Hygiene Hypothesis and the Whip Worm.

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Greetings everyone,

I read an article recently in the post register here in Idaho Falls on the whip worm and how it generates a different White blood cell response than the typical white blood cell that is produced with Crohn's Disease sufferers. From what little I gathered from this article, people that have Crohn's typically have an over-abundance of a less healthy cell called a T-1 Cell which is no good at all. Introducing the whip worm in the form of a medication will create a healthier cellular response of a type t-2 cell. does anyone have any further information on this I would love to read more on the subject.
 
Hi!

I've also been interested in the 'parasite' theory, ever since seeing a programme that investigated the low incidence of immune-related conditions (including asthma, eczema, allergies) in populations in 'less developed' countries where bowel parasites are prevalent.
In the programme, a lady with UC which was unresolved with all 'western' drugs, achieved almost full recovery after taking a monthly oral dose of a kind of hookworm. Ever since then I've never understood why this doesn't seem to be a more widely used treatment. I understand that you need clinical trials and so on, but this programme was on years ago. Surely the amount of side-effects suffered by so many on more conventional treatments would mean that more IBD sufferers should be offered this sort of treatment, even if on a trial basis.
The lack of posts on this forum from anyone using this therapy, and the higher number of posts by people interested in it speaks for itself! (I've not counted specifically, it's just the impression I get).
 
Thank you for your response. The article I read involved the whip-worm which is evidently a worm that is primarily found in pigs. In pigs they take off through breeding, but since the human body is different from a pigs body and thus foreign to the worm, they try and establish themselves and latch onto the inner wall of the intestine without being able to breed they soon die. the process usually takes a couple of weeks. During this time the human body creates the
T-2 cell to fight the invading parasites and people that suffer from auto-immune diseases seem to feel a bit better. This treatment seems to help with just about any kind of disease of the immune system. The article said this treatment could even possibly help those who suffer from Autism. I read that this treatment is currently in trials right now I just wish I knew where - sign me up. Ha-Ha
 
In medicine, the hygiene hypothesis states that a lack of early childhood exposure to infectious agents, symbiotic microorganisms (e.g., gut flora or probiotics), and parasites increases susceptibility to allergic diseases by suppressing natural development of the immune system. Because of this we fail to induce a Th1 polarized response early in life so as we grow up we are more prone to developing Th2 induced disease.[1] The rise of autoimmune diseases and acute lymphoblastic leukemia in young people in the developed world has also been linked to the hygiene hypothesis.[2][3]

There is some evidence that autism may be caused by an immune disease;[4] One study supports the hygiene hypothesis theory and cites the lack of early childhood exposure as a cause of autism.[5]





Contents
[hide] 1 History
2 Mechanism of action
3 Breadth of the hypothesis
4 Supporting evidence
5 Helminthic therapy
6 Alternative hypotheses
7 See also
8 References
9 Further reading
10 External links


[edit] History

Although the idea that exposure to certain infections may decrease the risk of an allergy is not new, David P. Strachan was the first scientist who gave the theory a scientific[weasel words] background in an article published in the British Medical Journal (now the BMJ), in 1989.[6] In this article, the hygiene hypothesis was proposed to explain the observation that hay fever and eczema, both allergic diseases, were less common in children from larger families, which were presumably exposed to more infectious agents through their siblings, than in children from families with only one child.

The hygiene hypothesis has been extensively investigated by immunologists and epidemiologists and has become an important theoretical framework for the study of allergic disorders. It is used to explain the increase in allergic diseases that has been seen since industrialization, and the higher incidence of allergic diseases in more developed countries. The hygiene hypothesis has now expanded to include exposure to symbiotic bacteria and parasites as important modulators of immune system development, along with infectious agents.[7]

[edit] Mechanism of action

Allergic diseases are caused by inappropriate immunological responses to harmless antigens driven by a Th2-mediated immune response. Many bacteria and viruses elicit a Th1-mediated immune response, which down-regulates Th2 responses. The first proposed mechanism of action of the hygiene hypothesis stated that insufficient stimulation of the Th1 arm, stimulating the cell defence of the immune system, leads to an overactive Th2 arm, stimulating the antibody-mediated immunity of the immune systems, which in turn led to allergic disease.[8]

The first proposed mechanistic explanation for the hygiene hypothesis cannot explain the rise in incidence (similar to the rise of allergic diseases) of several Th1-mediated autoimmune diseases, including inflammatory bowel disease (IBD), multiple sclerosis (MS), and type I diabetes. The major proposed alternative mechanistic explanation is that the developing immune system must receive stimuli (from infectious agents, symbiotic bacteria, or parasites) in order to adequately develop regulatory T cells, or it will be more susceptible to autoimmune diseases and allergic diseases, because of insufficiently repressed Th1 and Th2 responses, respectively.[9]

[edit] Breadth of the hypothesis

The hygiene hypothesis has expanded from eczema and hay fever to include exposure to several varieties of microorganisms and parasites, with which humans coexisted throughout much of our evolutionary history, as necessary for balanced and regulated immune system development.[10] In recent times, the development of hygienic practices, elimination of childhood diseases, widespread use of antibiotics, and relative availability of effective medical care have diminished or eliminated exposure to these microorganisms and parasites during development. Examples of organisms that may be important for proper development of T regulatory cells include lactobacilli, various mycobacteria, and certain helminths.[11]

[edit] Supporting evidence

The hygiene hypothesis is supported by epidemiological data. Studies have shown that various immunological and autoimmune diseases are much less common in the developing world than the industrialized world and that immigrants to the industrialized world from the developing world increasingly develop immunological disorders in relation to the length of time since arrival in the industrialized world.[12]

Studies in mice have shown that exposure of young mice to viruses can result in a decreased incidence of diabetes.[13]

In Cell : Homeostatic Expansion of T Cells during Immune Insufficiency Generates Autoimmunity they showed that when short lived T cells were replaced during a state of too few long lived T-cells (Memory T cell), because of lack of infections, the risk of developing autoimmune diseases will increase. They showed that in a state of too few long lived T-cells, because of lack of infections, not enough short lived T-cells could be produced by long lived T-cells during homeostatic expansion. Therefore, more auto reactive T-cells will divide in such a state, causing multiplying auto reactive T-cells with a greater risk of causing autoimmune diseases like type I diabetes or MS.[14]

One conclusion is that a clean environment, with lack of infections (like early life infections) increases the risk of an autoimmune disorder.

Th2 immune disorders such as asthma and other allergic diseases are probably related to the hygiene hypothesis. A baby has many Th2 cells, which stimulate the production of antibodies. When not sufficiently stimulated with early life diseases, the immune system will have too many Th2 cells present, leading to a greater risk of Th2 immune disorder. If a child is exposed to infection diseases then the cell defense will be stimulated via Th1 cells causing a reduction of Th2 cells and subsequently a reduction of antibody stimulation by Th2 and therefore a lower risk of developing an allergic disease such as asthma. Unfortunately, vaccination only uses the Th2 mechanism.[citation needed]

In developed countries where childhood diseases were eliminated, the asthma rate for youth is approximately 10%. In the 19th century, asthma was a very rare disease.

Longitudinal studies in the third world demonstrate an increase in immunological disorders as a country grows more affluent and, presumably, cleaner.[15] The use of antibiotics in the first year of life has been linked to asthma and other allergic diseases.[16] The use of antibacterial cleaning products has also been associated with higher incidence of asthma, as has birth by Caesarean section rather than vaginal birth.[17][18] However, the studies investigating these links showed only tenuous correlations between the factors described and the conditions they are hypothesized to cause.[citation needed]

Several pieces of experimental evidence also support the hygiene hypothesis. Work performed in the laboratory of Professor Anne Cooke at the University of Cambridge showed that mice of the NOD strain (which spontaneously develop type 1 diabetes mellitus) had a significantly reduced incidence of this disease when infected with the helminth parasite Schistosoma mansoni.

In November 2009 a group of researchers at the School of Medicine at University of California, San Diego, found that Staphylococci helped reduce inflammation.[19][20]

A double blind study performed on 2500 pregnant women in Uganda showed that infants of the women treated with anthelminthic medication for worm infections had double the rate of doctor-diagnosed infantile eczema.[21]

[edit] Helminthic therapy

Main article: Helminthic therapy

See also: Effects of parasitic worms on the immune system

The use of parasitic worms (also known as helminths) to treat the types of disease described by the hygiene hypothesis is being studied in the UK, USA and Australia.

Because of the promise shown by this research, two versions of Helminthic therapy, using Trichuris suis ova or Necator americanus larvae, have become available.

Helminthic therapy is the treatment of autoimmune diseases and immune disorders by means of deliberate infestation with a helminth or with the ova of a helminth. Helminthic therapy is currently being studied as a promising treatment for several (non-viral) autoimmune diseases including Crohn's disease,[22][23][24][25] multiple sclerosis,[26] asthma,[27][28] and ulcerative colitis.[29] Autoimmune liver disease has also been demonstrated to be modulated by active helminth infections.[30]

In addition to the treatment of immune disorders the anti-inflammatory effects of helminth infection are prompting interest and research into diseases that involve inflammation but that are not currently considered to include autoimmunity or immune dysregulation as a causative factor. Heart disease and arteriosclerosis both have similar epidemiological profiles as autoimmune diseases and both involve inflammation. Nor can their increase be solely attributed to environmental factors. Recent research has focused on the eradication of helminths to explain this discrepancy.[31]

As a result of the hygiene hypothesis helminthic therapy emerged from the extensive research into why the incidence of immunological disorders and autoimmune diseases is relatively low in less developed countries, while there has been a significant and sustained increase in immunological disorders and autoimmune diseases in the industrialized countries.[28][32][32][33][34] If helminthic therapy and other therapies using other types of infectious organisms, such as protozoa,[35] to treat disease are proven successful and safe the hygiene hypothesis has potentially large implications for the practice of medicine in the future.

[edit] Alternative hypotheses






This section may contain original research. Please improve it by verifying the claims made and adding references. Statements consisting only of original research may be removed. More details may be available on the talk page. (May 2012)


There are many other hypotheses which aim to explain the increase in allergies in developed nations, many of which are also related to the other. A few other major areas of focus in the literature include infant feeding, over-exposure to certain allergens and exposure to certain pollutants.[citation needed] Infant feeding covers a range of topics which include whether babies are breast fed or not and for how long, when they are introduced to solid foods and the type of these foods, whether they are given cow's milk and even the types of processing that the milk undergoes. Numerous articles[citation needed] have reported that over-exposure to certain allergens in occupational situations can cause allergic diseases, such as Laboratory animal allergy, bird lung, farmer's lung, and bakers lung (See Wheat allergy). The third of these theories suggests that pollution (such as diesel exhaust) might be responsible for the increase of these diseases; however, some also claim that developed nations have also been becoming cleaner, and much more so than in the bleak Dickensian years of the early industrial revolution.[citation needed]

For immunological conditions related to Strachan's original version of the hygiene hypothesis, such as atopy and asthma, the pool chlorine hypothesis was proposed by Albert Bernard and his colleagues as an alternative hypothesis based on epidemiological evidence in 2003.[citation needed]

[edit] See also
Hookworm in therapy
Antibacterial soap
Helminthic therapy (includes more discussion of hygiene hypothesis)
Diseases of affluence
 
There are a total of 3 microscopic organisms used in treatment of a variety auto-immune diseases, in particular we are going to be discussing CD and UC here. There is nothing gross or disgusting about them. We have billions of bacteria living inside of us and we wouldn't be able to live very long without them. We humans lived with other organisms, including helminthic parasites, for millions of years and only started getting rid of them over the last 70-80 years in the developed world. Undeveloped countries (most of Africa and South America) still have them and Crohn's and Ulcerative Colitis are virtually unknown there. Granted, they have a host of other problems and diseases but they don't suffer from auto-immune illnesses. Balance is needed. Modern humans survived to this day because we evolved to have strong immune systems that could keep the number of parasitic organisms in our bodies very low. Those that couldn't, died out and we are descendants of those who survived. Parasitic organisms in turn tried to live as long as possible and since the immune system fight invaders using inflammatory response, they evolved to suppress this inflammation and kept our immune system in check. Now that we got rid of them, after evolving to live in a symbiotic relationship with them for millions of years, our immune systems go haywire and go into uncontrolled inflammatory responses. There has been a lot of research on helminthic therapy over the last few years. I am working on a wiki site on which I am posting articles from major medical journals. If you google "open source helminth therapy" and then click on the "Helminth Wiki", on the "Studies & Papers" on top there's a link to google docs repository of all these articles. Some are very heavy on immunology but are highly interesting.

The 3 organisms used are: 1. Trichuris suis ova (TSO) is produced by a German company Ovamed, and distributed by a Thailand company Biomonde. It costs a few thousand euro (I think about 3 or 4) for a 3 month supply. It's basically eggs (ova) of a pig parasite that can't live in humans for more than a couple of weeks. It's extremely safe and the remission rates in CD and UC are over 55% which is amazing. However, it needs to be taken every 2 weeks and the remission lasts only while you're taking them. Good but very expensive.



2. Necator Americanus (human hookworm) Here's the description of the lifecycle of this organism:

Eggs are passed in the stool , and under favorable conditions (moisture, warmth, shade), larvae hatch in 1 to 2 days. The released rhabditiform larvae grow in the feces and/or the soil , and after 5 to 10 days (and two molts) they become filariform (third-stage) larvae that are infective . These infective larvae can survive 3 to 4 weeks in favorable environmental conditions. On contact with the human host, the larvae penetrate the skin and are carried through the blood vessels to the heart and then to the lungs. They penetrate into the pulmonary alveoli, ascend the bronchial tree to the pharynx, and are swallowed . The larvae reach the small intestine, where they reside and mature into adults. Adult worms live in the lumen of the small intestine, where they attach to the intestinal wall with resultant blood loss by the host .



It's really not as scary as it sounds. I received a tiny vial with what appeared to be 3-4 drops of clear liquid. I applied it to a gauze which I affixed to the inside of my arm with a band-aid. A minor itch developed (Benadryl really helped a lot to get rid of it). A few small red dots were visible for a few days after I took off the band-aid 12 hours later. There was no cough, diarrhea, pain or any other symptoms or side effects.



It lives in people for 3-5 years, though there were documented cases when it was eliminated after 1 year or lived for over 7 years. It's very cheap as it's a one time application every few years and the therapy provider guarantees infection for 3 years and will provide additional doses if needed. So the costs is extremely low, only a couple of dollars a day. Remission rates for CD in the small intestine are over 85%. I hope you realize that's nothing short of a miracle to have such high cure rates for CD.



3. Trichuris trichiura (human whipworm) Lifecycle:



The unembryonated eggs are passed with the stool . In the soil, the eggs develop into a 2-cell stage, an advanced cleavage stage, and then they embryonate; eggs become infective in 15 to 30 days. After ingestion (soil-contaminated hands or food), the eggs hatch in the small intestine, and release larvae that mature and establish themselves as adults in the colon. The adult worms (approximately 4 cm in length) live in the cecum and ascending colon. The adult worms are fixed in that location, with the anterior portions threaded into the mucosa. The females begin to oviposit 60 to 70 days after infection. Female worms in the cecum shed between 3,000 and 20,000 eggs per day.



There's nothing gross about this. Helminthic therapy provider washes the ova in an anti-microbial and anti-biotic solution and they are provided suspended in a few milliliters of a buffer solution. Essentially, I drank half a cup of clear liquid that tasted like water. That was not disgusting at all and I am very thankful I did it since I am now in complete remission.



Remission rates from UC and Crohn's in the colon are over 85% - again, a miracle to have such high rates. Remission rates from a combined therapy of both hookworm and whipworm, and raising vitamin D levels to at least 50ng/ml are over 90%.

This is some more info from a member of another site that I found extremely compelling.
 
Wow! You've been busy!
Too much for me to read right now, but I'll certainly give it some time when I can.
Thanks.
 
I have also been researching this treatment since my diagnosis with Crohn's 8 years ago. Now that I have tried and failed all conventional treatments, with my condition deteriorating rapidly, now is the time for alternative treatments. I am applying for a Stem Cell Transplant with Dr. Burt at Northwestern University in Chicago, although I am not too keen on going through chemo. Ideally I would like to try helminthic therapy first, seeing as how the risks are menial when compared to the risks of aggressive therapies.

But alas, the US has quite a bug up it's @$$ (pun intended) when it comes to allowing helminthic therapy. You have to find a doctor to agree to treat you while using helminths and order the necessary labs to be sure you do not become anemic. I've asked quite a few doctors, they all look at me like I'm crazy. IF you are lucky enough to find a doctor willing to comply, you would still have to travel outside the United States to receive your treatments, and I'm not sure what the laws are in regards to carrying the helminths back into the States with you. This would be quite difficult for anyone to accomplish, much less a very sick person... And quite costly.

I truly wish I could give this a shot before subjecting my body to chemo... but living overseas for a few months while testing out the parasites just doesn't seem doable. But, if I don't get accepted for the Stem Cell Transplant trial, I will be trying helminth therapy, as it will be my only option left before having my intestines removed.

If anyone knows of any caveats, loopholes, or trials going on in the states- Please, do share!

Good luck to you all!
 
Thank you for your response. The article I read involved the whip-worm which is evidently a worm that is primarily found in pigs. In pigs they take off through breeding, but since the human body is different from a pigs body and thus foreign to the worm, they try and establish themselves and latch onto the inner wall of the intestine without being able to breed they soon die. the process usually takes a couple of weeks. During this time the human body creates the
T-2 cell to fight the invading parasites and people that suffer from auto-immune diseases seem to feel a bit better. This treatment seems to help with just about any kind of disease of the immune system. The article said this treatment could even possibly help those who suffer from Autism. I read that this treatment is currently in trials right now I just wish I knew where - sign me up. Ha-Ha

A company contacted me about participating in a clinical trial of the whipworm about a week or so ago. I go for my first appointment Tuesday (I have Crohn's Disease)......The company that mailed me a letter is called Acurian.....they have a toll-free number (877) 632-6527. Not sure if they have them where you live, but maybe they can direct you!!
 
I have also been researching this treatment since my diagnosis with Crohn's 8 years ago. Now that I have tried and failed all conventional treatments, with my condition deteriorating rapidly, now is the time for alternative treatments. I am applying for a Stem Cell Transplant with Dr. Burt at Northwestern University in Chicago, although I am not too keen on going through chemo. Ideally I would like to try helminthic therapy first, seeing as how the risks are menial when compared to the risks of aggressive therapies.

But alas, the US has quite a bug up it's @$$ (pun intended) when it comes to allowing helminthic therapy. You have to find a doctor to agree to treat you while using helminths and order the necessary labs to be sure you do not become anemic. I've asked quite a few doctors, they all look at me like I'm crazy. IF you are lucky enough to find a doctor willing to comply, you would still have to travel outside the United States to receive your treatments, and I'm not sure what the laws are in regards to carrying the helminths back into the States with you. This would be quite difficult for anyone to accomplish, much less a very sick person... And quite costly.

I truly wish I could give this a shot before subjecting my body to chemo... but living overseas for a few months while testing out the parasites just doesn't seem doable. But, if I don't get accepted for the Stem Cell Transplant trial, I will be trying helminth therapy, as it will be my only option left before having my intestines removed.

If anyone knows of any caveats, loopholes, or trials going on in the states- Please, do share!

Good luck to you all!

Not sure if you subscribe to responses to this, but here is what I posted to another person: A company contacted me about participating in a clinical trial of the whipworm about a week or so ago. I go for my first appointment Tuesday (I have Crohn's Disease)......The company that mailed me a letter is called Acurian.....they have a toll-free number (877) 632-6527. Not sure if they have them where you live, but maybe they can direct you!!

p.s. they pay for everything, labs, all tests, all visits and they even pay you for participating in the trial.....my letter says up to $1,385 bucks to participate! Maybe this is what you are looking for.....fingers crossed
 
Thank you, so much, for sharing! I will definitely contact them tomorrow. I've already gotten the ball rolling for the Stem Cell Transplant, but my first evaluation isn't until September 10, and it will still be months of insurance approval and tons of pretesting before the transplant even gets started. So needless to say, I need something in the meantime, or a plan B in case I don't get accepted or something goes wrong.

And the location is actually quite convenient because I have an Aunt living in Ann Arbor, MI. Not sure how far that is from where you are or where the trial is taking place, but it's still more accessible and more affordable than the Stem Cell Transplant ($175K!!!). So if my insurance won't cover it, it's not an option, obviously!

Once again, I cannot thank you enough for sharing this information! I tried looking up the company online and found this-https://www.acurian.com/clinicalstudies.html

Not sure if it's the right one, but they didn't have any trials for crohn's, only IBS. I filled out a questionnaire to see if I was eligible and it said I wasn't. I guess because the trial is for IBS, not Crohn's disease? I could have looked up a completely wrong website, who knows! But I will still call the number you gave tomorrow, Thanks again.
(PM if you have any additional details that may help me find the right website/company. having more blonde moments than usual lately!) :)
 
Silly me.....never even thought to post the website......I have more blonde moments than I care to admit most days......the website is Trust1Study dot com or you can also email them at trials@acurianhealth dot com

Good luck!!!
 
I heard some doctor in California does give the whipworm to IBD patients. I have no clue who it is or if it's legal for them to do so. I would be interested in trying it from a reputable source and not via the Internet or another country.
 
There's a great pro-con article on ABCnews dot com called "Allergy Desperation: I'll Take a Parasite, Please" from 2009 that is really an excellent overview of the hopes and concerns of the medical community about this therapy.

Anyway,there's nothing illegal about using the worm eggs - it's not considered a medical therapy so it's simply not regulated by the FDA, just like probiotics. There are ethial considerations that may give doctors pause - giving someone parasites does technically violate their oath to "do no harm"... however, there are several companies listed in the article that sell the parasites, one of the companies started by a guy seeking relief himself who was so desperate, he literally flew to Africa and walked barefoot around latrines to infect himself... but it worked.

Unfortunately the time and cost of clinical trials in the US is so onerous, it's going to be difficult to find a pharma company to invest tends of millions of dollars to certify and then create a set of manufacturing quality controls for a therapy that is not likely to produce enough revenue to cover their costs before it goes off-patent. Making pills from powders is easy - making vats of live parasites and packaging them for delivery is much more complex...
 
Actually, there are 3 pharmaceutical companies currently "manufacturing" the whipworm because it is not just being used for Crohn's disease, it is being used to treat ALL autoimmune diseases, such as multiple sclerosis, diabetes type I, autism, and even rheumatoid arthritis. The potential to make serious money is there because all of these diseases are prevalent in our country. The study group I posted is not just in Michigan.....I was told today that it is a National Study across many states, so if you are interested in checking it out, call the number I gave and they will tell you if they have one in your area. Also, if you are in the greater Detroit area, the research place I am going to NEEDS more people to participate. If anybody is interested, please let me know and I will give you their number directly. I had my first appointment today....they drew blood, did an EKG, asked a bunch of questions, gave me a container to collect a stool sample that I have to bring back to them and gave me a check for $125 bucks. I go back in 2 weeks after all of the tests results come back and will be given my first dose, which may or may not contain the whipworm ova. After a total of 12 weeks, beginning with today's appointment, I go into an open-label study where I will definitely be given the whipworm ova and this will continue for a period of two years. At that point, they are hoping they will be available as an "approved" treatment for Crohn's disease. The eggs are microscopic, so you will not see them, nor will you know if you drank them. It would be like going hiking and you come across a mountain spring.....you are dying of thirst so you cup your hand and drink the crystal clear mountain water........you probably just ingested multiple bacteria..........
 
@Kimm0913 - do you know what restrictions there are in terms of the current regimine for participants? e.g., do you have to stop all current treatments during the trials, or only biologics, etc.?

Good luck!
 
I was not asked to stop any of my medications at all. They did ask what meds I was on and to be honest, I have not been on any meds in the past 6 months because I had a reaction to just about everything known to the Crohn's world. The only meds I currently take are Loperamide, Lyrica, Tylenol #3 and a sleeping pill. I honestly do not know if any meds preclude you from the study, but if you call the number, they do a screening over the phone to see if you qualify for the study based on the way you answer the questions. Sorry I could not be of more help.......
 
Actually, there are 3 pharmaceutical companies currently "manufacturing" the whipworm because it is not just being used for Crohn's disease, it is being used to treat ALL autoimmune diseases, such as multiple sclerosis, diabetes type I, autism, and even rheumatoid arthritis. The potential to make serious money is there because all of these diseases are prevalent in our country. The study group I posted is not just in Michigan.....I was told today that it is a National Study across many states, so if you are interested in checking it out, call the number I gave and they will tell you if they have one in your area. Also, if you are in the greater Detroit area, the research place I am going to NEEDS more people to participate. If anybody is interested, please let me know and I will give you their number directly. I had my first appointment today....they drew blood, did an EKG, asked a bunch of questions, gave me a container to collect a stool sample that I have to bring back to them and gave me a check for $125 bucks. I go back in 2 weeks after all of the tests results come back and will be given my first dose, which may or may not contain the whipworm ova. After a total of 12 weeks, beginning with today's appointment, I go into an open-label study where I will definitely be given the whipworm ova and this will continue for a period of two years. At that point, they are hoping they will be available as an "approved" treatment for Crohn's disease. The eggs are microscopic, so you will not see them, nor will you know if you drank them. It would be like going hiking and you come across a mountain spring.....you are dying of thirst so you cup your hand and drink the crystal clear mountain water........you probably just ingested multiple bacteria..........

Is this a phase 1 clinical trial? If so, I fail to see how they could get FDA approval and be on the market in 2 years.
 
Actually, I believe it is in phase 2.......I do double blind for 12 weeks, then open label for up to 2 years.....because it is not a chemical compound like most drugs are, it does not require as many clinical trials as a synthetic drug. This is considered a homeopathic treatment rather than a prescription drug, so the FDA regulations are not as tight or as long.
 
There is another clinical trial recruiting participants in about 60 cities across the US. You can find more about it here: http://clinicaltrials.gov/ct2/show/NCT01576471, including contact information in each of the cities.

I heard about this therapy years ago when I was first diagnosed (2004) from a wonderful doctor, but it was virtually impossible to get the treatment and I didn't feel great about trying to do it on my own with no medical supervision. Happy to see there are some clinical trials happening. It seems like the adverse side effects are extremely mild, particularly compared to some of the drug treatments we currently have. So, for me at least, its worth a shot. I don't have huge expectations, but I'm willing to try anything low risk with a decent shot of helping.
 
Yes, this is the study I am doing......I was just contacted by a company contracted by them to participate......I go next week for my first "dose".....since it is double blind, I will not actually know if I am getting the worm ova or if it is a placebo.....at 12 weeks, it will be open label and I will 100% get it. I will keep you all posted with what happens with this.....
 
Hi Kimm0913! I am glad you are participating in this trial. I have just found out about this therapy and may be interested in doing it. I have a couple questions. I live about an hour from Detroit. Is the info. below who I would contact? Also, I have just started Remicade. Will this prohibit me from participating? I am anxiously awaiting to hear if this therapy helps you! Please keep us posted!!


Clinical Research Institute of Michigan, LLC Recruiting
Chesterfield, Michigan, United States, 48047
Contact: Aaron Ryder 586-598-3329 [email protected]
Principal Investigator: Ronald Fogel, MD
 
I sent a message to the local coinc running the trial. I might not be eligible based on the criteria but I'll try.
 

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