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Re: Dr. Mercola/Marshall

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I am not on the Marshall Protocol, but I have read www.bacteriality.com from

top to bottom. (It promotes the MP). I have to say that after reading all of

the information on the site, I find it far more thorough and compelling than

Mercola's argument against it.

I've been troubled by Mercola in the past few years, and how very commercial

he seems to have become. He often claims that there is only ONE brand of a

certain supplement he recommends, and you can ONLY buy it from HIM. I was

also a bit disturbed that he was selling radar detectors - encouraging

people to speed. How many auto accidents could have been prevented had

not the participant been speeding? Why is a physician selling radar

detectors?

I find it disappointing that he no longer supports the AP, even though he

admits that he used it in the past and found it helpful, and that Dr. Brown

helped thousands of people. He claims that diet and lifestyle can fix

anything, but I was too far gone, too sick. The AP saved my life. I wish

that Mercola and Marshall and many others out there would come together,

remain open minded, and not let egos and firmly entrenched positions keep

polarizing the debate.

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i too am unsure re the MP. i did an experiment with D - taking it from

late Oct. to 2 weeks ago and during the last few weeks my arthritis has

gotten worse than it's ever been. the pain is incredible. in my 12 y

with RA it's never been this bad. so maybe there is something to the MP?

i wish i could get my 1-25 D tested to see. though mercola says it's not

an accurate reflection of D since it changes constantly. docs here won't

order 1-25D anymore.

monique

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Hi all,

It has been my understanding that Dr. Mercola is no longer seeing patients as he

is spending all his time on his newsletter in the hopes that he can get the

health system changed whereby people will be able to use what ever treatment

they wish. He is hoping that he can break the hold Big Pharma has on everyone.

Keeping the newsletter free to the public has made it necessary for him to find

a way to fund it continuance. He has chosen to sell products that he himself

would or does use. At least that is what he has claimed over the years.

I do not always agree with some of his points but overall I think he is doing a

great service in keeping us informed.

jmo,

carol_DM

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Hi All,

We are all different.

I am in remission/control of my Dermatomyositis and Mixed Connective Tissue

Disease with CREST syndrome.

Before and after going on AP, the sunshine was my best friend. It made me feel

much better.

Before reaching remission, I limited my time in the sun to avoid sunburn but

made sure that I got at least 20 minutes a day in direct sunlight (of course,

only on those days the sun actually shined) and felt much better for it.

Since reaching control, I can spend any amount of time in the sun. I recently

spent over 2 hours in direct sunlight sitting on the bow of a boat at the Great

Barrier Reef. No sunburn, no windburn, just plain joy and well being.

I guess we are all different in how we react.

We each need to do what is right for our own bodies.

take care all,

Carol

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