I presume that you did not have this done recently because whole genome sequencing now costs $499/€399/£352. https://www.dantelabs.com/   [End]
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A client of mine is 43 and has suffered horribly from lupus since she was 29 years old. I turned her onto bio-magnets and she has been doing meridian therapy for almost a week; following everything by the book… Last weekend, she became so ill she had to go to the emergency room, because her digestive system hardly works at all, and she suffers from severe constipation; just one of the many things that plague her because of the lupus. Within a few days of magnet therapies, her transformation has been to say the least awe-inspiring. She couldn’t even drink water before wearing the magnets ...
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Read https://www.curezone.org/forums/fm.asp?i=2400410#i https://www.curezone.org/forums/s2.asp?f=326&c=14&ob=v https://www.curezone.org/forums/fm.asp?i=2403730#i https://www.curezone.org/forums/fm.asp?i=2405398#i https://www.curezone.org/forums/fm.asp?i=2402296#i WS   [End]
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first of all,sorry for my english. i’m writing post here because i know what is suffer from body odor and i know what is listen bad comment from people.i’m 19 year old boy.Boy who is very famous, at school at university. i lived normally,before it started. i was 13 year when my BO started. it was first day at school after summer. and at classroom, classmates talking about bad odor. my friend ask me if i take bath,before school. OMG of course i had bath before i came at school.it was really bad urine odor. is smell urine and sometimes when i really don’t farted i smelled ! my life changed a ...
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These test are not complete genomics tests, they are just general test limited to about 1500 genome screening if that. If you what a clear DNA testing you need a 22,000 genome test. This deeply hits all 23 chromosomes and what lies between those chromosomes as well. My sons 22,000 DNA test revealed a deletion at his 22q13.3 at the long end of his 22 second chromosome. But general DNA test revealed nothing. Maybe it could generally give you some basic race traits but not anything health wise. A 22,000 genome test runs about $25,000 and also should include you mother and Father ...
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So we have come to see that James has fewer symptoms than other but one that we are most concerned of is his bodies inability to sweat normally as normal healthy people do. Simply holding hands and walking in a circle singing with classmates allows his body to heat up. A few times he has had small events that resulted only in him emptying his bladder and then going into a deep sleep for 15 minutes or so. We let his teachers know of this so they can encourage him to drink more water and have time to cool down. The last time he has a seizure was three weeks ago. It was very similar t ...
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My youngest child James was diagnosed with Phelan-McDermid Syndrome after five years of being bounced around from doctors to clinics, and then being told we would never find an answer. We took matters into our own hands and transferred to UVA Pediatric Neurology and Genetics, and after a 22,000 genome test they were able to identify our sons condition. We are hoping to develop a network here on Curezone and share with each others our story and how we were able to grow with our son and teach him. Below is the summery of PMS and answers some basic questions from the PMS Foundation at ...
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Resources for interpreting Promethease? I have watched the videos, read the links, but I still do not understand what I am looking at. Is there another service with more basic help/terminology for total newbies? Or any other resources? Thank you!   [End]
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if it doesn’t help you, try o p c (grapeseed) or fisetin. just don’t take reserpine.   [End]
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I’m desperate for some guidance with understanding my results from the 23andMe genetic test. Some of my SNP results are: rs1801133, versions are A or G, I am: AG -if I understand this correctly, I am heterozygous for this mutation rs1801131, versions are G or T, I am: TT -if I understand correctly, I am negative for caring a mutation with this gene rs2274976, versions are C or T, I am: CC -I don’t know what this means And I don’t know what else to really look for. I did the promethease.com report, but am struggling to understand that too. I’m overwhe ...
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Hi there, I just got my results from a saliva methylationtest back. It says i have one gene mutation called C677 that causes me not being able to methylate zinc or folate. Unfortunatly i have no idea what to do about it and when i google i can’t really find anything specific for this gene mutation. Im pretty desperate and was hoping someone in here has an idea of how i can fix this issue and get to better health? If you know something please let me know, i would be so grateful. I don’t know if this matters, but one thing i realised is, when i take high dosage of b12(mecobalamin 50 ...
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Hi Dave, Those "over methylation" symptoms are possibly hypokalemia or pottassium deficiency which is life threatening.  I have started Freddd's protocol and he heavily cautions to watch out for that when beginning, have some pottassium on hand and be cautious.  I am really learning a lot about starting methylation from him and here is the rundown of what to do: http://forums.phoenixrising.me/index.php?entries/my-understanding-of-freddds-protocol.1697/ check it out, it is very very interesting and helpful.  He has worked with lots ...
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Dave, Congratulations on going to AA!! With the amount of illegal and prescribed drugs in your system, it might be best to try a compound medication. It is non-addictive, is formulated to YOUR DNA, and NEEDS to be prescribed by your doctor. You mentioned that your medication has not ”touched your depression”, since compound medication is formulated for you, it has a better chance vs pills that are mass produced which may or may not help your depression due to your metabolic rate of digesting pills. There is a lot of information that can help you and eliminate a lot of the side effe ...
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This is something I was researching that you may take an interest in about methyl-b12. There are a number of reports of people having problems with taking it, yet it seems to be an important part of the healing process. http://www.kemikaliedetektiven.se/hmb/engelska/artiklar/b12.htm   [End]
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try a Brain Synchronizer. It helped me a lot when depression was bad. (no, I don’t sell them)   [End]
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Hi Dave, First, you know that there is no quick, overnight fixes for any ill condition that we are in. Longer you are in an ill condition longer it will take you to be in balanced condition. Please check your basal temperature for 3 days. You can search here on CZ on how to take basal temp. I suspect you have thyroid problems. You may need Iodine, but lets get the basal temp first. You also know that drugs are not curing your depression and anxiety. They are masking the symptoms and making your body more toxic. So plan on being drug free, but has to be done slowly. Fasting is th ...
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I’m beginning methylation and I’ve hit a rough patch. A bit of background: I spent many years in moldy homes and abusing drugs; mostly dissociatives and opiates. I really screwed my brain up with dxm 12 years ago and never got around to figuring out what to do about it. I’ve had ”brain pain” since the day I had a near death experience on dxm and weed. I’ve been pretty over exposed to antibiotics too. Depression since I was 10, and anxiety since I was 15. I’m 27 now. 4 years ago I developed chronic candidiasis and never fully recovered. I treated myself for it incorrectly and flooded my bod ...
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Hi do you know any Trusted lab. can make a DNA test for stool sample to figure out the gut bacteria (microbiota)?I found a site dealing with this mater :ubiome are some body tried it ? my best wishes nori641   [End]
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Do you know where I can get my raw data from 23andme interpreted? Thanks!   [End]
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DNA is an electromagnetic storage mechanism. There is no junk DNA. Do your research and do not worry. Worry and fear creates its own damaging frequencies that inform our state of being.   [End]
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How can I be skin white and sexy?   [End]
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This is a letter that was published in ”Dear Prudence”. I read her column and recognized it right away. So...I’m not sure if you are the original Dear Prudence letter writer and want more advice than you got from ”Prudence” plus those who comment on her columns or...?   [End]
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Corrected link: http://www.psychologytoday.com/blog/health-matters/201011/nutrition-and-depression-nutrition-methylation-and-depression-part-2   [End]
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Look at Methylation which could be part of the problem. There are many pathways http://www.psychologytoday.com/blog/health-matters/201011/nutrition-and-depression-nutrition-methylation-and-depression-part-2 Try some b vitamins like B12 and folic acid which help in the methylation pathway. Do a hair analysis test - I prefer Trace Elements for several reasons. Possibility of heavy metals playing a role, the only effective way to test is with a Heavy Metal Challenge from Doctors Data. Avoid fluoride in toothpaste, and mouthwashes, avoid fluoride treated water.   [End]
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Other thoughts: -NAC and Probiotics give me an initial bad reaction -I used to have bad stomach problem correlated with anxiety, but my stomach is mostly smooth now, though.   [End]
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Hey everything, this is my first post on this site! Some background: As a child, I was diagnosed with depression, asperger’s, GAD. I had an unhealthy diet and was on antibiotics a moderate amount. In my college years I used alcohol and marijuana often, until quitting both and settling for a good lifestyle/diet (meditation, paleo diet). Afterwards, I started feeling depressed and bored living at home, so I developed an opioid (kratom) habit that persists over 2 years later. Now, I am seeing a psychiatrist, but I seem to have an allergic reaction to many medications (including EMSAM, s ...
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23andme.com will give you ancestry info - maternal and paternal haplogroup - for 99 bucks. You’d need to be in contact with the sister to find out your uncles results. So going down that route would lead to communication being opened - which as SS has written - is something you need to decide whether you want to open up to that. I feel for you - families can be awful! I’ve had my fair share! The hardest thing in life is to ’let things go’ - we see a situation on the horizon which we know and sense will be stressful - yet we embrace it because we feel out of principle things need ...
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I don't know about the costs of DNA testing, but there are many sources available out there, these days. As far as interacting with the sister, if you aren't concerned about the uncle's Will (good for you!), then there is literally no reason (legal, or otherwise) to communicate with her.  Seriously.  And, if you choose this route, it means not answering her calls, responding to emails, blocking her texts, etc.  If she's toxic to you, there are the options of:  a) exposing yourself to manipulations or other toxic behaviors by allowing communications, ...
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I’m not worried about my uncles estate that will work out itself. I just wonder how to deal with this person who obviously lacks any respect. I would go ahead and take the test but I don’t feel like handing my genome to gobble. Is there a cheap test I can do to confirm my blood relation to my uncle without going through Big Sister?   [End]
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I'm so sorry that you're experiencing this stress, and you have options. First of all, it's important to understand what an "inheritance" is, legally.  It is a gift, and not an obligation.  So, if your uncle has known you your entire life, he's going to make his Will the way that he wishes.  If this sister is coercing him into altering his Will, that can be addressed through Estate Courts. If you have not been in contact with this sister, for whatever reason, you are under NO obligation to respond or even communicate with her if her discus ...
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I have a awkward situation on my hands. I have a half sister who has never contacted me in 40 years. Now out of the blue she calls me and tells me she has an extra 23&ME DNA test that she is ”offering” me for free. Turns out our uncle is about to die and has a million dollar estate. I heard through the grapevine she is suggesting I am not my father’s son. This is absurd because of all the family I look most like my father and not like my mother. I feel giving her a piece of my mind but I suspect she is conning my uncle that I am not his relative. And you thought your family was ...
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I should add that others who have taken these online DNA tests were diagnosed with the conditions that showed at the top the list...I suppose it is listed in order by the largest risk? This skin adhesion problem was at top of the list for me. These are risk factors determined by medical studies on chromosomes or not a genetic defect, which genetic counselors are not trained to access.   [End]
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I had my appointment with the genetic counselor. I thought genetic research was more advanced than it is in the USA. It does not cover all genes. The visit would have been a waste of time except I learned more about the online DNA health sites. The site I received a report from just analyzes the risks, not genetic defects. Genetic counselors do not know how to analyze the risks in these DNA health reports because they do not measure how much of a risk it is. Just because it is a risk, it does not mean it will happen. If it showed a larger risk of getting something, then these online report ...
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The DNA link seems specific to the lack of skin glue problem. I will see what the genetics counselor says about it?   [End]
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It might be resistent infection rather than dna link or any inflammation.   [End]
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Because one disease of the DNA problem explained above can be caused by certain foods (hormones or stress), I wonder if gluten was the trigger for me. It is possible when I get chapped lips from eating gluten that this problem with my lips happens due to DNA mutation. Since I had the vitamin A deficiency from celiac disease, I do not know if it is a combination of this DNA problem triggered by certain food (gluten in my case) AND vitamin A deficiency. I can’t believe this came up in my DNA when I was not even looking for it. I wrote many posts about skin glue (adhesion) and here it show ...
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longterm are you not completely cured yet?   [End]
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I just wanted to add that the promethease site showed that I do not have a lactose intolerance gene. I always wondered about that. It also shows if you have a high risk for psoriasis, but there are more than one gene for that. It does not analyze all your genes. I guess different dna ancestry sites include different DNA segments so you might get different dna genes analyzed depending on which dna ancestry site you used. All I know is that ancestry.com included the skin adhesion gene in their data... so promethease was able to analyze it.   [End]
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I ordered a ($99) DNA ancestry kit from ancestry.com, then uploaded my raw DNA file to promethease.com for a limited DNA health analysis ($5). You have to wait a few weeks to receive the results of your DNA test from ancestory.com before you can upload your raw DNA file to promethease.com. Or you can have a genetics counselor prescribe this test. Since I do not think health insurance covers DNA tests, the ancestry/promethease option is probably cheaper. Also, ”As basal cells reproduce and mature, they move towards the outer layer of skin, initially forming the stratum spinosum. Intercel ...
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Interesting.. I don’t know if I can really do much else with going to doctors and such. I’ve already been to the derm and doctor multiple times. I am currently still on my parents health care plan and I’m sure there getting sick of me going to the doctor only to figure out that there’s nothing wrong with me. Most people just think that I’m a crazy hypochondriac. I just want to know what’s wrong with me damnit. Anyways, that that’s out of me, keep us updated. It sounds pretty promising to say the least. Keeping my fingers crossed that it’s reversible.   [End]
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I only had a limited DNA saliva test . A problem came up related to the SNP known as rs2076295 (T;T) on chromosome 6p24, which encodes the protein desmoplakin (part of desmosome). Desmosome is an adhesive intercellar molecule that tightly links adjacent cells for cell-cell adhesion. It is part of a dynamic structure that involves other proteins, such as plakoglobin and plakophilins, which tether the cytoskeleton to the cell membrane. Desmosomes (and desmoplakin) are important in maintaining the integrity of tissues that experience mechanical stress, and there is strong evidence that ma ...
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I think I am going to try Niacin since it works for overmethylation.   [End]
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I tested through 23andme andI am curious if anyone knows of any natural treatments for this gene mutation (MAO-A++). I feel like if I could treat this naturally then some other issues I have may get better such as adrenal fatigue, candida, etc... I have read that some autistic children are prescribed Respen-A but I feel hesitant about that. Any thoughts?   [End]
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you could check some previous messages of onwards for example or sd 2345 on parasites forum. great advice   [End]
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good point pet, Dr. Ben Lynch feels that “repairing the digestive system and optimizing the flora should be one of the first steps in correcting methylation deficiency”, and that especially includes treating candida because of the toxins it releases, inhibiting proper methylation. Generally speaking infections can lead to impairment of methylation path no mater if bacterial fungal viral...   [End]
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How do u take care of the parasites?   [End]
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A lot of the mthfr practitioners have gotten bad reviews.... One was even a sexua| predator. Many are changing their stance to fixing other issues first (gut, minerals, absorption,....) before tackling methylation. Many find a short cut helpful. I’ve been researching this for a long time and did the 23andme myself. Tons of mutations. The consensus on what to do exactly is not clear. Many think that the snps will improve by working on key imbalances, not necessarily targeting the snps. Snps don’t show what’s actually happening bc u don’t know if they are active or not. It just sh ...
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Very nice information. Thank you for sharing it. Thanks pmd   [End]
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There was something on the 23andme reporting ( I think it was there, maybe it was a different site) that was a marker for not being able to tolerate common vitamins. I definitely fall into this category. I take only about 4 things very sporadically out of a few hundred things that I tried over the years. I did read about trying a different form of B12 and that is definitely in my future as well. Just finishing up 4 more days of homeopathic and then I can order some of the methylation supplements. Also on the back of my mind is something I read( maybe from Andrew Cutler or on Curezon ...
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Hmm.. I have endless liver congestion with no clear reason why. Where should I start again in terms of testing?   [End]
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Interesting that you didn’t do well with the B12. There is a way to determine which B12 is best suited to you genetically...i will post up the info later when i find it. When i followed the guide for me and my boyfriend as per our gene results, i found that i could tolerate a small amount of methyl B12, and he could not at all (why i think i had better energy on it and he didn’t) The gene result combinations meant that Hydroxycobalamin B12, and Adenosylcobalamin B12 were better suited than the standard Methylcobalamin B12. I bought them in powerful liquid form for sublingual made b ...
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Hi, I had asked for a support forum to be created for people following a gene-test protocol for improved health...commonly called Nutrigenomics. This forum has been created to pool together our experiences with this route of health and healing, and for anyone with genetic conditions who are trying health protocols to alleviate symptoms. Many get their gene tests from 23andme.com, which is the cheapest by far that you’ll find online. There are other practitioners who also offer gene testing for specific conditions. The gene results synchronise nicely with Curezone’s general protoc ...
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I also have the CBS defect. I think this explains why I never did well with taurine even though I have the endless liver congestion. I plan on trying methyl folate soon. B12 though I never did well with, maybe it was the wrong form. I had shots and pills both and neither did anything for me. MSG strangely does not bother me. Benzoates on the other hand I cannot stand at all. Yasko seemed too expensive for me at this point. I just want to dip my feet in the waters and see if anything significant happens, then I can bankrupt myself later if it will be worthwhile. Maybe I will mess ...
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You’re singing my song! After multiple iv chelations, I ran into a methylation block(caused by my cbs upregulation)-my body was shutting down. After testing with Yasko and reading about methylation on Phoenix Rising, I pursued Yasko’s Rnas for a while- nutrigenomic bypass, which was truly helpful but expensive! Aiming for nutritional balancing on my own, I have benefitted from loads of zinc, bp5p, folate and b12 for the MTHFR. the slow MTHFR(going backwards) -over methylation- and the up regulation of the CBS component Causes all kinds of misappropriation and overall diffuse loss- stemmin ...
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Just regular black tea. I know it is not recommended on Nutritional Balancing   [End]
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What kind of tea are you drinking?   [End]
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I dont know exactly - is still a new subject for me. But from what i’ve read I have a strong belief that solving gut issues and other infections in the body is a huge step to improve methylation. If parasites can ’steal’ minerals and put a lot of toxins in - that impair detox - this made a lot of sense to me.now. its clear now that only taking liver herbs for some having this issue is not a solution. about infections - for years I had a lot of symptoms that went far more than all in your head. i have a strong phisical feeling that something is wrong inside but for years i could not co ...
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Hm,seems you also had a lot of issues... I’m just in the middle of the process and each day learn new things. I cant make a complete cleanse as adrenal and liver is still aproblem for me. The hardest part was to figure out what is going on and methylation was just apart of the problem. Re- deworming stuff : I had bad experiences trying some ”brands” because not being able to find out exactly the culprit and target the treatment. example: tried supps for worms and candida which included flax seeds and psyllium and got super constipated just to find out later that a bacteria overgrowt ...
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I agree with what you said and I’m game for anything that will work. When I first got sick I had high EBV titers, but they said that it wasn’t an active infection, just indicative of an old infection. EBV is something that has been on the back of my mind for a while. There was a youtube video somewhere of a girl who used a homeopathic remedy to cure it but I could never find the remedy name. My experiences with intestinal flora have turned into an odyssey. It started out when I went off dairy and gluten two decades ago and started passing intestinal plaque every day. Hard stool that con ...
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Dave, I’m just curious: Do you think methylation issues or MTHFR can be ”cured” or fixed? And how did you find out about your infections - how did you know? Thanks for this!   [End]
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Did you have the chance to check his site? Dr. Ben Lynch feels that “repairing the digestive system and optimizing the flora should be one of the first steps in correcting methylation deficiency”, and that especially includes treating candida because of the toxins it releases, inhibiting proper methylation. Generally speaking infections can lead to impairment of methylation path no mater if bacterial fungal viral... In my case was multiple cause parasitic bacterial fungal and finally viral put the cherry on top...Maybe something is still in your system causing this EBV for example ...
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it’s all quite interesting, seems like you are on the right track and found some culprits to your health. I wish you the best of luck! And I’d love to hear about what you try and what you learn, feel free to share if you have the time along your genetic journey :))   [End]
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I mean, I guess I get it - if you can’t properly detox - metals, etc. can create spectrum issues. I’m dealing with this with my four-year-old right now. She is on NB and has sensory and spectrum stuff (as well as anxiety and depression). I should get us both tested.   [End]
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What’s the relationship between ASD and methylation?   [End]
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Can you provide a source for this... that parasites can lead to false DNA testing. I’m not agreeing or disagreeing, just curious. I know that with parasite testing they test for parasite DNA and these can be very inaccurate, but with human DNA tests???? Also there was a CDC report some years ago that upward of 90% or more of Americans were infected with parasites as most people here know, so you can’t correlate parasites with gene mutations. Well, you could but it would be like correlating parasites with people that breathe, i.e. not very significant. From the very basic reading I ...
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I wish I knew more than I do, but I’m only one step ahead of you in that I had the test done, other than that I don’t know what I’m doing. I guess I can be a good guinea pig and post results when I actually start doing something about the test results. I just post here from time to time because I’m into all the same things as you guys are doing except for the fact that NB did not work out for me at this point. I have done so many things in the past including the NB diet, but my body went through all sorts of shifts that now I cannot do the diet and the supplements didn’t really seem to ...
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sd2345 wow really interesting information!   [End]
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Hello, My ND doctor recommended one of these tests and I have yet to move forward with it. What was your plan with the test results? and with the 20 gene mutation defects it shows you, was your plan to follow a certain protocol to address them? Are you planning on incorporating the recommendations alongside your NB protocol? Didn’t quite understand what it all meant and how it works and if it’s really all that necessary? My doctor said that for example some of the supplements I am taking, I may not need to take based on what my gene test finds and some I may need to add in, she ...
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I know a lot of people here are just getting started with parasite cleansing, but this is not new to me. I spent a good 6 years or more dong parasite cleansing. I’m not sure if they are all out yet, but I haven’t seen any in quite a while, even though I still have symptoms. Also the herbs that used to cause really bad die-off reactions don’t cause anything to happen now, whatever that means. I am suspecting protozoa now and not helminths, but it’s just a feeling I have no proof yet. I’m skeptical like you with the gene tests, but I feel like it’s something I have to at least try jus ...
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Take care of intestinal parasites, and all this may fall into place for you. I have been researching MTHFR gene mutations for a while now......not one of the sufferers that I personally spoke to of this ”gene mutation” have not had parasites.....so rather than concentrate on the gene issue, and having a reason for the detox issues, I choose to look at what may cause the mutation to show up in tests, just as in mineral imbalance......just throwing it out there......look at your gut issues before the ”why and how” to a possible gene mutation. The parasites that inhabit our gut can lead to ...
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Oh so you recommend doing 23 and me and then that other web site? Okay - cool. Sorry I can’t help with the other info. Good luck!   [End]
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I’m one of those weird people who refuses to join FB. I did the 23andme test for the same reason. Their health reporting is not so good/detailed. But the mthfrsupport.com reporting was excellent. It will import your 23andme data right into their system and spit out a report for $20. Edit: I have 20 methylation related mutations not mthfr.   [End]
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I can’t recommend anyone, but I’m sure there are loads of MTHFR forums on Facebook that you can join and ask. Just curious - what testing did you do? I’m looking at 23andme b/c it’s the cheapest to do MTHFR testing.   [End]
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I just got my results back and did the promethease report, geneticgenie report and the mthfrsupport report. By far the mthfrsupport report was the most complete, and I have 20 mthfr mutations. So what to do. It looks like so far the options are trying the Yasko protocol on my own, reading phoenixrising and trying ideas there or have a consultation with someone, but the prices are pricey. I’m leaning toward a consultation, so if anyone can recommend someone that would be great   [End]
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verry useful information. thanks a lot for this. thanks 99thin   [End]
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It is not my intention to start a debate, here, but there are incalculable sources of illness and emotional dis-ease, from processed foods to heavy-metal poisoning to physical/emotional childhood trauma. There is not, nor can there be, a single approach to whole-self healing and recovery. I have known many people who put physical and supplemental protocols at the tops of their agendas and, regardless of the iodine and meatless diets, these people were still sick because they were sick in their souls as well as their physiology.   [End]
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I haven’t read this entire thread, but I get the gist that this young man is experiencing terrific depression and anxiety, and I ”get this.” The human organism is a whole being - physical, emotional, etc. I completely agree with the response, above, to not only consider meditation, but begin using various coping mechanisms for the anxiety like: * getting (or, staying) in ”The Now” * tell yourself exactly what you are feeling and where you think it morphed into anxiety * EFT tapping - this really does work when it’s practiced properly * physical movement - whether you ”feel” li ...
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People have suggested things for you to put in your mouth.  I’ll make a suggestion for things to heal you as spirit which most people think of as your mind. Try some meditation.  Take at least twenty minutes a day for this form of inner peace.  Find a meditation that works for you.  I use grounding and centering in my meditation.  Here’s an article on meditation and abuse - and it does raise its ugly head in adulthood after forgotten childhood abuse - I know: http://worldpulse.com/node/58217 Just eight weeks of mindful meditation can rewire the ...
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Thank you everyone for all the quality information. I suppose I should mention, I did experience physical and sexua| trauma for about 6 months as a toddler at the hands of a babysitter. After it was discovered, my parents did put me through therapy for about a year, and with that combined with my young age I don’t really have any residual problems from that that I know of. alao I am male, if that makes any difference. I’m almost convinced though that this has something to do with environment or genetics since my dad, my grandpa, my great grandfather, and myself have all had almost the s ...
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If someone can prove to me that drugs are needed other than in a crisis situation to save someone’s life, then I’m all ears. Once the life has been saved, proceed to clean out the CAUSE of disease and get rid of the drugs. The final phase of healing is when the organs will regenerate AFTER the bugs, radiation and other poisons have been cleaned out of the organs. There are many con artists in the natural healing field, too. Why do they say their products work well for some and not for others? It’s the degree of toxicity of the body that determines how well any of the nutrients work. W ...
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Agreed, toxic congestion is one of the biggest causes of ailments. Cleansing, fasting, detoxing using nature’s finest ingredients is a superior route to general medical care and attention. I went through this route many years ago and symptoms at the time were not as exacerbated as they are now, despite regular cleanses, fasts, colonics and of course diet, toxic-less exposure to perfumes etc. When one protocol doesn’t eliminate symptoms we have to look at other causations. As i have listed in the previous post, and am finding relief at last after so many years. ’Stressors’ that bri ...
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All illness stems from pathogen or parasite.   [End]
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Oh, boy, the medical and how much it costs to do all this study when all you have to do is kill the bugs, clean out the liver and colon, let the rest of the body clean out by itself (because it will after these 2 organs are clean), and get your health back. How they have buffaloed people and taken their money!!! They’re right, but they sure do love to take your money then not tell you how to get well. I wouldn’t go the detour route and pay them a cent.   [End]
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Go to http://www.oldfashionedspices.com and get some dewormer. Take a couple of tablespoonfuls of his dewormer a day. That’ll tell you real quick if you’ve got parasites, and I’ll bet dollars to donuts you DO. Trying to help you.   [End]
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Your problem is that you have been parasite and poisoned and your parent’s were before you were born. Drugs, immunizations with chemical poisons in them. All kinds of poisons and parasite eggs that we ingest and know noting about. solvents tha tmake parasite eggs hatch in our bodies. Then the parasites get into the liver and cause panic attacks. there is nothing genetic about it except for the fact when you were in the womb, your mother passed on those poisons to you. A good 99% of people have parasites now and just become victims of the medical with their drugs. Get rid of all diseas ...
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Agreed - methylation issues, pyroluria, ADHD, etc etc can all easily contribute to symptoms you describe. If you’ve had no trauma and nothing particularly bothering you - you’ve gone down the therapist and oral antixylotic route - it’s worth DNA testing. Also the urine test for kryptopyrolles is worth persuing too. GAD gene converts glutamate to GABA - GABA is the neurotransmitter which is INHIBITORY - calms us down..stops mind-racing...etc. Within the ’YASKO Methylation Cycle’ diagram - genes such as GAD, MAOA and MAOB, SOD, CBS, MTHFR, COMT, VDR, NOS are all the important one ...
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I’d get tested for methylation defects. These are genetic and are implicated in or can cause/lead to nearly everything you described. I used 23andme.com for the DNA profile (best bang for the buck, by far - $108) and geneticgenie.org for the methylation profile (free/donation). Good luck!   [End]
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I never really thought about that. Considering some aspects of my life I suppose it’s definitely possible. How would you find out if that was a problem?   [End]
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Have you ever considered you may have a worm burden??????????????   [End]
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I’m new to this forum and hope I am posting in the right spot. I’m here because I am just about to start college and for the past 6 months I have been experiencing severe anxiety or inner tension as well as a very apathetic demeanor. For the first few months I thought it was just because of an issue I had had in my early childhood being brought up again to my conscious mind and stressing me out. I tried Lexapro and that helped a little but only to kind of numb the feelings, not really make them go away. There were a few therapists I went to and they didn’t really help either because I didn ...
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I have been on the candida diet for.....9 months now. I was extremely strick for months and months, with lots of allergy testing. I now mostly eat everything except white flour/rice, nothing white and sugar. I still use xylitol on my cereal. My doctor told me if I stay below 20 or 30 grams of sugar, I’ll be ok. I probably get less than 10. I feel good and am taking IgG2000DF, probiotics, kefir, and just retested with metametrix and saliva test. Hoping the yeast in the gut has gone down, just paranoid about getting the vaginal yeast. Early on, it was so bad. I know mine was from par ...
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http://content.nejm.org/cgi/content/full/361/18/1760 Paper about one genetic link found...but I think scientists are still learning and what is known today about immune system is probably less than 1% of what is still unknown, out there waiting to be learned.   [End]
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There is very strong evidence that it is genetic. The genes identified so far point to the immune system cells being unable to identify and/or kill candida as well as in people who are not genetically susceptible to it. The genetic link does not change the fact is that for almost all people if they had never in their life received antibiotics, they would be very unlikely to get it, as it was rare 100 years ago - and if even they did get it in some other way (e.g. sexua| transmission) it would be a much much milder case. I have seen no real evidence that its caused by allergy to yea ...
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I am cured now sicen 1 year.I am taking probioticsto prevent it,but i would like to know if is genetic,its very important for me,because my father has always it too.And what about allergies to yeast and allergies to yeast in the intestines?how i know if i have this?can this causing candida overgroth?   [End]
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When you have this it means your metabolism is slow and yes it’s linked to candidiasis in fact many believe this is the cause of it, i’d recommend following the anti candida diet but what would really help is getting in a good excersise routine as this would stimulate you and get metabolism going very quickly. Might wanna consider taking enzymes depending on what you are eating to help break food down quicker   [End]
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can candida cause hypothyroidism??? My doctor tested me for this, and in fact she said I have this and now have to take something called NatureThyroid. It’s no big deal, I have none of the symtoms of hypothyroidism so I can just take this stuff which is easy with zero side effects. My sister has the hypothyroid thing too, she’s 52, I’m 50 and just says it is really common in women this age. She doesn’t have the candida though. I have the candida which stemmed from parasites, not antibiotics.   [End]
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Greetings, you will find a lot of help on these forums but by the sounds of it you are having problems already and it’s in the family I wasn’t able to get it tested by doctors but am well on the way to recovery now after 2 months of work. In a way i know when i got it bad as i get it on my penis and can see it although the real debilitating problems occur in my gut and i’ve developed some sensitivities to wheat, white rice and other foods. Do the full cleanse and change your diet take the anti fungals and supplement with good quality probiotics and you will see improvement but it might ta ...
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Hello, i have been sufering systematic candida overgroth more than 24 years,my floaters by candida are very severe,i have hypotyrodism by candida too.It has arruined my life .My father and son had and have it. Maybe is some genetic by my father.Is there any genetic testing for intestinal candida OVERGROTH?.Or can be any allergy/intolerance to yeasts in general or in the intestines ,so i get candida overgroth??is there any test for ths too? regards   [End]
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The person who wrote that article should read this book. The Genie in your Genes, by "Dawson Church" It was recomended by Gary Craig of the EFT newsletter. I am only about 25% through the book, but I think it’s interesting and worth reading too. In essence, the book is about how your genes change for the better, or worse in relation to your health depending on your external environment, and how you process the everyday changes, and stresses in your life. This starts with your childhood. A study was done on a group of children that found that children who lived in a dys ...
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LONDON (Reuters) - Genetic tests to assess disease risk are proliferating but many are a waste of money and tell people little more than they would know from studying family history, medical experts said on Friday. A host of companies now offer tests, typically costing hundreds of dollars, to calculate genetic risks for common conditions like cancer, diabetes and heart disease that involve multiple genes. But Christine Patch, a genetic counselor at Guy’s and St Thomas’ NHS Foundation Trust and a member of Britain’s Human Genetics Commission, said most had little clinical relevance. ...
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BRAVE NEW WORLD ON THE MOVE OCTOBER 28, 2004. Mandatory gene testing for newborn babies...states adopting laws...NY expands its program...from the AP dispatch below, it appears that parents have no choice in the matter...have a baby in a hospital, the test is done... What about the science behind this coercive program? It stinks. The word GENE has become a code symbol for ”we know what we’re doing, we’re linking diseases to specific genes, we’ve done the studies...” If you can find an old out-of-print book, NOT IN OUR GENES, grab it and read it. It details the fake science a ...
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