Comments for Proper ME News, no PSYCHO babble http://meworld.wordpress.com Sat, 27 Dec 2008 20:16:42 +0000 http://wordpress.com/ hourly 1 Comment on MErry Christmas by meagenda http://meworld.wordpress.com/2008/12/25/merry-christmas/#comment-124 meagenda Sat, 27 Dec 2008 20:16:42 +0000 http://meworld.wordpress.com/?p=275#comment-124 A peaceful Christmas to you, Simon. Let's hope the coming year will be a better one for all of us and the year in which this illness finally receives proper recognition and research. Suzy A peaceful Christmas to you, Simon. Let’s hope the coming year will be a better one for all of us and the year in which this illness finally receives proper recognition and research.

Suzy

]]> Comment on The Lightning Process … by MinnieME http://meworld.wordpress.com/2008/11/27/the-lightning-process/#comment-120 MinnieME Wed, 17 Dec 2008 13:25:59 +0000 http://meworld.wordpress.com/?p=259#comment-120 LP is just as worse and as much crap for ME as CBT and all the other silly therapies that only work if you DO NOT have ME. Very simple. So stop promoting LP. LP is just as worse and as much crap for ME as CBT and all the other silly therapies that only work if you DO NOT have ME.

Very simple. So stop promoting LP.

]]> Comment on The Lightning Process … by lpparent http://meworld.wordpress.com/2008/11/27/the-lightning-process/#comment-119 lpparent Sat, 13 Dec 2008 02:16:36 +0000 http://meworld.wordpress.com/?p=259#comment-119 I have just been through the 3 days of the lightning process as a carer with my daughter who has had ME for nearly 2 years. It is a very real disease with her losing out on school, on the floor in agony if she doesnt have permanent pain killers, in a wheel chair due to not being able to walk without pain and being absolutely knackered with any activities. We were just as sceptical about the LP at first, we forked out for the £560 and went along. My daughter to her credit gave it her all and was extremely positive - afterall what did she have to lose - the doctors had tried everything else including 2 MRI scans. To explain the background to the LP you have to understand NLP, the LP is essentially using NLP to affect your bodies biological chemicals. To control the adrenaline and keep your immune system and lymph system working so toxins as not trapped. This is done by working on catching negative thought processes and turning them 180 degrees into positive ones thus changing your whole bodies chemical imbalance. After day 1 my daughter no longer had any pain, for the first time in nearly two years she took no painkillers. Had she done that the day before she would have been on the floor in agony. Thats not to say it was all in her head, far from it she used her mind to release her bodies own built in painkiller by altering her neural pathways. After day 2 she walked a mile then went home and played the wii fit, with the biggest smile I think I have ever seen. The week before she would never have been able to do this, certainly not without a lot of pain and certainly not without crashing. She walked back with a cane for balance and somewhat unstable but taking our time we made it. After day 3 she was feeling great, working on how to take this back home with her to her life and how to get back into school. Her balance was much improved and I cannot thank the LP practioner enough. If you know anyone who has ME I would refer them to the LP without a shadow of a doubt. Yes there is a cost involved but we have spend a fortune on fancy foods, painkillers, gadgets and all kinds of other "cures" in the last 2 years. £560 is money well spent to see my daughter back to normal health, in fact I believe the LP will enhance her life to much better than before. A truly great process - using your mind to change your body to overcome a truly physical disease. I have just been through the 3 days of the lightning process as a carer with my daughter who has had ME for nearly 2 years. It is a very real disease with her losing out on school, on the floor in agony if she doesnt have permanent pain killers, in a wheel chair due to not being able to walk without pain and being absolutely knackered with any activities.

We were just as sceptical about the LP at first, we forked out for the £560 and went along. My daughter to her credit gave it her all and was extremely positive – afterall what did she have to lose – the doctors had tried everything else including 2 MRI scans.

To explain the background to the LP you have to understand NLP, the LP is essentially using NLP to affect your bodies biological chemicals. To control the adrenaline and keep your immune system and lymph system working so toxins as not trapped. This is done by working on catching negative thought processes and turning them 180 degrees into positive ones thus changing your whole bodies chemical imbalance.

After day 1 my daughter no longer had any pain, for the first time in nearly two years she took no painkillers. Had she done that the day before she would have been on the floor in agony. Thats not to say it was all in her head, far from it she used her mind to release her bodies own built in painkiller by altering her neural pathways.

After day 2 she walked a mile then went home and played the wii fit, with the biggest smile I think I have ever seen. The week before she would never have been able to do this, certainly not without a lot of pain and certainly not without crashing. She walked back with a cane for balance and somewhat unstable but taking our time we made it.

After day 3 she was feeling great, working on how to take this back home with her to her life and how to get back into school. Her balance was much improved and I cannot thank the LP practioner enough.

If you know anyone who has ME I would refer them to the LP without a shadow of a doubt. Yes there is a cost involved but we have spend a fortune on fancy foods, painkillers, gadgets and all kinds of other “cures” in the last 2 years. £560 is money well spent to see my daughter back to normal health, in fact I believe the LP will enhance her life to much better than before.

A truly great process – using your mind to change your body to overcome a truly physical disease.

]]> Comment on In MEmoriam ME sufferer Nicola McNougher by Comment by ShowalterdontlikeME that says it all … « Proper ME News, no PSYCHO babble http://meworld.wordpress.com/2008/09/17/in-memoriam-me-sufferer-nicola-mcnougher/#comment-118 Comment by ShowalterdontlikeME that says it all … « Proper ME News, no PSYCHO babble Thu, 11 Dec 2008 21:08:22 +0000 http://meworld.wordpress.com/?p=248#comment-118 [...] in reasonable terms why they deny the existence of ME. No apology from them would ever be adequate. Someday they will be seen for what they are – dishonourable charlatans. Deepest sympathy to Nicola’s family and [...] [...] in reasonable terms why they deny the existence of ME. No apology from them would ever be adequate. Someday they will be seen for what they are – dishonourable charlatans. Deepest sympathy to Nicola’s family and [...]

]]> Comment on In MEmoriam ME sufferer Nicola McNougher by ShowalterdontlikeME http://meworld.wordpress.com/2008/09/17/in-memoriam-me-sufferer-nicola-mcnougher/#comment-117 ShowalterdontlikeME Sat, 06 Dec 2008 01:48:43 +0000 http://meworld.wordpress.com/?p=248#comment-117 The Wesselyian school of thought, for all they have said and written over the last two decades, have never really explained in reasonable terms why they deny the existence of ME. No apology from them would ever be adequate. Someday they will be seen for what they are – dishonourable charlatans. Deepest sympathy to Nicola’s family and friends. The Wesselyian school of thought, for all they have said and written over the last two decades, have never really explained in reasonable terms why they deny the existence of ME. No apology from them would ever be adequate. Someday they will be seen for what they are – dishonourable charlatans.
Deepest sympathy to Nicola’s family and friends.

]]> Comment on The Lightning Process … by terri http://meworld.wordpress.com/2008/11/27/the-lightning-process/#comment-116 terri Tue, 02 Dec 2008 23:59:29 +0000 http://meworld.wordpress.com/?p=259#comment-116 LP made me so ill I was bed bound for weeks.The cost of this scam was outrageous. It is just a money grubbing scheme run by unscrupulous people who pretend to have recovered from M.E. They don't have a recognised medical qualification between them. LP made me so ill I was bed bound for weeks.The cost of this scam was outrageous. It is just a money grubbing scheme run by unscrupulous people who pretend to have recovered from M.E. They don’t have a recognised medical qualification between them.

]]> Comment on Christmas cards 2008 … by Smiffy http://meworld.wordpress.com/2008/08/18/christmas-cards-2008/#comment-115 Smiffy Mon, 01 Dec 2008 20:04:05 +0000 http://meworld.wordpress.com/?p=243#comment-115 Thank you for posting this. My cards came very quickly and I think they're lovely. Biomedical research into M.E. receives no UK government funding, so needs every penny it can get. Thank you for posting this. My cards came very quickly and I think they’re lovely. Biomedical research into M.E. receives no UK government funding, so needs every penny it can get.

]]> Comment on The Lightning Process … by Smiffy http://meworld.wordpress.com/2008/11/27/the-lightning-process/#comment-114 Smiffy Mon, 01 Dec 2008 19:27:45 +0000 http://meworld.wordpress.com/?p=259#comment-114 The members of my M.E. group who have done this questionable and unscientific 'therapy' have relapsed dreadfully. They have each spent over £500 on it; one young man is on benefits. None of them have had a refund or any follow up at all. Anyone who 'recovers' doing this or any other form of psychobabble never had the serious neurological illness M.E. in the first place; there is no diagnostic test for M.E.. The members of my M.E. group who have done this questionable and unscientific ‘therapy’ have relapsed dreadfully. They have each spent over £500 on it; one young man is on benefits. None of them have had a refund or any follow up at all.

Anyone who ‘recovers’ doing this or any other form of psychobabble never had the serious neurological illness M.E. in the first place; there is no diagnostic test for M.E..

]]> Comment on ME News by anonymous http://meworld.wordpress.com/about-2/#comment-113 anonymous Mon, 01 Dec 2008 13:24:50 +0000 http://meworld.wordpress.com/about-2/#comment-113 st.clair - i wish you would witter on some more - interesting to read your comment - be interested to know more. st.clair – i wish you would witter on some more – interesting to read your comment – be interested to know more.

]]> Comment on The Lightning Process … by Joe http://meworld.wordpress.com/2008/11/27/the-lightning-process/#comment-112 Joe Thu, 27 Nov 2008 17:36:37 +0000 http://meworld.wordpress.com/?p=259#comment-112 i know lots of people who had ME who are better who've done the LP. Your article doesn't make sense, I think you've misunderstood a few things. i know lots of people who had ME who are better who’ve done the LP. Your article doesn’t make sense, I think you’ve misunderstood a few things.

]]>