Tuesday, March 21, 2017

Slight Delay


Well the blood work that was required before I could start the protocol revealed that I have hyperthyroidism that needs to be resolved first. I am a little bothered by the fact that this is a fairly common condition amongst MS patients, yet, was not something that was included my regular blood work. So, I'm not really certain how long this has been the case, and many of the symptoms are very similar to those experienced with MS. The earliest available appointment with the endocrinologist was April 5th, so that's the first delay. Even after seeing the doctor, I'm not sure how long will it take for the proper medication to be prescribed and correct my thyroid condition. Michael expects it to be about 3 months after seeing the doctor. I'm hoping it will be earlier as I'm still excited and hopeful about the protocol.

In the meantime I finally received my vitamin D3, and have been told that daily taking 10k units would be safe. So I have started that and patiently waiting to see the endocrinologist.

Wednesday, March 15, 2017

Selecting the Dr.

While the information regarding the Coimbra Protocol all state the importance all state the importance of including an individual trained by Coimbra. The following link lists the current doctors: Doctors


Having a doctor that speaks English did limit the options, so I sent an email message to both Florida and Ireland asking if it would be possible to perform the protocol using Skype. This seemed logical as the results of the blood work are what is important, not actually physically seeing the physician. The time difference between myself and Miami made Dr. Cawley the logical choice. On top of that, how can one go wrong with the name Michael?


Do on March 15, 2017 had a Skype call with Dr. Cawley. I though the call would last between 5-10 minutes, even with the questions I had written down to ensure that they would not be forgotten. I was pleasantly surprised that we talked for nearly 30 minutes. I must admit that I found his bedside manner much more relaxing and comforting than I had expected, but that might be because he is an ND and not MD. In addition to assisting others with the protocol, he is a patient himself because of suffering from MS since the late 90's. While remaining very cautious and not offing unrealistic expectations, his reliving his own experience helped bring cautious hope to the situation. So I have submitted my blood work to be examined with tentative plans for another Skype meeting around the 21st of March.


Hearing his accounts of what he has experienced as well as seeing how he seems to be today brings hope. Trying to ensure that I am not giving myself false hope or unrealistic expectations, I do believe that being in the proper frame of mind not only helps, but is necessary. I do understand and appreciate that there are readers out there that are skeptical of this protocol. I do not mean to turn this into an overly religious discussion or anything, but it is my belief that God provided mankind with a limited amount of knowledge and it was his responsibility to discover what is unknown. It is possible that could be accomplished with science and medicine or maybe it is understanding how to properly utilize what nature provides. I have tried science and medicine for the past decade, and now will try the other option. Yes, I am trying to remain realistic and not get overly hopeful, but I must admit that I am excited.

What is the Coimbra Protocol

So in the first post I have given a brief history of my MS and the purpose of this blog is to document my experience with the Coimbra Protocol, which I have not yet explained. So here goes....


Dr. Cicero Galli Coimbra is a Brazilian Neurologist, Professor and Researcher who has become popular for treating Multiple Sclerosis and auto immune disease with high doses of vitamin D3 combined with a combination of other supplements and diet recommendations. Dr. Coimbra does not claim to cure MS [some of his patients will tell you differently] but he has proven that his treatment does stop it progression.

The Dietary Restrictions
All patients must discontinue eating or drinking dairy products or calcium enriched foods or beverages. Complete restriction is critical! This includes foods that are formed by milk, cheese, cheese spread, yogurt, curdled milk, cream of milk, caramel, milk pudding, condensed milk. Also includes products made of soy milk enriched with calcium (for reduction of the amount of calcium ingested due to the use of high doses of vitamin D in your treatment) .  Coimbra also encourages patients to avoid excessive or routine consumption of bananas. Of course this includes discontinuing any calcium supplement.

Hydration is Critical
​Drink at least 2.5 liters [85 ounces] of fluids, preferably water, daily to avoid excessive concentration of calcium in the urine. From Dr. Coimbra "Ingest high amounts of liquids (at least 2 and a half liters of liquids daily, including water, juices,, soft drinks, teas, etc.). This higher quantity of liquids assures a urine volume around 2.000 ml which allows calcium dilution eliminated in the urine, and avoids excessive concentration of urinary calcium ( as when calcium is diluted it does not get deposited in the kidney, preserving renal function). 

Calcium, Vitamin D and Auto Immune Disease
Dr. Coimbra believes that lack of vitamin D has led to an increase in occurrence of a growing number of diseases that affect all the organs and systems of the human body', where the most notorious ones are: infectious and autoimmune illnesses, cancer, cardiovascular illnesses, hypertension, diabetes, depression, autism, infertility, spontaneous miscarriages, and pre-eclampsia. Vitamin D deficiency leads to loss of control of 229 functions (genes) as well as in cells of the immune system, reducing the system’s potency to fight infections and allowing immune aggression against the organism. Individuals prone to developing autoimmune illnesses appear to be partially resistant to Vitamin D. Once they get ill, higher doses of vitamin D are needed in order to make the illness inactive. Not only to compensate this partial resistance, but also to "erase" the false information that part of the body sees as a micro-organism intruder by the immunological system memory.


Contrary to what occurs with high doses of steroids and with the use of immunosuppressive agents used as part of traditional treatment, the administration of vitamin D3 increases the power of immunological system in combating infections. When taking extremely high doses of D3 the absorption of excessive amounts of calcium present in food or supplementation can be a problem, at least that has been the common belief. But Dr. Coimbra has determined that these higher doses of vitamin D "completely open the door" to allow the passage of calcium from the interior of the bowel to the blood stream, obliging the organism to get rid of excess calcium through urine elimination. Calcium excess, concentrated during urine formation, could be deposited in the kidneys, and could cause loss of renal function and make the individual dependent on haemodialysis to survive. This is why the water intake he prescribes, as least 2.5 liters [85 ounces] of fluids preferably water, is so critical.

Independent Testing
Dr. Coimbra has claimed amazing results with his treatment and unfortunately very little is done in the US or the UK to prove or disprove any of his claims since our the medical industry has little interest in the subject.​ Researchers from the University of California, San Francisco have done some basic work on MS patients and have reported a reduction in brain lesions and disease activity in multiple sclerosis patients who had higher levels of vitamin D. This conclusion came after a 5 year study, involving 469 men and women with MS. All participants underwent yearly blood testing for vitamin D and brain magnetic resonance imaging (MRI) to evaluate disease progression. The researchers determined that with each 10 ng/ml increase in serum 25-hydroxyvitamin D, there was a corresponding 15% reduction in the risk of new brain lesions characteristic of MS. They also noted a 32% lower risk of areas of active disease as indicated by “white spots” or areas of inflammation visible on MRI images.

Sunday, March 12, 2017

Deciding to take the first step

A brief history about myself.

I was diagnosed with Relapsing-Remitting MS (RRMS) on valentines day in 2006; however, it seems that symptoms started showing as early as 2002. Treatment for the first couple of years included Beta interferons, unfortunately, there were still several relapses. Thankfully the doctor finally switched to Tysabri back in Nov, 2010. During the fall of 2015, the only relapse while taking Tysabri was experienced. For those that are not aware of this medication, it comes with a whole set of possible side effects that must be considered. A few months ago a friend suggested researching the success of using Coimbra protocol in treating a number of diseases, including MS.

It may be surprising to discover there are actually books regarding the protocol published and available on Amazon. There were even more items returned when conducting a similar search on YouTube. Eventually it was decided to begin the Coimbra Protocol. The motivation for this blog is two fold, first to help put thoughts, feelings, and even fears to paper. Secondly, to hopefully provide additional information for other patients of MS as they are trying to decide if this treatment might be right for them.

I do not live in a part of the world where there are currently doctors trained to administer the protocol. Thankfully, I have reached out to a couple whom have expressed a willingness to use Skype and WhatsApp instead of requiring a visit in person. Laboratory results are expected in a week, which will immediately be forwarded on to at least one of the doctors previously mentioned. Currently, the plan is for weekly updates to the blog, but that could change depending upon how things are progressing within the treatment. Some links for additional sources of information that proved to be useful will be posted in the next couple of days while waiting for the lab results.