Topic: Dr. Andy Wright & Dr. Lida Mattman to speak in Chicago, March 12-13
TX Lyme Mom
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The AutoImmunity Research Foundation is hosting a medical conference in Chicago on March 12-13, to be held at the Chicago Midway Airport Conference Center for the convenience of air flight schedules.
Here is the link to the official conference announcement, which includes an on-line registration form. Patients are invited to attend, but space is limited.
In addition to talks by Dr. Andy Wright of the UK and by Dr. Lida Mattman, there are at least two department heads from the NIH who will be present, one of whom is giving the keynote address. (Dr. Mattman is the author of the medical textbook, "Cell Wall Deficient Forms: Stealth Pathogens", CRC Press.)
Also, the FDA will be sending a couple of representatives, but those names have not been officially announced yet.
Lyme disease will be on the program agenda, but this conference is not focused solely on Lyme disease per se because the conference agenda includes many other chronic, degenerative diseases, all of which are believed to have an infectious etiology with occult, cell wall deficient pathogens, also.
The main focus of the conference will be on the Marshall Pathogenesis and on the Marshall Protocol (MP), which is an innovative and promising treatment program for putting these chronic diseases into remission.
There will be several recovered and recovering sarcoidosis patients present as living testimonials to the effectiveness of the MP program, which involves low-dose, long-term antibiotics in combination with another new drug, Benicar, which is being used off label and which potentiates dramatically the effectiveness of the low-dose antibiotics.
To get a preview of what the MP treatment program is all about, here is the link to the ARF homepage, which contains two other links: (1) the SarcInfo website and (2) the Marshall Protocol website. (Click on the appropriate icons for each.) http://www.autoimmunityresearch.org/
It may also be of interest to note that Dr. Trevor Marshall gave an oral presentation this last fall at the ILADS meeting in New York, so many of the LLMDs have already had a chance to hear him and to learn about this promising new therapy program.
posted
Thanks for the info. Wish I could go. Will be interested in hearing the approach taken by the NIH representatives. Hope someone will go and report on the session.
Posts: 8430 | From Not available | Registered: Oct 2000
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Andy Wright, Bolton UK - a collection of several videoclips of moving filamentous and granular structures filmed in blood of chronically ill UK patients diagnosed with CFS and/or chronic Lyme disease (52 Mb) - A MUST SEE !
Emma
Posts: 37 | From Whitehead, Northern Ireland | Registered: Feb 2009
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TX Lyme Mom
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Emma, Thanks for posting the link to Dr. Wright's amazing photoes. He is bringing even newer and more exciting images to this meeting, we've been told -- something which he feels is a real breakthrough and which carries forward Lida Mattman's earlier work into a new age, thanks to new imaging technology and his innovative techniques.
The timing couldn't be better because there will be officials from at least two different branches of NIH in attendance to see his presentation. We are hopeful that this event will mark the beginning of a new era in the understanding of all of these occult intracellular infections with CWD pathogens.
In fact, the news about Dr. Wright's latest breakthrough hadn't even reached us yet at the time that our conference program was first announced -- that's how very new it is.
I'm hopeful that there will be at least a few representatives from the Lyme community in attendance.
To obtain the best airfare rates, one needs to purchase airline flight arrangements at least two weeks in advance, so the time is growing short to take advantage of the very lowest rates in airfares -- which would be this coming Friday, Feb. 25.
Chicago Midway airport is a convenient location for the conference because Southwest airlines goes there, as do many other airlines, so it makes it even easier to get a non-stop flight at attractive rates -- providing one books early enough.
As a reminder, here's the link once again to the official conference bulletin and registration form:
posted
I am thinking about traveling to it to listen in and take down what I could. I am not doing the MP, but some folks in my support group are. I was initially hesitant when I knew it was not strictly on LD and that I did not recognize the names aside from Dr. Marshal. I was also uncertain to say the least about NIH involvement, but hopefully it is productive for us all.
Thanks TX lyme mom about the reminder about ticket cost. Bob
Posts: 77 | From Morris County, NJ | Registered: Jul 2004
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TX Lyme Mom
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Bob, Dr. AW is the UK Lyme specialist. He's one of the speakers in the plenary session. He is bringing some brand new slides to the meeting and will be talking about his newest discovery, which helps demonstrate the pleomorphic differences between Bb when it's in the body vs when it has been cultured in the lab.
Lida Mattman has published a PubMed article on how to culture the CWD form of Bb. She's the author of the medical textbook, "Cell Wall Deficient Forms: Stealth Pathogens" (CRC Press) and is a retired Professor from Wayne State University. Her interest in Lyme disease stemmed from the fact that her daughter suffered from it.
She's 92 years young and still going strong. Her talk is bound to hold your interest. (I heard her speak in 1996 at a meeting in Boston and her talk then was excellent.) This is an opportunity you won't want to miss.
Southwest Airlines flies into Chicago Midway airport, so there might still be some good air fare rates, even on late flight reservations.
What is so unique about the Marshall Protocol is that the use of Benicar potentiates the effects of the antibiotics so that the phagocytic WBCs, which have been paralyzed and parasitized by Bb, can now begin to do what they are supposed to do and actually start to kill it. The Herxes even feel different, according to patients who have tried other antibiotic protocols before.
The Marshall Pathogenesis, upon which the Marshall Protocol is based, represents a whole new paradigm of medical thought.
There will (hopefully) be a DVD recorded, but that's not the same as actually being present and having the chance to meet and to talk to people -- especially to the recovered sarcoidosis patients, who have some remarkable stories to tell.
posted
Good info.! I am going to look into this today and really want to go. I will keep you posted.
Posts: 77 | From Morris County, NJ | Registered: Jul 2004
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TX Lyme Mom
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Bob, Good. I hope to meet you there.
You can easily recognize me in person by my "avatar" (photo) at the MP website. I use the same screen name there that I do here, so you shouldn't have too much trouble in figuring it out.
Please be sure to introduce yourself to me as a "LymeNet member" so that I won't get you confused with the other MP website members.
MammaLyme
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I contacted them and they will be taping the event. I told them I would like Dr. Mattman and Dr. Wright. Posts: 2173 | From Maryland | Registered: Jun 2001
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Tx Lyme Mom: I confirmed I will be there! I hope to meet you as well. I am more and more interested to the point where I am getting excited about the prospects of the MP.
Also, maybe you can help me on something simple. I tried to access the Quest link you provided on the MP site to view the Panel Info. for the D-Metabolites. (under www.sarcoinfo.com)It won't let me saying the site is down. Several minutes later it linked me to the site that required an id to view test results (like a doctor would). Is this the right link or can you re-direct to this info? I'm hoping to have my Dr. order the test on Monday so I can have it for the conference
Thx Bob
Posts: 77 | From Morris County, NJ | Registered: Jul 2004
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TX Lyme Mom
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Member # 3162
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Bob, The MP website went down a couple of days ago for a few hours. After they got it back up and running again, there were still a few glitches though. Hopefully, those glitches have all been fixed by now, so try again, and maybe you will have better luck this next time.
I bought a bright Lyme-green colored neck scarf and a matching Lyme-green broach pin to wear so that folks can spot me easily in the crowd. My hair is short, salt and pepper colored, but with more salt than pepper.
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