It was porphyria. In a new ebook, this acclaimed author of 18 health books and former physics professor reveals exactly how Bruce Lee died from a porphyria combination effect of hash and the medicinal drugs he took. New ebook states that he was very ill with porphyria his last month with weight loss, anxiety/panic, sleep apnea, seizure, and other symptoms. All other hypotheses of “hypersensitivity to aspirin or other drug”, or heat stroke or epilepsy all tie in with porphyria causation as explained for the first time today. See www.wellatlast.com for more info on this breaking ne ...
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If people don’t know, his work shows that porphyria is a common, NOT rare disorder and is often the main cause or contributing factor of many problems including: food sensitivities chemical sensitivities anxiety fatigue and fibromyalgia asthma epilepsy weight gain blood sugar problems chronic pain adrenal fatigue autism and other   [End]
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To learn how to overcome or improve porphyria and related problems see Dr Rochlitz’ new interviews: https://www.youtube.com/channel/UCi8OMtlfXPbOf9aZFht_vvQ There are 3 and a fourth one will be up soon. This is my fave: overcoming neurological problems including chronic pain: https://www.youtube.com/watch?v=9P5r6rp2LXg   [End]
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About a year ago I searched online intensively to try to figure out what the “cotton balls with legs” are (I’ve also passed many of them) and nobody really knows. I also have a documented, chronic, worm infection, so the two things could be related.   [End]
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I hope you’re still here I know it’s been years since this post was made. I have the same exact thing. I have no clue what it is. But hundreds and hundreds have come out. I need help figuring out what it is. Thanks Jamie   [End]
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The acclaimed holistic health author and educator and former physicist, Dr Steven Rochlitz has just published a new theory on a cause of Type II Diabetes. It contains his hypothesis that the hiatal hernia [HH] and/or vagus nerve imbalance [VNI] affect the pancreas and thus blood sugar levels. He reports that upon correcting--with simple body methods--the HH and/or VNI, he’s seen rapid normalization of both low and high blood sugar readings, and low body temperature as well. This is not a “permanent” correction, as there are many things to do regarding the HH and VNI. The metabolic di ...
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The “cotton balls with legs” are most certainly NOT “bananas”. I have passed the same exact things and I have not eaten bananas for years. It is for sure some sort of parasite.   [End]
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This interpretation guide from Metametrix will explain more about how various toxins, especially heavy metals cause abnormal balance of porphyrins in urine. https://www.gdx.net/core/interpretive-guides/Porphyrins-IG.pdf A. Cutler, PhD Chemistry talks more about urine porphyrins as a test for heavy metals in this interview with Mark Schauss. http://www.letstalkrealhealth.com/dr-andrew-cutler-phd-mercury-detoxification/   [End]
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JFK is said to have had Addison’s Disease, but Dr Steven Rochlitz book on Porphyria reveals that JFK was diagnosed by his White House physician, Dr Janet Travel as having episodic adrenal failure for unknown reason and that he did not have Addison’s. Dr Rochlitz new 3rd edition of his book, Porphyria: The Ultimate Cause... examines JFK’s entire medical history of episodic adrenal [partial] failure as well as his life-long chronic pain, GI, immune, allergy, asthma, neurological, muscular, bladder and other complaints and asserted that JFK had porphyria his whole life. Porphyria is a ...
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On January 6, 2017, Dr. Steven Rochlitz — former Physics Professor and leading holistic health consultant and author, announced the publishing of the 3rd edition of the magnum opus of his 11 health books, Porphyria: The Ultimate Cause of Common, Chronic and Environmental Illnesses, with Breakthroughs in Diet, Supplements and Energy Balancing. In it, he has made the historic proclamation that US President John F. Kennedy had porphyria, and stated all the reasons why after studying his medical records and history of lifelong pain and many chronic symptoms—the cause of which was never f ...
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My BIG apology to you White Shark! I thought you were stupid to think that the legs and cotton balls are fibers of banana, but after repeated experiment myself, I have to admit that they indeed are caused by banana. I was wrong and stupid, and you are right indeed, so I am really sorry. Kindly accept my apology. You don’t see them if you don’t eat banana, or eat no more than 1 a day. But as long as you eat up to 3 a day, you’ll no doubt see them. They totally like worms, so I was led to believe that I was infested with worms. But as long as I keep away from banana, they are gone no matte ...
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My BIG apology to you White Shark! I thought you were stupid to think that the legs and cotton balls are fibers of banana, but after repeated experiment myself, I have to admit that they indeed are caused by banana. I was wrong and stupid, and you are right indeed, so I am really sorry. Kindly accept my apology. You don’t see them if you don’t eat banana, or eat no more than 1 a day. But as long as you eat up to 3 a day, you’ll no doubt see them. They totally like worms, so I was led to believe that I was infested with worms. But as long as I keep away from banana, they are gone no ...
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On Lyme’s, Babesia, Artemisia, and the key—Porphyria Leading health educator and author, Dr. Steven Rochlitz has recently released two crucial enewsletters to his readers that should be read by all. So I am passing some of this on here. A former physics professor, Dr. Rochlitz uncovers what’s really going on often with chronic illnesses. He’s helped many with “chronic Lyme’s Disease” to finally get well. He says that many with Lyme’s are told that they have “Babesia coinfection” and “need” to take Artemisia/wormwood herb or compounds derived from it. Dr. Rochlitz says this i ...
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Historic Proclamation on the Causes of Allergy and Other Chronic Health Problems Porphyria & Mast Cell Disease are also the ultimate causes of why so many people react to many foods & environmental chemical and EMFs. Please be advised that Steven Rochlitz—the former physics professor and holistic health educator and author—on Nov. 3, 2015—made an historic porphyria and MCD proclamation to readers of his first porphyria [and MCD] book, PORPHYRIA: The Ultimate Cause of Common, Chronic and Environmental Illnesses. With Breakthoughs in Diet, Supplements and Energy Balancing. The proclam ...
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Historic Proclamation on the Causes of Allergy and Other Chronic Health Problems Porphyria & Mast Cell Disease are also the ultimate causes of why so many people react to many foods & environmental chemical and EMFs. Please be advised that Steven Rochlitz—the former physics professor and holistic health educator and author—on Nov. 3, 2015—made an historic porphyria and MCD proclamation to readers of his first porphyria [and MCD] book, PORPHYRIA: The Ultimate Cause of Common, Chronic and Environmental Illnesses. With Breakthoughs in Diet, Supplements and Energy Balancing. The proclam ...
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Most stupid thing I heard today!!! :P   [End]
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After being chronically ill for many years, with pain, anxiety, blood sugar-type problems, high blood pressure, a racing heart at times, and skin blistering from the sun, I came across an awesome, free, radio interview of an American author of the most amazing book, discussing crucial health information on porphyria and related topics, at this link: http://foodforthought.naturalhealthradio.co.uk/media/2015-04-07_professor_steve_rochlitz_.mp3 The British nutritionist said she was “in awe” of all the new info. If it does not display, you can find it on the author’s testimonials pag ...
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can you write a few words about what the basic dietary philosophy is here that really helped you out? Thanks   [End]
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Thanks Garfield. I had a similar experience after following the book’s recommendations! And when people follow the diet changes and self-energy balancing, there is nothing else to buy. No gizmos or such... You are right: a glimpse at the testimonials page shows how far ahead of the field Dr. Rochlitz’sbooks are. It says at wellatlast dot com: Allegra DiMuzio [USA]:”I received your fabulous book... I must say, that in all my life, I have never read anything like this!! Speechless..... Will be reading it over many times. It is brilliant! Randall Langston M.D. (Env. Med Spe ...
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I agree with #185190, the breakthrough information in this book was my life saver, after suffering for 30 years with fatigue, allergies, MCS etc. and not being able to find out from doctors or alternative practitioners what my problem/s were, let alone what the cause was. Doctors would give me medication, which I was invariably allergic to and felt as if I was being poisoned by it, and on several occasions I was told I was an hypochondriac or I had an imaginary disease, so I decided to stop going to doctors and get on with things in my own way. I managed to get through and survive ...
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Treatments fail for Lyme sufferers often due to hidden factors. The main one being porphyria. Any overgrowth (Lyme bacteria, Candida, Protozoan parasites, etc.--or the overuse of drugs, herbs etc., according to Dr Rochlitz will in some 20% of us result in chronic porphyria. See wellatlast dot com The person then becomes more chronically ill and more ”allergic” to foods, supplements, drugs, env. chemicals, stress, sun, etc. Supplements are often problematic because they induce Cytochrome P450 enzymes [heme proteins] which wlll then trigger porphyria in many people [whether or not t ...
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I am so pleased to have heard about your Porphyria Group. It’s going to be of great benefit to myself and my whole family.   [End]
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One idea: we could search what is the green substance they realise after getting out of you... It could be a indicative of that is that.. Other thing: they sure look like plants aka very similar to fungus. Fungus are intolerant to salt as well, but most patogens are, so that is not so relevant... But i found very curious that all that have those cotton balls have candida symptoms. Guys, someone else to help me? Ten, are you there? Let’s get to the bottom of this!   [End]
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Lyme as PARASITE ‘Wild’? Dr F R Klenner cured lyme disease and trichinoses. The worms I researched today are new to me. I can only suggest doing both cures at the same. Research ’dr klenner lyme’ I have never been injected with antibiotics, with all the problems caused by them, I never will. Vitamins are more and no side effects   [End]
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I saw all those links in your previous posts. I can see a lof of sense in your theory. Thanks for reply. I have pictures here. I had then in the water one time too and other thing, if you leave them in the presence of air and check them in the next morning they turn green and make the things like the water around them green, it is very weird... But i am keep thinking if it isnt a coinfection of lyme or another thing. I almost have certain that i still have those things in me but i dont know why i have no symptoms. I didnt have symptoms like blurred vision or floaters in vision or headaches ...
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Guys, theres a reason it isnt known what they are...because its Lyme and nobody wants us to know. I have studied enough about Lyme, so White Shark go eat some bananas and leave your opinion out of this. Okay guys, and white shark. http://www.youtube.com/watch?v=oO1SOAn373A&NR=1 Now, here is MICROSCOPIC lyme colony, look familiar?? http://youtu.be/yfPg_kcFyZA Lyme is the biggest conspiracy out there, everyone in power and the medical community want to stay in control... I have seen these things first hand, I got em saved in a jar. I check em under the microscope, t ... [Image Embedded Here]
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Quit posting your BS stuff about bananas. I hope you turn into one.   [End]
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Yeah, thanks! I saw this page. Unfortunnatly, it is so little information.. Thanks a lot for reply   [End]
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I found a webpage that has pics of them. Apparently they are nematodes of some type in some stage between egg and adult. It is not lyme bacteria. Look here: http://www.altcancer.com/oldam3.htm   [End]
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Another thing, we have to be open minded. Doctors say candidiasis doesnt exist and they are wrong. So, how can i be sure that they are right about lyme? How can i be sure that lyme couldnt grow or isnt a parasite? There is no way to be sure because we not have data of this, we not have research of this and if it is a bacteria and they know it for sure, how come they dont cure people or antibiotics dont work? For me, the right thing is question about everything and consider every possibility. Of course not every possibility, because i think it is the 50 post i saw you saying that is banana ...
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thanks!   [End]
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MAN, i told you IT IS NOT BANANAS. Sorry, but here you go again with this, always. I spent a long time without touch a banana and they come out. So, you theory is non sense. sorry to answer that way, but it not bananas. If it is maybe i have a banana tree in me because i was not eating bananas.   [End]
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There’s no way those are banana fibers. Sure, they look similar, but there aren’t even that many dark fibers in a banana in the first place. And clearly whatever this is always forms somewhat of a distinct pattern when wrapping itself around the gel like substance. To me, it just even naturally looks like some type of organism...not a piece of fruit.   [End]
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No parasite looks like that. Lime is caused by microscopic bacteria ... not by a ”cotton ball”. ”Cotton balls” with ”legs” are pieces of banana, poorly chewed, undigested. Try eating only banans one whole day. Check your stool the day after. You will find many ”Cotton balls” with legs. Those ”legs” are natural banana fibers, colored by bile and digestive juices. Our digestive juices color everything brown. Check banana and you will see identical fibers inside banana. Banana is soft, so people can swallow large pieces without chewing it very well. That is why you can ...
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Sorry, but that was not my question. I currently feel good. I just wanna know what those creatures are. Thanks for reply   [End]
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Get a parasite cleanse. Continue antifungals like coconut oil fasting , olive leaf extract and oregano oil and eat green veggies and some brown rice, some chicken.   [End]
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http://curezone.com/forums/fm.asp?i=2117616#i another one with those.   [End]
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there some months that fell ”cured”. I have been trying to help friends online everyday, talking by usings apps of chat, facebook.. To the day i started all this journey and finally felt ”normal”, I STILL can’t find out any information of what those are (cotton balls with legs). I had all the symptoms of candida, i expelled over 10000 of this. I emailed everyone, some persons online, one or 3 doctors that i found that know about all this nightmare (candida, lyme, ...), friends on curezone, lyme disease guys, ... BUT i cant find nothing about this. None one answer, all i know i had yeast in ...
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Honest to God, I think it would be easier being abducted by aliens, than finding a compentant doctor or naturopath who is well practiced with this disorder. I think I have this and need to be tested for it. I live in So. Cal. But I also have a lot of other health conditions that go along with it, and ones that many MD’s don’t want to deal with, so I would prefer finding an MTHFR naturopath is possible. I’m willing to treat with one out of state, if they are willing to treat long distance. I have gone to MTHFR.net and MTHFRsupport.com, but there really aren’t that many to choose from. ...
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Ophthalmologists treat patients with optic neuritis. Have you tried consulting them? They’d be able to guide you better in this regard. For mild or moderate pain, analgesics that can be purchased over the counter, such as Tylenol and Motrin, are recommended. For more severe pain, prescription pain medication, such as Demerol, Darvon and Percocet are used. For serious stabbing and jerking pains that some neuritis sufferers experience, anticonvulsants, which prevent and reduce convulsions, are prescribed. Some of the same drugs used to treat epilepsy, such as Diazepam and Neurontin, can be u ...
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I don’t believe it is possible for your ozone therapy to be bad for you because you are a biological creature who thrives from the oxygen that you receive. But it is bad for the parasites who do not want to give up their happy home. It appears to me that you may be trying to take too much too soon. Ozone therapy like H2O2 therapy must be gradually applied in order to give the body a chance to adjust and fully use the oxygen you are giving it. I suggest that you decrease both your frequency and your dose and gradually work your way up. OxygenLynne   [End]
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I used ozone for my morgellons (lymes?), and I had heavy duty herx. I decided the die off could kill me, but it didn’t. You might try shorter sessions. Soaking in an epsom salt bath helps draw out the toxins. It always gets worse before it get better.   [End]
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Hello I have had two recent experiences with Ozone therapy and both times I feel horrible for weeks. My lymph becomes blocked; my ankles and just above the knee swell. I feel like I’ve been kicked in the ribs on my back. I have huge sweats while sleeping. I worry that perhaps the ozone kills lyme or some other anaerobic bug but then babeia or something aerobic takes over in full force. I also have cpn (chlamydia pneumonia and lots of other bugs like cytomeglo, hhv6) and finally my porphyrin count is high. So, is ozone bad for me or is this just a horrible herx because I feel worse th ...
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Hi, Does anyone know how to relieve the pain of optic neuritis, especially when exposed to the glare/glint of sunlight? Or if there is any way to mitigate this symptom of optic neuritis? Are there special sunglasses that could help? I am writing on behalf of my friend who has MCS, EHS, chemical-induced MS, glaucoma, occasional migraine blindness, porphyria and optic neuritis. She cannot tolerate the EMFs coming from computers which is why I am writing on her behalf. Any guidance would be most appreciated.   [End]
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Yeah, I did the kryptopyrrole test as above and to my surprise it was negative. Apprarently it can often be negative due to many reasons. But the urinary porphyrin test (I may have spelled that incorrectly) is slightly different, and there are a few different types of porphyrin disease, some so severe that death happens shortly after birth. So, I’m not totally clear on the differences but the ’gold standard’ tests besides the barely available genetic tests now being preformed in a Mt. Sinai New york hospital on a trial, is done at Phillip Auguste Laboratoire in France. www.labbio.net ...
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Over 80 percent of our Lyme patients have developed HPU (hemo-pyrrol-lactam-uria). The term falsely used in most US literature is KPU (krypto-pyrrol-uria) HPU disarms the immune system by catastrophic depletion of zinc, manganese, arachidonic acid, histamin, taurine. These losses are hard to detect with any current technology (only bone and CNS biopsies are reliable. Labs to consider: KPU urine test (Vitamin Diagnostics) alkaline phosphatase low normal copper: zinc ration greater than 1 in hair and urine low Omega 6 in red cell membrane fatty acid test white blood cell zinc, red ...
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From what I posted down a way’s today, from Klinghardt on Lyme: Many Lyme patients suffer from Pyrroluria, a metabolic illness where abnormal porphyrins carry out significant amounts of needed zinc and vitamin B6. Diagnosis is made with the appropriate test at Vitamin Diagnostics in New Jersey. Even though it is assumed that this illness is hereditary I have my doubts, since most Lyme sufferers have a degree of it. I suspect that the appearance of kryptopyrroles in the urine is induced by the illness. However, I am careful with excessive substitution of zinc. Zinc has a synergistic ef ...
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Yes, I did a kryptopyrrole test,which had come back negative.. but today the guy talking about porphyrin test said it’s actually quite different..so did my doc. I think they are sort of in the same family at least though. And the test at Phillip Auguste Laboratoire, is kind of the gold standard for this test and sure enough one of the markers....for precoproporphyrin, is a marker specifically for heavy metal toxicity too, or Hg as you mentioned. Here’s a short link to read if interested.. http://www.ncbi.nlm.nih.gov/pubmed/16782144   [End]
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I know I already answered this way back when before you even bought the F165. The reason I know this is that about the time I made notes in the EPFX about Porphyrins. Anyhow just like then, and I am pretty sure I said Hg toxicity then too, I also remember Niacinamide and TMG.. more from Andy: http://onibasu.com/cgi-bin/search.cgi?query=andrewhallcutler++Porphyria+&submit=Search%21&max=20&sort=score&idxname=am&idxname=fdc&idxname=amc&idxname=dc   [End]
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never heard of it. but in my mind, most of the issues you are talking about sound like symptoms of other underlying disorders. so if rifing helps get to the bottom of it, its worth any temporary discomfort. just don’t overdo it. John   [End]
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I was told today by a very nice and informative ’expert’ on porphyrin disorder, that due to other genes I carry such as hemochromotosis, gluten intolerance, fructose intolerance etc, and my sx, that I ’probably’ have porphyrin disorder. He also said that rifing is not good for ppl who are porphyrics due to the electrical imbalance causing flare ups etc and/or electrostatic muscles ie/charged up muscles, I am not quoting exactly but it was along those lines. Do you have input on this topic at all? Everywhere I turn, one says black the other says white.. I am about to set up to rife the ...
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I’ve had similar skin problems. Tried all external ointments and oils and nothing helped. Took out sugar including fruits, starches etc. cleared everything within week. Had the skin problems for over 1.5 years. I am eating now close to raw and love it. My skin looks great.   [End]
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Hi... Here is a questionaire that may help you diagnose whether you have candida troubles. (Everyone has candida.) http://www.thecandidayeastanswer.com/page/page/4577805.htm You can also down-load free e_book.   [End]
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Ya know... it should be your decision to stop your antifungals. Some of them have pretty nasty side effects. It’s possible that you’ve got something systemic going on internally too. If that’s the case, if you plan to discontinue the antifungal rx’s, you need to replace it with something that you can take internally. Neem soap and the neem oils are non-toxic, but are for external uses only. The neem capsules are good for internal uses. I keep neem and reshi on hand for colds. Whenever we have a cold that just won’t go away, we hit it hard with the neem and reshi (4 caps each every 4 ...
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thank u lolite for your response. yes i can get that stuff at a local whole food store in my area. so should i stop taking the rx medicine (even though its working) and start taking that neem oil? i just bought some oregonoyl oil for internal (drops).   [End]
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I knew I had some form or porphyria. My face is sinking in all over. I have everything from a 2 inch long ditch looking thing over my eyebrow, to chicken pox scar looking indentations all over my face, of different sizes, with new one appearing every dya. I have been seen by countless dermos, had biopsies and such no one has been able to diagnose it. Long story short, I have other autoimmune health problems. I used to post regularly on the candida forum. A regular poster there by the name of Raider told me about a forum she started on curezone called Healers Who Share and how muc ...
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Do you have a healthfood store or an Indian market near you? Get some neem soap and neem oil and bathe in the neem soap. Put a few drops of the neem oil with the soap or in a body wash and bathe with that, alternatively. Warning: the neem oil smells absolutely foul. But the neem is really good stuff. If your healthfood store sells neem capsules, then take that internally, 2-3 caps 2-3 times a day. Neem is has anti-fungal, anti-bacterial and anti-viral properties. It doesn’t have the harmful side effects that the rx antifungals have.   [End]
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I have had jock itch then I broke out in these rashes around my armpits and under my breast and around my groin-thigh area.. some on my stomach and sides as well. Ive been going to a school doc (im in college its cheaper) and they prescribed to me Ketoconazole pills and Nystatin cream. I had an allergic reaction to the keto (shivers--- skin felt very sensitive... itchy even more etc.) So i stopped taking that kept taking the nystatin and still am takin it. Went back to see doc .. got perscribed Griseofluvin. I apply nystatin and goldbond twice daily on all effected areas and today is my th ...
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I had my first porphyria (acute intermittent) attack when I was 27, which was fifteen years ago. My first attack manifest itself as weeks of losing weight, constipation and flu-like aches and pains. This the worsened until until I couldn’t walk properly and my urine went a dark red colour. I went to the hospital and because I previously had gynae problems it was assumed that it was something to do with gynae. They were going to do an exploratory operation but then my blood pressure went sky-high and so they cancelled my op and gave me medication to to lower my blood pressure. However, the ...
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I had my one and only attack about 2 years ago. It manifested itself as severe nerve pain as if someone was peeling the flesh off my bones. The first hospital gave me pain meds that actually made it worse....they thought it was just in my head. Finally the second one figured it out. I was in the hospital for 6 weeks and lost 35 pounds. Essentially I was left with a lot of nerve damage i.e. drop foot in both feet, loss of fine motor skills in my hands, loss of saliva, inability to cool myself off as I lost the ability to sweat. Some of my saliva, sweat have come back and my feet move ...
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Well I checked this Porphyria forum, started 28 months ago, but no posts in it. It looks like I’ll have to give it a jump start. They figure if it wasn’t for PCT, there would be no vampire legend, and you would all be drinking tea . lol Symptoms: Clear blisters on face and hands exposed to sunlight, easily bruised skin, slow healing skin trauma, pissing heavy, colored, at times purple. Here is a link to the American Porphyria foundation to get started. http://www.porphyriafoundation.com/about_por/types/types03.html   [End]
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Ok, fellow heppers, now how many have porphyria related to your HCV? I could find no talk of it in the forums, but it is common among HepC sufferers. Quote ”PCT is one of the hepatic porphyrias. Large amounts of porphyrins build up in the liver when the disease is becoming active. The disease becomes active when acquired factors, such as iron, alcohol, hepatitis C virus (HCV)” And HCV can’t be treated until the PCT is taken care of first. ”Peginterferon success rate of treating HCV is at 4.5% for people with PCT and HCV” Well I checked the Porphyria forum, started 28 months ago, ...
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