holy smokes, when you were describing your symptomes, I feel like aha! I have that! Is lyme one of things that you really know when you have it? I’ve had some major cognitive dysfunction for the past couple years..
Lyme can enter your central nervous system in 24 hours and start wreaking havoc immediately. But it can also mimic many other diseases. Find a doctor with experience diagnosing and treating Lyme!
Jeremy, thank you for the blog. I have had chronic Lyme for 6 years. I think if you haven’t seen improvement by now, it’s not working. For me, a couple days of Doxy takes care of any flare ups. I do that 4-5 times per year. I suspect Ill have it the rest of my life.
has anyone actually been cured by MMS? I see all these youtube tapes of people taking MMS, but none actually say that they are cured. I think Jim might have all of us fooled on this product, no one documented has ever been cured of anything by MMS
OH! Be careful about the amount of coffee that you use. I once used way to much and my heart was so off kilter. Racing and pounding. Hopefully the Zappers have improved oveer the years. Never found any help with Hulda Clarks, but I did use some ohter products that I liked for cleansing.
Jeremy I would advise you to use the Zapper strapped around your neck with probes sitting on the carotid arteries. See Bob Beck protocol. People I know have used the zapper and cured severe depression and migraines. It works really well with MMS as the cells seem to absorb the chlorine dioxide easier. Keep up the great work.
Hi Jeremy, A great way to get rid of the brain fog and brain herx is coffee enemas. It sounds gross, but it made a difference for me. It sounds like the MMS is killing the Lyme, but your body is not able to get rid of the toxins so they are staying inside you making you feel worse. Google coffee enemas. It helps your body get rid of all the stuff the MMS is killing. For me I could not do the MMS if I did not do coffee enemas. I had to do it daily. It might make you feel better.
Thanks Jeremy again!. This particular blog was so needed. You are definately suffering the same as me with the head stuff. I am very depressed and feeling full of dispair and its hard to go through. The MMS has made this worse but I want to stick with it so having your blog to watch is very helpful and reassuring that it isnt just me. My husband is getting bad stomach pain and finding it difficult but he is sticking at it now he has seen this. You are helping lots of lymies. Thankyou.
It always amazes me that even when you’re feeling so awful and disoriented, you still offer words of encouragement, perspective and advice to others. You’re doing a wonderful thing here, Jeremy. Thank you, too, for the reminder that MMS can make things a whole lot darker before revealing any light. Those of us using it or supporting people who are need to remember that. Thanks again.
Ooops! disregard my previous post. I found your update . Even if you aren’t successful with this protocol. Please keep the videos coming. It may form a pattern that at least gives some results in the end, or maybe the protocol could be combined with another therapy in the future…And even if you keep your own Vlogs and don’t post them, just keep doing them . Okay I think we all like to watch though. Thank you for sharing them with us.
March 27th, 2009 at 3:29 pm
Anne
holy smokes, when you were describing your symptomes, I feel like aha! I have that! Is lyme one of things that you really know when you have it? I’ve had some major cognitive dysfunction for the past couple years..
March 27th, 2009 at 8:24 pm
Lyme can enter your central nervous system in 24 hours and start wreaking havoc immediately. But it can also mimic many other diseases. Find a doctor with experience diagnosing and treating Lyme!
March 28th, 2009 at 11:16 am
Dan
Jeremy, thank you for the blog. I have had chronic Lyme for 6 years. I think if you haven’t seen improvement by now, it’s not working. For me, a couple days of Doxy takes care of any flare ups. I do that 4-5 times per year. I suspect Ill have it the rest of my life.
March 29th, 2009 at 7:23 am
Carlo
I’m feeling your pain brother. Everything you have said i have felt the same. How do you feel now ?
April 1st, 2009 at 11:35 am
Samantha
has anyone actually been cured by MMS? I see all these youtube tapes of people taking MMS, but none actually say that they are cured. I think Jim might have all of us fooled on this product, no one documented has ever been cured of anything by MMS
April 2nd, 2009 at 7:33 am
Carlo
OH! Be careful about the amount of coffee that you use. I once used way to much and my heart was so off kilter. Racing and pounding. Hopefully the Zappers have improved oveer the years. Never found any help with Hulda Clarks, but I did use some ohter products that I liked for cleansing.
April 2nd, 2009 at 8:47 pm
Violet
Jeremy I would advise you to use the Zapper strapped around your neck with probes sitting on the carotid arteries. See Bob Beck protocol. People I know have used the zapper and cured severe depression and migraines. It works really well with MMS as the cells seem to absorb the chlorine dioxide easier. Keep up the great work.
April 6th, 2009 at 4:31 am
Violet
Hi Jeremy, A great way to get rid of the brain fog and brain herx is coffee enemas. It sounds gross, but it made a difference for me. It sounds like the MMS is killing the Lyme, but your body is not able to get rid of the toxins so they are staying inside you making you feel worse. Google coffee enemas. It helps your body get rid of all the stuff the MMS is killing. For me I could not do the MMS if I did not do coffee enemas. I had to do it daily. It might make you feel better.
April 8th, 2009 at 3:41 pm
Carlo
Thanks Jeremy again!. This particular blog was so needed. You are definately suffering the same as me with the head stuff. I am very depressed and feeling full of dispair and its hard to go through. The MMS has made this worse but I want to stick with it so having your blog to watch is very helpful and reassuring that it isnt just me. My husband is getting bad stomach pain and finding it difficult but he is sticking at it now he has seen this. You are helping lots of lymies. Thankyou.
April 11th, 2009 at 7:12 pm
Tim
It always amazes me that even when you’re feeling so awful and disoriented, you still offer words of encouragement, perspective and advice to others. You’re doing a wonderful thing here, Jeremy. Thank you, too, for the reminder that MMS can make things a whole lot darker before revealing any light. Those of us using it or supporting people who are need to remember that. Thanks again.
April 13th, 2009 at 3:19 pm
Tim
wrote a lyme brochure with the help of 2 Lyme specilists. will email to anyone.
elaine in va
April 15th, 2009 at 2:18 pm
Jane
Ooops! disregard my previous post. I found your update
. Even if you aren’t successful with this protocol. Please keep the videos coming. It may form a pattern that at least gives some results in the end, or maybe the protocol could be combined with another therapy in the future…And even if you keep your own Vlogs and don’t post them, just keep doing them
. Okay I think we all like to watch though. Thank you for sharing them with us.