A few months ago I started investigating ‘outside of the box’ in regards to what is making me (and everyone else with fibromyalgia, CFS/ME) unwell. I was never ‘comfortable’ with the fact that there are over 200+ co-existing conditions and symptoms that come part in parcel with these illnesses and felt that there had to be root causes that were not being thoroughly investigated. At first, I came across the whole mold and mycotoxin area and felt there was something in this. I started to look for testing, as we are living in an area with whisky fungus (our homes, cars, patio stones are turning black from this! So we are breathing it!!). All I could find was a hair analysis kit. Then, by fluke (or I like to think Divine Intervention), I came across what is called ‘pathogenics’ and there is testing for over 1000 different pathogens. And ding ding ding! The fibromyalgia, CFS/ME pathogen connection completely made sense.
For me and the journey I am on regarding a) finding out what the ROOT causes are of my health issues and b) treating them and feeling better I have come to the realisation that:
- I am not going to find answers and help on the health system
- That it is going to cost money
- If I don’t take radical action regarding my health, nobody else is going to…
The health system is great in many ways – and antiquated in many others. Doctors on the westernised health system are tied to the options provided through big pharma. In many cases these treatments cause more side effects than help – certainly as is the case with fibromyalgia and CFS/ME. (As Dr Bruce Lipton says, ‘There is no such thing as side effects, they are DIRECT EFFECTS). When less than 10% of the people using the 3 FDA approved drugs for fibro are finding relief? (And many are experiencing major side effects? There is something radically wrong with this situation…)
As well, tests through our health system can be shockingly, wildly inaccurate. For example, a magnesium test to check for deficiency? 99.7% inaccurate! We get these results and walk away thinking, ‘well, that’s not it, then!’, meanwhile, it could very well be the issue. (80% of Americans are deficient in magnesium. I know my diet is not fantastic, yet my mag test can back as fine…I know for a fact this is not the case!).
What is Pathogenics?
My Experience (so far…)
I have had well over 60 pathogens detected – from cytomegalo virus to Epstein Barr, meningitis strains, a variety of different fungus, including different candida strains and so much more.
For myself, the first consultation? Well, I was in tears. And not tears of pain, either. (There are no bloods taken, pathogens are detected immediately and treatment starts within a few days (once your specific remedies are made).
Tears of finally feeling vindicated in finding the whack of pathogens I was dealing with…hepatitis, meningitis, cytomegalo virus, poliomyelitis, just to name a few. (There were 29 found in the first consultation, if you would like to see my list of pathogens detected, go here). No wonder I was feeling sh*t!
As well, my husband had a weird ‘rash’ on his ankle that doctors had prescribed antifungals and corticosteroids and they did nada…when tested, he immediately had hepatitis show up. Hepatitis C, in fact. (And within a month of treatment (which was 2 days of a few drops of remedies in water)), his ankle has healed, I kid you not.
I have also seen people who have gone for a consultation with rosacea and psoriasis on their face, return a month later – with their faces completely cleared. (Skin can be one of the most difficult areas to treat so often takes much longer). Dealing with invisible illnesses such as fibro and ME/CFS and the erratic fluctuation of ever-changing symptoms doesn’t make it always easy to see whether there has been improvements easily, however, that is what the FibroMapp app is for – tracking, monitoring, recording and creating reports. For myself, there has definitely been a many improvements in regards to sleep, fever, migraines/headaches and body aching to name just a few. And seeing tangible and physical results on others has been, well, no less than amazing!
I think one of the things that was most incredible was that 2 days after taking the remedy for the candida geotrichum fungus I was treating, I actually felt like I ‘woke up’ out of a coma – ie, brain fog.
Remedies are made with distilled water and a bit of vodka (optional) and can be taken with any medication and alcohol with no side effects. For me – and for many people, treatment only lasts a day or two for each pathogen being treated – of course, everyone is different – for some people who are extremely sensitive, it can take a few weeks.
It is important to note that this is not a miracle cure that happens overnight. With conditions like fibro and CFS, we have a MULTITUDE of pathogens that needs to be cleared out, so the process can be slow going – but definitely worth doing, in my opinion.
I think that it is imperative to look at other options outside the box in regards to getting help – because they DO exist!
For more information about pathogen detection and treatment in the UK go here.
As well, Dr Jess Armine, from Pennsylvania does a different type of testing for pathogens and treatment – as well as methylation therapy and many other things that are helping people to recover from fibromyalgia, CFS, Lyme Disease and many other ‘incurable issues’. Dr Armine also comes to the Manchester area in the UK. He is a functional and integrative medicine doctor who works with bio-individualized medicine. For more information, please go here.
Dr Chris Pickard is also rather an amazing guy when it comes to helping (and healing) people with fibromyalgia, CFS/ME and many other issues. There are many videos that he has done on YouTube. He looks at gut health, which is a critical component of many aspects of our health – from inflammation and pain to IBS, arthritis and so much more. His business is called Body in Balance and some of the work he can do is remote as well. He’s in the London area.
I hand on heart believe now that pathogens are the missing link and the connection to fibromyalgia and CFS/ME. I have no doubt about it. In fact, I have been doing my best to get the word out to as many researchers, charities and doctors as possible – only to fall on deaf ears. The thing is, it all just makes sense! I am calling this the ‘new medicine’. And one without side effects and masking symptoms, let alone actually detecting the issues to begin with. I cannot encourage people enough to look into getting treatment – this can change your life. Seriously.
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