A very good point Maddie. my clients so far had it for several years so I suppose the "trigger" illness damage had had time to recover. I need to think about that, thanks for raising it.Hi, Steven. I read the information at the link given, and I didn't find a guarantee anywhere. I saw a price for one session + one follow-up within 3 months, but I looked in vain for either a money-back or a complete cure guarantee. Would you post a link?
I think you've got an internally consistent theory here, but you might have left out a piece. That being the bit where the triggering invader not only requires us to rest, but also immediately starts damaging us faster than we can repair ourselves.
Madie
It is my belief that the symptoms and biology related to having the illness are that a specific or several parts of the body no longer work they should and that the immune system overloads, causing traces of things to appear ether through lack of production or overproduction. When the body is allowed to go into recovery it will then start producing the right things. I feel that too often the mass of differing symptoms overwhelms the search for the root cause. When I first approached this it was the multitude of symptoms and effects that initially I found somewhat daunting. It was when i started looking for the similarities that the root cause came to me. Quite frankly it was my lack of a medical background that let me see past the technicalities!
"SHE DIED AS A RSULT OF ACUTE RENAL FAILURE ARISING FROM THE EFFECTS OF CHRONIC FATIGUE SYNDROME"
Sorry I didn't respond to the guarantee, this was someone posting out of context my other services. I always try and guarantee my work so that the client has piece of mind and knows the cost up front. It also ensures that I get feedback if they are not fully happy with the results and that enables me to refine and develop the treatment.A very good point Maddie. my clients so far had it for several years so I suppose the "trigger" illness damage had had time to recover. I need to think about that, thanks for raising it.
Sorry replying to too many people at once. What I meant to say was that no other things being wrong were mentioned. I have many people visit when they have had all the tests any nothing has been found (not talking ME here). They look devastated but to me that is great news.Steve it is a myth that people with ME do not have abnormal test results see my previous post on this thread .
you said quote ..... The great news is that the tests can't find anything wrong with you!
Steve
the ONLY thing your therapy could help with in this illness, is reduce stress levels, which can improve quality of life, and that may well be useful.
This illness reacts severely to any form of stress, and by that I mean "stressors" not merely emotional stress, and so it seems your mood can make your symptoms worse
http://en.wikipedia.org/wiki/Stressor
some may disagree with me on this of coruse, but it's logical and seen in other illnesses, too to an extent.
I.e. your body picks up any form of stress as indication of what it believes is infection, so ramps up the "attack" on what it wrongly thinks is an ongoing infection...making you worse.
But, it's only to a degree that such occurs with emotional stress, and it sure as hell doesn't cause it nor can you be cured by removing emotional stress. It is merely a "worsening factor".
This is where some psychiatrists have fallen, or deliberately walked into, a logical trap (or just bloody made stuff up to suit themselves).
This illness is NOT caused by mental stress, worsening of health due to mental stress (amongst other forms) is a *symptom* of the illness, not cause, and primarily, infection is the worst trigger for worsening this illness.
The pain I had when I had Norovirus infections twice in a row earlier this year, was horrific, I really should have asked for morphine-type of pain relief, but didn't want more hassle or to infect the emergency doctor who'd need ot have come out.
I've had kidney stones, meingitis, been eletrocuted and fried by red hot metal, I used to be able to control/deal with pain very well from meditation and other things I've learned, I know what pain is bloody well like and M.E. pain in severity is bloody awful.
AND
I've experienced horrible crap most folk hopefully will never know and yet that horrible crap sure as hell never triggered illness for me, I dealt with it very well actually.
One may have "bats in one's belfry" but it doesn't turn you into a plague ridden zombie!
You hear folk liek myself and others on this forum and its ilk, people who have courage, determination, who were once bright, driven, peopel above the norm, for many of thsoe who were "normal" or have it too severe are bloody DEVASTATED by this vile illness
ie it whinnows the wheat from the chaff (*), so you get higher reporting of this illness form folk with gumption etc
(*)no offence meant, there is no such thing as "ubermensch"
this leads to again, bloody stupid misinterpretations of such data, that it's "driven folk" who suffer from ME because their mindset "drives them into burning out"
BULLSHIT!
Oridnary folk get it too, but they mostly suffer in silence because they are so shattered or too afraid because of the evil hysteria, prejudice, abuse and sheer bloody bigotry we suffer.
it is no different to the crap HIV, AIDS, Tuberculosis and Multiple Sclerosis patients suffered in times by.
Mind doesn't cause illness except by destructive *actions* (ie drug addiction): the mind experiences and interprets the effects of illness.
M.E. drives folk to suicide, it's that bad, but that's the only way the Mind causes severe issues in this case.
However, since M.E. is a *lethal* illness, it causes organic death, and it is from best we know to day, largely an autoimmune disease, you had best be VERY careful about how you speak/treat folk with this illness for obvious reasons.
Please read this,
You have now seen an official, English death certificate. You know know that M.E. is a lethal organic illness.
If you wish to provide counselling, stress relief and such to sufferers, I wish you well
sorry to quote myself but I would like this answeringSo what about someone like me who has had numerous abnormal blood results and immune system results that do not fit any other illness thus I have an me/cfs diagnosis as I do not quite fit in a box ?
I do work that is all about the whole person. Our neurology has an overall controller, the unconscious. In the main it gets everything right and is great at helping us survive. Sometimes it gets it wrong and over reacts. So for instance with Hayfever 8 out of ten people don't get it so it can't be the pollen, it has to be that persons reaction. I can help them turn off that over-reaction permanently it takes about 15 minutes!Yes, but how does hypnosis treat any biological imbalances.
Perhaps, your lack of medical background is causing you to believe something that you shouldn't!!
Treatment relies on rapport and trust between us. I also need to get the person past the sceptical stage, so if I cannot explain it well enough that they understand how it works - then it won't!I do guarantee it as a kick start to recovery and back it up with a free review session. Obviously at the first session I would not carry out treatment if the client was not suitable,
who would you class as not suitable ?
(my bolding)... It really doesn't matter whether the ones I helped had ME CFS or Fibro or were misdiagnosed with it, all I know is they have a far better life and had suffered for many years. I wish you well and thank you for your input to the debate.
I also need to get the person past the sceptical stage, so if I cannot explain it well enough that they understand how it works - then it won't!
I can do nothing right on here. My point is I investigated a theory treated 4 people who were diagnosed with it and they all recovered. I expected a bit of support and encouragement on here - yes that does make me naive. Thanks for the debate, I'll leave now perhaps it was just a fantastic coincidence, and that all the people I treat with other illnesses have great coincidences as well.(my bolding)
It does matter when you write about specifically helping those with ME/CFS on this forum. This is a forum for those correctly diagnosed with this devastating illness. If you have helped patients who have the extremely abnormal lab tests that point to ME/CFS, then tell us about those patients and their before and after tests.
Sushi