taking advantage

I've said before and I'll say it again, if people just stopped jumping on every money making bandwaggon there is regarding ms perhaps we would be a lot further than we are.

Its a disgrace really,


The medics have had 70 years to come up with something and failed time to give alternative and holistic medicine a go,all they have done iscertify their own existance, wrong way of looking at it   the medical world needs to back off

Let the young forward thinkers through.

Candida and misaligned Atlas or just Candida

I think that there are two types, no ms just these conditions, so NO CURE required for ms that is

2nd 0f 2 (previous post)

The drug he speaks of is Neprinol which kills systemic CANDIDA



Another nail hit on the head eh!

1st of 2 (on MSS message board)

How I cured my wife's Chronic Fatigue and Tiredness.

MSsido
12 Mar 11
0:35

My main aim is to cure my wife of MS.
My experiences of Doctors and Specialists are that they can only see through blinkers. They only see what they want to see and everything they see involves dangerous drugs with nasty side effects which happen sooner or later.

My wife has been told she is in the Secondary Progressive stage of MS by the specialist.
She was diagnosed by symptoms, lumbar puncture for antibodies and MRI scan of the brain showing multiple scarring. She has had MS for 38 years at least.
For 10 years now she has had constant overwhelming tiredness and poor memory with constant walking difficulty. She would collapse when walking (with help) within 50 yards. This has been constant so no relapse effect here.

She now has no chronic fatigue or tiredness and has a very sharp memory since the day after starting the treatment that helped me.
We walked together up the road last Sunday and she was not even tired when we got home.

My wife had been thinking of asking her doctor to put her on a course of steroids but the next day after starting the treatment she said it was no longer necessary which was quite a surprise to me.

Our Story:

Having been to hospital with heart problems I soon realised that most doctors were very poor at diagnosis (to put it politely). The Health Service Journal had a chat board open a couple of years ago on the subject but soon had to close it due to the embarrassment of finding that doctors agreed that they were useless at diagnosis. They diagnose correctly in less than a third of cases according to their own figures. If this happened in industry 9 out of 10 doctors would find they would be soon out of a job.

So I decided the only way to find out what was wrong with me and to get appropriate treatment was to do it myself.

That was the best decision I have ever made in my life.

I come from a very technical background and one of my jobs was to protect a major University from Computer virus infection. I did this job for many years and became very familiar with how infections bypass immune systems. I even designed a disk based immune system to protect computer disks from infection. (most people would not realise that computer disks can have their own immune systems.

Despite having had a heart attack I am now not on any NHS prescribed drugs and the Atrial Fibrillation I had for 40 years has gone.

The correct way to diagnose what is happening is to simplify things. (Doctors take note)

1) The way I see MS is that it is primarily caused by inflammation. That is simple.

2) To have MS the blood brain barrier has to be breached. That is simple too.

3) Before we get into drugs that stop the myelin sheath being damaged we should take a step back and fix the blood brain barrier first.

4)The chances are that the blood brain barrier is being damaged by something, most likely inflammation.

5) So by reducing inflammation we might actually fix the Blood Brain Barrier and stop MS in its tracks. ( at this point most doctors will come up with countless other ideas of what it might be, However we will keep it simple and assume that the simplest thing is the cause and think about more complicated things later if this does not work.)

On the basis that inflammation is the root cause of most "autoimmune diseases" The same treatment may well work for all, my wife started taking the same treatment that I had used to successfully treat myself.

And Bingo! It seems to work.

So what treatment could help heal the blood brain barrier?

Steroids reduce inflammation and worked very well for my wife but cannot be taken on a long term basis so they are out of the question.

NSAIDs like ibuprofen cannot be taken on a long term basis.


Inflammation cannot happen if the blood is flowing quickly.

So an anti-inflammatory which is not a drug and has no nasty side effects which thins the blood (allowing it to flow more quickly) would be ideal. (Inflammation causes the blood to thicken anyway I believe)

I am not allowed to mention the product here due to posting rules.

I will attempt to get double blind trials started but expect to get fierce opposition from the establishment for obvious reasons. The EU in any case has introduced unhelpful new laws to protect the drug companies.

Good luck all.

He is right

A man called Noel Batten in Australia states ms is a medical mistake, and I go along with that theory.

His case on Tiffany is very very relevant

ignore the word cure as there isnt one needed

I cured myself of MS

By LISA SEWARDS, Daily Mail
Last updated at 09:52 04 July 2006

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Dermot O'Connor claims he has freed himself from MS

Conventional medicines says multiple sclerosis is incurable. This man insists he beat it with diet, ancient Chinese exercises and mind over matter. Wishful thinking - or truly extraordinary breakthrough?
In 1998, Dermot O'Connor, 36, from Dublin, was diagnosed with a severe form of multiple sclerosis (MS) - the 'incurable' and degenerative neurological disorder.
He left his job to dedicate himself to fighting the condition. Eight years later, in perfect health and symptom-free, he has written a book telling how he achieved this through nutrition, acupuncture and forms of mind and body medicine.
As an international banking consultant, Dermot O'Connor was chronically stressed, short on sleep and always running late. But he was used to being in control. Imagine his horror when he made the first phone call of the day from his office in 1998 and heard himself slur: 'Hello, itsch Dermoch O'Connor, can I schpeak with Carlosh?' His colleagues laughed. 'What have you been drinking?' they joked. 'I hadn't been drinking, so I put it down to tiredness,' recalls Dermot. But he spent the rest of the day trying not to speak, then got an early night.
'The next day I heard the words: "New Zealand had lost rugby's Tri-Nations Championship for the first time since its inception" on the radio. 'I put my speech to the test with that phrase. I certainly couldn't have said that the previous day. Now, after much sleep, I felt totally confident. "New Zhealand losht rugbysh Trinashions championshipsh for the firsht time sinsch itsh incepshion." My speech was even worse.
'I was terrified. No matter how hard I tried, I couldn't shape my mouth correctly to pronounce the words.' The next day, Dermot flew to Germany on business, only to find his health deteriorating rapidly. At one point during a presentation he was literally struck dumb. A colleague had to step in.
Back home in Dublin, he had a series of hospital tests. At first, consultants thought he'd had a stroke, as one side of his face had dropped. But an MRI scan showed lesions on his brain and a lumbar puncture confirmed the dreadful diagnosis: multiple sclerosis. 'I felt all the energy drain from my body,' recalls Dermot. 'I was familiar with MS. I would often say that I would take any health condition ahead of MS. And here I was at the age of 29 with exactly that.
'It seemed one of the cruellest of all illnesses. Once it got a grip on you, there was no release. You spent the rest of your life fighting a losing battle. I knew the comedian Richard Pryor had MS and was confined to a wheelchair and could barely talk.'
Multiple sclerosis is an 'incurable' degenerative disorder of the nervous system. Many symptoms first appear between the ages of 20 and 40. One in 600 people in the UK has it.
Nerve fibres are normally insulated with a protective sheath of fatty tissue called myelin. In MS, there is patchy loss and scarring of this myelin sheath, so nerve messages cannot travel normally from the brain to different parts of the body, leading to numbness, fatigue, speech or swallowing difficulties, loss of balance, blurred vision, muscle spasms and unstable walking.
'By the time I left the hospital my speech was back to normal,' Dermot says, 'so I convinced myself that nothing was wrong. Then, two weeks later, on a business trip in LA, I awoke and found that I'd lost sensation all over my body, except for a feeling of a tight band around my waist.'
Back in Dublin he saw a neurologist, who gave him a number of tests. One involved pushing and pulling against his arms. 'I was so determined to pass this test that I pushed him back so vigorously that he almost fell over,' says Dermot. 'To my mind I had performed all the tests admirably. But then he slowly took off his glasses, and said: "Listen, you have got MS." '
On average, an MS attack comes once a year. Two within two weeks suggested that Dermot had a very aggressive form. 'I was told to go away and cry and to come back the following week with any questions. As I sat in the waiting room, I could see the varying degrees of decline as people before me struggled on walking frames and in wheelchairs. I wondered how long it would be before I was wheeling myself in for my appointment.
'While medication can slow down the decline by 30 per cent, nothing can halt MS indefinitely and often this medication has side-effects and sometimes it doesn't work. The cause of MS is unknown, which makes it more difficult to come up with a cure. I thought it would be better if my life just ended.'
This feeling was reinforced when he bought books about MS: 'They seemed to be just guidebooks to decline - detailing all the ghastly symptoms including being wheelchair-bound and, finally, facing death.
'I developed a morning ritual where I would test each of my faculties to confirm which had declined and by how much. Sure enough, as each day passed, my legs got weaker, my eyesight seemed worse and I was developing pain sensations all over my body.
'I remember when my foot fell asleep and I was stricken with fear. Was I about to lose my ability to walk? As feeling and movement came back into my leg, I was momentarily relieved. But worst was the fear of the unknown.
'It was as if a giant was holding me in his palm, about to close his hand and crush the very life out of me at any point he chose.'
Dermot started to look at his lifestyle. He had been filling every minute of every day with work, lectures and study, then exercising by running or lifting weights well into the early hours of the morning, collapsing into bed around 4am.
For the previous seven years, he had worked in more than 70 countries, hopping in and out of time zones, fighting off jet-lag to perform under high pressure conditions.
He frequently gorged on junk food - colleagues called him 'the human dustbin'. He also felt 'emotionally' unhealthy: whenever he felt that he had suffered an injustice, he would harbour a huge amount of resentment - just as he did after being diagnosed with MS.
'I knew I needed quickly to make myself mentally stronger,' he recalls.
So he turned to various 'alternative' disciplines, including Neuro-Linguistic Programming (NLP), which 'reprogrammes' the brain to change negative thoughts. He also studied the work of Irish hypnotherapist Dr Sean Collins.
Dr Collins was researching the effect of the mind on the body and had just completed his first book Tipping The Scales. He argued that while making one change to your life might not be enough to conquer an illness, the cumulative effect of various changes could tip the balance in your favour.
The first change Dermot made was to take up Shengong ? a Chinese form of meditation. Then he changed his diet, cutting down on saturated fats and eating more whole foods and oily fish, an approach devised by American neurologist Dr Roy Swank.
'Within three weeks of changing my eating habits, I noticed some dramatic changes in my health,' says Dermot.
'My energy levels became higher, my thoughts were clearer, my memory improved and I started to sleep better at night. Critically, the numbness in my body from the previous MS attack waned and eventually disappeared.'
To Dermot, it seemed the original diagnosis had been turned on its head. He went back to his neurologist six months later and was told it was a temporary remission. Dermot never went back.
The next time he and his neurologist met, they were sharing a platform at an MS Society conference where they were clearly from opposite schools of thought.
'He came from the angle that MS sufferers can get temporary relief from drugs, but it is simply incurable,' says Dermot.
'I believe I didn't get into remission from rapid deterioration by chance. I believe I have actively created my remission. In just six months, I was measurably fitter, faster and stronger. My energy was higher than I had ever known it before, and I had increased mental clarity. Not only was I symptom-free, but I was in the best physical shape I'd been in for almost ten years.'
Dermot continued to study alternative approaches, training as an acupuncturist, dietary therapist and NLP master practitioner.
He also studied Chi Kung, a form of exercise, at Xi Yuan hospital in Beijing, the leading Chinese medicine hospital. 'I witnessed very sick people at Xi Yuan hospital move, breathe and meditate themselves back to health,' claims Dermot.
'From all this, I put together the pieces of the jigsaw to create the foundations of what I call the Healing Code.'
He has now left banking and opened clinics in Dublin and London. He claims success with illnesses ranging from serious conditions such as Parkinson's disease to chronic migraine.
It is now eight years since Dermot was diagnosed with MS. He claims his health has improved year on year and that he remains symptom-free.
Dermot appears to have confounded the prognosis. The history of medicine is full of stories of patients who defy expectations.
As Lucy Jeanes, of the Royal College of General Practitioners, explains: 'Self-empowerment and lack of stress is almost always therapeutic in chronic conditions.'
MS experts also point out that remission from the disease can last for many years.
And while Dermot himself was was not on medication, health professionals get worried when patients use alternative treatments to the detriment of conventional treatment.
'Inspiring'
Dermot's story is 'inspiring', says Matthew Trainer, spokesman for the Multiple Sclerosis Society. 'He has certainly found an approach that works for him. Every person's experience of MS is different.
'Seven out of ten people with MS have tried a complementary therapy. Some find benefits in them, but we recommend you consult your doctor to make sure these therapies are not to the detriment of any mainstream treatment.'
Lucy Jeanes agrees: 'It is essential that these treatments are used with conventional medical treatments and not instead of them.'
For Dermot, the first vital step is to understand and perfect the psychology of health recovery: 'So we begin implementing the Healing Code with a question: Is your mind ready to be well?'


Read more: http://www.dailymail.co.uk/health/article-393949/I-cured-MS.html#ixzz1RIObnV3C

headache/pain/spasm/blood flow