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
https://youtu.be/IJP7UuDpMGE
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.
STUDIES:
Effect of myrrh and thyme on Trichinella spiralis enteral and parenteral phases with inducible nitric oxide expression in mice
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4708024/
Analysis of the Beta-Tubulin Gene and morphological changes of the Microsporidium Anncaliia algerae both Suggest Albendazole Sensitivity
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4308492/
Electron microscopic changes in Enterocytozoon bieneusi following treatment with albendazole. (HIV)
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC501614/
Microsporidia infection of the cornea--a unique and challenging disease.
https://www.ncbi.nlm.nih.gov/pubmed/24104931
http://emedicine.medscape.com/article/221631-overview#showall
Infectious Diseases Articles
http://emedicine.medscape.com/infectious_diseases
Thursday, May 18, 2017
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 YouTube.com
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.
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 YouTube.com
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 wikiwild@gmail.com
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.
If you would like a copy of the slides from this presentation please send me your email to wikiwild@gmail.com
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:
https://www.ncbi.nlm.nih.gov/pubmed/28221130
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.
PUBMED ARTICLE FIRST RECORDED HUMAN INFECTION FUNNILFORMIS MOSSEAE:
Evidence for polymicrobial communities in explanted vascular filters and atheroma debris.
www.ncbi.nlm.nih.gov/pubmed/28411089
Excerpt:
"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.
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:
https://www.ncbi.nlm.nih.gov/pubmed/28221130
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.
PUBMED ARTICLE FIRST RECORDED HUMAN INFECTION FUNNILFORMIS MOSSEAE:
Evidence for polymicrobial communities in explanted vascular filters and atheroma debris.
www.ncbi.nlm.nih.gov/pubmed/28411089
Excerpt:
"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.
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