Watch Under Our Skin for free short time only

Hello all,

This is an oppotunity to watch "Under Our skin" for free.

 The Producers of this film are allowing a FULL and FREE Viewing on Mercola.com! Please show your support by purchasing a copy of this film! Quantities are limited! Click HERE to purchase Under Our Skin for only $19!
By Dr. Mercola

Unrelenting pain. Headaches, muscle aches, swollen joints, rashes. Loss of coordination and muscle spasms. Intermittent paralysis. Cycles of disabling symptoms that persist for years, causing ceaseless suffering and frustration for patients and their families.

This is the picture of chronic Lyme disease. And yet, many physicians tell their patients there is "no such thing," referring them to psychiatrists, misdiagnosing them, or even accusing them of fabricating an illness or simply seeking attention.

An award-winning documentary called "Under Our Skin" exposes the hidden story of Lyme disease, one of the most serious and controversial epidemics of our time.

Each year, thousands go undiagnosed or misdiagnosed, often told their symptoms are all in their heads. This film brings into focus a troubling picture of a health care system that is far too willing to put profits ahead of patients.

The History and Discovery of Lyme Disease

Lyme disease rates are escalating at breakneck speed, among humans as well as animals. Today, Lyme disease the most common vector borne disease in the U.S., far more common and dangerous to the average American than West Nile virus. In fact, there were almost 40,000 reported cases of Lyme in 2009,1 which by all accounts is a gross underestimate.

The CDC estimates the real number of cases may be up to 12 times higher, suggesting as high as 480,000, making Lyme far more prevalent than AIDS. The number of Lyme cases reported annually has increased nearly 25-fold since national surveillance began in 1982.2

Lyme disease was named after the East Coast town of Lyme, Connecticut, where the disease was first identified in 1975.3 The disease was first referred to as "Lyme arthritis" due to the presentation of atypical arthritic symptoms. By 1977, the black-legged tick (Ixodes scapularis, also known as the deer tick) was linked to transmission of the disease.

Then in 1982, Willy Burgdorfer, PhD, discovered the bacterium responsible for the infection: Borrelia burgdorferi. The bacteria are released into your blood from the infected tick, while the tick is drinking your blood.

We now know there are five subspecies of Borrelia burgdorferi, more than 100 strains in the U.S. and 300 worldwide, many of which have developed resistance to our various antibiotics. Although many still attribute transmission exclusively to ticks, according to Dr. Deitrich Klinghardt, one of the leading authorities on Lyme disease, the bacteria can also be spread by other insects, including mosquitoes, spiders, fleas, and mites. This may be the reason so few Lyme sufferers recall being bitten by a tick.

Borrelia burgdorferi is a spirochete,4 a cousin to the spirochete bacterium that causes syphilis. In fact, they look very similar under a microscope. B. burgdorferi's corkscrew-shaped form allows it to burrow into and hide in a variety of your body's tissues, which is why it causes such wide-ranging multisystem involvement.

The Invisible Illness

Many Lyme patients who battle this disease on a daily basis appear healthy, which is why Lyme disease has been called "the invisible illness." They often "look good," and their blood work appears normal, but their internal experience is a far different story. Patients struggling with Lyme disease usually become adept at hiding their pain from others as a way to cope and restore some degree of normalcy to their lives.

Part of the problem with diagnosing and treating Lyme disease is that it is so easy to misdiagnose.

Lyme disease is called "the great imitator,"5 mimicking other disorders such as multiple sclerosis (MS), arthritis, chronic fatigue syndrome, fibromyalgia, ALS, ADHD and Alzheimer's disease. In some cases, Lyme patients can even develop paralysis or slip into a coma. The only distinctive hallmark unique to Lyme disease is the "bulls eye" rash, but this is absent in nearly half of those infected. Laboratory tests are notoriously unreliable.

Fewer than half of Lyme patients recall a tick bite. In some studies, this number is as low as 15 percent. So, if you don't recall seeing a tick on your body, that doesn't rule out the possibility of Lyme disease. According to TBDA:

"Although the bulls eye red rash is considered the classic sign to look for, it is not even the most common dermatologic manifestation of early Lyme infection. Atypical forms of this rash are seen far more commonly. It is important to know that the Erythema Migrans rash is a clear, unequivocal sign of Lyme disease..."

Besides the rash, some of the first symptoms of Lyme disease may include a flu-like condition with fever, chills, headache, stiff neck, achiness and fatigue. For a complete list of symptoms, refer to the Tick-Borne Disease Alliance6 (TBDA), but some of the more frequent symptoms include the following:

Muscle and joint pain
Neurological problems
Heart involvement
Vision and hearing problems
Migraines

The "Lyme Paradox"

Dr. Klinghardt believes one of the factors that's led to increased Borrelia virulence is the dramatic increase in electromagnetic fields (EMFs) and microwave radiation from cell phones and towers, wireless Internet, power lines, household electrical wiring, etc. Reduction of exposure to these fields is a key part of his Lyme treatment protocol, which I'll be discussing shortly.

One of the reasons blood tests are so unreliable as indicators of Lyme infection is that the spirochete has found a way to infect your white blood cells. Lab tests rely on the normal function of these cells to produce the antibodies they measure.

If your white cells are infected, they don't respond to an infection appropriately. And the worse your Borrelia infection is, the less likely it will show up on a blood test. In order for Lyme tests to be useful, you have to be treated first. Once your immune system begins to respond normally, only then will the antibodies show up. This is called the "Lyme Paradox" – treatment before diagnosis.

Dr. MacDonald's Syphilis Model

The behavior of Borrelia may be more similar to its cousin Treponemapallidum, the spirochete responsible for syphilis. Both take different forms in your body (cystic forms, granular forms, and cell wall deficient forms), depending on what conditions they need to accommodate. This clever maneuvering helps them to hide and survive.

Perhaps the most compelling evidence for Borrelia as a far greater player than previously thought comes from the work of Alan MacDonald, MD, who's been studying parallels between Lyme disease and syphilis for the past 30 years. MacDonald found the DNA of Borrelia in seven out of ten brain specimens from people who died of Alzheimer's disease.7

Astonishingly, the DNA was "fused" with human DNA, into one molecule! Syphilis is well known for causing symptoms across multiple body systems, including neurosyphilis, the psychiatric form of the illness.

Syphilis remains relatively easy to treat, as long as it's diagnosed early. But its cousin Borrelia seems to be upping the ante. Dr. Klinghardt stated in one of our interviews that he's never had a single patient with Alzheimer's, ALS, Parkinson's disease or multiple sclerosis who tested negative for Borrelia. Those are all diseases with no known cause. Could Lyme disease be the missing link? And if it is, why hasn't there been a stampede of researchers in pursuit of the truth?

Attorney General Finds IDSA Lyme Guidelines Flawed and Panel Corrupted

A handful of people are the gatekeepers for information about Lyme disease. Most of those occupy positions within the Infectious Diseases Society of America (IDSA), which publishes guidelines for a number of infectious diseases, one of which is Lyme.

The IDSA's most recent clinical practice guidelines for Lyme disease8 they claim Lyme is easily cured with, typically, two weeks of antibiotics, requiring 28 days in rare cases. They also claim there is no scientific evidence for chronic Borrelia infection. However, the literature choices they list in their reference section clearly reflect their bias. Of the 400 references they cite, half are based on articles written by their own people.

Their literature review in no way represents the total body of science related to the study of Lyme disease.

Connecticut Senator Richard Blumenthal has long been a strong advocate for people with Lyme disease.9 While he was Connecticut, Attorney General Blumenthal conducted an investigation into the IDSA's panel members and 2006 Lyme disease guidelines.

These guidelines have sweeping impacts on Lyme disease medical care. They are commonly applied by insurance companies to restrict coverage for long-term treatment and strongly influence physicians' treatment decisions. Insurance companies have denied coverage for long-term treatment, citing these guidelines as justification that chronic Lyme disease is a myth. Blumenthal's investigation found conflicts of interest were rampant in the IDSA, with numerous undisclosed financial interests among its most powerful panelists.

The IDSA agreed to create a new panel to review the ethics of the 2006 IDSA panel, overseen by Blumenthal's office. But this ended up being nothing more than a pacifier. The end result was a Final Report published on the IDSA site10 finding the original guidelines "based on the highest-quality medical/scientific evidence available," stating the authors "did not fail to consider or cite any relevant data." Senator Blumenthal continues to fight the establishment, however, and has taken his battle to the Senate.

http://articles.mercola.com/sites/articles/archive/2012/10/13/under-our-skin-documentary.aspx

Watch "Under our Skin" for free at above link I think offer is on for a short time only not sure try watching asap.

 Copyright 2012-2013  LymeGirl all rights reserved.

More eyesight improvement wow!

Hello all,

Just to keep you updated my youngest who was born with congenital Lyme had an eye sight test just like the eldest.
Well the vision is above 20/20!!!
So those blasted spirochetes also have not caused irreparable damage to the eyes.
In fact the eyesight is better than ever before. Last eye test the vision was just 20/20 but now better!
We are sure this is because of treating the spirochete infection.
I could not be more pleased as in my extended family that were infected all had eyesight problems that were getting increasingly worse most were becoming blind and not one member of the medical profession put two and two together.
My brother was told he was going to have to have an operation because he had the start of Cataracts and could become blind!
Now he has been treating himself with MMS because he was infected his eyesight is 20/20!!!
Not a sign of a supposed cataract at all!
This is all very good news for us.
Those blasted spirochetes cause so much long lasting damage if left untreated, we are all just so glad we are all being treated now and cleared of the infection.
Lyme girl

You can read here about my other dauhters eyesight improvement http://diaryoflymegirl.blogspot.co.uk/2012/09/eyesight-improvement.html


  **Always consult a LLMD (Lyme Literate Doctor) or your own health care professional.** 
 
 Copyright 2012-2013  LymeGirl all rights reserved.

MMS treatment not just for drinking

Hello all,

I have just realised that I forgot to mention how else I am treating myself and how my children are treating themselves with MMS to treat the spirochaete infection.
As the spirochetes live in the mouth we do the mouth protocol about 3 times a week.
For brushing 5 drops of activated MMS and half a glass of water added and then brush teeth and gargle (as you would with mouth wash)
Then 3 drops activated MMS and place mouth over glass and breath through nose only very important (do not sniff MMS in glass) for 5 minutes only no more than that.

We also have MMS baths

The reason to have a MMS bath is because the Spirochaete could go under the skin to escape any other treatment one is doing internally i.e drinking MMS.

In addition to taking oral doses of MMS it is possible to absorb MMS through the skin directly into underlying muscle. Whereas oral doses provide Cl02 gas primarily to the red blood cells, MMS that sinks through the skin provides Cl02 gas directly to the liquid plasma of the blood. See 3000 protocol also. More Cl02 is circulated and more rapid benefits can be expected. If you are not acquainted with the reported benefits from taking activated MMS doses, read the article: "Introduction to MMS"  When using this bathtub strategy, your full skin surface will be in contact with Cl02 gas for 20 to 30 minutes.

 For some people this strategy has produced a breakthrough. By soaking for 20 minutes in tub water laced with activated MMS, people who had been unable to rise above a 7 drop oral solution were able to increase the supply of Cl02 gas in the blood stream without nausea. Rationale? Bacteria and pathogens on or below the skin level are killed by the MMS and they move outward, away from the body. Most debris moves outward and floats away rather than being adrift in the blood stream. Do not neglect oral doses during your occasional tub experiences. Take at least a six drop dose just before the tub bath. Don't worry about whether you just ate - or didn't eat. Any Cl02 losses caused by food in the stomach is minor and relatively unimportant.

Pathogens removed through the internal use of MMS (as when we drink it) can only get out of the body by passing to the liver and on to elimination. This works fine until you reach the (temporary) nausea barrier. Nausea indicates that MMS is killing more pathogens than the elimination system can handle, resulting in temporary-but-serious nausea.

Bathing in MMS water enables cleansing of pathogens that are on the skin surface or just under it. Cleansing at these outer levels seems to avoid overloading the internal elimination systems. Pathogens killed near the skin surface more-often move outward through the skin and float away. Do continue with normal MMS oral doses, of course.

1. WIPE OUT THE TUB. Otherwise the MMS ClO2 gas in the water will go to work on any soap scum and bathtub-ring, reducing or neutralising the Cl02 available to the body. By the second bath, the tub will be clean due to the MMS cleansing action. Put no soap or other chemicals in the water. Adding more water does not weaken the CL02 that is being generated. Some people add 1/4 cup DMSO. (Not required but it may assist deeper penetration of the Cl02 gas.)

2. ACTIVATE MMS IN A CUP OR GLASS before adding to the tub water. Place 30 drops of MMS in a cup. Add 2.5 teaspoons of lemon juice or citric acid (150 drops). Plan for a 20 to 30 minute minute tub sitting. If you have open skin sores or severe body wounds, consider reducing the MMS to 20 drops mixed with 100 drops of citric acid or lemon juice (1.5 teaspoons) so that sensations of heat or burning will be reduced. Open sores usually heal quickly due to the disinfecting action of MMS. The 1 to 5 ratio is the normal MMS protocol.

3. MIX THE MMS WITH THE ACID AND SWIRL IN A CUP Wait 3 minutes. While waiting, draw 5 to 8 inches of hot water for bathing. Do not add soap, perfume, shampoo nor children's toys. The amount of water doesn't matter. It is good to drink a separate 6 or 8 drop dose as well.

Diseases caused by bacteria or viruses will almost always be resolved through repeated exposure to MMS Cl02 gas.

Diseases caused by genetic or nutritional deficiencies may not be helped by MMS because MMS supplies no nutrients.

4. ADD THE ACTIVATED MMS into the tub water. Stir it. Almost immediately all germs in the water will be eradicated. Some companies provide swimming pool systems that use this same strategy. Water does not reduce the amount of ClO2 gas that is being produced. Tub half full or very full doesn't matter because the same amount of Cl02 gas will be produced by the activated MMS.

5. Get into bath. One side, then the other. Splash water onto the entire body - arms, neck, hair, face - all over. If a history of cold sores, then wipe tub water on the lips and nose repeatedly and wherever they were once visible. If water splashes in the eyes, just wipe it away. MMS doesn't harm eyes - unlike shampoo. With a cup pour tub water onto the scalp.

6. ADD MORE HOT WATER. Heat opens the pores and MMS penetrates into the muscles. Massage the scalp with tub water. By the 3rd bath, skin moles may begin to crumble.

7. WIPE AWAY TUB DEBRIS 

In the presence of Cl02, parasites and germs will flee or die.

We also actvate 3 drops of MMS and dilute with water and use it as an eye wash, because the spirochete also live in the eyes and can cause blindness if left untreated. Also I feel that when treating the spirochete infection they will migrate to the eyes and it is best to treat all areas of the body to not give them a chance.

We have been doing all of the above and drinking the MMS for 14 and half months now. 

I am positive the MMS has helped myself and my children dare I say it the MMS has virtually cleared our bodies of the infection.

I cannot definatly say we are totally clear yet because well it takes time and the infection can go dormant so it is best to carry on treating for a least a year after one feels better and feels like they are cured.

Lyme Girl

 **Always consult a LLMD (Lyme Literate Doctor) or your own health care professional.**  

http://jimhumble.biz/20-tub-baths.html

 Copyright 2012-2013  LymeGirl all rights reserved.

Congenital Lyme/ Spirochete Rash

Hello all,

I thought I would just blog this for others to see a congenital lyme rash something you would probably be hard pressed to find anywhere.

This rash is not the bulls eye rash as we are lead to believe what the Lyme rash should look like.
Also this rash is not from a bite no, it is a rash that appears anywhere on the body diffrent places and appears in cycles every 6 weeks or so.

"Congenital Lyme/Spirochete rash"

We thought before we knew about spirochete infection that it was an allergic reaction or something along those lines but no it is not know now.

Yes creams and ointments were applied but to no avail creams and ointments did not help.
The rash is not itchy or scaly it just come and goes in cycles.

Since treatment with MMS for 14 months the rash stopped until about a week ago and it suddenly reappered.

Maybe this is the die off like my stripy leg http://diaryoflymegirl.blogspot.co.uk/2012/08/stripy-leg-swollen-foot.html

At least we know now the mystery of the disappearing/reappearing strange rash that would appear anywhere on the body.

Well we shall monitor this rash and see how quickly it clears up.
My stripy leg took about 4 days and has not come back since.

Lyme Girl

**Always consult a LLMD (Lyme Literate Doctor) or your own health care professional.** 

 Copyright 2012-2013  LymeGirl all rights reserved.

Eyesight improvement

Hello all,

I just had to blog this information as well it is amazing news!

My eldest who has been treating congenital Lyme/co-infection with MMS for 14 months, went for an eye test the other day.
She has always had a problem with the right eye and for about a month could not see out of the right eye about 2 years ago.
We were expecting either the eyesight to have deteriorated or she would need glasses we really did not know.
She had an eye test age 8 (before I had even heard about Spirochete infection) and then eyes tested as 20/20 vision.
Then the right eye lost sight, could they find what was wrong? Nope.
Anyway right eye got better and sight was restored.
Then we started the MMS treatment and as I have said before it is her choice to take MMS because she is Gilleck Competent (Knows her own mind).
Well 14 months later eyes both of them have not lost any sight.
The eye test she has just had showed she has now above 20/20 vision!
This is amazing no glasses, eyes perfectly healthy and improved sight than when she was 8!!!!
All I can say is yep the MMS worked.
Even if we had not of taken MMS and chosen antibiotics I am sure we would of seen the same healing but maybe at a much slower rate who knows.
We are just so grateful that something that was passed on to her is now being cured by MMS.
Goodness knows what her sight will be like in 6 months as they just want to test her again just to make sure!

Lyme Girl

 **Always consult a LLMD (Lyme Literate Doctor) or your own health care professional.** 

My Progress

Hello all,

I was a person who could not drive my car for long distances, i found it hard to move around my own home.

Cooking for myself was out of the question, dressing , bathing totally would wipe me out.

Working on the computer was a big no no.

Conversation very limited, my brain fog was getting worse by the day.

Muscle cramps were very bad and would cripple me to the point I would not be able to get out of bed.

Now I have more strength in all areas of my body, I can stand for longer, I do not have muscle cramps, conversation ability is now second to none (maybe some are not so pleased i am now a chatter box).

My I.Q has increased by at least 50% I am becoming more able to look after myself.
I can drive longer distances and do more around the home.

Pacing really helped me to increase my activities and i can now contemplate light exercise like Yoga or Pilate's or Tai Chi.

I have invested in a Wii, i use Wii sport and i find this has helped me to become more active and I am finding i can do more and more on the Wii than I could of ever of done before treatment.
I was in the shops the other day and I found my children were guiding me and speaking to me like I was a baby, I said "stop treating me like a child"
 my eldest said "sorry but you have never been able to do the things you are doing now we are not used to this"
I apologized and realized yes I am doing more.

Yes I am waiting for the other shoe to fall and that this is too good to be true but every day i am getting stronger and stronger better and better.

The other shoe is not going to fall off it is not all going to go belly up I have to trust this.

Yes my progress is very good and I would probably never be where i am today if I had not of found out about Lyme and Spirochaete infections and if I never connected the dots with the fact that I was bitten 30 years ago by a beastly horse fly.
I owe everything to MMS and Jim Humble and of course guidance I got from a higher source my angels.
Wrongs are being righted.

See for yourself if MMS helps you no matter what ails you.

You can either believe that an autoimmune disease is your body attacking you that something has gone wrong with your immune system or believe that there is something more and perhaps it's a parasite living off you.
Unfortunatley the tests for these infections are useless hopeless at best do not just rely on a positive test result go find a Lyme Literate doctor (LLMD) try the tests if you want.
It does not matter if one chooses MMS or antibiotics it's worth a go.
Yeah there is a lot of dis-information flying around out there, there is a Spirochaete/Lyme cover up yes, many do not trust MMS be careful who you do really trust and research for yourself.
I do not receive a cent/penny from Jim Humble or sales of MMS  
 I have written this blog for others to gain knowledge and know where to get help no one should suffer any longer.
With the financial climate the way it is at the moment, the rising costs in health care, the austerity being imposed on us all, benefit cuts, scrapping of disability benefits (UK), disabled hate crime on the rise.


You just need to look at this Blog http://johnnyvoid.wordpress.com/ to see how bad things are going to get for the sick and disabled in the UK at least. Or this blog  http://diaryofabenefitscrounger.blogspot.co.uk/

I wanted to help as many as I possible so that we can all not be reliant on government help, big pharma and lead normal healthy lives.
If you are already treating a spirochete infection excellant and you have done the right thing you will not regret it.


**Always consult a LLMD (Lyme Literate Doctor) or your own health care professional.**

 Copyright 2012-2013  LymeGirl all rights reserved.

Exercise, Healing from Lyme & Co-infections

"No I do not mean vigorous exercise like tennis"

Hello All,

I was in a quandary about what exercises are OK for those who are taking medication or treatments to heal from Lyme and co infections.
As one can herx which can be very debilitating on it's own seeing as one can suffer from old symptoms or new symptoms which can last a few hours up to a month or more.
It depends on each individual some herx some do not.
If I do repetitive exercise or exercise too vigorously or put too much stress on the limbs I suffer very badly.
When I was younger after the horse fly bite, I used to horse ride regularly and after a month or two of horse riding I would end up in hospital the doctors had no idea what was wrong with me and basically put it down to me being either lazy or trying to get off from going to school.
I could not walk my hips were extremely painful.
Everyone wrote me off.

Now I am treating myself I would like to do some form of exercise to keep me mobile and I decided to see how people with M.E and CFS keep mobile and active if possible.
After researching M.E and CFS I discovered that most of the medical profession do not believe M.E/CFS is an illness that it is caused by the the sufferer because of their belief, basically it does not exist All made up.
I am shocked and dismayed by this how dare anyone suggest M.E/CFS sufferers make it all up!
The sufferers are not treated properly and told to exercise the illness away!
Also have cognitive therapy and talk about the belief!
No one can exercise an illness away especially the type of exercise regime M.E/CFS sufferers are recommended to follow, if anything this type of exercise could be potentially fatal in some cases.
The exercise regime is G.E.T Graded exercise therapy which is just impossible for anyone with an autoimmune disease which is what M.E/CFS is one of the many.

Pacing

I found a website that recommends "pacing" exercise.
 This I felt was more like it for anyone who has a autoimmune disease or anyone who is treating the spirochaete infection.
Now I could be wrong don't hold me to this.
Pacing is when the sufferer basically paces themselves to remain as active as possible, but to avoid relapses with  too much over exertion.
To try to increase activity levels every few days as long as you remain within the limitations the disease imposes.
Pacing in practise means stopping an activity as soon as it becomes unpleasant not a nice tiredness, or when arms and legs begin to feel weak, or when one begins to feel ill or sick
It is advisable to rest for a while at the first sign of muscle weakness. Learn to listen to your body.
You must rest when you need to this is very important.
See your energy levels like a bank so lets say you have an energy level of £500 and every day when you get up assess your amount in your bank.
So if you do find getting dressed and bathing very tiring and lets say it depletes £100 out of your energy bank make sure when you do these activities you rest for as long as it takes to build up your energy again.
As you take breaks and rebuild your energy bank any amount left over from the previous day can be added to your total.
If you use up the whole £500 in one day you will work in a minus or debt and that cannot be recouped.
allow space between your most tiring activities .
If you deplete your energy account too much or you have a busy day make sure you have at least 3 free days to recoup your energy bank.
You want to make what limited  energy you do have go further day by day. Be patient with your body as it has a lot to deal with if you are treating yourself with MMS or antibiotics or other treatments. Your Immune system needs a helping hand from you.
You may find you need to limit the amount of time you spend on the phone or computer or T.V as all these are energy zappers.
Or limit the amount of time you spend with others ie. spouse, children etc.
 If you have just started treating the Lyme/co-infections be very aware of your limits, yes it is very exciting when you do start to get your energy back and strength but do not make my mistake.
When i first started to take MMS wow I felt great but I did not listen to my body and I paid for that and it took a good 3 months to recoup my energy bank.
I do use walking poles to prevent tierdness if i have a lot of walking to do or if I go shopping in the supermarket I do borrow the electric scooter as I do not want to deplete my energy bank too much.
I have learnt to be patient with my body and I know after treatment with MMS I will eventually not need to use the walking poles or electric scooter. I will be able to be as fit and active as "Mandy" on the film "Under our Skin" I keep that in my mind so I carry on treatment.

Listen to your body
Take rest days 2 or more if you need to.
Be patient with yourself don't run before you can walk.
Experiment with what you can do and what works for you.
Keep a diary of your daily activities include your emotional state, foods eaten, any stress you had.
If you have started treating yourself and are dealing with the Herx's be extra kind to yourself.
You will see with perseverance you too will be active and fit and stronger but treatment takes a long time and antibiotics can take 5 years or more.

MMS well I do not know exactly how long that takes with chronic Lyme and co-infections I am a test case I suppose and from my experience so far of 14 months and HBO it would seem the time is probably 1/2 the time of antibiotics.
Could be that it is different for each individual.
I do work part time from home, have two children so I suppose I was a little more active than some. I am not saying working part time was doing me any favours before treatment and my children were doing more and more for me before treatment with MMS. i was having to get my food delivered to my home and I was getting to the point where I was going to give up working all together.
happily those days are now long gone thanks to MMS!



**Always consult a LLMD (Lyme Literate Doctor) or your own health care professional.**