Re: A/P, Marshall Protocol & so much more.

[Guest guest]

Hello Carl. 

 

 In my opinion, since I started with A/P and made great strides the first two

years, then switched over to M/P and made more leaps, I think that doing both in

that order were most important in my healing.  A/P got rid of the initial load

of bacteria and M/P helped to mop up the rest.  Both had great impact of the

body.  If I had it to do over again, I would do the same exact thing in the same

exact order. 

 

 M/P is another version of A/P meaning I used the initial drug of minocin only

during A/P and then on M/P I kept using the minocin and gradually added several

more antibiotics as I increased gradually in the different phases. 

 

The reason I went on M/P is that in addition to scleroderma, I also had a

diagnosis of (MCTD) that is mixed connective tissue disease & R/A.  This means

that I had co-infections at the same time.  That is not unusual and most people

do have co-infections.

 

The addition of other antibiotics was necessary to weaken all the different

bacteria, I may have been harboring for so many years in my body.  There are

more (cell wall deficient microorganisms) than just micoplasma pneumonae whic I

had, lurking in our bodies. I was a  bacterial & viral soup.  I think by doing

both I was able to get rid of most, if not all of the offending microorganisms. 

 

Some people  (in addition to antibiotics) need antivirals & antifungals as

well.  It all depends on what you are infected with.  Apparently, I chose the

right path because initially when I proved to also have a viral infection, I was

given Acyclovir. Some people will need antifungals also. 

 

While I was recuperating, I also had all my metal fillings in my teeth removed

and replaced with porcelain.  I also added dietary aids like whey protein for

the anemia, vitamins and made diet changes.  I did mild exercises at first and

increased my mobility as well.  I used laughter therapy and positive thinking. 

I believe healing of the body encompasses an entire commitment to get well and

that the mind is a powerful tool in that aspect. Depression is a symptom of

disease and I worked to remove all doubt that I wouldn't heal.  Sleep & rest was

very important.  I spent a lot of time doing both. 

 

 I also kept myself hydrated to help eliminate the toxins.  When I had severe

diarrhea, I did not take anything for that symptom, nor for the profuse sweating

at times and chills.  These were all signs that my body was in the middle of

detoxing.  That is why just treating the symptoms only does not cure the person

and they may feel okay while the symptom is masked, but they never get rid of

the cause of the disease,  which primarily is the infection.  I chose to ignore

the symptoms as I knew they would be of temporary duration during the cleansing

process.  Apparently, I was right.  All symptoms are now gone.  I think by

eradicating the source of the disease, mainly the infectious origin, you take

care of the symptoms as you go along.        

 

Not all people need it, but I  certainly did.   I am in remission today.  I

might add that at the second year point, while I  had made great strides, I

listened to my body and knew I still had a way to go as I was still battling the

infections.  By adding the extra medicines, I was able to clear out all the

infection. 

 

Scleroderma is a terminal illness unlike R/A.  I was diagnosed as terminal from

the get-go.  The way I saw it, I needed to do all the protocols until I was

totally free of disease.  That is what I needed to do to remain alive. 

 

Since I don't know what your disease or (diseases are),  I can not guarantee

that doing both will have the same effect with you.  That is something to

discuss between you & your doctor depending on what exactly ails you.  Each of

us is unique and individualized treatment with antibiotics is personal.  Good

luck with your recovery. 

 

The decision to remain on Minocin at half dose three times a week is all mine. 

No one recommended it.  I just told my doctor that I wanted to stay on the

Minocin to keep my body clear of re-infection and so he prescribes the Minocin

for me. When and if I ever go off the medication, will be strictly up to me.  My

body will let me know when & if to stop. 

 

Right now, Although I am in the remission phase, the healing process is still

ongoing.  I am nearly totally restored, but still feel vulnerable to further

attacks by bacteria.  i want to have the strongest immune system possible and so

I have just started a new vitamin & healthy diet regimen.  I have made further

lifestyle changes. I moved to the tropics where I don't have to battle the cold

weather.  At one time, I was so cold intolerant that I could not even go for a

walk all winter.  I live close by to the ocean where the breezes keep my air

fresh & clean.  I installed a pool in my yard and every day when the sun is

behind the trees and I am not in direct sunlight, I go in and ot my aquatic

exercises.  I take care of my mom who is 96 and has alzheimers, so I cannot

always leave to do my exercises in the clear carribbean water, so the pool is

the best I can do at this time.   The trees around me all bear fruit in their

season and that is

basically what I eat.  I also drink the whey protein powder.  I eat meat, but

have never been a huge meat lover.  I eat all manner of dairy, eggs, vegetables

and  drink it all down with homemade limeade with natural limes from the trees. 

 

I think every change that  I made and continue doing, has had a huge effect

on regaining my health.  I take continuing to live my life to the best of my

ability, very seriously.  I nearly came to losing it.  When I was initially

diagnosed, I had been given about 5-6 months left to live.  That was  in

November of 2005.  It is almost October 2010 and I have conquered  Systemic

Scleroderma, MCTD and R/A.  I am now as healthy or healthier than I was 30 years

ago. 

 

I noticed that you e;mailed me privately.  I would appreciate it if you shared

this answer and all future questions through the Rheumatic . so

everyone can benefit from the information.  My job is to let everyone know of my

success story. You may also share this on the RBF site.  That is the roadback

foundation.org. site. My best to you, Dolores  

 

I thank you for your co-operation in this.        

From: yeoldelunatic <yelunatic@...>

Subject: Marshall Protocol

martysfolks2004@...

Date: Sunday, September 26, 2010, 7:58 AM

Hi, if I had read correctly, I beieve it said that you have used the Marshall

Protocol after seeing Dr. Whitman. I am considering seeing Dr. Whuitman. What

was your experience with him, did he help you? Also, what Dr. did you see that

treated you with the Marshall Protocol? What made you decide to go on it? Did it

help? Sorry for so many questions. I live upstate NY and am looking for

different treatment options.