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Marshall Protocol Thread Locked

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14 years 5 months ago #19555 by martini
Marshall Protocol Thread Locked was created by martini
I wonder why you were so quick to close that thread about the MP treatment. You didn't even give me a chance to answer any questions.

I'm not here to harm any one. I was just giving my experience. If you know something works that cures your condition would you keep it to your self or share it with others? Well that's what I was trying to do.

Is this the same Marshall Protocol treatment the is run by Trevor Marshall. The same Trevor Marshall that has no medical training and the only doctrate he has is in engineering.

Yes it is the Trevor Marshall treatment. He might not be a MD, but whatever I had nothing else to look forward to and I tried it, even though I was hesitant about it my self. Nothing else worked, this was my only option. And 2 years later I can say it's working.
Its a doctorate in biotechnology engineering I think. You don't see many physicians thinking of cures or treatments. Its usually the scientists that do that. And the MD's use that knowledge.

And if you go to the link listed above you can read the page for
medical personnel.
mpkb.org/home/physicians/emergency


Im not sure what your point is with this Melinda.


I've never seen MAR Tini on here before. He's been a member for 10 hours and is apparently recommending a product or program and providing a webpage link to it.

I thought I explained that. Did you only read parts of that thread? I did say the reason i signed up to the forum is tell every one how I treated my ITP.
I just signed up to tell every one about my what worked for me. And I really hope it might work some one else. But I'm not forcing any one. Just telling about my experience.

Is MAR Tini actually Trevor MARshall? Or someone who stands to gain from this product?
Yeah, lol. I'm Trevor Marshall. I have nothing better to do than sign up to forums so that people can try my treatment.
And I'm also wondering what is there to gain other then the fact I'm hoping MP will help someone like me.
And what product is there to gain from.

Whatever, I wish you all luck with prednisone or other corticosteroids. May it not give you too many side effects. And I hope your spleens are in tact and not being taken out by surgeons just so they can have nice vacation.
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  • Sandi
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  • Sandi Forum Moderator Diagnosed in 1998, currently in remission. Diagnosed with Lupus in 2006. Last Count - 344k - 6-9-18
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14 years 5 months ago - 14 years 5 months ago #19557 by Sandi
Replied by Sandi on topic Re: Marshall Protocol Thread Locked
The thread was locked due to the controversial nature of the subject matter. I did not delete it, so you did get to share the information that you set out to give. At this point, if anyone is interested, they can follow your link and look it up themselves.

If you would like a chance to override my decision, please contact PDSA@PDSA.org. I will permit open dialogue if you have consent.
The topic has been locked.

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The Platelet Disorder Support Association does not provide medical advice or endorse any medication, vitamins or herbs. The information contained herein is not intended nor implied to be a substitute for professional medical advice and is provided for educational purposes only. Always seek the advice of your physician or other qualified healthcare provider before starting any new treatment, discontinuing an existing treatment and to discuss any questions you may have regarding your unique medical condition.