I don't have the time or energy to get into any arguments over the MP, but I think it's important that anyone considering it should first read what others have gone through -- check out the comments on this site from both ex-patients, and ex-MP volunteers:
http://heartscanblog.blogspot.com/2008/03/marshall-protocol-and-other-fairy-tales.html
Also, Mark London has written a thorough analysis of the MP here:
http://stuff.mit.edu/people/london/universe.htm
Thanks, dannybex. For anyone who's wondering whether or not the above links are worth the energy of reading, I'd highly recommend the first and then just reading through the comments. Many with significant experience with the MP share their thoughts on it, and it's very enlightening. There are basically three main takes on the MP and TM (Trevor Marshall):
1. It's complete nonsense and very dangerous. Those who get relief get it from Benicar, which is anti-inflammatory.
2. There might be something to the MP, but the cultishness of it, lack of studies, and TM's resistance to questions makes it difficult for any scientific progress to be made. The "study site" is not interested in failures, which makes it difficult to get an accurate read on what's going on.
3. The MP is a great protocol that can heal autoimmune disorders...other people just aren't disciplined enough to follow through with the instructions until they see improvement.
The vast majority of comments are either in the first catagory or the third.
I have seriously considered the MP twice now: once when I first became very severe (after about 4 years of milder CFS) and then again about a year ago. The first time I was in the third category, even though I never ended up starting it. I avoided vitamin D, which wasn't too hard because any sunlight or daylight already caused me problems. My new doctor was very excited about the MP. Blood tests didn't show the results she expected, and she kept wanting to do them over as I became life-threateningly ill, until finally we decided that I needed my blood and needed to focus on just staying alive for a while. Changed doctors.
During that time I was on the forum I can attest to the cult-like nature of it.
About a year ago I started seriously looking into MP again, deciding that if I did so I would be
very cautious and would take what was said on the forum with a few tablespoons of salt. My reasoning was since I cannot tolerate even the smallest amounts of vitamin D (whether supplemented or from food) without irretractable, body-wide pain (very different from my regular pain) that I may as well try an experimental treatment that is for low vitamin D levels. Yes, I "stuck with" attempts at vitamin D supplementation for weaks thinking it was just a detox reaction, but the pain would only continue to worsen. My doctors were confounded because vitamin D generaly relieves pain instead of causing it.
So I figured, my D levels have been extremely low for years and I can't raise them since I can't get any into my system, may as well give this protocol a go. So I spent months researching it, talking about it with my caretaker and naturopath, and having them research it.
In the end I decided that my symptoms were opposite the protocol. VItamin D gave me severe symptoms that did not wax and wane from day to day likea "herx" would. Vitamin D never made me feel better, only worse, contrary to the theory of "you feel better for a little while because..." And finally, low vitamin D just wasn't working for me. It had been 3 years of extremely low levels, and I was still as ill as ever. TIme to try something different.
So I went the opposite direction and decided I was willing to do whatever it took to get D back into my system. My naturopath agreed that trying vitamin D shots was an excellent option since oral vitamin D was intolerable, and she assured me that we would take necessary steps to make sure my pain didn't become overwhelming. It was all set to go until I read about a cod liver oil that was raw, fermented, and packaged in glass. I figured I'd try that first, just to see. I did get the characteristic pain for a few weeks, but it was not as bad as before and then it slowly went away.
Have I had drastic improvement? No. There may be some improvement on my ability to tolerate daylight (NOT direct sunlight) though since that's been cyclical over the past few years there's no way to tell. What I do know is that vitamin D is necessary for dental health (in
one study vitamin D supplementation alone reversed many children's tooth decay) and since my teeth are full of cavities that's my focus right now.
So that's my story as it relates to the MP. I urge anyone considering it to make sure they do a lot of research
outside of the two MP sites, and if they decide to move forward to do so cautiously, keeping your head about you and making sure that you keep doing what
you think is best for your health without being pressured in to anything. All symptoms are explained away as herxing, and many people have ended up hospitalized....some have died. So it's imperative that you have enough layman medical knowledge to know when a symptoms is concerning enough to stop treatment or to seek answers elsewhere.
Last I heard ou are not permitted to take any other supplements or medications while on the MP. That alone makes it impossible for most of us.