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  #161 (permalink)  
Old May 10th, 2008, 10:40 AM
carla is a bit itchy
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KR,
I think you should send an e-mail to the Miracle Mineral Organisation to ask them. I wouldn't like to say if it safe to take for weeks or not.
Heres the link for their contact form.They usually reply within a day or two.
carla xx

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  #162 (permalink)  
Old May 13th, 2008, 05:49 AM
Gator is about love for mankind and helping others.
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Smile Mms -

Hi Knight-Ryder,

Sorry it took so long to answer. I have been down due to an injuryto my neck and I couldn't log in until today.

It is possible to download Jim Humble's book. Part 1 is free and Part 2 is $9.95 from mmslymecure.com; I think.

A maintenance dose means when we are cured, adults take 6drops 2X per week.

Jim is working on a Lymes cure now. He has suggested that for Lymes; Mix a dose and sip it over a period of 2 hours; mix another dose do the same throughout the day and so on.

I take 6 drops per dose as many times a time as I can tolerate up to 30.drops This helps with the nausea. However, I have been taking it for a couple of months and nausea is not a problem now unless I ramp up to 15 drops per dose.

This is going to be a long term treatment and hopefully will cure us or at the very least make us much better.

Hope you are seeing some results by now. It is the cheapest most effective treatment I have found.

My problem is getting in the vit c and antioxidants which need to be taken 4 hours apart from the MMS.

I usually take them first thing in a.m. and last thing in p.m.

Hope this helps.

Hugs,
Gator
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  #163 (permalink)  
Old May 18th, 2008, 01:20 PM
carla is a bit itchy
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Hows everyone on MMS doing ? I couldnt be without it now. I m just taking a few drops twice a week and its keeping my symptoms down.
carla xxx
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  #164 (permalink)  
Old May 20th, 2008, 01:37 AM
Gator is about love for mankind and helping others.
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Smile MMS Update

Hi Carla,

I'm happy youu are able to keep your symptoms down now.

I am continuing to take MMS at least twice a day, but I am working on taking it every 2-3 hours as suggested for Lymes. I am doing fine with it now.

I am better when I take it except that I seem to be more tired.

Maybe the MMS is not the cause of the exhaustion since I am struggling with all kinds of allergies and the neck and head injury. I am getting a massage on Saturday and doing physical therapy 2x a week and exercises at home.

I am so tired, I can't keep up with everything so I just don't. I need to be cleaning, cleaning, cleaning, but just not able. I have no help which makes it very hard.

So, I read my Bible, pray, try to obey God in everything and leave the consequences to him.

Hugs and prayers,
Gator
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  #165 (permalink)  
Old May 20th, 2008, 07:05 AM
carla is a bit itchy
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Thanks Gats, No wonder your so tired with all them injurys.
I hope you get well soon.
carla xxx
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  #166 (permalink)  
Old July 2nd, 2008, 12:46 AM
jonsi is live and let live. Let's get through this!
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Default update please!

Hi Carla,

I'm wondering if the MMS is still having positive effects for everyone who is using it. I hope so!

In the white light,
~jonsi
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There is a reason I have "Morgellons". Helping and teaching others how to survive in our toxic world may be the reason. Hang in there everyone who has this.
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  #167 (permalink)  
Old July 2nd, 2008, 06:07 AM
carla is a bit itchy
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Hi Jonsi,
Ever since the day I drank it too quickly and became very sick I've had a hard time taking it .
I get a stomach ache just looking at it now.I can manage one or two drops every few days at the most .
I felt like I was on my way to being normal again before that happened too.
I d been out of the house every day that week and wasn't getting tired after half an hour like I do now.
Now I wonder if it was the morgs way of defending themselves and if I should risk nausea again.
Of course I should but I'm scared.
carla xxx
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  #168 (permalink)  
Old July 2nd, 2008, 05:33 PM
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I suggest that everyone that is just doing MMS to get better to realize that they are probably are not going to get better as their have been lyme patients that have taken MMS now solely for the last 2 years and have gotten worse. I am not saying that everyone is going to have this happen to him or her but it is my suspicion that it will. Using an antibiotics combination like that described in the book healing lyme is a way better thing to do. Not only will it kill the spirochetes that every morgellons sufferer has but will also improve the immune system and increase the antioxidant levels in the body so as to treat the viral infections that come with the ride. A cup or two of Aloe vera is also very helpful to take everyday as well. Flushes out toxins and increases intestinal

Then doing an occasional MMS pulse would be beneficial as well. BTW dont take some of those mood stabilizers as they are antipsychotics and will only make your immune system worse.

Paul
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  #169 (permalink)  
Old July 15th, 2008, 03:00 PM
carla is a bit itchy
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Quote:
Originally Posted by paddel View Post
I suggest that everyone that is just doing MMS to get better to realize that they are probably are not going to get better as their have been lyme patients that have taken MMS now solely for the last 2 years and have gotten worse. I am not saying that everyone is going to have this happen to him or her but it is my suspicion that it will. Using an antibiotics combination like that described in the book healing lyme is a way better thing to do. Not only will it kill the spirochetes that every morgellons sufferer has but will also improve the immune system and increase the antioxidant levels in the body so as to treat the viral infections that come with the ride. A cup or two of Aloe vera is also very helpful to take everyday as well. Flushes out toxins and increases intestinal

Then doing an occasional MMS pulse would be beneficial as well. BTW dont take some of those mood stabilizers as they are antipsychotics and will only make your immune system worse.

Paul
Well I think MMS is the best thing I have ever used as a treatment. I've had Antibiotics in the past and I think they made me worse and depressed me.
A lot of us can't afford antibiotics or find a doctor who will prescribe them long term, so MMS is the only option.
carla xx
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  #170 (permalink)  
Old July 15th, 2008, 10:35 PM
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Hi Carla

I am still on MMS and it is helping me I think. I was on antibiotics for about 5 month once didn't help very much.

Have a good day
Nick
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