Below is a list of answers to your questions.

Replacement Sunscreen from Arbonne

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Big News!
I've discovered that the Swiss formula Men's facial moisturizer has the same active ingredients as the old  Swiss SPF 30 formula that was so helpful in protecting skin from the fungus when having to go into an infected box or to wear when having to go around people you want to protect. I still had some of the discontinued  SPF 30 formula (since I only used it at the beach occasionally) so I actually tasted them both and they tasted exactly the same! I  then checked the ingredients and sure enough, the active ingredients are the same. I put some of each on my arm and can't tell the difference so I think is a better replacement than the sunscreen for face I had recommended as a replacement earlier. Here is the product number. *If you already bought the sunscreen for face you can still use that, but this one is going to go on easier and cost less because it will water down and spread better.

 Men's Facial Moisturizer Broad Spectrum SPF 20 Sunscreen #638  If you have not previously ordered the recommended skin products, send me an email requesting the link to purchase. 

Prayers for your healing,

Megan

Updated 2015 Newsletter

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If you want to write to Arbonne about bringing the products they discontinued back, send an email to the following addresses:


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December 2014 Newsletter

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Stopskinmites.com

Newsletter December 2014

 To answer your most common question… yes I am well with no symptoms and have a normal life again. Well, maybe not normal, since I still get to dwell on this condition on a daily basis helping others get out of the suffering.

I have been meaning to send this Newsletter for quite awhile but with working 3 other jobs it seems to always get buried on the list.  I am still hoping that someone else who has gone through this and learned the protocol can take over some of my consultations. I have not had a break since I started consulting in 2008. I mean, no vacation in 8.5 yrs including the time I was suffering! I receive weekly emails where the person wants to end their life due to the intense suffering or a divorce is threatening because only the wife feels anything. No matter how badly I need it, this is just not something I can ignore and go have a holiday. (yes, these do get forwarded to me).  If you have been successful using my protocol, you qualify to help others.  Please contact me if you are qualified and interested in helping others.

There are just a few things I want to share that have repeatedly come up in consultations. One is to do with Cat’s Claw application. Cats Claw works but application is the key to it working.  After much analysis, I have discovered why the Cats Claw always works on the rest of the body but sometimes not on the scalp.  (Note Cats Claw is impractical to use on the scalp except on isolated spots; not usually the entire scalp).  The answer finally dawned on me while dealing with Sarcoptic Mange on my dog. This experience with my dog was so similar to what I went through with this fungus because I could not find anything that worked on him. I tried everything non-toxic that I could find on the internet instead of giving him dangerous internal pesticides.   I got a slight case of the mange from him on one arm that went away in an hour using the Cats claw. Cats Claw worked on Sarcoptic mange mites!!!!  

One person selling a nontoxic mange treatment online sold a shampoo for prepping the skin for the mange treatment. I believe the mange treatment was basically Borax washing powder dissolved in water mixed into hydrogen peroxide and some herbs. I rang up my credit card to the tune of about $500 putting me farther into debt but with my best friend suffering, what could I do?  After 5 months I gave up and in desperation tried my own protocol on him. To my amazement the Cats Claw and Cotz and a strong solution of PCO (1-2 parts water) has worked the best so far topically on the mange. The good news about his condition was that the dog mange mite can only live about 36 hours without a host so the environmental aspect is far easier than the fungus/ Collembola infection where the fungus can exist for years.

The idea of prepping the skin to better take in the mange treatment (since mange also lives deep under the surface)  made me realize that the only time I have seen the Cats Claw  not work is when it can’t get into the skin deep enough to get to the root of the problem. The two things that cause the failure in getting results are:

  1. The presence of moisture in the skin (IE water)
  2. Oil the skin.

Both conditions will not allow the penetration of the Cats Claw needed to get results. Because the scalp must secrete enough oil to lubricate hair, there is far more likely going to be oil on the surface of the scalp compared to the rest of the body. Along with being the hottest area other than the crotch, the scalp starts to secrete the oil the minute you finish washing it.  (The body is always trying to bring things back to balance.)  It may enhance the application of Cats Claw to wipe the area to be treated with a cotton pad saturated with 90%+ rubbing alcohol to remove any trace of oil on the surface of the skin. Of course this is besides making sure the skin is really dried out prior to applying Cats Claw.

 I have always been pondering what could take the Cats Claw faster and deeper into the skin other than dryness of the skin. I am not sure if it will help but if you already have the Kool N Fit Spray, you might try spraying that where you are going to treat just prior to the Cats Claw. The ingredients have something that quickly and deeply penetrates the skin since it is made to help muscle pain which is much deeper. I have no feed back or experience with this, so you need to decide if you want to be a Guiney pig and try it. I tried DMSO but as I and many found out it is extremely damaging to the skin. Weakened skin means less capability to fight the fungus infection so that is not an effective option.

 The most common place for symptoms is still the scalp on almost everyone. I have been told by one person that Genitrex, a homeopathic pubic lice treatment, greatly helped the scalp so if anyone wants to try it please let me know.  I usually do not suggest anything that has not worked on at least 12 people consistently and brought permanent change so unless I hear that this is a breakthrough I will not put it into the protocol. Lots of things give temporary relief from symptoms, but most of them weaken you so the fungus comes back with a vengeance IE one step forward 2 steps back.

The other gift discovered on one of my other jobs was a cushion I got because the seat on the vehicle gets so hot I could not sit on it. I bought a seatcushion on Amazon and then realized this may be helpful for those having to sit somewhere that they fear may be infected or the fear they will infect it.  It will also minimize sweating that is escalated while sitting on something that does not breathe. The cushion is only about $12-16. It is small and light enough to be taken with you and does not contain cloth. It is plastic mesh and allows air flow so sweating is minimized.  You can most likely spray it with rubbing alcohol to disinfect it. The cushion can be found on my website underOTHER USEFUL PRODUCTS. There is also a mesh office chair at Costco for $99 that is a good replacement for an upholstered chair. http://www.costco.com/Metrex-Mesh-Task-Chair.product.100117458.html

The other thing I want to mention is that if the topical protocol has given you relief and you have seen areas scab and heal then you know it can do the job.  It is just a matter of continuing UNTIL you get rid of every spot infected.  People are used to instant results and stop doing the protocol before they are clear or they start losing patience and start experimenting with other things again. I am always surprised when they admit that it did kill and heal the fungus on their arm for example, and then say it did not work on another part of their body. That has to be re-infection from something or incorrect application. They know it works from their own results but then don’t understand they are still suffering due to some flaw in the application or stopping before the fungus is completely gone which then causes a resurgence.

One person left her house because she could not get the environment under control. (house was too large and others felt nothing). She went to stay at a clinic for environmental illness. There she did find relief but told me she still did my protocol using Cats ClawCotz and Bodywash. The only thing that she could not do was the PCO laundry soak. She said they were using Dimethylbenzyl Ammonium Chloride which surprised me since we tried that for disinfecting our clothes and got boils from the chemical.  People are normally at the clinic because they have chemical sensitivity so the clinic does not permit strong smelling substances that could affect the other patients. If you want to know more about the environmental clinic in Texas, please contact me.

People are concerned when they move what to take with them. I suggest that anything not cloth or leather is easy to clear unless it is a very rough or a porous surface. If a dresser drawer or wooden bed frame is suspect, you might consider painting or varnishing it to seal it and then take it with you without worry.

 A common anguish is the question: Do we have to throw that expensive (fill in the blank) in the dump?

 I suggest that you at least remove questionable items from the house until you are clear and then introduce them back into your environment 1 item at a time. Try to wrap the item in plastic to store it if you can to keep it from infecting where you are storing it. Furniture and bed stores usually have large thick plastic bags so you might try getting a furniture or mattress bag from them. (*NOTE covering an infected mattress is dangerous but covering a new one so you don't ever infect it is wise.) If you begin to feel any symptoms immediately remove the item from your house.  You know what to do so you can treat yourself quickly and prevent getting a full blown re-infection.  If exposure were to happen, you would peel off your clothes and bag them to soak them in PCO or the bleach (See Treatments). Jump in the shower, wash down with Bodywash and treat the area with at least the Cotz if not Cotz and Cats Claw.  If you need to touch the item again to get it to the dump, protect yourself by coating your face with Cotz and your body with Swiss Formula sunscreen including your hands. BTW never use Swiss Formula Sunscreen on your face since even way below your eyes on your chin it can burn your eyes. (*Note Because of their company policy, I cannot use the brand name of the Swiss formula products in a news letter)

 Eyes Problems: If after using a tiny drop of No More Tears Baby shampoo on a finger nail and scrubbing your eyelashes and rinsing well you still have symptoms in your eyes, you might try using over the counter Stye drops or the Vetericyn eye gel. (*Note this is for animals so use at your own discretion. It is really mild and can be used in the eye of an animal but liability wise I have to warn you.) If that does not work go to an eye doctor and get an ointment.  Do not mention bugs/crawling but merely that your eyes are itching. Be sure you are clearing everything that touches your face near your eyes IE glasses, makeup brushes and applicators, etc. The best way to clear glasses is soaking in a mason jar. Fill it to the top with the same PCO solution dilution you use for your laundry soak. Keep a pair of glasses in there and rotate out the ones you wear till your symptoms around your eyes are gone.

Nose and Ear problems: One person who has gotten over this wrote in this suggestion:

“it helped tremendously to prevent mites' nocturnal migration and reproduction in my sinuses by using Cotz, both as a lining in my nostrils and also applied to foam earplugs in my ears. This thwarted their breeding cycle. Soon after that, I found the EM-1 killed them on contact if used in my ears and held inside with earplugs all night. But the Cotz was pretty effective for this, if folks can't source the EM-1.
Main thing is to never leave ears & nostrils unprotected at night, & keep 
Cotz as a lining in nostrils 24/7.Weird thing, as an aftereffect of having the SM, my teeth went into crisis. I lost 3 molars in the 2 years directly following the infestation. Maybe because the stress caused me to clench my jaw more at night. Have you had any other reports of increased dental problems from clients? “

 Teeth and gums: The above statement is something I never even considered but frankly it was absolutely true in my case. I began grinding my teeth in my sleep (what little sleep I had) during the ordeal as I am sure many have. This pounding caused my gums to recede for the first time in my life. I had healthy gums (no gum disease at all and no pockets. All my teeth were healthy with no cavities (I have all my own teeth, and no implants or root canals, only some fillings from my childhood. For more on what I recommend for teeth care you can now purchase a kindle version of my  book on natural hygiene on Amazon for $4.49 here). This grinding at night was the only explanation the dentist came up with for what was happening to my gums. He told me the pounding and grinding was affecting the gums ability to stay adhered to my enamel. He recommended wearing a bite at night that cushioned my teeth to lessen the impact.  Now that I think about it, this grinding stopped when I got over the fungus and collembola problem.  I did not have to have any teeth pulled but this condition definitely affected my oral health.

Treating the car:  Only fog by cracking the door and filling the car just until it is full of the fog to the point where visibility is obscured. There should be no air movement IE fans, air conditioner, etc during the fogging. Remember that any air movement or any heat that makes the active ingredient in the fog evaporate, weakens the treatment. Spray down seat belt to the point that it is soaked through and through as well as spraying headrest, seat and floor with 90% + rubbing alcohol. (Note* Protect yourself from breathing fog or rubbing alcohol.)  Right after you spray place a thick construction bag over the head rest and seat and then cover that with a thick towel that can be daily treated in a soak. Leather is more difficult to clear but you can try. There are custom neoprene (wetsuit material) seat covers that can be put on new cars to protect from ever getting anything into the seats.  The seats are completely sealed and water proof by this material. The company that makes them is called Wet Okole. http://www.wetokole.com/. They are expensive but worth protecting a new car or trying to seal an existing infected seat that is leather. Warning one person told me she had a cushion made out of this material and it got infected but better that than a new car seat since at least you could take it off and soak it.

Many say that their crotch is completely infected and so they complain they cannot use the Cats Claw with the dropper on such a large area. One person said they sprayed it on for convenience because it was such a large area but admitted it was not working. Spreading it superficially over a large area does not work because it is needed deep under the skin. You could just as easily use the Bodywash left on overnight for a surface treatment if that is all you needed. Most people with pin pricking and nerve symptoms need to get deep into the skin to kill the fungus so surface treating is just waiting time and money. I strongly suggest a lighted 10x magnifying mirrorespecially for the crotch area. It was my experience that the symptoms radiate out through the nerves from a center that is the true cause of the problem. Even if it is not a huge visible difference, with close observation you can see broken skin or raised skin at the problem spot.

Deeply treating the center of the symptom area is far more productive than surface treating the whole area with Cats Claw. Cotz can generally be used on the whole area along with baby powder with great results as long as the fungus problem spots are also deeply treated. Remember no tight clothing IE pants that do not allow skin to breathe and stay cool and dry.  I now only recommend people wear cotton and fibers that let the skin breathe. Better to treat clothing than wear clothing that creates a green house effect on your skin which is just what makes the fungus thrive.  Consulting with one victim I discovered her problem with re-infection was caused by wearing pantyhose. The trapped moisture and heat was what kept her suffering with the problem.

 Finding Bleach that works for soaking laundry remains a challenge. I have been told that Lowes Home Improvement carries something incleaning sections of the store. The brand is Styleselections that is working and is 8.25 % chlorine. Also at Lowes 30 Seconds Cleaning Solution for cleaning outside is 9% but costs $19.00. The same person told me that Clorox is down to 5 % chlorine so no wonder it is not working. I also noticed a basic bleach at K-Mart under the brand Home Basics. Avoid all bleaches that say Concentrated or New Improved Formula since they do not work at all on this condition. Remember that older bleach bottles of even the right kind can also lack adequate strength to clear things since the active ingredient loses its strength after about 4 months on the shelf. You could still try to use them but would need to use a higher concentration than what the bottle says.

Although I suggest you can use the PCO soak for multiple loads in the same day (see treatment page) I do not recommend storing the solution unless you can do that in air tight containers. There must be no air between the liquid and the lid. Also the amount of dirt for the dirty clothing affects the strength of the PCO. Keeping the mixed soaking solution in a covered Tupperware tub will not work since air will cause the active ingredient in the PCO to weaken and evaporate to the degree that it does not clear what you are soaking. Trying to soak less time in a stronger solution or longer time in a weaker solution also has proven to not work. Every time I learn that someone is leaving the clothing in the soak for longer periods like all day or overnight it does not work; I can't explain why but it has been consistently true.

The other helpful thing I would like to teach everyone is how to test food and items to see if they make your body stronger or weaker. This can be a powerful tool in avoiding what is keeping a person from enjoying their God given right to be healthy.  Everything you consume through your mouth, skin, lungs, eyes, or ears affects your immune system and the strength of your body.  This is some of what I teach in my book on natural hygiene (available here). In my book I point out that health is the automatic result of removing whatever is weakening the body. This may be food, vitamins, what your bathe with or put on your body. It can also be what you listen to and who you surround yourself with. In subtle ways, even colors can strengthen or deplete your physical body. All these things can either strengthen or deplete you. Each person’s body is unique; what can be strengthening for one person can be poison to another.

 A simple way to test everything you are exposing yourself to is called muscle testing.  It takes the help of another person to do it. I recommend that you be blind folded or at least tightly close your eyes so you can’t interfere and bias the testing. No matter how hard you try not to interfere, your beliefs and opinions as well as likes and dislikes will give you false readings. You will need a large plate or tray to place the items on to insure you can’t guess by weight or touch what is being tested. Hold the empty plate at your solar plexus so that what you are going to test can be placed on it;   (This is the area right in front of your Diaphragm which is the directly above your belly button right below your ribs.)  Now with the other arm you are not using to hold the plate, raise your arm to shoulder level either straight in front of you or straight out to the side whichever is easiest for you. Have your helper push down on your arm while you try to resist. Try with all your strength not to let them push your arm down. This is to develop a base line of your physical strength to compare to. Now have your helper place one item at a time that you want to test on the plate. Be sure this is without the any awareness of what is being tested as this is critical to obtain any accurate results.  Have your helper again try to push your arm down to test your strength with the item on the plate. The item will either make you stronger, weaker or there will be no change. Have your test helper place the tested items in three piles for stronger no change and weaker.  I suggest you definitely eliminate from your diet and life anything that makes you weaker. It is also wise to replace anything that does nothing to help you but does not hurt you. Replace what does nothing with what strengthens you and design your own diet of strengthening foods. (*Note sometimes a particular item will test week if the brand is a problem or the produce is somehow contaminated with toxins or pesticides.) Logically if what you are eating or taking depletes your strength (IE your life force) you are spiraling away from vibrant health. Amazingly you will discover that many of the supplements you take to make you healthier not only don’t strengthen, but weaken you. Supplements are concentrated foods so if they weaken you they have a bigger negative impact than foods.

Diet: Many ask what diet they should be on. I really believe that it is only necessary to restrict the foods and drinks that trigger an alkaline reaction in the body. These may even test well for you since long term they do strengthen but be aware the fungus seems to be strengthened by alkaline triggering foods. This includes  things  like orange juice, lemon juice (especially those tree ripened create an alkaline reaction in the body even though they are citric acid), coconut milk and coconut water, alkaline water, (might want to get PH strips-health food stores carry them- and test your drinking water) vinegars, apple juice etc.  The other things that trigger symptoms are things that irritate and excite the nerves so that includes stimulants and sugary foods like sweets and dried fruits. Caffeine and alcohol are also problems since one irritates the nerves and the other turns rapidly into sugar in the bloodstream. Grapefruit juice, pomegranate and cranberry juice seem to help as long as they do not have sugar in them. In fact if you feel a surge in the fungus in your system try drinking  these juices since they can shift your PH quickly.

I have been sent contact information about an MD specializing in mold  in Florida and am going to discuss sending people to him for testing. He seems to be open to researching things so that is a step in the right direction. I will send out a supplement newsletter if anything promising comes from my contacting him. If you are in Naples area of Florida and want to try to get testing done with him, please email me at This e-mail address is being protected from spambots. You need JavaScript enabled to view it . 

And finally, to give you some encouragement… I asked a couple of victims to share the encouraging truth that not only I got well, but others can and do get over this by doing what I did.

Dear Megan,
I can never thank you enough for all you've done for me. Truly there is no one else on earth who knows as much or cares as much as you do about helping people with this horrible affliction.. Everything you said about this has been true and accurate, as I've learned along the way.
I got well by applying your advice and using all the products you recommend, and using them the way you instruct. It has been a life-altering experience to go thru this and I'm sure no one would understand unless they've been thru it themselves.
I am greatly empowered by the knowledge and tools you've shared.
Earlier this year I was traveling thru an airport (I can travel now because I'm WELL!) and sat on a chair in the boarding lounge. After a few minutes in the chair, I suddenly felt a tickly-crawly sensation starting all over my body. I realized in horror that I was sitting in a chair that had been used at some point by a person infected, and I was reacting to this! I didn't want to get infested and then visit my family and expose them!
I had my RE9 Body Wash product with me in my carry-on, and I quickly got up and ran to the restroom where I went into the stall, wiped down my whole body with wet paper towels soaked with the Body Wash, and changed my clothes. I went back to the boarding lounge and sat in a different chair, and I was fine...there were no more symptoms because I acted quickly and did the right thing.
What if I didn't know how to deal with this? It's spreading all over the world. I'm now empowered to be able to help myself and my loved ones if they're ever exposed.
Thank you always, for saving my health...and probably my life, too!
TWD
Sept. 22, 2014

Review/Testimony for Megan Wells

I am so thankful for finding Megan Wells and her website, which is the only course of action that relieved my suffering .

Her 3 part protocol of:

          •  fogging the house

          •  caring for the skin

          •  laundry procedure

is miraculous and works!!

Along with the above protocols, my telephone conferences with Megan made all the difference in the world.  Through direct conversation with Megan, the procedures were clarified.  In addition I felt comforted and valued.  I finally found someone to listen, who had lived successfully through the same nightmare experience, and who had successfully treated the skin, the house, the laundry.  Doctors and dermatologists, as well as pest control companies were of no help to me.  Often they tried to discredit what I was experiencing.  Megan was the voice of experience, strength and hope that I could connect with.

Before discovering Megan, I was lost, trying many things over the internet for my hair, body, laundry, and home.  At best, none of these suggestions worked.  At worst, I was damaging my skin, body, etc, while spending a fortune with no results.  

With the gentle, holistic, natural products that Megan suggested, I felt relief for the first time from my symptoms.  I was getting better.  My skin, which was very damaged before Megan's protocol, is now healthy and strong. Today, I still use many of the products for bathing, shampooing and treatment of the skin because they are good for my skin. 

I found that Megan Wells is willing to go to any lengths to help others.  She is truly serving humanity with her website, protocol and consultations.   I trust her totally. 

For example:  I was visiting my daughter out of town and forgot the body wash. I needed it desperately.   Megan called the company, found a consultant near me.  The consultant met me the next day with the body wash, that I purchased, so I could continue the protocol uninterrupted. Thank you, Megan!

Megan Wells has gone above and beyond in her care warmth and consulting with me.  I truly believe in her and thank God that she has shared what she has found to be effective in getting rid of this condition.  Because of Megan, her website, her sharing, I am healthy and free today to live life to the fullest.  Thank you again, Megan.  I am forever grateful!!

Sincerely,
L J

Another confirmation client sent that what I discovered about this condition is true…

“hospital pathology an biology dept confirmed finding the following on tape of my husband my bodies: a) fungus- they want tape samples to determine the kind as we gave them photos of the tape, b) mites and c) something they said was organic and they could not identify - they want more tape samples- we believe this is the collembolan”

 Hoping for your healing and always praying for you all,

Megan

Newsletter 2015

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Stopskinmites.com

Newsletter 2015

I have been made aware, by numerous emails from victims, that Arbonne discontinued selling the SPF 30 Sunscreen for body  product number #950. This is very big concern since after careful analysis the Arbonne replacement SPF 30 for body does not have the same ingredients so there is no way of knowing without trial and error if it can do the same job. I have had 1 person tell me it did not work but I do not know if they applied it correctly,  which you all know is critical.  I am sending this notice out because I have not had a chance to update my website about this.  I hope to get help with that shortly.

However don’t panic , remember that the ONLY job the old Arbonne SPF 30 sunscreen for body did was protection from bugs bothering you while in the process of getting rid of them with the fogging and also providing a layer that protected from re-infection when touching things infected with the fungus.

As mentioned on my site, the original SPF 30 was only used as a sort of a hazmat suit. By that I mean it was a good safety measure when entering an infested area or touching infected things or not wanting to infect others. It was not used for getting rid of the fungus or Collembola but was a safety measure during the process.  The Cotz SPF 58 can and does doe the same thing as far as protecting and I have always recommended that on the face with the old Arbonne SPF 30  on the rest of the body as a hazmat suit. However Cotz is very impractical (stains everything) and expensive to use for the whole body as a hazmat suit. 

 BTW: Remember to cut open the flat end of the Cotz tube when you think it is empty. There is a lot left in the tube for you to use if you do this and then fold the cut end over  with a close pin or paperclip to keep it from drying out. You can keep cutting it shorter and shorter to reach what is left in it.

 I am grateful the Arbonne Bodywash (soap) that is so critical is still available. Arbonne has also discontinued the Glow With It which is really disappointing since it now has positively shown to heal the residual itching from the fungus damage without resurrecting the fungus if any is still present in the skin. In lots of lots of cases it has been what finally stopped the last of the symptoms.

 It may convince the company to bring these 2 products back if all of you send a letter to Arbonne asking for the Glow With It #955 and SPF 30 sunscreen product number #950  be put back on the sale. Please do not make any medical claims in your letter since that is a touchy subject with the AMA and FDA that can be misinterpreted since legally there can be NO medical claims for these products. Saying that can only serve to hurt my site and prevent getting the products back.  Just say you had great results with a skin condition you are suffering from and want to buy it again. You can say you found the products extremely beneficial because they are.  Last week Arbonne sent out a notice to everyone in the company that people using the new SPF 30 formula don’t like it as well so even sunscreen users are complaining... so there is hope. I am begging everyone receiving this letter to please do this even if you are over it. Do it for those who are still struggling and need it and for those yet to come.

 I am somewhat encouraged that the NEW Arbonne face sunscreen # 8915 main ingredients are the same as the Cotz and may work the same way.  This new Arbonne face sunscreen has the same main active ingredients as Cotz but instead of the 10% titanium dioxide 3% zinc it has 1.7% titanium dioxide and 4.4% zinc. It is possible it may be helpful but someone willing to experiment with an active case of the fungus/collemobola needs to try it and let me know so I can let others know.  If it does work, then it definitely can replace the Arbonne SPF 30 because Cotz also protects along with helping suffocate the fungus so this new Arbonne face sunscreen may be an improvement even over Cotz if it costs less and does not stain like Cotz.  I suspect that due to a reduced strength it may not be as strong as Cotz for the topical fungus treatment over Cats Claw but it almost certainly could be useful in replacement of the SPF 30.

I would  also suggest for those of you who were using the discontinued SPF30 sunscreen that you substitute the Arbonne bodywash in place of the sunscreen for now  if you don’t want to try the new face sunscreen number 8915. What I mean by that is, re-applying the body wash as a thin film after the shower and leaving it on and letting it dry.  In other words, applying it  with wet hands as a thin even film left on when there is need to be protected or to protect others. The bodywash and  discontinued Arbonne sunscreen did have some common ingredients so this is worth a try. I really do not like to recommend any products that have not passed the test of at least 12 people getting positive results so this loss is challenging.  My entire purpose for my website was to prevent others from having to experiment and waste time and money. I only have what works on my site in the treatment protocol. I do not know the result of leaving the bodywash on for extended periods since it is not made for that. I did use it as a coating when I ran out of the sunscreen when I was a victim but not for long periods since it was just until the sunscreen arrived.

Until the environment is cleared by daily fogging and getting rid of infected items that can’t be cleared, it is very important to keep the bugs off to keep them from re-infecting you. To keep the bugs off until you clear your environment and clear the attracting fungus from your skin, you can use spot fogging for 1 or 2 seconds in an area before you go into it. NOTE *Please try not to breath the fog since it can eventually irritate your lung tissue and if you get a sensitivity to it and can no longer use it, you will be in trouble. You can also use Now Brand  peppermint oil  (the cheapest strongest quality one I know of) on your clothing, feet, hair, etc that will repel bugs as long as it smells. Also burning candles and incense scares bugs and keeps them away from where you must sit for prolonged periods if you are home.

So in review I am suggesting three replacement strategies for the discontinued SPF 30:

  1.  To protect from fungus re-infection:  Reapplying  Arbonne body wash and or trying the new Arbonne  SPF 30 Face sunscreen # 8915
  2.  To repel bugs: Use Now Peppermint oil on your clothing, shoes, and hair and reapplying when it no longer smells or Spot fogging area before you enter (can be just creating a faint cedar smell so you are not breathing it).

Dealing with infected feet

Almost everyone who contacts me has the fungus on their scalp and feet. Shoes are a problem because they hold in heat and moisture; just what the fungus loves.  The Crocs or other rubber shoes are maybe easier to disinfect but they do tend to create sweating and that is counterproductive. Remember dehydration is what kills fungus and moist heat makes it grow. I realized a simple easy to soak and dry shoe might be what are called a Tai Chi slippers or shoes. I have linked these to Amazon so you can see what they are.  They make them for men and women. You might be able to find them locally.  They are thin cotton with a rubber sole and they would soak and dry faster than any other cloth shoe and may breathe better than tennis shoes although they do not have cushioned foot bed. Just a suggestion if you are looking for a cheap shoe during the process of getting over this and you need to treat what you wear each time. Spraying any shoes with rubbing alcohol including Croc’s and flip flops is not working to clear them. These need to be also soaked for an hour like the rest of the laundry and linens to be certain they are disinfected.

I just received the golden news that there is a bleach that is working for everyong found at the CVS drug store chain. The brand is Total Home. This is good news since so far all the "New Concentrated" bleaches, which now is most of them, do not work at all.

I wanted to remind everyone that if you are not actively using your fogger to clean it out to store it. You can run warm soapy water through it to clean it for storage or if you have been using it for many months it may also require this as maintenance. One person from Hong Kong asked me to include her email about foggers for other countries with different power sources. See below: From Hong Kong

“If possible, pls mention in your coming newsletter that there are 110V and 240V fogger for selection. People who wants to order it need tell Cedarside which one they need as otherwise, the fogger would break down and they have to buy another one again. Money is not the most important issue, time is. Like us, we had lost a week's time to fog and we have to use longer time to eradicate the problem. And now, it seems the result is not as good as we first fogged”.

I recently watched an 11 hr special called the Truth About Cancer for my other consulting work where all the leading doctors (MD’s) doing new treatments were interviewed.  I was amazed to see that everything they were saying that was considered groundbreaking in the series was already in my book You’re Not Fat You’re Swollen that takes only about an hour to read. The revolutionary news was what I have been saying and teaching about cancer for the last 50 yrs.

 I wrote down names of these brave and cutting edge doctors that seemed to be interested in all kinds of innovative research. I will be writing them and asking if they will research this fungus. We shall see. At least they had grown past the pill and bill insanity that most MD’s are doing where they do no diagnosing at all only prescribing with you as a guinea pig. The let’s try this and see what happens to you MO.

I still hear some are trying to wear polyester which I have not recommended for many years. Fabrics that allow skin to breathe and airflow against the skin are preferable even though the cloth is more easily infected. Fabrics that do not breathe make the fungus worse as well as any tight clothing. You know this because you will see that except for your head, crotch and feet that are hotter and sweat more, the places the fungus tends to grow are in areas where sweat is held against the body like straps, waistbands and where there is elastic against the skin. Until you are over this, try to wear loose clothing and clothing that allows air against your skin especially where you have the active infection. You have to treat cotton or linen after each use, but then you should do that with any clothing. At least with fabrics that breathe you are not increasing your problem.  Also be aware of sitting or sleeping against plastic. There needs to be air flow so even though it is cloth you will need to treat, ALWAYS have something that allows air between the plastic and your skin like a mattress pad thick towel etc. This applies to your  air mattress, un-upholstered chair, car seat and head rest as well.

 

Here are some great tips from woman that now helps me with the newsletters that I helped get well. I think they are worth including here:

 "for chairs...plain plastic or metal is best. Even my plain wood chairs had to be treated for fungus a hundred times altho they were always in the room when I fogged, because the wood really absorbs fungus and the seams can be hiding places for mites.
I tried many things to clear my wood chairs of fungus, including a PCO/water spray, but what worked best is the Dawn Blue Ultra dish soap mixed in water in a spray bottle and scrubbed on the wood. I had to do it regularly for a while.
For a temporary mattress with extra easy handling, people can buy a beach float mattress...the deluxe type with a built-in pillow, and use it on the floor as a bed. These can be washed daily with the Dawn dish soap and water, fogged, sprayed with rubbing alcohol, or whatever it takes to have a bug-free bed!
The microfiber sheets you recommended worked really well, altho I eventually stopped using sheets and instead just rolled up like a taco in an acrylic blanket which was perfect, and could be fogged 6 nights a week before bedtime and then PCO soaked on the 7th day.

(Please note that I believe the Dawn dish soap has very toxic chemicals in it) Megan

If you are not having decreased symptoms on daily basis in both environment and skin then there is definitely something being done wrong in the protocol?  I know this not only from the feedback from those who have been helped, but also with my own experience of being re-infected and getting over it again and again in the beginning of my own healing back in 2008.

And yes to answer the most common question. I am well and working many jobs so I have my life back other than financially. Still digging my way out of that pit.

If anyone has website skills I could really use help with SEO on the StopSkinmites.com website. The most common complaint I get is how it takes (3-4 months) to find me.

My prayers over all of you that you will have your life back and then reach back and help the others.

Kindness is the best religion,

Megan

Newsletter December 2013

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Newsletter December 2013

First I want to thank those of you who have written me expressing your appreciation for being helped by my site. It makes my sacrifice of time and money to keep this going worth doing. When you are relieved I feel relieved. I have recently (as of this month) updated and simplified the protocol found on the Treatments for Collembola page.  Even though there is other valuable information found in previous newsletters, please disregard all previous suggestions found in the older newsletters and follow the Protocol currently found under Treatments for Collembola. Do not use anything not mentioned in the current treatment protocol since I have streamlined and eliminated the products not absolutely necessary so that victims will focus on just what works the fastest and costs the least.  Products for fogging and clothing treatments found there are still the first step and are essential for any progress. These have been confirmed over and over as working quickly as reported back to me from victims on a daily basis. Next most helpful is the bodywash which continues to bring amazing email praises. Topically, the Cats Claw and Cotz and baby powder treatments continue to show the best results topically even on advanced cases where victims have had unhealed lesions for years.

One victim who convinced a dermatologist that she did not have scabies and was not delusional was told she had a condition known as folliculitus but she was also told the crawling sensation was from her hair follicles rubbing against clothing and not from a bug. Of course this diagnosis did not explain the crawling on this victims face or scalp where no clothing is there to rub (her main symptoms) so that was my first indication that yet another dermatologist was wrong. I did a Google search on folliculitis and found it is, as it turns out, just a fancy medical term for skin infection of the hair follicles but then I realized that knowing this terminology might be advantageous when it comes to dealing with a dermatologist.

One of the only symptoms folliculitus does not cover is the crawling which we know is related to Collembola and other microscopic fungus loving insects that may be attracted to the areas infected with the skin fungus.  No matter what anyone says, based on so many victims (including myself) getting positive ID of bug specimens in the environment (but not on or in the skin), we know that Collembola is involved.  I have been saying for years now though that the fungus, not a bug, is the initial cause. The bugs are incidental but I know from experience and feed-back from others the bugs are spreading the fungus once they come in contact with it on an infected person and are the source of the crawling sensation.  We also know that this is an epidemic, so the common reasons people would normally get folliculitis do not logically apply to this. Most common cases are caused by bacteria which is not true in this case since no fungus loving insects would be attracted if it were a bacteria. Also this is most likely spread from spores in the air or by physical contact and not from the common causes stated in the article I have posted later in this newsletter which mostly address bacterial causes. The causes listed in the article would NEVER trigger a widespread epidemic in almost every state in the US and now in so many countries where victims have contacted me. (IE China, Japan, Taiwan, Australia, Canada, UK, Ireland, Hungary, India). Recently I was told by a victim that his dermatologist admitted telling 34 victims with his same symptoms that they were delusional and this was just so far this year. This is one small city in the US so just imagine what the reality of the number of cases in the US actually is and the number of misdiagnosed victims. UGH!

I am bringing the term Folliculitus to your attention since this medical terminology may be useful in going back to a dermatologist and getting an accurate sample of the infecting fungus; something we desperately need so this plague can be studied by scientists or Universities, if not by the uncooperative medical professionals. I have received 100’s emails from victims where a scraping or biopsy did show an unidentified fungus, however, the only positive ID of what exactly the fungus was came from a different kind of diagnostic equipment (see previous newsletter found under Updates on stopskinmites.com). Note* I have posted this article on this later in this newsletter along with my comments.

Unfortunately, when I studied the prescriptions this last victim got from her dermatologist, they were acne medications plus a symptom suppressing cortisone cream. I had a quite a few try some of what was prescribed because it was supposed to be drying (a benzoyle peroxide wash and cream) but unfortunately the feedback by everyone was that it did nothing to help (big surprise). Note *Feed-back has shown that any cream is counter-productive even if it contains some antifungal properties. Many have been hurt by prescription creams for scabies that made them worse. So far, only what can dry up this fungus works.

I tried the strongest prescription antifungal creams for weeks when I was suffering in 2006 and none of them worked for me. Most of what was prescribed to this victim was really damaging to the immune system (just my un-medically based opinion) based on studying the side effects posted on the net. One product was just symptom suppressing and 2 of them had side effects that caused an increase in vulnerability to skin infections. The prescriptions appeared to be aimed at bacterial not fungus infection so that is a warning if anyone is going to try dealing with a dermatologist again.

I did get an email from someone mentioning they thought they had some results from a pharmaceutical called Nystatin. http://en.wikipedia.org/wiki/Nystatin. Quote from Wikipedia: “When present in sufficient concentrations, it forms pores in the membrane that lead to K+ leakage and death of the fungus. Ergosterol is fairly unique to fungi, so the drug does not have such catastrophic effects on animals or plants”..

This may be worth exploring since it does not seem to have the side effects of most antibiotics. I would not suggest any Nystatin creams or ointments since the side effect is itching. Logically this would be a night mare on top of a nightmare.

Antifungal creams don’t work because I still strongly believe that the fungus causing this condition is not normal fungus based on how it has spread all over the US and the world and because no one to date has positively identified it in the regular medical community. This is even after a year of study by the US Center for Disease Control and Kaiser Permante who then turned over the results to the US military and then after much criticism for not releasing the findings, made a statement that all the victims were delusional.

Below is the article copied from the internet on the condition called folliculitus: Please note the Yellow highlighted statements in the article are highlighted because, interestingly, they match what I have been saying now for years on my site. I have also put my added comments and concerns highlighted in aqua throughout the article copied and pasted below.

Folliculitis - Topic Overview

What is folliculitis?

  1. Folliculitis is an infection in the hair follicles. Each hair on your body grows out of a tiny pouch called a follicle. You can have folliculitis on any part of your body that has hair. But it is most common on the face and scalp and areas rubbed by clothing, such as the thighs and groin. This does not seem to explain the common foot symptoms reported to me since it does not seem there are hair follicles on bottom of feet but it is possible that those symptoms on the bottom of the feet could be nerve ending symptoms from the fungus in the nervous system.

What causes folliculitis?

It usually is caused by bacteria. It also can be caused by yeast or another type of fungus. (See definition of fungus I pasted below) Based on the fact that fungus loving insects (which have been confirmed) are attracted, it must be a fungus and not bacteria. It is a concern that most dermatologists will try treating this as a bacterial infection when it is fungus or possibly a cross between a fungus and bacteria (GMO) God forbid.

You may get folliculitis if you have damaged hair follicles. Shaving or wearing clothes that rub the skin can irritate the follicles, which can lead to folliculitis. (I have observed that tight clothing makes the fungus worse) They also can become blocked or irritated by sweat, machine oils, or makeup. When the follicles are injured, they are more likely to become infected. (Again I have said anything that weakens the skin makes this condition worse)

You are more likely to get folliculitis if you: The below causes are not the cause in this case because of the epidemic proportions of this condition and the fact that it appears to be approaching worldwide

  • Use a hot tub, whirlpool, or swimming pool that is not properly treated with chlorine.
  • Wear tight clothes.
  • Use antibiotics or steroid creams for long periods. The cortisone creams are a form of steroid creams and that is what many dermatologist prescribe so there is a contradiction here since this says using these kinds of creams long term can cause folliculitus. http://www.mayoclinic.org/medical-edge-newspaper-2011/oct-28a.html Steroid creams have been used for the past 50 years, but are not a cure because they have no effect on the underlying cause of inflammation. They can, however, be very effective in helping to control skin flare-ups and relieve symptoms, such as itching and irritation” 

*Note this says that this cream usually prescribed by a dermatologist only temporarily relieves symptoms and can cause folliculitus if used long term and long term use would likely be the case since it does nothing to remove the cause.

  • Use or work with substances that can irritate or block the follicles. Examples include makeup, cocoa butter, motor oil, tar, and creosote.
  • Have an infected cut, scrape, or surgical wound. The bacteria or fungi can spread to nearby hair. We already know this is contagious.
  • Have a disease such as diabetes or HIV that lowers your ability to fight infection.  This does not match my data for the past 6 yrs since most of the victims that I have been contacted by are healthy before they get this which I still believe is related to the alkaline chemistry of a healthy immune system.

What are the symptoms?

Folliculitis usually looks like red pimples with a hair in the center of each one. The pimples may have pus in them, and they may itch or burn. When the pimples break open they may drain pus, blood, or both. (The comment on when the pimples break open was not the case with me and most victims that have contacted me so must be more related to bacterial than fungal infection cause),

"Hot tub folliculitis" most often appears about 72 hours after you've been in a hot tub or spa. Many small pimples appear on your stomach and sometimes on your arms and legs. You might have a mild fever and have an upset stomach. Most of the time, this kind of folliculitis goes away on its own in 7 to 10 days. Definitely not this

How is folliculitis diagnosed?

Your doctor will check your skin and ask about your health and activities. He or she may do tests to find out what is causing your folliculitis (PLEASE GET TESTED FOR FUNGUS) and to make sure you don’t have a different problem, such as impetigo or heat rash. Testing a sample of the fluid in the pimples or a sample of tissue can help your doctor learn what is causing the infection. Ask the doctor for an identification of the exact fungus not just an unidentified fungus confirmation as many have received from their doctors to date which gets us nowhere….

How is it treated?

Mild folliculitis usually heals on its own in about 2 weeks. You can take care of yourself at home with: We all know from experience that this does not apply at all with this condition

  • Warm compresses made with white vinegar or Burow's solution. These may ease itching and help healing. Not with this fungus… and the warm moisture can make it worse as well as the alkaline nature of vinegar that we have seen just aggravate this and Burrows solution is for bacteria.
  • Medicated shampoo Has not so far worked for anyone I know of in last 6 yrs. It can be used to treat folliculitis on the scalp or beard.

Here is a definition of fungus I copied from the net:

Fungus

A fungus is an organism that can grow on living and nonliving things This is what I have been saying… that this can not only grow on nonliving things but can also be spread this way. Fungi (the plural of fungus) include many types of organisms including yeasts, mold, and mushrooms. Fungi that cause problems for people include yeasts and molds and other types of fungi.

In some situations, fungi can infect and damage tissue, such as skin, hair, or nails. Fungi also may be involved in infections throughout the body, such as in the central nervous system or the bloodstream.!!!! This is what I have been saying that this is not in the blood or digestive tract but in the nervous system.

The inhalation of fungal spores (airborne) or the local colonization of the fungus (skin contact) within the epidermis can lead to infections.

Folliculitis - Topic Overview

(continued)

If the infection doesn't go away, you may need anantibiotic or antifungal cream. If your infection is severe, your doctor will prescribe antibiotic or antifungal pills. (So far as I know, no one has been prescribed antifungal pills by an MD or dermatologist so I do not know what that might be or if they would even work on a genetically modified fungus. My pharmacist friend that was head of Kaiser Permanente Pharmacies for the state of Hawaii who tried to help me with this told me antifungal pills can really damage your liver and or kidneys. Your liver is what keeps your blood stream clean and your blood stream is like a stream in nature that nourishes and cleanses all it touches in this case that is all your cells….

Call your doctor if you have folliculitis and: Think carefully before you do this since I went to 9 dermatologists with no help… just loss of time and money

  • It spreads or keeps coming back.
  • You have a fever over 101°F (38°C).
  • The infected area becomes red, swollen, warm, or more painful.

If the infection doesn't go away or keeps coming back, laser hair removal may be an option. Laser treatment destroys the hair follicles so they can't get infected. (This is ridiculous in my humble personal opinion like cutting off your hand to take care of a splinter)

How can you prevent folliculitis?

There are many things you can do to prevent folliculitis or keep it from spreading. Another comment about how this is contagious

  • Bathe or shower daily with a mild antibacterial soap. This is not a bacteria and no one so far has had that work only the  Bodywash helps in a permanent way Also, bathe or shower after you exercise and after you work around chemicals.
  • Avoid sharing towels, washcloths, or other personal items. If you have folliculitis, use a clean washcloth and towel each time you bathe. (This is what I have been saying about clothing and linens for years now)
  • Don't scratch the bumps. (This is what I have been saying about treating instead of scratching)
  • Avoid shaving the bumps. If you must shave, change the razor blade each time Shows how contagious this is even on your own body. Try using depilatory creams and lotions, which remove hair without shaving. (These products are not recommended for use more often than once or twice a week.) I would not do this since they are toxic and weaken the skin
  • Avoid using oils on your skin. Oils can trap bacteria in the pores of your skin and can cause folliculitis. (This is what I have been saying and everyone who has used oils and who has had permethrin creams prescribed has been hurt by this, except the essential oil brands I have shared on my site that work because they have very little oil in ratio to their active antifungal properties because of their quality and refinement. Seems like this would be clearly malpractice based on a misdiagnosis of scabies and prescribing creams… something that should be avoided for filliculitus).
  • After you use public hot tubs or spas, shower right away with antibacterial soap (This does not apply to fungus and does not work). If you own your own hot tub, follow the manufacturer's instructions for keeping it clean.

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If, after studying all that I have written,  you want to try going back to a Dr. and you have carefully considered the fact that they do not really have the answer but are willing to go to try to get a positive ID of the fungus, below is what I suggest you do. I still recommend you follow my protocol however, since based on my own experience and enormous amounts of  feedback, I know it is the best there is so far out there for getting your life back.  

PLEASE DO NOT TELL THE DOCTOR about my site since they do not like anyone cutting in on their territory and they may attempt to remove my site.

1. Make an appointment with a dermatologist. Either a new one or the one you have already seen

Even if you have not been helped by them they should be more attentive since now they will

know you know they misdiagnosed you IE scabies, delusional, dry skin, etc

2. Tell them you have Folliculitis and say that your symptoms match but that it is a fungus not a bacterial infection. You can’t tell them how you know it is a fungus since if you mention bug crawling symptoms they will go back to their old “you are delusional routine”.  Only tell them about the fungus symptoms (IE all but the crawling sensation including but not limited to stinging burning pinpricking itching etc. Tell them it feels like it is affecting your nervous system.

3. Get a scraping or better yet a skin biopsy to identify the exact fungus that is causing the folliculitis. I am not sure you will get any answer since the labs are only are educated to ID human pathogens not plant pathogens or anything like a newly created genetically modified fungus.

4.  Warning: Do not mention bugs or crawling symptoms. They will do nothing for you and ridicule you. If they can help you with just the fungus ID that would be a miracle. The bug crawling is easy to get rid of with the fogging product that worked for me and everyone that has used it correctly. Also, when you no longer have any fungus infecting your skin or environment, the bugs will not be attacking you since that is the only reason they are attracted to you and your house or car.

5. I would not take a prescription called Doxycycline which they may try to give you since that is for bacterial infections. Here are the side effects for you to be educated http://www.drugs.com/sfx/doxycycline-side-effects.html I would possibly ask for an antifungal pill if they insist on giving you something internally but Google the side effects before you decide since weakening your immune system means weakening your ability to ever get over this.

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If you do get a positive ID or get prescribed something that you find works beyond temporary symptom relief (which is what most doctors are schooled to do) please email me and tell me what it is. I am always trying to find a shorter way out but at least there is a way out (my protocol). Even though it does take effort and time it is tried and true if done correctly. I do not post any suggestion unless 100’s of victims have reported results.

I recently had to clear out my house of 24 years because I sold it at a big loss to get out from under my crippling mortgage. While going through a box I felt that old horror when my forearms began to burn and itch. I jumped up and ran to do my protocol. I immediately bathed with the Bodywash, disinfected my clothing with PCO and treated my arms with Cats Claw, Cotz and baby powder. (I keep all these on hand for emergency and have found many other great uses for these things). It worked like a charm and I am relieved to have proven with my own experience once again that this protocol works. What is alarming though is that this thing was still contagious in a box after 6 yrs of being closed up!  When I was sure I was normal after giving it a couple more days, I coated my hands, arms, torso, neck and shoulders with the SPF 30 sunscreen and my face with Cotz and dove back into the same box and felt nothing and did not get it again! Another reassurance the there is nothing better out there than what I discovered and have shared with others through my site.

I have a few suggestions that I remembered that are helpful:

  1. You can buy a very high 30x magnification magnifying glass for very little. It is called a jeweler’s lens and costs less than $5.
  2. I highly suggest you buy a 10x magnification lighted mirror on a stand so you can more accurately treat spots. You can see where the epicenter of the problem is if you can see the skin better since the nerve symptoms tend to make you believe it is an entire area when it sometimes is possible to treat a smaller area or even just a spot and benefit/relieve the whole area.
  3. Gold Bond Baby Powder: This is new and contains zinc powder which is also a beneficial ingredient in the Cotz and I have feedback that it is superior to regular baby powder in the protocol. It may also be sprinkled on to things you sit on to help that way.
  4. Try using ice for intense itching and burning relief. Be sure that it is not adding moisture so put the ice in a Ziploc or if using an ice pack be sure cloth surrounds it so you are keeping your skin dry. Spraying the Kool 'N Fit as a temporary relief of burning and itching can be useful while away from where you can treat or for convenience in the middle of the night. It does work to stop burning and itching for up to 4 hrs and is drying on the fungus. Also try spraying some on a cloth and breathing it through your nose to stop those symptoms.
  5. You can pinpoint areas infected under the skin when no surface symptom can be seen by lightly rolling your skin between your thumb and forefinger along an area. The area with fungus under it will be tender and painful and the areas with no fungus underneath will not. The center spot of the nerve pain generating out will be coming from the most tender or painful of the area in this procedure. There is a slight swelling that is not easily perceived except by this type of checking. It will help you to know to what extent the fungus has spread under an area of your skin where there are no surface symptoms yet and help with treating it.
  6. You might try to have a neuro-surgeon (nerve specialist) look at you and see if an MRI or other testing on the nervous system would show the fungus infection in the nerves. We know this is infecting the nerves and these types of doctors also treat nerve infections. Most doctors no longer diagnose, they just prescribe. What’s wrong with this picture? Shouldn’t they try to find out what is wrong so they can fix it correctly before they prescribe? Beware if they do not try to diagnose and just try to experiment on you with drugs someone has asked them to push.
  7. It is confirmed from feedback that highly alkaline triggering foods and drinks can set off an outbreak of the fungus. Drink Cranberry juice to quickly shift your PH. (I like an organic frozen concentrate made by Cascadian Farms that can be mixed with grapefruit juice for a less sweet juice. I like the fresh not from concentrate grapefruit juice by Simply found in the health food stores. This combination or cranberry and grapefruit juice is a great source of vitamin C. You can also add unbuffered vitamin c powder to this juice for added benefit.

The other winner are Pomegranate juice  to quickly shift your PH. Do not drink any kind of alkaline water or alkalizing drinks like coconut water while trying to overcome this since the fungus likes alkaline and coconut in any form including the oil is a trigger for this fungus. Here again is an alkaline acid food chart. Pick healthy foods that are not high alkaline. http://www.rense.com/1.mpicons/acidalka.htm Things that excite/irritate the nerves like refined sugar, alcohol, caffeine, can also trigger symptoms. Unfortunately pro-biotics also seem to exasperate the fungus as well as oxygen treatments.

  1. Much damage gets done to the skin due to not only the fungus, but also all the toxic treatments that people try before they find me. At the end of doing my protocol, there may be some itching and possibly even burning that can be due to damage to the nerves and skin and not due to any residual fungus. There is another skin product made by the company that makes the Bodywash and SPF 30 sunscreen called Glow With It that I have added to the skin product page on the website.  It was formulated to repair sunburned skin. This product has shown promise in healing the fungus damaged skin. It can be found right next to the sunscreen when you go to order from the company. It appears to be formulated with some of the same basic ingredients found in the Bodywash and Sunscreen that work so well. We know that like the other two skin products from this company, it does not exasperate the fungus and may be able to quickly heal the skin of these residual symptoms.  Warning*I would not try this product until all crawling symptoms are gone. It is not a replacement for the Cats Claw or other topical treatments in the protocol along with keeping the skin dry at the end.  However, when you are almost clear, it may speed up healing the skin and quickly eliminate the last of the topical symptoms. There have been limited trials of this so please let me know if you too have good results. If for any reason you are not benefited for residual fungus symptoms, save it for your face later since it is a fabulous and healing face lotion that I like as well as this company’s $85 a jar repair night cream. * If you have the SPF 30 on your skin rinse it off before applying the Bodywash since the combination of these 2 products can give you an itchy red rash. In this case you would not follow my instructions to apply the bodywash to dry skin since your skin will already be wet from rinsing off the sunscreen.
  2. On a spiritual level, this is like some kind of possession. You must stay firm in your heart and mind that your body is yours and nothing has the right to live off of your energy. Make a strong statement that you will not allow this to take over you or your life. Be determined and pray for strength. Picture the body you were born with and tell your body that anything that was not part of your original DNA at birth does not belong and needs to be eliminated. I believe the body has a hard time identifying that this is foreign to it and that it is something to be gotten rid of (because it is genetically altered). Since the fungus likes what your immune system likes it seems to try to become part of the body. The visualization of your body’s original blue print might be helpful to your immune system in identifying and fighting what seems to be trying to live like it is part of you and off of you. The body understands what you tell it and communication is a big part of how the body works.
  3. Post Traumatic Stress Syndrome. I am sure there is some of this experienced by everyone who has suffered with this. It can be as mild as thinking that everyone one you are around is itching because of you to any insect landing on you making you panic. As far as the itching going on in others, I have learned that everyone is itching all the time we just never noticed before. This is the same phenomena that takes place when you decide to buy a car and then see that model everywhere even though there are not suddenly more of those cars on the road. You can tell if the person itching around you has a problem or is normal by watching how they react to the itch. If the itch goes away once it is scratched it is just a normal itch. If the once scratched it itches more it is a symptom. It took me awhile to relax about the normal itch or a real bug really crawling on me. For awhile I was even elated and relieved every time I saw an ant on me. Even this residual nervous reaction goes away with time once you realize you are just over reacting and the problem is in your hypersensitivity. This of course only applies when you are well past the real symptoms.

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Because of so many requests, I am going to undertake making this website into a printed booklet entitled Getting Your Life Back and hopefully with the help of one of the recovered victims who offered to help me with editing, this might happen in the near future. She has also suggested a video of me demonstrating the protocol and /or an added CD in the booklet of me explaining it. This would help many more people and help me get some time back for living my much cherished normal life again. I have not had any time off now for the past 6 yrs since I just can’t ignore the agony I know is in every cry for help. I get in a steady stream all day long every day of the week. So far, there is no one else willing or experienced enough to do the consultations.

It has also been suggested that I consider offering 30 minute paid consultations for $50 that can be booked back to back to make up the hour but those would not involve my studying an intake since I spend additional time on to do that and time is something I just do not have any extra of since I continue to work 3 other jobs.  I have not offered those in the past since I have seen that it is not possible to cover everything in just 30 minutes but maybe this will help some people with follow up questions that have already had an hour with me.

If you are interested in the option of an additional 30 minute paid consultation, please email me and let me know. If there are enough requests we will change the policy to include these. I have tried to put everything any one needs to get over this on my site for free but, I  also understand that my guidance can be comforting and save people from making huge mistakes that cost them both time and money.

Although the fact that this has gone worldwide is alarming, it is now my hope that someone, a doctor or scientist, in another country will do some research on this. It is obvious, based on no results here, that there is some kind of blockage in the US. I still wonder if our government is protecting some powerful corporation who may have had a hand in causing this condition. My prayer is still that this might someday be covered under health insurance and that the validity of the suffering involved is somehow verified and acknowledged. This is sorely needed to help heal the separation this causes in families and relationships because only certain people are affected in a household.

Lastly, if anyone who has recovered and gotten their life back is interested in helping others still suffering, please email me.  I need others who can answer emails, give hope, and answer questions for those still suffering.

Always praying for all of you,

Megan

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