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Seems to work A-ok. I take the colloidal silver about 15 minutes before breakfast. I take the MMS before bed 15 - 20 drops in a pint of apple juice and water. Nasty lump on my back has disappeared after about 4 months at this level. The respiratory problems have disappeared. I will take it for about 6 months at this level. I was sensitive and it took me months to get to 15 drops. It was the only show in town. I suffered from the reactions but My God I was feeling better almost right away.
i would take that stuff.. its like bleach.. it kills the bad but also the good
i have bad health issues and have tried EVERYTHING
stop trying to kill the bacteria virus parasites etc that are in ure body .. this is useless..instead increase the strength of ure body so that it can deal with the challenges it faces.. if u just remove all threat the body gets weaker
i assure u this is the best way to go
there are lots of ways to do this .. if u need any info message me
LDN is working for me. You tube….”Controlling Lyme Disease.” I have shared some info, on another’s space there. After the $100,000.00 mark, waste of money, it cost me only $40.00 and my DR’s fee.
Yes continue the MMS! I have the feeling MMS fights everything in your body on all levels. From what I hear you say, it looks like your body is fighting towards the total annihilation of the Lyme disease. The purple spots you saw, the feeling of being disconnected to what you experience.. Thats pretty heavy stuff. Again, I think the MMS grabs the core and works towards total curing instead of briefly feeling better.
Jeremy, have you ever heard of Activated Charcoal. I cannot live without it. For me, it neutrilizes the toxins that get in the stomach from the cleansing process from the MMS. Please look up the health benefits of activated charcoal on the web and make an informed decision for yourself.
I started with MMS a week ago and am interested in your journey. In response to your question if the MMS is causing the reactions, I have not had the reactions that you have had. I did get diarrhea at 7 drops and need to cut back. I am treating parasites. You body may have problems detoxifying (adrenals?). Hope to see your next installment and hope you are feeling better.
Hi. I’ve been watching your videos. I’m not sure how you’re doing now or where you live, but I am seeing an alternative doctor who specializes in lyme disease. You seem to be interested in alternative treatments. Do you live anywhere near NY?
Your doing great !!!! I’ve had Lyme for 20 years and was with Dr. B for 8 years. I have to tell you that your very toxic with heavy metals..etc. That alone can create your brain fog and other symptoms. I’m just starting MMS as I my CD-57 is a 42. With your CD-57 increasing the way it is your doing the right routine with your MMS. I would get back on it ASAP and look into doing some chelations,if you’re close to New York City,look into Dr. Jeffrey Morrison for your chelations.
Andrew
Hi Jeremy, Just a thank you. I know how hard it is to get anything done. Let alone concentrate on one thing for more that 3 minutes. Thanks for putting the energy into this.
crowninformation, Jeremy may have to stop and start the tape (redo sections) to help him stay on track, and have it be cohesive. Neurological Lyme symptoms are terrible and you can’t think straight. That is probably what the jumping around is.
Hi,
Another chronic Lymie here. I’m 31 and apparently have had LD since I was 11 years old.
Re-infected 6 years ago, and again 4 months ago.
I have RMSF and Mycoplasma also.
I have ordered my MMS but waiting for the right time to start it. Happened upon your video blogs and I’m really getting excited about this stuff, after reading so much about it. But I see that you haven’t posted in 2 months now and I’m nervous … are you okay? Did you restart the MMS?
Keep up the good fight.
Dawn
Jeremy, take a break. My son was on the Marshall Protocol for 17 months and it got to a point where his body was very stressed, which ended in several journeys to the ER. He too did not take it slowly but pushed it to the limit. He has been off the MP for several months now and has stabilized. He is going to go back on the MP at a much slower rate. I too have Lyme and have taken Mino by pulsing it for over a year now. Thinking of trying MMS. Best of luck to you, will keep following.
HI I also am taking MMS. I think you need to take 3 x a day around the 10-12 drops mark. Try as I might I cannot get above 12 drops 3 x day without “adverse” reaction. You should develop a cough which would run for around ten days or so. I am also taking probiotics to replace stomach bugs which we need to function properly, and will start taking colloidal silver as well to get rid of any deep seated fungal infections (usually present thru overuse of antiB’s. They are natural-born opportunists)
Hi Jeremy. I’ve been following your videos and hope you are feeling better. I also am taking MMS for lyme, altho much less (6 drops twice a day) and trying to detox as much as possible each day. I believe that you may be hitting the protocol too hard with the amount of MMS you are taking and the Shoemaker detox protocol (too intense). No wonder you feel so much worse. I prefer to take a more patient approach taking epsom baths, chlorella and clay thru the day and cholostyramine before bed.
Its been six months since this video… is everything OK?
*wouldnt is what i ment
Seems to work A-ok. I take the colloidal silver about 15 minutes before breakfast. I take the MMS before bed 15 - 20 drops in a pint of apple juice and water. Nasty lump on my back has disappeared after about 4 months at this level. The respiratory problems have disappeared. I will take it for about 6 months at this level. I was sensitive and it took me months to get to 15 drops. It was the only show in town. I suffered from the reactions but My God I was feeling better almost right away.
Keep on fighting, hope you will get better.
did you start the coolidal silver? how is it working? especially with th e mms ?
i would take that stuff.. its like bleach.. it kills the bad but also the good
i have bad health issues and have tried EVERYTHING
stop trying to kill the bacteria virus parasites etc that are in ure body .. this is useless..instead increase the strength of ure body so that it can deal with the challenges it faces.. if u just remove all threat the body gets weaker
i assure u this is the best way to go
there are lots of ways to do this .. if u need any info message me
all the best
Use DMSO and apply it via the skin.
Look up Dr. Bob Beck, it clears out everything.
LDN is working for me. You tube….”Controlling Lyme Disease.” I have shared some info, on another’s space there. After the $100,000.00 mark, waste of money, it cost me only $40.00 and my DR’s fee.
You left out a third option. #3. It’s not working.
Yes continue the MMS! I have the feeling MMS fights everything in your body on all levels. From what I hear you say, it looks like your body is fighting towards the total annihilation of the Lyme disease. The purple spots you saw, the feeling of being disconnected to what you experience.. Thats pretty heavy stuff. Again, I think the MMS grabs the core and works towards total curing instead of briefly feeling better.
Jeremy, I forgot to say activated charcoal eases the symptoms from Herxheimer symptoms so that they are more tolerable. Contact me if you wish.
Jeremy, have you ever heard of Activated Charcoal. I cannot live without it. For me, it neutrilizes the toxins that get in the stomach from the cleansing process from the MMS. Please look up the health benefits of activated charcoal on the web and make an informed decision for yourself.
I started with MMS a week ago and am interested in your journey. In response to your question if the MMS is causing the reactions, I have not had the reactions that you have had. I did get diarrhea at 7 drops and need to cut back. I am treating parasites. You body may have problems detoxifying (adrenals?). Hope to see your next installment and hope you are feeling better.
Hi. I’ve been watching your videos. I’m not sure how you’re doing now or where you live, but I am seeing an alternative doctor who specializes in lyme disease. You seem to be interested in alternative treatments. Do you live anywhere near NY?
I had no idea MMS had such a hard time curing Lyme disease! It seems to cure colds and flus in minutes.
Your doing great !!!! I’ve had Lyme for 20 years and was with Dr. B for 8 years. I have to tell you that your very toxic with heavy metals..etc. That alone can create your brain fog and other symptoms. I’m just starting MMS as I my CD-57 is a 42. With your CD-57 increasing the way it is your doing the right routine with your MMS. I would get back on it ASAP and look into doing some chelations,if you’re close to New York City,look into Dr. Jeffrey Morrison for your chelations.
Andrew
I got that Herxheimers syndrome taking chlorella. Did you have any problems on it ?
Hi Jeremy, Just a thank you. I know how hard it is to get anything done. Let alone concentrate on one thing for more that 3 minutes. Thanks for putting the energy into this.
crowninformation, Jeremy may have to stop and start the tape (redo sections) to help him stay on track, and have it be cohesive. Neurological Lyme symptoms are terrible and you can’t think straight. That is probably what the jumping around is.
Hi,
Another chronic Lymie here. I’m 31 and apparently have had LD since I was 11 years old.
Re-infected 6 years ago, and again 4 months ago.
I have RMSF and Mycoplasma also.
I have ordered my MMS but waiting for the right time to start it. Happened upon your video blogs and I’m really getting excited about this stuff, after reading so much about it. But I see that you haven’t posted in 2 months now and I’m nervous … are you okay? Did you restart the MMS?
Keep up the good fight.
Dawn
Hello Jeremy
Check out Transfer Factor Plus Advanced Formula.
It will increase your NK-cell level.
Sincerely
Bengt
Sweden
I think you should get back on the MMS adn cut the dosage back but go to three times a day would make sense to me. Keep us posted
Jeremy, take a break. My son was on the Marshall Protocol for 17 months and it got to a point where his body was very stressed, which ended in several journeys to the ER. He too did not take it slowly but pushed it to the limit. He has been off the MP for several months now and has stabilized. He is going to go back on the MP at a much slower rate. I too have Lyme and have taken Mino by pulsing it for over a year now. Thinking of trying MMS. Best of luck to you, will keep following.
great series! Have you tried LDN (low dose naltexrone)? That’s supposed to be good for cd57 levels.
HI I also am taking MMS. I think you need to take 3 x a day around the 10-12 drops mark. Try as I might I cannot get above 12 drops 3 x day without “adverse” reaction. You should develop a cough which would run for around ten days or so. I am also taking probiotics to replace stomach bugs which we need to function properly, and will start taking colloidal silver as well to get rid of any deep seated fungal infections (usually present thru overuse of antiB’s. They are natural-born opportunists)
Hi Jeremy. I’ve been following your videos and hope you are feeling better. I also am taking MMS for lyme, altho much less (6 drops twice a day) and trying to detox as much as possible each day. I believe that you may be hitting the protocol too hard with the amount of MMS you are taking and the Shoemaker detox protocol (too intense). No wonder you feel so much worse. I prefer to take a more patient approach taking epsom baths, chlorella and clay thru the day and cholostyramine before bed.