My Experience with MMS for Lyme Disease
conniekillbug asked:
I took MMS, Miracle Mineral Supplement, for treatment of my Lyme disease for approximately four months. In this video, I report what I observed during those four months. Since I made this video a couple of weeks ago, I have re-started MMS temporarily for an acute infection, and have had NO herxheimer response, other than a bit of fatigue, at a dose of 30 drops a day. This is atypical of my response with the chemical, as previously, I could only tolerate 15 drops a day (at most). I believe my …
Caroline
July 3rd, 2009 at 3:22 am
Gerald
ymv1020: I’m all for alternative treatments, but even Hulda Clark admitted her “Zapper” made people with CFS and HIV much worse.
She also recommends washing your hands with LYE, which is drain cleaner!
Don’t waste your energy reading or following any of her protocols. I speak from experience.
July 3rd, 2009 at 7:05 pm
Cameron
Hey guys….PLEASE register at the Oprah Winfrey website and let her know how much you would like to see her do a show on Lyme disease. Dr. Oz thinks the “UNDER OUR SKIN” documentary is wonderful but a show about Lyme won’t be done unless she sees lots of interest. Request that LLMDS and patients be the guests so that we can be heard. Also, Daryl Hall would make a great guest. OPRAH needs to hear about YOUR experience with Lyme disease. WE ARE ALL IN THIS TOGETHER !
God Bless,
Elaine
July 4th, 2009 at 2:31 am
Patsy
You say you only took 6 drops a day for an extended period which, in the book, says it’s only a maintenance dose.
Why didn’t you take a larger dose as recommnded by Jim Humble to eradicate pathogens in your body?
Hope you get well soon.
July 5th, 2009 at 11:43 am
Dutch
hello, i just got the dr. hulda book. i wanted to ask you, in what page does it talk about the adrenal gland cleanse. thank you
July 8th, 2009 at 6:18 pm
lewis
I have started MMS treatment to help cure severe systemic candida which I have suffered chronically for 5 years now. I am taking 10 drops morning and night and do notice the constant low-grade nausea effects. I have only taken the MMS for less than a week so I’ll hold on for a while yet. I eat only whole, organics, lots of bitter green, no sugar and value sleep, effectively making me an alien amongst most others.
I wish us all well with our recoveries.
Love over fear.
July 10th, 2009 at 9:57 pm
Bethany
Check out Dr. Bob Beck, on Google Video.
He is the real deal, I’ve tried it for a nasty Mycoplasma infection, it works!
I can’t wait to try this on a wart on my toe.
July 11th, 2009 at 3:47 am
Nancy
If you have questions please ask me.. I want to help:)
July 11th, 2009 at 4:31 am
Emery
is this stuff dangerous iv got cancer going to start on mms soon help me
July 11th, 2009 at 5:38 pm
Nancy
Thanks Ledfootjohnny, I appreciate your kind words
I am doing pretty well, it is sometimes a struggle but God is getting me through. Blessings, Connie
July 13th, 2009 at 3:42 pm
Gerald
Keep up the good work Smarty you’ll be rewarded.I know it’s got to be hard but you look pretty tough.Don’t stop here keep looking and praying.
July 16th, 2009 at 11:43 pm
Michelle
I’m very skeptical about chlorella as being beneficial for certain people. if you have an abundance of heavy metals like mercury, lead, deposits in your body, chlorella can exacerbate the problem. check out “andy cutler protocol” for more on that.
July 17th, 2009 at 9:13 pm
Joan
Hi Connie – Given that it took 5-6 years of intense treatment for a few of the Under Our Skin ‘people’ to be able to remove their PICC lines, don’t you think that MMS was removing ‘unwelcome guests/heavy metals, etc” from you causing you to feel unwell? And that, in time, once your body is clear enough to do it’s own healing, that your adrenals would have the steam to heal along with everything else?
July 21st, 2009 at 4:31 am
Julie
Why do we have to do this? What’s happening with doctors letting insurance companies run the show? Dont they have a union? I lost my faith in the medical field. When I die from LD, I guess they will say “natural” causes on my death certificate?
July 23rd, 2009 at 11:49 am
Nancy
dr hulda book the cure for all diseases shows how to do a kidney cleans/adreanal glan cleans, ect
July 24th, 2009 at 2:35 pm
Sherry
Blajing, I use mostly just chlorella. It has one of the best track records for toxin binding. Apple pectin, french green clay, and activated charcoal are also popularly used for Lyme neurotoxins. There are others. If you have detox problems, you may need a more powerful binder such as Cholestopure.
July 26th, 2009 at 8:37 am
Kevin
What are you using for detox binders?
July 26th, 2009 at 4:41 pm
Dutch
JCham, I have not used DMSO with MMS. I have heard that MMS is much more powerful when used with DMSO. Thanks for the suggestion!
July 28th, 2009 at 6:59 am
Samantha
Connie, Have you tried using DMSO with MMS?
I am using DMSO, Samento mixed with Concentrace trace minerals in water and 2000IU D3 with 2400mg Calcium. This seems to be helping with lyme plus my cavitations. I tried cholestaramine(sp?), but DMSO seems to work better for me. I also use Chlorella for binding heavy metals and energy boost. Readers may want to try googling Lyme+ cavitations, Mercury, DMSO.
Just some thoughts. I’m not a doctor.
Hope it helps.
Josh
July 30th, 2009 at 8:08 pm
Patti
Hi Anton,
The first two years I had this disease, I cried almost everyday, and suffered from severe anxiety and depression. Now, while I still have my difficult days, I feel OK most of the time. Life is still hard, but I feel much more emotionally stable, which is a huge improvement over how I used to feel! Peace, Connie
July 31st, 2009 at 8:11 am
Violette
hi connie, im just wondering how u feel most of the time? as in emotion’s and thought’s, due to this disease.
peace, anton
August 2nd, 2009 at 11:21 am
Louise
connie I am the one u are reffering too in your video heheh – tis moi…..the horsewomen…..Im onto a new treatment tahnks to our friend Roger and ist teh ondamed…..will keep you posted but so far herxing a ton!!! It is supposed to address all these residual issues we are left with with lyme taht get us from 80% recovered to 100% HPA everything…so its MMS and ondamed now….for me….
August 5th, 2009 at 7:58 pm
Daniel
LDP…Thanks for your insights. I do think for some that the “endless herx” phenomenon is something to think about. If detox mechanisms are compromised, a person may not heal. I don’t know if that is the case with me, but I know it is with others that I have seen.
August 7th, 2009 at 9:28 am
Bethany
pkwebman…Yes, I’m single. Too busy trying to get well to be involved with anyone!
August 9th, 2009 at 8:05 pm
Vichelle
Thanks for you post. I have not tried MMS yet but have done salt/c, doxycycline, samento, cavitation surgery, removal of amalgam fillings et al. Connie, What you said about adrenal insufficiency sounds like what I am dealing with too. I have a lot of fatigue and lack of motivation to get out.
I have been doing some rife therapy. I built a phanatron Ray tube. I would like to send you a picture, if you are interested. It definitely is helping me. I just need to find the right frequency for lyme.
August 12th, 2009 at 8:40 am
Mary
r u single connie.
September 12th, 2009 at 10:54 pm
I have been taking MMS for about four months now for chronic lyme infection. (I think I have had it for less than two years} I started with two to three drops three times a day and as I added drops I switched to Jim Humble’s new recommended regime, which is fewer drops many times a day. So after four months I am up to 60 plus drops per day. I take drops every two hours starting around 8 am and ending at midnight. I start with just 3 or 4 drops in the morning and end with 9 or 10 drops per dose in the late evening, since I am much more sensitive to the drops in the morning. Immediately after starting MMS I noticed that the soreness in my legs started to improve. I have been gradually gaining strength and feeling more mobile and more energetic over the entire period. I have had no major herxheimers reaction, but from time to time i have developed severe soreness in my legs and once in my neck for a few days. In the beginning I felt often extremely uncomfortable from the MMS. I experienced a kind of queasy feeling starting about 45 minutes after taking the drops and diarrhea off and on whenever I would work up to more than about 7 drops at one dose. However I only actually felt nauseous enough to actually throw up one time and it was an entire day of throwing up and having the runs. But it passed and I am continuing to gradually increase the drops. Incidentally my Doctor here in Maastricht has me on Nattokinase simultaneously. He says that lyme creates a protein case made of fibrin around itself in order to protect itself from the immune system or from antibiotics or MMS, and that Nattokinase disolves the protein case in order to reach the bacteria. I am also starting on Lumbrokinase as well, since my online research says that it is also extremely effective at breaking down fibrin biofilm.
Incidentally my chronic yeast infection has disappeared completely after about three weeks. My athletes foot fungus has disappeared and my actinic kertosis seems to be improved as well. So I am continuing with this treatment and I hope that it eventually clears out the lyme.
To anyone wanting to try MMS I can only emphasize that you should start with a very small dose, say one drop three times a day, work up to one drop every two hours, and when you feel comfortable with that up to two drops and continue. As soon as you feel nauseous or diarrhea lower the dose, and when you feel better, start moving to up the drops again. It is a bit like two steps forward and one step back, but you must be patient and persistent. Don’t try to push it too hard, just take it easy, but be persistent.
So I will try to report back in a few months and let you know how this turns out.
September 12th, 2009 at 11:36 pm
I hope you continue to improve! There are many who insist MMS cured their Lyme and I hope you will be another! Please remember that others may have a different reaction…
Blessings,
Jenna
November 1st, 2009 at 5:02 pm
Iam from Romania,I suffer from a kind of disease since 2004,when a huge kind of bee has bitten me and a huge rush appeared.at that time I had no ideea about Lyme disease and since then,after a short period of strange aches in my legs and arms and joint aches tat would move from a joint to another,the nightmare began,with extreme fatigue that would last two mounths ,followed by a total recovery,than a new episode after six mounths,again recovery for six mounths and so one…one episode put me in bed for seven mounths,I thought I would die!!!!!I saw no healing perspective!my mental state deteriorated,especialy concentration began very difficult ,one winter I had not even the power to bo to look outside the window.Last two years I had the episodes milder,for only one mounth or less,I could even concentrate to the computer.Here we’ve got a special kind of vitamines and minerals,a total of 60 I think!it was prescribed to my mom for another condition,but I thought it couldn’t harm me so I took two tablets a day,for as long as the condition lingered,and I noticed the condition was much more mild and easy to bear!I must say it was the only treatment I took,as here nobody knew what was happening to me,so they prescribed me no treatment instead of antidepressing pills.The medicine is called VITAMAX,u can find it in Europe and I don’t know,it may be a coincidence,but I fought much better with the disease and now I am fully recovered(I don’t know though for how long)anyway I take these pills daily even now,when I feel totally fit,to prevent the condition coming again,as it always reappers in autumn and winter!I wish full recovery for all of u,as I know how it feels to be so sick!