more then I use to and my anxiety is so much worse.

[@DrMartinRutherford]

We work with people from all over the world via Zoom. If you are interested in a consultation to review your case you can find out more at powerhealthconsult.com

[@raindrops1047]

My CFS is so bad, have no energy to listen. Can someone summarize for me please.

[@kathyhanson3277]

You are the only answer to my prayers. You have the answers to every question I have ever had

[@aegisgfx]

Why, they didnt give any solutions. Although I have to admit they do understand the problem quite well. Its also worth noting that chiropratic is total BS, so if they are using that as part of their treatment, then they are not using a science based approach

[@debbiechristian506]

Thank you so much! I hope you can evaluate me when you get some more openings. God bless y’all for your work and for educating us. You have given us hope, and that is priceless.

[@xifanie]

This makes so much sense now. I've been diagnosed with psoriasis at 2yo, but I've always, as far as I can remember, had severe digestion problems, insomnia, very poor memory, concentration problems/ADHD, and while some things have improved with better diet and digestion (acidity and enzyme supplementation), my body still has as much trouble getting enough sleep, still refuses to produce its own stomach acid and enzymes (at 24yo this is not normal), and my memory isn't that great yet... which just tells me that I've really been in a perpetual state of Fight or Flight or Freeze since I was 2yo. Thank you so much for this video. Now I'm off to learning more about the amygdala and meditation practices that have been proven to shrink it over time.

[@Truerealism747]

How are you now

[@nobodynothing2594]

How are you now? What things helped you?

[@xifanie]

​ @nobodynothing2594 ​ @tomsale5142 I've been able to drastically reduce stress from my life, mostly through self-awareness, relaxation (walks, warm showers, baths, near-infrared phototherapy), and really upping my magnesium intake (flax, dark chocolate, bananas). Mentally I'm in a much more positive place while my body has been falling for the last 4 years and doctors have no idea what's going on. At least not letting the stress of illness get to me as much allows me to still be a decent wife and friend

[@tja6040]

YOU MENTIONED THE COMPLETE HISTORY, OF AN INDIVIDUAL'S MEDICAL PROBLEM. WHEN DID SYMPTOMS FIRST BEGIN? THAT IS SO KEY TO FIGURING OUT A GOOD AND FITTING DIAGNOSIS. UNFORTUNATELY, IT SEEMS TO BE DISREGARDED BY MANY DOCTORS TODAY. THANK YOU . ENJOY THIS CHANNEL. GOD BLESS.

[@aegisgfx]

you have proof of these 'gods'?

[@aharowna3539]

@@aegisgfx There *IS* only one true God and Yahowah is the name (YHWH). Study the original writings. There is only one source to 'this truth' You'll find all you ever need in His Towrah = Teaching, Guidance, Instruction and Direction. It's NOT RELIGION, nor law etc. It's Yah's "Prescription For Living" The Towrah, accurately spelt or sometimes written: Torah consists of The Towrah, Prophets and Psalms. The most concise & accurate you'll get on this planet is found in: The Bless Yahowah website, however I'm warning anyone who maybe reading this: it's 100% necessary to have 'an open mind'...99.9% of people won't and don't. It's a beautiful website, easily followed with zillions of incredible links and resources for anyone out there genuinely seeking the truth. I sincerely hope you all do! May Yah Barak (bless) you. Shalowm from Angel (UK), BTW it's written over 3,500yrs ago by God (Yahowah - Yah for short) only thousands out of billions will ever find this, or take it on board. Sadly that equates to approx just 1 person per million of this current world's population. Therefore that already rules out all christians and their fake/tampered with/corrupt bibles and teachings. Even the word bible comes from the Greek 'biblios'...look it up & verify this yourself please! No letter J existed until the 17th century = No one named Jesus lived, however Yahowsha did and is His real name, not to diminish Him at all, He was a part of Yahowah (a diminished part made flesh) & did His part..for us. I could say so very much more, but I urge you to please start by looking up the aforementioned website. It will blow your mind (if your open and receptive)...not dumbed down or duped like the majority of folks. It's the only thing that will give your soul (nepech) eternal life. Many people just don't care, they're only interested in the here and now. Trust me - if you want to truly know God...then Yah wants to know you too. It's more about your eternal soul and what blissful life awaits, this here now is but nothing compared. He however has 7 Mo'ed Miqra'e 'Invitations to meet with Him' throughout the year and 5 Terms & Conditions, but it's always only ever an individual's choice to say yes or no. Walking away from religion, politics, military & institutions are all a part of it - sadly it's too much for most people to comply with. These above are ALWAYS only ever about man's power and control over the masses of people and exactly why Yah is opposed to them all. YES...He opposes religion and bowing down or fearing etc. Look up His name in Ancient Pictograohic Hebrew Letters...it's incredible. It's an arm and hand reaching down to lift 2 people up to Him & also with an open palm. There's a tent peg in the centre of them, representing home and family & security. His name says it all. He's YOUR DAD and is only asking for you to stand up - eyes looking up & awake, arms stretched up to be picked up and raised up to Him for a real Father & Child relationship together. I maybe see you there one day - and trust me too, it's actually far sooner than the majority of people know about. 2026-2033 are certainly going to be what's classed as The Worst 7 years of Hell on Earth. No...I'm not an end time nut or scaremongering - this is all verifiable, evidence & reason based knowledge. Just start digging underneath the surface and you'll find it too. Google Apophis for example - NASA have been tracking this for years & it's real. It's too mentioned over 3,500yrs ago. How and Why!!?? Study it please.....

[@JenniferJacksonxminecraftlifex]

Thank you for this presentation.

[@jaderose5127]

Thankyou both for your presentation and expertise it has proved very supportive giving greater understanding of this complex condition.

[@deboruth]

You seem to use "chronic fatigue" as a synonym for "Chronic Fatigue Syndrome." That is not correct. "CFS" is the name CDC chose to rename the outbreak of Myalgic Encephalomyelitis at Incline Village NV winter of 1984-85 wherein "fatigue" is merely a by-product of biologic dysfunctions including mitochondrial dysfunction, neurologic dysfunction, cognitive difficulties, and immune abnormalities. This is very different from being chronically fatigued.

[@tammydesmet1678]

Ive looked up research papers on that because a g/f of mine ended up w fibromyalgia (i actually diagnosed her said to tell ur doc to check for it.. cause ive had it for 14yrs.. but the cfs came on horribly chest pains etc.. well back to my point.. my g/f ended up almost in a coma and dyin because her brain had swelling!! I freaked! So researching it..(thru actual research papers.. i found in the uk theres been deaths due to em/cfs.. but they i guess r covering it up.. it was found in ths autopsy n not written down. It was weird.. why? So they dont have to take it as serious? Or what.. well she finally recovered.. but she almost died..😢 scares me SumThin fierce cause i get the horrible chest pains w mine.. its almost like feelin ur a ticking time bomb.. will it pass.. or will the encephelomyolitis make something finally swell n kill u.. hopefully they figure out how to resolve it for real soon..

[@tammydesmet1678]

Ps. Deborah.. thank you for the break down of that too.. ( im gonna write it down) 😉 but ty for that. Someone who knows what theyre talkin about 😎⚘ awesome!!

[@Dreadtheday]

Mrsa for 18 years, 1/2 fmf, immunodeficient in G & a, Hives, dermographia, hysterectomy, survivor of incest, EBV at very high levels. Psoriasis.... no chill.... ibs, fibroids, tumors, type B ovarian Low grade cancer. I csnt burp either. Ater a while you dont want to give a medical history..... too msny words. Mild seizures, nausea, blurred vision. Dad overdosed, mom has 4th stage cancer, brother is serving 39 years. I feel alone. ..

[@hisalone7166]

Love the new look!!!! FYI.....I've just started using Super Beets and they have helped me tremendously!!!!! Blessings, Beverly

[@MsJanetLouise]

GarysOnlyGal ***Hello, where did you order from?

[@JLU-wm8ir]

MINE WAS 2 YEARS MONO.. ALWAYS FEEL LIKE CRAP.. I HAVE THE CHILDHOOD TRAUMA. A FAMILY MEMBER MURDERED ON MY 13TH BIRTHDAY AND MORE. SORRY FOR THE CAPS BAD VISION

[@susanvaughan-schiele210]

I cant even concentrate enough to follow or make sense of this video.

[@cowsonzambonis6]

Really interesting video! I'm toward the beginning of my search to figure out why I am so fatigued, etc, and this gave me a lot of things to research and discuss with my doctor.

[@danpalmer1202]

I have wicked orthostatic tachycardia, enlarged spleen, gastrointestinal distress (awful pain and food intolerance), sleep disturbance, brain fog, syncope...etc...lost my job, denied disability benefits, AND I'M ONLY 42! Cleveland clinic has no clue what to do. I feel like I'm dying

[@danpalmer1202]

@Tzaikore Masbi I have developed more intense symptoms suggestive of a neuroendocrine tumor. I have begun vomiting blood and have blood in stool. I've got an endoscopy coming up

[@kimberlyhortz6471]

You will have to keep applying. If you take Lyrica. They will give it to you because the Lyrica can make you fall asleep. It took me 3 times failing then they give it to me.

[@LizBrownYoga]

This was a very long winded way of concurring with the new push for brain retraining but you don’t actually state what you propose the solutions are?!

[@kimbee1964]

I’ve heard it all from doctors...inflammation is always the key in the blood work as evident by an abnormal Rheumatoid factor indicated on the blood work.

[@davidkruse4030]

inflammation means little. its obvious cfs patients have inflammation. what is causing it is the mystery

[@hdd1977m7]

I have CFS and my RF is normal. All of my regular blood work results are normal.

[@donnaallgaier-lamberti3933]

I also appreciate that you are trying various backgrounds. I am guessing since you are exploring options you desire feedback because you want to improve. The gray one is okay (actually the best of all options in my opinion) the black background was just awful against the whilte coats (glaring sorry!) This office desk background (for me) is just too busy and distracting. (All the busyiness confuses my brain) I just cannot watch this (but I did listen!!) Aside from that minor issue, I LOVE LOVE LOVE your programs and topics. Your topics are SO pertinent and "right on" to the challenges I face (Hashimoto's/chronic adrenal fatigue/mold exposure and my husbands low thyroid/brain issues. I listen to every program even though they are not my issues because there are so many autoimmune connections. I learn every time. I am VERY interested in knowing more about the brain exercises that you do. My husband is seeing a GREAT Functional Medicine Neurologist here in Michigan. But as retirees our budget is limited so we have to do as much as we can on our own. I just listened to "The Broken Brain" series and we just read two brain books. We do out best; we eat the AIP Protocol and working on healing his gut, he takes the recommended supplements, he is detoxing his high lead, he is taking thyroid hormones now and is working to increase his time on the elipitical to increase blood flow to the brain. His focus now is on his brain....So brain information is very pertinent to us. He is Italian and ate the Italian way...he had a HORRID gut his entire life a 6 out of school bought with what they called Hepititus (which his blood tests now say is negative so more likely Epstein Barr according to our FMP.) Anyway these are our concerns and ideas for future programs. Thank you for ALL of your hard work and for your educational approach. We watch every program and share them with others.

[@stevecampbell9381]

P pl

[@lisakaylanemorris]

Nice talk! I too crashed into severe illness at age 48. I am 49 now... I had a kidney stone jus a lil too big so I had to have lithotripsy and ureter stent.. 2 surgeries in 10 days and then acquired a super bug urosepsis. Ugh.. Great, then needed to take probably the strongest IV anti biotics for 6 weeks.. Finally the ordeal was over and 2 weeks later I woke up one morning with POTs. Before this happened I had been through alot of stress.. As a child, I was adopted out at the age of 6 and as an adult I had a horrible marriage to a cheating, thieving, drug addicted alcoholic.. Finally got free from that! Anyhow back to now! About 4 mo after I experienced pots, my thyroid went out, and I acquired frozen shoulder. Ouch.. Anyhow at one point, I could not stand up for more than 1 minute. I couldn't hardly breathe for months, I could barely eat anything and lost 35 lbs. My head was ringing, my muscles twitching or locking up, migraines, brain fog, panic, shuddering, depressing, suicidal thoughts and sooo much more! A complete nightmare where I was in agony and seriously wondered how it was even possible for me to be alive in this physical state. Soo fast forward to today.. I have done limbic system retraining, meditation, and I eat no gluten, sugar or dairy or man-made preserves or msg. I also researched the HECK out of whatever was happening to me to come up with my own thoughts and understanding. I am pretty sure I may have ganglion autoimmune neuropathy or something like that.. Haven't been tested... Not sure I want to do cancer, immune suppression drugs or steroids as the side effects are great and the drugs are not a cure. Anyhow, I am not well, but I can now stand up several times a week pots free.. Sometimes just for an hour or two, sometimes most of a day.. I can walk for 15, 20 mins now on most days. I can go shopping at least once a week now.. My headaches are almost gone, brain fog almost gone. Frozen shoulder is still there.. Ouch, alot of pain still with me.. Like CRpS... But overall I have improved and I am hopeful for more improvement over time. I still spend a lot of time in bed or on the couch, but I feel more comfortable so I can do sewing, or reading now when I am resting. But I continue to be hopeful.. I just need to figure out this chronic regional pain syndrome! Your video was helpful Thanks!

[@g.s.5868]

you could have tried lemon juice / apple cider vinegar = dissolve stones naturally

[@LM-iv8wl]

I love the new format you guys are great

[@geraldevans378]

Kudos for the video content! Sorry for the intrusion, I would love your thoughts. Have you researched - Dinanlinson Rebooting Health Approach (do a search on google)? It is a great exclusive guide for getting rid of chronic fatigue syndrome minus the hard work. Ive heard some great things about it and my friend after many years got amazing results with it.

[@susanjannarone135]

I find it politically incorrect that my family sees only the days I’ve survived, ignoring my quality of life. My husband died from a pharmaceutical. I believe I am ill due to pollutants, mercury amalgams, pesticides and possibly viruses given to me. I often reflect that my life has been primarily trying to figure out how I got sick and why the government never investigated. I’ve always tried very hard to “act” normal. Seems when China did/didn’t release COVID resulting in long COVID it might be best for me at age 72 to pose as a long COVID patient because big Pharma makes money on that. My life exemplifies our country failing in areas such as NIH CDC, EPA, etc. I’m still not able to find a doctor and not much has changed for me. Profitable disease is addressed. Period. That’s why cancer’s metabolic treatment is supported by private funds.

[@tracysirls9462]

I’ve been to so many Doctors and all of them tell me the same thing.. “ I don’t see anything wrong” I live in Orlando FL. Do you guys have a recommendation as to who has the knowledge similar to yours? I so tired of being tired. Can’t cook, play with kids, hold a conversation with my hubby. I can’t run or work out anymore. :(

[@tracysirls9462]

I’m *

[@milkweed07]

maybe i keep missing the actual point and if someone can clarify for me... you address the brain...ok ? but no videos say how? or am i just missing it in these long presentations about the same thing over and over.

[@LisaLeeLeeBlue]

Alllll the same symptoms from the abuse to the ulcers to the constant fight or flight to the short term memory loss and fog to the anemia to the inflammation to the crazy tired all day and then can’t sleep at night and on and on. I have a chance to get a realllll life nowww!!!!

[@kathygreen6043]

Hello. This video was made before Covid. Do you have any updated information on viruses triggering CFS/ME? This is my third bout. All three occurred after specific medical events

[@glarson1527]

When my C1 is out of line. I have a major Chronic Fatigue. Chiropractor Rock

[@mdee860]

Read article from Hope Rising/ Open Med. Foundation - it's called: Can CCI/Aii be Causing my ME/CFS & POTS. This article was a game changer for me. I have both upper & lower neck damage from a car & a horse accident. The link was sent to me by a stranger from the Netherlands!!! We were both listening to an ME Seminar & made comments & then he made a comment that struck me. About 4 days later - he sent the link! But I hear you - when my neck slips out of alignment - it's like major short circuit - so painful, brain fog, spasms, tachycardia, etc., etc., etc.

[@UpNorthFreyja]

Thank you for this video. I was officially diagnosed with chronic fatigue in 2006, though I can see that I was suffering from it in 2001, at least... I won't go into all the details, of course, but I definitely had a major trigger in that year when I had an acute illness of some sort (I didn't go to a doctor, but my guess is that it was a mild scarlet fever - which caused an undiagnosed miscarriage - next period was 6 weeks later, totally out-of-character for me.) That was also the time during which I was diagnosed with an underactive thyroid. I also have possible heavy metal toxicity from 6 years of weekly allergy shots when I was a teen. (No amalgam fillings thankfully.) I have also had various emotional traumas including an emotionally abusive marriage, the subsequent divorce and battle and several other major emotional traumas since. I also identify with the perfectionism you mention, but I would argue that perfectionism is the result of childhood traumas, not something separate (though I understand that someone currently with perfectionism might not be able to pinpoint that one.) Anyway, thanks for the video. I will be sharing some of this information when I see a doctor in a couple weeks to see about finding a treatment for myself as well as for my daughter who also exhibits symptoms of chronic fatigue (having undergone some of the same traumas that I have had myself.)

[@sealily6015]

Lori - I hope you and your daughter get well.

[@06eyM3]

Loved this, thanks!

[@patriciajoyner9871]

I wish I could go to the clinic .but Nevada.....

[@DrMartinRutherford]

We actually are able to work with patients from all over via Zoom. You can get information on how to schedule a consultation at powerhealthconsult.com

[@diesel4125]

I'm confused. Is one of them really tall, or is the other one sitting down? My brain foggy brain can't get past this question. I have to close my eyes in order for me to take in a single word.

[@turnitupmike]

One is very tall and one is very short

[@addhoc256]

I want to add the possibility of brain-inflammation.

[@addhoc256]

And B12 .

[@addhoc256]

I must say I totally respect a doctor talking about his own disease. That is really cool.

[@KidCity1985]

Absolutely, Dr Ron Davis has proven this.

[@EmilyPorter]

Do any of these videos have suggestions for calming down the the brain at home?

[@Roger-cb3fv]

Hi, I know of only one really great treatment for calming the brain which worked for me to calm my Amygdala down. Google "Linden Method" It's brilliant and he came to the same conclusions these Doctors have in regard to Anxiety. Goodluck

[@aegisgfx]

It has VERY bad reviews on Amazon

[@Truerealism747]

Dr Sarno tms great vid

[@Ray-iy1li]

I have been diagnosed with M.E & have always had a lot of stress in my life as well as childhood trauma. I can recall some symptoms back to when I was a teenager insomnia & back pain, I had some fatigue in my 20s but thought it was normal Exhaustion from working a very physical job and long hours. Then had some relationship & work stress through out my mid to late 20’s with more & more fatigue. I went out one night with friends for drinks and then the next day I had GI issues what I believe to be sibo & got allergies over night too as well bowel changes. But I eat sugary snacks all day like I’m im needing a quick dopamine release or the need to have alcohol. But when I have alcohol I then don’t need to snack on the sugary foods… how can you tell the difference from M.E or low dopamine? Or can you have low dopamine with M.E?

[@Truerealism747]

Yes can have both do you have hypomobility had CFS 1997 since fall pelvic pain.fybromylagia 6 years fatigue not as bad now have you killed your Candida?

[@dirty-d-rodney8458]

Hi Sir can you recommend someone in the New Jersey area?

[@DaisyKmua]

Does this also entail fibromyalgia or just cfs? I understand how it all comes from that fight or flight issue but how can you tackle that issue.. I live in Belgium so I can't visit you but I'm seeing g a neurologist soon I'd like to have something good to suggest.

[@69birdboy]

Try losartan

[@roygriend5143]

Search for b1 video's

[@bea29able]

The problem is not sleeping!

[@fuzzacker.]

CFS/ME sufferers need it in a nutshell toooo long.

[@kanthasastry4116]

how do you get the amygdala to calm down?

[@cheri7054]

Does taking Berberine destroy good gut bacteria?

[@ilonabaier6042]

i had chronic fatigue and when i stopped using statins the problem was solved

[@mmedeuxchevaux]

i'm gIad you feeI better, but you didn't have "chronic fatigue syndrome".

[@kennethmoore3783]

Diagnoses are not diseases

[@lilmisspeace]

Second comment, question to be accurate. Do you think a Borderline Personality diagnosis could have been chronic fatigue that was misdiagnosed?

[@diesel4125]

yes

[@Stopnormalizingviolence]

CFS/ME and borderline are often comorbid. I'm diagnosed with both.

[@Italian69Boi]

I found out my Chronic Fatigue was Chronic Acidosis, since MDs are useless. My blood was so acidic. I think my gastroparesis and pancreatic insufficiency was the cause. My bile ducts are clear but bile wasnt getting released. Everytime I ate or exercised id get burning hands and feet and my fingertips would pulse and id get shortness of breath which doctors just said i was anxious. One time my whole body burned and i couldnt breathe i think i was close to metabolic acidosis that time. I had diarrhea all the time too. And the acid causes potassium to be dumped out of cells which lowers BP. And my guess is my mineralcorticoid (aldosterone) receptors were somewhat downregulated from constant stimulation, causing worse potassium levels and worse acid levels. So all i needed was calcium pill and a little more sodium. So i suffered for 2 years fir nothing

[@g.s.5868]

at least you found a solution to your problem... gastroparesis is mostly a thing of eating the wrong foods like patatoes , lectins, nightsades & fat, that force your pylorus to close (food cannot leave) and relax your lower esophageal sphincter = GERD

[@joeshmoe7899]

What about resetting the brain? Ketamine, marijuana, etc?

[@mandymonroe6295]

Neurofeedback, I bet.

[@tammydesmet1678]

Yes!! I very much agree w u on that! Cause its coming from our brain.. then mess w the other parts of whatever other probs go w it. (I got fibromyalgia too) so what is it substance p lacking or too much in the spinal column..etc)

[@turnitupmike]

I think Ketamine WITH a more comprehensive treatment may have a role in centralisation of pain and polyvagal neuroplasticity.... however it won't address mitochondrial repair/gut health/ spine posture / toxins, pathogens etc ....

[@allanknight843]

Speaking of BS

[@aegisgfx]

Meh, they know what they are talking about.. most of what they are saying is accurate, but if they are using Chiro to treat it, then that part is for sure BS