MMS – Magical Mineral Solution LYME DISEASE test results from IGENIX


I have read multiple sites where people want to see “proof” that MMS is actually working to fight viral and bacterial infections.

Here is living proof:


The first result was 1 month before I started taking MMS on 02/07/2011 – lyme disease diagnosis “POSITIVE;” the 2nd result A.K.A. the “follow-up,” 3 months after taking MMS DILIGENTLY, 8 hours per day every single day) on 07/11/2011.  EVERY SINGLE BAN BUT 1 IS COMPLETELY GONE.  NOT ONLY HAVE THE “STRENGTHS” (INDICATED BY THE AMOUNT OF “+” MARKS ELIMINATED, BUT GONE ENTIRELY).

Current-  It has been almost a year since my last test, and I need to get a follow up.  The last time I took MMS was in January of this year.  I haven’t taken it for the past 6 months, and I just started it up on June 14th of this year.  I will be taking it again to be sure everything isdefinitely gone.

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MMS UPDATE 2011 – TEST RESULTS NEGATIVE! MMS HAS CURED MY LYME DISEASE!


HOLY SHIT! UNBELIEVABLE! MY CHRONIC LYME DISEASE RESULTS ARE NOW NEGATIVE! UNBELIEVABLE! DUDE, MMS – MAGICAL MINERAL SOLUTION REALLY WORKS! I TOOK MMS FOR 3 MONTHS, FOLKS & MY CHRONIC LYME DISEASE IS UNDETECTABLE!

So either is plausible:

1. It’s GONE!
2. Counts have dropped too low to where it’s not detectable

Plan: To get re-tested in 2 months (this will have made it so that I would have waited an additional 3 months to get tested) to rule out #2.

If accurate, then:

Scenario 2:  There is a chance that I might still have lyme and the counts are just too low to be detected.  Furthermore, I could “relapse” and results could be hypothesized to show on the re-test in 2 more months.  Even so, with this scenario, the MMS has still worked!  It’s done it’s job!  The next action step would be to continue to take the MMS as long as I can tolerate it, knowing that it’s going to interfere with my thyroid absorption, but knowing that it’s working to kill the lyme faster than any other drug or remedy.

Scenario 1:  It’s GONE!

What do you think, folks, is there a chance being on MMS for the 3 months that I was, taking it every day 5-8 hours per day, CURED my lyme disease? MMS is supposedly the world’s “most powerful” antibacterial!

MMS MAY HAVE CURED MY LYME DISEASE!

PS-  Symptoms summary (Note:  This is only 1/3 of the symptoms I begin with before starting MMS):

Summary: Frequent/Unresolved, Occasional, & Resolved:

Remaining (Note:  This is only 1/3 of the symptoms I begin with before starting MMS):

Frequent/Unresolved:

-Ear-node pain (I would describe it as “ear-jaw, or “ear-node” pain – it’s a constant, dull, aching pain (pressure) behind ears) – occurs at random times for intermittent hour-stretches of time – when it is really bad, it extends to the upper jaw, causing me to clench both my teeth, jaw, and hands; then I get a headache, which often turns into a migraine and will occasionally extend to the neck and upper back, resulting in throbbing, knotting, and burning).
-Joint pain and stiffness in hands/fingers (Occurs on both sides, though slightly more painful on the right.  X-ray for arthritis twice  – both negative).
-Extreme fatigue (varies day-by-day and can strike out of nowhere)
-“Tired” dry eyes and tear ducts (Eye doctor said that my tear ducts dry up every “2 seconds” instead of “13″ seconds.  Additionally, my eyes have lost their “vitality,” ie: vivid/whiteness, and sometimes by the end of the night I look stoned.
-Headaches/Migraines (I get them a few times a year for a week straight)
-Lump in throat sensation (It will randomly feel like I have a golf ball or large-size piece of food stuck in my throat)
-Ringing/buzzing/occasional “swooshing” in ears (Occurs in 1 ear at a time and is known to occur in both ears, though it happens 75% more of the time in right ear)
-Extreme sensitivity to heat and cold (When others are warm, I am uncomfortably hot and sweaty, and when others are comfortable, I am cold)
-Mouth sores (I get little canker sores — clear bubbles in my mouth at random times — usually a single or couple bubbles at once typically behind my front bottom lip)
-Oversensitivity to sound
-Oversensitivity to light (I now have to wear a hat with a visor all the time and sunglasses)
-Dry hair (feels like straw)
-Brittle nails (they no longer grow)
-Foul-smelling boogers (Sounds strange, but is definitely something I have noticed since very early on when I became sick)
-Continual, re-occurring, slow healing infections (I get a lot in my fingers)
-Asymmetrical tonsil (On right side of mouth – Dr. states it looks and feels the “size of a grape”)
-Hypothyroidism (NOT Hashimoto’s)
-Abnormal ANA titer 3x (Negative for rheumatoid factor, ie: scloderma, lupus, arthritis, etc.)

Occasional:

-Clenched teeth/jaw
-Clenched fists (when this happens, it is most noticed upon waking up in the morning)
-Neck/shoulder pain (I will often wake up with EXTREME stiffness in my neck/shoulder area and my neck/shoulders will just randomly burn, especially at night)
-Enlarged neck/throat (lymph) glands (Especially when I work out, even minimally, ie: lifting dumbbells for a half hour)
-Tingling in hands/feet/face (I thought maybe I had MS -Multiple Sclerosis because of the random “tingling” – The face has tingling & numbness around lips and jaw bone upon touch and considerably more noticeable in cold weather)
-Increased anxiety
-Increased depression
-Unexplained weight changes (Extreme gain and loss — fluctuates between 118 and 127 – highest: 136 lbs in a very short periods of time)
-Unexplained hair loss (Noticeable in shower)
-Worsened vision (Blurry, worse at night. Developed astigmatism)

Resolved:

-Weakness in limbs (This has occurred twice.  I was so weak I could not even get up, and I thought I might have to be admitted to the ER.  Also at this time I was sweating – DRENCHED profusely)
-Unexplained menstrual pain and irregularity
-Vertigo (Two single occurrences, 2008 & …)
-Night sweats (Mostly occurred in 2008, but should not be ruled out because they occurred frequently)
-Vivid dreams and nightmares (Fall 2008)
-Hot and cold flashes (Fall 2008 – Occurs periodically often while laying in bed, or perhaps that’s when I notice it most like many of the other symptoms)
-Difficulty falling asleep and insomnia
-Random nose bleeds (Occur twice a year for a week-long stretch and will gush – Last time I went to the ER)
-Extreme dry mouth (Cotton mouth, and it doesn’t matter how much water I drink)
-Fainting (I had my blood drawn and entirely blacked out)
-Cold hands, feet, and nose (Occurs in fall and winter and is out-of-proportion compared to the normal person)

-Bloating (Occurred in Dec 2010- Jan 2011)
-Diarrhea (Occurred in Dec 2010- Jan 2011)
-Constipation (Occurred in Dec 2010- Jan 2011)
-Unusual abdominal cramping (Occurred in Dec 2010- Jan 2011)
-Big toe pain when walking – Gout?

-Allergies/Sensitivities (I have developed an allergy to dust and developed food sensitivity to blackberries and some soy-made products)
-Random rashes (Allergies?  I have eaten the foods before and never developed a rash – now I am getting more rashes when I eat things.  The last rash was on my left kneecap, which did not subside with Benedryl “quick strip.”  The rash remained on my leg for 3 solid days and was triangle-shaped).

2:30PM:  A follower and reader on my facebook states:

“It could have just mutated and they are not looking for the right bands… I hate to tell you that, but it is very possible you still have lyme if you did not take antibiotics.  I am on my 2nd week of 4 weeks of iv antibiotics..This time around seems to be helping so far.” – FB Follower

A clear skeptic she seems to be of any natural “treatment.”  You will have that.  At this point, I am pretty much convinced that the MMS has in fact been effective – how effective I do not know until I get yet a 3rd test to confirm the “negative” diagnosis of the 1st follow-up.

My response:

“I was tested through IGENIX, the top lab in the United States.  IGENIX has the best testing technology and the most sensitive testing.  Additionally, they test for more bans than any other facility.  Either the test was a false-negative, my counts are too low to be detected, or it’s GONE.  At any rate, the MMS has done its job, and it’s worked to treat my lyme disease.  I am going to get re-tested in 2 months (That will have made it 3 months since my last test) to confirm that the results are really correct.  If they come back “positive” then I will not know if the 2nd test was a false-negative, or if the lyme had not cleared fully.  If the test comes back negative again it is certain that my lyme is cleared – that or scenario 2 still exists and the counts are just too low, but I will be inclined to believe that if the confirmation test for this follow-up test to test #2 in 2 months comes back “negative” as this last test did, then my lyme is GONE.” 

MMS is said to be the #1 most powerful killer of bacteria, etc. and is said to be a major threat to the FDA who would lose a TON (Millions of dollars) of money if word got out that MMS is in fact a natural “curer” to most ailments.

Update as of 8/29/11:  Last week I spoke with Dr. Harris, the lead doctor at IGENIX Testing Labs and he said he has never seen anyone “recover” as fast as I have and asked me what I used to treat this lyme.  He stated that no one to his knowledge had recovered that fast even using conventional pharmaceuticals.

I am convinced now that MMS is in fact a “miracle cure.”  Through this illness I had lost nearly everything (I would have described myself as being “emotionally, mentally, physically, and spiritually “bankrupt,”) and I am now slowly regaining the faith I had lost in myself and the Universe.  After having used this “miracle” supplement, I can honestly say it’s been blessing.  Thank you Jim Humble, and thank you God/HP!  It works!

MMS Update – 94 Days (3 months, 2 days) – Thyroid medication conflicts!


I am still taking the MMS every day, but for the past 14 days or so I have been taking about about 5 drops versus the recommended 8 (1 drop per hour, working your way up to 3 per hour).  The reason for this: Concern.  Three things have been happening:

My thyroid scores (which have been normal since I’ve been taking Synthroid to stimulate thyroid hormone) have gone back to hypothyroid, making me wonder whether the MMS may be effecting the adsorption of the medication; two, I have been very bloated, retaining I would assume water and salt, which I believe to be from the MMS, which is primarily salt, and three, I have been super tired and sluggish – another symptom of hypothyroid.

My thyroid, with the thyroid replacement hormone, was functioning fine before I started taking MMS.  Since taking MMS, the symptoms of hypothyroidism have come back, making me miserable – ie, huge bloating (most noticeable in stomach, then face, then fingers – making me look heavier than I am), fatigue/sluggish, etc.

It’s a paradox however because the MMS seems to be working to kill off many of my other symptoms, including:

-Hot and cold flashes (Occurs periodically often while laying in bed, or perhaps that’s when I notice it most like many of the other symptoms)
-Extreme dry mouth (Cotton mouth, and it doesn’t matter how much water I drink)
-Lump in throat sensation (It will randomly feel like I have a golf ball or large-size piece of food stuck in my throat)
-Mouth sores (I get little canker sores — clear bubbles in my mouth at random times — usually a single or couple bubbles at once typically behind my front bottom lip)
-Neck/shoulder pain (I will often wake up with EXTREME stiffness in my neck/shoulder area and my neck/shoulders will just randomly burn, especially at night)
-Enlarged neck/throat (lymph) glands (Especially when I work out, even minimally, ie: lifting dumbbells for a half hour)
-Tingling in hands/feet/face (I thought maybe I had MS -Multiple Sclerosis because of the random “tingling”)
-Foul-smelling boogers (Sounds strange, but is definitely something I have noticed since very early on when I became sick).
-Continual, re-occurring, slow healing infections (I get a lot in my fingers)

Since taking MMS, the symptoms listed above have gone from occurring frequently to rarely.  I will still keep my eye open on their occurrence and frequency.

I am torn at the moment in terms of which action to take, ie: continue taking MMS and continue to getting more bloated (It’s making me look 15 pounds heavier than I am) and allow it to effect my thyroid to where I am exhausted every day, or not take it and run the risk of all my symptoms returning and my lyme bacteria forming “cysts” (right now they should be in the non-cyst form because I have been “aiming ‘bullets'” at them so-to-speak with the MMS, and I had not taken any other medication before to try and fight off the infection, so they received a straight shot of MMS, which I have continually been pumping into my body now for the past 3 months.

I do not want to stop taking it and make a mistake, but the effecting my thyroid absorption is very problematic and all of the symptoms that go along with that alone!  I almost feel like I am stuck in a catch-22 – like I either have to have hypothyroidism (which is bad – many of my symptoms alone are related to hypothyroidism by itself) or have lyme disease, which is even worse.  So basically I feel like I need to rid my lyme (most importantly) but in the meantime I am struggling with hypothyroidism because the MMS appears to be messing the absorption up!

With that being said, I feel like I cannot win… I wish there was something out there just as powerful as MMS that did not conflict with my thyroid medication… even if I knew of something though, I have already started the MMS, and I trust that it’s working so I don’t think I would want to take it.  Stuck!

Emily’s Symptoms:

Current/Unresolved Issues:

-Ear-node pain (Constant dull, aching pain behind ears – random times for intermittent hour-stretches of time – when it is really bad, it extends to the upper jaw, causing me to clench both my teeth/jaws and hands, then I get a headache, and then my upper back and neck start throbbing, knotting, and burning)
-Buzzing in ears (Occurs in 1 ear at a time and is known to occur in both ears, though it happens 75% more of the time in right ear)
-Asymmetrical tonsil (On right side of mouth – Dr. states it looks and feels the “size of a grape”)
-Joint pain in hands/fingers (Occurs in both hands, though slightly more painful on the right side.  Was x-ray for arthritis twice  – both negative).
-“Tired,” dry eyes and tear ducts daily (Eye doctor said that my tear ducts dry up every “2 seconds” instead of “13” seconds.  Additionally, my eyes have lost their “vitality,” ie: vivid/whiteness, and sometimes by the end of the night I look stoned when I am not even around smoke or anything to irritate my eyes.  This also effects my ability to ride a bicycle because of the dry air)
-Extreme fatigue (varies day-by-day and can strike out of nowhere)
-Abnormal ANA titer 3x (Negative for rheumatoid factor, ie: scloderma, lupus, arthritis, etc.)
-Hypothyroidism (NOT Hashimoto’s)
-Dizziness/increased motion sickness (Occurs every few days randomly)
-Extreme sensitivity to heat and cold (When others are warm, I am uncomfortably hot and sweaty, and when others are comfortable, I am cold)
-Unexplained hair loss (Every time I take a shower, more hair sheds than necessary)
-Dry hair (feels like straw)
-Brittle nails (they no longer grow)
-Oversensitivity to light (I now have to wear a hat with a visor all the time and sunglasses)
-Facial flushing (MRI showed inflammation in cheeks)
-Unexplained weight changes (Extreme gain and loss — fluctuates between 118 and 136 lbs and changes in a very short periods of time)

Note:  All symptoms started Fall 2007.  Most symptoms occur worse on the right lateral part of my body, but all symptoms are unilateral.  I am more inclined to notice symptoms while laying in bed at night and in the morning although they occur during the day and are noticeable, but I am trying to stay busy and function (very difficult).  I often stay home because I am so tired and ache (ear-node/jaw/back/neck/shoulder).

Recent Past (Latent?):

-Hot and cold flashes (Occurs periodically often while laying in bed, or perhaps that’s when I notice it most like many of the other symptoms)
-Extreme dry mouth (Cotton mouth, and it doesn’t matter how much water I drink)
-Lump in throat sensation (It will randomly feel like I have a golf ball or large-size piece of food stuck in my throat)
-Mouth sores (I get little canker sores — clear bubbles in my mouth at random times — usually a single or couple bubbles at once typically behind my front bottom lip)
-Headaches/Migraines (I get them a few times a year for a week straight – Note:  At a separate time when I get the nosebleeds)
-Neck/shoulder pain (I will often wake up with EXTREME stiffness in my neck/shoulder area and my neck/shoulders will just randomly burn, especially at night)
-Enlarged neck/throat (lymph) glands (Especially when I work out, even minimally, ie: lifting dumbbells for a half hour)
-Tingling in hands/feet/face (I thought maybe I had MS -Multiple Sclerosis because of the random “tingling”)
-Foul-smelling boogers (Sounds strange, but is definitely something I have noticed since very early on when I became sick).
-Continual, re-occurring, slow healing infections (I get a lot in my fingers)
-Night sweats (Mostly occurred in 2008, but should not be ruled out because they occurred frequently)
-Cold hands, feet, and nose (Occurs in fall and winter and is out-of-proportion compared to every person in the room)

-Random nose bleeds (Occur twice a year for a week-long stretch and will gush – Last time I went to the ER)
-Vision difficulties (Worsened, blurry far away vision – worse at night; developed a slight astigmatism)
-Increased anxiety
-Increased panic in crowded places
-Difficulty falling asleep and insomnia
-Increasing depression
-Vivid dreams and nightmares
-Allergies/Sensitivities (I have developed an allergy to dust and developed food sensitivity to blackberries and some soy-made products)
-Random rashes (Allergies?  I have eaten the foods before and never developed a rash – now I am getting more rashes when I eat things.  The last rash was on my left kneecap, which did not subside with Benedryl “quick strip.”  The rash remained on my leg for 3 solid days and was triangle-shaped).
-Weakness in limbs (This has occurred twice.  I was so weak I could not even get up, and I thought I might have to be admitted to the ER.  Also at this time I was sweating – DRENCHED profusely)
-Fainting (I had my blood drawn and entirely blacked out)
-Dandruff (I have never had dandruff my entire life)
-Unexplained menstrual pain and irregularity
-Unusual abdominal cramping (This has happened a couple times. I will get pain in my abdominal region when I am not on my period)

June 19th, 2011. MMS Update – 90 days.


-Need to get back to structure so that I can continue to take MMS consistently
-MMS taste still awful!
-I take it with water for effectiveness
-Ear-node pain the most pressing symptom (MRI approval pending)
-Boogers no longer smell; less finger and finger nail infections (MMS is definitely working here)

Bloating has occurred because stomach looks fat yet my weight is 121-122 lbs!  MMS causing possible water retention?  (Making me not want to use it) – Going to try doing some sit ups and seeing if it helps…

Over all, seems to be working!

June 13th, 2011. MMS Update :)


MMS seems to still be working well.  I have been taking it daily 5-8 times per day (I have slacked slightly, but I am still taking it consistently) since March 2011.  It has killed most of my symptoms minus the ear-node pain, which extends to the jaw when painful.  I will keep everyone posted asap.  Super busy, but please stay tuned :P