I am a recovered fibromyalgic who left the care of medical profession to discover the cause and cure of this horrific condition, and I understand this condition from the inside and back out again. This is a good description of symptoms. Symptoms can often be mistaken for the cause, and treatments that help do not cure. Do not give up from failed hope. Keep going! See You Tube video:
"Curing Chronic Fibromyalgia - Choosing What Works" by author Valerie Lumley
I have Lyme and thought that I tried MMS with no effect. I've begun to wonder now if I was sold some water or a placebo, instead of MMS. I couldn't tell I was taking anything at all. Nada! Nothing happened or changed at all. Does MMS smell a certain way? Any way I can recognize it? Thanks.
mms smells like bleach and turns a dark yellow when properly mixed at 1 drop mms to 5 drops citric acid 10% start at 1 drop twice a day work up to 6 drops twice a day or more
Wow i didn't realize how recent your last vlog was. Okay. I am joining the crowd and wondering...What's the latest? You mentioned improvements as being circulation, but I think your speech and thinking/cognitive has improved also? possibly? or maybe you are just getting use to being on camera :P. Great job. Please keep the vids up, even if you continue to struggle... These are improvements! The vids are GOLD to someone who has no hope!
Jeremy, Jeremy where art thou Jeremy?? (incidentally my son's name also)!
Please come on and tell us something - anything - even if you have given up the MMS quest, you will not lose face. You have tried! Nothing ventured, nothing gained as the saying goes!
If we don't hear from you again I'm sure we ALL wish you the very best in your fight against Lyme disease.
I am so glad you are doing these blogs. I have had lyme for 6 years and my 15 year old daughter and my husband have it too. We live in the UK but got it in on a trip to Florida. You are really helping me to reassure my family that the increase in symptoms is due to us using the mms and to helping us stick with it. Thanks. Keep it going! Has your Fatigue been really bad now you have increased?
Thank you for posting your experience. Have you heard of or tried the Marshall Protocal? If so, did you experience any luck? Are you still taking antibiotics while trying this new treatment?
I have had Lyme for 11 mnths and have started antibiotics for 9 weeks now. I commend you on sharing your battle, and look forward to your blogs. I hope and pray that this could be an answer for you and all of us with Lyme. Good luck and good health.
hey your symptoms resemble mine alot. And Ive as much or more than you in treatment. Had symptoms for at least 25 years. Looking foward to your input going to start next week.
I have been battling Lyme for five years. My symptom list is an exact clone of yours. Most people with Lyme that I have talked to have more of the classic Lyme symptoms. It sounds like you have tried a lot of things to get better. Have you tried a Rife machine? Good luck with the MMS.
Hello Jeremy, I'm starting MMS in less than a week, wanted to keep you in loop - if you're interested - as I am attempting to rid my body of herpes and the length of treatment is much shorter so you can see how I fair. Also Jim's book II says re: lyme: "The best results so far has been with MMS activated with the citric acid solution...Small doses every two hours seem to be the best results giving the immune system plenty of help...it might take as long as a year to overcome the lyme disease."
This has been flagged as spam show
I am a recovered fibromyalgic who left the care of medical profession to discover the cause and cure of this horrific condition, and I understand this condition from the inside and back out again. This is a good description of symptoms. Symptoms can often be mistaken for the cause, and treatments that help do not cure. Do not give up from failed hope. Keep going! See You Tube video:
"Curing Chronic Fibromyalgia - Choosing What Works" by author Valerie Lumley
ValerieLumley 1 year ago
thanks top job
Mackamoos 2 years ago
I have Lyme and thought that I tried MMS with no effect. I've begun to wonder now if I was sold some water or a placebo, instead of MMS. I couldn't tell I was taking anything at all. Nada! Nothing happened or changed at all. Does MMS smell a certain way? Any way I can recognize it? Thanks.
londerosa 3 years ago
Trying to contact Jeremy York by e mail. Do you have his mail address ?
69erronan 3 years ago
smells like chlorine a little trust me you might not have mixed it right i am having diareah today i took vit c to hopefully stop it
REAL88E 2 years ago
mms smells like bleach and turns a dark yellow when properly mixed at 1 drop mms to 5 drops citric acid 10% start at 1 drop twice a day work up to 6 drops twice a day or more
meadowofpeace 2 years ago
This has been flagged as spam show
@londerosa
"I've begun to wonder now if I was sold some water or a placebo, instead of MMS."
It doesn't matter. MMS doesn't work. Worse than that: it's toxic.
MomoTheBellyDancer 11 months ago
Wow i didn't realize how recent your last vlog was. Okay. I am joining the crowd and wondering...What's the latest? You mentioned improvements as being circulation, but I think your speech and thinking/cognitive has improved also? possibly? or maybe you are just getting use to being on camera :P. Great job. Please keep the vids up, even if you continue to struggle... These are improvements! The vids are GOLD to someone who has no hope!
periwink 3 years ago
I have a phase contrast microscope, and I am seeing these invaders, there dead and gone, from MMS in just a few days.
I am toxic from the death, but I no longer finding any moving bugs in my live blood. Bottom line, it works man, it appears to work!
jamescase13 3 years ago
James, what do you mean "moving bugs"? are you talking about the spirochetes? or are you suffering from another ailment, other than Lyme?
periwink 3 years ago
Jeremy, Jeremy where art thou Jeremy?? (incidentally my son's name also)!
Please come on and tell us something - anything - even if you have given up the MMS quest, you will not lose face. You have tried! Nothing ventured, nothing gained as the saying goes!
If we don't hear from you again I'm sure we ALL wish you the very best in your fight against Lyme disease.
Megan
Megan1710 3 years ago
Jeremy, How are things I've been checking daily for your next blog. Hope all is well. If you can we would love to know how you are.
Many blessings.
Lisa
supernags1 3 years ago
I am so glad you are doing these blogs. I have had lyme for 6 years and my 15 year old daughter and my husband have it too. We live in the UK but got it in on a trip to Florida. You are really helping me to reassure my family that the increase in symptoms is due to us using the mms and to helping us stick with it. Thanks. Keep it going! Has your Fatigue been really bad now you have increased?
goin2improve 3 years ago
how are you, jeremy? looking forward to your next update.. blessings, heather. :)
heiwalove 3 years ago
Aloha!
Now about a month in....I feel more of a herx verses in the beginning!!!
I need to start dry brushing...thanks for the reminder! Love my sauna too! smiles!
Cold hands and feet! me too.. and the hot sweats too! GREAT to hear that your circulation is improving!!! smiles!
Do you add anything to your mix--after you added water? like lime or lemon or something else?
at 15 drops, the taste is getting gnarly for me...
keep up the progress!!
much love~
Fawne
smilesoflove 3 years ago
Thank you for posting your experience. Have you heard of or tried the Marshall Protocal? If so, did you experience any luck? Are you still taking antibiotics while trying this new treatment?
caliyya 3 years ago
I have had Lyme for 11 mnths and have started antibiotics for 9 weeks now. I commend you on sharing your battle, and look forward to your blogs. I hope and pray that this could be an answer for you and all of us with Lyme. Good luck and good health.
Lisa
supernags1 3 years ago
Improved circulation is awesome!!!!!!
mrsjamietodd 3 years ago
hey your symptoms resemble mine alot. And Ive as much or more than you in treatment. Had symptoms for at least 25 years. Looking foward to your input going to start next week.
divinicus1001 3 years ago
I have been battling Lyme for five years. My symptom list is an exact clone of yours. Most people with Lyme that I have talked to have more of the classic Lyme symptoms. It sounds like you have tried a lot of things to get better. Have you tried a Rife machine? Good luck with the MMS.
mhjacobs1 3 years ago
Wrote a very informative brochure with the direct input of 2 Lyme specialists. Will email to anyone.
Elaine in VA
ecftube 3 years ago
Thanks for the update JY. Very insightful.
rharkins123 3 years ago
thank you so much for sharing your journey with us. i'm following your updates with immense interest. best of luck.
heiwalove 3 years ago
Hello Jeremy, I'm starting MMS in less than a week, wanted to keep you in loop - if you're interested - as I am attempting to rid my body of herpes and the length of treatment is much shorter so you can see how I fair. Also Jim's book II says re: lyme: "The best results so far has been with MMS activated with the citric acid solution...Small doses every two hours seem to be the best results giving the immune system plenty of help...it might take as long as a year to overcome the lyme disease."
ben093u8 3 years ago
I got rid of a oral strain pretty quick on MMS hope you can do the same
nate4kate 3 years ago
Mister, it's great that you're seeing even small improvements. One improvement at a time. You're going to get there.
lillulabelle 3 years ago
Hi Jeremy,
Just wrote a post and lost it...
here's a quicks summary...
GREAT you're tolerating the MMS
improved circulation is significant
appreciate these videos.
We'll see what next week brings!
take care, D.
lymeliterateRN 3 years ago