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DMAE and PABA
An Alternative to Gerovital (GH3), the Romanian Youth Drug
By Ward Dean, MD
In Romania, Gerovital, or GH3, has been used for over 50 years to help people look and feel younger. It has attracted thousands of people each year to the spas of Romania and Western Europe where this therapy has been widely used. GH3 is a modification of the local anesthetic, procaine. It was developed for anti-aging uses by Professor Ana Aslan in Romania in the 1940s (Fig. 1). The discovery of procaines potential anti-aging properties was a serendipitous finding. Prof. Aslan was experimenting with the pain-relieving effects of procaine on patients with severe arthritis by injecting it into the arteries (!) which supplied blood to the area of the affected joints. She logically theorized that procaine, being an anesthetic, would relieve the joint pain. She was surprised to find that in addition to dramatic relief of joint pains, many patients also noted (1) improved memory, (2) less depression, (3) more energy, (4) restoration of normal hair color, (5) improved skin tone, and (6) a generalized feeling of well-being. (1)

These provocative results encouraged Prof. Aslan to carry out additional studies to test the effects of procaine on thousands of people. She did this at the Romanian National Institute of Gerontology and Geriatrics which she founded in 1950 — the first government-sponsored aging research institute in the world. Aslan found that by adding benzoic acid as a preservative, and potassium metabisulfite as an antioxidant, the procaine molecule was stabilized, and the effects were even more dramatic than with procaine alone. She called her improved form of procaine Gerovital, or GH3. She later added pyridoxine (vitamin B6), mesoinositol, and glutamic acid to this formula, to form yet another version called Aslavital. Aslavital was reported to have even more powerful and beneficial effects on memory, atherosclerosis, and other degenerative conditions than the original Gerovital H3. (2)

Gerovital
H3 is approved by the Romanian equivalent of the FDA for use in the treatment of numerous diseases, including: (1) prevention and treatment of the aging process; (2) depression; (3) arthritis; (4) asthma; (5) gastric and duodenal ulcers, (6) osteoporosis, and many other conditions.



In 1987, I traveled to Romania to attend and present a paper at the Romanian National Congress of Gerontology and Geriatrics (Dean). (3) I was interested in learning more
about Gerovital and Aslavital — to see first-hand how it was administered, meet patients undergoing the therapy, and review the scientific studies that had been performed. I was impressed by the body of scientific research that supported the use of procaine, Gerovital H3, and Aslavital as prophylactic and therapeutic agents against the aging process.

How Does Gerovital Work?
Procaine, as Gerovital H3 and Aslavital, has numerous documented mechanisms of action. These include (1) inhibition of monoamine oxidase (an enzyme in the brain which increases with age); (4,5,6) (2) nootropic properties; (7) and (3) antioxidant action. (8)

When procaine enters the body, it is broken down into para-aminobenzoic acid (PABA, a para B-vitamin), and diethylaminoethanol (DEAE), both of which are naturally present in the body (Fig. 2). Both of these substances are biologically active and have numerous beneficial effects of their own. Although the majority of the research involving Gerovital and Aslavital attribute the benefits to the procaine molecule, there is still controversy as to whether the effects are due to the procaine molecule itself, or to its breakdown products, PABA and DEAE. (9)



Anti-Aging Effects of PABA
PABA has been used as a component of many commercially available sunscreens due to its ability to block damaging ultraviolet rays. Skin damage due to sunlight causes or accelerates many of the characteristic skin changes that we attribute to aging. (10) PABA, both topically and orally, is truly an antiaging substance in terms of protecting
the skin from the sun.

PABA is a naturally occurring, water-soluble compound which is found in many foods as a cofactor of the vitamin B complex (associated with folate). It first became popular due to the writings of pioneer nutritionists like Gaylord Hauser, Lelord Kordell, and Adelle Davis. (11,12,13) Several decades later, life extension scientists Durk Pearson and Sandy Shaw extolled the potential virtues of PABA in their best-seller, Life Extension — A Practical Scientific Approach.

Is PABA a Vitamin?
By definition, a vitamin is a biologically active organic compound that is essential for an organisms normal health and growth, a deficiency of which results in a deficiency disease or disorder. Though PABA has many vitamin-like qualities, it fails to meet the strict definition of a vitamin. Early animal studies did, however, demonstrate that PABA increased lactation in rodents and increased the weight of chicks that were fed a diet with low levels of folate. These early studies suggested that PABA was essential, and it has erroneously been described as a B vitamin by many nutritionists and health educators in dozens of books. PABA is actually a structural part of folic acid. Although PABA is not technically a vitamin, it does appear to have a number of interesting and potentially valuable uses.

The Anti-Gray Hair Vitamin
One very interesting application for this versatile substance is its potential to restore hair to its natural color. In 1941, Dr. B. F. Sieve reported that administration of 200 mg of PABA per day for two months resulted in marked darkening of the hair in 30 patients with gray hair. (15) Brandaleone and colleagues (1944) reported that 2 of 33 individuals with grey hair had significant hair color change when administered 200 mg of PABA with 100 mg of calcium pantothenate (vitamin B5) and 50 grams (approx. 2 ounces) of brewers yeast for eight months. (16)

Dr. Chris Zarafonetis (1964) of Temple University followed these investigations with a report that described 5 cases of dramatic hair color change and hair regrowth in 20 patients with markedly gray hair, who were taking 6-24 grams of PABA per day for other conditions. (17) The hair color changes were serendipitous results of this therapy.Zarafonetis concluded that consumption of 6-24 grams of PABA per day for at least 6 weeks restored the natural hair color of 25% of people with markedly gray hair. He did not speculate on the mechanism for hair color restoration and pointed out that the effects were highly variable and might require extended periods of administration.

Zvak (1986) confirmed that forty years ago, large doses of PABA were clearly shown to darken grey hair; the regained color was lost within 3-4 weeks of stopping the treatment.(18) While it is clear that the hair color restoration effects of PABA were less than universal, any therapy which results in 10-25% reversal of an irreversible condition (like hair grayness) must certainly be considered significant.

PABA as an Antioxidant
It has been well established that PABA is a potent neutralizer of singlet molecular oxygen, a potent free radical which is a common by-product of normal metabolism. (19)
In theory, use of antioxidants protects cellular membranes and mitochondrial DNA from free radical attack. The mitochondria are the energy-producers of the cells. Mitochondrial degradation results in reduced cellular energy production which causes numerous undesirable physiological conditions, which may include fatigue and the aging process itself. As an antioxidant, PABA also provides protection against ozone, smoking, and other air pollutants that damage other cell structures and membranes through oxidative stress. PABA promotes cell membrane fluidity by preventing such oxidant damage.

PABA as an Anti-Crosslinking Agent
The crosslinkage theory of aging was proposed by Professor Johan Bjorksten in 1974. Bjorksten believed that the aging process was due to crosslinks (undesirable bonds induced by excess free radicals) which formed between molecules). Bjorksten theorized that these crosslinks progressively impaired the function of the body, the end
result of which was aging. (20) PABA appears to slow and in some cases even reverse crosslinking in the protein structures of connective tissues such as collagen.

Collagen crosslinking
— in addition to resulting in the loss of flexibility with age, and perhaps the aging process itself — also is the primary process in a number of fibrotic diseases, including: Peyronies disease (formation of fibrotic plaques of the penis, usually in men over 50, resulting in painful, crooked erections, rendering intercourse difficult or impossible); Dupuytrens contracture (wherein the flexor tendons of the fingers of the hands become fibrotic and contract, rendering the fingers useless); and scleroderma (a rare condition
characterized by heavily crosslinked skin and tissues, with disabling systemic results). Zarafonetis (1964) found PABA to have a marked therapeutic effect in these conditions, in doses of 12 grams per day. (21) Zarafonetis also used PABA to treat dermatitis herpetiformis (200 mg, 4-5 times daily), and vitiligo (a depigmenting disease). By slowing crosslinking, PABA may promote greater body flexibility in normally aging individuals.

Potential Side Effects and Cautions
High-dose PABA is generally well-tolerated, its most significant adverse side effects being diarrhea and nausea, which resolved with cessation of use, or lowering of the dose. As PABA is water soluble, it is rapidly excreted in the urine, and must therefore be administered in divided doses throughout the day. High-dose PABA should be discontinued when taking sulfa antibiotics (like Bactrim or Septra).

PABA Summary
Pearson and Shaw described PABA as an antioxidant which could: (1) slow crosslinking; (2) enhance flexibility; (3) promote membrane fluidity; (4) provide protection against ozone, secondhand smoke and other air pollutants; (5) alleviate the inflammation of arthritis; and (6) restore the original color of hair in perhaps 10-25% of cases. Pearson and Shaw reported they consumed as much as three grams of PABA per day. (14)



DMAE
Dimethylaminoethanol (DMAE) is a substance that is closely related to DEAE (Figure 3) — the other metabolic by-product of GH3. DMAE is a naturally occurring nutrient found in such brain foods as anchovies and sardines. It stimulates the production of choline, which in turn allows the brain to optimize production of acetylcholine (Fig. 4). Acetylcholine is the primary neurotransmitter involved in learning and memory.

DMAE is a mild cerebral stimulant, which was at one time approved by the FDA as being possibly effective for the following conditions:



Learning problems associated with underachieving and shortened attention span.

Behavior problems associated with hyperactivity.

Combined hyperkinetic behavior and learning disorders with underachieving, reading and speech difficulties, impaired motor coordination, and impulsive/compulsive behavior, often described as asocial, antisocial, or delinquent.


The learning problems mentioned above, although usually childhood disorders, are also not infrequently seen in adults. They are usually treated with much more potent and addictive amphetamines (like Ritalin). DMAE is a safe and non-addictive form of therapy for these conditions. DMAE produces a mild stimulant effect, which develops slowly over a period of several weeks. There is no drug-like letdown or depression if the substance is discontinued. (22)

DMAE for Adult and Childhood Learning Disorders
For those children and adults who suffer from ADD, ADHD, and other learning disorders (and even for those who dont) I recommend DMAE (dimethylaminoethanol). DMAE has been used for years to improve behavioral disorders in children, and may have positive effects on intelligence and grades as well.

In 1958, Dr. Leon Oettinger, Jr., found that DMAE:



Accelerated mental processes

Improved concentration span

Abolished early morning fogginess

Relieved lassitude and mild depression with obvious letdown when it was discontinued

Was useful in schizophrenia of long duration (with prolonged treatment)

Decreased irritability and reduced overactivity, leading to a much better overall social adaptation and improved scholastic functioning

Increased attention span

Did not cause drowsiness

Improved IQ!


Furthermore, he found that DMAE had numerous advantages over the amphetamines (like Ritalin) in that there were no effects on heart rate or blood pressure and no induced jitteriness. Instead of causing anorexia (loss of appetite) like the amphetamines, he found that DMAE actually improved appetite in many patients and caused no
interference with sleep. In fact, he found that DMAE actually reduced sleep requirements. Dr. Oettinger concluded that DMAE was a most useful tool in the handling of the child with behavioral problems.(23)

In 1960, Dr. Stanley Geller reported on a double-blind study of 75 children, that DMAE in doses of 50 mg twice daily resulted in improved functioning capacity, puzzle-solving
ability and organization of activity. (24)

In another double-blind study of fifty children who had been diagnosed as suffering from hyperkinetic syndrome, DMAE was administered in doses up to 500 mg/day (300 mg in the morning, another 200 mg at lunch). The author concluded that DMAE, when administered at doses of 300-500 mg per day for 12 weeks to moderately disturbed hyperkinetic children (six to 12 years of age) produces greater overall improvement in comparison to patients similarly treated with a placebo. 25)

DMAE for Chronic Fatigue, Depression, and to Enhance Dreaming
Kugel and Alexander reported that DMAE had also been demonstrated to be useful in the treatment of chronic fatigue and depression in children, (26) and Sergin reported the phenomena of DMAE-induced lucid dreaming, and speculated on its effects in normalizing brain function and mood. (27)

DMAE Improves Movement
Disorders and Prevents Adverse Effects of L-DOPA in Treatment of Parkinsonism
In 1974, Dr. Edith Miller added DMAE in doses ranging from 300-900 mg per day to the regimen of Parkinsons patients who had begun to exhibit adverse effects from high dosages of L-DOPA. DMAE administration resulted in a complete resolution of the L-DOPA-induced abnormal movements in a majority of the patients. Dr. Miller concluded that DMAE seems to be the first effective measure to combat L-DOPA-induced dyskinesias safely and effectively without interfering with the beneficial effects of L-DOPA
therapy. (28)

In a subsequent study, Dr. E. Daniel of the Portland VA Hospital used doses of DMAE ranging in dosages from 400 to 600 mg/day in a variety of patients with involuntary movement disorders, including benign essential tremor, tardive dyskinesia, and even blepharospasm (eyelid twitching). Use of DMAE resulted in improvement in all symptoms, with the exception of those suffering from Huntingtons chorea. (29)

DMAE Inhibits Formation of Aging Pigment
One of the most dramatic and well-documented effects of DMAE is its ability to inhibit the formation of aging pigment (lipofuscin). Lipofuscin is believed to be formed by the inefficient metabolism of fatty acids, and its accumulation in the cells is one of the most obvious and regularly reported cytological (cellular) changes with age. Lipofuscin
accumulates with age in all body tissues. Although no known adverse effects are known to result from lipofuscin accumulation, it certainly does no good, acting as intracellular garbage. Even if it is not harmful, lipofuscin is often cosmetically unacceptable, as it is the brownish pigment that causes liver spots on the backs of the hands of many people over 50 years of age.

DMAE not only can prevent the formation of lipofuscin, but it also actually flushes it from the body. Many people gauge the rate of lipofuscin removal from their hearts
and brains by watching their liver spots disappear with long-term supplementation of DMAE. It usually takes about six months for significant changes to take place — many spots resolving completely.



Life-Extending Effects of DMAE
Richard Hochschild, designer of the H-SCAN (probably the most well tested system designed to measure human biological age), evaluated the potential life-extending effect of DMAE on old mice. DMAE administration in the drinking water resulted in a reduction in mortality and an increase in both mean and maximum survival times (Fig. 5). (30)

Conclusion
In his book, Secrets of Life Extension, John Mann wrote that GH3 may not be the key to extraordinary life extension, but it appears to help, treat and delay the onset of many of the symptoms and side effects of aging. It can be a useful adjuvant to other longevity agents, and will, most likely, potentiate their effectiveness.(31) I agree with Johns assessment.

Gerovital and Aslavital are unapproved by the FDA, and are therefore largely unavailable in the US. Nevertheless, it is still possible for people who wish to avail themselves
of this therapy by asking their physicians to prescribe it for them through a compounding pharmacy. Although not approved for anti-aging use, physicians can legally prescribe drugs that are not approved in this country, but which are not specifically illegal.

An alternative is to use a PABA-DMAE complex containing the ingredients that Prof. Aslan found to work synergistically with her formula. DMAE and PABA in the proper concentrations may have effects as dramatic as those of GH3 itself, and may provide a variety of independent positive effects as well. Consequently, since DMAE and PABA are both readily available, inexpensive dietary supplements, this may be a satisfactory (and perhaps, a superior) alternative.

References
1. Aslan, A. Theoretical bases of procaine therapy (Gerovital H3 and Aslavital) in the prophylaxis of aging. Romanian Journal of Gerontology and Geriatrics, 1: 1, 5-15, 1980.

2. Stroescu, V. The experimental and clinical pharmacology of procaine, Gerovital H3 and Aslavital. Romanian Journal of Gerontology and Geriatrics, No.4, Volume 9, pp. 427-437. 1988.

3. Dean, W. Biological Aging Measurement -Pre-Requisite for effective human aging intervention. Romanian Journal of Gerontology and Geriatrics, Supplement to No. (1, Vol 9: 26. 1988.

4. MacFarlane, D. Procaine HCl (Gerovital H3): A weak, reversible, fully competitive inhibitor of monoamine oxidase. Fed Proc, 1975, 34: 1, 108

5. Hrachovec, J. Inhibitory effect of gerovital H3 on rat brain monoamine oxidase, Fed Proc, 1972, 31: 2, 604.

6. Aslan, A. Theoretical and practical aspects of chemotherapeutic techniques in the retardation of the aging process. Romanian Journal of Gerontology and Geriatrics, 1: 4, 3-11, 1983.

7. Stroescu, V., Constantinescu, I., Brezina, AI., Sotirescu, D., and Vrabiescu, AI. Experimental studies into the nootropic effects exerted upon the central nervous system by Aslavital versus procaine and Pyracetam. Romanian Journal of Gerontology and Geriatrics, No. 2, Volume 7, pp. 115-121, 1988.

8. Rusu, C., and Lupeanu, E. Inhibitory effect of Gerovital H3 and Aslavital on the production of the superoxide radical. Romanian Journal of Gerontology and Geriactrics, Supplement to No. (1, Volume 9, pp. 99-100, 1988.

9. Aslan, A., Turcu, E., Simion, N., Dobre, V., Strungaru, C., Stroica, E. Experimental Researches regarding the pharmacodynamic characteristics of procaine hydrolysis pro- ducts- DEAE and PABA. Romanian Journal of Gerontology and Geriatrics, Supplement to No. (1. Vol 9, 101-102, 1988.

10. Gilchrest, B.A. Skin and Aging Processes. CRC Press. Boca Raton, 1984.

11. Hauser, G. Look Younger, Live Longer, Crest Books, New York, 1962.

12. Kordel, L. Eat and Grow Younger, MacFadden Books, 1962.

13. Davis, A. Lets Eat Right to Keep Fit. Harcourt, Brace Jovanovich, New York, 1970.

14. Pearson, D., and Shaw, S. Life Extension A Practical, Scientific Approach, 1982, Warner Books, New York.

15. Sieve, B.F. Clinical achromotrichia. Science, 1941, 94: 257.

16. Brandaleone, H., Maine, E., and Steele, J.M. The effect of calcium pantothenate and para-aminobenzoic acid on gray hair in man. Am J Medical Science, 1944, 206: 315.

17. Zarafonetis, C. Darkening of gray hair during para-amino-benzoic acid therapy. J Investigative Dermatology, 399-401.

18. Zvak, C. The Science of Hair Care, 1986, Marcel Dekker, Inc., New York.

19. Allen, J.M. Rapid Reaction of Singlet Molecular Oxygen with P -Aminobenzoic Acid (PABA) in Aqueous Solution. Biochemical and Biophysical Research Communications, July, 1995.

20. Bjorksten, J. Crosslinkage and the aging process, in: Theoretical Aspects of Aging, by Morris Rockstein (ed), Academic Press, NY, 1974.

21. Zarafonetis, C. Antifibrotic Therapy with POTABA. American Journal of Medical Sciences, 1964, 248:550-561.

22. Pfeiffer, G.C. Parasympathetic Neurohormones. Possible precursors and effect on behavior. Int. Review of Neurobiology, pp. 195-244, 1959.

23. Oettinger, L. The use of Deanol in the treatment of disorders of behavior in children. J. Pediat, 1958, 53: 761-675.

24. Geller, S. J. Comparison of a tranquilizer and a psychic energizer. JAMA, 1960, 174: 89-92.

25. Coleman, N., Dexheimer, P., Dimascio, A., Redman, W., and Finnerty, R. Deanol in the treatment of hyperkinetic children. Psychosomatics, 1976, 17: 68-72.

26. Kugel, R. B., and Alexander, T. The effect of a central nervous system stimulant (Deanol) on behavior. Pediatrics. 1963, 31: 651-655.

27. Sergin, W. Use of DMAE in the induction of lucid dreams. Med Hypotheses, 1988, 26: 4, 255-257.

28. Miller, E. Deanol (DMAE) in the treatment of levodopa-induced dyskinesias. Neurology, February, 1974, 116-119.

29. Daniel, E. Mood alterations during deanol therapy. Psychopharmacology, 62: 2, 187-191, 1979.

30. Hochschild, R. Effect of dimethylaminoethanol on the life span of senile male A/J mice. Exp Gerontol, 1973, 8: 4, 185-191.

31. Mann, John. Secrets of Life Extension, Bantam Books, New York, 1982
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Date: Wed, 5 Sep 2007 14:40:49 -0400 (EDT)
From: Lee Denis
To: John Hutchison
Subject: Fwd: BEDBUGS!
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Lee Denis wrote:
Date: Tue, 4 Sep 2007 20:26:37 -0400 (EDT)
From: Lee Denis
Subject: BEDBUGS!
To: Dave Brown


Hello Dave,

It's Lee Denis here. I made a sucessful transition to BC Housing at Hall Towers, but nobody told me that these places are not just for seniors anymore, and they are mainly taking in Level 2 Disability people now. But these people do not have the supports that you provide at Lookout...its not a good thing. I pity the elderly. Maybe when I'm 60 I'll get safer and go private if the place turns into a 'Welfare Hotel'...too scary to contemplate!

I got so depressed today I almost felt like asking if I could return to Cliff Block! But no, it's early days yet and I'm just depressed because I developed a bedbug problem.

I have no idea how I got them...does anyone? But it was only about a month ago, so nobody will blame Cliff Block at least.....

They travel along the heating system, which is the old apartment kind that goes from room to room on the floor.

They use the same Pesticide people that Cliff Block uses, only they come EVERY THURSDAY! Don't forget Dave, there are two towers and over 200 residents, so I would say it is reasonable. Unfortunately, they were totally successful in eradicating the cockroaches that used to be in the two towers, and cockroaches are the only local enemy for a bedbug. Cockroaches will eat the eggs that they lay in the cracks in the tiles.

So, here we go....first I wanted to see if the fact that a dead bedbug gives birth...so I put a live one in a glass, then poured salt on the thing to see if that would kill it, but no - it crawled around on the salt. It did die eventually, as I had injured it in the capture. After a week or so a black sqiqqle lay beside the dead bedbug.

I had thought all the black sqiqqles I had been cleaning up in the cracks in my tile floor were dead fruitflies! Silly me.

The black sqiqqles are actually the larvae, or whatever the proper name is for such a thing. They have a sort of intelligence, as I have watched them climb my wall, UP of coarse, to try and get to wood table. They love wood, more on that later.

So, cleaning the cracks in the flooring of anything like a black sqiqqle is a good idea.

A few days later I looked in the glass and the sqiqqle was GONE..but I could vaguely make out the outline of a bedbug...the babies are translucent! Invisible to us. And they can move fast!

So, that is one experiment I tried.

The second experiment was to put a live one in the glass with 2 dead ones to see what would happen. After one day it has burrowed it's way into the dead one's belly to get at the blood!

Now I will tell you what a very bad infestation feels like...lonely. How can I visit anyone? I cannot see my 85 year old mother now, she is so very scared of getting a bedbug infestation, she knows that she could not stand the work.

The work - yes 8 or 9 loads of wash...plus purging all belongings that may be infested. I've done the wash thing 3 times now. Now I live with everything in plastic bags...it's all washed. I had to undo my new home and make it into an armed camp! It's so hard for me to move the furniture out from the wall each time so I just leave it out from the wall for the next fumigation!

Plus there is the cat...I cannot just leave for 6 hours. Blue kindly took me in to your lobby the first time (I wore clean clothes and took every precaution not to infest you)...but this time I must go to the 19th floor lobby with the cat...there is nothing there but an empty room and a wonderful view! But I cannot keep bothering Lookout. The manager at Hall Towers, Steve, is a wonderful man and is very helpful...in his way. He looks after BOTH BUILDINGS, so everything he does is 'on the run'...a very busy and hard-working man.

So, we have black sqiggles that seem to have the intelligence to climb a wall to get to my wood table. Here comes the clincher, THEY LIVE IN WOOD. My son, Shawn, lives in the West End of Vancouver where there is a bad infestation everywhere and they all are buying wrought iron and glass tables...and iron beds...

You must check all your wood furniture Dave, or get the pesticide people to check it. Some of those tables are bad looking. Also, it says on the sheet of paper they leave that nobody can bring in used furniture unless they check it first. I believe we should follow the instructions on that sheet of paper to the letter.

I did find out that heat to 117 degrees Farenheight will kill ALL STAGES of the bedbug...I am still dubious about the freezing.....

I read a book on pests and apparently in the 1930's there was a worldwide infestation of bedbugs and England suffered badly. Sweden put people up in tent cities in the parks while they fumigated they buildings and they were seriously thinking of building hotels for the people to stay in thru the winter fumigations.

Denmark came up with a good idea, they painted the walls in an oily substance almost to the ceiling (bedbugs cannot climb a smooth surface) and the made some sort of concave molding for the walls.

Another thing I read, I can copy this if you like - you can be in an iron bed all safe and sound, and they bedbugs will climb the wall and the ceiling and DROP onto you - their food.

These bugs are prehistoric, they live to eat and breed.

Everyone says I'm too 'into' this thing and I should take my mind off of it. But I cannot really have company in my infested apartment and feel good about it and I cannot really visit people for the same reason. I feel like I'm in some sort of isolation! Quaranteen if you will. I am lucky that my girlfriend, Corinne, is brave enough to visit me! It's very depressing. It's also a lot of work, a LOT of work...the laundry MUST be done!

I have no idea if they will be gone after my 3 fumigations. I am expecting the second fumigation on Thursday...they use very strong poison....I was in the room a hot 3 minutes before my bowells exploded when I returned home after fumigation number one. I put my bare arm on the table and my arm burned because there was a wet spot of spray!

My first thought was that the SECOND fumigation was the IMPORTANT one, as all the big ones would have died, and they the second wave of poison would kill all of the hundreds of hatching egg things. Think Dave, if you see 3 big bedbugs and a female lays 300 eggs in 3 hours...in all the cracks in the floors and in the wood - they the HATCHING EGGS must be the important spray.

BUT I caught 2 big guys just today...I just pick them up now I'm so used to them...and I have no idea where the big ones came from!

I don't think anyone has the answer, unless we bring back pet cockroaches! They are like aliens and they are truly creepy bugs...then again, I guess if we look at any life cycle of a bug, yes, it's creepy...

I hope this information helps you...I'm at the library, so I'll try and get that book on the 1930 infestation and copy the pages, it's a good read.

I really need a mattress for Thursday or Friday Dave...my Mom will buy me a metal daybed and I will cover the mattress with plastic, but she cannot affort to get it for my until after the 3rd spray. My foamy is so infested that it must be thrown away!

I'm 57 years old and starting to feel the effects of sleeping on the floor, up and down, up and down...God.

OK Dave, any questions, just ask!
or email me at:

Thanks for listening,
Lee Denis




Lee Denis
e-mail

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Copyright © 2002 Infinet Communications Group

CURES UNTILL TELOMERASE IS TESTED OK

DO YOU HAVE CANCER?
TRIHERBA BLACK SALVE HELPS:

Skin Cancers, and Malignant Growths
Prevent Tumorous Cells from Multiplying
Prostate and Colon Cancers
Breast Cancers
As a Cancer Preventative
Skin problems, such as Tumors, Viral Moles, and Warts
Boost the Immune System
Viral Disorders and Internal Growths
Detoxify the blood & body by inducing oxygen into the system


For many years Black Salve products have been used to help malignancies, not only in humans but also in animals. The above are but some of the uses for these products.



Why Choose TriHerba Black Salve
And Black Tonic Over Other Salves?

Please Note: For those of you who are familiar with TriHerba Black Salve and Black Tonic, you are already well aware of it's cancer healing power. For those of you who have used other salves, you should be aware that the TriHerba Product Line utilizes the original formula. We believe it to be superior over other brands on the market. Thank-you, Smart Health Center Staff.


Testimonial: I cannot rave enough about TriHerba Salve. Within one week it removed numerous skin malignancies - DC Edmonds, WA

Testimonial: I've had cancer of the colon. I know for a fact that TriHerba Tonic has slowed down the growth. X-rays revealed this. I can't praise TriHerba Products enough - H.M. Sheridan, WY

Here are some other uses for TriHerba Black Salve and Black Tonic:

To prevent early Viral Diseases in animals
To treat abnormal tissue growths in various animals
To remove plaque from teeth and diseases from the gums
To treat sarcoids on horses
For Yeast Infections (Candida) in women
If You Have Cancer Or Are At Risk
TriHerba Natural Herbs & Minerals Can Help!


What Is TriHerba Black Salve And Black Tonic?

Black Salve and Black Tonic contain natural herbs and enzymes known to neutralize carcinogens prior to their stimulating any tumor growth and preventing tumorous cells from multiplying once they have started.


How Does TriHerba Black Salve And Black Tonic Work?

Black Tonic is taken internally for virus related disorders and internal growths and works directly on the immune system acting as both a preventative and an immune booster. It generates purification of both blood and the body by inducing oxygen into the system and affected areas, thus helping to ward off any viruses or malignant growths both internally and externally. It appears that the herbs have the ability to remove unnatural and foreign substances from the body.

Testimonials reveal that Black Salve works effectively when applied topically on areas malignant, toxic or virus related. Sometimes it will turn red around the area of the tumor, mole, wart or sore, of whatever is being treated. This is a normal process and in the center it will be a whitish gray color, this means the salve is working. The salve penetrates and travels the area to its roots, killing all foreign matter and drawing it out. Sometimes the infected core itself will come out in one piece, or it may slough off on the bandage. It works differently on different types of malignancies, virus types or skin problems.

It has also been known to alleviate yeast infection (Candidas) in women, remove plaque from teeth and diseases from gums, and help alleviate colon problems.


Ingredients and Sizes:

The ingredients in the TriHerba Black Salve are as follows: Sheep Sorrel, Red Clover, Bloodroot, Chaparral, Graviola, Galangal, Zinc Chloride, Pine Tar, Emulsifying Wax, DMSO, Wintergreen Oil, Stearic Acid, Polysorbate 20, Glycerin, Olive Oil, Charcoal and Purified Water.

The ingredients in the The TriHerba Black Tonic are as follows: Sheep Sorrel, Red Clover, Graviola, Galangal, Bloodroot, Chaparral, Zinc Gluconate, 36% Alcohol and Purified Water.

These products are produced by a Canadian manufacturer that meets all the Health Canada Standards and the Food and Drug Administration's Good Manufacturing Practices.

TriHerba Black Salve is intended for external use and is available in a 1.3oz/40ml jar. For convenience, we also produce TriHerba Black Tonic for internal use which is available in a 3.4oz/100ml bottle. Many people use both products simultaneously depending on what the ailment is. Instructions for each or both are always shipped with product orders.

TriHerba Original Black Salves has 30% more product packed
inside each container vs other salves on the market!


1.3 oz Black Salve: $69.97 / 3.4 oz Black Tonic: $69.97

ORDER HERE

All orders are shipped within 48hrs, and come with a 30 day
100% Money Back Satisfaction Guarantee! (Minus S&H Fees)

TriHerba Products
Black Salve
History
Graphic Testimonials
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Links Of Interest




Disclaimer: None of the information presented on this site should be considered for the purposes of diagnosis or treatment of any health-related condition or concern, nor should it be perceived as individual medical advice or as a substitute for medical care. If you think you have a medical problem, please consult your physician.

Copyright 2001-2007 © TriHerba Marketing Inc Scratch Web Design






DR. WOLZ ZELL OXYGEN® + Royal Jelly

RETAIL PRICE $58.00 OUR PRICE $36.00



Ingredients: One vial , 3 tablespoons, contains 150 billion Enzyme Yeast Cells Dr. Wolz® and 300 mg fresh royal jelly
Vitamin B1
3.2 mg
regulates the carbohydrate and fat metabolism

Vitamin B2
3.4 mg
controls the respiration and visualization

Vitamin B6
2.0 mg
enzymatic function

Vitamin B12
3.2 mcg
blood-forming

Vitamin E
33.0 mg
cell protection, fosters the circulation of the blood

Vitamin C
218.0 mg
enhances the defenses and the physical power

B-Carotene
10.0 mg
cell protection and detoxification

Biotin
160.0 mcg
skin and nails

Niacin
5.0 mg
skin and metabolism of the nerves

Folic Acid
0.4 mg
blood forming; protein metabolic

Pantothenic Acid
3.6 mg
contributes to the formation of Coenzyme A

Ergosterol
11.0 mg
Provitamin D

Trace Elements:
Selenium
120.0 mcg
protection against free radicals

Chrome
50.0 mcg
cholesterol metabolism

Zinc
1.4 mg
cell metabolism

Iron
0.3 mg
blood-forming

Other Contents: molybdenum, manganese, copper, cobalt.

Minerals:
Calcium
29.0 mg

Potassium
220.0 mg

Magnesium
11.0 mg

Sodium
25.0 mg

Phosphorous
210.0 mg

Amino Acids: 20 amino acids are present, including methionine, cystine.

Enzymes: Superoxide dismutase, catalase, proteases, invertase, cytochrome, oxidase, alcohol dehydrogenase.

Other biological substances: glucanes, mannanes, DNA, RNA, Q6, peptides

Enzyme Yeast Cells Dr. Wolz®

Yeast cells are structurally similar to human cells. They also consist of a cell membrane and a nucleus. However, the vital power of yeast cells is much stronger than that of human cells. It is important to note that there are many types of yeast and that one yeast cell is not necessarily the same as another.

For example: Baker's yeast continues to germinate within the human body and, therefore, when it is processed, is not best for human consumption. Brewer's yeast is also heated and often dried into powder, flakes and tablets. This heating and drying process destroys the enzymes and most of the vitamins.

Enzyme Yeast Cells Dr. Wolz®, on the other hand, are cultivated in fruit juices which are rich in vitamins and in wheat germ extracts.

As a result of the unique process, the yeast cells remain biologically active, but they do not multiply in the body. The entire extraordinary rich contents of vitamins, enzymes, and trace elements in the yeast is provided to the body. And because the Dr. Wolz cultivation procedure results in especially thin cell walls, their essential components are more bio-available.

These are some excerpts from scientific studies and research on Dr. Wolz's ZELL- Oxygen® in Germany.

"In his research and day to day clinical practice, Professor Dorling, of Hamburg, Germany has demonstrated that yeast cell preparations are effective in many respects, promoting:

better oxygen utilization through improved cellular respiration
improved assimilation of nutrients
the restoration of biological intestinal flora and detoxification following antibiotic and chemotherapy treatments.
improved metabolic function
increasing resistance, vitality, and contributing to a fresher, more youthful appearance
Professor Jurasunas of Lisbon, Portugal, who has treated thousands of cancer patients indicates in his study on Zell-Oxygen that he has successfully treated numerous cases of anemia, chronic constipation, diabetes, Crohn's disease, and leukemia.

He uses Zell-Oxygen to reduce the side effects of chemotherapy and radiotherapy.

He recommends the following mixture to be taken 3 times a day.

20ml Zell-Oxygen (1 vial)

10 ml liquid Chlorophyll ( buy from health food store)

20 ml fresh red beet juice. ( buy in the kosher section of supermarket.) Borsch

100ml water. ( rinse vial with filtered water)

The chlorophyll will increase the oxygenation processes in the body by 20%.

This combination is used to reduce the side effects of chemotherapy.

The red beet juice is specifically used so as to enhance the respiration of damaged cells. Zell-Oxygen is known for its action in increasing the blood supply to the brain. It also helps the intestinal flora as well as the liver, by promoting detoxification and restoration.

Prof. Jurasunas found that patients suffering from cancer were always found to have their liver affected and even damaged. Cancer produces extra amounts of hydrogen which can be removed if detoxification and stimulation of the immune system are occurring.

Caution: If you are pregnant or planning to become pregnant, please consult a healthcare professional before beginning any supplement regimen. Stop use and consult your healthcare professional if an allergic reaction occurs.
A Stock Enterprises Company
Herbs4Healing ~ 134 Crooked Lane ~ King of Prussia, PA 19406
Phone: (610) 275-2153
Site design & maintenance by BRK Web Designs, Inc.
Copyright © 2000-2007 Herbs4Healing, Inc. All Rights Reserved
NOTE
The information on this website is for informational purposes only and is not intended to be a replacement for medical advice from your personal physician.































































































Accept Credit Cards

REAL CURES UNTILL GENETIC ENGINEERING AND TELOMERASE IS UNDERSTOOD

Previously the Cancell Home Page


Cancell NCI Test Fraud| Cancell Effectiveness Study | Cancell Super Antioxidant
Home | Test Kit | The Solution | Comparison Table


--------------------------------------------------------------------------------
Cancell™ like products, Cantron and Protocel, are safe alternative cancer treatments. They both have the same ingredients, but slightly different ratios of those ingredients. Cantron and Protocel are manufactured by different companies. Ed Sopcak, who coined the name “Cancell” has passed away. There is no product currently sold under the name Cancell.


How Cancell Works
Both Cantron and Protocel work by reducing the ATP energy in each cell of your body. (This is also one of the cancer fighting effects of Paw Paw and Graviola.) Our cells have an electrical potential that effects how the cell processes energy producing substances mostly blood sugar and oxygen from our blood supply (the red area in the graphic below).



By reducing this voltage level from 70 to 110 mv to something in the 50 mv region, normal cells can still function. However, cancer and viral cells cannot process energy at this low voltage level and start to starve. The process of starving is a slower process than being poisoned which is why Cancell works slower than chemo and why there was a dramatic reduction in the weight of tumor cells in the two day NCI test of Cancell, but only a small number of dead cells. Had that test run longer, all the tumor cells that showed such dramatic weight reduction would have starved to death. For more on the NCI test, go to the Comments on the NCI Test Summary for Cancell page.

For more information on how Cancell works, go to:

How Cancell works, a summary of the full text
The full text by the developer of Cancell (not concisely written)
Cantron Introduction and Prices
Manufactured by Medical Research Products (MRP), Miami, FL. MRP has been manufacturing Cantron since 1984 when they received the formula from an associate of the developer, James Sheridan. This associates name was Don Wilson. MRP also has the support of the HOPE group (Humanitarian Organization of People for *Entelev) who receives no financial compensation for their efforts. MRP changes $60 for a one month supply (8 ounces) and $190 for a little more than a four month supple (32 ounces). Shipping is $5 the continental United States.

They offer a full refund even on opened bottles regardless of how long ago you purchased it. For detailed protocols and ordering information, proceed to the Cantron Alternative Cancer Treatment page.

*Entelev was the name that the developer, James Sheridan used for Cancell.

Protocel Introduction and Prices
Manufactured since April 2000 by an undisclosed company and distributed by Renewal & Wellness, LLC Simpsonville, South Carolina. They have two versions of Protocel, JVS-23 and EJS-50. They claim that EJS-50 works faster on most cancers and works better on:

Leukemia, especially ALL
Rhabdoid brain tumors
JVS-23 is reported to work better on:

Kidney cancer
Primary brain tumors
Breast cancer
Bladder cancer
Auto-immune diseases
The following prices are presented as JVS-23/EJS-50. For a two month supply $109/$136 and for a four month supply $202/$252. Shipping in the continental United States and Canada is $8. No refund if either:

The bottle is open .
Protocel was ordered more than 30 days ago.
You fail to notify them by phone prior to returning the product.
A 10% restocking fee is subtracted from the amount returned. For Protocel ordering information, proceed to the Manufacturers section at the bottom of the Protocel Alternative Cancer Treatment page.

On this web site, information about Cancell is presented on two separate pages:

The Cantron Alternative Cancer Treatment page
The Protocel Alternative Cancer Treatment page

--------------------------------------------------------------------------------

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To search for a phrase, use quotes. Results appear in a Google page. All results, except the first few commercial results, if any, are from alternativecancer.us.