True CFS is not caused by nutritional deficiency & is not simply a case of chronic tiredness, it also involves pain, exhaustion, etc. As a doctor, you should know this. I have a background in health science & have been using my knowledge to give me the best chance of overcoming my CFS & while I also have a healthy diet (inc. my 5 portions of fruit & veg per day) & my consultant has ruled out deficiencies of any possible kind, I'm still in the throws of chronic fatigue. You can only do your best.
I too have been diagnosed with FMS/CFS. Since 1999 I have been under treatment with variations from medication to nutrition, diet, exercise as well as suppliments. We have yet to put either into remission.This year we finally found pinched nerves as well as bulging discs due to facet joint damage etc. So any information on help I am more than open to just as so many others are.
I haven't heard of anyone else having their jaw snap but mine does the same thing. also my left eye feels weird, the vision is distorted and is very often red and sore for no apparent reason. my friends still ask me to social events but i know that i am not able - the terrible aching and pain that this disease causes is unbearable. i have tried cannabis and find it helps if i keep it to a minimum. am about to try a different diet so will keep you all updated
the is no turning back. a little 10 year old girl was raped and murderded in 1945. her body was not found until 1947. then a boy last week read this and did not copy and paste this message. the dead girl appeared in his room haunting him and killed him. if you do not copy and paste this onto 10 vidoes in 30 minutes the dead girl will apear in your room tonight and haunt you and kill you. well you better start to copy and paste to be saved 3 days ag
can tmj cause fatigue ? im always tired and I always get pain in my left side on the face around my jaw and ear and eye...my jaw snaps alot and i can feel that my left side of the jaw is bigger than the right
I recovered. The highlights: Fluoride sits in your pineal gland, slowing down melatonin production. If you stop sleeping, you'll never recover. I went on the raw food diet. My PH went up to 6.6. (my lowest was 4.5 yikes! At 8 oclock, all our lights are turned off. From 10-12 oclock, your liver does magnificent work. If you have any questions, please ask. I wish someone could have told me all this, instead of experimenting over and over. Also feel free to look at my blog about my experience.
There are multiple sites and videos on Youtube explaining how each portion of the Beck Protocol functions to help those suffering from viral diseases and has personally helped me with my CFS. Visit the Unleash Health site and channel for more information on the Protocol and therapy!
helo doc! hello guys! it was about at my 17 years that I started being unproductive in school, sleeped so many hours but no refresh, couldn't have a regular workout with teamates, didn't have the mood to hang out with friends and generaly it affected everey aspect of my life.CFS was eating my life for about ten years... I am now allmost 29 and I am all back to real life again. What helped me was doing cardio to the max at any given time and consuming q10 capsules and extra virgin olive oil daily
I am 55 years old, and I liked this video, is very important for our health, and we need to sleep more than we think, I am learning english with this. Thanks.
I am 22 years old an I used to cycle 80 kilometers everyday without fail and it made me so so so fit. I was put in a mental hospital because I was on a medication that gave me restlessness for a whole year where I couldn't sit still for even a second. Then they put me on another medication that made me throw up for the whole 3 months I was in there, thus destroying my immune system, thus giving me M.E which I have had for over 1 year now.
I have also been diagnosed with CFIDS in 1999 and CLL in 1982 (still surviving that one). Over Christmas, like everyone else, my diet consisted of high fats, increased carbs and the result has been a significant increase in fatigue. This man is making great sense and I hope people with significant fatigue issues will start with their diet and a nutritional assessment.
i have cfs and ended up in an ambulance one night from severe tachycardia, shaking, chills, i felt like i was dying. turns out i was malnourished because my colon was not absorbing nutrients, my electrolytes were through the floor. now i'm taking supplements and it's been helping some but i'm getting a colonoscopy to figure out why my colon isn't working right.
cant bloody sleep at all-when i want to-when you're suppose to.....up all night (anxiety/chronic pain).....but when i dont want to sleep, i cant keep my eyes open.......
I guess doc is right.. everything isnt that complex as it seems... but ironically, its dificult to eat well, regularly at the same times.. sleeping well when you are drowning in bills and... even check up the cortisol level- my GP will look at me as im crazy.. last time had to beg her to check up my blood cause i thought its first thing to find the cause of fatigue..:(
if you're talking about california.... and lack of sleep..it because people are KILLING themselves to pay sky high mortgages/rents. I work with people that leave work at 4am then start a DAY job at 5am for another 8 hours ..then go home to attend their homes
"nap" then return to their night job with a few hour sleep ..and continue on. GREED is killing us ! A home should NOT be killing people..A home should be a good place it shouldn't be used as a money mill .
@orbtaybal CFS sufferers typically have a lack of energy during the day which is attributable to the fact that they simply can't get proper restful sleep. This causes day time drowsiness/fatigue that may resemble the symptoms of narcolepsy.
As a person suffering from CFS myself, I have undergone many "treatments" including a sleep study for narcolepsy, which of course came back negative - even though I awoke around 10 times during the test.
Does anyone here believe that our bodies can heal themselves?
When we scratch ourselves, we dont have to do a thing for our bodies to heal that scratch. All we need to do is put in the right fuel and have the right mind-set and we can beat it. If you dont believe this, I am on a 200 day challenge to prove that i can beat my ME/CFS (which I have had for over 5 years), just watch my video: ME (Myalgic Encephalomyelitis) and CFS (Chronic Fatigue Syndrome). There IS a cure - Day 1 of 200. Alex
I am a recovered fibromyalgic who left the care of the medical profession to discover the cause and cure for this horrific disease after 15 years of failed treatments. I understand this illness completely from the inside and back out again. Symptoms are often mistaken as a cause and what can help does not cure. Please, do not give up and keep going. See my You Tube video "Curing Chronic Fibromyalgia - Choosing What Works" and my best wishes to you all!!!
"I am a recovered fibromyalgic who left the care of medical profession to discover the cause and cure of this horrific condition, and I understand this condition from the inside and back out again. Symptoms can often be mistaken for the cause, and treatments that help do not cure. Do not give up from failed hope. Keep going! See You Tube video:
"Curing Chronic Fibromyalgia - Choosing What Works" by author Valerie Lumley"
I have ME/CFS (have had it for over 5 years) and I believe there is ONE cure, and that's the right diet, but we dont often know what the right diet is. We think cow's milk is good for us and salt / fats aren't, but there is a lot we as a society need 2 learn about real healthy nutrition. I am on a 200 cleanse 2 prove that I can be rid of the illness in a month, Watch my videos 2 find out more: "ME (Myalgic Encephalomyelitis) and CFS (Chronic Fatigue Syndrome). There IS a cure - Day 1 of 200".
I am a recovered fibromyalgic who left the care of the medical profession to discover the cause and cure of this horrific condition without drugs, and am living proof you can cure this and take back your life. Symptoms are mistaken for the cause and treatments that help do not cure. Please, do not be discouraged by failed hope and keep going!!!
Valerie Lumley, Recovered Fibromyalgic and author of
"Curing Chronic Fibromyalgia - Choosing What Works"
I am a recovered fibromyalgic who left the care of the medical profession to discover the cause and cure of this horrific condition without drugs, and am living proof you can cure this and take back your life. Symptoms are mistaken for the cause and treatments that help do not cure. Please, do not be discouraged by failed hope and keep going!!!
Valerie Lumley, Recovered Fibromyalgic and author of
"Curing Chronic Fibromyalgia - Choosing What Works"
I am advocating these , because when you have been through so much, many associated issues which manifested later in life as disease and find something that really works and empowers you well you share it. We are not taught to relax, society is more, do , have - pressure:( These CD's and MP3's do work) - I use daily and feel so good, in control and free of much angst. Minds can work wonders with guidance
There are multiple sites and videos on Youtube explaining how each portion of the Protocol functions to help those suffering from primarily viral diseases and has personally helped me with my CFS. Please visit the Unleash Health site for more information on the Protocol and therapy!
in Berlin University Clinic (Charité) and also in England CFS is more and more recognized as a debilitating disease. The syndrome is more the general definition for all cases- but there are people who cannot recover, even if they rest. There are some possible physical causes. Greetings! Mike
I do all the things I should, I eat healthy, vegetables, fruits, all kinds of meats and fish, pasta, milk products, protein drinks.. Try to sleep up to 8 hours, but I have a hard time falling a sleep, although my body is exhausted, my mind isn't. I fall a sleep once or twice a day, my body has no chance of doing anything else but relax or sleep, and my heart starts pounding really hard and fast. Just walking up the stairs could be very hard. I don't know whats wrong, could CFS be it?
@iris0093 Whatever it is, the best bet is altering lifestyle. Hearing your symtoms, the 1st thing I thought was get enough exercise so your relaxed at night. Burn off any anxiety.
Also gotta say, pasta, milk and meat is not healthy. Go for brown rice & beans. And as for protein, the real concern is to not get too much.
It's not "CHRONIC FATIGUE" it is "MYALGIC ENCEPHALOMYELITIS" and it is a much more serious condition than what these people are trying to make out. Whoever reads this, I implore to go and do some real research on this condition, please Google "A hummingbirds guide to M.E." and against all odds, stay away from garbage DISINFORMATION about this condition as it only harms the people who are seriously affected by the 'true' condition M.E.
As the way of all things, what effect do you suppose its question, knowledge, understanding and application by billions of persons will have on the state of global economics, science, the humanities, education, government and business?
.
The underlying law of nature is the most important subject any person can investigate and learn about, can proceed to understand, and can then come to personally apply in life.
my Chronic fatigue this star I have a heart test i do have in 2007 and it caused me to have kidneys damage and i have pain all over my body and legs, arms pain, i can not do want i did before and I can not wakk to good if i did walk i will have pain and chest pain, hip pain, caused me to have diabetes, abdomen pain, assessment 1.chronic fatigue 2. chronic hip pain 3. chronic renal insufficiency , weakness all the time.
It's like describing a zebra as "An animal from Africa" and then failing to ever nail down what a zebra is, because virtually all the animals in Africa qualify for "Animal From Africa" syndrome.
Please let us know AFTER you have done some REAL Research and KNOW what CFS is...not what it is NOT. Thank You.
The CFS criteria was only a partial collecton of outward indicators that would enable doctors to recognize the "possibly unique clinical entity" when they saw it, and ORDER special tests.
But the medical community warped the purpose of the description and made the definition into the disease... .
"CFS" is a syndrome that was coined for specific reasons, and in response to parameters of depleted RNase-L, B Cell abnormalities, zero sed rate, high platelet debris and a bunch of other stuff that the CDC had no explanation for.
Contrary to what many people think, the description is not the matrix of what CFS is.
i believe that too much sugar is probably the no 1 cause for chronic fatigue in western society because we know that people eat too much sugar and even lots of fructose. a body of such a person is permanently afraid of being bombarded with sugar and does the absolutely right thing by producing as much insuline as the body can take without shutting down completely. the alternative would be even worse.
Thank you so much for this video~!!! what an eye opener. I have been searching for answers for a long time to help my husband who I believe has CFS. I will be sure to get him the cortisol test. Is there shots or pills he can take to replace his cortisol level if we find they are low?? Donna
Thanks for this videos, i really almost lost my judgment about most doctors as prostitutes for the drug industry. This man is really telling something safe, simple and truthfully.
Most corporation wants to harvest money on our health. Tobacco-industry, Big pharmaceutical and fast food are just some to mention.
Codecs Alimentarius wants to erase nutritions and vitamins in most food that gets import/export. This is something that will give us great problem in the future of our food.
Many CFIDD patients do not sleep at all for weeks or months. People who were ill as children may, after nearly 50 years, lose their body's abnormal insomnia tolerance. The part of the brain that causes neurally mediated hypotension breaks down farther with age until with unremitting insomnia, it may not work well at all. I have had tests that showed no nitrogen and zero percentile of nitrogen--no protein digestion. Immune dysfunction caused by radiation or dioxen are impossible to counter.
but in my case my cognitive abilities started decline rapidly over some days to the point were i could not even read three words plus i had a burning sensation when i was going to sleep am sure it was stress because the cognitive decline continued even after i stopped doing hard revision my question is can any visual stimulants be the cause of the condition and how much damage can stress do to the brain and can all be repaired
I have had CFS and fibro as well as EBS. I think it's extremely important to mention, after 10 years of this, I finally fell apart and Celiac was found. Please, have people look deeper! These illnesses are sometimes only symptoms!!
Fibro is a mystery to the medical field and no one knows the complete story. Fibro is a symptom of deeper issues and evidence is showing more and more that it's intestinal illness. Check out SCD diet, GAPS diet webpages and you can see how the gut affects the entire system, including how it causes fibro/CFS, MS, autism, mood disorders, insomnia........This is how I addressed fibro successfully.
I think Dr. Bellonzi is correct in his treatment of fibro, but there is more to it. Diet can not be ignored and sugar, grains, chemicals and most carbs cause fibro pain. Until this is addressed the gut can not absorb nutrients needed to reverse fibro or any other disease. The liver is maxed out too and that needs attention. GAPS, SCD and others address the core of fibro.
Oh yes.....lots of stomach and gut pain!! It's very easy to not get a proper diagnosis. She should keep a symptom diary and find a smart doctor. The norm for finding the underlying causes of fibro, celiac, etc..is over 10 years. Don't waste time!!
I spent 2 years paralyzed as a teenager diagnosed with CFS. The medical community offered no hope and told me i was going to die within 2 years. 18 years later i was a competitive runner with my city's track club coming in 2nd place for the entire year. 2 years after that - i am paralyzed again. my diet has not changed. my stress levels have gone down yet here I am bedriden getting bone marrow biopsies and getting around in a wheelchair. I don't think a few tweeks of the diet will fix this.
The inability to sleep is not the issue. For the past 10 years my wife has had extended periods where she slept 16-20 hours per day. Other symptoms have included; muscle pain, headaches, dizziness, lack of concentration, sensitivity to light/sounds, irritability, etc.
These problems appear to grow worse in direct relationship to her monthly cycle, which suggests a relationship to hormones. She has been prescribed prozac, paxil, aderall, even lithium. Nothing seems to break the pattern.
I got Mono last summer. I thought I recovered quite fast. I was back lifting, then fell in the gym one day. After that I had random pains, extreme fatigue, and crazy panic attacks. I gotta pin point the cause of this crap.
for anyone who reads this in time, a product called delimmune V has excellent effects on recovery from mono.
Its a whole lot of a particular dead bacterium that will stimulate the receptors in your gut to release a massive amount of anti bodies into your system
Dr. Bellonzi is looking at the "big picture" to what is CAUSING CFS/ME. We may not know the exact cause(s) of CFS yet, but he does point out most of the known possibilities. good job doc!
I have been diagnosed with CFS... I have had it for 8 months now. I miss out on alot of school,family activities,and hanging with friends. The thing I have found to help a little... Is to do some things,workouts,do activities to overwork the stress you may have. It doesn't get rid of it... But it does help.
I've checked basically everything that could be checked in my blood ,and also got depression checked, which I don't have. Cognitive behavioral therapy has helped me overal to get into a balance and to accept, another think what's helping right now is taking vitamine b12 injections and folic acid pills, anyone who is interested can send me a PM, I will give the full information. They now think that even though yoú re not low on that stuff, that we might need more. I've improved a lot on my CFS.
hello there, your comment interests me. i have supposed CFS i have had it now for 6 months i have has all blood test which were all negative and do not have depression. i do feel down , but this is only because of my condition. Please tell me more about what you are doing to help yourself
There are some good books out there I liked 'beat fatigue with yoga' by Fiona Agombar it tells you a lot about the condition. It could be stress so you need to find what works for you here could be an intolerenace or lack of a vit or min try magnesium it has helped me, could be hormones, blood pressure, hyperventilation or diet. A good diet, de-stressing and gentle exercise will help many, 'The complete book of nutritional health' is great and so is yoga. Talk to a Dr and do research
I had Candida and the thyroid imbalance and all that. I could not get rid of candida no matter what the drug or nutritional supplement and or diet. Since I have been taking Iodoral and have been getting rid of mercury my symptoms have improved. My Candida antibodies have dropped as well, it is really amazing.
Many Lyme disease patients have been diagnosed with CFS. Wrote a Lyme disease brochure with the help of 2 Lyme specialists. Will email to anyone interested.
Not only Lyme Disease, but also Babesia, an emerging illness. It is also transmitted by ticks, but the symptoms of Babesia are somewhat like Malaria. I have tested positive for Lyme on the most stringent test, the Western Blot Test, and positive for Babesia, but I have my doubts about how much each one contributes to my misery. My CFS is textbook as far as symptoms go. I take blood thinner shots, Heparin, twice a day because Heparin has been found to kill Babesia (in vitro). It does help.
Read Explaining colours to a blind man. Not only will it enlighten many as to what living with a mental illness and chronic fatigue syndrome is like, it also gives comfort to those sufferers who think there is no hope and that they are alone. It is very informative, sometimes shocking but also very funny in parts. All in all, a good read and highly recommended.
I have 3 different kinds of metal in my body -- a bb (from a bb gun) in my face, a sewing needle (i have no idea how it got there, but I swear to you it's there - a doctor saw it in an Xray when I was in 6th grade and decided to leave it there because it would be too intrusive to remove) in my wrist, and titanium in my skull (fractured orbital).
Could any of these things cause a risk to me in the future?
This goober has no concept of what Chronic Fatigue Syndrome really is. I hope he gets real Chronic Fatigue Syndrome. I would bite him if I thought CFS were infectious.
BCCButters, have you read anything about Helmenthic Therapy? It's a disgusting idea at first, but it makes a lot of sense. Look it up on Wikipedia, and contact me, if you wish. I'm thinking of trying it because I have so many crossover symptoms with MS.
Sorry to hear you are sick. Have you tried Vitamin Therapy? I take the USANA Essentials, Active Calcium, their Bi Omega product (fish oil) and at least 3,000 IU of Vitamin D a day. I was taking 10,000 IU until my count was normal. I feel great!!
Regarding Helmenthic Therapy, if you have tried everything else, then I cannot see how it would hurt...but I see your point, probably a little disgusting. Although, I think they do still use maggots and leechs for certain medical procedures, too.
Dr byron Hyde makes a difference between M.E and CFS. I think most physicians mean the same thing, but this one is talking way too much about fatigue. I think this is the difference Dr. Hyde is talking abut. The Dr on this video is not talking about M.E. He doesn´t mention any neurological problems that are present in the diagnostic criterea. Nothing about orthostaic intolerance etc. Only fatigue. ME/CFS is so much more than just fatigue!
Well that was simplistic "Figure out what's causing you to be tired and take care of that and you'll be fine."
What an idiot! Yes I sleep, yes I eat, yes I exercise, yes I practice stress management, etc... Sad fact is I got EBV and have been wiped out for 19 months.
I would recommend getting a full Allergy test as well. Your body might be using allot of energy fighting other allergies. Sometimes if you remove these allergies it gives your body enough energy to get on top of the real cause of the problem! wheat allergies for example can prevent the uptake of vitamins and minerals in to your body , leaving you tired. You may have a couple problems that youre dealing with, removing one will help allot.
@hoki424: That was smart to start with just one minute a day - a good habit developer. I advise all my client to exercise for one round a day. A round of boxing is only three minutes.
What I found is when I got CFS, i got a new allergy, house dust allergy. XD. I take pills for it, but it aint helping me fully. It's the best to take out all those factors indeed, but it 's not a full cure.
The WHO (Myalgic Encephalomyelitis is defined by the World Health Organisation as a neurological illness (code WHO-ICD-10-G93.3 ) and several countries, such as Canada recognize ME/CFS as a neurological illness/disease. In Europe, the government of Norway and Catalonia (Spain) have come to the same conclusion and they are starting biomedical centres to treat the patients. No psychiatrist is involved in these centres
Um, fatigue is not the only symptom with the actual disease called chronic fatigue syndrome. There is a list of at least thirty other symptoms sufferers have. It's not just about being tired and not getting enough sleep...how offensive.
The World Health Organization has called CFS (M.E.) a Neuro-Immune Disease. The WPI also refers to it this way. There is a cause for the horrors of CFS, we just have not found the biological answers yet. We could say that this "syndrome" is caused by an unknown disease perhaps. No matter what we say, the experience of living with CFS is filled with crippling physical symptoms that feel like an unimaginable terrifying disease. I too have CFS and work so hard to help! ~Love to all~
@psychetruth If the cause is not known yet, it does not mean it will not be found. Multiple Sclerose was diagnosed as "no real illness" as well because in the beginning there was no known cause.
@psychetruth Well, technically, a disease is a 'dis' 'ease' - meaning not at ease. Anything that causes a sustained lack of 'ease' (regardless of it's nature) is a disease (an impairment of health or a condition of abnormal functioning).
I am a CFS sufferer myself (for 20 years now), and found this video to be of some value as it points out the truth of the nature of chronic fatigue, and is another positive step toward finding a realistic solution to this debilitating condition.
well said! chronic fatigue for me is an overlapping of hormonal, immune system and nervous system problems..i have a lifelong T3 thryoid hormone deficiency (diagnosed at 30 yrs!), candida (a fucking Horrid problem which gets into you when u have a low immune system), and yeah accompanying all this is lifelond severe depression and failure to get a career, a love life..loss of a life..etc..made some progress but cant beat the candida and beating the candida i think is fundamental to vitality
i have always believed that the mono i had at 16 had a huge to-do with why i am chronically fatigued...it hit me hard, that mono...i am now 38 years old and struggle for energy. if i have energy, it only lasts a few hours at most.
what i am wondering about is...what if we don't have much money (due to wanting to sleep more than work!?!?) to get proper testing...i am on state paid insurance...would they test for cortisol? thank you...
my wife had Chronic Fatigue for 7 years, she was one of the worst cases world wide. We switched to organics and she was of perfect health within 3 weeks. Our whole family has never looked nor felt better. Our receipies are sourced from Sally Fallon's Nourishing Traditions which we highly recommend. Try it yourself, better nutrition worked for us, seriously you have nothing to loose.
Put CFS behind you, give it a try. ORGANICS and NOURISHING TRADITIONS BOOK.
No offense but I find it very hard to believe your story. If you're wife was one of the worst cases in the world, she'd be almost dead. I know one of the worst cases in the UK and she is hospitalized, being tube fed and basically paralyzed.
Also I don't see how switching to organic food can cure one of the worst cases of CFS in 3 weeks - that's ridiculous.
Sounds to me like you're just trying to promote a book.
The video is excellent and Dr. Bellonzi is spot on.
Absolutley agree with you Zild. I have a very severe case - been going through such a bad patch at the moment, that im in bed nearly 24hrs a day, and have been into ER 4 times in one month for episodes of becoming extremely weak, cold, with severe blood pressure drops to the point where i needed an ambulance - & that was just from getting up to get a drink. Now i have eaten more 'perfectly' in the past than most people i've known. All organic food, vege juices, it didnt 'cure' me at all.
Never give up looking for a cause of your CFS. Every case of CFS has a cause, you just need to find the cause and treat it.
Do you have a good doctor doing loads of tests?
I bet if you had a proper thorough physical exam with loads of tests for infections, adrenal fatigue, thyroid problems, hormonal imbalances, vitamins & mineral deficiencies, chemical/heavy metal poisoning, gut problems, etc, etc. you would find some treatable abnormalities that could help.
Nobody mentioned taking calcium supplements and calcium is very important together with magnesium not only for bones but for several other reasons. I am taking Cal-Mag stress formula by NOW and Amino Complete and zinc and antidepressants I must say I feel a litte better.
i woke up with a sore throat, headache, im still sleepy, and at night when im sleeping my body suddently wakes up and starts having these wierd pains...i need help...plus when im waking up my body is so dizzy tat it justs wanna faint...and now my throat has this stingy, burning,rash like feeling...i need help
hi! well it sounds to me you have the MONO (mononucleosis). I had it for like a month and your symptoms sound just like mine back then. my advice: go to an ER, get the monotest and rest, get plenty of rest and fluids since there is no cure for this virus. It needs to go away on its own. Hope it helps, take care.
This comment has received too many negative votesshow
You should also be more specific about FM. Fibromyagia is not caused by CFS/CFIDS or chronic fatigue symptoms. FM is sometimes accompanied w/ chronic fatigue but neither is exclusive in and of itself.
You are using scare tactics here. Perhaps another video with more information to this painful and widespread condition?
My Dad was fatigued for quite a while - very low energy. He started using a CPAP breathing machine at night. He is full of energy now. He is a smoker, so that is surely the cause.
The point is to be responsible, find out about physical conditions and their causes yourself, then seek help based on a self knowledge of the condition. Placing your trust solely in commercials and doctor advice is responsible.
I have CFS and you are being irresponsible when you lump other chronic fatigue issues with CFS/CFIDS.
I suggest you clarify because people w/ sleep issues that have chronic fatigue do not have high ebv titers. Ebv causes mono which is DX'ed as EBV after 4 months which is DX'ed as CFS after a year of symptoms.
I always think it's funny when a consumer leave a comment protesting an alternative health professional since they "know better" because they have disorder, syndrome, etc.
The fact is that whatever the conventional doctors have told you, you still have the
True CFS is not caused by nutritional deficiency & is not simply a case of chronic tiredness, it also involves pain, exhaustion, etc. As a doctor, you should know this. I have a background in health science & have been using my knowledge to give me the best chance of overcoming my CFS & while I also have a healthy diet (inc. my 5 portions of fruit & veg per day) & my consultant has ruled out deficiencies of any possible kind, I'm still in the throws of chronic fatigue. You can only do your best.
SuperMissblueeyes 1 month ago
I too have been diagnosed with FMS/CFS. Since 1999 I have been under treatment with variations from medication to nutrition, diet, exercise as well as suppliments. We have yet to put either into remission.This year we finally found pinched nerves as well as bulging discs due to facet joint damage etc. So any information on help I am more than open to just as so many others are.
midnightwolf31 5 months ago
@midnightwolf31 take provigil/nuvigil. works wonders for CFS, I have no side effects!
sirloynes 3 weeks ago
masterbation makes this ilness worse, try to stop
moynul123 5 months ago
@moynul123 Or sex?
GemsofEarth 5 months ago
@GemsofEarth nope sex will rejuvenate the body 2 very different things
moynul123 2 weeks ago
I haven't heard of anyone else having their jaw snap but mine does the same thing. also my left eye feels weird, the vision is distorted and is very often red and sore for no apparent reason. my friends still ask me to social events but i know that i am not able - the terrible aching and pain that this disease causes is unbearable. i have tried cannabis and find it helps if i keep it to a minimum. am about to try a different diet so will keep you all updated
carolecotterill 6 months ago
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the is no turning back. a little 10 year old girl was raped and murderded in 1945. her body was not found until 1947. then a boy last week read this and did not copy and paste this message. the dead girl appeared in his room haunting him and killed him. if you do not copy and paste this onto 10 vidoes in 30 minutes the dead girl will apear in your room tonight and haunt you and kill you. well you better start to copy and paste to be saved 3 days ag
jewell011 6 months ago
can tmj cause fatigue ? im always tired and I always get pain in my left side on the face around my jaw and ear and eye...my jaw snaps alot and i can feel that my left side of the jaw is bigger than the right
raoorz 6 months ago
NO SUCH THING AS BULLYING IT IS AN ADDICTION
NOT POSSIBLE NOT POSSIBLE KIMA AND ANNE OPRAH WINFREY DAUGHTERS
DRAWING PINS
whotaughtyou 7 months ago
tell you what helps....
cannabis.
ThatBoyFL 7 months ago
Dr., I am sleeping but I keep sleeping late min.around 12:00am and when I wake up I feel very tired . Also ,I get a bit dizzy as well.
quelita28 8 months ago
I recovered. The highlights: Fluoride sits in your pineal gland, slowing down melatonin production. If you stop sleeping, you'll never recover. I went on the raw food diet. My PH went up to 6.6. (my lowest was 4.5 yikes! At 8 oclock, all our lights are turned off. From 10-12 oclock, your liver does magnificent work. If you have any questions, please ask. I wish someone could have told me all this, instead of experimenting over and over. Also feel free to look at my blog about my experience.
PamelaViktoria 9 months ago
Dr. talk about PDK. remedies
lrmodranoel 9 months ago
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Nice videos this you tube world just gets bigger every day! When you
have time come visit my chann
TheNitricOxide 10 months ago
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Nice videos this you tube world just gets bigger every day! When you
have time come visit my chann
pheromoneaction 10 months ago
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Nice videos this you tube world just gets bigger every day! When you
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TheHcgdietplan 10 months ago
There are multiple sites and videos on Youtube explaining how each portion of the Beck Protocol functions to help those suffering from viral diseases and has personally helped me with my CFS. Visit the Unleash Health site and channel for more information on the Protocol and therapy!
Thank you!
unleashhealth 10 months ago
helo doc! hello guys! it was about at my 17 years that I started being unproductive in school, sleeped so many hours but no refresh, couldn't have a regular workout with teamates, didn't have the mood to hang out with friends and generaly it affected everey aspect of my life.CFS was eating my life for about ten years... I am now allmost 29 and I am all back to real life again. What helped me was doing cardio to the max at any given time and consuming q10 capsules and extra virgin olive oil daily
mariotubegr 11 months ago
Swine flu casued CFS for me
Finanski9 11 months ago
@Finanski9 Yikes!
sirloynes 3 weeks ago
MITOSYNERGY Search mitosynergy on u-tube or google it Mitosynergy Check it Out
Mitosynergy 11 months ago
I am 55 years old, and I liked this video, is very important for our health, and we need to sleep more than we think, I am learning english with this. Thanks.
Pimentone22 1 year ago
I am 22 years old an I used to cycle 80 kilometers everyday without fail and it made me so so so fit. I was put in a mental hospital because I was on a medication that gave me restlessness for a whole year where I couldn't sit still for even a second. Then they put me on another medication that made me throw up for the whole 3 months I was in there, thus destroying my immune system, thus giving me M.E which I have had for over 1 year now.
nz804 1 year ago
Great vid! Thanks.
dasmikeify 1 year ago
I have also been diagnosed with CFIDS in 1999 and CLL in 1982 (still surviving that one). Over Christmas, like everyone else, my diet consisted of high fats, increased carbs and the result has been a significant increase in fatigue. This man is making great sense and I hope people with significant fatigue issues will start with their diet and a nutritional assessment.
freedom4nan 1 year ago
good advice. thank you.
VenusAsABoyFilms 1 year ago
i have cfs and ended up in an ambulance one night from severe tachycardia, shaking, chills, i felt like i was dying. turns out i was malnourished because my colon was not absorbing nutrients, my electrolytes were through the floor. now i'm taking supplements and it's been helping some but i'm getting a colonoscopy to figure out why my colon isn't working right.
jwallbanger 1 year ago
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kzkleyoile 1 year ago
No way out man Asian women #lushfmlk.info#
rileystephak 1 year ago
i would trade this demon for the extreme tinnitus i have hands down..!
RascalLamb 1 year ago
@RascalLamb it's not fun, trust me.
sirloynes 3 weeks ago
cant bloody sleep at all-when i want to-when you're suppose to.....up all night (anxiety/chronic pain).....but when i dont want to sleep, i cant keep my eyes open.......
VUPdingCLICK 1 year ago 3
@VUPdingCLICK yes! what is that about? me too!
MsLiberty101 1 year ago
@VUPdingCLICK Nuvigil/provigil...miracle pills for cfs!
sirloynes 3 weeks ago
I guess doc is right.. everything isnt that complex as it seems... but ironically, its dificult to eat well, regularly at the same times.. sleeping well when you are drowning in bills and... even check up the cortisol level- my GP will look at me as im crazy.. last time had to beg her to check up my blood cause i thought its first thing to find the cause of fatigue..:(
irenakolek 1 year ago
lots of info, thank you xx
chikinkilaydee 1 year ago
CHEMTRAILS!!
Amaraka13 1 year ago 2
@Amaraka13 you're my man.. ;)
mariotubegr 11 months ago
if you're talking about california.... and lack of sleep..it because people are KILLING themselves to pay sky high mortgages/rents. I work with people that leave work at 4am then start a DAY job at 5am for another 8 hours ..then go home to attend their homes
"nap" then return to their night job with a few hour sleep ..and continue on. GREED is killing us ! A home should NOT be killing people..A home should be a good place it shouldn't be used as a money mill .
plutoplatters 1 year ago
@plutoplatters " is because"
plutoplatters 1 year ago
@plutoplatters Epstein Barr virus is also killing us in Calfornia :)
sirloynes 3 weeks ago
Please screen for Narcolepsy, as you may know 1 in 2000 people are affected of which usually goes undiagnosed for years.
'Chronic fatigue' sounds like the usual misdiagnoses.
Please screen for HLA-DQB1*0602.
Stanford Center for Narcolepsy, has much information on this subject .
Thank you.
orbtaybal 1 year ago 2
@orbtaybal CFS sufferers typically have a lack of energy during the day which is attributable to the fact that they simply can't get proper restful sleep. This causes day time drowsiness/fatigue that may resemble the symptoms of narcolepsy.
As a person suffering from CFS myself, I have undergone many "treatments" including a sleep study for narcolepsy, which of course came back negative - even though I awoke around 10 times during the test.
It's not a simple condition by any means.
wumpee72 1 year ago
If you have CVS or Firbomyalgiae look up the research after XMRV.
DoomNoMore 1 year ago
Does anyone here believe that our bodies can heal themselves?
When we scratch ourselves, we dont have to do a thing for our bodies to heal that scratch. All we need to do is put in the right fuel and have the right mind-set and we can beat it. If you dont believe this, I am on a 200 day challenge to prove that i can beat my ME/CFS (which I have had for over 5 years), just watch my video: ME (Myalgic Encephalomyelitis) and CFS (Chronic Fatigue Syndrome). There IS a cure - Day 1 of 200. Alex
alexsantoro 1 year ago
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I am a recovered fibromyalgic who left the care of the medical profession to discover the cause and cure for this horrific disease after 15 years of failed treatments. I understand this illness completely from the inside and back out again. Symptoms are often mistaken as a cause and what can help does not cure. Please, do not give up and keep going. See my You Tube video "Curing Chronic Fibromyalgia - Choosing What Works" and my best wishes to you all!!!
ValerieLumley 1 year ago
"I am a recovered fibromyalgic who left the care of medical profession to discover the cause and cure of this horrific condition, and I understand this condition from the inside and back out again. Symptoms can often be mistaken for the cause, and treatments that help do not cure. Do not give up from failed hope. Keep going! See You Tube video:
"Curing Chronic Fibromyalgia - Choosing What Works" by author Valerie Lumley"
ValerieLumley 1 year ago
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I have ME/CFS (have had it for over 5 years) and I believe there is ONE cure, and that's the right diet, but we dont often know what the right diet is. We think cow's milk is good for us and salt / fats aren't, but there is a lot we as a society need 2 learn about real healthy nutrition. I am on a 200 cleanse 2 prove that I can be rid of the illness in a month, Watch my videos 2 find out more: "ME (Myalgic Encephalomyelitis) and CFS (Chronic Fatigue Syndrome). There IS a cure - Day 1 of 200".
alexsantoro 1 year ago
I am a recovered fibromyalgic who left the care of the medical profession to discover the cause and cure of this horrific condition without drugs, and am living proof you can cure this and take back your life. Symptoms are mistaken for the cause and treatments that help do not cure. Please, do not be discouraged by failed hope and keep going!!!
Valerie Lumley, Recovered Fibromyalgic and author of
"Curing Chronic Fibromyalgia - Choosing What Works"
ValerieLumley 1 year ago
This has been flagged as spam show
I am a recovered fibromyalgic who left the care of the medical profession to discover the cause and cure of this horrific condition without drugs, and am living proof you can cure this and take back your life. Symptoms are mistaken for the cause and treatments that help do not cure. Please, do not be discouraged by failed hope and keep going!!!
Valerie Lumley, Recovered Fibromyalgic and author of
"Curing Chronic Fibromyalgia - Choosing What Works"
ValerieLumley 1 year ago
I am advocating these , because when you have been through so much, many associated issues which manifested later in life as disease and find something that really works and empowers you well you share it. We are not taught to relax, society is more, do , have - pressure:( These CD's and MP3's do work) - I use daily and feel so good, in control and free of much angst. Minds can work wonders with guidance
Free report and samples to Nurture you.
Google Relaxationforme U-tube yourbraintraining
PositiveHarmony 1 year ago
GREAT VIDEO!!
jeanie1963 1 year ago
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He is a really good doctor, wish they were all like that!
bambolina2005 1 year ago
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There are multiple sites and videos on Youtube explaining how each portion of the Protocol functions to help those suffering from primarily viral diseases and has personally helped me with my CFS. Please visit the Unleash Health site for more information on the Protocol and therapy!
unleashhealth 1 year ago
Goddamn this makes me want another Snickers bar.
YouFoolWarrenIsDead 1 year ago
VERY INTERESTING, YOUR RUGHT ON THE DOTT! I SUFFER FROM THIS I HAVE R.A., AND I HAVE A STRESSFUL LIFE!
sickpainevil 1 year ago
in Berlin University Clinic (Charité) and also in England CFS is more and more recognized as a debilitating disease. The syndrome is more the general definition for all cases- but there are people who cannot recover, even if they rest. There are some possible physical causes. Greetings! Mike
FallaciesDetective 1 year ago
I do all the things I should, I eat healthy, vegetables, fruits, all kinds of meats and fish, pasta, milk products, protein drinks.. Try to sleep up to 8 hours, but I have a hard time falling a sleep, although my body is exhausted, my mind isn't. I fall a sleep once or twice a day, my body has no chance of doing anything else but relax or sleep, and my heart starts pounding really hard and fast. Just walking up the stairs could be very hard. I don't know whats wrong, could CFS be it?
iris0093 1 year ago
@iris0093 Whatever it is, the best bet is altering lifestyle. Hearing your symtoms, the 1st thing I thought was get enough exercise so your relaxed at night. Burn off any anxiety.
Also gotta say, pasta, milk and meat is not healthy. Go for brown rice & beans. And as for protein, the real concern is to not get too much.
Gary1111001 1 year ago
It's not "CHRONIC FATIGUE" it is "MYALGIC ENCEPHALOMYELITIS" and it is a much more serious condition than what these people are trying to make out. Whoever reads this, I implore to go and do some real research on this condition, please Google "A hummingbirds guide to M.E." and against all odds, stay away from garbage DISINFORMATION about this condition as it only harms the people who are seriously affected by the 'true' condition M.E.
-Logical Correctioner
PostHuman2113 1 year ago 2
@PostHuman2113 the symptoms of ME do not fit me, especially the physical symptoms. The CFS symptoms do fit me, so not all CFS is ME.
sirloynes 3 weeks ago
this guy scares the shit out of me the way he talks its like hes talking into u
TripalipO 1 year ago
Blah blah blah blah
What is this video doing for me ?
blah blah blah blah
eutuve 1 year ago
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THE MOST FUNDAMENTAL QUESTION OF ALL:
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What is the underlying law of nature.
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The underlying law of nature is the most important subject any person can investigate and learn about, can proceed to understand, and can then come to personally apply in life.
TedDGPoulos 1 year ago
my Chronic fatigue this star I have a heart test i do have in 2007 and it caused me to have kidneys damage and i have pain all over my body and legs, arms pain, i can not do want i did before and I can not wakk to good if i did walk i will have pain and chest pain, hip pain, caused me to have diabetes, abdomen pain, assessment 1.chronic fatigue 2. chronic hip pain 3. chronic renal insufficiency , weakness all the time.
richard04654 1 year ago
Part 4:
which really solves nothing.
It's like describing a zebra as "An animal from Africa" and then failing to ever nail down what a zebra is, because virtually all the animals in Africa qualify for "Animal From Africa" syndrome.
Please let us know AFTER you have done some REAL Research and KNOW what CFS is...not what it is NOT. Thank You.
bodieangels 1 year ago
Part 3:
The CFS criteria was only a partial collecton of outward indicators that would enable doctors to recognize the "possibly unique clinical entity" when they saw it, and ORDER special tests.
But the medical community warped the purpose of the description and made the definition into the disease... .
bodieangels 1 year ago
Part 2:
"CFS" is a syndrome that was coined for specific reasons, and in response to parameters of depleted RNase-L, B Cell abnormalities, zero sed rate, high platelet debris and a bunch of other stuff that the CDC had no explanation for.
Contrary to what many people think, the description is not the matrix of what CFS is.
bodieangels 1 year ago
you are NOT addressing CFS !!!
YOU are talking about plain vanilla chronic fatigue
There is a HUGE difference...
The REAL ME/CFS Community already HAS done everything you are talking about to NO avail...
I don't hear you checking for the extremely LOW SED rate? low NKcell function? low B cell lymphocytes? depleted RNase-L ?
Maybe YOU need some education B4 you speak...
as IF YOU are Education on a subject. dear Sir ~
bodieangels 1 year ago
i believe that too much sugar is probably the no 1 cause for chronic fatigue in western society because we know that people eat too much sugar and even lots of fructose. a body of such a person is permanently afraid of being bombarded with sugar and does the absolutely right thing by producing as much insuline as the body can take without shutting down completely. the alternative would be even worse.
1schwererziehbar1 1 year ago
@1schwererziehbar1 The no 1 cause for CFS is the epstein barr virus still running through your body.
sirloynes 3 weeks ago
Thank you so much for this video~!!! what an eye opener. I have been searching for answers for a long time to help my husband who I believe has CFS. I will be sure to get him the cortisol test. Is there shots or pills he can take to replace his cortisol level if we find they are low?? Donna
donnadohogne 2 years ago
Chronic Fatigue Syndrome can be controlled and neutralized utilizing the Beck Protocol and blood electrification microcurrent therapy.
unleashhealth 2 years ago
Thank you for this insightful video. Please do have a look at our channel as we have many specialised chronic fatigue syndrome videos
freedomfromme 2 years ago
Thanks for this videos, i really almost lost my judgment about most doctors as prostitutes for the drug industry. This man is really telling something safe, simple and truthfully.
Most corporation wants to harvest money on our health. Tobacco-industry, Big pharmaceutical and fast food are just some to mention.
Codecs Alimentarius wants to erase nutritions and vitamins in most food that gets import/export. This is something that will give us great problem in the future of our food.
Check it out
Totalreformer 2 years ago
Just exercise cardio and such >.>
naveslaikss 2 years ago
Many CFIDD patients do not sleep at all for weeks or months. People who were ill as children may, after nearly 50 years, lose their body's abnormal insomnia tolerance. The part of the brain that causes neurally mediated hypotension breaks down farther with age until with unremitting insomnia, it may not work well at all. I have had tests that showed no nitrogen and zero percentile of nitrogen--no protein digestion. Immune dysfunction caused by radiation or dioxen are impossible to counter.
DadsBlueAngel 2 years ago
but in my case my cognitive abilities started decline rapidly over some days to the point were i could not even read three words plus i had a burning sensation when i was going to sleep am sure it was stress because the cognitive decline continued even after i stopped doing hard revision my question is can any visual stimulants be the cause of the condition and how much damage can stress do to the brain and can all be repaired
mugara16 2 years ago
Thanks for sharing your medical expertise with us. I will ask my physician to check my cortisol levels.
rebeccamesslna 2 years ago
Please know that people suffering this horrible illness would like nothing more than to have the strength to get out of bed and live their life.
rebeccamesslna 2 years ago 15
I have had CFS and fibro as well as EBS. I think it's extremely important to mention, after 10 years of this, I finally fell apart and Celiac was found. Please, have people look deeper! These illnesses are sometimes only symptoms!!
yarwnna 2 years ago
can you expand on that?
JASONMOORE87 2 years ago
Fibro is a mystery to the medical field and no one knows the complete story. Fibro is a symptom of deeper issues and evidence is showing more and more that it's intestinal illness. Check out SCD diet, GAPS diet webpages and you can see how the gut affects the entire system, including how it causes fibro/CFS, MS, autism, mood disorders, insomnia........This is how I addressed fibro successfully.
yarwnna 2 years ago
I think Dr. Bellonzi is correct in his treatment of fibro, but there is more to it. Diet can not be ignored and sugar, grains, chemicals and most carbs cause fibro pain. Until this is addressed the gut can not absorb nutrients needed to reverse fibro or any other disease. The liver is maxed out too and that needs attention. GAPS, SCD and others address the core of fibro.
yarwnna 2 years ago
have you had spasms! like very bad! as my girlfriend incresed her "amitriptalean" cant fully spell it. but it was very heart breaking top watch!
JASONMOORE87 2 years ago
Oh yes.....lots of stomach and gut pain!! It's very easy to not get a proper diagnosis. She should keep a symptom diary and find a smart doctor. The norm for finding the underlying causes of fibro, celiac, etc..is over 10 years. Don't waste time!!
yarwnna 2 years ago
I spent 2 years paralyzed as a teenager diagnosed with CFS. The medical community offered no hope and told me i was going to die within 2 years. 18 years later i was a competitive runner with my city's track club coming in 2nd place for the entire year. 2 years after that - i am paralyzed again. my diet has not changed. my stress levels have gone down yet here I am bedriden getting bone marrow biopsies and getting around in a wheelchair. I don't think a few tweeks of the diet will fix this.
TheChildprodigy147 2 years ago
That's brilliant. I wish I would have thought to tell her to spend less time in bed.
I assume your advice to Farrah Fawcett would be to spend less time having cancer.
waltersquality 2 years ago 4
@waltersquality You're inability to actually hear what is being said is mind boggling.
steviesama 1 year ago
The inability to sleep is not the issue. For the past 10 years my wife has had extended periods where she slept 16-20 hours per day. Other symptoms have included; muscle pain, headaches, dizziness, lack of concentration, sensitivity to light/sounds, irritability, etc.
These problems appear to grow worse in direct relationship to her monthly cycle, which suggests a relationship to hormones. She has been prescribed prozac, paxil, aderall, even lithium. Nothing seems to break the pattern.
waltersquality 2 years ago
@waltersquality Nuvigil and Provigil, work wonders for CFS!!
sirloynes 3 weeks ago
I got Mono last summer. I thought I recovered quite fast. I was back lifting, then fell in the gym one day. After that I had random pains, extreme fatigue, and crazy panic attacks. I gotta pin point the cause of this crap.
BaileyLush 2 years ago
for anyone who reads this in time, a product called delimmune V has excellent effects on recovery from mono.
Its a whole lot of a particular dead bacterium that will stimulate the receptors in your gut to release a massive amount of anti bodies into your system
LostMente 2 years ago
So this immune response is the reason for all the physiological components? Thanks for the info:)
BaileyLush 2 years ago
@BaileyLush Nope. 15 years after mono, still exhausted!
sirloynes 3 weeks ago
Great Video - Thank You! :)
jonathancreates 2 years ago
B complex, B12, in high doses
1000creation 2 years ago
@1000creation: Please be careful with this recommendation, because excessive B doses will result in the body creating other vitamin B's deficiencies.
4chango 1 year ago
Dr. Bellonzi is looking at the "big picture" to what is CAUSING CFS/ME. We may not know the exact cause(s) of CFS yet, but he does point out most of the known possibilities. good job doc!
youlance29 2 years ago
Vince is the best Doctor with sensible intelligent solutions...
tskimmi 2 years ago 2
I have been diagnosed with CFS... I have had it for 8 months now. I miss out on alot of school,family activities,and hanging with friends. The thing I have found to help a little... Is to do some things,workouts,do activities to overwork the stress you may have. It doesn't get rid of it... But it does help.
XxSavotagexX 2 years ago
wow this has really helped me!
i think i may have cfs as im always low on energy but i really want to be more active.
ekahamsa 2 years ago
I've checked basically everything that could be checked in my blood ,and also got depression checked, which I don't have. Cognitive behavioral therapy has helped me overal to get into a balance and to accept, another think what's helping right now is taking vitamine b12 injections and folic acid pills, anyone who is interested can send me a PM, I will give the full information. They now think that even though yoú re not low on that stuff, that we might need more. I've improved a lot on my CFS.
MerinaWish 2 years ago
hello there, your comment interests me. i have supposed CFS i have had it now for 6 months i have has all blood test which were all negative and do not have depression. i do feel down , but this is only because of my condition. Please tell me more about what you are doing to help yourself
cpettet 2 years ago
Hello :)
I've sent you a comment to your inbox, I hope you got it and that it's useful to you.
MerinaWish 2 years ago
Hi
There are some good books out there I liked 'beat fatigue with yoga' by Fiona Agombar it tells you a lot about the condition. It could be stress so you need to find what works for you here could be an intolerenace or lack of a vit or min try magnesium it has helped me, could be hormones, blood pressure, hyperventilation or diet. A good diet, de-stressing and gentle exercise will help many, 'The complete book of nutritional health' is great and so is yoga. Talk to a Dr and do research
jadonblade 2 years ago
@cpettet take provigil/nuvigil...life altering pills, no side effects for me, but i'm awake and more alert than ever!
sirloynes 3 weeks ago
I had Candida and the thyroid imbalance and all that. I could not get rid of candida no matter what the drug or nutritional supplement and or diet. Since I have been taking Iodoral and have been getting rid of mercury my symptoms have improved. My Candida antibodies have dropped as well, it is really amazing.
kruseman44 2 years ago
Many Lyme disease patients have been diagnosed with CFS. Wrote a Lyme disease brochure with the help of 2 Lyme specialists. Will email to anyone interested.
ecftube 2 years ago
Not only Lyme Disease, but also Babesia, an emerging illness. It is also transmitted by ticks, but the symptoms of Babesia are somewhat like Malaria. I have tested positive for Lyme on the most stringent test, the Western Blot Test, and positive for Babesia, but I have my doubts about how much each one contributes to my misery. My CFS is textbook as far as symptoms go. I take blood thinner shots, Heparin, twice a day because Heparin has been found to kill Babesia (in vitro). It does help.
stillwaterguy04 2 years ago
Could you send that brochure to me? Not that I didn't get that checked, but I find it interesting. I've had CFS for about 3 years now.
MerinaWish 2 years ago
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Read Explaining colours to a blind man. Not only will it enlighten many as to what living with a mental illness and chronic fatigue syndrome is like, it also gives comfort to those sufferers who think there is no hope and that they are alone. It is very informative, sometimes shocking but also very funny in parts. All in all, a good read and highly recommended.
hsttraindriver 2 years ago
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check out my channel for the cure of CFS if you have been affected by a biotoxin, lyme or have MCS.
YourHealthTube 2 years ago
You mention metals in the body here.
I have 3 different kinds of metal in my body -- a bb (from a bb gun) in my face, a sewing needle (i have no idea how it got there, but I swear to you it's there - a doctor saw it in an Xray when I was in 6th grade and decided to leave it there because it would be too intrusive to remove) in my wrist, and titanium in my skull (fractured orbital).
Could any of these things cause a risk to me in the future?
NumbNutz12000 2 years ago
This goober has no concept of what Chronic Fatigue Syndrome really is. I hope he gets real Chronic Fatigue Syndrome. I would bite him if I thought CFS were infectious.
stillwaterguy04 2 years ago
"This goober has no concept of what Chronic Fatigue Syndrome really is."
Modern, western medicine doesn't, either.
BCCButters711 2 years ago
BCCButters, have you read anything about Helmenthic Therapy? It's a disgusting idea at first, but it makes a lot of sense. Look it up on Wikipedia, and contact me, if you wish. I'm thinking of trying it because I have so many crossover symptoms with MS.
stillwaterguy04 2 years ago
Sorry to hear you are sick. Have you tried Vitamin Therapy? I take the USANA Essentials, Active Calcium, their Bi Omega product (fish oil) and at least 3,000 IU of Vitamin D a day. I was taking 10,000 IU until my count was normal. I feel great!!
Regarding Helmenthic Therapy, if you have tried everything else, then I cannot see how it would hurt...but I see your point, probably a little disgusting. Although, I think they do still use maggots and leechs for certain medical procedures, too.
BCCButters711 2 years ago
Dr byron Hyde makes a difference between M.E and CFS. I think most physicians mean the same thing, but this one is talking way too much about fatigue. I think this is the difference Dr. Hyde is talking abut. The Dr on this video is not talking about M.E. He doesn´t mention any neurological problems that are present in the diagnostic criterea. Nothing about orthostaic intolerance etc. Only fatigue. ME/CFS is so much more than just fatigue!
annikapet 2 years ago
Comment removed
agatka2007 3 years ago
Well that was simplistic "Figure out what's causing you to be tired and take care of that and you'll be fine."
What an idiot! Yes I sleep, yes I eat, yes I exercise, yes I practice stress management, etc... Sad fact is I got EBV and have been wiped out for 19 months.
nabadm 3 years ago
I would recommend getting a full Allergy test as well. Your body might be using allot of energy fighting other allergies. Sometimes if you remove these allergies it gives your body enough energy to get on top of the real cause of the problem! wheat allergies for example can prevent the uptake of vitamins and minerals in to your body , leaving you tired. You may have a couple problems that youre dealing with, removing one will help allot.
NAPALMJUNKY 2 years ago
actually what he is saying makes good sense...after four years of being treated by the system i have totally gone the natural way ..
vitamins,rest, nutrition, exercise(starting with 1 minute per day)..
and i am now seeing good results.. dont knock it till you try it.. dont get sucked into the medical systems crap
hoki424 2 years ago
@hoki424: That was smart to start with just one minute a day - a good habit developer. I advise all my client to exercise for one round a day. A round of boxing is only three minutes.
4chango 1 year ago
What I found is when I got CFS, i got a new allergy, house dust allergy. XD. I take pills for it, but it aint helping me fully. It's the best to take out all those factors indeed, but it 's not a full cure.
MerinaWish 2 years ago 2
AMERICAN GENOCIDE
ramvan55 3 years ago
The WHO (Myalgic Encephalomyelitis is defined by the World Health Organisation as a neurological illness (code WHO-ICD-10-G93.3 ) and several countries, such as Canada recognize ME/CFS as a neurological illness/disease. In Europe, the government of Norway and Catalonia (Spain) have come to the same conclusion and they are starting biomedical centres to treat the patients. No psychiatrist is involved in these centres
Sunshineray1 3 years ago 3
Hi, could you please give me the contact details or websites of these biomedical centres if you have them? Sorry if this has come through twice.
thanks, Rach
racheclare72 3 years ago
your website is not working
piyushsoniccc 3 years ago
His website changed since this video was made. I updated the link in the video description. It works now.
psychetruth 3 years ago
If you think the chronic fatigue is caused by bacteria, can a antibiotic kill the bacteria and stop fatigue
piyushsoniccc 3 years ago
maybe fnding the right antibiotic is not just like finding sand on a beach, ever thought about that? Duh
uffx3 3 years ago
Um, fatigue is not the only symptom with the actual disease called chronic fatigue syndrome. There is a list of at least thirty other symptoms sufferers have. It's not just about being tired and not getting enough sleep...how offensive.
normaeinstein 3 years ago
CFS is not a disease. It is syndrome.
A syndrome is a set of symptoms without a known cause. A disease has both a set of symptoms and a cause.
Syndrome does not equal disease. This is why they call something syndromes and some things diseases.
Example:
Chronic Fatigue Syndrome - No cause.
Irritable bowel Syndrome - No cause.
Lymes disease - known cause.
Sexually transmitted diseases - known causes.
psychetruth 3 years ago
I suggest you do some reading. You will find that CFS is a disease with multiple causes. IBS for example has a thyroid connection.
If Chronic fatigue did not have a known cause, people would not get any better with Antibiotics/Antivirals, hormones and or nutritional supplements.
Actually the real name of Chronic Fatigue is Chronic Fatigue Immune Dysregualtion.
Chronic Fatigue-Known Causes
IBS-Known Causes
kruseman44 3 years ago
Hello Friends,
The World Health Organization has called CFS (M.E.) a Neuro-Immune Disease. The WPI also refers to it this way. There is a cause for the horrors of CFS, we just have not found the biological answers yet. We could say that this "syndrome" is caused by an unknown disease perhaps. No matter what we say, the experience of living with CFS is filled with crippling physical symptoms that feel like an unimaginable terrifying disease. I too have CFS and work so hard to help! ~Love to all~
DrFrankyDolan 1 year ago 36
@DrFrankyDolan Epstein Barr? That's my problem.
sirloynes 3 weeks ago
@psychetruth If the cause is not known yet, it does not mean it will not be found. Multiple Sclerose was diagnosed as "no real illness" as well because in the beginning there was no known cause.
DoomNoMore 1 year ago
@psychetruth Well, technically, a disease is a 'dis' 'ease' - meaning not at ease. Anything that causes a sustained lack of 'ease' (regardless of it's nature) is a disease (an impairment of health or a condition of abnormal functioning).
I am a CFS sufferer myself (for 20 years now), and found this video to be of some value as it points out the truth of the nature of chronic fatigue, and is another positive step toward finding a realistic solution to this debilitating condition.
wumpee72 1 year ago
well said! chronic fatigue for me is an overlapping of hormonal, immune system and nervous system problems..i have a lifelong T3 thryoid hormone deficiency (diagnosed at 30 yrs!), candida (a fucking Horrid problem which gets into you when u have a low immune system), and yeah accompanying all this is lifelond severe depression and failure to get a career, a love life..loss of a life..etc..made some progress but cant beat the candida and beating the candida i think is fundamental to vitality
vincent4500 3 years ago
i have always believed that the mono i had at 16 had a huge to-do with why i am chronically fatigued...it hit me hard, that mono...i am now 38 years old and struggle for energy. if i have energy, it only lasts a few hours at most.
what i am wondering about is...what if we don't have much money (due to wanting to sleep more than work!?!?) to get proper testing...i am on state paid insurance...would they test for cortisol? thank you...
meghandsheamas 3 years ago
@meghandsheamas take provigil or nuvigil...worth every penny, and life altering too, no side effects!
sirloynes 3 weeks ago
CFS cure??? We believe so 110%
my wife had Chronic Fatigue for 7 years, she was one of the worst cases world wide. We switched to organics and she was of perfect health within 3 weeks. Our whole family has never looked nor felt better. Our receipies are sourced from Sally Fallon's Nourishing Traditions which we highly recommend. Try it yourself, better nutrition worked for us, seriously you have nothing to loose.
Put CFS behind you, give it a try. ORGANICS and NOURISHING TRADITIONS BOOK.
RGO22574 3 years ago
No offense but I find it very hard to believe your story. If you're wife was one of the worst cases in the world, she'd be almost dead. I know one of the worst cases in the UK and she is hospitalized, being tube fed and basically paralyzed.
Also I don't see how switching to organic food can cure one of the worst cases of CFS in 3 weeks - that's ridiculous.
Sounds to me like you're just trying to promote a book.
The video is excellent and Dr. Bellonzi is spot on.
Zildjian285 3 years ago 3
Absolutley agree with you Zild. I have a very severe case - been going through such a bad patch at the moment, that im in bed nearly 24hrs a day, and have been into ER 4 times in one month for episodes of becoming extremely weak, cold, with severe blood pressure drops to the point where i needed an ambulance - & that was just from getting up to get a drink. Now i have eaten more 'perfectly' in the past than most people i've known. All organic food, vege juices, it didnt 'cure' me at all.
sypher7 3 years ago
Sorry to hear that sypher.
Never give up looking for a cause of your CFS. Every case of CFS has a cause, you just need to find the cause and treat it.
Do you have a good doctor doing loads of tests?
I bet if you had a proper thorough physical exam with loads of tests for infections, adrenal fatigue, thyroid problems, hormonal imbalances, vitamins & mineral deficiencies, chemical/heavy metal poisoning, gut problems, etc, etc. you would find some treatable abnormalities that could help.
Zildjian285 3 years ago
Actually one person already died of the inflammation from CFS.
MerinaWish 2 years ago
@RGO22574 I've eaten organically most of my life and nope, no cure for my CFS!
sirloynes 3 weeks ago
Nobody mentioned taking calcium supplements and calcium is very important together with magnesium not only for bones but for several other reasons. I am taking Cal-Mag stress formula by NOW and Amino Complete and zinc and antidepressants I must say I feel a litte better.
agatka2007 3 years ago
thank you, you've helped me keep my hopes up
blountore 3 years ago
thank you. and God Bless You.
gugegago 3 years ago
Too high and too low cortisol is very
prevalent particularly if you have anxiety
and stress problems. Don't rely on hormone
replacement if you can bring your adrenals
hormones back into working order naturally.
realnoid 4 years ago 2
this is wat im beev having
i woke up with a sore throat, headache, im still sleepy, and at night when im sleeping my body suddently wakes up and starts having these wierd pains...i need help...plus when im waking up my body is so dizzy tat it justs wanna faint...and now my throat has this stingy, burning,rash like feeling...i need help
umf013 4 years ago
hi! well it sounds to me you have the MONO (mononucleosis). I had it for like a month and your symptoms sound just like mine back then. my advice: go to an ER, get the monotest and rest, get plenty of rest and fluids since there is no cure for this virus. It needs to go away on its own. Hope it helps, take care.
equirnam 3 years ago
@umf013 Mononucleosis?
sirloynes 3 weeks ago
what about caffeine?
maciejwrotek 4 years ago
I shot a video w/ Dr. Bellonzi talking about Caffeine yesterday. It will be uploaded sometime next week.
See the video "Caffeine is a Mental Disorder? - Psychology w/ Sandy".
That video actually has some good nutrition facts about caffeine even though it's a psychology video.
psychetruth 4 years ago
@maciejwrotek : Caffeine pulls vitamin B-8 out of your body.
4chango 1 year ago
Dr Bellonzi is always interesting in his videos. Lucid and easy to view and listen to. Another informative video post. Very appreciated information.
mooker5600 4 years ago 2
I totally agree.
NitnitNameerf 4 years ago 2
Good information. We need more of Integrative Medicine.
naz220 4 years ago 3
I've been listening to your videos for a few months, I just wanted to thank you for taking the time to do these I enjoy them very much!
revisedtara 4 years ago 3
This comment has received too many negative votes show
You should also be more specific about FM. Fibromyagia is not caused by CFS/CFIDS or chronic fatigue symptoms. FM is sometimes accompanied w/ chronic fatigue but neither is exclusive in and of itself.
You are using scare tactics here. Perhaps another video with more information to this painful and widespread condition?
todieandwither 4 years ago
We shot a FM video. I just haven't edited it and posted it yet.
psychetruth 4 years ago
Thanks for the video!! I really hope people check out this video and see an alternative health specialist before agreeing with conventional medicine.
Wisdombychoice 4 years ago 5
My Dad was fatigued for quite a while - very low energy. He started using a CPAP breathing machine at night. He is full of energy now. He is a smoker, so that is surely the cause.
crem88 4 years ago
@crem88: Did he have sleep apnea?
4chango 1 year ago
cool
ryanreenter 4 years ago
The point is to be responsible, find out about physical conditions and their causes yourself, then seek help based on a self knowledge of the condition. Placing your trust solely in commercials and doctor advice is responsible.
c16467 4 years ago 2
"...is irresponsible." I meant to write.
c16467 4 years ago
I have CFS and you are being irresponsible when you lump other chronic fatigue issues with CFS/CFIDS.
I suggest you clarify because people w/ sleep issues that have chronic fatigue do not have high ebv titers. Ebv causes mono which is DX'ed as EBV after 4 months which is DX'ed as CFS after a year of symptoms.
todieandwither 4 years ago
I always think it's funny when a consumer leave a comment protesting an alternative health professional since they "know better" because they have disorder, syndrome, etc.
The fact is that whatever the conventional doctors have told you, you still have the