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.

XMRV, Lyme Disease, and Chronic Fatigue Syndrome – CFS. MMS WILL TREAT.


As everyone may or may not be aware of the fact that I have lyme disease, specifically chronic lyme disease.  I did a posting on this a year or two ago and how I believed lyme to be linked with the “XMRV” virus before researchers even made the connection (my entry dates back, before the research).

I want to get tested for the XMRV virus (it is said to cause lyme disease, fibromylagia, chronic fatigue syndrome – CFS, ms, etc).  It is the root cause of these chronic diseases.  Unfortunately there isn’t a standardized test for XMRV yet, not that the government will pay for anyway.  There is an excellent lab by the Whitmoore association, but the test costs $600.  As I stated, it is not covered under insurance.

I have had a return of lyme, or “XMRV” symptoms since I stopped taking the MMS… the MMS was the only “drug” (all natural) that seemed to keep my CFS/lyme/XMRV under control… I am going to once again resume taking it, every single day for 5-8 hours per day.  I also would like to get my follow-up lyme test that I have been talking about, but I cannot afford that, either, which is also out-of-pocket, $200.00, tests #188 and 189.

A lot is going on in my life right now, and the health issues are once again surfacing.  My most recent blood test, from 6/11/12 states:

Hematocrit 47.0 H
MCHC 31.7 L
MPV 10.8 H
Neutrophils 40 L
Lymphocytes 51 H
Thyroid TSH .05 L

My results are once again, since I have stopped taking MMS, out-of-whack.

Anyone who would like to connect with me is welcome to send me a Facebook message.  Search for “Emily Anne Cox,” or emilyacox@aol.com.  I won’t approve your friend-request without a personal message.  I also have a youtube series “MMS- Magical Mineral Solution.”  My username is Not2bforgot10

I look forward to hearing from you!

I will continue to advocate for my health and learn more about my condition and ways to improve my health.  I will be resuming my MMS – Magical Mineral Solution A.K.A. “Water purification drops” to treat my lyme/fibro/XMRV.

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 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

Fri June 3rd, 2011. MMS – “Magical Mineral Solution” DAY 74- Healing FIBROMYALGIA/ LYME DISEASE.


A reader believes that I am having cardiac problems resulting from late stage lyme disease.  He wants me to be on cautious of a heart attack.  I am having major ear-node pain.  When the pain is really bad, it extends to my upper jaw.  The pain comes and goes and its intensity varies from a 3 to 5 on 1-5 scale with 5 being the most severe.  I also get occasional hand-joint pain, in the hand and fingers.  My ear also buzzes and rings for about 20 seconds a few times a week.  Most of my symptoms for some reason seem to be worse on the right side of my body.

I also have an asymmetrical tonsil inside my throat, which I first noticed about 1 year after I had become sick.  Dr’s have wanted to conduct a CT SCAN to see if it could be a growth or tumor, but I am trying to avoid this due to the high radiation exposure.  The CT SCAN is the last thing I would like to do.

Fatigue comes and goes and is extreme.  I can be tired after having done only one thing.  A walk around the corner can leave me exhausted.  Whenever I try working out with 10 lb dumbbells I end up with swollen lymph glands in the neck and throat.  Sleep doesn’t make a difference.  I get about 8-9 hours of sleep on average.  I fall asleep between 12 a.m., sometimes between 1-2 a.m.

So in summary, ear-node pain (when intense, extends to the jaw), joint pain (hand/fingers), buzzing in ear, headaches, and extreme fatigue are the major symptoms.  There are several others.  The pain is unbearable.