Holistic Therapy: Lupus (Systemic Lupus Erythematosus)

Before I say anything about this Holistic treatment on Lupus I would like to thank Ted from Bangkok, Thiland for posting this Lupus treatment on the internet.

I am 20 years old and I have been diagnosed with Lupus when I was 18. I have been taking pills for 2 1/2 years now and I was devastated. I've been to four different Rheumotologists - The best ones here in New York city and all of them told me the same thing. They told me that I'm going to have Lupus for the rest of my life and that I am going to have to take medications for the rest of my life so my Lupus conditions won't get worse. That's a lie!!! This is a true story of my life experiences I want everyone with Lupus to read about. Wether your conditions are mild, moderate, or severe. The things that Ted from Thailand said has saved me from this disease. I really thank you Ted.

My father had severe Lupus ever since I was 7 years old. My father took all his medications and went to the doctor for blood tests once a month and his Lupus became worse. First it affected his legs and he couln't walk well and when he walked fast he ended up falling on the ground. When I was 11 years old my father was hospitalized because at home his head was extreamely red and he had blood in his brain at the time. He stayed in the hospital for two months. He became a little bit better and he was released from the hospital. He was still very sick and he was getting worse as months went by. But when I was 18 years old my father ended up in the hospital for good. My father was 54 years old back then. For two years my father went from hospital to nursing home constantly and for two years I did not see my father home as I used to before that. I prayed everyday and I told god I want my father and everyone else who is sick to get better one day and live a healthy and normal life at home with their family.

That did not happen for me. My father took all his medications, two pnemonia vaccines, several surgeries, he was also on morphienes and in two years after he was transferred from hospital to nursing home he passed away at the age of 56 on December 11, 2004.

I have been diagnosed with Lupus when my father was in the hospital. I was given Plaquenil 200mg. I took it 2 times a day with Bayer asprin 81mg one a day. I took the plaquenil and the asprin for a year and a half. I developed arthritis on my shoulder, fingers, arms and legs. Two doctors gave me plaquenil at the time. My arthritis was getting worse and worse. My doctor told me it was because of the lupus so I decided to go to another doctor he gave me prednisone and it made me sleep all the time I told my doctor and he told me keep taking it as your body adjusts to the medication. I went to the fourth doctor, he told me to take Methylprednisolone 4mg, Chloroquine phosphate 250mg, and the Bayer asprin once a day. In 6 months I felt very week, my memory was not good, and everyone who saw me knew I was sick because my face had changed and I looked sick. I was tired of all this. For two years I was looking for the cure of Lupus and I came across what Ted wrote here so I told myself I will give it a try. I am taking a little more than what Ted mentioned above. I am taking Calcium/Magnesium 500mg/250mg, Vitamin E 400IU, Vitamin C with bioflavonoids 1000mg, vitamin B complex 50mg, Niacin (in the form of nicotinic acid) 100mg, Zinc 30mg, L-carnitine 500mg, Alpha Lipoic acid 60mg, and N-Acetyl-L-cysteine 600mg. I take all of these once a day along with Echinacea 3ml daily, RNA/DNA supplement 100mg/10mg daily. I know that Ted mentioned Cellfood but it's very expensive and I cannot afford it, and I also take Kyolic aged garlic 600mg 3 times a day for my arthritis. The only vitamin I am not taking is vitamin A. I have taken these vitamins and suplements for a month now and was shocked to see my blood test results. I compared my blood test results from last month (I was taking the medications) and This month (when I am taking my vitamins and supplements) I saw a big improvement on the results. The first blood test was terrible that was when I was taking my medicine. And my blood test results now are perfect with everything being at the normal range and it's as if I do not have Lupus at all. With these supplements and vitamins I feel strong, energetic, and my memory is perfect because I remember things clearly now and as a college student my grades are up too, I am very Happy now that I got my Lupus cured but I will still be taking my vitamins and supplements.

Thank you Ted from Bangkok Thiland for putting this on the internet.

Borax treatment for Lupus: I am on day 5 of my 1/4 tsp borax & 1/2 tsp baking soda w/ acv treatment for my Lupus & it is Working!! I have severe skin problems, butterfly rash, redness on farhead, etc., it is really getting less noticeable each day.

Still have alittle brain fog & head pains, some joint pain but all lesser, I did camphor 10% alcohol rub (couldnt find powder), with eucilyptus, and it did help. Im wondering if after 2-3 wks all symptoms are gone if they come back again??

Want to contact Lupus patients in Pakistan especially if someone is following Ted's cures.

I have been using the vinegar and baking soda for lupus, also seasalt and borax. Since I have been using it I have had a cold and cough. I have had it for over a month now and feel better from the symtoms I had from Lupus, but the cold and cough won't go away am wondering if it is part of the detox. Also what is the maintenance once you have taken the vinegar and baking soda and borax.

Dear Ted, Re: SLE - Lupus remedies feedback (baking soda, borax, ACV and coriander)

I thank God for you and for leading me to earthclinic when I started researching on lupus to understand what lupus was all about. Numerous renowned medical websites and my rheumatologist claim lupus causes are not known, there's no cure and advocate prescribed drugs are the only way to put lupus under control, some with lifetime consumption. I was deceived by such websites and my rheumatologist initially until I found your contributions in earthclinic. I've got a rheumatologist who is always quick to add dosages in the name of preventing flare-ups, by simply basing on unreliable numbers from laboratory tests which are not lupus-specific, scares me. You have imparted valuable truths and knowledge for healthy living. Thank you very much for being very patient, very kind and very committed in finding lupus cure and with me. I suppose this is not your job and you are doing this outside your working time, I truly appreciate you and all that you have done.

I'm in my mid-30s, I've got SLE with no organs implications. I'm weaning off prednisolone which I've taken for 2½ years, the side effects were getting more unbearable and worrisome and the frequency of pains and inflammation were on the increase without your lupus remedies, dropped plaquenil recently which caused blindness intermittently and I've tried traditional chinese medication for 5 weeks which gave me many other side effects, your lupus remedies gave me strong confidence to wean off prednisolone. I know long-term consumption of prednisolone will shut down my immune system and from a patient's point of view and experience, I concur with you that I should not suppress my immune system. Insofar I strongly believe there's no way I can wean off prednisolone without your lupus remedies. Your lupus remedies deal with the causes and hence the pain reduction or elimination and in my opinion, they do it speedily relative to the other treatments I've tried. I hardly change my diet to know and monitor what works for me and against me.

When I first read about your borax treatment on earthclinic, I had much faith in it even before I tried it. The very mention of lupus nanoinsects feeding on heavy metals caused me to link it with the nose infection I had about 8 years ago and I thought it made so much sense. I developed this nose infection shortly after I joined a MNC selling valves when I had to come into contact with them. I had 1 dent on each side of my nose, they looked like my flesh has been eaten up. Before this nose infection was cured 7 years ago, the scalps were never dried up and were growing bigger by and by. I had a biopsy done 7 years ago and I just found out recently I had discoid lupus then.

Over the last 6 months, I've tried your lupus remedies separately to see and feel my body's response to each of them:

1) 1/8 teaspoon of borax in 1 litre of water on empty stomach - I drank 250 ml 4 times a day and eating fresh coriander on empty stomach everyday to chelate mercury which feeds the lupus nanoinsects

When I first started borax treatment, I took it 4 days consecutively. I didn't see any lupus nanoinsects (tiny black dots) surfacing from my skin and I didn't have diarrhea, I used a see-through glass container to collect my stools hoping to see these tiny black dots. My stools are usually light brown to medium brown but during these 4 days, my stools were totally covered by so much of these tiny black dots (I broke down the stools with water to make sure they were not black stools to begin with) and I also experienced constipation and had piles. I understood from you that the dead lupus nanoinsects also cause inflammation hence the constipation and the piles did not make me stop the borax treatment. No more piles for subsequent borax treatments. I had loss of appetite and I experienced drowsiness whenever I take this borax treatment and I welcome drowsiness because I could sleep only 2-4 hours a day for the last decade. For a few months, I was very aggressive on borax treatment because I knew I had 'sticky blood', evident by the big blood clots from my periods. I made the mistake of not unclotting my blood first to allow the borax treatment penetrate into all my cells. The lupus nanoinsects were kinda wrapped up inside the blood clots. I used asprin as per your advice to unclot my blood and I have much lesser 'black blood' during menstruation now, which I've learnt from you that it is an indication of lowered levels of bacterial infection. I'm less dependent of borax treatment now that I don't see tiny black dots from my stools.

2) ½ teaspoon of baking soda in ½ mug of water on empty stomach once in the morning and once before bedtime in the evening to provide unfavourable terrain for mycoplasmas growth

Recently, I had a very speedy recovery from flare-up using this. I had a huge flare-up (intense pains and inflammation everywhere in my body) caused by eating vegetables not cleared of chemicals previously sprayed on them and sugar intake. The chemicals and sugar seem to fuel mycoplasmas growth very fast, gauging from the speed and intensity of pains and inflammation spreading all over my body. Bearing in mind I've been taking prednisolone and plaquenil faithfully since 2½ years ago, they didn't help one bit in any way whenever flare-ups occur. Then I took baking soda treatment and borax treatment on empty stomach, on an alternate basis with 1 hour interval 3-4 times each and only had one meal for the day before I took medicine, the pains and inflammation reduced by 80% at the end of the same day. The next day and the day after, I simply take the baking soda treatment as per normal without taking borax treatment, no more pains and inflammation by the 3rd day. I didn't see any tiny black dots from my stools during these 3 days, figured baking soda treatment did the job. The existence of lupus nanoinsects or mycoplasmas give rise to the same kind of pains and inflammation.

3) 1 teaspoon of baking soda + 2 tablespoons of apple cider vinegar + 8 teaspoons of freshly squeezed lemon juice + 250 ml of water on empty stomach

Prior to asprin intake, this ACV treatment has made my blood less sticky, the blood clots became smaller. Together with baking soda treatment, the white coating (candida) on my tongue is getting less concentrated, I see more redness on my tongue. From https://www.earthclinic.com/remedies/acvinegar.html#why, I'm sure it also helps me in many areas which I'm not aware of.

I shout "YEA! YEA! YEA!" to the abovementioned lupus remedies.

God Bless You

Pharma drugs basically don't treat the cause, it has always been to treat for the symptoms. It has and always will be the most profitable venue for a pharma drugs, to get people to buy drugs like they were an addictive drugs until you go to the grave. What can be more profitable than that? It is even legal to say the least, which is hugely more profitable than selling heroine since you can sell them legally.

If you read many of my postings, it is the cause that I am trying to treat. Strange alien sounding medicine sounds more like toxic chemicals to me and I think finding the cause of the lupus and treat ourself for the cause is really the best ways toward a more healthy body.

The lupus issue I think that helps is to get regular bowel movements, alkalizing the body, vitamin D supplements, being the top of my lists in dealing with lupus but at least without the crutches and the extreme expenses of Pharma drugs.

I am glad to read that we are waking up. I was diagnosed with lupus along with several other ailments, which only devoloped during taking medication for an operation and having to wait on the waiting list for 8 months. I am in the process of trying to figure out my diet and allergies too. I am nearly back to normal. but i really believe the damage has been done already. So its no more medication for me. We are all guinea pigs. I believe a number of the drugs that I had been taken have since been taken of the market. We all need to think twice before taking medication.

Without getting confused in lupus remedies, I am going to make it simple and concentrate on major supplements that resulted in major improvements.

I have seen lupus to improve most significantly from only four things being the most important. These are the bare minimum:

1. Alkalizing pH. 1/2 teaspoon of baking soda taken twice a day in 1/2 glass of water on an empty stomach. Urinary pH MUST be at LEAST 7.0

2. Vitamin D3 2,000 i.u.- 20,000 i.u./day. Magnesium is synergistic with the vitamin D at about 250 mg of mangesium citrate. Vitamin D I found accidentally after I noticed lupus tend to worsen during winter with less sun, and when early summer arrive, the lupus was reduced. Excess sun exposure is still not recommended for lupus, but vitamin d seems to increase the immune systems.

3. 1/8 teaspoon of borax taken weekly diluted in 1 liter of water taken in divided dose throughout the day.

4. No acid forming supplements! Vitamin B6 (pyridoxal hydrochloride) and Nicotinic acid, were the biggest problems in creating a lupus, not because they are vitamin B, but because they are acid forming. One is a hydrochloride, the other is the nicotinic acid. If they are other that are alkaline forming, they are relatively toxic to both staph and strep.

5. Contaminated water supply. Yes fluoride, chlorine, but I also found free heavy metals contaminants to be the big cause also. Certain water had unknown chemicals and switching them to mineral water did major improvement were seen in the condition of lupus.

6. No sweets, too much meats, pizza, steaks, oily foods, white flour, and fried foods. They make the condition so much worse as they too are acid forming.

Those are the big six that resulted in major improvements. You can do the other things later. I have as yet to fine tune this, but lupus is still rare where I live. If I get any more information on lupus, I will update them as it comes along.

Before I forget to mention, Shara from Philadelphia..if you are still reading this post, I highly recommend you get tested for Pompe's Disease...otherwise, something you are taking is causing the rapid muscle breakdown and brown urine, which is called rhabdomyolysis, ..high fluoride in teas and other sources such as drugs can do the same thing.

Ted, you have some good information posted on this site and I will like to add to it...after developing an autoimmune disease myself, I researched extensively on the issue. In the end, I decided that the majority of all autoimmune appear to be linked to a retrovirus, gluten, mycobacteria, silica, or all of them together. Retroviruses can be kept in check with vitamin E and selenium, and killed with fresh coconut meat. The gluten issue is related to strep and staph. Strep bacteria are used in mice to induce autoimmune disease. You can do what is called a BlAST search on pubmed...for a protein/protein interaction, and you will find that the gluten protein resembles the protein coat of strep and staph bacteria...that can trigger disease....be aware that most yogurt has a harmless strep added..but this is not good for autoimmune sufferers...that is why dairy is an issue...along with the fact that strep and staph bacteria are present in milk and yogurt. These bacteria loves low body temperature...so in a hypothyroid situation, (such as that caused by fluoride or triclosan in your antibacterial soap) they run rampant. Be aware that the reason most autoimmune sufferes have B-vitamin deficiencies is when strep/staph are involved, that is because that is WHAT THEY EAT, in combination with chromium(strep and staph need B vitamins and chromium to survive)...So if you cook on stainless steel and take high doses of B-vitmains..you are feeding strep like crazy..try eating a banana and see if your symptoms worsen..haha .Next comes the silica...this is the one that you probably have never heard of...fluoride is added to water in the form of a fluorosilicate..the fluoride reduces white blood cells, but at the same time, the silicate reduces the ability of a person with autoimmune to fight off mycobacteria. Mycobacteria thrive on silica..and some foods are high in silicon...that is how they form the scar tissue...haven't you heard of the breast plant issue with silicon and autoimmune? Anything ground up (such as seasonings), many medicines in capsules, etc..and even table salt, which also has silica added to it to make things "pour" will be a problem with autoimmune sufferers..and you will form scar tissue. The mycobacteria uses the silica in this way in a destructive manner, especially in the presence of fluoride...to make scar tissue. Studies show that TB patients cannot fight off tuberculosis (which is also caused by a mycobacterial infection) if silica is being consumed. You can research this if you want to. I have read that mycobacteria are vulnerable to citrate, tetracycline, monocycline (which, unlike tetracycline, penetrates tissues),and copper. So what does all of this add up to??? I wanted to see if I can make my symptoms completely disappear WITHOUT ANY SUPPLEMENTS...yes you heard me right. It happened...but the problem is, it is a very restrictive (but simple) diet: Elimate all sources that feed mycobacteria, retroviruses, and strep/staph. This boils down no fluoride, silica, and gluten, and foods with B-vitamins added. No fluoride is hard...spring water low in fluoride, do not cook on non-stick cookware in any form, and avoiding high fluoride foods such as chicken, soy, and canned meats. Reduce silica means avoiding seasonings that pour or that you sprinkle on food, and high silicon foods...(i.e.use fresh herbs only for seasoning). Low/No HCL in the stomach is generally caused by fluoride toxicity...you end up with HF instead of HCL inthe stomach, which sets up hypothyroidism, and that will now allow strep/staph, and retroviruses to thrive...also the problem with red meat is this..the stomach is lined with a sodium layer..when you ingest red meat, it pulls the sodium from the lining stomach, and creates a inflammatory condition...because of lack of sodium...mycobacteria thrives on sodium, making the problem worse...but you need sodium to digest your food. And finally, the gluten issue: by avoiding gluten, your body does not launch an autoimmune response to type IV collagen...gluten once again, looks like the protein coat that covers strep and staph..but also that makes up type IV collagen, which is present throughout your body, including your kidneys...and this collagen gets attacked. This is a very general and short version of what i could say, but I hope many find this information useful. Feel free to email for more info. and clarification.

I was diagnosed with Systemic Lupus and Rheumatoid Arthritis 14 years ago. My grandmother told me about ACV and the many ways it could help arthritis, sleeping problems and stomach problems. I take 1 tbsp. once daily with just water and all of my physicals for the SLE & RA have come back great. I have no deformity in my joints and have not had a flare up in over 7 years. I also had several bleeding ulcers & was having to take daily stool samples to my doctor, but my physical showed scarring but no ulcers. I also use ACV as a toner for my face and my pores are smaller and my age spots are nearly invisible. I have printed out several pages of literature on ACV and have over 20 friends on this daily regimen and all of them can tell the difference and have been taken off their medications for their illnesses from arthritis to high blood pressure & cholesterol. I am a 48 year old grandmother that works with a younger market and I work circles around all of them. ACV helped me with my SLE, RA, Ulcers, Chronic Fatigue, Crohn's Disease and IBS.

WARNING!

Concerning taking Vitamin D, one must be careful when taking it. It is important that it is balanced with Vitamin F. Some doctors will diagnose people with lupus when they actually have sarcoidosis, and diagnose them with sarcoidosis when they actually have lupus. The 2 are not the same, although they are both thought to have a type of mycobaterium involved, but not the same mycobacterium. Vitamin D would be very helpful for lupus but detrimental for sarc. The difference appears to be due to whether or not the mycobacteria has infected your macrophages. If this is the case, your active vitamin D levels will actually be high, even in the presence of low stored vitamin D. A good rule of thumb may be to have both the stored and active levels measured. If taken vitamin D causes you dizziness, this can also be a clue that you active levels may already be high. In this case, it needs to be balanced with Vitamin F.

re: Corn and Pellegra Email Posted by Rhonda -- Traveller's Tales Italy (edited by Anne Calcagno) has a very moving and detailed account by an American botanist of how the importation of maize (corn) from Mexico to Italy after the discovery of the new world led to pellagra among the Italian peasantry. Unlike the southwest Indians who ground the corn and processed it with ash (calcium bicarbonate "lime" and other mineral salts to release the nutrients, in Italy the corn was simply ground in a standard way to make corn flour. It was then used for polenta, which became a staple of the peasant diet and led to pellagra . This is a stunning piece of social history that will be of interest to many people. "Sagra di Polenta" is the name of the chapter. The author is Gary Paul Nabhan.

I was just browsing through some of the information posted and wanted to add my "5 cents".

I should mention, if you do use blackstrap molasses to "blacken your hair," be careful that you do not develop a vitamin B3 deficiency, WHICH IS known as pellagra, which apparently is important for the diet for those with Lupus.

For the man who treated Lupus on a gluten free diet...take heed, that this goes right back to a probable involvement of strep as this is the main bacteria that feeds on B-vitamins, as it is essential for them to live. This is especially true if you eat corn poducts because corn alone can induce pellagra if the corn has not been fortified(i.e.canned corn or corn on the cob, corn chips, or unfortunately for all its good intentions..organic corn producers that do not fortify their processed foods. If you have Lupus and you're going luten free and eating unfortified corn, you're inching closer to pellagra.This one instance where eating a wholesome food (corn) will give you disease (pellagra) if eaten in large quantities and it is not fortified.

... Also, for Lupus people, they tend to be sensitive to electromagnetic frequencies. I have personally found that simply not putting a cell phone or a cordless telephone up to my head greatly improved my autoimmune symptoms than just with diet alone. It turns out, that electromagnetic frequencies also block melatonin synthesis.

Finally, if you have lupus and Raynaud's and live somewhere where it is cold, Raynaud's is closely linked to low thyroid function on exposure to cold weather. Raynaud's has been cured by treating the thyroid. City tapwater has caused most of the lupus symptoms for me...its the pipes and the water that flows through them.

I was diagnosed w/SLE at 12. I'm 43 now and 20+ years on hemodialysis. No kidney function,transplant didn't work,EVER. Chems A+. Still have some sort of autoimmune disease. unknown. Going gluten free,etc. I think diet, environment, bad DNA caused my lupus. They plugged me full of prednisone, which caused ESRD--dialysis. Now I'm stuck because my kidneys don't exist, and I'm trying to fight off another autoimmune. Ted, you're a genius. I hate American Medicine and their 'pimps'. ADVICE: Get lupus before it gets your organs--dialysis, transplant,death.