I’m very glad you are looking into the Marshall Protocol and the science that forms it’s backbone. There are many Canadians on the MP. If you write a post at the following website:

http://www.curemyth1.org (Th1 refers to bacteria) …..the patient advocates on the site, who work for free, may be able to put some of them in touch with your personally.

However, if you are a health professional, you can likely communicate directly with other MP medical professionals by joining the “Private Section for Medical Professionals” on the Marshall Protocol study site. Once a member of the forum, I’m sure you could set up a time to speak with other professionals over the phone. The forum is the first on the MP study site (go to http://www.marshallprotocol.com). Once you enter the forum there are instructions on how to become a member.

Those are my two top suggestions!

Best,

Amy

I definitely think the MP could help you. I would advise you to read as much as you can about the MP. You can create an account at CureMyTh1.org right away and ask any other questions you might have.

One thing that is lost on a lot of people is that these diseases and symptoms have a common underlying pathology.

If you take a look at the patient interviews you see in the sidebar, a lot of your (former) fellow sarcoidosis patients have co-morbidities as well. In particular, Jane Taylor’s is pretty great. She had a number of co-morbidities and her interview has a chart, which shows her levels of ACE changed before, during, and after the treatment.

The earlier you do the MP, the easier it will be. If your doctor won’t do the MP, I recommend finding one who will.

Best,
Amy

My first symptom was acute anterior uveitis. Blood work at the lab came back with ACE elevated at 73 (normal 15-60) and my chest CT scan came back with a couple small nodules but nothing in lymph nodes in chest.

I’ve read a few studies that uveitis is a first symptom and there’s a very strong (90%+) that I’ll develop chronic sarcoidosis.

Do you think the Marshall Protocol could help me? Would it be smart to start before other organs get involved?

I’m sorry to learn about your struggle with sarcoidosis. Although your have taken prednisone for several years, which has unfortunately slowed your immune response, we have had many study subjects who have successfully weaned off prednisone and been able to use the MP to recover from sarc.

As for your questions:

1. No, there are no restrictions. In my opinion, it is always worth giving the MP a try no matter how sick you may be. As you may have read, sarcoidosis is a bacterial illness and those people have been sicker for longer periods of time or taken corticosteroids usually have higher bacterial loads. However, as mentioned above we have had people who were on prednisone for decades, successfully weaned off it, and done well on the MP. No one is turned away from the study based on age, disease, anything. Everyone is welcome to participate.

2. You should ask that question at the following website where the patient advocates should be able to provide you with a list of doctors that administer the MP in Pennsylvania:

http://www. curemtyth1.org (Th1 refers to diseases caused by bacteria). Unfortunately I happen to know that Pennsylvania is essentially the only state in the US that does not have too many MP doctors! A lot of people in that state find they have to travel to New Jersey or New York to see a doctor. But post about your situation on curemyth1 anyway since new MP doctors show up on a regular basis.

3. You can order DVDs of the last two Marshall Protocol Conferences by going to the study site http://www.marshallprotocol.com and clicking on the “add” for videos on the left hand top of the screen.

You can also order the video you just watched “An Overview of the MP” on DVD at:

http://www.marshallprotocol.com/forum39/9999-12.html

Many of Dr. Marshall’s video-tapped presentations at various conferences can be viewed at this link:

http://mpkb.mp-dev.com/doku.php#publications_presentations

Hope this helps!

Amy

I’m 55 and have sarcoidoses of lungs since 1993.
I was getting a prednisone for 3 years before I got release from the first burst.
After 13 years of the release the illness is back now and I’m getting a prednisone every 6 months for the last 2.5 years.
I’ve just read about the Marshall protocol and it sounds promissory.

I have a couple questions to you.

1. Are there any age or health restrictions for the MP’s treatment?
2. Are there any doctors in Pennsylvania (USA) who can support the MP’s treatment?
If yes could you please provide their names and addresses?
3. How can I order a video about the MP?

Your response will be greatly appreciated.

Regards,
David

Sorry not to write you back sooner. I just got back from Portugal where I gave a speech related to the MP at the International Congress on Autoimmunity. It went very well and interest in the MP ran high which was exciting.

In any case, thank you for you kind comments about my work and I’m so glad you found the video interesting.

As far as your brother goes - he would be a fantastic person to educate about the MP. I very much agree that it’s sometimes difficult for doctors to keep up with the latest research in the field of molecular biology - especially because they arn’t trained to approach disease from a molecular perspective in med school. But as you can tell, Dr. Marshall has been able to may key discoveries about chronic disease by using in silico modeling and it’s imperative that we try to communicate the result to doctors.

I hope that your brother takes an interest in the MP. I’m sure some of the tenets of the MP are not what he’s used to hearing from the mainstream doctors around him, but if he keeps an open mind he is in the place to help so many patients.

That includes you! I would be so happy if he would agree to put you on the MP. Like you said, maybe you could serve as a test case so that he can see how you react to the treatment (almost certainly improving over time) and it will boost his faith that it will work for others.

Thank you so much for speaking to your brother about the MP. I have your email address and if you or he has any specific questions about the MP don’t fail to email me at my private email (which is listed in my bio on the homepage) and let me know how I can be of help.

By the way, you may want to convince your brother to join the “Private Section for Medical Professionals on the MP website. Once a member of that forum, he can directly correspond with other doctors who have patients on the MP. Information on how to become a member of the forum can be found here:

http://www.marshallprotocol.com/forum24/32.html

Best,

Amy

I love your video! Very helpful! I don’t fully understand it all being a non-med major… but my brother who is a doctor and on the board at Kelsey Seybol clinic here in Houston, TX needs to hear this. I will email him the video website. Doctors need to be connected with molecular science discoveries and successes… to update them… and help so many more patients… whom other wise would be sent home without a reason for their pains and fatigue. My name is Carol Dickinson. My brothers name is Dr. Robert Dickinson. I wish there was a way you all could get together. Kelsey Seybold is one of the largest Hospital (St. Lukes) linked Clinics in Houston if not Texas and possibly the US. If they could know what you knew… WOW!!!… What wonders they could do! Is their any way I can make this connection easier. What can I do to make this happen? I will send him your video website. Please email at carol.dickinson@earthlink.net if you have any suggestions what so ever that I… we… can make this happen. They are one of the largest in Houston… and I am his sister.

I have written to you before about my medical history of Inflammatory Disease … I have extremely high 1,25 Dihydroxyvitamin level (95). Loss of large intestine due to bleeding ulcerative colitis for 14 years till 27 years of age (on asulfadine and prednisone). Colon removed at 27, I am now 52. Still tired, brain fog and various body pains and inflammations. If I can introduce this to Rob… I could also be helped. He could use me as his ginea pig following the Marshal Protocol.

Thanks you so much for all your tireless passionate work, which is evident. Maybe I was meant to be sick… just so I could get the Marshal Protocol into the largest Hospital/Clinic system in Houston Texas… the largest medical center in the world.

Much love in Christ,
Carol Dickinson

carol.dickinson@earthlink.net

There are people in Ireland who are on the MP and have doctors who are willing to prescribe the treatment. The best way to find a list of such doctors is to write a post asking for the “Ireland MP doctors list” at the following website:

http://www.curemyth1.org (Th1 refers to diseases caused by bacteria, hence the name)

The patient advocates on the site should be able to provide you with the list and are also available to answer questions about the MP free of charge.

Best,

Amy