Effective Treatment of Chronic Fatigue & Fibromyalgia

[@ChrisLee-rf5is]

Decades of low quality sleep. Long hours of sleep but never once wake up refreshed. It's been a sad life.

[@nancyhalloran3044]

Boy can I relate! Have you found anything that has worked

[@benxamin13]

Medical Medium, check him out.

[@raulpujol3847]

Lovely Video clip! Excuse me for chiming in, I am interested in your initial thoughts. Have you heard the talk about - Dinanlinson Rebooting Health Approach (just google it)? It is a smashing exclusive product for getting rid of chronic fatigue syndrome without the normal expense. Ive heard some amazing things about it and my work buddy after many years got cool results with it.

[@tessgirl383]

Antiviral agents should not be used for the treatment of chronic fatigue syndrome/myalgic encephalomyelitis (CFS/ME). Do Not Do Recommendation Details Recommendation: Antiviral agents should not be used for the treatment of chronic fatigue syndrome/myalgic encephalomyelitis (CFS/ME). Interventions: antiviral agents

[@tessgirl383]

Those are nice guidelines

[@NganLe-tb8bt]

I pray everyone here recovering and restoring your health and happiness. Much love 💕.

[@gabbym7219]

Thank you God Bless you 🙏

[@suepete]

I wish he'd call it was it really is: Deep, dark, drop-dead fatigue that causes the inability to function. It isn't "chronic fatigue," or even "fatigue." It is Chronic Fatigue Immune Deficiency Syndrome, also known as Myalgic Encephalomyelitis (neuroimmune disorder). The false name has had a significant negative impact on what others have understood about my disease. I have been second-guessed, told it was in my head, etc. etc. ALL because the name is WRONG!

[@gaylegibson4324]

Exactly!!!!! 😩😩

[@Jon-dh3ki]

Chronic fatigue is accurate in my opinion.

[@nikhilwagh7314]

Yes since then i having different different dreams also. Can anyone please help me with this 😔

[@denisedevoto5703]

I agree. Chronic fatigue doesn't cover it. It is a bone numbing fatigue!

[@allie54774]

Oh really? I did not realise what people refer to it to was as important as that. I call mine cfs all the time just because its what I was told I had. But I will try to retain this information! Thank you. I'll look into it a bit more.

[@upstairsbedroom5506]

I was diagnosed with ME/Fibromyalgia two years ago, and after being fit and hardworking my entire life, it has ruined everything....It is refreshing to hear someone be understanding, sensible, and offering an insight to becoming more well....

[@Fckubr00]

How were u diagnosed?

[@ramon2008]

What brought it on ?

[@harvestblades]

Would be curious to hear more about this & if this or other "treatment" has worked for you.

[@nomade438]

Thanks for sharing I so resonate

[@jennifersilves4195]

When I quit eating gluten I was able to get out of bed and exercise and work.

[@dawndaniel22]

I love this man.. He explained more to me than any Dr in the last 15yrs

[@Uniquettt]

But remember your Doctor can not give you that length of time.Coming here and trying to do your own research is the best way for me

[@josef.torrealba6992]

This was great, thanks, I've been looking for "what are the symptoms of myalgic encephalomyelitis?" for a while now, and I think this has helped. Have you ever come across - Diyadelyn Ziyily Idea - (search on google )? It is a great one of a kind guide for getting rid of chronic fatigue syndrome (CFS - Also known as myalgic encephalomyelitis or ME) without the normal expense. Ive heard some incredible things about it and my co-worker got excellent results with it.

[@Uniquettt]

@@josef.torrealba6992Primary Symptoms Also called “core” symptoms, three primary symptoms are required for diagnosis: Greatly lowered ability to do activities that were usual before the illness. This drop in activity level occurs along with fatigue and must last six months or longer. People with ME/CFS have fatigue that is very different from just being tired. The fatigue of ME/CFS: Can be severe. Is not a result of unusually difficult activity. Is not relieved by sleep or rest. Was not a problem before becoming ill (not life-long). Worsening of ME/CFS symptoms after physical or mental activity that would not have caused a problem before illness. This is known as post-exertional malaise (PEM). People with ME/CFS often describe this experience as a “crash,” “relapse,” or “collapse.” During PEM, any ME/CFS symptoms may get worse or first appear, including difficulty thinking, problems sleeping, sore throat, headaches, feeling dizzy, or severe tiredness. It may take days, weeks, or longer to recover from a crash. Sometimes patients may be house-bound or even completely bed-bound during crashes. People with ME/CFS may not be able to predict what will cause a crash or how long it will last. As examples: Attending a child’s school event may leave someone house-bound for a couple of days and not able to do needed tasks, like laundry. Shopping at the grocery store may cause a physical crash that requires a nap in the car before driving home or a call for a ride home. Taking a shower may leave someone with ME/CFS bed-bound and unable to do anything for days. Keeping up with work may lead to spending evenings and weekends recovering from the effort. Sleep problems. People with ME/CFS may not feel better or less tired, even after a full night of sleep. Some people with ME/CFS may have problems falling asleep or staying asleep. In addition to these core symptoms, one of the following two symptoms is required for diagnosis: Problems with thinking and memory. Most people with ME/CFS have trouble thinking quickly, remembering things, and paying attention to details. Patients often say they have “brain fog” to describe this problem because they feel “stuck in a fog” and not able to think clearly. Worsening of symptoms while standing or sitting upright. This is called orthostatic intolerance. People with ME/CFS may be lightheaded, dizzy, weak, or faint while standing or sitting up. They may have vision changes like blurring or seeing spots. Other Common Symptoms Many but not all people with ME/CFS have other symptoms. Pain is very common in people with ME/CFS. The type of pain, where it occurs, and how bad it is varies a lot. The pain people with ME/CFS feel is not caused by an injury. The most common types of pain in ME/CFS are: Muscle pain and aches Joint pain without swelling or redness Headaches, either new or worsening Some people with ME/CFS may also have: Tender lymph nodes in the neck or armpits A sore throat that happens often Digestive issues, like irritable bowel syndrome Chills and night sweats Allergies and sensitivities to foods, odors, chemicals, light, or noise Muscle weakness Shortness of breath Irregular heartbeat

[@AlmazulVortex]

@@Uniquettt The truth is that doctors do not know how to revert chronic disease.

[@MissJetson5]

@@Uniquettt Thank you for this information. I'm 25 years housebound. Tried grocery shopping a short time ago and had to call for a ride. It was frustrating and very embarrassing. This helps validate what goes on while others just do not understand. :'... While this is by far one of the smallest of my symptoms (grocery shopping), reading this one thing really hit home. No one believes taking a shower can be so difficult. I resort to sitting down in a bath and using hand held shower to rinse. Most often need to lie down for at least 2 hours after. And getting dressed consist of yoga pants and a hoodie. Hair very rarely gets more than a comb through. I haven't given up yet. Hope is all this cruel depletion of energy/life leaves me with.

[@HellasGD88]

Wow an actual Dr that cares.

[@nainiramulu4595]

Thanks from my heart, Doctor. I observed tremendous positive results just after 2 weeks of following your treatment. My condition is improving noticeable, after suffering for 20 years. Thanks again.

[@gallakochar4245]

Wow.. Naini…

[@Frosty-273]

Did you get the information from just this video or from the link/payed treatment? I seriously need whatever I can get to help start to change my life desperate for a better life 😓

[@Eana-of-Sussex]

Have you found relief yet? Jus seen your post from 2 months ago..

[@zccau2316]

what is his treatment?

[@ronilittle7028]

Bless you sweetheart! I love this Dr,!

[@tonifelise3]

It would help if we had a competent medical industry, instead of one built on keeping people sick and billing insurance companies.

[@Freesoul54]

My life was before severe /ME and after. Ambitious , sporty , perfectionist& driven. Was famous for juggling 100 balls at same time. On top of the world . After emergency c-section With a baby ended up in wheelchair! Yes it is all in your head, you have depression etc after 3 year of different diagnosis like MS etc told me you have FM/ME. I cried atleast knew am not crazy. I know now that I burnt myself & my body out. I lost my career as pharm D. Still no one understand & gets me. Still do too much for my family . This year became 50, and DT2 as well due to reduced mobility . My cortisol has been x20 normal levels and that makes it difficult to lose belly fat. If I could live in deserted island , with no responsibilities and no one to expect too much of me, I would feel better. I am never pain free even with fentanyl patches , SSRIs etc .

[@oo6112]

😭😭😭Can I come to the island with you please

[@tousift7822]

I want to getisolated on an island as well where I don't have to explain or I don't have to oblige to others

[@tousift7822]

@saba r u a doctor??

[@MrsBDatCreole]

How are you now?

[@aineotoole3686]

Do you take B12? You can become deficient particularly during/after pregnancy and after surgery with nitric oxide.

[@henryboyd9542]

This is only the second time I have ever commented on another persons videos on KZbin. I would like to give you a huge thank you for conveying what I have been experiencing for the last 5 years of my life. Long story short, I spent six years in the military deploying all over the world and it caused me to blow a fuse along the way. I was recently diagnosed with CFS by the VA and I am just grateful to finally have a name for the multitude of symptoms I experience on a daily basis. Thank you again for making such a comprehensive video!

[@rahab-mercyjewel3846]

At first my legs started to feel heavy and gradually I started having a weighty feeling on my cheßt that makes me weak...please can you help?

[@83dangerweasel83]

Thank you for this video. I am crying watching it because I feel hope for the first time in years

[@Starshine_99]

I just have to find the money now for all of these supplements. Being on disability, it's hard to even find an extra $5. It's another component that makes this disease hard, no health to work, and no money to get the treatment, meds, supplements, or appointments to get better. Trapped. 😭

[@drina4706]

Yes! It's hard ....

[@charliegordon2266]

I tried all of this and nothing helped.

[@edie4321]

I feel you. I've been caught in this trap since 2005. I ran from the medical industrial complex in 2017, and still have not recovered. There are cures for ALL these things. This is why they hate Mother Nature. We must demand the cures, and an end to this system.

[@Truerealism747]

​@@charliegordon2266do you have hypomobility

[@Truerealism747]

​@@charliegordon2266do you have hypomobility

[@Ava-oc1dg]

I’m glad you said doctors are clueless diagnosis for thyroid and crohns took years. I believe I will probably die from old age before I am properly diagnosed for fatigue.

[@Truerealism747]

Do you have pain symptoms

[@Truerealism747]

Thyroid chromes causes fatigue in itself badly

[@ruthwhittingham4]

At last someone who gives hope and no nonsense information with great humour and positivity. Thankyou 👌

[@CambioJoe]

You may have chronic fatigue if you’ve fallen asleep watching this video while taking notes... twice and then still never got to the end.

[@Miss_Tika1]

Absolutely

[@debrahendriks4098]

Oh my goodness…….youve GOT IT! Isn’t it awful..

[@kavitadeva]

Narcolepsy??

[@JJ-yu6og]

What a great personality he is!! He is so real!! Love his attitude!!

[@arealperson8084]

@@Christianmoney1 Shut the fuck up

[@MsHeaddy]

I read years ago that approximately 78% of people with fibromyalgia had previously suffered a severe neck injury. I can say it’s 100% true in my situation.

[@ishouldbesleeping1354]

Oh wow! Me too!

[@PurplePinkRed]

Holy crap! You might be onto something!

[@barbarateresarhiannonsreal1756]

Yes, neck injury here as well.

[@ciobicaalin499]

Did You tried prolotherapy ?

[@larapalma3744]

Yes

[@JessicaRode]

I wish he could be my physician I love him! Bravo.

[@meg9598]

Wow I wish my doctor knew this! I’m going to try to do it myself as I live in the UK. Thanks for putting it out there I ‘m so grateful

[@Truerealism747]

As it worked

[@IBLV2DOU]

Wish we had a good rheumatologist near our home. And one who recognizes stress, from pain and missing life, actually cared about people. I take pain meds, and they help a little. I dropped one med completely. I blew a fuse years ago. Been in pain 23 years, I’m about done. Maybe it’s time to look into holistic help. You’re a great Teacher, and it’s refreshing to finally hear someone believe we are sick. 🙏

[@Truerealism747]

Any better do you have Asperger's

[@toni-leepadman3777]

Why did you ask that Tom? Actually curious and not being a twat

[@storkdoctor11]

Listen to this man ! I actually have primary adrenal failure ( Addison’s disease ) and damn near lost my life in Addisonian crisis …. This , after I became so acutely disabled that I knew I was dying and had 6 separate points of entry over 8 weeks into the hospital / medical system ( missed EACH time !) This has been my life x 12 years now. And I’m steroid dependent for life now . But …… that said , it’s like this man has been following me around . This is THE best medical synopsis I’ve heard in two decades . Well done , sir !!

[@mdee860]

I agree with you, Dr. Teitelbaum actually "gets us." Brilliant video. Wow, all those Drs. in the audience were tough on him. He was trying to take a very complex disease & inject a bit of humor into the subject - but it was like pulling teeth to get them to laugh.... until the choc. analogy! PS: I wish he would make just 2 or 3 pills that include all of the supplements he mentioned.

[@gillhall7590]

I should have added, that I took low dose steroid (5mg)for 8months, until the inflammation subsided. And as I added vitamin B1 I reduced steroids, until I could manage very well without them. If you get a rare flare up, take short dose steroids if required, to settle things down again.

[@soundrastone2800]

😊

[@areneesouder]

Think my adrenaline was shot a long time ago due to constant trauma and stress, and this illnesses and no help. My heart rate stays over 100 even at rest. I was a perfectionist and would rather do everything myself than to trust others to do it and do it right... Now I'm bedridden for all these years and can't with basically little to no help cuz people don't understand around me, yet I keep trying to keep my and their spirits up, and laughing.

[@bevnae]

I’m slowly coming out of this so I don’t have quite yet enough energy to go into any detail, but please please start reading up on the work of Ray Peat. He’s a biologist that really understands this, and he’s not selling you anything. Good luck.

[@manyBlessings2all]

@@bevnae thank you bevnae 😘🤗 💜 may you be well & happy asap ✨

[@stephg4273]

Maybe look into CFS HEALTH program or dnrs/ans rewire

[@sherryd.3425]

I have 45 years in, my friend. Do not quit! You are alive and you are amassing huge quantities of information. Your knowledge and your story might be useful to help others in your family and community, including me, to avoid the same pain. Knowledge will save us. Joy to you and yours.

[@MsFiFix1]

Omg!!! You have to read the mind body syndrome by doctor sarno which describes this situation perfectly. Please read I know it applies to you.

[@schoolofhot]

I’ve had CFS my whole life (I was a sick baby), long story short, he’s right. Don’t even fight it. The only reason I still go through bouts of CFS is when I stop doing some of these things! He’s a wealth of knowledge. Listen to him and don’t quit, it can take years but you’ve gone years stressing your body out.

[@tracysmith245]

so was i very good video never had vit d

[@deannang455]

It runs in our family. Been tired and hard to sleep forever. Symptoms he lists are just normal for me all 37 years on this planet.

[@organicfireorganicfire1236]

Look into the amazing liver and gallbladder flush by Andreas moritz

[@organicfireorganicfire1236]

@@deannang455 look into Andreas moritz liver flush.

[@Jazz-ch9uj]

Hi! How have you been? Could you tell a little bit of your story?

[@radiancelee1977]

So basically eat well (anti inflammatory diet, or high protein), know your energy limits, make sure you're not vitamin deficient, try to limit infections or rid of them as soon as possible, do low intensity exercise when you can and limit stress

[@oo6112]

Ive been doing all this and still suffering. I cant afford to go completely vegan. I wish i could. No one in my house eats like me. I workout for a few weeks. Then i crash and cant go for weeks. My pain is just relentless. Ive lost a lot of muscle mass in my legs.

[@radiancelee1977]

Since I'm a targeted individual I understand why its been happening to me. They using radiation microwave weapons to do experiments on citizens

[@yournamehere6939]

@@oo6112 which vitamins and mineral supplements are you taking?

[@mustafanaser9789]

@@oo6112 you crash everytime after training? Then you have a false approach. I would recommend just to train in the beginning 1 minute. You should begin at a very easy workout like instead of normal pushups you should do pushups on the wall. If you feel much better with that then increase the intensitiy but just a little bit.

[@oo6112]

@@yournamehere6939 vitamins for muscles, bones, inflammation, immunity. Im good on the vitamin dept.

[@PaperclipProphets]

This man is a medical miracle! His talk was a wonderful blessing, thank you🙏

[@RaelanAgle]

I'm so grateful for everything that Dr. Teitelbaum does spread awareness and information about this illness! Amazing. It's exactly people like him and videos like this that inspired me to start my own KZbin channel sharing my 10 year journey with CFS and eventual full recovery. Great information - thanks so much for sharing it!!

[@Jade-bf5we]

I have begun following you recently Raelan via KZbin. Your videos have begun to help me immensely.

[@LR-px9ms]

a plug in?

[@peopleplacesandperspective5564]

I was listening to your story tonight for the first time. 💫

[@MisterstereoOso]

What a wonderful presentation ! Many thanks from an appreciative Englishman 🍷🙏

[@alexhouston899]

Amazing finally I have found a specialist who knows what they are talking about. thank you the nutrition section was so useful and I have had more information from this conference than all of the days and weeks researching on papers and the internet. thank you

[@jennifergold2529]

I wish to use this medium to recommend this great herbal doctor called Dr Onyeneke on KZbin he cured me from fibromyalgia which i have been suffering from for the past 8 years now God bless you sir indeed herbal medicine is the best way of healing.

[@astaraoneill9166]

This explains so much. I have so many of the symptoms, including some I’d never known were correlated with Fibro...I wake up every night due to a completely numb hand, some times several times. I have hot AND cold flashes. They’re almost never related to the actual temperature, and with the cold flashes, it takes forever to get warm again.

[@jonprue]

I had that too but instead of just a numb hand it was my entire body! That was crazy! It was actually intense anxiety and what happens is your blood flows to your core muscle groups causing the numbness in extremities. Search “improvement path anxiety” on KZbin here and you’ll probably see some things you’ve dealt with. Hope that helps

[@Miss_Tika1]

@astaraoneill9166 - Same here

[@mdee860]

Thank you Dr. Teitlebaum. This is such a great, informative video. It really should be a 'Mandatory' course for Continuing Education credits for Drs. & Nurses. All 'Teaching Hospitals' should make this video available to their students online & on demand. It's that good. 👏👏👏

[@Peter-zw8yn]

This guys the man, would love him to be my consultant.

[@victoriadolci6463]

There seems to be 2 ways that CFS people are affected. Those who cannot sleep well and those who sleep too much. I believe they are both the same disorder just expressing differently.

[@ksize3147]

Victoria Dolci, I agree. It is the lack of deep restorative sleep that is missing. The deep sleep that restores and repairs your body, the sleep that makes you feel rested....restorative sleep ( stage 4).

[@alexedgar6539]

Yes. I will sleep 12 to 20 hours deeply and solidly when my me is active.

[@VyvienneEaux]

I have experienced both modes of sleep distrubances. The oversleeping, I believe, is a consequence of sleep disturbances preventing you from getting quality deep (stage 4) sleep. For me, I tend to have a lot of nightmares (which occur during stage 3) that wake me up before I can get stage 4 sleep, and then I go back to sleep repeating the cycle. Other periods of my life, when I have a lot of responsibilities, I have so much anxiety about sleeping for too long and about the nightmares that I can't seem to fall asleep.

[@schmeegil2240]

Same I can sleep 16hrs with 10 minutes waking every 2 hrs to realign myself and matteress

[@catherinewylie6959]

I have FMS and relapsing and remitting chronic fatigue but mostly I am tired if I do even half of what normal people can get done. I can get a good night's sleep and then still need an afternoon nap that can last 1-2 hours,

[@1bigreddog1]

Excellent Presentation! Thank you

[@DjSumitM]

I am hypnotherapist, and now treating a client with CFS. I am finding your video extremely helpful and I am glad that my client is showing progress. Hypnotherapy and your wisdom is working greatly. Thanks you.

[@Truerealism747]

Helping pain ?

[@DjSumitM]

@@Truerealism747 pain and tiredness

[@nateneyasamuelslaw4620]

Where are you located? Can Hypnotherapy really help with pain? If so, how?

[@DjSumitM]

Hi @@nateneyasamuelslaw4620 I am located in Europe. Hypnotherapy can help with pain but not with the reason of pain. I have helped my client and friend to manage pain because of cancer. Pain is a sensory signal to your brain that you need to do something that is wrong. In some cases we know what is wrong (wound/cancer/ or someother ailment) which can not be treated immediately, in that case hypnotherapy can help to manage the pain, You're most welcome to get in touch and we can talk about it in details.

[@DjSumitM]

yes@@Truerealism747

[@Zee7897-e3f]

I am force to say you ,,,SIR,,,,you are giving so informative , ,emotional ,, humen friendy ,, and whith full of your own attention to giving more and most beatifull lecture on conference.......I am your big fan since now ......you are genius on earth .........

[@kreeastichattopadhyay2965]

Thank u.Now I understand my cfs and fibromalgia,neurotic pain,thyroid problem,lack of sleeping problem,neurotic pain,weight gain,lack of exercise and unable to say people NO all are interrelated.

[@tousift7822]

I am a m and I am stuck and I have pressure saying no to ppl what should I do I don't know

[@sherryd.3425]

@@tousift7822 Oh, don't answer the phone! Look at the text message. Mom and your children and maybe your Significant Other get a call back if they use the appropriate code word for emergency. No one else. Anyone over eighteen may be blocked at anytime from your phone forever, if they tire you. Blame me. Sherry said no. You can't do it. Your mental health won't allow it. See Sherry online. Right here. (It's so much fun setting boundaries for other people's friends and families. Give it a go. It is empowering.) I hope you're well in the here and now. Don't let the CFS blues drag you under.

[@bananamustache3071]

100% most of these what I have found to actually help me, especially all the nutritional stuff. Thank you for what you do.

[@ronilittle7028]

Oh,I love this DR.! He is the most thorough, and complete, of any I have ever seen in my many years! He doesn’t miss a thing! He is truly a godsend!❤

[@harvestblades]

I don't know why I am just seeing this after all the searching I have done. Has anyone gotten results with what he says in this? I am 44 & male. I have had Fibro for around 6 years now, & have had migraines since I was twelve that has become worse vs better as I age. The combination of the two has done its best to ruin my life & has almost cost me my life as I can no longer bear continuing to fail my wife & nine children. It has gotten to the point that I have apologized to my wife for marrying her & starting a family that I had no business starting. Going onto a low carb & even better an animal only diet has given me the most benefit. I have worked construction for most of my life, but things have gotten so bad holding a job is damn near impossible. With the chronic migraines it has been hard enough. I also love training jiu-jitsu & Muay Thai, as well as weight training. I need to really spend extra time warming up before class/session, & a half hour after I stop moving my body seizes up & I move like my 85yo grandfather (literally hunched over, & stiff until I can warm everything up, but the pain is still there), & mornings are hell.

[@VyvienneEaux]

There were so many points where what he was describing described me exactly, in weird ways. For instance, I have long described the onset of my muscle pain as "it feels like the muscle randomly tenses and hardens up until it exhausts itself and starts hurting, even when I'm not using it." I have also noticed cognitive improvements when I switched from veganism to eating meat again after months of intense cravings (this is probably the only time I'll admit to having been vegan, because vegans who stop, no matter how sick, are relentlessly bullied by vegans). Additionally, I crave loads of salt and can't seem to hold onto any water. I could go on for pages.

[@PurplePinkRed]

Are you watching Goatis? Former vegan who only eats raw meat now. He opened my eyes! The community there is very supportive.

[@astaraoneill9166]

OMG, I’m the same with salt cravings and frequent urination! I always say it’s a miracle I don’t have high blood pressure, but it’s actually good!

[@serif392]

Do you also need to drink a lot of water. Could be pre diabetic.

[@astaraoneill9166]

@@serif392 I also eat TONS of salt and urinate about every hour.

[@lynettebright5299]

I used to eat salt right out of my hand when I was a teenager.....I think Ive had this all my life. My bp is normal, thankfully

[@LB-yj6lj]

Love this man

[@katpea3641]

My CFS/FS started immediately after contracting Epstein Barr syndrome in 1999. I learned how to manage my fatigue symptoms and they only flare up when life gets extremely busy or stressed. However my fibromyalgia pain i have not been able to relieve. I'm very fortunate that i am able to work full time, I'm self employed so i take a 2 hour lunch every day to help manage fatigue and pain.

[@yournamehere6939]

How are you doing? Have you found a solution to your pain? I also had to stop being an employee and had to become self-employed in order to not get fired for not being able to work an 8-12hr shift

[@leaveittolefty]

my husband's rheumatologist prescribed Cymbalta/Duloxetine for fibromyalgia (he has RA) --he is like a new person! so happy he got relief!

[@donnag7288]

My fibromyalgia response well to swimming everyday. Once a month I see an Accupuncture. Also low sugar , practically no carbohydrates. Have been working for over 30 years and trying to make it three more years .

[@kildee0170]

@@leaveittolefty I was on it to, had to stop it after being on it for couple years, you would have thought I was coming off crack or something like it, never been so sick in my life, I went through severe withdrawal symptoms. I'd never take that again.

[@sherryd.3425]

@@donnag7288 Good for you. It took me many years to figure out no carbs (diagnosed in 1983). Also, I had to reduce dietary fiber to almost nil. I found that quiet, regular daily exercise was essential, and that walking and basic yoga stretching were my go tos.

[@mcooper4043]

I love this video, this man has truly blessed me with his free knowledge! I have listened over and over and i know have it!!!! Plus he is hilarious! Thanks so much!!!!! Many blessings.....

[@robinlong1653]

After listening, I realized I met this Doctor in the 1990's as I used to do educational support for this. I've had this 35 going on 36 years.

[@maxjurish2589]

DAMN! A doctor that thinks beyond the box!! A million cheers doc! I've had cfs/fms since '99. I always said that it was the brain throwing a switch for survival but didn't know which part and the bio part. I thought it was the mitochondria. Thanks doc👍

[@christinecollins3131]

Wow. The fact that you had to leave med school it home. I made it through law school (with the ridiculous loans), only to fall apart a few short years later. It's devastating.

[@Glower22x4]

The best presentation and guidance for this condition I ever had, thank you 💖

[@aug.jam.1]

I've tried about everything by now to get rid of my chronic fatigue after having my colon removed due to ulcerative colitis 4 years ago + severe depression 2 years ago + Covid 1 year ago after which I believe I got CFS and so far had 3 failed suicide attempts. Doctors either don't believe me or don't give a shit and I can barely do any work at work or at home and have aches all over my body. And will try anything this man said during 2024 no matter what. I'll post an update monthly under this message to let everyone know if it is any good. I'm very skeptical though as nothing so far helped but still have a bit of hope left....

[@samuelJHolmes]

How are you getting on?

[@aug.jam.1]

@samuelJHolmes thanks for asking Samuel. I am taking exactly what the doctor in this video said for about 3 weeks now and I do feel a bit more energetic, I do have to supplement during week/working days with Ritalin once in a while as I do have bad days where I still have no energy for nothing However coincidentally I was talking with my wife yesterday how in general I do feel a little better. Not very much, but all little bits are welcome. I will at least keep this regimen of taking the following supplements for at least 6 months as I do see/feel some potential: Vitamin D, Omega 3 Fish Oil EPA/DHA, D-Ribose, CO Q10, Thyr (Thyroid) support blend, N-Acetyl Cystene, and additionally because of my previous and current medical problems I do take additionally Iron, additional multivitamin, vitamin C and Tramadol for my chronic pain. None of these substances I am exceeding max daily intake so that should be fine. I must say all in all it is quite expensive, but I see it more as a possible investment for my future. Also I am heavily focussed on working my mental issues with spiritual teachings from various sources, but especially from Mahayana Buddism although I don't focus on the religious part of teachings necessarily, listen and read a lot of books from philosophers like Alan Watts, Eckhart Tolle, Jiddu Krishnamurti, Ram Dass and doctors like Gabor Maté and people like Andrew Huberman, they have helped me all a great deal keeping my positivity up in dificult times. Sorry for the long winded post. I hope in case you're struggling with the same you find a solution soon as well!!

[@samuelJHolmes]

@@aug.jam.1 Really pleased that you have seen some benefit. My mum is the sufferer and I have to care for her whilst doing my job. Desperate to find something that can build some momentum. Did you get the supplements individually/privately, or did you buy the mix promoted in this video?

[@aug.jam.1]

@samuelJHolmes I bought it all separately through Amazon, some different brands but with the same strength dosage as the doctor describes, also look for his website, I think he mentions it there in a bit more detail. Since I live outside the US it made more sense to me to get it through Amazon due to shipping fees and times. I sincerely hope it has some positive effect on your mother as it is incredibly difficult to live with and also for the family to deal with this situation. I'm wishing your mom and ofcourse yourself all the best from the bottom of my heart and hope that you find a solution real soon.

[@aug.jam.1]

@@samuelJHolmes i bought them all separately through Amazon. That was the cheapest for me as i so not live in the US

[@Jazzidun]

I recently got diagnosed. Oh, the doctor hit the nail on the head. I was prescribed multiple anxiety medications, talked to slowly as if I was a nut case. I kept pressing until I finally had 2 doctors who understood my symptoms.

[@doreenlane9352]

Iv had fibromyalgia 28 years M E 17 years nothing helps .

[@dianawalker1622]

Doreen I very had fibromyalgia since age 9, I'm 66 now. Cfs comes and goes. 10 operations requiring demerol or morphine, 2 horrible car wrecks, lost the ability to work, age 19, lost every family member I ever had but one son. Just trying to live on my own after losing 2 husband's has been unbearable. I pray every day God will take me home. The pain I have had to live with all my life is so unbearable.

[@mar-mar3700]

Your knowledge, explanation and guidance are amazing.

[@brandypopejohnson2072]

This dude is giving the Science 🧪 🧬

[@chasingclouds7101]

This is what's been eating me up!!

[@MrsBDatCreole]

How are you now?

[@drelfredealberts5517]

SOOO HANDS ON...WILL DO ALL THE HOMEWORK. tHANK YOU.GOD SPEED

[@ivettesantana4319]

Omg thank you for this talk! I am now connecting all the dots and will go to a dr and written timeline because I cannot cope anymore on my own.

[@taleofawhale6964]

Thank you dr Teitelbaum. I have been suffering from fibromyalgia since 1973 and nearly died. You gave all the answers I needed to understand and accept my condition.

[@Truerealism747]

How did it nearly kill you

[@Tluv_1955]

Very helpful content Thankyou

[@africkinamerican]

It's not only the hypothalamus that controls peristalsis... nerves do as well and spinal subluxation, MAY play a role in slowed transit.... that is *definitely* the case with me. Subluxation could be purely mechanically caused or can arise secondary to the other causes such as infection/inflammation, according to what Ive heard from chiropractors. Inflammation in and around the spine and its surrounding tissues can impact the operation of the nerves, even the vagus.

[@Truerealism747]

Hypomobility can do this then

[@darlingstuff1560]

Arrogant & INCORECT. I sleep for hours...have 2 nights in a day briefly waking between. Had this for 62 years so long sleep is an established BRAIN HABIT

[@Goated12348]

I sleep 9-10 hours but am still exhausted every waking minute

[@drina4706]

Try taking GABA. It will help you get deeper, more restorative sleep.

[@gabbym7219]

No !!! Don't take Gabba, I was in high doses of Gabba bc my pain was chronic, my sleep was/is bad and my fatigue is killing my mind . With the time my memory has changed A LOT (😢) but my mood, omg!!! was horrible, I was mad, angry, everything bothered me and I started being aggressive. The Psychiatrist prescribed that but he never ever explained to me about the side effects. I just done taking that medication, trust me, can be good in low dose and short period but that's it. Now makes me scare when I hear about Gabapentin

[@jopainting1668]

I agree, do NOT take GABA.

[@tanyaluchko9003]

@@gabbym7219so, what to take?

[@figment9625]

I went keto and I take a pile of supplements and probiotics. Dr. Berg videos.

[@healthyman01]

Thank you Dr. for your unconditional help.

[@karrde666666]

the worst part is the normal people that say they have chronic fatigue, brings down everyone that really does have it with migraines,pots etc

[@lorrainedettbarn9384]

Thankyou I not only found knowledge but humor.

[@atiqrahman7289]

Lot of information----- multi-faceted.

[@florabraswell8423]

That’s what l was diagnosed with fibromyalgia and chronic fatigue years ago doctor’s didn’t even care about that , never thought it could have been something more serious did not do blood test brain scans or anything now l still have terrible symptoms going on with no medication for the pain management symptoms and lam a lot older and suffering everyday

[@Truerealism747]

Are you hypermobile diagnosed Asperger's today 27 years CFS 6 years of fybromyalgia for me there same thing neurosthenia

[@audreythurman3496]

This is me I'm so tired and I'm not doing anything I get tired getting up, laying down, tying my shoes, I'm so sleepy. Help

[@JANAlifestylevlogger]

My question is what do you eat on your regular day?

[@fordrac1ng81]

exercise a minimum of 30 minutes 5 days a week. It'll help after a few weeks. Needs to be very strenuous though, not just going on a walk. You need to be sweating.

[@stefanmitrovic973]

Excellent Video! Sorry for the intrusion, I would appreciate your thoughts. Have you heard the talk about - Dinanlinson Rebooting Health Approach (search on google)? It is a smashing one off product for getting rid of chronic fatigue syndrome minus the hard work. Ive heard some awesome things about it and my buddy at last got amazing success with it.

[@argenisacosta8296]

Appreciate Video clip! Forgive me for butting in, I would love your thoughts. Have you researched - Dinanlinson Rebooting Health Approach (Sure I saw it on Google)? It is a smashing exclusive product for getting rid of chronic fatigue syndrome without the normal expense. Ive heard some amazing things about it and my m8 got astronomical success with it.

[@tonylars4128]

Kudos for the Video clip! Apologies for the intrusion, I am interested in your initial thoughts. Have you thought about - Dinanlinson Rebooting Health Approach (do a search on google)? It is a smashing one of a kind guide for getting rid of chronic fatigue syndrome minus the normal expense. Ive heard some pretty good things about it and my work buddy after many years got cool success with it.

[@zozo6820]

BEST DESCRIPTION EVER THANKS FOR THAT !!!!

[@suebrown5665]

Many thanks, light bulbs popping on, very useful points. Be well everyone!!

[@MC-yx9oe]

Might want to look into oxalates which dark chocolate is high in

[@amirouchehocine7504]

If you are watching this at any time. I have had a gradual Chronic fatigue syndrome that was mild but still making me exhausted every little day despite how much I sleep which made me live like a zombie every day not able to work or study neither aocialize. I second the doctor, Carbs and food with high GI are your worst enemy, just avoid them for now. Eat a lot of vegetables and leafy greens. Take vitamins, you will start noticing that your sleep improves. Moreover, Take a lot of Herbs tea that help to calm and sleep better, like Tulsi, Chamomile, Lavender and lemonbalm, if your sleep gets better you will feel much better during the day. Moreover, herbs like Curcumin(taken with black pepper ) will help you to reverse the effect of stress and fatigue over time. Read about them! and wish you all the best in your lives :)

[@desjoshbpbo8212]

Please seems it’s startled after treating malaria..what can I do ..

[@newschaser6414]

Wow thx, I think i have mild CFS too 😢

[@kathyalexander3905]

Thank you!

[@Doughkat777]

I have self identified as asexual since middle school. I have also had CFS symptoms most of my life. My doctors think I have had this disease most of my life but was misdiagnosed with major depression. No one questioned why I had major depression while constantly tired and constantly complaining about everything being painful. 🤦‍♀️

[@Vancouver_1986]

THANK YOU. Depression isn't a good diagnosis for this neurological immune system disease.

[@lalitaholmesstressfreefast1897]

Thank you for this clear and concise explanation. Mine started by the fuse slowly becoming weekend by years of trauma, then that drop dead flu, followed by an injury and living in a toxic environment. Which then blew the fuse. I had been doing SHINE and didn't realise it. It was really once I addressed all the reasons I blew the fuse that I completely recovered from Lupus, Fibromyalgia ad CFS.

[@robindraterang5870]

Hello dear I need your help.

[@sergiorrwodz]

How did you recover? Can you share with us?

[@lalitaholmesstressfreefast1897]

@@sergiorrwodz i used a memory reconsolidation process addressing all my physical, emotional, environmental and psychological stressors and trauma.

[@Truerealism747]

Who did you do this with thanks

[@lalitaholmesstressfreefast1897]

@@Truerealism747 Robert Smith the creator of Fastereft. I have trained as a practitioner now if you would like to ask any questions

[@atiqrahman7289]

Impressive presentation.

[@simonnattrass2171]

Was going to skip past this until I realised it was Dr Teitlebaum

[@dotperry7443]

I have very much enjoyed his presentation. I was diagnosed with Fibro a couple of years ago . I also have Lupus , sleep apnea along with many other problems.. My only issue with his talk is the sleep part. I'm almost totally opposite thank goodness. I can sleep pretty much anywhere anytime 😊

[@toni-leepadman3777]

Me too but never jump out of bed feeling refreshed and ready for the day. I have also read that fibromyalgia can make you more sensitive to pain but I have a very high pain tolerance

[@banzobeans]

2:52 Can someone please explain what a "good night‘s sleep" means exactly?

[@Shericams]

Poverty is too much a problem to make any of this possible for someone emojis inwell or trying to get well so good luck today dealing with this issue

[@latonyaleach3026]

Very informative and first time I’ve felt some relief in knowing am not crazy! I have to find a doctor who believes in Fibromyalgia but will start Shine method for now!

[@nicolecross4834]

I hardly eat anything at all because I carnt stay awake long enough or have the energy to eat,I'm young a n d sleeping my life away,I lost my job everyone's angery at me,saying just get up and do stuff,but I turn white the second I stand I WANT TO LIVE PLEASE PLEASE PLEASE HELP

[@savannaheckstrom7296]

Hi Nicole, I’m 19 and in the exact same boat, had to put all my dreams of college, moving out and working aside because I’m in constant pain. I’m 104lbs rn cuz I can’t eat I just don’t have the energy. Trust me I feel what you’re going through. What helps me is writing notes for myself that i can look to when people don’t understand and give you shit ( which of course is constant ), for instance “you’ve been presented with this challenge for a reason” or “ my pain is real and valid” stuff like that. What has helped me so far is removing as many unsupportive people from my life as possible and REGULAR THERAPY, there’s also Facebook groups for chronic conditions and it’s helped me cuz being so young and so sick can get lonely. But most of all don’t stop, don’t stop going to all the shitty doctors, don’t stop saving for expensive naturopath care, don’t stop trying those difficult diets. No one knows exactly how this disease works but many people have found routines that allow them to have a good quality of life, it’s so hard but try not to loose faith ❤️

[@rob141]

If you have a problem when you stand it's probably POTS(postural ortho static tachycardia) just Google it, but you need more sadium(salt)

[@andrewdove9867]

Hang on in there Nicole! Sitting on the sofa with my 5 year old, wondering how I’m going to get the energy to get off it and make us lunch.... arrrgggg! Keep plugging away at it. Get angry get sad but keep going. With a bit of luck and a healthy diet things might get better for you. Best of luck.

[@kfl611]

My sister has Chronic Fatigue & Fibromyalgia, she says she has to exercise and that helps her combat being tired and in pain all the time. Well she has neck and back pain, I sent her this web page link. Hopefully it will help everyone. It sounds crazy if you don't have energy, that exercising will help you get more energy, who knows, maybe it gets your juices flowing correctly in your whole body.

[@kimberlya9591]

Research this Dr if you think you have fibromyalgia. Dr. Paul St. Amand. There is help and you will be surprised of the simplicity to heal. The medicine he uses to heal is guaifenesin. Like Mucinex, but don’t use mucinex, there’s other stuff in there you don’t need. Read his protocol. You’ll be amazed. Search him here on KZbin.

[@lynb87]

Interesting about the salt. My husband has fibro and his sodium levels were borderline low. He mentioned this to the doctor but they thought it was irrelevant.

[@jessicadubois9945]

Mine goes low all the time.

[@favianalatorre1836]

My sodium is also low and doctor's can't figure out why.

[@deannang455]

Been like this since I moved during the pandemic. C19 made it worse. No energy and its 3am, but this is normal to be up.

[@areguapiri]

Stop the covid lunacy.

[@allaboutstress]

Brilliant and Thank you

[@tigressnsnow]

First questions I ask myself when I wake up after falling asleep during the day. 1. Where am I? 2. What day is it? 3. What's the time? 4. And why am I on a plane and where is it going?

[@user-ki7ud2mk8h]

Lol. Classic. Also: Who am I? Where's my car?

[@tigressnsnow]

Do I have a car? Can I drive? What's my name again? Lol

[@karine8738]

Same hete 😳 are you better ?

[@theonecounttheonecount8477]

Killing the yeast overgrowth is the key. It's gruesome pain, and utter exhaustion.

[@Truerealism747]

Still got pain sinuses are clear now do you think it's anywhere else

[@Nawidmusarat]

Nice video and I learn a lot thank you very much Nawid

[@KevinFreist]

i don'tknow anything but my experience. i had the drop dead fatigue . i was know to all as "flash". no longer . i found that i am likely b1 deficient . i am vegetarian . cooked anything is usually low if not depleted of b 1. i had physical nerve trauma on upper right extremety in 2013. subsequent surgeries did more damage. moringa has been my savior since i quit drs. after 6 years of missdiagnosis and detrimental treatment , i was done. no improvement. i started eating raw dry moringa ( 6 to 8, 00g caps a day.) it has too many positive qualities to list but one great benefit is good levels of b 1 and the supporting enzymes . total package of nutrients . when i stop or scale back on moringa , my arthritis , swelling , edema , neuropathy , pain and no energy all come creeping back. after 2 or three days if 6 caps , i can function and get things done , then after relax with out agonizing pain. look it up .i grow my own now.it saved my life. if i didn't find it by the grace of Gods providence , i don't know how i would be today it i would be at all.

[@bonitocraftsarg]

Excellent dr.🎉

[@yournamehere6939]

I got fed up with the medical system and looked for my own treatment plan, I take zero medications, my pain is down 98%, I’m sleeping a lot more, my chronic headaches and migraines are gone, and my chronic fatigue is 80% better

[@a11j]

so what are you doing that is helping if you don't mind sharing.

[@yournamehere6939]

@@a11j Hi. I started looking into vitamin supplements that other people posted were helpful for their symptoms. I researched each one and after 6 months I had a regimen I have been using for the last 7 years and so far, they continue to help. I’m being tested for Sjogren’s Syndrome and Lupus and getting my thyroid hormones tested and God willing, will get a full diagnosis. I’ve been diagnosed with fibromyalgia already. The vitamin supplements have saved my life, yet, I understand that if I have an autoimmune disorder, then there’s still more I have to take care of. When I started my vitamins I was ready to apply for disability, my symptoms have improved 90-95% within 6 months of starting on them. Thanks to Dr Google and comments from other suffers 🥰

[@a11j]

@@yournamehere6939 awesome, do you mind sharing which vitamins? And also any other vitamins you think I should look into. I am currently following up with functional medicine doctors and will also be soon doing tests. Please let me know how the test go!! Anything you share is helpful including your routine. Thanks!!!

[@yournamehere6939]

@@a11j I take the recommended dose of Vitamin A, B Complex, B-12, 2000 IU D-3, E, K2, colostrum, acetyl L-carnitine, Cq10, magnesium oxide, magnesium citrate, magnesium malate, magnesium threonate, zinc, and selenium. I researched them All, did trial and error for several months, and these are the ones that have my pain and most symptoms under control. Please do your own research 🤓

[@a11j]

@@yournamehere6939 Thanks, yeah I am going to look at it, I already take B-12, D3, Elderberry, Vitamin C daily.

[@Miss_Tika1]

Thank you Doc🙌🏾🙏🏾🙌🏾🙏🏾🙌🏾🙏🏾

[@USALibertarian]

What exactly are his proposed treatments?

[@Eclipse2-l8f]

I LOVE YOU, DR T. Thank you so much for this info!!!! You are AMAZING!!!! I've had CFS since 1983 and gave up till I heard your seminar

[@roar321]

What has it fdone for you.

[@ayeshakhan-du1pb]

How do we got hold of him

[@karine8738]

What did you do to help you ?

[@Eclipse2-l8f]

@@karine8738 // i listened to Abraham Hicks "everything is ok" or close to that title, on KZbin. Sounds strange, but its true

[@karine8738]

@@Eclipse2-l8f thanks I will 👍

[@rbar3623]

I have narcolepsy with cataplexy-so I have no trouble sleeping. But I also have all the symptoms of fibromyalgia. I have leaky gut, about 90 food intolerances, muscle pain and tenderness, allergies, excessive weight gain, and chronic fatigue. The muscle pain is becoming intolerable. I have treatment that is working for the sleep disorders, but now need help with the muscle tightness and pain.

[@sherryd.3425]

Have you had a full nutrition workup? With your gut issues you may not be absorbing key vitamins and nutrients adequately. Unless you are paying out of pocket or have truly stellar insurance, a full blood screening is very expensive and your doctor may have to request each test specifically. Look up B12 deficiency and see what huge effect that can have on your body. Some newly trained doctors don't even know to ask about that anymore. It's not a routine blood test. You will often notice commenters mention no carb and low fiber diets. This diet seems to reduce stress on digestion and improve absorption of nutrients. It's us old timers that recommend it.

[@rbar3623]

@@sherryd.3425 I had the alcat test in 2009 when insurance still helped pay for it. It came back with 90 severe food intolerances, about 40 moderate, and 40 low intolerance. I took the foods out of my diet and within two week I lost twenty pounds of fluid and my joint inflammation was gone. I have had just about every test done on me. Everything normal except for sleep studies and the alcat test. I can’t reach deep sleep or control rem sleep properly. Diagnosed officially narcolepsy with cataplexy 2014.

[@sherryd.3425]

@@rbar3623 Very interesting. I have a sleep disorder as well (genetic) 2-6 hours a night in graduated, 6-week cycles. I dream with my eyes open while appearing semi-functiona; and present to others during 2-3 weeks of that cycle. Sleeping medications only create conditions for serious physical injury. I have over 100 food intolerances and 40 chemical intolerances, but only 3 allergies. I'm old and sensitivities seem to become more pronounced with exposure as food and product fads wax and wane on the market. I have always had severe stomach and digestion problems. The only useful diet I have ever found, and I have tried them all, is don't eat. That diet is unfortunately a permanent cure for all that us. The next best thing I've found is the anti-diet made just for me. I have had several minor bowel surgeries over the years to clear areas of chronic blockage due to inflammation/infection. Small areas of scar tissue build up on the lineing of the bowel and given too much pressure, more inflammation and infection result. Muscle and joint pain have been life-long comorbid symptoms. They are not, of course, exclusive to bowel or gut issues. My diet: avoid yeast, sufites, nitrates, fiber, most carbs, and anything that makes you say yuck! Eat twice as much of anything else you like that doesn't cause you pain. Don't assume that your unhappy gut is letting you benefit from all the nutrients you are putting in there. The vehicle of the nutrients is very important. Vitamin tablets, capsules, gels, powders, sublingual liquids, and shots enter the body in different ways and with different speeds. Also with different ingredients. If you have multiple intolerances to foods, sometimes the inert ingredients in tablets and pills can trigger a reaction in your body that inhibits absorbtion. For example, to benefit from an iron supplement, I have to double dose a prescription supplement that is triple-coated to dissolve deep in my lower bowel. My kidneys have the burden of filtering off the excess iron, but if I don't take it I quickly become anemic and very vulnerable to illness. It's a calculated trade off. We each have to make our own choices. Thank you for sharing your story of your testing. It might help someone. I hope your pain eases in the future or that you find a cure. I find that the depression that results from chronic pain and immune system problems requires the most diligence. Better days!

[@Truerealism747]

Can I ask you what do food intolerances do to you

[@maureentorres9153]

I love this Doctor!

[@Uniquettt]

Long but very informative and clear presentation from speaker .Thank you for uploading

[@BernadetteDevlin-l6w]

This man is so fantastic . Puts drs to shame

[@NganLe-tb8bt]

Wish I've seen this video 8 years ago when I first became debilitated with extreme fatigue. The explanations here make perfect sense and actually correct in terms of how I had this chronic fatigue. But now by God grace, I've been recovering wel especially this last year and a half.. I feel I'm about 80-90 recovering. Thank God. I'm doing everything the doctor says in this talk and more. Recently from Dr Berg suggestions I added zinc 30 mg, fulvic acid, and D3. These have given me strength and stamina at the next level that the other supplements couldn't give me. Cell food also gives me nice clean strength but I'm a little hesitant about it.

[@sushirolltiger]

I am suffering alot and bed ridden. Please can you guide me.

[@NganLe-tb8bt]

@@sushirolltiger I was like you 8 years ago. What symptoms do you have? Did you listen to the video to figure out how it it can help?

[@NganLe-tb8bt]

@@sushirolltiger Don't give up. There's hope, just need to get started with small steps and go from there. You can reach out to me.

[@Truerealism747]

@@NganLe-tb8bt did you have much pain the fatigue isn't to bad as it was with minerals

[@NganLe-tb8bt]

@@Truerealism747 no I didn't have any pain, but my fatigue was severe. Are you having lots of pain?

[@walgorafi1]

This is the greatest dr described the cfs perfectly with advice l carnitine and co q10

[@DMac-uv1bl]

I’ve tried nearly everything he suggests with no improvement, sucks because I was really optimistic and hopeful. I eat well, don’t overdue it, do stretches and some yoga every morning, walk in my neighborhood two to three times a day, am in good physical shape (blood pressure, not overweight etc.) and am dog tired, dizzy, incoherent nearly all the time and it’s getting worse and worse. What medication can help me? My sleep isn’t the best and I take a medication for that it’s the fatigue that’s the most debilitating for me. There needs to be a medication FDA approved for ME/CFS if there is one I’m all ears. Seems in the past all my doctors wanted to give me was an SSRI and I hate those. I invite all those that are taking medications that help them. No disrespect but I’m not looking for a diet type plan, just medication. Thank you,

[@youknowcrimedontpay9257]

When did you put the comments in?

[@allisonmarch3783]

It is hard. I have gradually gotten better, but I know what it is like to get so excited about an answer that does not work. I highly recommend setting an intention that you will find the right people, resources and your own ideas that will help you get better. I have done that so many times and then run into someone who tells me something new or pivotal. Ok these are somethings that have helped me the most: -FLORA - Floradix Iron & Herbs - for anemia -magnesium - for sleep -an adrenal tonic (standard process) - adrenal fatigue -EMF device (I felt insanely better and clearheaded when I started using one) -HPA Adapt - for general cognitive support -I take a multivite and vit D3+k as well. I am always looking and considering more supplements etc. bc I am still not 100%, but I so lucky compared to others.

[@DMac-uv1bl]

@@allisonmarch3783 Hi Alison thanks for responding I’m glad to hear that things have worked out for the better for you. I’ve tried a few of the things you have and with very limited if any improvement. I am curious about a few of the others listed and will look into that. Thanks

[@sherryd.3425]

@@DMac-uv1bl Hello, D Mac. I was diagnosed in 1983. Please don't be discouraged or depressed. CFS and Fibro are blanket categories. They really just hint at what might be going on and push you in a direction to look for relief. If you have searched multiple channels for information, you may have noted that very scary words are casually inserted into the narrative, but not explored or elaborated upon. The words are autism, chemical toxicity, food sensitivity, and genetic predisposition. We are in a rich country and we are literally unable to absorb or benefit from the nutrition in our bountiful food, and we can pass that flaw on to our children. We are, however, bright and tenecious internet trolling individuals. Sherry's quick list of lifetime lessons from family and friends: Sleep is priceless: Never take sleeping medication, prescribed or otherwise. It never induces the right kind of sleep, and might just cause you injury. If you sedate a malnourished, fatigued, semi-depressed individual, what will happen? They will fall down, run into walls, and possibly drown in the shower.

[@MsFiFix1]

@@allisonmarch3783 what is an emf devise

[@SocialWorkerLiz]

Thank you!

[@AshleaRay]

I’ve been tested for everything under the sun for the last 9+ years and it’s been pure hell. I’ve felt hopeful and still kind of do, I feel tired a lot I think because of my pain level. I don’t have a sleeping disorder but I’ve just been labeled with fibromyalgia. I have a list of things he speaks of except for the sleeping disorder. Including the numbing and tingling, I’ve had horrible testing for that because they think that you have something else I’ve had 3 nerve studies. All my tests come back negative. Also, for the last couple weeks, I’ve had the worst flareup I have ever had. It’s crippling.

[@janeteddddd]

Stay away from ,v,@××!nes and c,ontrast dyes..they are toxic in the body. Cause all kinds of health problems.

[@jemsuk3784]

Try carnivore with organs might help

[@jemsuk3784]

Maybe some dark raw honey for antioxidants and some berries

[@jemsuk3784]

Look into kefir and other fermented milk products preferably made with raw goats milk or a2 cows. Highest diversity probiotic food. This condition might be related to Microbiome dysfunction and leaky gut. Kefir can lower zonulin which controls intestinal permeability. Gluten also increases zonulin in some people so maybe avoid that too.

[@jemsuk3784]

Take a look at hormonal and trace mineral profiles as they are a lot more important than people think as multiple hormones control mitochondrial function and trace minerals influence hormones.

[@canyoncreekster]

Auravedic med recommends Shilajit for CF.