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Friday, November 3, 2017

Attention KRATOM and opiate USERS - A BIO HACK to reduce your tolerance

Agmatine Sulfate supplement can reduce your tolerance to opiate and opiate like pain medicine (Kratom).

I recently found Kratom was not working effectively as my tolerance required doses to increase over time from 8g to 15g per dose. When my third and or fourth dose of Kratom at 15g was not working anymore, I switched to Oxycontin and Ibuprofren for 7 days. On the 8th day it was time to switch back to Kratom.

I started the day with Agmatine Sulfate 1760mg on an empty stomach in the morning. Ceasing all Oxycontin intake I resumed Kratom therapy at just 8g per dose one half hour later. I has been 2 days and the Kratom is working again at this lowered dose. I take at least one additional 890mg dose of Agmatine later that day, on the second day (and every second day) this becomes two doses for an additional 1760mg.

I am pleasantly surprised. More related information and references below for those interested:

Effects of Agmatine on tolerance to and substance dependence on morphine in mice.


Agmatine reverses pain induced by inflammation, neuropathy, and spinal cord injury


How to take Agmatine

Agmatine is a metabolite of L-Arginine, but acts very differently. Do not take with L-Arganine.

Also dont take Agmatine with Yohimbe since Yohimbe deactivates the a2 adreneric receptors, whereas Agmatine activates/binds to that same receptor.

It shows promise for alleviating neuropathic pain and drug addiction but without opiate use has been known to increase perceived pain. Agmatine supplementation can also protect from strokes and benefit cognitive health.


Monday, July 3, 2017

Pleomorphism and Yellow Colloidal Silver a Radical Solution

A wealth of information has been coming in as of late and I believe it is a direct result of me challenging the universe and asking the question "Why have I received the knowledge that I have acquired so late? Can I please have the knowledge disseminated to me in an accelerated fashion."

This prayer was answered and information continues to pour in. This information is challenging all of my existing paradigms that I have come to learn, but only because I remain open to the possibilities.

Much of the knowledge that we have acquired has been manipulated to be upside down and backwards. The internet allows us a glimpse into knowledge and truths that we may not have otherwise been exposed to. Before this information we had to blindly trust people in positions of authority. Doctors included.

Now the potential exists that we might actually break the chains that have been placed on us and rethink the existing paradigms.

This has led many to question even the shape of the earth and although we wont address this here, it goes to show we are living in fascinating times that would have us questioning everything we have ever learned.    

Although I am still of the globe earth model I admit I do not know, but I am more interested in information that I can use and apply to my life. I now realize I must approach everything with the untainted curiosity of a child and assume nothing.

I can no longer take anything for granted.

I recently came across a theory in orthobiology that is at least 60 years old, but has been experiencing  a modern resurgence. So much so that a microscope retailer has begun selling microscopes which incorporate an ultraviolet light. This allow for otherwise unseen particles to be seen.

When using this equipment you can witness amazing transformations that pull the rug out from under conventional and accepted theories of modern medicine.

Modern medicine, bacteriology, is founded on the idea of Mono-morphism. This currently accepted germ theory believes that once a germ is a particular germ it always stays that way.

According to this way of thinking a streptococcal germ is always a streptococcus. It only has one (mono-) form, it doesn't change into anything else.

Pleomorphism on the other hand maintains that "germs" occur in many forms beginning with the Protit, which can change into a virus, which can then change into a bacteria, which can also then change into a fungus.

Any of these forms, bacterial, viral or fungal can and do eventually, break all apart, and turn back into the Protits from whence they came. It starts all over again, life. The Protit never dies.  

It has been observed that when blood pH is 7.4 and above that pathogenic bacteria will not inhabit the body. The implications are astounding. If this is in fact true and seeing is believing then everything we think we know about disease must be rethought. Take a look here:

If that wasn't enough to swallow there is also a powerful new treatment option that has been brought to my attention.

Yellow Colloidal Silver is toxic to ingest but appears it can be beneficial if used correctly.

I cannot tell you that this is completely safe. You will have to do your own research.

People with radical diseases are often looking for unconventional radical solutions which I will blog about as I come across them. 

Apparently it can be used under the tongue and then spit out as well as introduced in other ways without ingesting.

The following is a quote from a gentleman named Normand Boivin who brought this substance to my attention shows how to make it in a video linked below. He states:

" Most of you have learned about colloidal silver, now all you need is a simple recipe to produce it for yourself !

I am here to help people to make their own anti virus and anti bacteria medication

This is my recipe to produce yellow ionic colloidal silver Ag+, silver atoms positively ionized can go deeply in the body for example in the nerves, antibiotic can't go there.

That's also better than silver oxide AgO2, this molecule is much bigger than ionic yellow colloidal silver Ag+.

Since 6 years i got the Lyme disease and i have no more symptoms, i can return to normal life !

Share this video at large so every one can make it in the kitchen.

Medical science discovered it half a century ago and it really look like an universal panacea killing viruses and bacteria. "

Stay tuned and I will make you aware of all of the cutting edge information I come across so that you can do your own research.

Tuesday, June 13, 2017


 I woke yesterday with what I call a yeast headache which is commonly located right above the right eye in the center of the brow. In my continuous research the timing of finding the following study couldn't have been more appropriate.

 I decided to add Aspirin to follow my 400mg dose of Fluconazole. Since it has upset my stomach in the past, I started with half a 325mg dose.

 Some improvement led me to adding in the other half and this worked so well that I have added it to my protocol. These headaches often lasted for up to 3 days.

 What appears beneath the link below are excerpts from the same article which discusses Aspirin, NSAIDS, and their antifungal, antibiofilm activity in detail.

Aspirin, one of the oldest and most widely used anti-inflammatory drugs, also dramatically decreases biofilm formation by C. albicans. Moreover, some aspirin concentrations (50 to 200 μM) producing significant levels of antibiofilm activity in vitro fall within the range of those frequently achieved by therapeutic doses of aspirin in humans

Aspirin, whose antifungal properties have been reported previously (9), drastically reduced the viability of planktonic cells

For example, addition of aspirin to relatively mature, 24-h biofilms reduced their metabolic activity at 48 h by over 80%

In a further series of experiments, mature, 48-h biofilms grown in the absence of aspirin were transferred to fresh growth medium containing different concentrations of the drug and incubated for further periods of 5 to 48 h. All of the aspirin concentrations tested (75 μM to 1 mM) significantly inhibited biofilm activity after 16 h (Table ​(Table3).3). After 48 h of additional incubation, biofilm activity was reduced by 20 to 80%. Moreover, physiological concentrations of the drug (75 to 200 μM) reduced biofilm activity by 20 to 80%, suggesting that aspirin could have a significant inhibitory effect on mature biofilms in vivo.

Aspirin (acetylsalicylic acid) has a short half-life in circulating blood (about 20 min) and is rapidly deacetylated to form salicylic acid in vivo (34). Sodium salicylate and related compounds such as aspirin are known to have a variety of effects on microorganisms. Growth of certain bacteria in the presence of salicylate can induce multiple resistance to antibiotics. Paradoxically, it can also reduce resistance to some antibiotics

The activities of antifungal agents can also be affected by salicylate. A combination of fluconazole with either sodium salicylate or ibuprofen results in synergistic activity against C. albicans

Some strains of S. epidermidis secrete mucoid extracellular polymers (polysaccharides, proteins, and teichoic acid) that promote biofilm formation and become important components of the biofilm matrix. Salicylate can inhibit the production of some of these components by as much as 95%

Aspirin and etodolac also significantly reduced the viability of biofilm cells. Indeed, aspirin appears to show an even greater effect on viability than on biofilm formation; presumably, aspirin-treated biofilm cells are largely incapable of cell division but still retain some metabolic activity

Aspirin reduced biofilm formation substantially, as determined by quantitative measurements, but in areas of the catheter disks where biofilms could be observed, large numbers of yeasts and hyphae were present, just as in untreated controls. However, examination of the cells at higher magnification revealed that aspirin-treated fungi had very wrinkled surfaces

Sunday, June 11, 2017

Submitting Specimens to CDC for Diagnostic Assistance

DPDx is a Web site developed and maintained by CDC's Division of Parasitic Diseases and Malaria (DPDM) that uses the Internet to assist laboratorians and pathologists in the diagnosis of parasitic diseases, both in the United States and abroad.


PLEASE NOTE: Effective immediately, the DPDx Team will require a CDC 50.34 submission form to be filled out and submitted with images for diagnostic assistance in order to generate a formal, written laboratory report.  This form must be submitted in a secure method to protect patient information. 

The CDC has a Sharefile system that should be used to submit the form and images.  Please email the DPDx Team to request a one-time link to the Sharefile server to submit a case for diagnostic assistance. 

The Team will include a CDC CSID number for the case in the subject line when they email the link and that number will be used for any subsequent correspondence (when necessary). The following steps describe the submission process:
  • Send an email requesting diagnostic assistance to  DO NOT include patient identifiers or images in the email requesting diagnostic assistance.
  • The DPDx team will respond by email with a CDC Sharefile link, open this link in your browser.
  • Upload your case images and CDC 50.34 submission form.  Other supporting documents and communications such as questions, etc. can also be uploaded as word or text files.
  • The DPDx team will receive notification once the files are uploaded and will respond via email with a preliminary diagnosis using the CDC CSID number assigned. 
  • An official, final diagnosis will be generated only if the CDC 50.34 is submitted.
If the electronic communication system of your institution is incompatible with using the web-based CDC Sharefile, the form should be printed and faxed to (country code +1) 404-718-4195, attn: DPDx Team, or submitted using your institution’s own web-based secure file sharing system, unless the CDC IT Security Team detects that it does not meet HHS requirements for patient data transfer. The images may be submitted by email; however the file name of the images should not include patient identifiers.

To access the most recent form (CDC 50.34), please click here.
This assistance is free of charge (except for U.S. Federal agencies and the U.S. military). If you have an urgent case, please do not delay case management and treatment.

 Please do not include patient identifiers (P.I.) in email inquiries.
Please send your diagnostic request to

Wednesday, June 7, 2017

Oral Spirochete Bacteria must be dealt with

The following statements are collections from around the internet in dealing with Oral Spirochete bacteria and novel ways of dealing with implant infection. It is believed by some that this is the origin point of Lyme Disease as well as source of relapse.

The author believes this is at minimum a source of Lyme disease relapse potential and must be dealt with. I am open to suggestion on additional methods verified or not in the comments, so please follow, comment. and subscribe. 

None of these statements have been verified and do not necessarily reflect my opinion. Not intended to treat or cure any disease. Some statements offer differing opinion and may conflict. Some deletions and elaborations in parenthesis have been made where the author disagrees with the opinion expressed (albeit of minor importance to the message).

So why put this information here? The importance of attention and research into this area is paramount.

Also implants and root canals cause artificial areas which are not directly connected to the blood supply, therefore antibiotics and other ingested treatments cannot reach into these gaps.

An alternate possible way to treat infected implants is by using a current as outlined here:  

Video description:

"A diseased mouth infected with spirochetes. 90% of our patients are infected with these creatures which are able to do remarkable things.

Lyme disease and syphilis both very debilitating illnesses are cause by a spirochete.

Why had dentistry chosen to think of the sulcus as a unique habitat somehow divorced from the body?

These spirochetes are microscopically indistinguishable from syphilis or Lyme disease spirochetes. Oral spirochetes have been found in the brains of Alzheimer's patients.

We believe that oral spirochetes are the primary injurious agent in two other chronic diseases that plague man, heart disease and diabetes.

These things breed by the trillions in the gingival sulcus and invade into the body by millions moving via the de-epitheliazed gingival sulcus into the blood stream then into cells found along the blood stream. Primarily the endothelial cells lining blood vessels, and the Islets of langerhans cells in the pancreas.

We have not seen anyone with heart disease or diabetes who are not infected with oral spirochetes. Recent papers have proven the Alzheimer's plaques are created by these spirochetes which breed in the crevice between the tooth and the gum and under plaque bacteria.

The use of tooth cleaning agents will not remove these spirochetes. The only effective methods we have found is Dakins solution. Vigorous rinses for at least two minutes with Dakins or Dakins in a WaterPic®.

The use of the Dakins which is a 20:1 dilution of Clorox bleach is by far the most effective technique for killing spirochetes in between the teeth as well as the more accessible areas.

Brushing and flossing is not enough. Spirochetes form spores which require daily disinfection of the crevice between the tooth and gum.

One thing which will dissolve plaque(the vegetative bacteria which cause tooth decay) off a tooth surface without friction is Clorox diluted in water at a 20:1 water/Clorox ratio.

This material is cheap effective and absolutely works but no one can sell it to you for a high price, so not one cent of marketing money will be spent to educate the public!

This is tragic in the extreme. We have research grade microscopes to show the spirochetes.

The only effective techniques involve using bactericidal materials such as Clorox and high concentrations of baking soda... Other things such as hydrogen peroxide, povidone iodine, chlorhexidiene, and table salt have drawbacks in daily use.

 Tooth pastes are valuable in stopping and treating tooth decay (I recommend glycerin free toothpaste with no Fluoride such as Earthpaste as well as frequent Xylitol use), but flossing and brushing with tooth paste or oral rinses with items such as OTC mouth washes, will not guarantee a kill, and in comparison to Clorox are very expensive over a lifetime.

Patients wonder if Clorox is toxic. While it tastes terrible, it is harmless when diluted to 0.3 percent, that is a 20:1 dilution of 6% Clorox. Clorox turns into
table salt in the stomach if swallowed (unverified statement). 

There will be some initial stinging of the skin in the mouth when first used! That goes away when the skin heals after a few uses. Use at night before going to bed and do not rinse the mouth after.

If irritation develops move to mornings. Use at night when saliva flow shuts down will keep the material killing for a longer time when not rinsed out..

Finally, we have tried them all and brushing with copious amounts of baking soda forcing it into the gums and in between the teeth one time daily and then using a WaterPic® with the dilute Clorox solution will give the best results.

What are those results? Absolutely no leakage of the seal where the tooth come out of the skin. The Gum is a specialized tissue designed to seal the skeleton where it come out thru the skin.

The teeth are the only part of the skeleton which is out side the skin... So it cannot heal itself.

Never eating sugar or carbohydrates between meals will assure no tooth decay in those with normal saliva."

Second Video description: - "Spirochete Killer William D Nordquist searches to find a compound to kill oral spirochetes in the plaque in the gingival sulcus (the pocket round teeth) colloidal silver, Betadine (iodine), and discovers 25% bleach solutions were used unsuccessfully.

A surprisingly simple food with a combination of eight natural herbs turned
out to be a potent spirochete killer (unfortunately not detailed in the video.)

The purpose of the search was to find a substance that would kill the spirochetes in gingivitis and periodontitis before a dental cleaning.

This would prevent dangerous bacteremias caused by dentists cleaning. Research has shown that bacteremias cause damage to the blood vessel lining that takes time to return to normal."

A person in another related video mentions: "Good video, I will make a link to this. I advise to take borega-complex it is helping in just 4-6 weeks a whole cure is 12 weeks. In all cases 100% result, not only by own experiences but also shown by the LTT."

Periodontal Disease and its Relationship to Systemic Disease   - view it here (2hours in detail) for those who wish to gain a greater understanding of the problem:
 Video description:

          " Periodontal Disease and its Relationship to Systemic Disease has recently come to be one of the most important topics in medicine. This video was made for physicians and detists who treat chronic inflammatory autoimmune diseases. "

My notes taken:

Samples collected from molar

Spores survive antibiotics, cysts 1 micron

These spirochetes are anaerobes

Vita D may further suppress immune system upon body's conversion. I am experimenting with sunlight.

Oral spirochetes cause bone loss, cause implants to fail, potential to migrate
Chemical irrigation water pick hipocleanse or bleach see Dakins solution.

Debridement and CO2 laser for high populations vaporizes and cauterizes gingival sulcus (GS).

Tip of laser guide will clog and needs to be cleared by an experienced dentist.

Periodontal disease populates epithelial cells (loaded with spirochete) in GS.

Bleeding points and probing cause bacteremias so antibiotics are used. Flagyl and Amoxicillin started 2 weeks before treatment. (I believe Tinidazole is superior to Flagyl).

Brushing and flossing not enough.

How to make Dakins solution. see

Some other possible methods for controlling bacteria in the mouth may be through oil pulling as outlined below. We do not know how oral spirochetes react to said methods.

If you can oil pull with ozonated coconut oil this would be a superior substitution to the method in the link below. Wheat grass has also been used effectively by those who cannot stand the taste of coconut oil. I have used Xylitol to fend off an impending dental infection.  

Thursday, May 18, 2017

Studies on Fungal ParMicrosporidiosisasites Worth Noting (Dynamic Page)

 As we go forth in this brave new world of ours, we are discovering new infective agents responsible for emerging disease as in the case of Funnelilformis Mosseae a fungus that until April of 2017 had only been recorded as affecting plant species.

 Last month in PubMed, a leading resource for clinical trials, we discover that todays Funinilformis has the ability to infect humans.

 I did a short video on this which links to the study in the description

 It is important going forward that we pay attention to treatments with regards to fungal infections and other species of parasites as there are few promising drugs in the pipeline and there will be more emerging disease if the theories on genetically modified organisms being the causative agent are correct.

 I hope to make this a dynamic page that will continuously update as I locate any studies of importance. You may wish to bookmark or RSS this page now as this will perpetually grow as I locate studies with focus on all species of parasites.

 I fear we will have to devise our own treatments ahead of the pace in which big pharma provides the doctors with their continuing education. These studies may be key in helping you to finding what works when nothing else does.

 I think we need to pay special attention to the additional fungal infections that patients with HIV are susceptible to as these reflect what a weakened immune system is capable of contracting, so don't discount them solely because you don't have HIV.

 Remember Funnelilformis now affecting humans suggests that the former laws and paradigms may no longer apply.


 Effect of myrrh and thyme on Trichinella spiralis enteral and parenteral phases with inducible nitric oxide expression in mice

Analysis of the Beta-Tubulin Gene and morphological changes of the Microsporidium Anncaliia algerae both Suggest Albendazole Sensitivity 

Electron microscopic changes in Enterocytozoon bieneusi following treatment with albendazole. (HIV)

Microsporidia infection of the cornea--a unique and challenging disease.

Infectious Diseases Articles

Saturday, May 13, 2017

MOLD, LYME, MORGELLONS - What you should be doing NOW

There are a lot of things you should be doing as I can attest these diseases are all closely related.

The only difference is how many coinfections do you have with your illness. If you are at the stage of visible parasites or relapsing bacterial infections you will need anthelmintic medication.

See my Ivermectin video at ClintFromNYtoVA channel on 

More videos are on the way as well as blog posts.

We are going to talk about why I use certain items and don't use other items mentioned on the internet. Half of the stuff on the internet is wrong.

We are going to break them all down one by one in the future so follow this blog. Follow my work and you will find the answers.

You can start a few things right away, and eliminate others.

No sugar, no bread, limit dairy to unsweetened yogurt, no processed foods or quick carbs.

Nascent Iodine is very useful but NOT with thyroid meds. 1mg per day, incrementing slowly to a max of 20mg. Go slow. Take it on an empty stomach and then eat a fatty meal (I eat avocado) 30 minutes later.

SSKI is a potential huge mistake waiting to happen.

Make sure you are on a multivitamin, multi-mineral supplement, but know this is not enough.

800mg loading dose Fluconazole (FLZ) then 400 mg daily. I take it with Doxycycline (Doxy) 200mg twice daily and Biaxin 500 mg twice daily. I take my Doxy on an empty stomach so 90% is absorbed. I am also rotating anthelmintics and DEC.

Nystatin is useful.

I get my meds from several Indian Pharmacies. If you contact me I can tell you where to get from the source that I do for less if you do not have insurance or a willing doctor.

Biofilms are tricky, If you are not attacking the bacteria, you should NOT be using enzymes to battle biofilms. If you are on antibiotics why aren't you on Enzymes? Nattokinase, Serrapeptase, Bromelain on empty stomach on wake.

If you use antibiotics and you aren't on 3 different types, ask why, and prepare to find a new doctor. You must add probiotics to your diet daily with food.

Magnesium is essential if your are inflamed. A pinch of Epsom Salt in each liter of water helps inflammation. Less is more. FIND your tolerance. REVISION: as much as Epsom Salts helped me to determine how quickly magnesium would help me, Trans dermal Magnesium Chloride would be the better way to go and does not interfere with medications.

 5000mg Flax seed oil daily if you are inflamed. 4000mg Modified Citrus Pectin daily for at least 2 months.

Increase zinc substantially but slowly if you find yourself urinating frequently all of the time. Increase copper but take it 12 hours after zinc. Selenium, D3, K2 every other day. REVISION: In light of new evidence against D3 supplementation for the immunocompromised, I am no longer recommending it. Minimize calcium and dairy.

4000mg Monolaurin. Eat everything coconut and coconut oil is good for skin also but messy.

The 'bugs' eat your manganese and deplete your zinc and copper. If you starve yourself of minerals you get sicker and thing begin to fail in your system. Plus they move on to their second favorite mineral anyways and so on.

Boost your minerals and gut flora with resistant starches and powdered vegetables. Look it up or wait for my segment on it. 

Half the stuff on the internet is wrong and it all depends on your co-infections. The internet tends to generalize as do people who should know better.

If you cant afford the Fluconazole get Xylitol which I call the poor man's Fluconazole. BUILD your tolerance slowly.

If anything makes you herx, back it off, if anything gives you diarrhea reduce it the amount but don't stop these things.

You didn't get sick in one day. This has been happening for some time, you just didn't know what was happening until it got out of hand.

I know you are angry but your health cannot afford to be as stress and worry only make it worse. Stay tuned. Stay Calm.

Thursday, May 11, 2017

Notes from Dr. S. Fry Conference in San Francisco Spring 2017

Dr. S. Fry Conference in San Francisco Spring 2017

If you would like a copy of the slides from this presentation please send me your email to 
Put FRY SHARE in the Subject Line and I will provide you with a link to download this. Your email must be correct to get access.

For a limited time only.

Tuesday, May 9, 2017

GMO. Taking the Focus off of Food for a Better Understanding of Our Barve New World.of Emerging Disease

When GMO is mentioned people generally think food. This is the first error in understanding the scope of the problem and connection to emerging disease.

The Organisms are what you need to be concerned with. The practice of deploying these GM Organisms in agricultural pest control has been widespread and overt for some time.

It is unregulated and experimental. Yet the focus is intentionally misdirected toward food and away from the imminent danger.

We are beginning to see evidence of creatures that shouldn't ever have come into existence in nature and their direct links to chronic illness.

Cross species modification and the horizontal gene transfers that these organisms are capable of are the genesis for today's emerging diseases which resemble and include

Lyme Disease is frequently misdiagnosed as CFS and Fibromyalgia. Its common co-infections such as Bartonella are evolving faster than available testing.

If you have long red streaks that appear like scratch marks on the skin, crazy uncomfortable eye symptoms you could be infected with an emerging disease often overlooked.

There are now over 40 species of potentially infectious Bartonella bacteria:

Lyme Books less than 6 months old state that there are 23 species. This bacteria is evolving rapidly and is a common co-infection in Lyme disease.

Standard testing for Bartonella infection is available for only 2 species. You could easily test negative and have this disease.

Scientist will throw the words 'discovery' and 'evolution' around to make it seem that these organisms have always existed. Our technology as limited as it may be, has been a bit too advanced for some time for oversight to be probable.
Living beings have 'evolved' rapidly in the last 30 years. The timing of which is not at all coincidental but correlated.

Disease agents that were once confined to singular kingdoms are now infecting others. Funneliformis mosseae was a fungus that only affected plants until recently. The first recorded cases of human infection were published in April of 2017 in medical journals.


Evidence for polymicrobial communities in explanted vascular filters and atheroma debris.


"The main contributing prokaryotic species in atheroma debris suggest a diverse and novel composition...
Additionally, Funneliformis mosseae, ... was detected in the coronary hard plaque from two patients

Today's form of this fungus posses mixed DNA which led to it initially being mistaken for a protist organism on first 'discovery' by people who should know better.

Mixed species do not have offspring and should NOT exist.

Yet this genie is now out of the bottle and this cannot be undone. The industries responsible will be not be held accountable without the people demanding it. The people cannot demand for something they vaguely understand.

The consequences are widespread emerging disease and there are not enough effective pharmaceuticals in the pipeline to assist. It has never been more important to keep your immune system healthy than it is today.

Monday, April 17, 2017

DNA Transfer and Emerging Infectious Disease.

I believe there may be a correlation to the emergence of new infectious diseases to the time period where cross species modification has become so common place. It is occurring on a large scale today.

The following scientific article postulates that we now have more than 100 different genes from different species, even kingdoms if you will, yet alludes that evolution is responsible.

If evolution is responsible then why have humans evolved so quickly in the last 3 decades?

Is it possible that there has been cross species contamination resulting in new infectious diseases?

It seems there is a great deal of skepticism with regards to this topic.

I doubt emerging infectious diseases of the last 3 decades would have occured had we limited genetic modification to the same species.

We have delicious and healthy bananas because of genetic modification within the species.

It is the practice of multiple cross species modifications that concerns me and its not just happening in salmon.

It being performed across bacteria, nematodes, fungi, et al, that are used in crop pest control across a wide range of unregulated products. 

Agrobacterium and bartonella were once two of a very small number of bacteria that were capable of horizontal gene transfer. Now there are many more.

As we become more plant like, insect like, fungus like, etc., it opens up the possibility that we become affected by pathogens that used to be limited to just plants and insects.

Any diseases which resulted from these actions would be by default an emerging infection.

I dont believe that nature or evolution is responsible for these new forms of organisms with DNA that have become so genetically complex.

Conjugative DNA transfer into human cells by the VirB/VirD4 type IV secretion system of the bacterial pathogen Bartonella henselae.

This was a recognized potential for concern for some time now.

Health Considerations Regarding Horizontal Transfer of Microbial Transgenes Present in Genetically Modified Crops (2005):

Genomic changes associated with the evolutionary transition of an insect gut symbiont into a blood-borne pathogen (2017):

Vertical transmission of Bartonella schoenbuchensis in Lipoptena cervi

What is it regarding expanding horizontal and vertical gene transfers connection to emerging diseases that makes it so difficult to comprehend? Or is it just too scary a topic to consider?

More importantly if cross contamination of genes is responsible for emerging infectious diseases, is there anything that can be done to contain it?

No, there is no way to put that genie back into the bottle so they will just continue to scramble for new drugs and when they find them you might get treatment. The problem is that they are not finding drugs that work at all.

And the emerging infectious diseases beat plays on....

Friday, March 24, 2017

Chronic Morgellons Scalp gets a medically recognized name.

If you discount the alluded racial bias, this sounds like a part of what we have come to know as the scalp breakout condition common to Morgellons and it has a name!

The article I reference below is from a medical journal and states the alopecia (hair loss) as

I am slowing hair loss dramatically and my scalp conditions have resolved. 

The similarities described in the condition outlined below are stikingly familiar to those experiencing symptoms of Morgellon scalp.

Maybe these conditions are not one in the same but I've bolded the similarities to what Morgellons sufferers go through.

Here's where it gets really cool:

Newer pathologic hair findings include: pigmented casts,black dots, and "3D" yellow dots . Newer associations include: keratitis-ichthyosis-deafness syndrome, Crohn disease and pyoderma gangrenosum. Older associations include arthritis and keratitis.

Are you ready for the name?

Say the following 5 times quickly:

Folliculitis et perifolliculitis capitis abscedens et suffodiens

"Folliculitis et perifolliculitis capitis abscedens et suffodiens is a rare disease of unknown etiology. It is a suppurative process that involves the scalp, eventually resulting in extensive scarring and irreversible alopecia. The condition is also known as ‘acne necrotica miliaris’ or ‘Proprionibacterium’ folliculitis...

The clinical picture is determined by fluctuating painful fistule-forming conglomerates of abscesses in the region of the occipital scalp. 

The cause of scalp folliculitis is not well understood. It is generally considered to be an inflammatory reaction to components of the hair follicle, particularly the micro-organisms.

These include: bacteria (especially Propionibacterium acnes, but in severe cases, also Staphylococcus aureus), Yeasts (Malassezia species) and mites (Demodex folliculorum).

The initial histopathologic finding is an exclusively neutrophilic infiltration followed by a granulomatous infiltrate. The treatment of the disease is usually difficult and often disappointing.....

The main reason is considered to be the disordered keratinization and further occlusion and accumulation of keratin at the hair follicle.

After a dilatation followed by rupture, not only a granulomatous inflammatory process accompanied by the attraction of gigantic cells, partially phagocyting the keratin masses are induced in the hair follicle, but also an inflammatory bacterial process derived from a superinfection, most frequently caused by Staphylococcus aureus and Staphylococcus epidermidis, which are considered to be the main factors in the chemotaxis of neutrophils."

Now for the treatment (not cure) and its a doozy....

"Successful treatment with Isotretinoin 1 mg/kg body mass could be achieved only after regular systematic administration in the course of 3–4 months.

Eruptive purulent form of the disease, has been controlled with combination therapy: systemic antibiosis with metronidazole and clindamycin, dermatosurgical removal of single nodular formations, and isotretinoin 1 mg/kg body mass for 3–5 months."

I will be honest, the treatment sounds almost as bad as the condition.

Plus this is similar to just one aspect of Morgellons.

Many with the Morgellons condition experience healing in the scalp afterward a short period of time and treatment with antifungals and antihelmintic drugs. 

There's also a cancer scare statement contained within this documented scalp condition so be prepared. It could be suggested at any time by your doctor that you should treat with chemo and radiation. Dont fall for it. We all should know better by now.

At least we have a starting point and a name (holy heck and how) and medical journal references.

You can bring it to your doctor and see if he can pronounce it.

Be prepared for the doctor to place emphasis on the disease affecting men of African-American or African-Caribbean descent.
So you may have to bring the second article that indicates other races.


Here it acknowledges "but the condition also has been reported in other races and in women. "

And one for good luck...


The drug used to treat the condition, Isotretinoin, sounds like a weaponized modification of Vitamin A.

"Isotretinoin is available only from a certified pharmacy under a special program called iPLEDGE. You must be registered in the program and understand the risks and benefits of taking this medicine.

It is dangerous to try and purchase isotretinoin on the Internet or from vendors outside of the United States.

Isotretinoin in just a single dose can cause severe birth defects or death of a baby. Never use this medicine if you are pregnant or may become pregnant."


Newer treatments reported include tumor necrosis factor blockers (TNFB), quinolones, macrolide antibiotics, rifampin, alitretinoin, metronidazole, and high dose zinc sulphate (135-220 mg TID). Isotretinoin seems to provide the best chance at remission, but the number of reports is small, dosing schedules variable, and the long term follow up beyond a year is negligible; treatment failures have been reported. TNFB can succeed when isotretinoin fails, either as monotherapy, or as a bridge to aggressive surgical treatment, but long term data is lacking. Non-medical therapies noted in the last decade include: the 1064 nm laser, ALA-PDT, and modern external beam radiation therapy . Studies that span more than 1 year are lacking.


So is this an accurate depiction of what happens to the scalp of Morgellons sufferers? Post your assessment in the comment 


What to do immediately if you experience an episode of Morgellons Scalp?  

Discontinue all sugar, and carbs (including bread and pasta) for 3 days. Keep track of how you respond to this diet change. If there is improvement, it can rule out certain possibilities and shed light on what is causing your symptom and eliminate some possibilities.

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Mold, Lyme, and Morgellons The Subtle Differences. Therapy Options (Part one - 10 pass ozone)

Lyme is defined by Borellia bacteria infection. Co-infections are everything else that come with it. Borellia can originate from many vectors not just ticks as we have been led to believe. Left untreated it often soon becomes accompanied by co-infections that include several other bacteria which we will discuss in future writings.

Morgellons, remains unrecognized by the medical establishment so many doctors act as if it does not exist. It is comparable to Lyme on steroids with a nasty twist.

In both cases a Lyme Literate Medical Doctor (LLMD) will be your best chance at getting medical treatment. When dealing with any doctor try to avoid being the first one to use the word 'Morgellons'. Approach your condition as Lyme with additional symptoms. Stick to the symptoms and avoid speculation of what you think it is or repeating what you've read on the internet.

Some have been labeled delusional by doctors and once this appears on your medical record, each doctor that follows will see this diagnosis and may be biased.

Here is a good resource to help you find a doctor willing to assist: 

But what about mold sickness? The following is information on the tests to request alongside additional resources:

As I stated in an earlier post, a few years ago I moved to (The Republic of) Panama from Virginia. I now find myself living in an area where there is no Lyme and there are no LLMDs. At the start of it all, I attempted to get medical assistance but I was told I am fine and there is nothing wrong with the exception of allergies. I was given a prescription for three different eye drops. What an excellent pharmaceutical salesman that doctor was!

Mold Sickness and Morgellons both are accompanied by sensations of crawling, stinging, or biting. Often you see nothing but would swear something just bit or stung you. Lyme victims often lack this symptom.

Mold can cause a flat red lesion about the size of a dime with a dot in the middle. It appears somewhere isolated on the body. Unlike an insect bite which is often raised, the resulting macular lesion is not raised. It takes weeks longer to resolve than an insect bite and may or may not itch. Just as it finally heals another may appear somewhere else on the body.

Lyme has been stereotyped with an erythema migrans rash as pictured in the next link below. It is nicknamed the 'bulls eye' rash but it doesnt always look like a bulls eye and varies in size.

The rash can vary in size but heals from the center towards the edges, referred to as central clearing. About half of Lyme victims do not notice any rash.

A Lyme co-infection named Bartonella will cause a rash with long wide streaks to appear in a vertical or horizontal pattern. These marks appear like scratch marks but the 'streaks' can appear almost instantaneously.

"There are currently over 40 documented species of Bartonella, identified as causing human diseases—including cat scratch disease; Carrion’s disease; trench fever; endocarditis; bacteremia; myocarditis; bacillary angiomatosis; and various ocular diseases

Clinical signs and symptoms of infection vary widely depending on both the specific tissue infected and the immune status of the host. Bartonella henselae is the most common ocular pathogen, although B. quintana, B. grahamii and B. elizabethae infections each have been reported to infect the eye."
Mold is a fungus. In Spanish they do not distinguish from mold, mildew, fungus, ringworm, yeast, candida, or even edible mushrooms. It is all called 'hongos'.

There are certain molds that exist in yeast form at body temperature. These are known as dimorphic fungi as they can exist in different forms depending on the temperature of their environment. These are adaptable and some are pathogenic to humans.

Dimorphic fungi comprised of known and yet to be classified type play a central role in Morgellons. 

Researchers are often confused by the undocumented DNA sequences being discovered in fungi today. Upon closer examination, they contain DNA resembling multiple types of organisms.

These are difficult to classify as they can have characteristics of a protozoa with parts resembling yeast and other organisms.  

Below is a link to an interview with Dr. S. Fry describing a new organism, protomyxzoa rhematica, with mixed species traits as "similar to malaria, similar to babesiosis, even more complex genetically, sort of in between a helminth [parasitic worm] and a protozoan."

I am confident that more will emerge going forward.

The fungus like growth attracts fungi consuming insects which will bite you. You may find multiple types of insects taking an interest in you. After all you smell like food. The bite from an infected insect injects bacteria and microscopic nematode larvae just under the skin.

A healthy immune system can respond to the invaders where a Mold Sick individual will be unable to.

Treat insect bites as soon as possible to prevent larvae maturation and dissemination. Place a generous dab of antibiotic ointment on the bite area about the size of and thickness of a dime. Loosely cover it with a band aid so the ointment doesn't get wiped away, but leave space for the ointment to bulge a bit.

Continue to do this and try to keep ointment atop it for at least 24 hours consecutively. Reapply ointment as needed to keep a layer on the bite with new band-aids as needed. 

In a pinch where you have no antibiotic ointment, you can wipe the area with alcohol and then dab some petroleum jelly.

The idea is to cause any microscopic nematode larvae introduced under the skin to surface seeking oxygen. They then get coated in ointment, suffocate, and die.

Untreated the larvae mature, reproduce, disseminate, and create additional bacteria. Each type of larvae are known to have symbiotic relationships with certain bacteria. Where there is one you will find the other.

This is one of the most overlooked aspects of Lyme and or Morgellons by many doctors, including the ones familiar with these diseases. Many fail to address parasites and fungal issues and prescribe one or more antibiotics.

Antibiotics encourage fungal growth. Many on antibiotics get better temporarily only to get sick again as these bacteria producing nematodes often go unaddressed.   

A course of Doxycycline administered quickly after initial infection may prevent Lyme, but there have been cases that show this is not always the case.

Both Morgellons and Lyme begin with a vector but present with slight differences. These differences can help you to determine which you are dealing with. Both are slowly advancing conditions and get worse if left untreated.

If you can recognize early warning signs there are many steps you can take to treat and prevent co-infections. The later you wait to treat, the more co-infections that will follow.

Morgellons often initially presents as a yeast or fungal infection. For men this may manifest as the jock-itch from hell that wont resolve using topical anti-fungal and yeast creams. It may manifest as ringworm that keeps returning regardless of the amount of Terbinafine your doctor prescribes.

Sufferers of Morgellons and Mold Sickness can experience intermittent crawling, and biting sensations occur as infection affects the nervous system. Yeast grows explosively in budding chains and this too affects the nervous system.

A major difference with Morgellons sufferers when compared to Lyme is a major widespread insatiable itch that is relentless.

Through each stage of each of the three infections, I experienced varying degrees of this sensation known as formication.

There are other symptoms common to Mold Sickness, also found in Lyme, which include cluster headaches, tinnitus, sneezing, and increased tear production. Vision problems and red eyes were one of my earliest symptoms.

An important point to make is that Mold Sickness can precede Lyme which can precede Morgellons.

All three can experience some form of lung pain. The way this presents can be a big clue as to which is affecting you.

Morgellons produces pain on inhale that slowly progresses often unilaterally at first. It comes and goes. Then it gets worse and eventually progresses to the adjacent lung. In Morgellons nothing shows on an X-ray or CT scan of the area and you are told that you are fine but may be given some pills to help you 'feel better'.

For myself it has responded to Biaxin (Clarithromycin) 500mg bid.

Mold Sickness may show visibly on X-ray or CT scan in cases of invasive Aspergillosis.

Lyme lung pain is different still and is often described as a feeling of 'air hunger' or not being able to absorb oxygen.

In Lyme a bacterial co-infection named Babesia is often the culprit. Babs, as we like to call her, brings night sweats, vivid dreams, and waking in the wee morning hours. She leaves you breathless but not in a good way!  

Skin may also eject tiny specs or barely visible grains which can be felt but not always seen and although some Lyme sufferers experience this condition they may have Morgellons and not know it yet.

One of the late and most upsetting symptoms of Mogellons are visible fibers of multiple colors protruding from the skin. The disease is classified by this symptom but this is flawed logic as it occurs late after exposure. 

Going forward I believe it will become widespread knowledge that carriers of Morgellons have pupils that fluoresce in UV light and testing can be done at home with a UV flashlight costing under $10.

Morgellons sufferers can also experience visible parasitic infections from untreated bites from multiple vectors. These often manifest as worms but can include mites, flies as in myiasis, and anthropod like creatures, and in some cases collembolan.

One way you can determine if you have actual mites crawling on the skin is to cease consumption of all bread products, sugar, and starches for a week. It may only take a few days to get an answer as in my case all crawling stopped in three days of the dietary change.

If the crawling sensation responds to this by stopping, then it is being caused by yeast (dimporphic fungi) and or bacteria and not by the larger parasites. It truly does feel like mites crawling all over and can be very deceiving.

Morgellons sufferers commonly experience scalp lesions and rash, and other skin lesions in other parts of the body well before any visible fibers appear.These are slow to heal and never really return to the original skin color leaving a blemish well after healing.

Friends and associates of mine with various degrees of Mold Sickness, Lyme, and Morgellons have shared with me some success stories which have helped them achieve remission of their condition.

Since it takes five years of being symptom free to medically define one as cured we will have to wait and see if they are cures but we can explore the ones that help.

I also have discovered some things that slow the progression of the diseases on my own through research, as well as clinical detection methods for testing for these conditions to know if you are afflicted and the differences.

I must disclose that I am not a doctor and just a guy on the internet who has been inspired to bring you some helpful information from the conjecture of myself and others with these afflictions. I give no medical advice and you are ultimately the one responsible for whatever action you decide to take going forward.

There is little scientific evidence that tells us anything definitive about these conditions no less how to cure them. I have shared in your suffering so I wish to offer as much help as I possibly can.           
Going forward we are going to take a closer look at some successful treatment stories from myself and others and what they did to get there. This first one is one of the most promising. 

I wrote a recent email to a clinic in Salt Lake City which I heard was the cheapest in the United States for this treatment but I am not aware if this is fact. I have no affiliation with the clinic but have provided a link to their site in case you wish to take a closer look at what they offer.

Rather than attempt to explain something that I myself have yet to attempt I encourage you to direct your questions about the therapy directly to the clinic at the link below to see if it is right for you.

I have attempted only direct intravenous ozone therapy and reached a point of stalemate to where I was not improving after 8 weeks only to then find out that this form of ozone treatment carries high risk, whereas the one below is a more proper application of ozone therapy with high rates of reported success.

The email below is my inquiry to this clinic. It details what I have been through and reflects my own personal story so as I wear my heart on my sleeve I wish to share it with you: 

"I am inquiring about 10 pass ozone therapy cost and the time it would take to complete this. 

I would naturally travel to Salt Lake and would also like to know what hotels are closest to your office to taxi as needed.

I have multiple infections that began manifesting beginning with long term mold exposure starting in August of 2014 which led to mold sickness.

The suspected dimorphic fungi became systemic and weakened my immune system which then invited multiple co-infections.

Just when I thought I had cured myself of the mold sickness and discontinued Fluconazole, then following month specific Lyme symptoms developed.

More recently there are the beginning of symptoms of that strange condition the medical system wont recognize.

It is often referred to as starting with an 'M'. It is the disease that will automatically get me labeled as delusional if I so much as mention it and therefore I dare not.

I have not progressed downhill rapidly because I have continuously researched medical journals for close to a 1000 hours and counting for the duration of this illness.

I have been self treating with Fluconazole and multiple antibiotics and anthelmintics. 

I do try to be cautious but nobody should be placed in a position where they feel as if there is no other option.

Had I trusted any previous doctors I have dealt with to date, I would likely have a detached rectus in my left eye but because I began self treatment, my eye feels better than it has been in a little over 2 years.

Every trip to any conventional specialist has been a complete waste of time and money as they continuously misdiagnose, and refuse to listen.

If I had eye allergies as they suggested, then why did a Doxycycline / Fluconazole combination clear up my eye?!

I would prefer not to continue to ingest potentially toxic drugs and begin to work towards restoring my gut flora.

In addition to this, I also have good reason to believe that I have am dealing with a Propionibacterium acnes infection in my spine.

This has manifested as a slow progression of chronic pain which has been escalating for 28 years.

L5/S1 is confirmed herniated by MRI, yet the thoracic region dosent show anything remarkable. The pain in the thoracic region sometimes feels as if it migrates between T9/10 and T4/5.

There was no trauma to my spine and it all began a few years after my first dental implant at the age of 20. I am now 48 years of age.

I have not been officially diagnosed with anything (except herniation at L5/S1) because the specialists have failed me.

Rather than test for anything that I have specifically asked for they have deceived me by testing for things that I did not request and then attempted to refer me to additional specialists.

The irony is that I am paying 100% out of pocket so why is it I cant obtain the specific tests that I have asked for?

I know this must be as difficult to believe as it is for me to disclose.

Please let me know what problems you can help with and what I should and or should not expect from ozone treatment.

I am frustrated but keeping calm and making progress, but nobody should have to do this alone."

There is a very good chance that you are not delusional and its a sure bet that you are not alone.

Your stress levels directly correlate to how fast the disease will progress or how quickly you may recover. I assure you panicking and pointing fingers will only make the situation a whole lot worse quickly.

Be careful. There is a lot of misinformation about these conditions on the internet and we will discuss this in the future also. Some even telling you not to bathe. You should absolutely try to keep yourself as clean as possible, but there is no reason to go overboard or resort to dangerous chemical treatments. You didn't get this overnight and there is no speedy cure.

The best first thing you can do is to avoid sugar, breads, and most carbs and begin taking Xylitol in 1/4 tsp increments until you can handle up to 4 tsp per day. This will cut down the yeast and many invasive bacteria as it will consume the Xylitol thinking it is sugar, but will not be able to convert it into energy causing it to starve.

Subscribe to this blog as well as my YouTube channel ClintFromNYtoVA and feel free to share it with others. Keep hope alive and know that we will one day find the answer and if there are people to hold accountable we will do so. I wish you recovery and peace of mind.

Until next time do yourself a favor and stay calm.

This blog is dynamically being updated as well as all of the previous posts on Morgellons as I review them and think of better ways to express my ideas and communicate my thoughts. So check the old posts also as there has likely been something new added to them recently.

If you wish to help me in my efforts to find a cure or simply appreciate the information I continue to bring to you, I ask that you donate what you will using the Paypal link below. Thank You.

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Sunday, March 12, 2017

Mold sickness, then Lyme, and my Descent into Morgellons - My story and steps taken

This blog will begin to move into the direction of analyzing treatments that people claim have helped or cured them.

In August of 2014 I moved to Panama. The infection would be triggered by mold sickness. I may have become infected in VA. 

I began to have a film cover my eye and reduced my vision slowly and became irritated. 

A painful epididymal cyst in my testicle was diagnosed. I now suspect this was a mold spore.

Alternaria was clearly visible in the home. I've read cases where dogs testicles have swollen from exposure. It infected my left eye.

I began to develop a ringworm type rash on the face and body.

3 months slow incremental dosing of Nascent Iodine to 15mg daily cleared the cyst, bran fog,  cluster headaches, restored energy, and has rejuvenated my thyroid.

Terbinafine 500mg bid /15d was tried initially and attacked a fungal infection in a muscle behind the left eye. I felt it working one hour after taking it as the muscle behind my left eye tingled and itched. 

Itraconazole 100mg /11d helped clear the 'film' that was forming on the cornea.

From the start I appeared to have very few isolated spots of tinea versicolor on arms.

A few subcutaneous nodules appear from time to time taking weeks to resolve much like in Sporotrichosis yet I dont believe it is.

Unlike S.schenckii which causes Sporo there is no suppuration in the forearms and these do not progress to pustules nor gummata in the arms.

There appears to be a hematogenous spread from these hard yet painless nodules in the forearm to soft painless enlargements appearing like stops on a metro rail map within swollen veins. I would guess these are near lymph nodes.

After this first course I saw an ophthalmologist who stain tested the eyes for fungal infection and completed a thorough examination with a slit lamp. I believe at the time there was still candida in the eyes which he some how missed. It was likely small or I developed it shortly after.

I should have seen him before the Itraconazole but the timing just worked out this way.

There is 5-10% permanent damage, to the ciliary muscle. The left eye is not able to focus as accurately as it did before.

I will attempt the Bates method to restore the ciliary muscle and improve my focus.

Doxycycline 100mg bid used would later prove his diagnosis of allergies as incorrect.

I discovered Fluconazole had better penetration in the eye. It is over the counter here. It cleared all skin rash and resolved floaters. The final problem of a stationary foreign object on the cornea resolved and I was ecstatic.

Combining Fluconazole with Nystatin pulsing helped kill the excess yeast in the gut (herx city). Combining it with Doxy pulsing restored the sclera from red to white rather rapidly.

Doxycycline is known to make Fluconazole go from fungistatic to fungicidal.

6 months of continuous daily use of Fluconazole 400 mg and cured, or so I thought....

Oil pulling with ozonated Coconut Oil and Xylitol quickly and effectively arrested and cleared a failed dental implant infection that was beginning to hurt.

I suspect P. Acnes bacteria which normally resides on the skin traveled through a dental implant that I got in my 20's and caused the chronic pain in my spine that I have suffered from for 28 years. While I treat mold, lyme, and Morgellons symptoms I have also begun taking Augmentin tid for 100 days as was outlined in this clinical study:

I cannot recommend dental implants. I plan to have remaining ones removed.

Throw away your glycerine toothpaste and get a non-glycerine one like EarthPaste.

The glycerin coats teeth and prevents remineralization and healing of teeth.

I am finding it difficult to trust an industry that willingly gave us mercury fillings and marketed them as silver and will admit no harm. When I was a child I always thought they were silver. If only I knew then what I know now!

I am sorry to inform you that Lyme may cause you to lose your teeth anyway. Ask to see your teeth if you have them removed. You will notice the decay started on the inside and they are hollow rotting from the inside out.       

From the outside this often appears as a cavity at the base of a tooth.

I figured if I had parasites then no other method for healing could work until I get rid of the parasites. 

5 cycles of Ivermectin (4 days on 3off, 3days on,4 off, 2days on 5 off, 2days on 5 off). The 5th was of an extended length that I wont mention the length because I cannot justify doing a fifth cycle. This will knock out what it can knock out in 4 cycles.

I now use  Ivermectin to quell any recurrence of itch and it works in one dose and quickly. A 6mg single dose now works for me and I dont need it often as long as I remain on Fluconazole 400 mg / d.

I believe Ivermectin has helped remove some nematode(s) in the GI tract. I did several antihelmintic drugs in a modified Klinghardt protocol. The protocol can be found below.

Colloidal silver drops in the ear remove any irritation within days and for weeks at a time.

I began experiencing lung pain which at the time I thought was Aspergilosis.

I went back on Itraconazole for 28 days. It had been 2 years from the first time I used it.

In January I got an S.schenckii (Sporotrichosis) similar folliculitis in scalp sores which scabbed, rash by ears, sores inside the left cheek, and facial hair.

I believed I had mites crawling all over my scalp,face,and ears, yet it made little sense to me that I was affected and not my wife.

I figured if it were mites it wouldnt care what I ate. I stopped all sugar, carbs, breads.

The sensation rapidly resolved (yet others do have mites or Bartonella or yeast causing the sensations). It was not mites in my case although there are many sufferers of this condition with fibers, mites, worms, bacteria, yeast, and viruses.

I have become host to invaders which likely attract new infections which feed on the previous arrivals. I have become the dinner plate.   

Pores and skin fluoresce in UV light. Florescence occurs in the back of the throat between the tonsil walls and in pupils.

Tea tree oil soap as well as sulfur soaps have reduced areas which fluoresce on my skin.

28 days of Itraconazole at 100 mg bid should have helped S.schenckii or Aspergilosis but there was no improvement and continued breakout during. 

A friend recommends Clarithromycin 500 bid for the lung pain. This helped greatly is less frequent with reduced intensity and is 95% better. I still battle this.

Far IR Sauna has cleared grains of sand and a few arthropod like creatures.

These will still emerge dead if I massage the area. Collembola?I have no idea. They are visible and crunchy.

I am also on my second 14 day course of Mebendazole 100 bid. I am on Tinidazole 500 bid 2 wk pulse at a pre fibrous stage of this condition.

Cover any new insect bite with antibiotic ointment (for 24 hours) to suffocate injected nematode larvae. They will surface and die, else disseminate. This is why some end up with worms.

Morgellons sufferers have one or more uncommon dimorphic fungi which have disseminated throughout as well as multiple bacterial infections and sometimes viral ones.

I have been told that one person with this condition that they tested positive for Chaetomium globosum a dimorphic fungi (exists as mold at room temperature / yeast at body temperature)

A quick search at the link below and you will also see that they are scrambling for a drug that is effective against this invasive fungi, so maybe there is something to this. I will continue to investigate.

This mold is modified and used in crop pest control.

This and other dimorphic fungi get in hair follicles. The yeast may cause tingling sensations as it grows.

I am slso on Diethylcarbamazine 100 qid and stabilized oxygen drops throught the day (the jury still out on these).

This is not evolution. It is GMO disease:

More information will be added with tips from myself and others to follow. It has been a wild ride and a fascinating time to be alive. Follow along and lets defeat Morgellons, Lyme, and Mold Sickness!

I am now using a modified version of the Klinghardt Protocol.

The Klinghardt Protocol from 2013 is listed below. I do not know what he uses todays and I have modified the folowing protocol and Ive personalized it as I have indicated above.

1. Biltricide 600 mg - twice daily (q. 12 hours) for two days
Absorption increases most when taken with a high carb meal. A high fat meal increases it almost as much. Take with grapefruit juice to increase absorption also.

2. Ivermectin 12 mg - one 12 mg (or four 3 mg) tablet(s) four times per day for fourteen days (take at the same time as Pyrantel Pamoate) on an EMPTY stomach.
Pyrantel pamoate (liquid – 4 teaspoons) 1000 mg per day at bedtime for fourteen days.

3. Albenza 400 mg - Two 200 mg tablets twice per day for fourteen days (after completing fourteen days on Ivermectin and Pyrantel). Take with food. (every 12 hours)

4. Alinia 1000 mg - Two 500 mg tablets twice per day for fourteen days (after completing Albenza) every 12 hours

(A's addition from Dr. Clark’s Book - Levimasole 100 mg (3 times/day) before meals)


5. Mimosa Pudica (Biopure) - ½ teaspoon 2x/day for fourteen days mixed drink, milk or juice

6. Arteminisin (Biopure) - 200mgs 2x/day for fourteen days.
ALWAYS take with 4 oz. of grapefruit juice 30 minutes before meals.

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Sunday, March 5, 2017

Mold, Lyme, Morgellons - START HERE (revised 26mar17)

 Hello and welcome to this blog which will begin to take a more definitive and focused approach towards the resources available for healing Mold Sickness, Lyme, and the condition that has become known as Morgellons.

It has been and continues to be an amazing journey and I have had success at keeping myself from developing full blown Morgellons. I am constantly learning of new things about these conditions as I spend countless hours researching published medical journals.

I am not a doctor and do not give medical advice but instead relay information based upon my own personal treatments. I was ignored by doctors and forced to take matters into my own hands. You are responsible for your own health.

I will begin in depth analysis of items that I have used successfully in future posts in this blog. The key is recognizing the condition before it progress to the next stage and break this chain of events at a core level.

Each infection has the ability to pave the way for the next unless you break the chain of events. You become the dinner plate for a host of different organisms which then attract its predators and this becomes and endless progression into a nightmarish condition.

Antibiotics alone often do not cure and are a common cause of the infection returning accompanied  with yeast overgrowth. Yeast overgrowth is a major if not the most important factor in how Morgellons progresses.

There are some clear and not so clear differences among the conditions, but one can trigger the others. I have suffered many of them in the order listed in the title. I still battle but I am winning overall and am confident all of these pathogens can be eliminated but it takes time and money.

Morgellons is a rich persons disease and I am not rich therefore I am always looking to save money in my treatments by eliminating supplements and tests that are unnecessary.

You should not have to wait for fibers to protrude from the skin or parasites to appear before taking action to break the chain to stop the progression. Many of the steps I took are effective for all three conditions as I have run the gamut but I will specify.

The further the progression of these conditions the more difficult and prolonged the required actions will be.

No single therapy is prefect for everyone but there are exciting developments which we will explore in detail on future posts.

A healthy immune system is  key to keeping the population of all Lyme bacteria in check regardless of infection. 

Minimizing stress supports a healthy immune system.

As you likely know, stress produces an excess of the stress hormone, cortisol, which weakens the immune system and gives disease the advantage to manifest.

This stressor can be mentally induced by how we choose to react to events in our life. It can also be sourced environmentally, as many have manifested Lyme and related complicated co-infections following heavy exposure to mold spores.

Anyone experiencing symptoms of any of these conditions should check their environment for mold. Anyone feeling better after going on vacation just to return to a poor state when home again should also check their environment for mold. This problem must be corrected immediately.

The Borellia infection which is definitive of Lyme often paves the way for other infections to follow.

But it is very possible that we already have many of these bacteria in our system and our immune system keeps populations check, similar to the way that our immune system kills cancer cells on a daily basis.

There was a time when only two bacteria were known to be able to transfer DNA into humans one of which is Bartonella a well known co-infection of Lyme. This also appears to be changing but science will often identify this as a previously unknown discovery as opposed to a known modification in the behavior of an organism.

I believe Morgellons sufferers are also infected with many bacteria common to Lyme as well as yeast from dimorphic fungi (mold which converts to yeast in the body). A fungi ridden body tends to attract larger parasites by actions in nature. A yeast ridden body brings with it a lowered immune system attracting many insects which feed on fungus.

This is not limited to the tick. It also includes spider, fleas, bed bugs, mites or winged insects. Basically every insect that bites us is capable of transmitting disease.

Infected insects can and do transmit nematode larvae along with bacteria when they bite. If the bite is left untreated the larvae can grow and disseminate into other areas of the body. Treated each one from the start as if infected.

I always place a generous amount of antibiotic ointment on each insect bite as soon as possible and then cover it with a bandage for 24 hours. This will cause any nematode larvae inadvertently injected by an infected insect, to surface for air and suffocate in the process. The larvae are microscopic and cannot be seen with the naked eye but some are visible by the time they grow to adulthood. Preventing reinfection is a key process in any parasite protocol.

Morgellons involves additional dimorphic fungal infections (mold when inhaled, converting into yeast form at body temperature) that may be missing in Lyme sufferers.

Lyme sufferers could be one fungal infection away from developing Morgellons and with the frequent use of antibiotics is always at risk unless that risk is somehow countered.

The medical community has barely begun to recognize Lyme as a chronic infection but turns an official blind eye to Morgellons often based of the symptoms and speculations the suffer labeling sufferers with "delusions of parasitosis" (DOP). Once labeled delusional on your permanent medical record future doctors may treat you accordingly.

A better approach if you do not wish to have to go it alone is to see and Lyme Literate Medical Doctor (LLMD). You can search for one here.

Most doctors including those in the LLMD group do not write prescriptions for medications which treat parasites, but some of the better ones do. Therefore attempt to sound educated and ask if the doctor incorporates anthelmintic treatment in his protocol when appropriate.

There are ways of obtaining these as I have purchased from for horses and India based pharmacies for the human versions of anthelmintic medications.

We will discuss the Klinghardt Protocol in a future post which details using anthelmintics in cycles as well as the importance of treating for parasites and why testing often fails.

Unknown and difficult to detect organisms with altered DNA are being discovered since the expansion of cross species modification of multiple types of organisms became widespread. Science will act like it has always been there yet went undetected. It will always use evolution as a deflection tactic to protect commercial interests. Its not just plants that are genetically modified but a broad spectrum of organisms.

The genetically modified organisms include insects, yeast, fungus, mold, bacteria, nematodes, and the like whose DNA has been altered in a lab. Many altered organisms have been introduced for the purpose of controlling crop pests and these are just the ones we know about.

Difficult emerging diseases infecting humans in the last three decades happen to correspond with the advent of cross species modifications.       
It is now estimated that humans may harbor more than 100 genes from other organisms including bacteria, archaea, fungi, and other microorganisms.

The following scientific article linked below states this is simply a by-product of human evolution.

It seems we have evolved a lot in just the last three decades which would suggest evolution is not responsible for this.

I postulate that horizontal gene transfers between the lower life forms on up the food chain is resulting in gene transfers between microorganism and human that didn't occur 30 years ago.

These unnatural modifications have created the perfect storm for gene transfers to become more prevalent across multiple species.

As we have DNA transfer from other species combine with our human DNA we will become susceptible to the infections that used to be solely species specific. If this is what is occurring all diseases resulting from this would manifest as "emerging" by default. We have entered into dangerous waters and we will not be able to place this genie back into its bottle therefore we must go on the defensive.     

The once was a time when genetically modified organisms were only produced using genetic material from similar species. This had been occurring for a very long time and was considered relatively safe and probably was.

What the general public tends to overlook when discussing genetically modified organisms that have been occurring safely for a very long time is that the long history of safe DNA tinkering was limited to the same species until recently.

"In 1971, the first debate over the risks to humans of exposure to GMOs began when a common intestinal microorganism, E. coli, was infected with DNA from a tumor-inducing virus (Devos et al., 2007). Initially, safety issues were a concern to individuals working in laboratories with GMOs, as well as nearby residents. However, later debate arose over concerns that recombinant organisms might be used as weapons. The growing debate, initially restricted to scientists, eventually spread to the public, and in 1974, the National Institutes of Health (NIH) established the Recombinant DNA Advisory Committee to begin to address some of these issues.

 People have been altering the genomes of plants and animals for many years using traditional breeding techniques. Artificial selection for specific, desired traits has resulted in a variety of different organisms, ranging from sweet corn to hairless cats. But this artificial selection, in which organisms that exhibit specific traits are chosen to breed subsequent generations, has been limited to naturally occurring variations. 

 In recent decades, however, advances in the field of genetic engineering have allowed for precise control over the genetic changes introduced into an organism. Today, we can incorporate new genes from one species into a completely unrelated species through genetic engineering, optimizing agricultural performance or facilitating the production of valuable pharmaceutical substances. Crop plants, farm animals, and soil bacteria are some of the more prominent examples of organisms that have been subject to genetic engineering."

This has been occurring on an ever increasing scale with commercial applications since the early 1990's and not just in plants but in an extensive array of species on every level.

Once the genetic material began to be taken from other species and spliced together in labs to create things that were never intended to exist in nature we have noticed a large increase in the emergence of these strange infectious diseases which are beginning to approach epidemic levels.

Is it coincidental that the time frame of new and emerging infectious diseases such as Lyme correlate with commercialization of modified organisms not limited to plants? 

The link below implicates evolution but why have we evolved so quickly in just the last few decades?

The medical field is only beginning to recognize this cross species transmission in the world of viruses.  

As we obtain more and more DNA transfer from other species we will become more susceptible to a wide variety of disease that once only infected plants, fungi, insects as we will contain susceptible DNA in our bodies from all of these species. Practically anything we were immune to before now becomes possible.   

 Additional reading:
 Genetically Modified Organisms 25 Years On

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