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The Lightning Process™ itself includes taking physical steps to symbolise the steps you are taking with your mind. This physical action is an additional aid to establishing new neural pathways in the brain. The practitioner would ask me if I wanted to leave the wheelchair to do the process, I said no. It was only near the end of the last day – when I had evidence that my body was reacting differently in other ways – that I said yes. He never asked twice in a row. The LP includes a follow up support call, and some practitioners will be even more available than that. Nevertheless, after the 3 days, you will still be back home on your own. You will need to be the one to decide how much you can do, as you are now. It Is The Practitioner’s Job To Raise Your Expectations, Thus Impacting On Your Immune SystemThe practitioner’s job is to create an environment which raises your expectation that your body can do more, thereby creating new neural pathways and impacting on your immune system. It is not their job to know your limitations. Please note, this it is not the practitioner’s job to make you do more at the level of health you are at (unless of course this is the reason you are attending the course). It is about using techniques to impact on your neurology, and thereby your immune system. It is about changing the level of health you are at so you can do more. If you feel easily pressured when others encourage you to do more, perhaps you could work on that before putting yourself in a situation where you might feel pressured. Or else, remind yourself at all times that you are paying to do the LP. How ill you are, how much support you have, – these will be factors in your decision as to whether or not to take the training. Doing The Lightning Process™ Felt Like A Risk At Such A Low Level Of HealthDoing the Lightning Process™ was a risk for me. A life-or-death risk. With severe CFS /ME, at a level where I could speak little and worked to be fed a meal, I was struggling to keep going with the care I had. Had I been made worse by attending a 3 day event – and this would have been the case if it hadn't worked – then I probably would not have had the support to allow me to recover to my previous level. My Personal Experience of Recovery Through The Lightning Process™I did amazingly well at sitting up and taking in information. There is no doubt that the energy created in the room, the techniques – both those clear to me, and those no doubt woven into the coach’s approach, enabled me to sit up longer and take in far more than I normally could do. Having decided to do it, I was going to give it all I had. I was familiar with most of the concepts, including...
However, part way through the 2nd day, I reached the point where the symptoms were horrendous. I couldn't sit up longer, I was in a lot of discomfort, I couldn't breathe properly – I was in a closed room, with other people and I had MCS. I remember thinking: The practitioner pushed the wheelchair outside to the wonderful fresh air. After a few minutes he asked, “Do you want to do the Lightning Process™?” I had learned the process by then, and I said “Yes. Why not?” After all, what did I have to lose? I did the process and I experienced an amazing shift. It felt like a miracle. Afterwards, I could sit up and I could once more take in the information. I had been taken back in my mind to a time when I felt well. It was such a powerful and real experience for me. It was as if something had been shut off that was keeping my body in a state of illness and turmoil. OK, now I was really interested. Now, I wanted to learn more. DisclaimerThe Lightning Process is not a process offered on the NHS in the UK, or accepted by the mainstream. Please Don't Pressure Your Loved One To Try A TreatmentIf you are reading this for a friend or family member, please do not pressure them to do the Lightning Process™ if they don't believe it will work for them. If you feel inspired to do so, pass on the information you find here. I know it is terribly hard to watch someone you love in pain. But, believe me, it is also hard as an ill person to feel pressured to try treatments that don't feel right for us, or don't feel right at this time. Sometimes someone who is ill with CFS /ME has found that trying endless treatments means they are not giving themselves a chance to get the rest that allows them to feel better, and can allow their body a chance to recover naturally. Many people with CFS /ME do improve or recover when they allow themselves to rest. |
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