Beat Chronic Fatigue: Top Natural Remedies Revealed

Cider vinegar and H2O2, as well as being careful with what I eat, have been the means to correct my ph. You need to check your saliva and urine, not just your blood. Blood ph can be good and saliva and urine can be low as a result of the body correcting the blood. Our system knows that the blood needs to be right for our body's sake, so our saliva and urine systems will lower to counteract it. Therefore once we get our saliva and urine neutral things are rosey! Now after 30 years of pain and confusion, I am a different boy!

I have been buying 50% H2O2 solution for spraying crops for insect and fungi control at a 3% mix. I rinse my mouth with straight water and then sip a mouth full of H2O2, hold it in my mouth and swerling it for a minute or so and then swallowing it. I chase it with another sip of water. --don't know why I do that :)

H2O2 works on my crops and has worked on me. Who can argue with that?

I went to the doctor a few months ago complaining of being so tired I didn't want to get out of bed. They checked my vitamin d levels to find I was at 17 when the lowest they would like to see you at is 50. I've been on 2,000 iu's of Vitamin D3 (make sure you use d3 not d2) and feel soooo much better. I actually have energy now! I started my husband on it and it has helped him tremedously as well. Most people are vitamin d deficient and EVERYONE should be on 1,000 iu'd a day at least! I haven't gone back yet to check to see what my levels are now. It has been about 3 months. Everyone has to ASK their doctor to check their vitamin d levels. I wonder how many years I have suffered needlessly. From what I'm reading, when you are as defecient as I was, your dosage should be higher than 2,000 iu's. I will go get my levels checked and then if they are still low, up the dose.

After only one month on iodine, starting at a few mg a day and more recently working up to 100 mg a day (as recommended by Dr. Guy Abraham for FMS and CFS patients; and in addition to avoiding as much fluoride as possible by drinking only distilled water and a no-flouride toothpaste, I am happy to report a reduction in brain fog by about 50-60%; all my chronically swollen lymph nodes are gone; my previously scaly feet and heels are now pedicure perfect; my body temperature is completely normal for the first time in a decade; my mystery fevers have disappeared, and I'm sleeping better.

I'm doing many other things: Ted's alkalizing formula; Lysine; multi vitamin, b vitamins, 3 grams vitamin C, and an additional brazil nut each day (for the selenium), progesterone for 2 weeks per month, 1 tbs nutritional yeast when I don't have b-vitamins, magnesium citrate (600 mg/day) and only use coconut oil and butter. However, I'd done most of those things before the Lugol's iodine solution -- which I take in 3 divided doses of 33 mg each.

The other thing I started soon after the Lugol's was taking 1tsp 2x day of turmeric. That may be an important factor, esp re. the lymph nodes if they were caused by bacteria/virus.

The painful swollen lymph nodes have been a problem for about a year, and were usually accompanied by a low grade fever.

My waking body temp was usually around 95.2, although sometimes is was 94 and others 96. It is now consistently 97.8-98. 2! A couple of times my evening temp has risen to 99 but I'm not worried about that because I didn't feel feverish.

However, I haven't seen much improvement in my energy levels. That said, having my brain back is a Godsend and I'd choose a working brain over energy any day. Nothing is worse than a malfunctioning brain.

It's only been a little over a month on the Lugol's, and only 3 days on the 100 mg. Today I am starting d-ribose and L Carnitine to help with the energy. I intend to continue the 100 mg of Lugol's for 7 weeks, which is what Dr. Abraham recommends to reach saturation, then will consider tapering back down to about 25 mg a day.

This does not contradict the flouride toxicity theory as a cause of CFS Fibro: Iodine/iodide is one way to help flush out flouride, chlorine and metals and that may be a reason it is working so well.

I also posted in this category about coconut oil a few weeks ago.

If you have pets a parasite infection is very possible. Two good herbal complexes to consider is Nature's Answer "Black Walnut Complex" and Kroger Herb "Wormwood Complex". Also add (rotate) Garlic (I like the oil softgels) and Oregano (softgels again). To help clear parasites & pathogens (dead or alive) from the gut take one spoon Milled Flax Seed with meal once or twice daily. You may also consider rotating or including Turpentine as it is one of the most powerful natural antimicrobial and antiparasitic.

Ginseng and Pantothenic Acid will improve adrenal function. Raw Bovine Pituitary will help both Adrenal & Thyroid glands.

One last item that will help by itself or especially in combination with the herbs or Turpentine is Zapping. There are many types of Zappers with a price range of under $50 up to several thousand. A good beginner is a 30 KHz Hulda Clark Zapper. You will experience an immediate increase in energy from Z'ing.

The Flax should help clear the die-off but you may need to take some Charcoal or Clay prior to meals to avoid headache and other bad side effects. Digestion should improve shortly after the Herbals/Turpentine/Zapping.

If you have a Mycoplasma Infection the Borax will be most effective as 1/4 cup in a hot bath rather than drinking. It would be most beneficial to add 2 or 3 grains of Sodium Thiosulfate at the beginning of the bath to remove heavy metals from the water and your body. Fluoride is a likely culprit in many CFS folks so water purification is a must, and the above baths will remove existing fluoride as well as other heavy metals. When supplementing Iodine, do so several hrs away from the bath.

SS Disability for CFS is not impossible to get, nor improbable, but many applicants do get discouraged because they are often too sick to the research, understand, and get through the process; which unfortunately is often lengthy and stressful; (and can take more then 2 years in cities with many applicants and very few disability judges). Anyone considering SS disability MUST read the info in the SS website (or have an advocate do so to/for them) so they know what is required. This is often "too much" for CFS'ers, so here's a brief summary of the key points (and some helpful tips):

REQUIREMENTS: All SS Applicants require a Medical Doctor's diagnosis; and requires you complete several applications forms over a period of many months (and usually Appeals forms too). The forms ask several key questions that act as evidence, which is used to determine the likelihood of a valid disability claim. The application process also requires your doctor's support (i.e him/her submitting a lot of paperwork on your behalf); so you simply must ask him/her directly, if he/she will support you! If he/she can't or doesn't want to, for any reason, either plead with them, or go find another doctor who will support you (then start seeing them immediately).

If you get past the first 2 (of 3) application stages, then (approximately 6-24 months after your initial application) you must see several SS doctors for interviews, exams, physical and mental/cognative tests. Stay aware: All SS reviewers are doing their best to eliminate you/your paperwork from their mile-high pile of applicants, so keep this in mind at all times when answering questions, and when seeing doctors (don't slack off)! You can only prevent your elimination by giving them plentiful, relevant precise evidence of your disability, so they can forward your file to the next reviewer. IF each reviewer gets adequate, convincing evidence of disability, they will (eventually) send you to a Disability Judge (the only impartial person in the process; but unfortunately, the last person to see your case file)! If you do not provide plentiful, relevant, convincing evidence (with ALL your applications & during exams), you/your papers won't ever get to a Judge (period)! BEWARE: The forms are designed so there is NOT NEAR ENOUGH SPACE for you to provide an adequate amount of evidence to validate your claim! Therefore you must attach additional sheets of paper full of relevant, convincing evidence of your disability!

TIP: Each SS Rep must be able to easily VISUALISE (from your paperwork) exactly how & why your illness prevents you from working. In addition, all your SS doctors will need to see evidence (with their own eyes), in your person, that you are indeed disabled! They will judge your disability by how you/your body responds (or is unable to respond) to various stimuli. (Note: Your doctor provided a diagnosis and medical records full of symptoms; but YOU MUST provide SS with evidence of their disabling effects on YOUR body, mind, and life; and such that they prevent you performing normally/adequately (in major areas of your life)!

WARNING: Don't consider applying unless you're seriously, chronically ill (longer than 6 mo's) AND you really REALLY NEED financial and/or housing assistance because you have no other option. Living on SS is very difficult; and HUD/Sec 8 is no prize (and has long waiting lists)! BEWARE: Many/most CFS treatments, meds, supplements, etc, are not covered by Medicare (but many/most can be deducted as medical expenses which helps with benefits). Going on disability is a Major Life Decision. BEWARE: Once you go on disability; if you later get well, and decide to go off disability, you'll (virtually never) be able get it again, no matter how disabled you become! However, once you're on disability, you are allowed earn up to @$900 per month without it affecting your SS disability status (but the work/earnings may also reduce/prevent you from getting other benefits/assistance).

BE FOREWARNED & BE PREPARED: 98% of all SS applications for CFS (and most other non-life-threatening illnesses) get denied on their 1st AND 2nd applications; so you must Appeal (in writing) after each denial, within the deadline written on your denial notice. If you get to round 3, plan to see at least 3 different SS Doctors, on their schedule (no rescheduling allowed). You MUST NOT miss any application or appeal deadline, or appointments no matter how sick/bedridden you are (so plan ahead: find/rent a wheelchair/gurney, and a driver on your appt day)! BEWARE: If you miss an application, deadline, or appt, you must restart the application process over again, at round 1 (at the back of the line). This is why many people need Advocates or Lawyers especially when their claim has been denied a second time.

Lawyer Legal Fees: If your claim is awarded with the help of a lawyer, the law allows them [if you agree via contract] to take up to @1/3 of your monthly disability award for the first 3-5 years or so. So be ready to negotiate attorneys fees; and don't hesitate to ask them to take your case pro-bono if you're in dire straits! Many Low Income and Indigent people can get free legal advice and legal help from most city/county Legal Aide Offices [on a free, reduced, or sliding scale), and also through many Foundations, Societies, Charities, Support Groups, Churches, and similar Orgs!

ADVOCACY: If you have family/friends/co-workers/church members (who can do research, and comprehend the SS disability criteria; and can see, apply, and transcribe how your illness/symptoms is disabling you, [and fits the criteria]) they often make great advocates as well! They certainly will make the process much easier on you/the patient! (Most lawyers do a phone interview or two, then they expect you to fill out forms, so they can build your case; if you cannot communicate effectively or fill out forms adequately, you must tell them this; and/or you must find someone else to help you communicate effectively! ).

This is how YOU CAN prepare your case while you are sick: 1) Start gathering witness testimonies (as many as possible): Ask all your family members, and friends, associates, neighbors, (even children! ) who know of/witness your illness, to write/dictate a reference letter to the Judge that A) states your relationship, and how you know one another (i.e. how long, from where, the nature of your relationship, etc). B)Then ask them to then write/dictate several paragraphs comparing/contrasting the "old" healthy you (your abilities, achievements, hobbies, sports, travels, physical/mental prowess, personality etc) with the "new" disabled you (always sick, doesn't call/go out, cant do activities/hobbies/sports/socials; and cant concentrate/remember things because of exhaustion/illness/confusion/fainting, etc; and describe how you have a totally different persona now [a very ill person]). 2) Next ask someone to find/make a lined "chart" with @8 columns (1 wide column for recording Symptoms; 7 narrow columns for Mon-Sun) for you to record your symptoms. On that chart (column 1) list every CFS symptom you have, starting with the most disabling and the most frequent; fill up as many pages as you can. NEXT: Near the very bottom of the last page, add 3 new Headers (in the Symptoms column); Functional Hours(how many hours you were up, functioning each day); below that your overall Abilityto perform hygiene tasks + food prep + basic household chores: (Unable, Minimal, Somewhat, Able). Below that, your Mobility Status (Bedridden, Couch/Chairbound, Housebound, NH needed help to leave house, ND needed a driver, NW/C/C needed Wheelchair or Scooter/Crutches/Cane, etc). Below that, include a key for any/all abbreviations you use on your chart. (Make at least 10 copies of this "weekly template", then put your original aside for making copies for next months charts).

NEXT: Date the page and fill in todays column, putting a check-mark next to every symptom you experience today (do this for each and every day from now on; this is evidence/testimonial proof, a legal record of your day-to-day ill-health). Fill in your charts daily; if you miss a day go back and fill it in to the best of your recollection; or write in why you missed your charting (too sick, too tired, too weak, too confused, I can't remember, I forgot, I lost the paper, I couldn't hold a pen, It was too depressing/confusing, I slept all day, etc). Once your charting habit gets rolling; on another page (or on a calendar or computer file, or diary, or phone-a-friend-and-dictate), start documenting/dictating how your symptoms prevented you from doing normal tasks/activities throughout your day(s) that week. Any kind of general or specific summary is OK (don't bother correcting your typos/mistakes; you're sick, don't waste precious energy unnecessarily). Example: Sunday: Too weak, can't get out of bed. Cant sleep, muscle spasms. Sickly, too exhausted to shower. Bad stomach can't eat today. Sore glands, to weak to eat/talk. Tues?; Soo tired, not sure what day it is, no energy, to weak to shower. Need rest. Ate tuna from can again. Mon : read 5 pages, can't remember any of it. Feel brain dead; can't calculate bills. Forgot to call bank again. Ears ringing, huge headaches 3 days now. To weak to cook, ask Dale to make pot of soup. Call mom, need help bathing ASAP. Thurs; Migraine, too sick/dizzy can barely move. Barfing all day, dry heaves FRI?: I dont know, I can't remember...

Make copies of everything; BEWARE: SS often looses paperwork, even complete files so do not give them your originals unless you have copies! If you are alone/immobile call the nearest church and beg for their help: most will send someone to help you!

Hope this help someone; Good Luck; Blessings to All

Since I have 3 amalgams, I also tried doing Mercury detoxing... I tried using Chlorella, high doses of Selenium, Kelp, MSM and Ted's Carbicarb... None of these really worked or ended the fatigue... Finally, I read on this website that Sulphur removes Mercury... Sulphur is something that I hadn't tried before, so I went to the health foodstore and bought these little dissolvable Sulphur tablets and took them as directed, which was 3 tabs under my tongue 3-4 times a day...

I remember that I was so exhausted on the day that I went to get the Sulphur tabs... And desperate to try anything that would help me... As soon as I purchased them, I popped them in my mouth and I felt instant relief... My heavy eyelids lifted up, posture lifted up, breathing sped up, energy came back and also a little itchy hive that I had on the crease of my arm near my veins, it went away... I went home with so much energy that I even went to the gym because I was so happy that I had energy...

It is clear to me now that the reason why Sulphur gave me energy is because I do have Mercury toxicity that was making me feel dizzy and suffer from Chronic Fatigue Syndrome... The dissolvable Sulphur tabs that I bought had a strength or potency of 30c... I continue to have energy taking these tablets... But I was also advised to take Selenium and Chlorella also to bind the Mercury and chelate it from my body! Mostly, I'm so happy I have energy to go out and also no more dizziness! Or itchy Hives!

Would love to hear an update on how the CFS is now Heather!

Will definitely add Ted's Borax Water. I've started Lugol's Iodoral 50mg tablet, plus 1 Tbsp Coconut Oil in my tea each morning and am already feeling more energy than I've had in 10 years - and it's only day 5!! Starting a second Tbsp in the PM into my food or warm beverage, or just straight. So beneficial. There's also been some incredible findings re coconut oil and reversing or stabilizing Alzheimers / Dementia from Dr Mary Newport who wrote, "Alzheimer’s Disease: What If There Was a Cure? The Story of Ketones." She's on YT too including a TEDx.

Studies have also shown aging. The reason why these unhealthy effects occur is likely because fish oils cause oxidation in the brain. One needs protection against the oxidation. I always take krill oil because it has much lower oxidation risk and highly absorbs. Fish oil has a tiny bit of astaxantin but not enough.

More importantly I take at least 4 mg of astaxanthin to protect myself from the oxidation that could come from the fish oil along with other beneficial effects. Alternatively, there are non fish oils but they seem more expensive.

As for cycling supplements, this usually applies to herbs or compounds not originally manufactured in the body, so with nutrients like Ribose you can take lots of it daily with only benefits.

As for your ADD/chronic fatigue/anxiety and depression issues, you definitely need to improve your natural detoxification system (which also improves energy); for starters I recommend 500mg L-Methionine + B-12/Folic Acid 1000/400 mcg + Dimethylglycine (DMG) 125mg. Take these together once a day preferably at the start of your day so you will have energy & clarity & a better mood thru the day.

I love this stuff.

I would definitely try the cortisol therapy, but perhaps there is a more natural way to stimulate the adrenal glands. Research has found that the nutrient Phosphatidylserine (PS) helps balance both high and low levels of cortisol. Usually our brains manufacture sufficient levels of PS, but if there is a deficiency of folic acid and vitamin B12, or of essential fatty acids, the brain may not be able to make sufficient PS levels. So get lots of fish, ridiculous amounts of dark green vegetables, and even rice and soy (or lecithin, I imagine). You can find PS supplements...they used to make them from cow's brains, but now they make a soy lecithin-derived one. (Phew!) At the very least, this nutrient would help with brain fog.

(My interest in chronic fatigue stems from having the Epstein Barr virus. I couldn't shake the fatigue for years and years. I did find getting fish oil and a teaspoon of chlorella everyday finally produced some results, which I would recommend to absolutely everyone!)

I have been rebuilding my health following CFS for many years but in June 07 I had "Influenza A" which really knocked me around. I thought I was recovering ok but the old CFS symptoms re -emerged ie headaches, brain fog, unrefreshing sleep, fibromyalgia, blurred vision, sleeping all the time. In November 07 I found EC and tried H2O2 food grade. At first I tried the inhalation method for a couple of weeks but progress was not really fast enough so I took it internally. Due to my low energy and fogginess I managed to take the upper end dose on the first day (normally people build up to this over a few weeks) ie. 150ml of .50% 1/4 tsp baking soda three times in one day. This is equivalent to 25 drops in 150ml of water three times in a day.
Results: first intake - nothing Second intake - my vision improved markedly over a ten minute period. It was as though a veil had been lifted from my eyes. Everything was sharper colors were brighter. I also began to feel more energy. (Since the flu my eyes have detiorated, I had to get a new prescription for my specs. And they had to make them 3 times because my vision varied so much from day to day. ) Third intake - nothing noticeable.
The following day I woke with a headache and fogginess and figured I was in for a detox reaction. This lasted until around 2pm and from then on I felt fantastic. I mean I felt exceptionally good. I felt like hugging strangers in the shopping mall. Giving money away, imagine no possessions and so on. It was exuberance, lightness, abundant energy. It lasted about 3-4 weeks. During this time I did some maintenance doses on a lower scale.
Results not: Anyway I have since had a garden variety bug and many of the symptoms have returned but to a lesser degree except for one debilitating condition that is worsening. When I eat - anything - I get a hangover and overwhelming fatigue for about 90mins. I have to sleep it off. I have tried various alternatives ie ACV & BS but to no avail. Does any one have any ideas what might cause this? I can't go out or for very long because if I have to eat I have to sleep.
I do not have any apparent digestive problems but it is probably connected in some way.

Thank you for your response...here it is 2021 and I just found it 4 years later....going to try it anyway as I have no energy and still want to sleep and sleep.

I get plenty of sleep, work at home, no heavy physical activity, but I do get out and walk or garden every day, and if the weather is bad, I'll do some aerobics inside.

I eat fairly decently, depending on how much I have to spend on food during the month. I don't eat a lot of meat, so try to get enough protein from other sources (dairy, nuts, brown rice).

These are the supplements I'm taking. Please tell me if you see anything wrong that I should take out of add. I know this is a lot, but I have to try to work as much as possible, and I just kept adding things that were supposed to help. For awhile, this worked, but now it seems to be harming me more than hurting me.

I thought one thing might be that I have a parasite, strongyloides, and some of these are also anti-parasitic, so maybe some of my problem is constant die-off, but if I stop taking them, the worms take over again and I get sicker.

Multi-Vit-Min tablet
Biotin 5000 mcg
Dopa Mucuna 15% L-Dopa
Potassium Gluconate 595 MG
C 1000mg
Hawthorne Berries 565 mg 2 x day
D3 3000 iu/day
CLA 1500 mg 2 x day
B-Complex & B-12
CoQ10 50 mg 2-4/day
MSM 500 mg 2 x day
Red Yeast Rice 600 mg
Iron Glycinate 28 mg take 1 every 3rd day since multi has iron in it too
Cal-Mag-Zinc (chelated) 3/day
Triple Omega (flaxseed, fish, chia oils) 3 x day
Serrapeptase 2-4/day
L-Tyrosine 1-3/day
Lugol's 5% - 1/2 drop/day (I'm very sensitive, so I'm working up to higher dosage)
Selenium 200 mcg 1 every other day (since I'm on such a low dose of iodine)
Diatomaceous Earth - 1 tablespoon/day
Borax 1/4 tsp./day dissolved in 1 liter of water and drunk throughout the day.