I’m so sorry your symptoms are escalating! I very much agree that it’s extremely important that you start the MP. You seem persistent and I am sure you will find a doctor.

I can recommend my own doctor in Manhattan. I hope you live in or near the city. I’ll send his information to you in a private email.

If driving to Manhattan is too long a trip I recommend that you ask for a list of doctors with patients on the MP at the following website:

http://www.curemyth1.org (Th1 refers to diseases caused by bacteria, hence the name). The patient advocates on the site, who offer help about the MP free of charge, will provide you with the list.

Also, are there any alternative medicine doctors in your area? Or could you possible switch primary care physicians and find someone who might be more open minded? If you are able to set up an appointment with another doctor in your area be sure to show him/her the following peer reviewed papers and conferences transcripts put forth by Dr. Marshall and team:

http://mpkb.org/doku.php/home#publications_presentations

Also, this article describes how to help convince a doctor to put you on the MP:

http://mpkb.org/doku.php/home:starting:physician:finding

Good luck and hang in there!

Amy

I am being investigated for neurosarcoidosis and having a gallium scan on Wednesday. I had the radioactive dye injected today. I was very curious because you are in Australia what doctor has overseen your treatment. If sarcoidosis is my diagnosis I would appreciate this information so i know that I am seeing a doctor that has already dealt with MP and sarcoid. I am very down about this diagnosis and would appreciate your help.

Thankyou in advance

Karen

I hope you mean that you are looking for a doctor who would treat your sarcoidosis with the Marshall Protocol. Be sure to read as many articles on this site, as well as information on the Marshall Protocol study site itself (www.marshallprotocol.com), so you understand the treatment as well as possible.

Rather than covering up symptoms of sarcoidosis, the Marshall Protocol targets the bacteria that have now been implicated in causing the disease. It also gradually restores the activity of the innate immune system.

Unfortunately, I don’t have a list of doctors who work with Marshall Protocol patients. I do, however, think that the patient advocates at the following website may be able to help you find an MP physician in India.

http://www.curemyth1.org. There is no fee to get advice from patient advocates as the MP is run by a non-profit foundation.

Good luck!

Amy

Thanks very much

I am confused by your comment?. Could you please clarify?

Thanks!

Amy

I wish you all the best and hope to see you as a member on the MP study site.

Best,

Amy

Thanks for your advice.

Cheers,
Sarina

I’m so glad that you’ve found the Marshall Protocol. It’s never to late to recover from your illness!

I cannot directly give you the name of an MP doctor in Australia as I don’t have access to such information.

You can visit the Marshall Protocol study site and request a list of doctors who already have patients in Australia on the MP at the following link:

http://www.marshallprotocol.com/forum11/11348.html

I also recommend that you visit the study site (www.marshallprotocol.com) and click on the “members” button on the upper right hand portion of the screen. There you can search for MP members by location. Search for other MP patients in Australia. If any live near you, send them a private message over the site asking them who their doctor is and if you can have his/her contact information.

If you still can’t find a doctor using those methods, then perhaps you can convince your current doctor to put you on the treatment? I recommend printing out articles from this site and the study site to show to your current physician.

You can also order a MP presentation book for doctors off the MP study site at this link:

http://www.marshallprotocol.com/forum2/11458.html

Here is a link to Dr. Marshall’s published papers in case you would like to show any of them to your doctor. I also recommend that you order the “Science DVD” off the MP study site and show it to your doctor.

http://www.trevormarshall.com/papers.htm

Last, but not least, it’s important that if you are serious about doing the MP, you fill out an application form to join the study at the following website:

http://www.curemyth1.org Th1 refers to disease caused by L-form bacteria, hence the name Cure My Th1. The patient advocates on the site will give you the form and also answer any questions you have about the treatment free of charge. Since some of the patient advocates are from Australia, they may be able to put you in direct contact with a doctor.

Good luck!

Amy