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#15 - 11/09/06 04:11 PM
About the Marshall Protocol
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BryanRosner
Forum Veteran
Registered: 11/08/06
Posts: 263
Loc: Mountains of Northern CA
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Although controversial, the Marshall Protocol, which was developed by Trevor Marshall, Ph.D., has helped many people. It takes into account specific aspects of the Lyme disease complex that (in my opinion) no other treatment can even come close to touching: attacking and killing cell-wall-deficient bacteria.
Many people feel that the Marshall protocol causes reactions/side effects that are too difficult to tolerate. However, the school of thought that I ascribe to is that these reactions are not "side effects of the protocol" but instead, they are herx reactions that result from challenging the Lyme disease complex. What do you think? What are your experiences?
More info:
http://www.marshallprotocol.com
http://lymebook.com/marshallprotocol
http://www.lymebook.com/marshall-protocol
_________________________
Bryan Rosner
DISCLAIMER: Bryan Rosner is a journalist, not a healthcare provider or doctor.
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#130 - 11/15/06 05:03 AM
Re: About the Marshall Protocol
[Re: BryanRosner]
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semperfi
New Researcher
Registered: 11/15/06
Posts: 2
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I agree. I did the MP mostly for almost two years. I did have elevated d125 which lowered during treatment. was sensitive ti light and had the classic herx during treatment. Some have problems. But, not sure if everyone that had problems, did it exactly. It was amazing how sun and light sensitive I was. Now no problems. Worked for me. And I have done all treatments ,availablr. I was tested by Igenex, a week ago. Results tomorrow. Been 6 months sice off MP. I think I feel a few monor symptoms coming back. Like thumb jiont hurting anf lower back. These my be age related.......I'm feeling 95%, but concerned about relapse. I have never been afraid of anything, in my life, before the lyme attack. Got my attention, I'm much more humble.It is like I was attacked by Satin.......I plan on doing the 2-3 week hammer on the MP once every 6 months, to insure it does not come back. Also, I believe in rife and the mag pulser, will get on a program for pulsing that treatment, inbetween the MP pulse. I still believe the rife, mag pulser, and MP, together, starting out slow on the MP, is the best way to treat. Basically you need to kill the bugs and let your body heal it self. Your immune system ultimately does the job. These treatments just allow the immune system to get on top of the attack. Thats why several treatments, like the salt c work, its your immune system eventually that takes over.
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#1589 - 05/09/07 05:27 PM
Re: About the Marshall Protocol
[Re: semperfi]
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mbwmax
Active Participant
Registered: 05/09/07
Posts: 21
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Its too early to say cure but I feel like I really have a shot now with ths one - too many folsk like Semper fi have gon eon to be well. I am sorry to hear some symptoms have returned but he knows what to do to quickly nip that in the bud. I DO believe the BEnicar makes the low dose way mor epowerful than all the IV and oral combos I took for over a year. I relpased right after all the IV's badly - it was nasty - way more pain than when I had started and with the first Benicar 80% of my pain melted away and most days I am pain free but i still feel crappy - and fatigues alot but I am only in Phase 1 - getting ready to combine ABX in phase 2 so will report bcak. My dr is seeing greta results in his Lyme, RA ,Fibro patients - many are off teh MP and feel great. I was really sick so I dont know if it will be a short or long haul. But if 100Mg of Mino every other day plus Benicar is keeping me from relapse something IS happening that didnt while on IV's.....Thanks for this site - its positive its about getting better and so far isnt taking me into the pits of negativity and helplessness that other boards do!
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#1591 - 05/09/07 05:58 PM
Re: About the Marshall Protocol
[Re: semperfi]
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mbwmax
Active Participant
Registered: 05/09/07
Posts: 21
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I agree. I did the MP mostly for almost two years. I did have elevated d125 which lowered during treatment. was sensitive ti light and had the classic herx during treatment. Some have problems. But, not sure if everyone that had problems, did it exactly. It was amazing how sun and light sensitive I was. Now no problems. Worked for me. And I have done all treatments ,availablr. I was tested by Igenex, a week ago. Results tomorrow. Been 6 months sice off MP. I think I feel a few monor symptoms coming back. Like thumb jiont hurting anf lower back. These my be age related.......I'm feeling 95%, but concerned about relapse. I have never been afraid of anything, in my life, before the lyme attack. Got my attention, I'm much more humble.It is like I was attacked by Satin.......I plan on doing the 2-3 week hammer on the MP once every 6 months, to insure it does not come back. Also, I believe in rife and the mag pulser, will get on a program for pulsing that treatment, inbetween the MP pulse. I still believe the rife, mag pulser, and MP, together, starting out slow on the MP, is the best way to treat. Basically you need to kill the bugs and let your body heal it self. Your immune system ultimately does the job. These treatments just allow the immune system to get on top of the attack. Thats why several treatments, like the salt c work, its your immune system eventually that takes over.
Semper Fi - I have been wondering about you b/c I read about you on the MP - and your story gave me hope - I have a few qws for you - 1) how long were you on it? It seeme dlike you did it for 1 year??? I wish it were going that fast for me! Also did you combine Rife and MP - id like to combine SaltC and maybe HBO or Rife with MP - but they scare you about combining...what has been your experience with that and what did you do at what levels...Also is your wife better form the MP? Back to 100%? Thanks for getting back if ou could - you were a real inspiring story that gave me hope!!!!
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#1703 - 06/01/07 05:47 AM
Re: About the Marshall Protocol
[Re: BryanRosner]
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GeneA
New Researcher
Registered: 06/01/07
Posts: 1
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HI my name is Gene I am new member. I got lyme two years. I have tried almost everything never got better. I would like to try MP but can’t find doctor who can help me with this. I live in Middlesex county New Jersey. Will be very appreciate for any advice
Thank You
Gene
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#1999 - 07/23/07 03:10 AM
Re: About the Marshall Protocol
[Re: BryanRosner]
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Alice_Quiroz
New Researcher
Registered: 07/23/07
Posts: 1
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Bryan: Once again you are saving lives. My daughter has been on the beam ray rife therapy (often referring to your first book) with great success but her autoimmune profile OUT OF CONTROL, so in June I read your second book, watched the DVD on Marshall Protocol (Trevor Marshall), and did an extensive review. My daughter was on HIGH DOSE D pharmaceutical drops that were "FEEDING" her lyme, within 24 hours of taking her off of these drops there was a dramatic change in her symptoms. Taking away all oral forms of vitamin D in foods and supplements she has had almost continuous "Herxs" or immunopatholy and I can only run her rife programs weekly. We are testing for the 25-hydroxyvitamin-D nad 1,25 hidroxyvitamin-D this week and her orthomolecular MD will help us add the Marshall Protocol. My daughter "Jewels" has a severe hypercoagulation disorder, has thrown several blood clots, a severe LPa disorder (genetic and worsened by Lyme your maker for a heart attack, Small Bowel malabsorption Crohns disorder (from bacteria not the usual on), to name a few. I expect in the next year as we progress and she endures this she will continue to use both her beam ray and marshall protocol. I applaud your efforts and hope more individuals understand the CWD side of lyme and possible recovery. One question is Trevor missing the spirochetes???
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#2513 - 11/11/07 03:30 AM
Re: About the Marshall Protocol
[Re: Alice_Quiroz]
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jtorgerson
New Researcher
Registered: 11/11/07
Posts: 1
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Bryan
I am new to this site. My son was diagnosed with Sacroidosis and had surgery on his lungs. He was put on a lareg dose of prednisone and his lungs cleared. However, he was still extremely tired and foggy. He was being treated at the Jewish Hospital in Denver. Three weeks ago he had a gan mall seizure. He was put in the hospital and through the MRI they discovered and tumor-AVP. They operated and told him he would be back to work in a month. He is still having seizures at least once a day and he sleeps non-stop. Extreme tiredness.
Could he be being misdiagnosed? They did test him for Lyme's disease but said that it came back negitive. Are there are different types if Lyme's disease that would require different types of tests.
He lives in Mesa, Arizona. Do you know of any doctors in that area or any area that are willing to think outside the box?
Judy
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#3120 - 03/06/08 08:09 PM
Re: About the Marshall Protocol
[Re: jtorgerson]
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Amber_in_TX
New Researcher
Registered: 03/02/08
Posts: 5
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Can you take Benicar if you have low blood pressure? My blood pressure runs about 90/60. Thank you so much, I really appreciate it!!!!
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#3274 - 04/05/08 11:06 AM
Re: About the Marshall Protocol
[Re: Amber_in_TX]
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kittysplaything
New Researcher
Registered: 03/30/08
Posts: 6
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You CAN take benicar if you have low blood pressure, I just recently read that part on the marshall protocol site. (It's really hard to navigate that web site!) Apparently people with low or high blood pressure will actually even out after being on the protocol for a while, I don't know how long it takes yet, I have a lot more reading to do over there.
Chrissy
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#3279 - 04/06/08 01:54 AM
Re: About the Marshall Protocol
[Re: GeneA]
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sammy1
New Researcher
Registered: 04/06/08
Posts: 1
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i live near you. did you ever find a doctor to help you with the MP? thanks in advance
sammy1
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#3419 - 04/30/08 01:49 PM
Re: About the Marshall Protocol
[Re: sammy1]
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kittysplaything
New Researcher
Registered: 03/30/08
Posts: 6
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Hi sammy1,
I dont know if you were asking me the question about if I found a doctor for the MP, but I did find out that a doctor in denville nj is doing the MP with one person so I'm going to go to that doctor when it gets closer to the fall and the days start getting shorter to make it easier to avoid the sunlight. If you want to find a doctor in your area click here: http://www.marshallprotocol.com/forum11/11348.html
Chrissy
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#3432 - 05/03/08 05:38 PM
Re: About the Marshall Protocol
[Re: kittysplaything]
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BryanRosner
Forum Veteran
Registered: 11/08/06
Posts: 263
Loc: Mountains of Northern CA
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I have quite a few videos now in my video blog on the MP:
http://www.lymevideoblog.com
_________________________
Bryan Rosner
DISCLAIMER: Bryan Rosner is a journalist, not a healthcare provider or doctor.
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#5459 - 11/07/10 01:46 AM
Re: About the Marshall Protocol
[Re: semperfi]
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drscott
New Researcher
Registered: 11/07/10
Posts: 1
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if you feel as though you were being hammered by "satan" perhaops you would be interested in healing ministry..which actually goes in to detail on how specifically to battle this "intelligence" i defeated lyme in one day once I knew what i was dealing with. i do have a sight, shining light ministries...this is not for everyone,.
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#5915 - 04/29/11 05:07 AM
Re: About the Marshall Protocol
[Re: BryanRosner]
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KeyLymer
New Researcher
Registered: 04/25/11
Posts: 1
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Dear Bryan,
I am newly diagnosed with Lyme (chronic) after much money wasted on doctors. My current LLND is caring and knowledgeable. She gave me a choice of treatments and I chose antibiotics because I wanted a quick fix, feeling like I was near the "end of the road" and if I didn't start something soon, I'd be dead.
Anyway, I think the Marshall approach has merit. The reason I say that is because, since my vitamin D is low and I can't tolerate oral D supplements very well, I tried soaking up some rays outside. Every single time I do this, I have about 3 to 4 horrible nights afterward - where I feel, once again, like I'm dying for sure. I always feel so much worse after taking or making vitamin D - either orally, or by exposure to sunlight (either outdoors or in a tanning bed). Low-grade antibiotics have seemed to help me at first, but even on them, I have horrible reactions after exposure to sunlight.
Question: Can the Marshall approach still be successful after trying a long course of antibiotics? And what about all the hoopla about low vitamin D causing deaths? Is that just hype?
I feel like my body is telling me "No D!" loud and clear - I'm just afraid to go against the current medical position on D. Of course, they are wrong about so many other things, I don't know why it concerns me, but it does. Please share your opinion on this. Thanks!
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#5916 - 04/29/11 05:47 AM
Re: About the Marshall Protocol
[Re: KeyLymer]
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BryanRosner
Forum Veteran
Registered: 11/08/06
Posts: 263
Loc: Mountains of Northern CA
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KeyLymer, you are right - the situation is controversial. I wish I knew for sure whether depriving our bodies of D would have ill effects. I don't know. What I do know though is that if what Dr. Marshall says is true, then we actually aren't D-deprived - we have too much on board and it isn't working right. Sorry I can't be more specific. I still stand by my opinions in my books.
Bryan
_________________________
Bryan Rosner
DISCLAIMER: Bryan Rosner is a journalist, not a healthcare provider or doctor.
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