Guest guest Posted August 19, 2002 Report Share Posted August 19, 2002 I suffered from Lymes for twelve years before diag. My gastrointestinal system shut down. I got myself up and going all natural. The abx make me much worse and I can not physically or mentally function. It is not due solely to herx. but mostly to the affect of abx on my body. I use abx on my daughters who got Lymes from me at birth. Yet when they do what they can on my regime they notice immediate improvement. It is not easy, yet it is good. My diagnosis: Lymes, Babesia, Toxoplasmosis, Cat Scratch Fever, Batonella. I drank from a well that had a seriously ill kitten in it, 1989 third trimester pregnant. Reinfected 1999 with tick bite in Jan, EM rash 7 inches over 7 days. My Regime 1. Cayenne Pepper for heat: buy the hottest you can get and work up to 1 tsp, in a shot of water 3x daily. 2. Homozon, internal oxygen: Purchase at azure.com, detoxes the kidney, liver and colon, adds intestinal flora and magnesium. non-toxic. Amazing stuff. 3. Food Grade Hydrogen Peroxide: I work up to eleven drops in a glass of water this adds oxygen to the body. I also wash my fruits and veggies in this, it oxygenates them and kills parasites to prevent reinfection. Warning! This must be diluted or it will burn you. Use knowledgeably. 4. Vit. C, crystallized; A pure form of Vit.C. To find your Vit. C tolerance level, start by taking doses until you get diarrhea, then cut back 500mg. This is your Vit. C tolerance level. Some people can only take about 3000 mg. I can take 12000mg. It is occasionally good to do a Vit. Flush. That is to take vit. C until you flush your body with some Diarrhea. 5. I take a high quality green drink everyday. 6. I am low on B12 levels and need shots. 7. I eat lots and lots of raw fruits and veggies and sprouts. These have great power to reverse the disease process. I balance my diet with whole foods, low protein, yet far from no protein. 8. Long periods of fruit and veggies juice fastings. I have done up to 40 days. 9. Extensive exercise. Biking is easy on the joints, gives you sunshine, deep breathing, fresh air and uplifts you spirits. I bike at dawn and at dusk. I also lift weights as I am able. 10. Somedays it is all to hard and I hold on to the post that said, just put one foot in front of the other, and that seems hard to do. On these days I force my self to get sunshine and during long winters I found a tanning bed (in moderation) to be helpful.. Somedays are very bad. This is my sign for fasting time. Usually within a day of fasting I show improvements. For the most part I am very enlighten and well. I fall back under stress. Blessings, Bernadette Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 8, 2005 Report Share Posted March 8, 2005 I suspect that I have chronic neuroborreliosis. I have been treating myself with my regime ( Noble's Regime) almost continuously for the last 3 years. My regime (see below) improves my symptoms tremendously, especially my brain fog – I get virtually no brain fog now. But I still get a substantial amount of aching/'burning' in my body. The soya isoflavones supplement ( a soy bean extract) that is in my regime contains genistein (an MMP-9 inhibitor, I think- this is the key action of the genistein, I think). I suspect that this soya isoflavones supplement also contains phosphatidyl serine( contained in soy beans) because my regime still works if I substitute the soya isoflavones that is in my regime with green tea (another MMP-9 inhibitor, I think) + phosphatidyl serine supplement but stops working if I substitute the soya isoflavones with green tea (another MMP-9 inhibitor, I think) only OR with phosphatidyl serine supplement only. I understand that phosphatidyl serine helps to protect neural tissues ( but not other body tissues ) from damage; I suspect that the phosphatidyl serine is helping to reduce damage to my neural tissues that is caused by Bb. It may correct to describe the action of the phosphatidyl serine in my body as `phospolipid-exchange therapy for the brain'. See Kane's Protocol. In Kane's Protocol( I think that this protocol has many similar actions to my regime) a sister compound to phosphatidyl serine, phosphatidylcholine, acts as `phospolipid-exchange therapy for the whole body', right? I understand that phosphatidylcholine helps to protect all body tissues from damage. So, my plan is to try substituting the soy isoflavones in my regime with phosphatidylcholine(`phospolipid-exchange therapy for the whole body?') + green tea(an MMP-9 inhibitor, I think) to see if it makes my regime work better still. For a start I am hoping that doing this will reduce the aching/'burning' I am getting in my body. Interestingly, ginkgo biloba( in my regime) and green tea are both supplements that have been recommended for LD by Dr. Burrascano in the past. Regards, Noble. Noble's Regime: a good treament for chronic neuroborreliosis? Every 3 hours or so, I take oral antibiotic: 250mg tetracycline or 500mg amoxicillin; + 300mg. of Holland & Barrett own brand Soya Isoflavones ( contains genistein, an MMP-9 inhibitor, I think ) ( ~1/3 of a capsule ) + 200mg. of Good'N Natuaral ( Holland & Barrett own brand )Feverfew ( a phospholipase A2 inhibitor & a TNF inhibitor. Can lower IL-6, I think. ) ( ~ 1/2 of a capsule) + 30mg. of Holland & Barrett own brand Ginkgo Biloba Standardized Extract ( Can lower IL-1B, I think ) + 8mg. of DHEA ( an immunomodulator. Can lower IL-6, I think )( a ~1/3 of a 25mg. tablet. ) + 1/2mg. of melatonin ( a 1/2 of a 1mg. tablet ) If I treat myself with the oral antibiotics ( amoxicillin, or tetracycline ) only, my symptoms do improve quite a lot for sure. It is just that my symptoms improve considerably more still if I put myself on my regime, which is the oral antibiotics + all the 5 supplements that are in my regime ( they are soy isoflavones, feverfew, ginkgo biloba, DHEA & melatonin ); but if I treat myself with the oral antibiotics + only 1,2,3 or 4 of the 5 supplements in my regime, the improvement in my symptoms that I get is at most only marginally more than the improvement in my symptoms that I get if I treat myself with the oral antibiotics only. I think that the chronic neuroborreliosis sufferer may get an autoimmune responses that is too strong. I think these autoimmune responses may cause hypercoagulation and anti-phospholipid syndrome and the like, which may lead to brain fog and abnormal VCS results ( due to reduced blood flow to the eyes ). As I have said, I suspect that I have chronic neuroborreliosis; I suspect that Bb is making my autoimmune response too strong and is disregulating my pro- inflammatory immune response. I strongly suspect that my regime can dampen down the autoimmune response and regulate the pro-inflammatory immune response; I suspect that my regime reduces hypercoagulation, brain fog etc - and that's why it improves my symptoms. I think my regime might improve the symptoms of some other suspected chronic neuroborreliosis/chronic neuroborreliosis sufferers for the same reasons if it they were to take my regime. What I suspect is that Bb 'toxins' (which may just be antigen complexes(e.g. 83kda?) containing OspB(phospholipase A2?) and OspA (binds plasminogen (which I suspect activates MMP-9)) that host antibodies are unable to bind to and to neutralise) CAUSE hypercoagulation, and therefore restricted blood flow, in chronic neuroborreliosis sufferers. And I think that if this restricted blood flow occurs in the eyes, it could explain the the abnormal VCS test results. I understand that Dr. Shoemaker also thinks that restricted blood flow in the eyes may be the cause of the abnormal VCS test results. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 8, 2005 Report Share Posted March 8, 2005 You might want to look into Nattokinase to disolve the fibrin if you suspect that hypercoagulation is a problem for you. If fibrin is a problem, meds will be better aborbed if you remove the fibrin. Might be the kick you need to get rid of aching in your body. http://cure2003.conforums.com/index.cgi? board=enzymes & action=display & num=1110295340 > > I suspect that I have chronic neuroborreliosis. I have been treating > myself with my regime ( Noble's Regime) almost continuously > for the last 3 years. My regime (see below) improves my symptoms > tremendously, especially my brain fog – I get virtually no brain fog > now. But I still get a substantial amount of aching/'burning' in my > body. > > The soya isoflavones supplement ( a soy bean extract) that is in my > regime contains genistein (an MMP-9 inhibitor, I think- this is the > key action of the genistein, I think). I suspect that this soya > isoflavones supplement also contains phosphatidyl serine( contained > in soy beans) because my regime still works if I substitute the soya > isoflavones that is in my regime with green tea (another MMP-9 > inhibitor, I think) + phosphatidyl serine supplement but stops > working if I substitute the soya isoflavones with green tea > (another MMP-9 inhibitor, I think) only OR with phosphatidyl serine > supplement only. > > I understand that phosphatidyl serine helps to protect neural > tissues ( but not other body tissues ) from damage; I suspect that > the phosphatidyl serine is helping to reduce damage to my neural > tissues that is caused by Bb. It may correct to describe the action > of the phosphatidyl serine in my body as `phospolipid-exchange > therapy for the brain'. See Kane's Protocol. In Kane's Protocol( I > think that this protocol has many similar actions to my regime) a > sister compound to phosphatidyl serine, phosphatidylcholine, acts > as `phospolipid-exchange therapy for the whole body', right? I > understand that phosphatidylcholine helps to protect all body > tissues from damage. > > So, my plan is to try substituting the soy isoflavones in my > regime with phosphatidylcholine(`phospolipid-exchange therapy for > the whole body?') + green tea(an MMP-9 inhibitor, I think) to see if > it makes my regime work better still. For a start I am hoping that > doing this will reduce the aching/'burning' I am getting in my body. > Interestingly, ginkgo biloba( in my regime) and green tea are both > supplements that have been recommended for LD by Dr. Burrascano in > the past. > > Regards, > > Noble. > > > Noble's Regime: a good treament for chronic neuroborreliosis? > > Every 3 hours or so, I take > > oral antibiotic: 250mg tetracycline or 500mg amoxicillin; > > > + > > 300mg. of Holland & Barrett own brand Soya Isoflavones > ( contains genistein, an MMP-9 inhibitor, I think ) ( ~1/3 of a > capsule ) + > > 200mg. of Good'N Natuaral ( Holland & Barrett own > brand )Feverfew ( a phospholipase A2 inhibitor & a TNF > inhibitor. Can lower IL-6, I think. ) ( ~ 1/2 of a capsule) + > > 30mg. of Holland & Barrett own brand Ginkgo Biloba > Standardized Extract ( Can lower IL-1B, I think ) + > > 8mg. of DHEA ( an immunomodulator. Can lower IL-6, I think )( a ~1/3 > of a 25mg. > tablet. ) + > > 1/2mg. of melatonin ( a 1/2 of a 1mg. tablet ) > > If I treat myself with the oral antibiotics ( amoxicillin, or > tetracycline ) only, my symptoms do improve quite a lot for sure. It > is just that my symptoms improve considerably more still if I put > myself on my regime, which is the oral antibiotics + all the 5 > supplements that are in my regime ( they are soy isoflavones, > feverfew, ginkgo biloba, DHEA & melatonin ); but if I treat myself > with the oral antibiotics + only 1,2,3 or 4 of the 5 supplements in > my regime, the improvement in my symptoms that I get is at most only > marginally more than the improvement in my symptoms that I get if I > treat myself with the oral antibiotics only. > > I think that the chronic neuroborreliosis sufferer may get an > autoimmune responses that is too strong. I think these autoimmune > responses may cause hypercoagulation and anti-phospholipid syndrome > and the like, which may lead to brain fog and abnormal VCS results ( > due to reduced blood flow to the eyes ). As I have said, I suspect > that I have chronic neuroborreliosis; I suspect that Bb is making my > autoimmune response too strong and is disregulating my pro- > inflammatory immune response. > > I strongly suspect that my regime can dampen down the autoimmune > response and regulate the pro-inflammatory immune response; I > suspect that my regime reduces hypercoagulation, brain fog etc - and > that's why it improves my symptoms. I think my regime might improve > the symptoms of some other suspected chronic > neuroborreliosis/chronic neuroborreliosis sufferers for the same > reasons if it they were to take my regime. > > > What I suspect is that Bb 'toxins' (which may just be antigen > complexes(e.g. 83kda?) containing OspB(phospholipase A2?) and OspA > (binds plasminogen (which I suspect activates MMP-9)) that host > antibodies are unable to bind to and to neutralise) CAUSE > hypercoagulation, and therefore restricted blood flow, in chronic > neuroborreliosis sufferers. > > And I think that if this restricted blood flow occurs in the eyes, it > could explain the the abnormal VCS test results. I understand that > Dr. Shoemaker also thinks that restricted blood flow in the eyes may > be the cause of the abnormal VCS test results. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 10, 2005 Report Share Posted March 10, 2005 Yes, I have been meaning to try Nattokinase. Thanks. > > > > I suspect that I have chronic neuroborreliosis. I have been > treating > > myself with my regime ( Noble's Regime) almost continuously > > for the last 3 years. My regime (see below) improves my symptoms > > tremendously, especially my brain fog – I get virtually no brain > fog > > now. But I still get a substantial amount of aching/'burning' in > my > > body. > > > > The soya isoflavones supplement ( a soy bean extract) that is in > my > > regime contains genistein (an MMP-9 inhibitor, I think- this is > the > > key action of the genistein, I think). I suspect that this soya > > isoflavones supplement also contains phosphatidyl serine( > contained > > in soy beans) because my regime still works if I substitute the > soya > > isoflavones that is in my regime with green tea (another MMP-9 > > inhibitor, I think) + phosphatidyl serine supplement but stops > > working if I substitute the soya isoflavones with green tea > > (another MMP-9 inhibitor, I think) only OR with phosphatidyl > serine > > supplement only. > > > > I understand that phosphatidyl serine helps to protect neural > > tissues ( but not other body tissues ) from damage; I suspect that > > the phosphatidyl serine is helping to reduce damage to my neural > > tissues that is caused by Bb. It may correct to describe the > action > > of the phosphatidyl serine in my body as `phospolipid-exchange > > therapy for the brain'. See Kane's Protocol. In Kane's Protocol( I > > think that this protocol has many similar actions to my regime) a > > sister compound to phosphatidyl serine, phosphatidylcholine, acts > > as `phospolipid-exchange therapy for the whole body', right? I > > understand that phosphatidylcholine helps to protect all body > > tissues from damage. > > > > So, my plan is to try substituting the soy isoflavones in my > > regime with phosphatidylcholine(`phospolipid-exchange therapy for > > the whole body?') + green tea(an MMP-9 inhibitor, I think) to see > if > > it makes my regime work better still. For a start I am hoping that > > doing this will reduce the aching/'burning' I am getting in my > body. > > Interestingly, ginkgo biloba( in my regime) and green tea are both > > supplements that have been recommended for LD by Dr. Burrascano in > > the past. > > > > Regards, > > > > Noble. > > > > > > Noble's Regime: a good treament for chronic > neuroborreliosis? > > > > Every 3 hours or so, I take > > > > oral antibiotic: 250mg tetracycline or 500mg amoxicillin; > > > > > > + > > > > 300mg. of Holland & Barrett own brand Soya Isoflavones > > ( contains genistein, an MMP-9 inhibitor, I think ) ( ~1/3 of a > > capsule ) + > > > > 200mg. of Good'N Natuaral ( Holland & Barrett own > > brand )Feverfew ( a phospholipase A2 inhibitor & a TNF > > inhibitor. Can lower IL-6, I think. ) ( ~ 1/2 of a capsule) + > > > > 30mg. of Holland & Barrett own brand Ginkgo Biloba > > Standardized Extract ( Can lower IL-1B, I think ) + > > > > 8mg. of DHEA ( an immunomodulator. Can lower IL-6, I think )( a > ~1/3 > > of a 25mg. > > tablet. ) + > > > > 1/2mg. of melatonin ( a 1/2 of a 1mg. tablet ) > > > > If I treat myself with the oral antibiotics ( amoxicillin, or > > tetracycline ) only, my symptoms do improve quite a lot for sure. > It > > is just that my symptoms improve considerably more still if I put > > myself on my regime, which is the oral antibiotics + all the 5 > > supplements that are in my regime ( they are soy isoflavones, > > feverfew, ginkgo biloba, DHEA & melatonin ); but if I treat myself > > with the oral antibiotics + only 1,2,3 or 4 of the 5 supplements > in > > my regime, the improvement in my symptoms that I get is at most > only > > marginally more than the improvement in my symptoms that I get if > I > > treat myself with the oral antibiotics only. > > > > I think that the chronic neuroborreliosis sufferer may get an > > autoimmune responses that is too strong. I think these autoimmune > > responses may cause hypercoagulation and anti-phospholipid syndrome > > and the like, which may lead to brain fog and abnormal VCS results > ( > > due to reduced blood flow to the eyes ). As I have said, I suspect > > that I have chronic neuroborreliosis; I suspect that Bb is making > my > > autoimmune response too strong and is disregulating my pro- > > inflammatory immune response. > > > > I strongly suspect that my regime can dampen down the autoimmune > > response and regulate the pro-inflammatory immune response; I > > suspect that my regime reduces hypercoagulation, brain fog etc - > and > > that's why it improves my symptoms. I think my regime might > improve > > the symptoms of some other suspected chronic > > neuroborreliosis/chronic neuroborreliosis sufferers for the same > > reasons if it they were to take my regime. > > > > > > What I suspect is that Bb 'toxins' (which may just be antigen > > complexes(e.g. 83kda?) containing OspB(phospholipase A2?) and OspA > > (binds plasminogen (which I suspect activates MMP-9)) that host > > antibodies are unable to bind to and to neutralise) CAUSE > > hypercoagulation, and therefore restricted blood flow, in chronic > > neuroborreliosis sufferers. > > > > And I think that if this restricted blood flow occurs in the eyes, > it > > could explain the the abnormal VCS test results. I understand that > > Dr. Shoemaker also thinks that restricted blood flow in the eyes > may > > be the cause of the abnormal VCS test results. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 11, 2005 Report Share Posted March 11, 2005 Once I started treating the endocrine malfunctions, mainly after I started taking ACTH shots, my blood started looking fantastic. It was amazing...Not thw whole picture I'm sure. I have also been looking into Nattokinase and also something I had never heard of before called Nat Cell http://www.Hepatitis Cfree.com/natMe.htm also www.natcellsuperstore.com yes, very expensive because it is sent in the frozen state. It really makes you think about the pills we take though, I heard this is what the athelites take or those who have money to burn.I'm specifically looking into the NatCell Mesenchyme -. Sometimes I get scared and think my children will say that I didn't try hard enough. I will go and read more of your words now. regards Peg Quote Link to comment Share on other sites More sharing options...
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