Ted's Remedies for Lupus

5 star (5) 
  83%
4 star (1) 
  17%

Dessert (USA) on 12/17/2007:
5 out of 5 stars

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

REPLY   7      

Florence (Olathe, CO) on 11/27/2007:
4 out of 5 stars

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.
REPLY   2      

Michael (Lakewood, NJ) on 06/30/2007:
5 out of 5 stars

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??

REPLY   3      



Mayla (Adelanto, CA) on 04/11/2006:
5 out of 5 stars

Ted's remedies cured my swelling of the joints and all the pain that I had due to the fact that I have Lupus and I am no longer taking any of my medications for it, I'm just on 17 different vitamins daily and I have changed my diet no read meat just lots of greens and fish,chicken not fried.
REPLY   5      

Shara (PHILADELPHIA, PA) on 01/10/2006:
5 out of 5 stars

Thank you so much!! I have been ill for my entire life but I was hospitalized when I was 13 yrs old. The Dr's had nothing useful to me other than a sugar and Saline drip and a lot of bed rest. They said that what I had looked like lupus but they could not peg it. Finally a few years ago I learned that Lupus ran in my family thus I believe that I may have a bastardized version of Lupus. My mother put me on a vitamin theorapy treatment of vitamins e,c,Lecithin, Bcomplex, multi, omega 3, Calcium, and many other things here and there. Just recently I have added Lipoic acid. I can honestly say that my lupus has not progressed as the Dr's were afraid of with out their treatment. They said that I would be in a wheelchair by the time I was 19 yrs old and now I am 29 and just having less episodes than when I was 13. I do still have episodes that consist of Extreme muscle break down, memory loss, Brown urine and extreme muscle cramping. Skin rashes are also a symptom along with facial sores that my have bonded with a herpes simplex virus. This mixture of herpes and lupus rash is a constant battle but I contain it by taking L-Lysine, Larrea Root, and Red Marine Algea. But still I am very vulnerable to virus attacks b/c of my immune system and when I contract a virus it sends me into an episode that can take me down for a week to a month depending on the virus. Anyway just wanted let you know that your information is very useful to me and I plan to use it daily
REPLY   5      

Aristo (New York, NY) on 10/05/2005:
5 out of 5 stars

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.

REPLY   8      
Return to Lupus