Re: Myrrh & tea tree oil treat fungus

[Guest guest]

Jen,i agree with khaya on the sunshine.  here at the ocean on the west coast, the n. side of our home grows green within one season, while the s. side does not.  the green is mold, same as fungus.  the sun shining on the s. side keeps it under control, while the area without the sunshine, mold grows.  so yes, i think the fresh air and sunshine would be great.

barbara

 

Hi Jen,

It's not a good idea to get any kind of oil into the eye, let alone something that stings! There must be something else you can use there ... But anything you use could easily get into the eye. What about fresh summer air? I once showed a rash on my face to Dr. B, and he said let the sun shine on it! This is a chronic rash, but it is better when I spend a lot of time outdoors. I don't think you want to look into the sun, either, but now that winter is almost over (maybe it's over where you are?) just being outdoors on a bright day might be helpful. Even with sunglasses. Just my humble opinion, for what it might be worth ...

Khaya

>

> Dear everyone,

 

> Do you know whether Myrrh oil  and tea tree oil are safe to  treat fungus on " eyelid " ?  I know it it safe to treat fungus on skin in general, but on eyelid, I am unsure as it is too close to the eye.  Pls. advise.  Thanks a lot.

> 

> Jen .

[Guest guest]

i know nothing about tea tree oil but ordered some in the 'more organic' section for shampoo.  is this something that should be used as medicinal shampoo for dandruff, etc.?  did i make a mistake in ordering this and using on a regular basis?

barbara

 

I know tea tree oil burnmy nouth so do not please

this is not regular oil i tis corrosif medecine very contrate not something to play with

 

kindly marie

To: " Lyme_and_Rife " <Lyme_and_Rife >

Sent: Thursday, March 8, 2012 8:54 PMSubject: Myrrh & tea tree oil treat fungus

 

Dear everyone,

 

Do you know whether Myrrh oil  and tea tree oil are safe to  treat fungus on " eyelid " ?   I know it it safe to treat fungus on skin in general, but on eyelid, I am unsure as it is too close to the eye.  Pls. advise.  Thanks a lot.

 

Jen .

  with rife. on abx, the abx will only work for so> long, because once they sense danger in our system, they go in hiding/cyst,> where they are safe. clever little bugs.>

> i believe, mms, is a cyst buster. *JIM, is my belief here> correct?????* so is a good product to help here.> > again, i was so much sicker when i got off the abx. it caused more> problems in my system. wish i had this site before i went to dr for

> treatment on abx.> > barbara> > > On Wed, Mar 7, 2012 at 1:07 PM, Chantel wrote:> > > **> >> >> > So in your opinion its better to be of the antibiotics while you rife?

> > > >> >> **>

>>> >>> >> Hi,> >>> >> your story sounds like mine. i've gone through over 39 yrs of every test> >> and med. they could do, several diagnosis like fibro, tested for lyme, but

> >> mine was negative, which means nothing. it really helps to have a positive> >> dx, at least you know why you feel crazy.> >>> >> when a lyme dr dx lyme he put me on 18 mos. of abx and many other meds to

> >> help the abx. after that i was actually sicker than before i went on the> >> abx. i also had more candida, which is a real problem. also, if you are> >> rifing, the abx cause the lyme to encyst, where the rife can't kill them.

> >> just something to think about, maybe do some research here on this site> >> because the abx will be counter productive to rifing. i know many rely on>

>> abx, but for me it just made it worse.> >>> >> also, i found detoxing made a big difference in moving me forward. there> >> is lots of info here on detoxing.> >>

> >> barbara> >>> >>> >>> >>> >>> >> On Wed, Mar 7, 2012 at 11:12 AM, Marie Benoit wrote:> >>

> >>> **> >>>> >>>> >>> Hi yes ,> >>> Me too , it looks like most of our history . Now that you know you will> >>> find a lot of help here we share much support and information .

> >>> I recovered from paralysi swith what I found here in thi sforum so> >>> gather yoru courage you are on yoru way out even thought ti looks very long> >>> to began with and very slow sometime

..> >>> Kindly Marie> >>>> >>> *From:* damarise ignitus > >>> *To:* lyme_and_rife

> >>> *Sent:* Wednesday, March 7, 2012 1:43 PM> >>> *Subject:* RE: My Lyme Story.> >>>> >>>> >>> Hi> >>> Wow, i feel a lote of empathy for you. I cannot believe you went through

> >>> all that, You were sick with so many things and not one doctor could> >>> diagnois you. At least your family doctor led you in the right direction to> >>> at least consider that you have lyme. and That is the cause of all your

> >>> illnesses. At least you know what you have and can

concentrate on a path> >>> that will help cure you. I wish you all the best. If you protocals seem to> >>> be slow, try to consider metal toxity also, having too much metal like lead> >>> and merucury can stop your progresss. i would also have a metal toxity

> >>> test. take care Damarise> >>>> >>> To: Lyme_and_Rife > >>> From: sanderschantel@...

> >>> Date: Wed, 7 Mar 2012 16:33:03 +0000> >>> Subject: My Lyme Story.> >>>> >>>> >>> My Lyme story> >>>> >>> March, 2012

> >>> For the past 10+ years I have been walking around feeling like a> >>>

Hypochondriac. I have had a lot medical problems, went to several doctors,> >>> had lots of test done, and I have never found a definite answer to what the> >>> problem was. Only their best guess based on symptoms. I have spent a lot of

> >>> money in MRI’s, CAT scans, ultrasounds, Upper GI, Physical therapy,> >>> chiropractors, and so on. It’s really frustrating not having an answer> >>> and feeling like no one believes me. Here is part of my story.

> >>>> >>> I have had several symptoms for years. In 2002 (?) I had severe> >>> migraines that caused black outs. I never found out why. In 2004(?) I was> >>> diagnosed with fibromyalgia . I had several years of extremely bad periods

> >>> that produced a lot of blood clots and severe pain which later led to a> >>>

hysterectomy in 2007. In 2009 my arm was going numb and I had a lot of neck> >>> pain. I lost a lot of muscle and had to do physical therapy. I was> >>> diagnosed with Degenerative disc disease. I have also been diagnosed with

> >>> High blood pressure, Anxiety, irritable bowel syndrome, migraines,> >>> depression, Insomnia, muscle spasms, not to mention Back pain and sore> >>> muscles for no reason. There are others but i cant remember. I suffer a lot

> >>> now with Memory loss and confusion. I loose track of what i am thinking. I> >>> have problems with my vision although when i go in the test are not bad. I> >>> have been told that my eye test show a question for Glaucoma. I cant

> >>> remember the last time i woke up without any pain. Not to mention it takes> >>> sleeping pills to give me an

almost good nights sleep. I know my body and i> >>> know when something is wrong.> >>>> >>> I recently found out I have Lyme from my family doctor. I was doing OK> >>> for a while until I had a Root Canal done on 12/8/11. I went in to the

> >>> doctor on 12/20/2011 because of severe stomach pains. I was at that time,> >>> so tired of being sick and not knowing why. I went in with a long list of> >>> all my complaints and my past diagnoses. After entering it all in it came

> >>> up Lyme. So he asked if i have ever been bitten by a tick. Then knowing> >>> that I have in the past he decided to do the test. I did not go back for> >>> the results, Instead I called and asked the nurse. She said everything

> >>> looks fine. (Never get your results from a nurse). Well I got even more>

>>> sick with a bad cough and severe migraines. I could not take the pain> >>> anymore so I went back in to my doctor on 1/31/12. He asked why i didn't> >>> come back for a follow up and to get my results. I explained that I called.

> >>> He then told me I had Lyme. The Western Blot AB IGM WB 41 KD Band was> >>> reactive. He put me on Doxycline and ordered a Brain MRI, An Upper GI, and> >>> an abdomen complete ultra sound. MRI was good except sinuses: Right

> >>> maxillary antrum mucous retention cyst. Upper GI showed Minimal> >>> gastroesophageal reflux. Ultra Sound shows Fatty infiltration of the liver.> >>> When it came back he said you have Lyme. He knew nothing more about

> >>> treating it besides putting me on Doxy. So he referred me to an Infectious> >>> disease doctor. Well, the

Infectious Disease doctor disagreed. He looked at> >>> the blood test that was given by my doctor. He said in his opinion I> >>> don’t have Lyme and I should not have been put on Doxycline. He ordered

> >>> the C6 peptide test along with others. When that came back he had his nurse> >>> call and she said, " you don't have Lyme. " Well I picked up my test so i> >>> could see it for myself. The Lyme total antibody had a reading of 0.14

> >>> which states that below 0.90 is Negative by their standards. I didn't take> >>> his advice and searched for another doctor. After being referred by another> >>> Lyme patient, I went on to an ND for a second opinion. During our 3 hour

> >>> visit, she said " Your not crazy. You have Lyme " . So later I called the> >>> infectious disease doctor back. After arguing

with him, he finally said " I> >>> cant tell you that you have Lyme. " Well that i understand. He goes by the> >>> CDC standards. Why is it so hard to get a true diagnosis. We should not

> >>> have to be so far gone in order for us to get the treatment we deserve.> >>>> >>> I remember being bit by a tick when I was young and a few times as I was> >>> older but I can’t recall when. I don’t remember ever seeing a rash. So

> >>> I have no idea how long I have had this. This is what I have learned. Most> >>> of everything I have ever had has been listed for symptoms of Lyme. I have> >>> had enough tests to know that so far, in most of the major organs I have no

> >>> damage. I feel that most can be healed. And with the support of my family> >>> and friends I can make it

through anything.. I also know that EMF> >>> electro-magnetic frequencies with the bed mat + sauna are a big part to> >>> healing. So is Rife. On top of that I am going to continue with the

> >>> Doxycycline until I'm out, eat better and try to find ways to detox. That's> >>> the plan for now. All we can do is go a step at a time. And Pray for more> >>> good days than bad.

> >>>> >>>> >>>> >>>> >>>> >> > >>

[Guest guest]

HI JIm,

yes it is the hair the sclap , the other si in control .

I do not breath it I am careful and aware of it .

Thank you JIm

KIndly Marie

To: Lyme_and_Rife Sent: Sunday, March 11, 2012 12:13 AMSubject: Re: Myrrh & tea tree oil treat fungus

Hi Marie,I am sorry, I don't understand what you are trying to say... Do you have fungus in your hair or scalp?If so, then yes activate 2 - 3 drops of MMS (no water) and place your hair over the glass,the chlorine dioxide (MMS) gas will rise to your hair and scalp... Don't breath this in, if you do turn your head away and breathe in some normal air as chlorine dioxide displaces oxygen.Some breathing in of MMS is okay and even healthy, but too much is not good as you need oxygen.. If this is for something other than hair or scalp, please say what!!Jim> > > >>> > > >>> **> > > >>>> > > >>>> > > >>> Hi yes ,> > > >>> Me too , it looks like most of our history . Now that you know you will> > > >>> find a lot of help here we share much support and information .> > > >>> I recovered from

paralysi swith what I found here in thi sforum so> > > >>> gather yoru courage you are on yoru way out even thought ti looks very long> > > >>> to began with and very slow sometime .> > > >>> Kindly Marie> > > >>>> > > >>> *From:* damarise ignitus <lorraina20pink@>> > > >>> *To:* lyme_and_rife > > > >>> *Sent:* Wednesday, March 7, 2012 1:43 PM> > > >>> *Subject:* RE: My Lyme Story.> > > >>>> > > >>>> > > >>> Hi> > > >>> Wow, i feel a lote of empathy for you. I cannot believe you went through> > > >>> all that,

You were sick with so many things and not one doctor could> > > >>> diagnois you. At least your family doctor led you in the right direction to> > > >>> at least consider that you have lyme. and That is the cause of all your> > > >>> illnesses. At least you know what you have and can concentrate on a path> > > >>> that will help cure you. I wish you all the best. If you protocals seem to> > > >>> be slow, try to consider metal toxity also, having too much metal like lead> > > >>> and merucury can stop your progresss. i would also have a metal toxity> > > >>> test. take care Damarise> > > >>>> > > >>> To: Lyme_and_Rife > > > >>> From: sanderschantel@> > > >>> Date: Wed, 7 Mar 2012 16:33:03 +0000> > > >>> Subject: My Lyme Story.> > > >>>> > > >>>> > > >>> My Lyme story> > > >>>> > > >>> March, 2012> > > >>> For the past 10+ years I have been walking around feeling like a> > > >>> Hypochondriac. I have had a lot medical problems, went to several doctors,> > > >>> had lots of test done, and I have never found a definite answer to what the> > > >>> problem was. Only their best guess based on symptoms. I have spent a lot of> > > >>> money in MRI’s, CAT scans,

ultrasounds, Upper GI, Physical therapy,> > > >>> chiropractors, and so on. It’s really frustrating not having an answer> > > >>> and feeling like no one believes me. Here is part of my story.> > > >>>> > > >>> I have had several symptoms for years. In 2002 (?) I had severe> > > >>> migraines that caused black outs. I never found out why. In 2004(?) I was> > > >>> diagnosed with fibromyalgia . I had several years of extremely bad periods> > > >>> that produced a lot of blood clots and severe pain which later led to a> > > >>> hysterectomy in 2007. In 2009 my arm was going numb and I had a lot of neck> > > >>> pain. I lost a lot of muscle and had to do physical therapy. I was> > > >>> diagnosed with

Degenerative disc disease. I have also been diagnosed with> > > >>> High blood pressure, Anxiety, irritable bowel syndrome, migraines,> > > >>> depression, Insomnia, muscle spasms, not to mention Back pain and sore> > > >>> muscles for no reason. There are others but i cant remember. I suffer a lot> > > >>> now with Memory loss and confusion. I loose track of what i am thinking. I> > > >>> have problems with my vision although when i go in the test are not bad. I> > > >>> have been told that my eye test show a question for Glaucoma. I cant> > > >>> remember the last time i woke up without any pain. Not to mention it takes> > > >>> sleeping pills to give me an almost good nights sleep. I know my body and i> > > >>> know when something is wrong.> >

> >>>> > > >>> I recently found out I have Lyme from my family doctor. I was doing OK> > > >>> for a while until I had a Root Canal done on 12/8/11. I went in to the> > > >>> doctor on 12/20/2011 because of severe stomach pains. I was at that time,> > > >>> so tired of being sick and not knowing why. I went in with a long list of> > > >>> all my complaints and my past diagnoses. After entering it all in it came> > > >>> up Lyme. So he asked if i have ever been bitten by a tick. Then knowing> > > >>> that I have in the past he decided to do the test. I did not go back for> > > >>> the results, Instead I called and asked the nurse. She said everything> > > >>> looks fine. (Never get your results from a nurse). Well I got even more> > >

>>> sick with a bad cough and severe migraines. I could not take the pain> > > >>> anymore so I went back in to my doctor on 1/31/12. He asked why i didn't> > > >>> come back for a follow up and to get my results. I explained that I called.> > > >>> He then told me I had Lyme. The Western Blot AB IGM WB 41 KD Band was> > > >>> reactive. He put me on Doxycline and ordered a Brain MRI, An Upper GI, and> > > >>> an abdomen complete ultra sound. MRI was good except sinuses: Right> > > >>> maxillary antrum mucous retention cyst. Upper GI showed Minimal> > > >>> gastroesophageal reflux. Ultra Sound shows Fatty infiltration of the liver.> > > >>> When it came back he said you have Lyme. He knew nothing more about> > > >>> treating it besides putting me on

Doxy. So he referred me to an Infectious> > > >>> disease doctor. Well, the Infectious Disease doctor disagreed. He looked at> > > >>> the blood test that was given by my doctor. He said in his opinion I> > > >>> don’t have Lyme and I should not have been put on Doxycline. He ordered> > > >>> the C6 peptide test along with others. When that came back he had his nurse> > > >>> call and she said, "you don't have Lyme." Well I picked up my test so i> > > >>> could see it for myself. The Lyme total antibody had a reading of 0.14> > > >>> which states that below 0.90 is Negative by their standards. I didn't take> > > >>> his advice and searched for another doctor. After being referred by another> > > >>> Lyme patient, I went on

to an ND for a second opinion. During our 3 hour> > > >>> visit, she said "Your not crazy. You have Lyme". So later I called the> > > >>> infectious disease doctor back. After arguing with him, he finally said " I> > > >>> cant tell you that you have Lyme." Well that i understand. He goes by the> > > >>> CDC standards. Why is it so hard to get a true diagnosis. We should not> > > >>> have to be so far gone in order for us to get the treatment we deserve.> > > >>>> > > >>> I remember being bit by a tick when I was young and a few times as I was> > > >>> older but I can’t recall when. I don’t remember ever seeing a rash. So> > > >>> I have no idea how long I have had this. This is what I

have learned. Most> > > >>> of everything I have ever had has been listed for symptoms of Lyme. I have> > > >>> had enough tests to know that so far, in most of the major organs I have no> > > >>> damage. I feel that most can be healed. And with the support of my family> > > >>> and friends I can make it through anything.. I also know that EMF> > > >>> electro-magnetic frequencies with the bed mat + sauna are a big part to> > > >>> healing. So is Rife. On top of that I am going to continue with the> > > >>> Doxycycline until I'm out, eat better and try to find ways to detox. That's> > > >>> the plan for now. All we can do is go a step at a time. And Pray for more> > > >>> good days than bad.> > > >>>> > >

>>>> > > >>>> > > >>>> > > >>>> > > >> > > > >> > >> >>

[Guest guest]

Marie ,have you tried apple cider vinegar on your head? It might help. dilute it half n half with water.Braggs ACD is the best Also rosemary essential oil is good for scalp and hair.janRe: Myrrh & tea tree oil treat fungus Posted by: "jimjax2" jimjax2@... jimjax2 Date: Sat Mar 10, 2012 9:14 pm ((PST))Hi Marie,I am

sorry, I don't understand what you are trying to say... Do you have fungus in your hair or scalp?If so, then yes activate 2 - 3 drops of MMS (no water) and place your hair over the glass,the chlorine dioxide (MMS) gas will rise to your hair and scalp... Don't breath this in, if you do turn your head away and breathe in some normal air as chlorine dioxide displaces oxygen.Some breathing in of MMS is okay and even healthy, but too much is not good as you need oxygen.. If this is for something other than hair or scalp, please say what!!Jim"Im not trying to counsel any of you to do anything

really special,except to dare to think, and to dare to go with the truth ,and to dare to love completely." -R. Buckminster Fuller