Beat Chronic Fatigue: Top Natural Remedies Revealed

Chronic Fatigue - Vitamin D

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.

I finally got relief for my ibs-d when I started taking L-Glutamine. I'd rather worry less about needing a change of clothes during the day than potential cancer.

Please make sure you read Jason Uttley's important article on Chronic Fluoride Poisoning. This article pinpoints fluoride as a very likely cause of Fibromyalgia and Chronic Fatigue. A MUST READ!

CFS is well known among those of us who have the mold-susceptible haplotype to be caused by toxic mold exposure in a water damaged building. For some, early on, simply getting out will restore health. For others, with lengthy exposures, it can take years and specialized medical treatment will be required. Doctors in general are not cognizant of this or will say it can't happen because they cannot get away from the concept that this is not an allergic reaction. 24% of the population has a mold-susceptible haplotype, and we are the ones who get extremely ill when living or working in a water damaged building (the water damage may not be visible.)

Amy: You are taking a very good regimen for the CFS but one word of caution is the problem of absorption. This very much seems like your case.

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.

Mitochondira are organelles in cells that provide oxygen and energy. Their decay and death leads to our decay and death over time. Astragalus protects them! Here is research to prove it: http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3291990/ I have found that with chronic fatigue it helps to take 3 capsules 2X a day - not near bedtime. Really chronic fatigue is just adrenal weakness. See Dr. Frank Shallenberger's Youtube vids to learn more about that.

My reply (above) got separated from the Original Post and now is confusing, so I'll add more info so others can benefit more.

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

In regards to ... "since we're all under the impression that Omega 3's are the ticket to health and longevity. Those scientists were perplexed and disappointed with the results: There was a significant trend toward the opposite: Lower IQ's in the babies."

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.

I have been taking 750mg D Ribose for couple yrs but still wasn't getting anything significant for energy. Recently I increased by using the bulk powder form by spoon & mouth or as a sugar substitute. Still needed more for energy so I began taking Ribose with Niacin and/or Niacinamide which converts to Nicotinamide Riboside which converts to NADH which is very important for energy and proper DNA or cell reproduction aka anti-aging.

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.

To Debbie-Anne of Australia, I have read on this web site that bloodroot and esiac tea can get rid of polyps. Good luck.

I have had some bad breath and chronic fatigue for quite a few years. I was just trying everything I could think of . The doctors were of no use. I used a cap full of drug store hydrogen peroxide to brush my tongue. I was pleasantly surprised to find my chronic fatigue was greatly reduced in just days. I have only been using it for about three weeks. I recently got some food grade which I reduced to 3%. I am going to start taking it by spray since I have asthma. The asthma seems a bit better just from the little bit I have used to brush my tongue. Oh yeah, the first night It was hard to go to sleep. I didn't know that this is a common effect.

Turmeric for Fatigue: I have Chronic Fatigue along with Mercury toxicity and started taking Turmeric for a tooth infection/ sensitive tooth. A GREAT side effect was energy! It only took a few days to get started. I take about 4 capsule in morning and 4 at lunch (homemade caps with turmeric from spice aisle). WARNING: Don't take before bed. I couldn't sleep for a few nights until I figured out it was giving me energy.

I love this stuff.

My sister was sick for 2 years with Mono that turned into Chronic Fatigue. We tried many things and nothing seemed to work. Finally a Naturopath told us that her immune system was over active which he said happens a lot in cases like these. He told us to take Marshmallow Root & Astragalus Root. We found a combination from Dr. Christopher's but that is just the one we went with, I'm sure there are others out there. She takes it religiously and has gotten back to her old self. I don't know how long she will have to take it, she's been on it for about 5 months and did try going down once and was able to, however when she tried going off of it she was getting the old symptoms back. It was such a blessing that someone recommended this to us. God Bless!!!

I just wanted to let you know that I after suffering from serious adrenal burnout and chronic fatigue and now found more energy by taking L-carnitine. I couldn't even get off the couch before and now I have 80% percent more energy. I also eventually added in q10 and that together with magnesium put me back to being the energizer bunny. I have read several times that people with CFS also have depleted L-carnitine. Hope this can help someone suffering from this horrible fatigue.

I recently read that people who suffer from chronic fatigue and fibromyalgia benefit remarkably from cortisol treatments (75 per cent showed significant improvement, and 62 per cent reported substantial improvement). This is because they have adrenal dysfunction, meaning their adrenal glands, which produce sex hormones and cortisol, don't work effectively. I suspect this is due to viral damage. Cortisol is that stress hormone... you get a shot of it in fight or flight situations for a quick burst of energy, decreased pain sensitivity, etc. Proper levels are important for proper glucose metabolism, regulation of blood pressure, insulin release for blood sugar maintanence, immune function and inflammatory response. Maybe this is why when you exercise it makes it worse because your cortisol levels should increase with aerobic exercise to help deal with the wear and tear. The bulk of cortisol release happens when we sleep, which would also explain why you might not wake up feeling refreshed. If you read up on cortisol, you'll see that if you don't have enough, you just don't have access to energy to burn.

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 am a 41 year old female with CFS for 7 years.

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.

I have chronic fatigue syndrome and I read that raw, unfiltered apple cider vinegar kills bacteria and can give you energy. Well guess what ? It does give me a burst of energy every time I add it in my water. If this apple cider can give a patient with CFS a burst of energy, imagine what it can do for someone who is healthy !

I have chronic fatigue and read all about molasses and acv..started taking 2 tblspns of both everyday and seems to be working. My skin is also smoother and healthy looking and I just feel better all over.

Mama to Many,

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 had a heap of luck with liposomal glutathione. Has to be liposomal. I also had luck with liposomal methyl B vitamins, I do have the genetic MTHFR mutation (A1298C and C677T) and I include high folate food and have that once or twice a week only. It's been really great for me.

WORKED TEMPORARILY

I'm really frustrated. I thought I had my CFS under control, but I obviously need something else, because what I'm doing just isn't working anymore. I'm so tired that on some days, I feel like I'm just going to die. My brain fog is so bad that some days I can't even concentrate long enough to watch a 30-minute t.v. show, much less work.

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.

I googled restful sleep so that I may be able to more properly deal with my chronic fatigue. The search came up with glycine and ZMA. I take the glycine and seems to work well mixed with a little Klonopin and Inderol/propranolol. I'm sure everyone is different so you may have to try and adjust it yourself. I started off taking only an 1/8 to 1/4 tsp glycine and 5 mg melatonin before bed without the other medicines and it seemed to also work well. If you wake during the night you can take another 1/8 tsp of glycine. I'm not a doctor so use your best judgement on this. Thanks.

Hi, I got ross river 20 yrs ago, fms, cfs, mcs real bad since. Charcoal can't hurt. Dont take it near food or meds. It should help clear out any unwanteds in your father's gut.

I eagerly tried d-ribose after reading "From Fatigued to Fantastic". The best price I could find was about $25 for a month's supply in powdered form. Because I am on disability and already spending $50 a month on supplements, I did not also get the co-Q10.

I used the d-ribose for two months. I took it without creatine but with L-Carnitine, and all the relatively affordable recommended vitamins.

It did nothing for my long term chronic fatigue syndrome, which is now significantly improved using Ted's recommendations for CFS Lugol's iodine protocol for 6 months following a healthy, wholesome diet devoid of processed foods, and putting the bulk of my focus into getting quality sleep. As a 20 year insomniac, sleep issues are the main thing the book really helped me to see the importance of getting a handle on in order to recover. (Doing whatever it takes to get a reasonable amount of sleep - melatonin, sleeping pills, ear plugs, eye mask, herbal teas, avoiding caffeine, herbal sleep remedies, exercise and sunlight when possible, etc.)

But, everyone is different and we have to keep trying different things so I'm not saying not to try D-Ribose. My chronic fatigue was very serious. I was completely bedridden for years. Perhaps in the future, when I'm actually trying to hold down normal responsibilities, I'll try d-ribose again to see if it gives me what I need to get through the day energy-wise.