Lyme disease

MMS and doctors who can't even practice what they learned in school... [Released : 09-11-2012 | Posted : 10-08-2012]

I just sent $10 [to the US~Observer MMS Defense Fund] and I'm not a rich person, but an organic farmer in Kansas. We are a small oasis surrounded by "Round-up" and have natural crops where thousands of birds and bees hang-out regularly on our one acre farm. I can also assure you I write about one letter like this every ten years. I've worked for a federal agency (and I'm proud of the work done there) and I'm the son of a private land owner (also proud of that work). IN BOTH cases though, we working citizens with educations and aspirations are always getting screwed over by someone "in Washington or on Wall Street" (a.k.a. big business).

 

In Feb 2011, I contracted what is likely to be Lyme Disease and after having correlated symptoms (and wasting a few thousand dollars on THREE doctors in two states), I found myself in a "haze" where my vision was suddenly going fast AND Tinnitus occurred in my left ear OVERNIGHT. The left side of my head then had (and to this day still has) "something" attacking it as I also had blurred vision, a pain deep in the center of the left eye, and daily discharges of heavy amounts of thick, disgusting phlegm. Even after biking 100 miles a week (rock steady for two months) the phlegm (to this day) occurs first thing EVERY morning when I awake and sometimes throughout the day.

 

"Neural Lyme" is the best guess but my Blue Cross insurance can't help me due to the ancient test they go by AND they won't allow NEW tests that are 98% (Vs. 40%) accurate to be run-- why? Nobody knows how to fix healthcare, but we do know WHY it's broken: "big oligopolies working for an oligarchy of the few," and this is even mentioned by a former WTO economist (among others one might hear speaking at TED). A good friend (and MD) I hunt with says, "we really are great at 'preventative' and 'emergency' medicine in the USA- BUT we suck in the middle." I also should add than he is a surgeon who doesn't HAVE to work "in the middle" (and he is glad for that fact). He is scared for his children and being a kid off the ranch, like me, he himself doesn't have a plan for his children WHEN they get bitten by that tick.

 

After all else was tried, money and jet fuel were wasted, and frustrations were hitting peak levels in my life-- a friend of my mother's mandated I try MMS as she had used it for HER Lyme for years and controlled it ever since while hoping one day for a cure she still can not find after many years of (like all of us) waiting. But she was happy and said that when using the MMS correctly, she was very little effected by her Lyme. So I did order and try it-- that was 19 months ago and I CAN say it works pretty good. I still have the phlegm hack (no matter how hard I work out) and the tinnitus is often still there but slight WHEN I use MMS regularly. This last Spring I ran out of the MMS product I purchased (from one of the "approved" sellers) and had to go three weeks without it. I thought that maybe whatever I had been "killing off" might be finally gone-- but it was not and it returned with a vengeance. I found myself back to that starting point where my head rang like a jet was right outside my back door; my eye was full of puss in the mornings, the shooting pains came back; and I generally felt as I had over a year prior before I started using this stuff.

 

Read full article.

 

(Taken from "MMS and doctors who can't evenpractice what they learned in school...",
A Letter to the Editor, By Russ Davenport, posted on USobserver.com.)


Only thing that helps for Lyme [Released : 07-05-2012 | Posted : 10-03-2012]

The “only” thing that helps me with over 50 yrs of Lyme Disease,not to mention all the other uses.


Lyme disease & Spirochete infections [Posted : 09-30-2012]

I was bitten by a Horse fly age 9 years old. Noone knew anything about Lyme back then. I was left un tested for any spirochete infection. But the infection slowly began to affect my body and my brain from then on, still noone put two and two together. When i was 22 I was diagnosed with Multiple Scelerosis. I have subsequently discovered that M.S is connected to Lyme disease in fact M.S is a spirochete infection not just an autoimmune disease.
 As Dr Lyda Mattman says "Multiple scelerosis should be renamed Multiple Spirochetes".  That is enough for me to know I was infected by the Horse fly.

 

M.S is chronic untreated  Lyme according to many Doctors out there.

 

I have been taking MMS for 15 months and wow! I am almost rid of the Lyme disease and co-infections. I say almost because these infections can go dormant for 10,20,50 years if you do not kill it all in the body system.

 

I am physically stronger, no need for walking aids anymore, my cognetive thinking is now second to none, i have no brain fog, my eyesight is above 20/20 vision, my corodination is brilliant, I can now hold a coversation, I do not have splayed feet anymore (something I have had since the bite age 9) My I.Q has improved by 60% (Lyme and co-infections affect the I.Q.

 

I am basically a normal healthy human all thanks to MMS and you Jim.

 

I have been spared a life of ever increasing disability and pain.

 

My children have congenital Lyme and co-infections and they too have been taking MMS for 15 months (their own choice as they are Gilleck competent)

 

They are fabulously well and also have cleared their bodies of Lyme and co-infections again they will carry on taking MMS for a while longer as i said because these infections can Lie dormant for a long time and we all want to be sure it is gone for good!

 

Both have been eyetested and their vision is above 20/20 their eyesight has improved greatly.

 

My eldest who was a snuffly baby (connected to a spirochete infection) no longer has sinus problems, the eyes are no longer affected (used to have constant eye irratation also connected to a Lyme, co-infection)

 

Our hair, nails, teeth are brilliant and fabulous with an infection all of these are affected.

 

We were on a limited time with my children it would only of been a couple of more years (by the time they reached age 18)  that they too would of been diagnosed with an autoimmune disease or become disabled, MMS has saved their lives too!

 

All of this because of a bite from a horse fly which are carriers of Lyme and other co-infections.

 

MMS is the saviour as well as Jim of course I am eternally grateful.

 

I will keep everyone updated about our further progress.

 

If anyone is concerned about long term use of MMS well if I had of taken antibiotics i would have to take those for up to 10 years causing damage and costing £800 per person per month, as far as i am concerened MMS causes no damage long term, no side affects and is better for the body and costs pence per dose it really is the better option to heal from chronic Lyme.


MMS [Posted : 08-31-2012]

I was bit by a deer tick over a year ago and everything I took to help cure my Lyme Disease did not work.

 

I stumbled on a MMS thread on the internet and read all the comment and even the scary stuff the FDA published on MMS. i felt like i was at deaths door and in constant pain so i said---why not try this stuff----well Im glad I did!!!

 

I started taking MMS in July 2012 - It has helped me. Its only been one month but it is starting to work and many of my symtoms are starting to go away. I still get sleepy and have a little bit of joint pain but on a scale of 1 to 10 = the joint pain is now a 3 when it was a 10 with out MMS. I am going to continue taking MMS for as long as it takes to completely rid my body of this lyme. 

 

I had the diarrea at first when starting the MMS but it went away soon and now I am taking 12 drops in the morning and 12 drops before bedtime. Thee MMS makes me sleepy sometimes when I drink it in the morning but That is the only side effect Ive been having. 

 

I will update my information in the future and report my progress so others can read about the good news.

 

Thank you Mr. Humble for all that you have done !!!!!!!

 

MMS is a blessing to me!!!

Nikki Mo
 


It works 100% [Posted : 08-06-2012]

I have a youtube video series on MMS and a live journal on wordpress for it. It works 100%. I have taken it over a year for my lyme disease, fibromylagia, CFS- Chronic Fatigue, likely XMRV. I am willing to speak with anyone about my experience with it. It works 100%.

 

-= Genesis II Church edit =-
Not2bforgot10 is the YouTube alias of a lady from the US who had great results with MMS when dealing with Lyme disease. You can watch more of her videos talking about MMS and Lyme at youtube.com/user/Not2bforgot10/videos?query=lyme

 

Her latest video in two parts on MMS vs Lyme (June 2012):
MMS UPDATE (1 OF 2) CURES LYME, HIV, HEPATITIS, HPV, ETC
MMS UPDATE (2 OF 2) CURES LYME, HIV, HEPATITIS, HPV, ETC

Not2bforgot10
 


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