I know there are lots of us unfortunate ME/CFS people on here (past and present) and would like your advice/knowledge/information about Phil Parker's The Lightning Process.
Having been severely affected with ME (since a flu virus in 2013) I have researched the full range of 'cures' to get me out of my 'Housebound Hell' of pain, fatigue and vertigo etc. Every so often, a different friend recommends the LP and I find myself on his website again.
In the beginning -with lots of research- I faced my illness with positive, determined CBT/NLP type approaches and attempted to get on with my life. I continued to deteriorate.
After an (NHS prescribed) year of Graded Exercise, I am worse and now medically retired. 
Can anyone tell me why people pay £650 for LP and risk causing a further relapse? I've read such mixed stories on their success and am curious. It seems to either be a miracle cure (how?) or causes permanent further damage.
How do I explain to my well-meaning friends that 'No, I don't want to sign up to something that will cure me' 
. It shows me as the typical obstructive ME patient who continues to subscribe to the 'false illness belief' (that is still being rolled out in the UK press 
) even though what I really fear is ending up being poorer, bed-bound and tube fed/catheterised.
Any thoughts? Would you risk it? Or did you and with what results? Would be interested to know if anyone was 'cured' and then had a later serious relapse and regrets trying it.