30/03/2025
May I ask, has anyone you know been diagnosed with MULTIPLE SCLEROSIS or ‘MS’?
If so, this info may be helpful to them. Two of my patients were medically diagnosed with this condition. Following their treatment with myself, each has shared their recovery story in detail. I will share one here and am happy to provide the other if requested.
A young lady of thirty-two years of age and mother of one presented with the condition known as Multiple Sclerosis formally diagnosed and confirmed by MRI other medical tests six months earlier stating “Neuromyelitis optica’ of the left eye and T1 Thorasic demyelinization; Extensive demyelinization left side”.
The medical prognosis: ‘Rapid progression’ causing loss of muscular co-ordination and function. Life in a wheelchair was inevitable.
To be honest, observance of her difficulty moving, unless something was to change, this was indeed the case in the not too distant future. Upon arrival for the first consultation the patient could hardly make her own way into the clinic. She physically struggled to walk and negotiating two steps was a major challenge for her. The patient was having ‘an episode’ every four days, each lasting from a few hours to a few weeks. Three types of episodes were experienced and sometimes these could be very intense.
MY TREATMENT and MEDICATION: Education and careful systemic detoxification
I gave my special detoxification and revitalisation program, specific nutritional supplementation and drew up a clear ‘action plan for her to follow’.
Results:
Patient returned two weeks later almost completely free of all symptoms.
Walked up the stairs and into clinic, tall, straight, moving freely and well poised.
Following all lifestyle changes suggested.
No headaches or other symptoms
Bowels working well everyday
Only two small ‘episodes’!
Two weeks later:
Patient is glowing and very pleased with the results thus far.
Four weeks later. Only two more small episodes since her last visit being four in total since treatment began more than eight weeks earlier.
Eyesight in left eye has improved, more colour but not form.
Eyes clearer, no headaches, can feel three toes on left foot now whereas was only one toe previously...
Walking most days with husband and son for 30 to 45 minutes.
Patient’s husband ‘in complete shock’ and the extent of his wife’s improvement and recovery! Patient has returned to full time work and is living a normal and more than active life.
Patient’s account below:
My name is Janet and I’m 32 years old. I suffer from an incurable disease called multiple scleroses or MS. I was diagnosed with MS in July. How this came about is as follows.
I thought I was getting a common eye problem called conjunctivitis, as I was a little run down, however, on Thursday night – I remember this particular night, as I ended up putting myself to bed relatively early after telling my husband of the amount of pain I was feeling in my left eye. When I woke the next morning I was taking our son to school and noticed my sight in my left eye blurry, and my eye felt as though I had been punched by someone in it. After dropping my son at school, I went to see my local doctor as I was starting to worry. Upon him turning off the light in his surgery to look into my eye, he noted a lot of blood behind my eye, however when he turned the light back on, I found myself unable to see out of my left eye. After the initial shock, I was seen by a surgeon that same afternoon, as first impressions suggested some sort of clot, worst scenario – on the brain. After test, after test, after test, with no actual diagnosis I saw an eye surgeon who’s sister-in-law had recently been diagnosed with Optical Neuritis, the first sign that can result in MS. Upon the request of this doctor, I had an MRI Scan which showed I had MS or black spot on my brain. However, only one was found and I was told I should not have any more episodes, this is common and some people have one episode and are find the rest of their lives.
I was told regular monitoring every 6 months MRI’s to keep it in check, that my sight would come back eventually and I shouldn’t have any more episodes. Exactly 10 days after I lost the sight in my eye, I woke up with pins and needles the length of my left side. My first thought was that I had had a stroke. I went straight to my Doctor who sent me to another specialist in Brisbane – a Neurologist who deals primarily with MS sufferers. He in turn was in shock over the rapid ferocity of demilinaiton in my left side. It was as if plaques had appeared overnight. I was given a grim outcome, told “what to expect” etc. etc. I was given a drug introveinously over 3 days – this drug was to take away some of the inflammation; a combination of Cortisone and Prenisone in massive, undiluted quantities. The side effects were staggering. I couldn’t urinate, I couldn’t stop shaking, I couldn’t have a bowel motion, I couldn’t eat and I still couldn’t walk or see out of my left eye, and I was hallucinating. I ended up worse than when I started. In the end I was on drugs to urinate, drugs to have a bowel motion, drugs to help me ease the pain I sometimes suffered – I was 32 and a wreck, a shadow of my former self.
I then decided I didn’t want to go on the Betaferon injections much to the horror of my Doctor. My husband, by chance met Dr Peter Edwards and I was brought up in the conversation. By this time, my episodes were happening that furiously and often if I was able to walk or function 2 days out of the week, I was ecstatic. My husband got me in to see Dr Edwards on the Thursday in February. I had trouble getting to his door. My hand was twisted into its usual knot, my leg wasn’t working at all, I was embarrassed to be in such a state, constantly apologising for my condition. In the hour, Dr Edwards changed my eating habits and I was given some supplements. My episodes decreased to 4 in 8 weeks with the longest episode lasting 2 days. Who would think, by changing some simple things and maintaining my eating habits I have minimised the amount of episodes I have. I still have only partial feeling in parts of my left arm and leg, however the decrease in episodes is amazing.
I would rate my general well being on seeing Dr Edwards 12 weeks ago as 10% – my general well being I would say is now 200%.
I wish my husband had met Dr Edwards when I was first diagnosed – maybe I wouldn’t have had to suffer to the extent I have. Anybody willing to give some something a go could be happily surprised. Just take a look at me, I now can keep up with my 6 year old again, all my thanks to Dr Peter Edwards for all his help and encouragement.
– Janet B.
Thank you Janet, well done!
