An allakine diet

[Guest guest]

In a message dated 10/22/2005 4:01:59 PM Eastern Daylight Time, acts92@... writes:

It would also be a good ideal to do a google search typing in "alkaline foods" and pull of food charts available that

could help you with your diet. Rule of thumb is that our diet should consist of 25A% acidic foods and 75% alkaline.

This is a very good idea because there are some foods that you may think would be acidic, lemons for instance, but they become akaline once eaten. I found a chart that shows the foods listed in categories, ie most acidic down to least acidic and the same for alkaline. I can't remember the site, but i'm a search would give lots of hits.

Good luck

Arlene

[Guest guest]

In a message dated 10/22/2005 4:45:51 PM Eastern Daylight Time, Aletha@... writes:

I would love to see the chart. I keep hearing of others that are keeping cancer at bay or putting cancers into remission with these types of diets and or juicing.

Althea

Just saw this website and it has the chart I was referring to.

http://www.naturalhealthschool.com/acid-alkaline.html

Arlene

[Guest guest]

In a message dated 10/22/2005 5:31:54 PM Eastern Daylight Time, marilyn1972@... writes:

Does honey turn to acid?

This site may help answer your question.

http://www.naturalhealthschool.com/acid-alkaline.html

Hope it helps

[Guest guest]

Marilyn:

It can be very challenging to maintain a more alkaline diet. If your diet allows, fresh lemons and Braggs Apple Cider Vinegar

are just a couple to mention of products you can take to help you be more alkaline.

It is very important to eliminate processed sugar and food items with processed sugars, corn syurp, etc. from your diet.

Sugars such as these turn to acid. It seems when you read the labels in the grocery store, about everything has sugar in

some form. Even in natural sugars (such as found in fruits) your intake should be in moderation.

For a sweetner, I use Stevea. It is all natural and also help with alkaline balance.

I recently was introduce to a product for assisting in keeping you more alkline called "Dr. Flanagan's - MEGA H".

It is in gel capsul form to take orally or you can do as I do, and open capsul and mix with 8 ounces of water. I have to take

6 of these a day to help me maintain a Ph balance of 6.9 to 7. The website for this product is: www.phiscienes.com

It would also be a good ideal to do a google search typing in "alkaline foods" and pull of food charts available that

could help you with your diet. Rule of thumb is that our diet should consist of 25A% acidic foods and 75% alkaline.

Hope this information will be of help!

Tom Armstrong

[low dose naltrexone] Re: Questions from Potential LDN user with Melanoma/O...My Personal Experience With Low Dose Naltrexone and CancerMy Name is Tom and my screen name is TomOnLDN. I will be in my thirdyear of Stage IV malignant melanoma which had metastasized to thelymph glands in my neck, shoulders and under my arms. CT's confirmedthat it had metastasized to the lymph's under my jaw on the left sideand around the spine at the back of my neck. The lymph node under myjaw is swollen the size of an unshelled walnut.Research on the internet in areas that the medical profession useeducated me to the fact that when there are tumors with the melanoma;they are larger than 1/16th inch in diameter and the cancer hasspread to the lymphatic system, it is in stage IV and conventiontreatments with chemo and radiation are no longer effective. In otherwords, it is to late by their thinking.Two weeks prior to finding I had stage IV melanoma, I also hadsquamous cell carcinoma which started on the top of my forehead andspread to and around my eye, into the sinus cavity and towards mymouth.So under my circumstances, I opted to go 100% natural. So I set outresearching cancer for the past three years. I my research, I camethe conclusion, especially from the methods I have been using, thatcancer and other diseases can not be necessarily cure, but managed tohelp keep in remission.I first started out with a good nutritional diet and keep myself veryalkaline. Cancer can only thrive in an acidic environment. Inaddressing my tumors, I decide to opt for the use of a drawing salve(black salve), in my case, Cansema. I documented in every detail,along with hundreds of pictures, the two years I used the salve todraw out tumors. Some of the tumors were as big as ½ too ¾ inches indiameter. The problem with this method, was that the tumors wereproducing faster than I could keep up with. In my research, thispossibly was brought on by edema which was cause by theaggressiveness of the salve.So I knew I was going to have to make some adjustments. One year intomy battle, the spring of 2004, I added to my therapy Wobenzym N fromMucos Pharma in Germany and approved for sale in the US. This is asuperb product that I still use to this day. Enzyme therapy is veryimportant in any disease or prevention of disease. I started out on60 pills a day to as little as 30 a day. I was introduced to twodifferent kinesiologist. One in Kentucky and one in Michigan, bothwho monitoring me the past two and a half years. It is with theirhelp, I was able to know how much Wobenzym N and other necessarysupplements I need to take as well as what was effective and what wasnot. They also monitored my diet as well.As well as all this was working for me, I still had flair ups in mycancer activity every time my immune system was compromised and I gotreal ill. So I decided that I needed to research more and look forsomething else that would enhance my immune system to keep thiscancer in remission. Then a friend of mine told me about being put onlow dose naltrexone for his non-Hodgkin's lymphoma in January of thisyear (2005). He knew very little about this product. So I started todo my home work. I found the Low Dose Naltrexone website and afterreading about the women's experience in France that had three month sto live due to melanoma that had spread to the brain, and lived fortwelve years afterward until she stopped taking LDN, I said this isthe product I want to take.I went to three doctors that I have known for some years, and nowould write me the prescription. Their excuse was that it was not FDAapproved for that use. I reminded them of other drugs that theyprescribed for other uses beyond would the FDA had approved them for,but that did not convince them. One even wanted me to have surgery. Iknew better or they were not well educated that surgery is to latefor stage IV melanoma.I ended up having to be paired with a doctor in Ohio who is on LDNfor MS to get my prescription. Once I received the LDN I had mykinesiologist test me. In testing my endorphin level, it was only at10%. Testing with LDN, I was not responding due to a malabsorptionproblem. I suggested that we try D-5 Extra along with the LDN. Whentested, my endorphin level went to 90%. I could absorb thenaltrexoneI started the low dose naltrexone in March of 2005. Prior to gettingon LDN, I contacted a serious upper respiratory infection that causedmy cancer activity to flair up 60%. My lymph nodes swelled as well.After starting on the LDN in March, I again, in April, contacted aserious upper respiratory infection, but this time my cancer activitydid not flair up! That told me it was working.My report from my kinesiologist this week, Oct 18, 2005, was thateven though I still had my cancer, it was not active. The naltrexonewas keeping it under control. She was amazed herself.So I even though I am on naltrexone, I still watch my diet. I thinkthat this is very important when fighting any disease that naltrexoneis being used for. It can do no more than help enhance theeffectiveness of the drug.As far as it keeping me awake at night, I do not have that problembecause I also take 3 mg of Melatonin at bedtime. It is importantthat one is in a good, deep sleep when taking LDN, Light of any kindcan disrupt the sleep pattern. Therefore the bedroom should be pitchblack at night or at least wear a sleeping mask.Today, I am thankful to God for giving me the wisdom and insight toeducate myself on how to manage my cancer. And I am also thankful forDr. Bahari for his dedication to the research of LDN, which in myopinion, could be one of the most valuable, life saving and lifeenhancing drugs every discovered that even someone going thealternative, natural route, would not even think twice about beforetaking it.Tom Armstrong>> Hello Jorn,>> There's a lot to be said for LDN. So far though I haven't seenmuch to> indicate that it can deal with Stage IV Melanoma rapidly enough tosave someone> whose brain, spine, and possibly liver are invaded. If I had aloved one with> a similar condition Here's what I would do:>> Go to _www.cancertutor.com_ (http://www.cancertutor.com)imediately and> make contact with Webster, the author of the site.>> Describe your son's condition to him along with his treatmenthistory. Ask> Webster if he knows of an aggressive and effective protocol forsuch an> advanced condition. Webster will respond quickly...sometimesinstantly. The site> isn't commercialized at all.>> There is a therapy at the site that's very rapid in terms ofdestroying> cancer cells. There'll be plenty of detoxification needed to ridthe body of all> the killed cancer cells, and that should begin right along withwhatever> protocol you choose....from Webster or Bihari or anyone.>> Find Stage IV Protocols on the site (it's easy to navigate) andrealize that> Cesium has been used successfully for decades in the treatment ofcancer.> It's safe because people who use it follow the instructionscarefully and with> expert guidance from the author of the site, if requested. Themain> consideration is keeping the body's minerals balanced. This isdone with the> Potassium that is part of the Protocol and with a blood screeningevery two weeks.> Webster is adamant in his instructions for following the protocolson the> site.>> The protocol calls for Cesium & Potassium, with Liquid DMSO actingas the> carrier of the minerals...whenever there is brain involvement.The DMSO binds> with the minerals, then crosses the Blood/Brain barrier with thecancer> killing minerals. Right now the cancer cells are in an extremelyacidic state.> The Cesium is very alkaline. Cancer does not survive in a highalkaline> environment. OK...that addresses the growth in the brain.>> If my child's spine was involved I'd wonder is the bone structureis> invaded. If not, how would we get rid of the growth before itdoes take over the> spine bones. Imagine the sudden loss of spine stability if thereis bone> invasion and those cancer cells are killed. There could a be acollapse causing> spinal cord impingment...resulting in paralysis from that pointdownward.>> If the spine bones are temporarliy safe from invasion, and thetumor is> small and not significantly impinging on vital nerves, I'd getCesium to do the> job on that tumor, as soon as possible!!>> If the spine bones are invaded with the cancer cells...I'd want asurgeon to> screw some rods to healthy spine bones which would bridge theaffected> joints and bones. Even as the surgery is being planned andscheduled I'd have my> son on the Cesium Protocol. Immediately after the surgery, I'dhave my son> on the Cesium.>> The question of whether Radiation Therapy is a right course ofaction for> the spine tumor is something I'd have to look at after I got afresh PET Scan> for my son. They can hit a tumor with a pretty narrow beam ofRadiation these> days. Obviously, if there's bone invasion, no Radiation could begiven> without the above surgery. Radiation is an unpleasantthought...but...>> If the spine tumor is large, but not in the bones, I'd considersurgical> removal if that seemed at all possible. If surgical removal is notan option,> and the fear is that bone invasion and/or paralysis is imminent, Imight give> serious consideration to the Radiation Therapy to quickly shrinkthe tumor.> The Cesium Protocol would commence immediately after theRadiation, and with> great emphasis on Detoxing the bloodstream before the onset ofToxemia.>> Now for the liver invasion. I'd get the Cesium into hisbloodstream ASAP if> the liver is to be saved. The liver does have amazingregenerative powers> of it's own. so l'd be praying that the invasion is superficial atpresent> time.>> We know the cancer tumors are symptoms of a process within thebody.> Before, during, and after the Cesium, or whatever therapy is used,I would be> giving my son "therapeutic" doses of the best known and mosteffective immune> boosters and other recommended supplements that I've seen on theCancerTutor> site, and elsewhere. The Cesium Protocol will be successful formy son, and the> immune systet has to be restarted and maintained. We have to getstarted> with the Cesium before any organs are too deeply invaded.>> I am researching the feasibility of LDN and Cesium therapies being> administered together. If I had to choose whether to use one orthe other...for any> Stage IV cancer...It would be Cesium every time. It's fast...it'ssafe. It's> been around quite a while. It's being used in foreign countriesby US> medical doctors who fled under pressure from the FDA federalies.>> The longer any therapy takes (like perhaps LDN alone)...the moretime the> cancer has to destroy vital organs. Chemotherapy for my son atthis stage> would be unthinkable and unconscienable. To undertake LDN Therapyalone could> lead to a page on a statisical chart at LDN headquarters if theLDN doesn't act> quickly enough to save organs and spinal bones. There's plenty of> verifiable proof of Cesium's efficacy as a fast acting cancertherapy. An added bonus> is that all cancer pain is amelioriated in 1-3 days. LDN,unfortunatley,> doesn't allow for heavy doses of pain meds. If my son had anyStage cancer, I> would be talking to Cancer treatment experts, not a moderator of aforum that> deals primarily with MS.>

[Guest guest]

Thanks Arlene,

I would love to see the chart. I keep hearing of others that are keeping cancer at bay or putting cancers into remission with these types of diets and or juicing.

Aletha

Re: [low dose naltrexone] An allakine diet

In a message dated 10/22/2005 4:01:59 PM Eastern Daylight Time, acts92@... writes:

It would also be a good ideal to do a google search typing in "alkaline foods" and pull of food charts available that

could help you with your diet. Rule of thumb is that our diet should consist of 25A% acidic foods and 75% alkaline.

This is a very good idea because there are some foods that you may think would be acidic, lemons for instance, but they become akaline once eaten. I found a chart that shows the foods listed in categories, ie most acidic down to least acidic and the same for alkaline. I can't remember the site, but i'm a search would give lots of hits.

Good luck

Arlene

[Guest guest]

Does honey turn to acid?

[low dose naltrexone] Re: Questions from Potential LDN user with Melanoma/O...My Personal Experience With Low Dose Naltrexone and CancerMy Name is Tom and my screen name is TomOnLDN. I will be in my thirdyear of Stage IV malignant melanoma which had metastasized to thelymph glands in my neck, shoulders and under my arms. CT's confirmedthat it had metastasized to the lymph's under my jaw on the left sideand around the spine at the back of my neck. The lymph node under myjaw is swollen the size of an unshelled walnut.Research on the internet in areas that the medical profession useeducated me to the fact that when there are tumors with the melanoma;they are larger than 1/16th inch in diameter and the cancer hasspread to the lymphatic system, it is in stage IV and conventiontreatments with chemo and radiation are no longer effective. In otherwords, it is to late by their thinking.Two weeks prior to finding I had stage IV melanoma, I also hadsquamous cell carcinoma which started on the top of my forehead andspread to and around my eye, into the sinus cavity and towards mymouth.So under my circumstances, I opted to go 100% natural. So I set outresearching cancer for the past three years. I my research, I camethe conclusion, especially from the methods I have been using, thatcancer and other diseases can not be necessarily cure, but managed tohelp keep in remission.I first started out with a good nutritional diet and keep myself veryalkaline. Cancer can only thrive in an acidic environment. Inaddressing my tumors, I decide to opt for the use of a drawing salve(black salve), in my case, Cansema. I documented in every detail,along with hundreds of pictures, the two years I used the salve todraw out tumors. Some of the tumors were as big as ½ too ¾ inches indiameter. The problem with this method, was that the tumors wereproducing faster than I could keep up with. In my research, thispossibly was brought on by edema which was cause by theaggressiveness of the salve.So I knew I was going to have to make some adjustments. One year intomy battle, the spring of 2004, I added to my therapy Wobenzym N fromMucos Pharma in Germany and approved for sale in the US. This is asuperb product that I still use to this day. Enzyme therapy is veryimportant in any disease or prevention of disease. I started out on60 pills a day to as little as 30 a day. I was introduced to twodifferent kinesiologist. One in Kentucky and one in Michigan, bothwho monitoring me the past two and a half years. It is with theirhelp, I was able to know how much Wobenzym N and other necessarysupplements I need to take as well as what was effective and what wasnot. They also monitored my diet as well.As well as all this was working for me, I still had flair ups in mycancer activity every time my immune system was compromised and I gotreal ill. So I decided that I needed to research more and look forsomething else that would enhance my immune system to keep thiscancer in remission. Then a friend of mine told me about being put onlow dose naltrexone for his non-Hodgkin's lymphoma in January of thisyear (2005). He knew very little about this product. So I started todo my home work. I found the Low Dose Naltrexone website and afterreading about the women's experience in France that had three month sto live due to melanoma that had spread to the brain, and lived fortwelve years afterward until she stopped taking LDN, I said this isthe product I want to take.I went to three doctors that I have known for some years, and nowould write me the prescription. Their excuse was that it was not FDAapproved for that use. I reminded them of other drugs that theyprescribed for other uses beyond would the FDA had approved them for,but that did not convince them. One even wanted me to have surgery. Iknew better or they were not well educated that surgery is to latefor stage IV melanoma.I ended up having to be paired with a doctor in Ohio who is on LDNfor MS to get my prescription. Once I received the LDN I had mykinesiologist test me. In testing my endorphin level, it was only at10%. Testing with LDN, I was not responding due to a malabsorptionproblem. I suggested that we try D-5 Extra along with the LDN. Whentested, my endorphin level went to 90%. I could absorb thenaltrexoneI started the low dose naltrexone in March of 2005. Prior to gettingon LDN, I contacted a serious upper respiratory infection that causedmy cancer activity to flair up 60%. My lymph nodes swelled as well.After starting on the LDN in March, I again, in April, contacted aserious upper respiratory infection, but this time my cancer activitydid not flair up! That told me it was working.My report from my kinesiologist this week, Oct 18, 2005, was thateven though I still had my cancer, it was not active. The naltrexonewas keeping it under control. She was amazed herself.So I even though I am on naltrexone, I still watch my diet. I thinkthat this is very important when fighting any disease that naltrexoneis being used for. It can do no more than help enhance theeffectiveness of the drug.As far as it keeping me awake at night, I do not have that problembecause I also take 3 mg of Melatonin at bedtime. It is importantthat one is in a good, deep sleep when taking LDN, Light of any kindcan disrupt the sleep pattern. Therefore the bedroom should be pitchblack at night or at least wear a sleeping mask.Today, I am thankful to God for giving me the wisdom and insight toeducate myself on how to manage my cancer. And I am also thankful forDr. Bahari for his dedication to the research of LDN, which in myopinion, could be one of the most valuable, life saving and lifeenhancing drugs every discovered that even someone going thealternative, natural route, would not even think twice about beforetaking it.Tom Armstrong>> Hello Jorn,>> There's a lot to be said for LDN. So far though I haven't seenmuch to> indicate that it can deal with Stage IV Melanoma rapidly enough tosave someone> whose brain, spine, and possibly liver are invaded. If I had aloved one with> a similar condition Here's what I would do:>> Go to _www.cancertutor.com_ (http://www.cancertutor.com)imediately and> make contact with Webster, the author of the site.>> Describe your son's condition to him along with his treatmenthistory. Ask> Webster if he knows of an aggressive and effective protocol forsuch an> advanced condition. Webster will respond quickly...sometimesinstantly. The site> isn't commercialized at all.>> There is a therapy at the site that's very rapid in terms ofdestroying> cancer cells. There'll be plenty of detoxification needed to ridthe body of all> the killed cancer cells, and that should begin right along withwhatever> protocol you choose....from Webster or Bihari or anyone.>> Find Stage IV Protocols on the site (it's easy to navigate) andrealize that> Cesium has been used successfully for decades in the treatment ofcancer.> It's safe because people who use it follow the instructionscarefully and with> expert guidance from the author of the site, if requested. Themain> consideration is keeping the body's minerals balanced. This isdone with the> Potassium that is part of the Protocol and with a blood screeningevery two weeks.> Webster is adamant in his instructions for following the protocolson the> site.>> The protocol calls for Cesium & Potassium, with Liquid DMSO actingas the> carrier of the minerals...whenever there is brain involvement.The DMSO binds> with the minerals, then crosses the Blood/Brain barrier with thecancer> killing minerals. Right now the cancer cells are in an extremelyacidic state.> The Cesium is very alkaline. Cancer does not survive in a highalkaline> environment. OK...that addresses the growth in the brain.>> If my child's spine was involved I'd wonder is the bone structureis> invaded. If not, how would we get rid of the growth before itdoes take over the> spine bones. Imagine the sudden loss of spine stability if thereis bone> invasion and those cancer cells are killed. There could a be acollapse causing> spinal cord impingment...resulting in paralysis from that pointdownward.>> If the spine bones are temporarliy safe from invasion, and thetumor is> small and not significantly impinging on vital nerves, I'd getCesium to do the> job on that tumor, as soon as possible!!>> If the spine bones are invaded with the cancer cells...I'd want asurgeon to> screw some rods to healthy spine bones which would bridge theaffected> joints and bones. Even as the surgery is being planned andscheduled I'd have my> son on the Cesium Protocol. Immediately after the surgery, I'dhave my son> on the Cesium.>> The question of whether Radiation Therapy is a right course ofaction for> the spine tumor is something I'd have to look at after I got afresh PET Scan> for my son. They can hit a tumor with a pretty narrow beam ofRadiation these> days. Obviously, if there's bone invasion, no Radiation could begiven> without the above surgery. Radiation is an unpleasantthought...but...>> If the spine tumor is large, but not in the bones, I'd considersurgical> removal if that seemed at all possible. If surgical removal is notan option,> and the fear is that bone invasion and/or paralysis is imminent, Imight give> serious consideration to the Radiation Therapy to quickly shrinkthe tumor.> The Cesium Protocol would commence immediately after theRadiation, and with> great emphasis on Detoxing the bloodstream before the onset ofToxemia.>> Now for the liver invasion. I'd get the Cesium into hisbloodstream ASAP if> the liver is to be saved. The liver does have amazingregenerative powers> of it's own. so l'd be praying that the invasion is superficial atpresent> time.>> We know the cancer tumors are symptoms of a process within thebody.> Before, during, and after the Cesium, or whatever therapy is used,I would be> giving my son "therapeutic" doses of the best known and mosteffective immune> boosters and other recommended supplements that I've seen on theCancerTutor> site, and elsewhere. The Cesium Protocol will be successful formy son, and the> immune systet has to be restarted and maintained. We have to getstarted> with the Cesium before any organs are too deeply invaded.>> I am researching the feasibility of LDN and Cesium therapies being> administered together. If I had to choose whether to use one orthe other...for any> Stage IV cancer...It would be Cesium every time. It's fast...it'ssafe. It's> been around quite a while. It's being used in foreign countriesby US> medical doctors who fled under pressure from the FDA federalies.>> The longer any therapy takes (like perhaps LDN alone)...the moretime the> cancer has to destroy vital organs. Chemotherapy for my son atthis stage> would be unthinkable and unconscienable. To undertake LDN Therapyalone could> lead to a page on a statisical chart at LDN headquarters if theLDN doesn't act> quickly enough to save organs and spinal bones. There's plenty of> verifiable proof of Cesium's efficacy as a fast acting cancertherapy. An added bonus> is that all cancer pain is amelioriated in 1-3 days. LDN,unfortunatley,> doesn't allow for heavy doses of pain meds. If my son had anyStage cancer, I> would be talking to Cancer treatment experts, not a moderator of aforum that> deals primarily with MS.>

[Guest guest]

Might I suggest juicing beets?  10 oz per

day of beet juice will raise Ph unlike any other food out there.  Also, a good

slice of watermelon daily will help maintain Ph.  When I was first diagnosed

with terminal cancer a year ago, my ph level was around 4.  It took 4 weeks to

get it to 5+ and another 4 weeks to get it between 6.5 and 7 fairly consistently.

  Urine Ph will follow saliva ph with about a 3 hour lag and generally .3 lower,

but that is OK. 

Regards,

Bruce Guilmette, Ph.D.

Survive Cancer Foundation, Inc.

http://www.survivecancer.net

But the fruit of the Spirit is love, joy,

peace, patience, kindness, goodness, faithfulness, gentleness and self-control.

Against such things there is no law. Galatians 5:22-23 NIV

From:

low dose naltrexone [mailto:low dose naltrexone ] On Behalf Of Marilyn Sawyer

Sent: Saturday, October 22, 2005

5:30 PM

To:

low dose naltrexone

Subject: Re: [low dose naltrexone]

An allakine diet

Does honey turn to acid?

[low dose naltrexone] Re: Questions from

Potential LDN user with

Melanoma/O...

My Personal Experience With Low Dose Naltrexone

and Cancer

My Name is Tom and my screen name is TomOnLDN. I

will be in my third

year of Stage IV malignant melanoma which had

metastasized to the

lymph glands in my neck, shoulders and under my

arms. CT's confirmed

that it had metastasized to the lymph's under my

jaw on the left side

and around the spine at the back of my neck. The

lymph node under my

jaw is swollen the size of an unshelled walnut.

Research on the internet in areas that the medical

profession use

educated me to the fact that when there are tumors

with the melanoma;

they are larger than 1/16th inch in diameter and

the cancer has

spread to the lymphatic system, it is in stage IV

and convention

treatments with chemo and radiation are no longer

effective. In other

words, it is to late by their thinking.

Two weeks prior to finding I had stage IV

melanoma, I also had

squamous cell carcinoma which started on the top

of my forehead and

spread to and around my eye, into the sinus cavity

and towards my

mouth.

So under my circumstances, I opted to go 100%

natural. So I set out

researching cancer for the past three years. I my

research, I came

the conclusion, especially from the methods I have

been using, that

cancer and other diseases can not be necessarily

cure, but managed to

help keep in remission.

I first started out with a good nutritional diet

and keep myself very

alkaline. Cancer can only thrive in an acidic

environment. In

addressing my tumors, I decide to opt for the use

of a drawing salve

(black salve), in my case, Cansema. I documented

in every detail,

along with hundreds of pictures, the two years I

used the salve to

draw out tumors. Some of the tumors were as big as

½ too ¾ inches in

diameter. The problem with this method, was that

the tumors were

producing faster than I could keep up with. In my

research, this

possibly was brought on by edema which was cause

by the

aggressiveness of the salve.

So I knew I was going to have to make some

adjustments. One year into

my battle, the spring of 2004, I added to my

therapy Wobenzym N from

Mucos Pharma in Germany

and approved for sale in the US.

This is a

superb product that I still use to this day.

Enzyme therapy is very

important in any disease or prevention of disease.

I started out on

60 pills a day to as little as 30 a day. I was introduced

to two

different kinesiologist. One in Kentucky

and one in Michigan,

both

who monitoring me the past two and a half years.

It is with their

help, I was able to know how much Wobenzym N and

other necessary

supplements I need to take as well as what was

effective and what was

not. They also monitored my diet as well.

As well as all this was working for me, I still

had flair ups in my

cancer activity every time my immune system was

compromised and I got

real ill. So I decided that I needed to research

more and look for

something else that would enhance my immune system

to keep this

cancer in remission. Then a friend of mine told me

about being put on

low dose naltrexone for his non-Hodgkin's lymphoma

in January of this

year (2005). He knew very little about this

product. So I started to

do my home work. I found the Low Dose Naltrexone

website and after

reading about the women's experience in France that had

three month s

to live due to melanoma that had spread to the

brain, and lived for

twelve years afterward until she stopped taking

LDN, I said this is

the product I want to take.

I went to three doctors that I have known for some

years, and no

would write me the prescription. Their excuse was

that it was not FDA

approved for that use. I reminded them of other

drugs that they

prescribed for other uses beyond would the FDA had

approved them for,

but that did not convince them. One even wanted me

to have surgery. I

knew better or they were not well educated that

surgery is to late

for stage IV melanoma.

I ended up having to be paired with a doctor in Ohio who is on LDN

for MS to get my prescription. Once I received the

LDN I had my

kinesiologist test me. In testing my endorphin

level, it was only at

10%. Testing with LDN, I was not responding due to

a malabsorption

problem. I suggested that we try D-5 Extra along

with the LDN. When

tested, my endorphin level went to 90%. I could

absorb the

naltrexone

I started the low dose naltrexone in March of

2005. Prior to getting

on LDN, I contacted a serious upper respiratory

infection that caused

my cancer activity to flair up 60%. My lymph nodes

swelled as well.

After starting on the LDN in March, I again, in

April, contacted a

serious upper respiratory infection, but this time

my cancer activity

did not flair up! That told me it was working.

My report from my kinesiologist this week, Oct 18,

2005, was that

even though I still had my cancer, it was not

active. The naltrexone

was keeping it under control. She was amazed

herself.

So I even though I am on naltrexone, I still watch

my diet. I think

that this is very important when fighting any

disease that naltrexone

is being used for. It can do no more than help

enhance the

effectiveness of the drug.

As far as it keeping me awake at night, I do not

have that problem

because I also take 3 mg of Melatonin at bedtime.

It is important

that one is in a good, deep sleep when taking LDN,

Light of any kind

can disrupt the sleep pattern. Therefore the

bedroom should be pitch

black at night or at least wear a sleeping mask.

Today, I am thankful to God for giving me the

wisdom and insight to

educate myself on how to manage my cancer. And I

am also thankful for

Dr. Bahari for his dedication to the research of

LDN, which in my

opinion, could be one of the most valuable, life

saving and life

enhancing drugs every discovered that even someone

going the

alternative, natural route, would not even think

twice about before

taking it.

Tom Armstrong

>

> Hello Jorn,

>

> There's a lot to be said for LDN. So

far though I haven't seen

much to

> indicate that it can deal with Stage IV

Melanoma rapidly enough to

save someone

> whose brain, spine, and possibly liver are

invaded. If I had a

loved one with

> a similar condition Here's what I would do:

>

> Go to _www.cancertutor.com_ (http://www.cancertutor.com)

imediately and

> make contact with Webster, the author of the

site.

>

> Describe your son's condition to him along

with his treatment

history. Ask

> Webster if he knows of an aggressive and

effective protocol for

such an

> advanced condition. Webster will

respond quickly...sometimes

instantly. The site

> isn't commercialized at all.

>

> There is a therapy at the site that's very

rapid in terms of

destroying

> cancer cells. There'll be plenty of

detoxification needed to rid

the body of all

> the killed cancer cells, and that

should begin right along with

whatever

> protocol you choose....from Webster or

Bihari or anyone.

>

> Find Stage IV Protocols on the site (it's

easy to navigate) and

realize that

> Cesium has been used successfully for decades

in the treatment of

cancer.

> It's safe because people who use it follow

the instructions

carefully and with

> expert guidance from the author of the site,

if requested. The

main

> consideration is keeping the body's

minerals balanced. This is

done with the

> Potassium that is part of the Protocol

and with a blood screening

every two weeks.

> Webster is adamant in his instructions

for following the protocols

on the

> site.

>

> The protocol calls for Cesium &

Potassium, with Liquid DMSO acting

as the

> carrier of the minerals...whenever there is

brain involvement.

The DMSO binds

> with the minerals, then crosses the

Blood/Brain barrier with the

cancer

> killing minerals. Right now the

cancer cells are in an extremely

acidic state.

> The Cesium is very alkaline.

Cancer does not survive in a high

alkaline

> environment. OK...that addresses

the growth in the brain.

>

> If my child's spine was involved I'd wonder

is the bone structure

is

> invaded. If not, how would we get rid

of the growth before it

does take over the

> spine bones. Imagine the sudden loss of

spine stability if there

is bone

> invasion and those cancer cells are

killed. There could a be a

collapse causing

> spinal cord impingment...resulting in

paralysis from that point

downward.

>

> If the spine bones are temporarliy safe from

invasion, and the

tumor is

> small and not significantly impinging on

vital nerves, I'd get

Cesium to do the

> job on that tumor, as soon as possible!!

>

> If the spine bones are invaded with the

cancer cells...I'd want a

surgeon to

> screw some rods to healthy spine bones which

would bridge the

affected

> joints and bones. Even as the surgery

is being planned and

scheduled I'd have my

> son on the Cesium Protocol.

Immediately after the surgery, I'd

have my son

> on the Cesium.

>

> The question of whether Radiation Therapy is

a right course of

action for

> the spine tumor is something I'd have to

look at after I got a

fresh PET Scan

> for my son. They can hit a tumor

with a pretty narrow beam of

Radiation these

> days. Obviously, if there's bone

invasion, no Radiation could be

given

> without the above surgery. Radiation is

an unpleasant

thought...but...

>

> If the spine tumor is large, but not in the

bones, I'd consider

surgical

> removal if that seemed at all possible.

If surgical removal is not

an option,

> and the fear is that bone invasion and/or

paralysis is imminent, I

might give

> serious consideration to the Radiation

Therapy to quickly shrink

the tumor.

> The Cesium Protocol would commence

immediately after the

Radiation, and with

> great emphasis on Detoxing the

bloodstream before the onset of

Toxemia.

>

> Now for the liver invasion. I'd get the

Cesium into his

bloodstream ASAP if

> the liver is to be saved. The liver

does have amazing

regenerative powers

> of it's own. so l'd be praying that the

invasion is superficial at

present

> time.

>

> We know the cancer tumors are symptoms of a

process within the

body.

> Before, during, and after the Cesium, or

whatever therapy is used,

I would be

> giving my son " therapeutic " doses

of the best known and most

effective immune

> boosters and other recommended supplements

that I've seen on the

CancerTutor

> site, and elsewhere. The Cesium

Protocol will be successful for

my son, and the

> immune systet has to be restarted and

maintained. We have to get

started

> with the Cesium before any organs are

too deeply invaded.

>

> I am researching the feasibility of LDN and

Cesium therapies being

> administered together. If I had to

choose whether to use one or

the other...for any

> Stage IV cancer...It would be Cesium

every time. It's fast...it's

safe. It's

> been around quite a while. It's

being used in foreign countries

by US

> medical doctors who fled under pressure

from the FDA federalies.

>

> The longer any therapy takes (like perhaps

LDN alone)...the more

time the

> cancer has to destroy vital organs.

Chemotherapy for my son at

this stage

> would be unthinkable and

unconscienable. To undertake LDN Therapy

alone could

> lead to a page on a statisical chart at

LDN headquarters if the

LDN doesn't act

> quickly enough to save organs and

spinal bones. There's plenty of

> verifiable proof of Cesium's efficacy

as a fast acting cancer

therapy. An added bonus

> is that all cancer pain is amelioriated

in 1-3 days. LDN,

unfortunatley,

> doesn't allow for heavy doses of pain

meds. If my son had any

Stage cancer, I

> would be talking to Cancer treatment

experts, not a moderator of a

forum that

> deals primarily with MS.

>

[Guest guest]

I would also like to suggest taking chlorophyl to

balance PH levels.

Cheers

Elio

--- " Bruce Guilmette, Ph.D. " <bruce@...>

wrote:

> Might I suggest juicing beets? 10 oz per day of

> beet juice will raise Ph

> unlike any other food out there. Also, a good slice

> of watermelon daily

> will help maintain Ph. When I was first diagnosed

> with terminal cancer a

> year ago, my ph level was around 4. It took 4 weeks

> to get it to 5+ and

> another 4 weeks to get it between 6.5 and 7 fairly

> consistently. Urine Ph

> will follow saliva ph with about a 3 hour lag and

> generally .3 lower, but

> that is OK.

>

>

>

> Regards,

>

> Bruce Guilmette, Ph.D.

>

> Survive Cancer Foundation, Inc.

>

> http://www.survivecancer.net

> <http://www.survivecancer.net/>

>

> But the fruit of the Spirit is love, joy, peace,

> patience, kindness,

> goodness, faithfulness, gentleness and self-control.

> Against such things

> there is no law. Galatians 5:22-23 NIV

>

>

>

>

>

> _____

>

> From: low dose naltrexone

> [mailto:low dose naltrexone ] On Behalf

> Of Marilyn Sawyer

> Sent: Saturday, October 22, 2005 5:30 PM

> low dose naltrexone

> Subject: Re: [low dose naltrexone] An allakine diet

>

>

>

> Does honey turn to acid?

>

>

>

>

>

> [low dose naltrexone] Re: Questions from

> Potential LDN user with

> Melanoma/O...

>

>

> My Personal Experience With Low Dose Naltrexone and

> Cancer

>

> My Name is Tom and my screen name is TomOnLDN. I

> will be in my third

> year of Stage IV malignant melanoma which had

> metastasized to the

> lymph glands in my neck, shoulders and under my

> arms. CT's confirmed

> that it had metastasized to the lymph's under my jaw

> on the left side

> and around the spine at the back of my neck. The

> lymph node under my

> jaw is swollen the size of an unshelled walnut.

>

> Research on the internet in areas that the medical

> profession use

> educated me to the fact that when there are tumors

> with the melanoma;

> they are larger than 1/16th inch in diameter and the

> cancer has

> spread to the lymphatic system, it is in stage IV

> and convention

>

=== message truncated ===

__________________________________________________________

Find your next car at http://autos..ca

[Guest guest]

Thank you, Bruce - I will try it.

[low dose naltrexone] Re: Questions from Potential LDN user with Melanoma/O...My Personal Experience With Low Dose Naltrexone and CancerMy Name is Tom and my screen name is TomOnLDN. I will be in my thirdyear of Stage IV malignant melanoma which had metastasized to thelymph glands in my neck, shoulders and under my arms. CT's confirmedthat it had metastasized to the lymph's under my jaw on the left sideand around the spine at the back of my neck. The lymph node under myjaw is swollen the size of an unshelled walnut.Research on the internet in areas that the medical profession useeducated me to the fact that when there are tumors with the melanoma;they are larger than 1/16th inch in diameter and the cancer hasspread to the lymphatic system, it is in stage IV and conventiontreatments with chemo and radiation are no longer effective. In otherwords, it is to late by their thinking.Two weeks prior to finding I had stage IV melanoma, I also hadsquamous cell carcinoma which started on the top of my forehead andspread to and around my eye, into the sinus cavity and towards mymouth.So under my circumstances, I opted to go 100% natural. So I set outresearching cancer for the past three years. I my research, I camethe conclusion, especially from the methods I have been using, thatcancer and other diseases can not be necessarily cure, but managed tohelp keep in remission.I first started out with a good nutritional diet and keep myself veryalkaline. Cancer can only thrive in an acidic environment. Inaddressing my tumors, I decide to opt for the use of a drawing salve(black salve), in my case, Cansema. I documented in every detail,along with hundreds of pictures, the two years I used the salve todraw out tumors. Some of the tumors were as big as ½ too ¾ inches indiameter. The problem with this method, was that the tumors wereproducing faster than I could keep up with. In my research, thispossibly was brought on by edema which was cause by theaggressiveness of the salve.So I knew I was going to have to make some adjustments. One year intomy battle, the spring of 2004, I added to my therapy Wobenzym N fromMucos Pharma in Germany and approved for sale in the US. This is asuperb product that I still use to this day. Enzyme therapy is veryimportant in any disease or prevention of disease. I started out on60 pills a day to as little as 30 a day. I was introduced to twodifferent kinesiologist. One in Kentucky and one in Michigan, bothwho monitoring me the past two and a half years. It is with theirhelp, I was able to know how much Wobenzym N and other necessarysupplements I need to take as well as what was effective and what wasnot. They also monitored my diet as well.As well as all this was working for me, I still had flair ups in mycancer activity every time my immune system was compromised and I gotreal ill. So I decided that I needed to research more and look forsomething else that would enhance my immune system to keep thiscancer in remission. Then a friend of mine told me about being put onlow dose naltrexone for his non-Hodgkin's lymphoma in January of thisyear (2005). He knew very little about this product. So I started todo my home work. I found the Low Dose Naltrexone website and afterreading about the women's experience in France that had three month sto live due to melanoma that had spread to the brain, and lived fortwelve years afterward until she stopped taking LDN, I said this isthe product I want to take.I went to three doctors that I have known for some years, and nowould write me the prescription. Their excuse was that it was not FDAapproved for that use. I reminded them of other drugs that theyprescribed for other uses beyond would the FDA had approved them for,but that did not convince them. One even wanted me to have surgery. Iknew better or they were not well educated that surgery is to latefor stage IV melanoma.I ended up having to be paired with a doctor in Ohio who is on LDNfor MS to get my prescription. Once I received the LDN I had mykinesiologist test me. In testing my endorphin level, it was only at10%. Testing with LDN, I was not responding due to a malabsorptionproblem. I suggested that we try D-5 Extra along with the LDN. Whentested, my endorphin level went to 90%. I could absorb thenaltrexoneI started the low dose naltrexone in March of 2005. Prior to gettingon LDN, I contacted a serious upper respiratory infection that causedmy cancer activity to flair up 60%. My lymph nodes swelled as well.After starting on the LDN in March, I again, in April, contacted aserious upper respiratory infection, but this time my cancer activitydid not flair up! That told me it was working.My report from my kinesiologist this week, Oct 18, 2005, was thateven though I still had my cancer, it was not active. The naltrexonewas keeping it under control. She was amazed herself.So I even though I am on naltrexone, I still watch my diet. I thinkthat this is very important when fighting any disease that naltrexoneis being used for. It can do no more than help enhance theeffectiveness of the drug.As far as it keeping me awake at night, I do not have that problembecause I also take 3 mg of Melatonin at bedtime. It is importantthat one is in a good, deep sleep when taking LDN, Light of any kindcan disrupt the sleep pattern. Therefore the bedroom should be pitchblack at night or at least wear a sleeping mask.Today, I am thankful to God for giving me the wisdom and insight toeducate myself on how to manage my cancer. And I am also thankful forDr. Bahari for his dedication to the research of LDN, which in myopinion, could be one of the most valuable, life saving and lifeenhancing drugs every discovered that even someone going thealternative, natural route, would not even think twice about beforetaking it.Tom Armstrong>> Hello Jorn,>> There's a lot to be said for LDN. So far though I haven't seenmuch to> indicate that it can deal with Stage IV Melanoma rapidly enough tosave someone> whose brain, spine, and possibly liver are invaded. If I had aloved one with> a similar condition Here's what I would do:>> Go to _www.cancertutor.com_ (http://www.cancertutor.com)imediately and> make contact with Webster, the author of the site.>> Describe your son's condition to him along with his treatmenthistory. Ask> Webster if he knows of an aggressive and effective protocol forsuch an> advanced condition. Webster will respond quickly...sometimesinstantly. The site> isn't commercialized at all.>> There is a therapy at the site that's very rapid in terms ofdestroying> cancer cells. There'll be plenty of detoxification needed to ridthe body of all> the killed cancer cells, and that should begin right along withwhatever> protocol you choose....from Webster or Bihari or anyone.>> Find Stage IV Protocols on the site (it's easy to navigate) andrealize that> Cesium has been used successfully for decades in the treatment ofcancer.> It's safe because people who use it follow the instructionscarefully and with> expert guidance from the author of the site, if requested. Themain> consideration is keeping the body's minerals balanced. This isdone with the> Potassium that is part of the Protocol and with a blood screeningevery two weeks.> Webster is adamant in his instructions for following the protocolson the> site.>> The protocol calls for Cesium & Potassium, with Liquid DMSO actingas the> carrier of the minerals...whenever there is brain involvement.The DMSO binds> with the minerals, then crosses the Blood/Brain barrier with thecancer> killing minerals. Right now the cancer cells are in an extremelyacidic state.> The Cesium is very alkaline. Cancer does not survive in a highalkaline> environment. OK...that addresses the growth in the brain.>> If my child's spine was involved I'd wonder is the bone structureis> invaded. If not, how would we get rid of the growth before itdoes take over the> spine bones. Imagine the sudden loss of spine stability if thereis bone> invasion and those cancer cells are killed. There could a be acollapse causing> spinal cord impingment...resulting in paralysis from that pointdownward.>> If the spine bones are temporarliy safe from invasion, and thetumor is> small and not significantly impinging on vital nerves, I'd getCesium to do the> job on that tumor, as soon as possible!!>> If the spine bones are invaded with the cancer cells...I'd want asurgeon to> screw some rods to healthy spine bones which would bridge theaffected> joints and bones. Even as the surgery is being planned andscheduled I'd have my> son on the Cesium Protocol. Immediately after the surgery, I'dhave my son> on the Cesium.>> The question of whether Radiation Therapy is a right course ofaction for> the spine tumor is something I'd have to look at after I got afresh PET Scan> for my son. They can hit a tumor with a pretty narrow beam ofRadiation these> days. Obviously, if there's bone invasion, no Radiation could begiven> without the above surgery. Radiation is an unpleasantthought...but...>> If the spine tumor is large, but not in the bones, I'd considersurgical> removal if that seemed at all possible. If surgical removal is notan option,> and the fear is that bone invasion and/or paralysis is imminent, Imight give> serious consideration to the Radiation Therapy to quickly shrinkthe tumor.> The Cesium Protocol would commence immediately after theRadiation, and with> great emphasis on Detoxing the bloodstream before the onset ofToxemia.>> Now for the liver invasion. I'd get the Cesium into hisbloodstream ASAP if> the liver is to be saved. The liver does have amazingregenerative powers> of it's own. so l'd be praying that the invasion is superficial atpresent> time.>> We know the cancer tumors are symptoms of a process within thebody.> Before, during, and after the Cesium, or whatever therapy is used,I would be> giving my son "therapeutic" doses of the best known and mosteffective immune> boosters and other recommended supplements that I've seen on theCancerTutor> site, and elsewhere. The Cesium Protocol will be successful formy son, and the> immune systet has to be restarted and maintained. We have to getstarted> with the Cesium before any organs are too deeply invaded.>> I am researching the feasibility of LDN and Cesium therapies being> administered together. If I had to choose whether to use one orthe other...for any> Stage IV cancer...It would be Cesium every time. It's fast...it'ssafe. It's> been around quite a while. It's being used in foreign countriesby US> medical doctors who fled under pressure from the FDA federalies.>> The longer any therapy takes (like perhaps LDN alone)...the moretime the> cancer has to destroy vital organs. Chemotherapy for my son atthis stage> would be unthinkable and unconscienable. To undertake LDN Therapyalone could> lead to a page on a statisical chart at LDN headquarters if theLDN doesn't act> quickly enough to save organs and spinal bones. There's plenty of> verifiable proof of Cesium's efficacy as a fast acting cancertherapy. An added bonus> is that all cancer pain is amelioriated in 1-3 days. LDN,unfortunatley,> doesn't allow for heavy doses of pain meds. If my son had anyStage cancer, I> would be talking to Cancer treatment experts, not a moderator of aforum that> deals primarily with MS.>

[Guest guest]

This is a link to the chart ..

http://www.thewolfeclinic.com/acidalkfoods.html