Silent Masters: Parasites, Molds/Fungi, & Bacteria

Link: http://www.rhrplus.com/education/ed_articles/skin_parasites.php

Strange Occurrence Of Skin Parasites
Restorative Health Research Plus™

Several years ago, shortly after I discovered that I had a problem with internal parasites, I started to notice a strange occurrence of skin parasites. I couldn’t deal with both internal and external parasites – the internal parasites was more than enough – the skin parasites had become a nightmare. I needed to get rid of them fast.

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Ever since I’ve been ill I spit/cough up copious amounts of mucus/slime. I’ve never got used to it. I’ve had it since day one.

I believe I need to address the mucus/slime in order to get to the parasites. I’ve always wondered whether it is the mucus/slime that is protecting the parasites, like a barrier.

Here’s what I am doing -

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I’m posting two pictures of what I passed in my stool. I don’t recall eating anything that resembled this. I’m wondering if perhaps, in fact, I passed some worms.

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I experienced a flare-up of symptoms today. I just don’t feel well at all. I’ve had a good run lately, whereby I’ve been feeling really good and my treatment is going well. I haven’t experienced a flare-up for a while, until today.

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I have an appointment with an Infectious Disease Specialist. I’ve had my results for over a year now and I’ve often wondered about visiting my doctor and showing him what I’d found out about my health. I had a lot of pent-up anger inside of me because of the way I’d been treated visiting doctors and being portrayed as delusional, paranoid etc. I felt by visiting my doctor it was perhaps a way of releasing this pent-up anger. To cut a long story short, when I plucked up the courage to go, he looked at my results, in awe I have to say, and without hesitation said words to the effect, “well, then it’s a trip to Infectious Disease for you". My doctor seemed to be very impressed indeed with my micrographs and notes. He couldn’t stop looking at them. He made a comment - ‘high powered micrographs’. He had no hesitation in making a referral to Infectious Disease. That came across loud and clear. I couldn’t believe it.

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As if I don’t have enough to contend with!! The parasites / infections / infestations are bad enough. All I need is for my endometriosis to rear its ugly head!

I had the period from hell on Friday. It started 2am, early hours of the morning. I’ve suffered from endometriosis (diagnosed as severe) since I was about 18 years of age. That’s when I first noticed the symptoms and the pains. It took 9 years for it to be diagnosed!

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When I received my results from RHRPlus it was one heck of a shock when I first read the analyst’s report and viewed the micrographs. But for me, now, I ony have relief that part of my nightmare is over. The part of NOT knowing is over.

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I’ve come to a stage where, although I’ve tried to explain in great detail, along with my results to my family members, they still show great ignorance and discomfort at the sheer mention of my health problems. If you can’t count on your own family at a time like this, then I don’t know when you can. It has almost been like fighting two illnesses.

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Here is a post I did some time ago regarding a large Nematode which was grown in culture from my stool sample. See previous post, here.

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I got in contact with Dr Kleeman in Germany. He is a doctor who has been working with lyme disease for 15 years and is a well known authority on the subject. I sent a blood test to another lab in Germany and it turned out positive for lyme disease. In Sweden, the doctors don´t believe in chronic lyme disease, so they don´t accept the testing either. All the lyme experts here believe that you can get small doses of antibiotics for a period of about 14 days and you will get cured from lyme disease. This is totally wrong. The lyme spirochetes are very well suited for survival and are mainly located in the organs, especially fatty tissues like brain and liver, and is also considered an illness of the small vessels in the body. From the tick bite they travel through the body and the blood vessels, go through the vessels and creates inflammation in the tissues. The inflammation makes it more difficult for oxygen to be delivered throughout the tissues. A way that you can see it is in the eyes. It is common for lyme disease patients to have red, dry and itchy eyes which are also very sensitive to sunlight. The redness is not just the eyes that are dry, but the actual inflammation of the capillaries in the eyes.

Since I am refused treatment in Sweden my parents had to take a bank loan for $20 000 for a two year treatment with antibiotics. I can´t take a bank loan myself since I don´t have any money because of the illness. Many other people have sold their homes in similar efforts to get better.

I went down there and got intravenous treatments two times a day for three weeks and got even worse. My mother went with me and helped me wake up and get out of bed for the appointments. My head felt like it was going to explode and my eyes got more red than ever. Dr Kleeman is a wonderful person as well as his staff, and they were extremely supportive. It´s the first time in ten years that I have experienced that, most doctors I have met are either ignorant or rude or sometimes both. I went back again to Sweden with a promise from my doctor that he would help me with the IV injections, but when i got back he changed his mind. So now I have to figure out how to solve that problem.