MULTIPLE SCLEROSIS AND INFECTION

Tuesday 10 July 2018

MULTIPLE SCLEROSIS AND INFECTION

'Dr. Gabriel Steiner had clearly shown that in about one in every ten brain-autopsies he could find spirochetes using his own silver-stain. We still use Steiner’s stain today to detect spirochetes, but for some reason we don’t acknowledge his discovery of spirochetes being associated with Multiple Sclerosis.'

https://durayresearch.wordpress.com/about-2/seven-provocative-findings-p5/

Further images of spirochetes from Steiner's work

The early history of MS and the MS society.

There is a whole history between Dr. Gabriel Steiner, Dr. Rose Ichelson and the MS society and Time magazine.

I wrote up the story on an old computer in 1992. Seems lost to the ages.

The story is basically is this: Dr. Steiner associates spirochetes in the brains of deceased MS patients in Germany in 1922 to 1933

Dr. Steiner is Jewish so he leaves Germany for Ann Arbor Michigan. Dr. Steiner is a revered teacher and takes on several graduate students. One of is students is Lida Mattman.

Dr. Steiner publishes only three more major papers in America on MS that associates spirochetes with MS. 1952-1956

Dr. Steiner worked on American MS patients and after finding spirochetes in American MS patients 1952, Dr. Steiner wrote a position paper on MS and named the spirochete myelaphthora or myelin-eating spirochete.

Steiner went on to state that he thought it was an entirely new species Borrelia.

At first the American medical community was excited,but the tide changed quickly. People who didn't understand science had the last word in a Time Magazine article in 1957.

Dr. Rose Ichelson was a microbiologist with 30+ years of experience, a woman who stopped two epidemics in Philadelphia and was mentioned by Eleanor Roosevelt as a female scientist that young girls should emulate.

Dr.Ichelson read Steiner's work with great interest.

Rose on several occasions cultured spirochetes from the CSF of MS patients and then published in 1956.

She gained the attention of TIME magazine who did an article in 1957.

That same year the inexperienced MS society was formed and was run by none scientists. They said MS was not caused by an infection because rarely did both identical twins or spouses get MS, therefore no infection was being passed. (Of course the infection is not passed from person to person but from TICKs to people.)

This statement shattered Dr. Ichelson's career and she was openly ridiculed, in a large part her struggle was because of her jealous boss, who literally stole a research grant out from under Rose to do his virus theory of MS.

Thus ending Rose's career in ridicule and internal politics. She died a few years later and all her lab books and papers were lost in a Philadelphia Town Hall fire.

The final insult from the MS society was ironically that the MS society after saying MS was not caused by an infection , they wholeheartedly embraced the Virus-theory of MS as put forth by Rose's ex boss.

Dr. Rose Ichelson PhD should be honored much in the same way Rosaline Franklin (DNA) is honored with an annual science award for research.Why Philadelphia doesn't wake up and make a statue of her I don't understand.

https://molecularsolution.wordpress.com/2011/02/20/spirochetes-found-in-multiple-sclerosis-patients/ ( a list of numerous published studies on spirochetes and MS)

The above was copied from Thomas Grier Facebook post with his permission to share. (https://www.facebook.com/thomas.grier1 ),

To learn more about the association of MS and other illnesses with Borrelia go to - Dr. Paul Duray Research Fellowship Endowment https://durayresearch.wordpress.com/

with special attention to - https://durayresearch.wordpress.com/about-2/seven-provocative-findings-p5/

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Lyme Life written in 2009

I started suffering with arthritis in mainly my large joints especially my knees 6 years ago. The symptoms varied and I remember saying that every joint was affected except my elbows to one doctor. I was told it would be hormonal and to take the usual supplements cod liver oil or glucosamine ( I would certainly recommend buying shares in the companies producing these supplements) They had no noticeable affect.

All my symptoms deteriorated significantly over a few weeks,4 years ago. Hips shoulders and knees being the worst and I started with muscle weakness in upper arms and upper legs. I had difficulty standing and walking across a room. I was unable to walk upstairs and my husband was making plans to convert to a downstairs bedroom. I had seen 5 doctors and 3 Rheumatologists and put on steroids for Poly Myalgia Rheumatica diagnosis. I had been diagnosed with Fibromyalgia and ME/CFS.

I have X rays and scans showing signs of osteoarthritis and Rheumatoid arthritis. ( later note.- the X rays done some years into treatment showed my hands completely normal no signs of inflammation or RA confirming how they felt - normal) I have been retired early from the Civil Service having lost my job not to mention my earning potential. My illness seemed to progress through my body not affecting the same joints left to right at the same time. I had bursitis in left hip, right hip, left elbow. I had synovial thickening in both wrists. At that time I could not lift and hold a magazine so lifting a kettle I could only do if a third full and with two hands. Each joint in my hands fingers feet and toes were affected. I had swallowing difficulties and many other symptoms. None of this describes the endless and awful pain whenever I moved or the tiredness but inability to get quality sleep.

Two years ago my GP gave me Amoxicilin for a sinus/throat/chest infection. All my arthritis symptoms improved. The course ended the symptoms deteriorated I started a second course the symptoms improved. The improvement was more significant than when I had started taking steroids. This led my GP to suspect Lyme Disease. I laughed because we do not travel abroad but she said they had had other cases in the surgery in the early stages of tick bite and Erythma Migrans rash. She said but you have not had a bite. I said oh yes I have I had two on my ankles with rashes, March 05 this was confirmed on her computer when I had seen a locum doctor. My worst symptoms were waking up feeling rigid and having to painfully flex every joint in my body before struggling to get up. The only other time I had experienced this was in May 2003 during a flu like illness like no other I had ever experienced. At that time I had a bite and similar rash on my right foot which lasted like the other rashes about four weeks. I had also consulted the surgery and it was dismissed as a virus. I walked our dog daily in the woods adjacent to our house where the deer roam, prime tick area. Thus started my very lengthy search about Lyme Disease leading me through Lyme Disease Action to a doctor who specialises in this illness. He confirmed my GP's suspicions. I never had a positive blood test but then they are antigen tests and there is much research that shows they are unreliable. In my case the year of steroids and many weeks antibiotics could have affected the results. So with a clinical diagnosis and following ILADS International Lyme and Associated Disease Society guidelines I continued on antibiotics for two years. Both my doctors continued to treat me despite of Health Protection Agency advising against long term antibiotics. I am now nearly 100% recovered I have no pain or muscle weakness. I can walk upstairs something I could not do for three and a half years. I can garden do house work and live a normal life. I still need to pace myself and with only a few months to 60 will not be looking to return to work. Life is such a joy. Sadly there is much controversy about Lyme Disease and doctors in UK are taught that it is so rare. Well where I live in Guildford I have been in contact with a dozen other people with it so perhaps not so rare as HPA would like us to believe. I am in touch with nearly 2000 other patients through a chat line Eurolyme most had been misdiagnosed with several other illnesses. Look at UK charity Lyme Disease Action if you want to read more about this illness. There are many MP's taking an interest in the problems surrounding diagnosis and treatment see above charity links into a recent meeting at the House of Commons.

Thank goodness there are some thinking doctors around who have courageously treated me against opposition and I have made such a miraculous recovery albeit rather a lengthy one. One day there will be many more people who are helped with their chronic illnesses when IDSA starts taking note of what our courageous LLMD’s are doing following ILADS Guidelines.

ME/CFS, Fibromyalgia, Poly Myalgia Rheumatica, Arthritis, Bell’s Palsy, MS,MN, ALS, Parkinson’s, Alzheimer’s, Heart Block, Stroke, Psychiatric, gastric problems the list is endless. Not all suffering from Lyme Borrelia but how many are even properly assessed for it.

UPDATE

UPDATE 10 January 2012

LOOKING AT LYME DISEASE - MSIDS

Tuesday 10 July 2018