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COPD 03 Nov 2013 00:09 #37169

Peg7
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I am 64 yrs old and was diagnosed 11 yrs ago with end stage emphysema (COPD). I use oxygen 24/7 at 3L, Symbicort and Spiriva. I also take Diltizem (generic for Cardizem) for high blood pressure and Lovastatin for high cholesterol.
I have had pneumonia 3 times in the last 2 yrs, had about 1/2 cup of fluid drained from my pleura sac the 2nd time I had pneumonia. This last time the carbon dioxide level was really high. Doctor said the next time I get pneumonia I would have to be ventilated.
I have taken MMS in the past and had good results even though I didn't think it was working for my disease. I had moles that disappeared, brown spots on my hands faded, dropped 1 daily dose of copd medicine, coughed up tons of stuff which helped my breathing. Looking back, it was working just stopped too soon.
So here I am again. I started taking MMS on October 25th. I stopped the nebulizer treatments that day as I was bringing up more junk with the MMS. I am juicing after (2 hrs.) treatment. I take probiotics and eat as much organic as is available in our area. Is this going to work onthe carbon dioxide?

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COPD 03 Nov 2013 05:11 #37176

paul
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Hi , Peg
Yes. you stopped too soon. :>) If you never stop, your lungs will clean out and you will never again contract pneumonia, oxygen transfer in and carbon dioxide out will improve to the point where you won't have to take extra oxygen. Once you've done the 1000 protocol. you can try the maintenance dosage morning and night, but never stop for the rest of your life.
You could consider carefully breathing fumes. That will get the chlorine dioxide straight into your lungs, where its need most.

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COPD 03 Nov 2013 19:01 #37196

Peg7
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Thanks Paul for your help. I will try the inhaling protocol today.

Still lots of mucous which I take as a sign MMS is working.

Haven't used my inhalers this morning. Will try not to use them today. My oxygen level last night at bedtime was 98%. I got the same reading this monring after I had been up for a while. But after a few doses of MMS it is now 97% which is still very good and higher than my normal.

Thanks again Paul.

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COPD 04 Nov 2013 22:35 #37218

Peg7 Topic Author Offline New Member Posts: 8 Thank you received: 8	Having terrible time today with MMS. My 2nd day of continuous dosing left me with horrible diarrhea and exhaustion. I have gotten 2 doses down this morning, have a headache, heart rate at 95 and blood pressure elevated a little. Think I am reacting to the citric acid but that is all I have right now. Is there anything else I can use?
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COPD 05 Nov 2013 01:11 #37220

JB13
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Hello Peg7. Sounds like you may be detoxing too fast. Could also be the citric acid as you said.

There is a new way to make MMS that uses 4% HCl for no taste or odor at low doses, Protocol 1000.

Read and watch:

mmsinfo.org/infosheets/POBOM_detailed.pdf

mmsinfo.org/videos/cdh_one_bottle.mp4

Please take Paul's advice to stay with it and when well, do daily maintenance doses forever!

Keep us informed of your progress.

Thanks!

• Easy, free way to support Jim Humble, Genesis II Church, MMS

• Jim Humble's MMS Books
• MMS Video Course
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COPD 05 Nov 2013 01:50 #37225

pam Offline Platinum Boarder Posts: 4593 Thank you received: 3702	Slow down, Peg - better to take fewer drops per dose and take a bit longer to get to the goal - you will continue to detox and if you're detoxing faster than your body can throw off the toxins, you will have some of these problems. Low and slow wins the race. The following user(s) said Thank You: paul
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COPD 06 Nov 2013 02:23 #37250

Peg7
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Thanks Pam and JB13 for your help. I have reduced the amount of drops and seem to be okey with the activator. I did the breathing treatment earlier. I had a doctor's appointment today and was very happy the carbon dioxide level had decreased 1 point below what it was in July when bolod work was done. I am having pain in my fingernails. I've had this once before when taking MMS. I wonder if it the MMS is taking care of an issue since I wore acrylic (sp) nails for too many years. They are looking healthier anyway.
Thanks

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COPD 07 Nov 2013 11:10 #37273

sjmc0330 Offline New Member Posts: 7 Thank you received: 0	Please keep us updated...I too have COPD and am going to start MMS!
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COPD 08 Nov 2013 13:28 #37291

acuneedler Offline New Member Posts: 11 Thank you received: 5	Is anyone else doing the breathing method (2 drops in the cup and inhaling through the nose and mouth 1 time)? I'm having a hard time with it. It seems to make my lungs worse. Don't know whether to keep it up or quit. This is the second time I tried it and this time it only took 24 hours to about shut my lungs down.
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