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Monday, February 2, 2009
Saturday, April 19, 2008
MAGIC SUGAR .POISON
GLOBAL RELEASE - ASPARTAME TOXICITY
Forwarded by Diana Buckland
by request of Dr. Betty Martini
PLEASE NOTE: This matter is regarding ABC Australia NOT ABC
Original Message
From: Dr. Betty Martini mailto:Bettym19@mindspring.com
Sent: Tuesday, September 07, 2004 1:03 PM
To: legal@your.abc.net.au
Subject: To ABC about Dr. Karl's propaganda attempting to convince
Australians the aspartame toxicity issue is a hoax
I am writing because ABC says that they will stand behind Dr. Karl and
this is regardless of the fact that not only is his information untrue but can
easily be proven to be false. First of all, obviously I know if I have lectured
for the World Environmental Conference. My invitation to speak is on www.dorway.com/nomarkle.html The full story is there as well under Update
World Environmental Conference.
This came about because a post I had written to a group of neurosurgeons
was picked up by a Nancy Markle. She changed the title and put her name on it.
A global networker by the name of Shoshanna Allison saw it and because her
husband was a victim (lupus, seizures, mood swings, etc.) placed it on 450 global
networks to warn the world. Her efforts saved so many thousands of people that
four support groups were set up for the sick and disabled. Today Aspartame
Detoxification Centers are in the
As a Legal Department, I don't have to tell you the power of the Pharmaceutical
Industry. They get what they want because they have a bottomless checkbook
(chequebook). In the case of aspartame, it was beyond not just being safe, the
FDA actually wanted the original manufacturer to be indicted for fraud. Both U.S.
Prosecutors, Sam Skinner and William Conlon, hired on with the defense team
and the statute of limitations expired. Let's face it, when the District Attorney
goes to work for the Godfather, expect acquittal. The Bressler Report, the FDA
Audit, on www.dorway.com explains some of the things that Searle did. Understand,
if you have a deadly chemical poison and you're trying to do studies to show safety,
it can't be done unless the studies are fixed. Aspartame breaks down to a brain
tumor agent, DKP, so when the rats developed brain tumors Searle would excise
the tumors, then put the rats back in the study.
When they died they would resurrect them on paper as the report points out.
I spoke with Jerome Bressler and thanked him for his report at which point he
told me that the studies were so bad that when the FDA retyped his report they
left out 20% of the worst part he had written. He also told this to Doctors H. J.
Roberts, and neurosurgeon Russell Blaylock. Dr. Roberts had his Congressman
demand the information from the FDA but they refused.
Originally Dr. John Olney, one of the most renowned neuroscientists on the
planet today, did studies on aspartic acid (l970) which is 40% of aspartame and
found it caused lesions in the brains of mice. He founded the field of neuroscience
called excitotoxicity. Dr. Blaylock wrote the book on it, Excitotoxins: The Taste
That Kills, www.russellblaylockmd.com An excitotoxin is a product that literally
stimulates the neurons of the brain to death causing brain damage of varying
degrees. Dr. Olney with the help of James Turner, Attorney in
The FDA refused to allow aspartame on the market for 16 years. But Don
Rumsfeld, now Secretary of Defense, was CEO of Searle and said he would call in
his markers and get it approved regardless of the fact the FDA said it was not safe
and caused braintumors. I might mention it also triggered mammary, uterine,
testicular, pancreatic and thyroid tumors, for starters. The FDA's own toxicologist,
Dr. Adrian Gross told Congress that aspartame violated the Delaney Amendment
because without a shadow of a doubt aspartame can cause brain tumors and brain
cancer. The Delaney Amendment forbids placing anything in food you know will
cause cancer.
The other FDA toxicologist, Dr. Jacqueline Verrett, told Congress all studies on
aspartame were built on a foundation of sand and should be thrown out. It was like
trying to do studies on arsenic and show it to be safe and they couldn't do it. In fact,
aspartame is a chemical hypersensitization agent and interacts with vaccines and
other toxins.
The FDA's own report shows 92 documented symptoms triggered by aspartame from
4 types of seizures to coma and death. Dr. Blaylock has a lecture on www.dorway.com
where he says to understand that the reactions to aspartame are not allergic reactions
– but toxic like arsenic and cyanide.
Don Rumsfeld was on President Reagan's transition team. The day he took office
he appointed Dr. Arthur Hull Hayes as FDA Commissioner to approve aspartame.
But Reagan knew it would take about 30 days to get Hayes to the FDA and in the
meantime the current FDA Commissioner could put an end to aspartame. So talk
about political clout - Reagan wrote an executive order making the current FDA
Commissioner powerless to do anything about aspartame. When Hayes got to the
FDA he over-ruled the Board of Inquiry of the best scientists the FDA had to offer
who said aspartame is not safe, caused brain tumors and the petition is revoked.
That's how aspartame got on the market. Now if you want proof of this and you
want to hear it right out of the mouth of Attorney James Turner all you have to
do is get a copy of the movie just released on aspartame, Sweet Misery:
A Poisoned World. You can get a copy from Cori@soundandfuryproductions.com
It is getting rave reviews and has already been shown in over 10 countries of the
world. In fact, its being marketed in
and Fury are now doing a sequel. Other movies are also in the making. This is one
of the greatest scandals in US History. Nobody has ever said it better than Dr.
James Bowen who told the FDA years ago that aspartame is mass poisoning of the
American public and more than 70+ countries of the world. You can read his letter
to the FDA on labeling on www.dorway.com Searle was afraid they couldn't get it
around the world if anyone knew about the FDA wanting them indicted for fraud.
So they got it approved in
Turner in the regulatory agency there. Parliament had a big blow out but did not
rescind the order. The story was in the Guardian. Then Searle was able to
rubberstamp it around the world. Letters have been written to ANZFA for years,
especially by Dr. H. J. Roberts and they just disregard them.
Like our FDA today they are nothing more than the handmaiden of the pharmaceutical industry. No matter how much evidence you give them they do nothing.
In Dr. H. J. Roberts first book on aspartame, Aspartame (NutraSweet) Is It Safe?
He quoted his first press release where he stated if something wasn't done then
we would have a global plague on our hands in five or ten years. It didn't take
that long for Dr. Roberts to declare Aspartame Disease to be a global plague and
publish the 1038 page medical text, Aspartame Disease: An Ignored Epidemic, www.sunsentpress.com
At the World Environmental Conference, Dr. Clarice Gaylord of the EPA said:
"We have an epidemic of MS and lupus and cannot identify the toxin.
" I said: "I'm Betty Martini of Mission Possible Intl, and I'm here to lecture on
MS and lupus and identify the toxin as NutraSweet/Aspartame." These diseases
are completely documented in the medical text as well as in Excitotoxins: The
Taste That Kills by neurosurgeon Russell Blaylock, M.D., and his new book, Health
& Nutrition Secrets To Save Your Life, www.russellblaylockmd.com
Just recently Dr. Blaylock released a press release on the MS and Aspartame
Connection complete with research. Go to www.wnho.net and clic on aspartame.
How serious is it? Basically what he is saying is that a good deal of the population
who have been using aspartame for years have subclinical MS and if not warned
can have full blown disease. And what is ABC doing - telling the people of
its all a hoax. I realize ABC in
the States and is the national, government-funded public broadcaster in
But this doesn't say very much for truth from Australia ABC.
This is why aspartame is so deadly. It is a molecule composed of three components,
40% aspartic acid (an excitotoxin), a methyl ester which immediately becomes
methanol (10%), a neurotoxin, and 50% phenylalanine, as an isolate a neurotoxin
that goes directly into the brain, lowering the seizure threshold and depleting
serotonin. Aspartame breaks down to a witches brew of toxins including
diketopiperazine, a brain tumor agent.
James Bowen, M.D. is a victim of aspartame with Lou Gehrigs and has explained
how the destruction works. Aspartic acid, the excitotoxic component of aspartame
does not cross the blood brain barrier but is secreted into the cerebral spinal fluid by
the choroid plexus located in the ventricles of the brain. There, in the brain's lower
area and upper terminus of the spinal cord is where Lou Gehrigs, Parkinson's Disease
and Multiple Sclerosis damage is most prominent. These critical locations bathed in
the toxin as it removes from the blood. From the
a narrow canal called sylvian aqueduct which fills with this secretion and washes
the roof of the hypothalamus. This accounts for the damage to the hypothalamus.
Dr. Madelon Price, Professor Emeritus of Neurobiology in Psychiatry, and
biochemist who worked with Dr. Olney for 30 years recently mentioned that
although aspartic acid does not cross the blood brain barrier, that many people
have compromised blood brain barriers. She said very important to her, is that
healthy people are at risk because certain areas of the brain, small organs that
about the ventricles of the brain, lack blood brain barrier protection. These are
the circumventricular organs (CVO) of the brain. The 3 principle ones are:
(1) the area postrema, located on the floor of the 4th ventricle, which controls
vomiting.
(2) the subfornical organ which hangs from the roof of the juncture of the 1st
and 2nd ventricles, which controls thirst and
(3) the median eminence/arcuate nucleus of the hypothalamus, located on the
floor of the 3rd ventricle, which controls the flow of many hormones. She said
this is the most important area and the one that got she and Dr. Olney involved
in the aspartame issue in the first place.
The capillaries that run through these organs are fenestrated - they have areas
of thinning in their walls (fenestre = window in French). Most capillary walls are
very tight and aspartate can only cross their walls by an energy dependent pumping mechanism. But aspartate can freely enter the CVO through the permeable
fenestra in the walls of the CVO capillaries. Releasing factors which control the
release of growth hormone, all the sex hormones (follicle stimulating hormone,
luteinizing hormone and prolactin), thyroid hormone and corticotropin among
others are controlled by this area of the brain.
Dr. Price mentioned the shrunken testes in experimental rats and also said it is well
known that women who ingest a lot of aspartame, stop menstruating and cannot get
pregnant. The baby animals that she and Dr. Olney injected or fed aspartate grew
up to be obese and infertile adults. That is because this area of the brain was affected.
As to methanol it converts to formaldehyde and formic acid and causes metabolic
acidosis. Dr. H. J. Roberts says the chronic methanol poisoning affects the dopamine
system of the brain and causes the addiction. Methanol is classified as a narcotic.
In the worst case scenario, a body builder and athlete, Charles Fleming was highly
addicted to diet drinks and other aspartame products. When he died they saw
the methanol poisoning and thought his wife poisoned him. This sweet Sunday
School teacher who helped the homeless was sentenced to 50 years in prison,
and is in the movie, Sweet Misery. Several aspartame experts have looked at
the autopsy and written affidavits that Fleming died of aspartame.
You may have heard about so many athletes dropping dead. The ones we have
investigated were using aspartame. Dr. Bowen explained aspartame and sudden
death in great detail. He says that aspartame and methyl alcohol poisoning are
noted for damaging myocardium and the specialized form of myocardium called
the cardiac conduction system. This kind of damage leads to susceptibility to
arrhythmias. The aspartame and methyl alcohol poisoning causes immense
damage to the mitochondria (life of the cell) and to MtDNA which perpetrates
the mitochondria damage. The myocardium and cardiac conduction system
never get to rest. They are constantly at work pumping blood, therefore they
are very highly concentrated in mitochondria to accommodate the metabolic
needs of this tremendous work load. Therefore, mitochondria damage is more
highly reflected in the heart. Damaged mitochondria produce increased amounts
of free radicals and other abnormal metabolites that produce arrhythmias.
Moreover, the person using NutraSweet may have a markedly decreased intake
of mineral and vitamin co-enzyme factors which also sensitizes the heart to
arrhythmias. It appears with athletes exercise is the last straw. You have unusual
demands on the cardiorespiratory system.
Dr. Blaylock says that magnesium protects the brain and heart from excitotoxins.
When an athlete runs he depletes magnesium. Its the last straw. The phenylalanine
in aspartame lowers the seizure threshold and depletes serotonin. Lowered
serotonin triggers manic depression, mood swings, insomnia, suicidal tendencies,
paranoia, hallucinations, etc. Psychiatric and behavioral problems are epidemic.
In fact, President Bush now wants everyone in this country checked for mental
illness. Congress has admitted that US children are poisoned and have given the
National Institutes of Health 2.7 billion to find out the culprit. See my letter to
NIH and their letter also on www.wnho.net click on aspartame. This is the site
of the World Natural Health Organization.
Dr. Roberts in Aspartame Disease: An Ignored Epidemic says: "Increased brain
phenylalanine can elevate norepinephrine levels becoming clinically manifest as
hypertension. A comparable phenomenon has been demonstrated in spontaneously hypertensive rats. Another plausible mechanism involves increased phenylalanine
metabolites, especially dopamine, in the presence of excess insulin. Tourian (l985) demonstrated that insulin potentiates the synthesis of phenylalanine hydroxylase
in tissue cultures.
He also says: "The documentation of essential hypertension in an insulin-resistant
state associated with hyperinsulinemia (Ferrannini l987) but independent of obesity,
is germane because many aspartame reactors have reactive hypoglycemia.
Furthermore, phenylalanine increases insulin release. In the face of continued
hyperinsulinemia, the down regulation of insulin receptors (and ensuing decreased
insulin actin) the increased reabsorption of sodium and sympathetic stimulation can
exaggerate hypertension."
Dr. Roberts in the l980's was selected as the best doctor in the
medical organization. He is Board Certified and Recertified in Internal Medicine,
a diabetic specialist. He says that aspartame can precipitate diabetes, stimulates
and aggravates diabetic retinopathy and neuropathy, can cause diabetics to go into
convulsions and even interacts with insulin.
What aspartame has done to the family is a crime. If someone does get pregnant
Dr. Bowen points out that aspartame is an abortifacient and also a teratogen
(causes birth defects). And if a live child is born he says aspartame may have
heinously damaged DNA for generations to come. DNA damage was proven on
the Trocho Study in l998, and also showed that the formaldehyde accumulates in
the cells with most toxicity in the liver but substantial amounts in the kidneys,
adipose tissue (reason for obesity -
fat cells), retina and brain. Aspartame also ruins female response and trigger
male sexual dysfunction.
Dr. John Olney told the Board of Inquiry of the FDA concerning children, and
they agreed with him, "I conclude that despite Searle's persistent tendency to
AVOID PERFORMING EXPERIMENTS OF APPROPRIATE DESIGN to clarify
the safety of the aspartate moiety of aspartame under "use" conditions, the few
items of relevant evidence they have generated since l974 serve to reinforce my
position that aspartame, together with glutamate, does pose significant risk of
destroying neurons in childrens' brains and exerting adverse influence on
neuroendocrine systems. Certainly the studies performed, thus far, do not even
begin to refute, disprove or rule out the brain damage and neuroendocrine risks
I have defined and documented with extensive evidence, nor do they demonstrate
that there is an adequate safety margin for the use of aspartame (plus Glu) in
childrens' foods. Searle has failed, therefore, to establish the safety of their
product for use in childrens' foods."
And so the best scientists the FDA had to offer revoked the petition for aspartame.
And if Don Rumsfeld hadn't called in his markers and Reagan hadn't appointed
Hayes to get it approved anyway by over-ruling the FDA Board, millions would
not have perished from the fatal diseases and tumors triggered by this neurotoxin,
and our children wouldn't be poisoned. As Dr. Blaylock says in Excitotoxins, even
if a child survives his mother using aspartame during pregnancy, by the time he
reaches puberty you will probably see behavioral problems. Aspartame reduces
IQ, triggers ADD, autism, ADHD and other horrors.
When studies are not fixed by Industry it's very easy to show how quickly
aspartame poisons. Dr. Baret in the
360 children by changing milk for aspartame laced juice, detailed in Dr. Roberts
medical text. All these children immediately demonstrated inability to concentrate, hyperactivity and such. Knowing that the only change made was adding aspartame
to the diet he removed it. In four days all the children went back to normal.
It doesn't take a rocket scientist to prove how deadly aspartame is, which is
why the FDA and the manufacturer has tried to prevent independent studies.
If you read the UPI investigation on www.dorway.com you will see that Searle
even threatened Dr. Richard Wurtman at MIT if he did studies on aspartame
and seizures, his research funds would be rejected, and they were. ILSE is their
front group that supplies research funds to universities who co-operate.
Research is negotiable. MIT now gets research funds but Dr. Wurtman no
longer speaks out about aspartame.
Finally in l996 when Dr. Olney made world news on the aspartame and brain
tumor issue, he was on 60 Minutes (also in
Walton joined him showing research on scientific peer reviewed studies and funding.
92% of independent, scientific independent studies showed the problems aspartame
causes, and if you removed 6 studies the FDA had something to do with since they
now are now the handmaiden of the pharmaceutical industry, plus one pro-industry
summary, 100% of independent studies show problems with aspartame. What
does say to industry funded and controlled studies saying aspartame is safe?
Like FDA toxicologist Jacqueline Verrett told Congress, all studies were built on a
foundation of sand and should be thrown out. I've gone to great length to provide a
good part of the story of aspartame and let you know that with it on the market, no
drug is safe. Aspartame interacts with just about every drug used to treat the
problems it causes as outlined in the medical text. I'm the messenger, founder
of an unpaid global volunteer force with operations in 50 states and over 22 countries
of the world educating the public on the deadly affects of aspartame, the information
from world experts. And what does ABC do - try to make out like its all a hoax, and
aspartame is safe as rain. Information is a matter of public record and cannot be
denied.
Are advertising funds more important that the lives of the people of
every bit of information can be checked out, and wasn't, how come ABC wants to lie to
the public? Currently suits have been filed against 14 large companies for poisoning the
public with aspartame such as Coke, Slimfast, Pepsi, Pfizer, Wrigleys and Atria. I'm also
working with class action attorneys and attorneys call often who are interested in
investigating. Four support groups help the sick and disabled. Aspartame Detoxification
Centers continue to increase. More and more movies are being made to get the
information to the public. Even in Sweet Misery, Turner admits that Searle even did
studies in Dr. Olney's lab showing brain damage and didn't even turn them over to
the FDA. They cared not about how many brain diseases their toxin would poison
and how much pain, suffering and death they would cause. A quarter of a million web
sites warn the public do not use aspartame. www.truthinlabeling.org explains
aspartame has a synergistic and additive effect with MSG. Their records show
how the glutamate industry used aspartame as the placebo for a quarter of a century
in studies with MSG to make the public believe that MSG reacted no differently
than the placebo, when in fact, both are excitotoxins. Searle even used people in
poor villages in
seizures, and show that aspartame destroys the brain and central nervous system.
Then they didn't publish the studies. Some of those people died. The pregnant
woman lost her baby. We have the affidavit from the translator.
Today the aspartame industry provides fake, frauds and front groups to mislead the
public. Dr. Stephen Barrett of quackbusters, one of the most well known for false
and misleading information on web has just been charged with racketeering. The
public has had enough.
Now ABC had a choice. I expected a full apology and the truth to be told to the
Australian people. My email sent to you on the 7th September, 2004 was ignored
– I informed you in that email that if I did not receive a full apology and the truth
to be told within 5 days (that is by the 12th September) after receipt of my email,
that this information will be placed on the world-wide web. The Australian people
will find out either way. In the end this letter may get to more people in
than ABC does. Be assured the aspartame industry and their bottomless checkbook (chequebook) and influence is not worth the life of even one child, much less the
mass poisoning of the world. Enough is enough. All the facts are a matter of public
record, and I would be happy to give you the phone numbers and emails of the
physicians for verification of the facts.
Dr. Betty Martini, Founder, Mission Possible Intl,
Parkway
Sweet Misery: A Poisoned World
Filmed in-person interviews with Doctors, Lawyers, people with aspartame
related health problems, advocates and many others. The film Sweet Misery reveals
one of the most pervasive, insidious forms of corporate negligence in the history of
the industrial revolution. The toxic long-term effects of aspartame are often dismissed
as a “hoax” by the sweetener industry and at least 5 other internet websites.
The real footwork however, unravels something less comforting than a mere “hoax”.
Sweet Misery is a documentary released by Sound and Fury Productions. http://www.soundandfuryproductions.com
FORWARDED AT THE REQUEST OF DR. BETTY MARTINI
by Diana Buckland Global Recognition Campaign/Multiple Chemical
Sensitivity/chemically induced illnesses, diseases & injury affecting civilians &
Kidneys for transplant being sold in North Cotabato town
| MLANG, North Cotabato (MindaNews/4 March) -- Poor residents in one of the Israelis and Arabs who undergo the kidney transplant operation at the |
Tambal sa Sakit nga AIDS Makadoble sa Gibating Sakit sa Kasing-Kasing
Nidhi Sharma - AHN News Writer
Syndrome” nga Abacavir, nakita sa mga eksperto nga makadoble sa
gibating sakit sa kasing-kasing sa mga pasyenting adunay AIDS diin aduna
usab sakit sa kasing-kasing. Matud pa sa mga pagtuon, diin 517 nga mga
pasyente nga adunay AIDS gawas sa 33,000 nga mga pasyente aduna
usab sakit sa kasing-kasing. Diha sa 517 nga mga pasyente, 124 kanila ang
nagagamit ug didanosine ug 194 kanila ang migamit ug Abacavir.
Ang resulta sa ilang pagtuon nga pinangunahan ni Jens D. Lundgren nga gikan sa
University of
maong mga medisina makatabang sa pagpataas sa sakit sa kasing-kasing. Sa
gisulat sa “The Lancet of Medical Journal” ang medisina nga Abacavir nakapataas
ug kaduha sa posibilidad sa sakit sa kasing-kasing ug ang laing medisina
nga didanosine nakapataas ug 50 porsiyento sa posibilidad sa sakit sa kasing-kasing.
Apan bisan pa niining mga pahimangno gikan sa mga maayo ug inila nga mga
eksperto, ang mga doctor mituo nga makatabang gayud ang maong mga
medisina aron mukonhud ang sakit nga AIDS.
Ang Abacavir naila usab sa tawag nga Ziagen nga gihimo sa kompanyang
GlaxoSmithKline PLC. Sa laing bahin, ang Didanosine, naila usab sa tawag nga
Videx, nga hinimo sa kompanyang Bristol-Myers Squibb. Ang maong tambal
giindorso sa Pangkalibutanong Organisasyon sa Panglawas kon
“World Health Organization" (WHO) isip tambal batok sa sakit nga AIDS.
Saturday, April 12, 2008
Neem Tree - Azadirachta indica
The neem tree could have been designed by a celestial committee (maybe it was).
A collaboration of genetic engineers, chemical engineers, pharmacists, agronomists,
and dieticians could not have produced a more interesting, and some say, valuable,
plant. I'll let you decide after reading this brief overview.
Azadirachta indica is "tailor-made for combating the serious problems
confronting mankind today" says the Neem Foundation. " Studies through
appropriate scientific channels are increasing and verifying the traditional uses
and are finding even more uses for neem. Although major studies to conclusively
prove neem's effectiveness are limited by financing and the general lack of
knowledge in the West about it, preliminary studies suggest exciting uses
for neem."
From the very beginning of recorded human history, people have used the
mysterious neem tree.
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Today, rural Indians call this tree their "village pharmacy" because it is said to
"cure" diseases and disorders ranging from bad teeth and bedbugs to ulcers and
malaria. The seeds, bark and leaves contain compounds called limonoids with
proven antiseptic, antiviral, antipyretic, anti-inflammatory, anti-ulcer and
antifungal uses.
Neem has a cousin that is a very familiar tree in the
Chinaberry. Many North Americans are familiar with the abundant Chinaberry
tree, Melia azedarach . Also known as umbrella tree, this naturalized western
Asian tree is a colonizer of disturbed sites throughout the South. It can be messy
with surface roots, brittle wood, and toxic berries. However, it has an ability to
grow in hostile sites and produce desirable shade.
Neem, on the other hand, is a sturdy, broadleaved evergreen. In the seasonally
dry hills of central
people and animals in villages and along roadsides. It will defoliate during periods
of extreme drought or freezing temperatures. Native to the dry forest areas of
India
and subtropics.
Mature neem trees are capable of withstanding mild freezes and can be grown
in some of the
and on the East coast as far north as central
must be grown potted and taken in during cold snaps.
I was shocked at the reported uses of the neem tree. Most of this is supported
by some scientific study. Much more investigation is needed,
however.
OPINION
DOK ALTERNATIBO
Nganong daghan sa mga masakiton ug diabetes, hypertension, toxic goiter, mayoma,
aneamia, cancer ug uban pang sakit ang naputos sa grabeng kabalaka? Kini dili
lamang sa dinagko kaung galastohan sa pagpaospital kondili tungod kay gipatoo
kita nga wala kini kaayohang mga sakita diha sa conventional medicine.
Natuman ang KASULATAN “ Ang mga nagpakamaalamon gipakawalay
alamag sa DIOS “ Magapangawot nalang ang ulo sa atong mga MD karon
kung imong pangutan on kung duna bay kaayuhan ang mga nsangpit nga balatian.
Mosiga nlang ang ilang mga mata nga ang tambal sa maong mga sakit dili nila
makaplagan sa ilang baga kaayong mga libro sa medisina kondili magagikan sa
mga taong kinasingkasing nangalyopo sa GINOO ug kaayuhan sa ilang mga
balatian-mga Natural Therapist. Ang gipakabililhon sa Medical Institutions
mao ang minugna sa tawo sama sa chemical drugs inay nga mosalig sa mga
tanom, ug kinaiyahan, mga minugna sa DIOS .Kini ang rason kung
nganong mas midaghan hinoon ang daghang sakit sa kalibotan
samtang nagakamoderno ang seyenya ug teknolohiya diha sa Medical
World. What a shame!
Ang kahakog ug pagpanlimbong nga kuno “ clinical test ”sa mga Multi-
national Companies nagapadasig sa pagdagsang sa diabetes ug uban pang
“HOPELESS”nga sakit diin usa na ka worldwide epidemic sa dugay na nga
panahon diin possible pa untang mapakgang pinaage sa honesty and good science.
Diabetes can quickly be reversed by naturally restoring the body's blood-sugar
control mechanism through banana bloosoms or neem tree leaves with natural
treatment program of alternative medicine. (Paminaw sa akong programa sa radio
alang sa dugang ebedensya).
Ania ang pamahayag sa usa ka Medical Doctor, author sa pinakahalinong libro,
MEDICAL MAFIA. “Ang mga medical establishment nakigkonsabo sa mga
drug multinationals kansang numero unong tuyo mao ang profits, ug ang ilang
gikahadlokan mao ang epidemic of good health. Daghang synthetic drugs
gikinahanglan ibaligya (ARON MAS MODAGHAN PA ANG SAKIT). Ug aron
mapatuman kini gikinahanglan ang pagpanlimbong, pagpanikas, ug korapsyon.
Doctors are the principal salespeople of the drug companies. Ginagantihan sila
ug mga research grants, gifts, and lavish perks. Ang mga mamalitay mao publiko
gikan sa mga masuso ngadto na sa mga tigulang diin ginapugos pinaage
sa balaod sa PAGPABAKUNA sa bisan unsang paage! Makapangutana siguro
kita nga ang awtoridad kaniadto sa mga nasod nga naulipon sa mga adunahang
nasod ginadili ang alternative medicine? KINI GUMIKAN KAY ULIPON
SILA SA INDUSTRIYA! Ang industriya di mabuhi sa mga herbs, vitamins, ug
homeopathy. DILI MAPATENT ANG HERBS TUNGOD KAY ANG GINOO
MAO ANG INVENTOR NIINI!. Mao kini rason ngano ginapamugos nila ang
synthetics- may dakong sapi diha bisan pa ug peligro kau kini gumikan kay
chemicals. They control medicine, and that is why they are able to tell medical schools
what they can and cannot teach.
" Guylaine Lanctot,
Bisan ang mga bangiitang MD sa abanteng nasod sama
sa AMERICA mitoo sa Alternative Medicine. “In my view,
cancer is a controllable chronic illness. Alternative doctors are not only
concerned with attacking the cancer; we're also supporting the body fully,
striving to make it stronger so that it can fight cancer for us, rather than
just sit on the sidelines, not being allowed to perform its usual cancer-controlling
functions."
"There is no better example of the weakness of our dominant medicine
than its clearly ineffective War On Cancer. By the same token, there is no
better example of the superiority of complementary, alternative
medicine than its management of this dread disease….we are equally
concerned about whether mainstream medicine’s demand for proof works
to maintain it at its current level of ineptitude."---Dr. Atkins, M.D.
Ania pa ang pagbulgar sa mga MD nga nakasinati sa MIND CONTROL
pinaage sa giingong Authority. Wa gayoy kalainan sa panahon sa
atong GINOO diin daghan sa mga tawo ang misalig kang JESUS inay
sa awtoridad nga way laing gihimo kondili ang pag atiman
lamang sa ilang kaugalingong interest..
“ First, we fall victim, not only to cancer, but also to the very clever
brainwashing of our number one ENEMY. The Medical Establishment and
the unending barrage of the conspiracy with the MEDIA and support groups
such as the American Cancer Society, the National Cancer Institute,
the American Medical Association and an unlimited number of organizations
that make their income from the crumbs that fall from the establishment’s
table. Dr Kelley DDS
Ania pa ang makabungog nga ebedensya nga dakong kalainan sa
Natural batok synthetic drugs nga gipaluyohan sa giingong
AUTHORITY.Mobilib ka sa mga MD nga way kukahadlok nga
misungag sa giingong “Authority” nga nagpakatag ug “Hopelessness”
sa kalibutan.
Sa kataposan, angayan tang pamalandongan kining confession sa usa
ka MD nga mibulgar sa tinood nga motibo sa institusyong ilang
gialagaran kaniadto.
"We have a multi-billion dollar industry that is killing people, right and left,
just for financial gain. Their idea of research is to see whether two doses
of this poison is better than three doses of that poison."
—Glen Warner, M.D. oncologist.
DOK ALTERNATIBO
XPERT N ALTERNATIVE MEDICINE
herbal,magsakit man tiyan, naa daw deperensya and iyang atay
0910-7890929
di mo-function ug tama, way daot sa ubang organs sama sa atay. Kung
Natural treatment lang ang iya nasunod, di jud unta madaot ug apil iyang atay.
Ang mga naandang synthetic drugs igo lang momaintain sa sugar level sa dug,
o pelegro pa kau sa complications gumikan kay chemical-base kini. Mao nadaot
pud ug apil ang atay.Dapat sudon nya ang formula nga natural. Maglaga sya
ug puso saging o mga dahon sa neem tree. Ibutang sa thermos ang nilaga.
Mas espeso mas mau. Kada baso timplahan ug 2 kutsara nga Dok B Complex ug
patakan ug 10 drops nga Dok F para mahulipan ang nawala nga enzyme
ug Vitamins gumikan sa pagpabukal sa herbal. Imon kini kada duha ka oras
sulod sa isa ngadto duha ka semana. Mao Kini ang nakapau kang
Mr. Arsenio Jomoc,2- times stroke diabetic, taga Panabo City nga igo lang
misunod sa atong Formula .Paminawa ang iyang kompletong testimonya sa
atong mga programa sa radio aron mas madetalye. Matod pa sa mga experto
ang diabetes ma-reverse lamang kung I- correct ang pancreas rather than
maintenance of your blood sugar level gamit ang droga.
Unsa man akong buhaton?Julie Ann of Tagum.0909-4455981
ug way chemical drugs nga mga anti acid ang imong imnun gumikan kay mga
chemicals sla nga makatiwas sa
(kon ulcer) sa imong ceccum o duodenum. Ang asukar brown man o white lakip
na mga producto sa white flour makapadugang sa acid sa tyan gumikan kay
KAWATAN sila ug mga minerals ug Vitamina A B C sa atong lawas.
Ang Urinary Tract Infection kon UTI epekto usab sa atong gihisgutan sa unahan
plus ang pag inum ug softdrinks lakip na ang pagkaon ug karne. Mga pagkaon
kini sa MICRO-ORGANISMS ug mopatay sa mga cells sa atong lawas. Kung
daghang dead cells modaghan ang pagkaon sa mga mikrobyo.Ang solbad niiini,
mopailalom ka sa WET FASTING program. Paminawa ang testimonya ni
Ms Evangeline Davis, empleyado sa
sulod lang sa 2 ka adlaw. Naglaga lang sya ug Bila-bila ug gitemplahan sa atong
ginatudlo nga Formula sa Radio.
nako malikayan ang kaon ug daghan, 0926-0413585
molikay ka sa pagkaon sa humay ug uban pang
acid sa stomach makapagana kau sa pagkaon
ka pag inum sa Dok B Complex nga
makorek ang acidity.Kung
pagkaon kay kompleto
ka mokaon makaon lang
aron dali
ang akong formula. Tested na kini gani daghan na ta ug mga testimony
atong programa sa radio.
nakau iyang ubo hangtod karon wala pa gihapon naayu gikan
namanunta mi sa nagkadaiyang doctor, naa may
apan wa jud maau. 0926-3395383
A. Kung chemical drugs lang ang imu saligan sa asthma o grabeng ubo, di jud
kini maulian gumikan kay chemicals kini. Ang pagsunod sa natural treatment sama
sa mga Chinese ug Indians makapahingangha sa imu gumukan kay puros herbal
lang ang gitambal maulian na ang ubo ug uban pang grabeng balatian nga di
makaya sa conventional or western medicine. Ang lagundi,
lamang sa mga herbal nga napamatud- an sa science of natural treatment nga makau
sa ubo. Lagaon sla ug ibutang sa thermos. Mas espeso mas epektibo. Kada baso
templahan ug Dok B- Complex ug Dok F aron paspas nga mosulod sa cells ug
mopagawas sa plema sa baga. Sa akong Clinical Experience Lau ra ang 1 week
para sa complete recovery.
nagadugo then nana, maam reteracion polomolok 0928-3146006
A. Mao kini ang epekto sa malnutrition. Ang kakulang sa natural nga Vit C ug,
Vit B complex mosangpot sa bleeding gums ug bukol. Ang mga taong kanunay
ga-asukar og ga-softdrinks. Kawatan kau sla ug nutrients nga gikinahanglan sa cells.
Bag o kini nga konsepto sa conventional Medicine apan akong napamatud an
nga kung i-correct nato ang nutrition dali ra kau makaricover and ingun niini nga
kaso. Dili paigo ang pag-toothbrush lang tungod kay naa sa slod nanukad ang
problema and that is in the cellular level. Pataki ug Dok F ang
naandang formula sa Dok alternatibo. Epektibo kau ni. Paminawa ang akong mga
regular program sa DXCP Gensan
DXGO
Lunes hantod Sabado. Pinasahe ang akong pagpresenta sa mga health issues nga di
ninyu madungan bisan asa. Sa inyung mga text 0906-8702338
He was a DOST Scholar and a bonafide Inventor (PATENT # 2-2007-000019),
a KPB license broadcast journalist and Doctor of Ministry in Alternative Medicine.
He is the FOUNDER and ORGANIZER of ALTERNATIVO Multipurpose Cooperative and Doktor Alternatibo Healing Ministry, Doktor Alternatibo Herbal Products
(BFAD LTO Registration RDI-RXI-FW-33)... He handles 8 clinics in Region XI.
Saturday, April 5, 2008
Sex Secrets:
| Unsaon Pagtagbaw sa imung Bana sa | |
Ang babaye nga makatagbaw sa iyang lalake ‘in the real sense’ matawag nga
'a complete woman'.Gusto mo bang pangitaon ka sa imung lalake inay
magpangita siyag kalipay sa uban.?
Kung mao, diay ‘sure formula’ alang kanimu diin makapakurog sa unod sa imung
bana!
Una, Ayaw kompyansa nga sa dihang makabalo ka unsaon mo siya paglipay sa
Kinahanglan mo sya lipayon sulod o guwa sa kwarto sa himaya. Ayaw gayod
ibaliwala ang
Karon, una ta hisgutan kini, ato una hisgutan kung unsa ka ingon nga
BABAYE, unsay angayan mong bag- ohon aron matagbaw mo sa kalipay ang
imung lalake gawas sa kwarto sa himaya.:
Respeto --mao gayod ang gipangita sa imung BANA. Kung dili mo sya
marespeto ingon nga imung bana, kawad- an ka usab sa pagpangga nga
angayan sa
(orgasm) ang babaye kay sa lalake. Ipakita kaniya ang pagtahod aron
tahoron usab nya ang imung pagkatawo ug labaw sa tanan ang imung tawhanong
panginahanglan sa
I-devote ang imong panahon sa imung bana, sa inyong relasyon tungod kay
mubo kau ang kinabuhi ning kalibutana ug angayang ipadaplin ta ang negatibong
emosyon ngadto sa tawong imong makauban sa tibook mong kinabuhi.
Kung gitinguha mo gayud ang paglipay kaniya, dapat aduna gayoy kabag-
ohan nga imung himoon ..
Dugang niini, lotoe sya o andame sya sa iyang paboretong pagkaon ilabe na
kung gikan siya sa trabaho nga kapoy. Makapahuwas kini sa stress diin usa
sa maoy hinungdan sa kawalay gana sa sex.Paimna siya sa HERBAL nga
pampagahi kung gusto mo syang modunar sa kama. Caution, ayaw gayod
pagamit ug mga synthetic –base nga pampagahi kay duna kini daghang pelegro
sama sa stroke o atake sq kasing-kasing . Niining paageha nagakakusog ang iyang
‘anticipation’sa sunod nga mahitabo ug mas Ganado sya sa pakighilawas.
Siya na siguro ang pinakamalipayong tawo sa kalibutan. I-andam ang
iyang gusto diha sa panimalay o sa gawas bisan dili nimu gusto aron ipakita
nga gatagad ka sa iyang interest ug makapatingala kaniya. Niini nga sestima
ganahan siya,.
Dinhi ta sa imong ‘looks’.- Ang lalake kanunay gusto sa babaye nga maanyag,
sexy, humot, ug naka-expose ang limpyo nga mga panit niini ilabi na sa
mga dapit sa liog, dughan, paa , dalungan labi na sa nipis nga sout ug makapadani
nga underwear. Bisan dili ka sama ug beauty sa mga mutya, maanyag ka gihapon
sa mga mata sa imung bana kung naka-make-up, naka-nighties, bag-ong nanghugas
o naligo ug gapahumot. Kung nagapangandam ka sama niini, mosantop sa iyang
huna-huna nga gipangandaman jud nimu siya ug motaas na ang kahinam niya nga
makighilawas sa imu kung makita ka niya nga nagapangandam.Gipakita mo nga
espesyal siya diha kanimu.Dali ra ganahan ang lalake bisan makita ra niya
tungod kay kinaiyahan sa lalake nga mapukaw ang gana sekswal bisan
sa pagtan-aw man lamang!
Sa kama, kung ganado na gani sya, ipakita nga interesado kang kopyahon ang
mga pagilok nga iyang gihimo sama sa paghalok sa mga sensitibong parte sa
lawas sama sa liog, dalungan, nipple sa totoy, pusod ,apan ang pinaka
importante mao ang pagdula –dula sa imong kamot sa iyang kinatawo.
Ang Lalake’ PENIS-CENTERED ‘. Dali kau ganahan kung imong pisliton ang
kinatawo ug kusog sibo sa iyang naandan. Kung di ka kamao ayaw pagpanuko
sa pagpangutana kung giganahan ba siya o wala. Importante nga ‘open’ mo
sa usag
Sa katapusan ayaw pagpanuko sa pagsunod sa iyang gusto bisan di makaya
pagsugod, ayaw jud pagnegatibo hangtod nga masulayan nimu ang iyang
gusto ipahimo sama blowjob o pag stimulate sa iyang G-spot o ang pag explore
ug sex positions. Mahinungdanon nga inyu una nga tun an ang usag
magkahibaw anay sa gusto o dili gusto diha sa pakighilawas ug kung sa
unsang paage kini himoon. Padayona pag sunod ang akong mga sinulat kung
unsaon pagpangita ang G-spot sa lalake o sa babae u g ang makapatagbaw nga
sex positions.
| Sex Secrets nga dapat mong mahibaw an Makapanilap nga sekretong di mo palampason
| |
| Nakabalo ka ba kung natagbaw ba imong pares diha sa pakighilawas? |
Ans sex mao ang pagtagbaw sa imong partner dungan sa imong personal nga
katagbawan.Apan kasagaran ang sex one sided diin ang
nagpalami sa iyang kaugalingon ug wa panumbalinga ang katagbawan sa kapareha.
Tungad niini, napalong ang gana ug dili nimu matagbo unsa gayod ang gipangita
nga katagbawan sa imung uban. Ang mosunod maoy mga sex secrets sa Indian
Kama Sutra nga makapahigmata kanimu.
1.Lipaya ang imung babaye ug lipayon ka usab niya!.Ayaw pagdalidali nga
magawsan ka pag una. Gahini gayud ug panahon nga pagilokan nimu ang
babaye pinaage sa paghalok o paghimas sa likod sa liog, sa dalungan, sa nipple
sa totoy, sa pusod ,ug sa clitoris labaw sa tanan ang pagtumbok sa G-spot.
May mga paage sa pagpagilok niini sama sa unsa ka hinay o kakusog ang
paghalok o paghimas .Basaha ang uban nakong mag sinulat mahitungod niini.
Niini nga paage, mapukaw mo ang iyang gana ug mailhan mo pinaage sa iyang
sagonson nga paginhawa,ug mga pisikal nga ilhanan sama sa pag utbo s nipple,
pagpanglibawot sa mga balhibo sa panit ug pagtubod sa kinatawo. Ayaw pagpadayon
sa sex kung dili nimu kini makita ug nagpasabot nga gakinahanglan ka ug dugang
minuto aron paganahan siya.
2. Ipakita nga gusto nimu siya. Ang babaye Ganado kung ipakita mo nga
gahinamhinam ka niya ug nga nagtagad ka sa iyang katagbawan labaw
kay sa imong kaugalingon. Ang lalake dali ra magawsan kung ikompara nimu sa
mga babae. Mao BAWAL gayud nga mag una ang lalake diha sa
kung masipyat ka isipon mo nga dako kaayong
ka pag una. Samtang nagapagilok ka sa iyang dungan, hunghungi kung
unsnimu siya ka mahal,ipabati kanunay nga gipanga nimu siya. Mas Ganado
ang babaye kung makabalo siya niini.
3. Paghimu ug mga surpresa sama sa bag ong sex positions. Sultie sya daan kung
unsaon nimu siya paglipay sa bag ong paage sa pagpalami kaniya. Ang imahenasyon
sa babaye maoy numero unong sex organ sa tawo.Niining paageha gipahinam mo
siya sa sunod mong buhaton ug sigorado gyud nga moagulo siya ug halos mulohod
kanimu aron makigdulog kanimo pag usab. Alang sa dugang impormasyon
pakigkita kanako personal alang sa mga espesyal nga tips. Dok Ed Delibo
Pagpangita sa G-Spot: Giya sa Firstimers
| How to find the G-spot? To support you around this, author has created a simple, step-by-step exercise that takes about an hour and a half |
Daghan ang wa kabalo asa dapita ang ‘ g spot’. Aron matabangan ka unsaon,
akong tagsa-tagsa-on ang proseso nga makapatagbaw sa babaye sulod sa
oras ug tunga nga ‘exercise’.
Imong mabantayan niining exercise ang taas nga ‘time’ ang gastoon una mo makaplagan
ang G-spot.Gituyo kini! Importante kayo nga adunay tamang oras ug erotic nga
environment
sa paghimo niini.Dinhi lamang nga paage imong makaplagan ang G-spot sa babaye.
Time nga gikinahanglan: Approximately 1-1.5 hours, mas maayo sa hapit
na tungang gabii nga wa nay disturbo o
(mas mayo sa hotel or motel)
Ang proseso nga andamon:
1) Pagtigom ug igong ‘energy’ ug mokaon sa mga pagkaong puno sa B complex,
Vitamin E ug Fulvic Minerals duha ka oras una ang exercise.
2) Ayaw pagbusog ug kan-on ug sud-an nianang panahona tungod kay mahago
ang imong tiyan ug mangawat kinig energy sa utok diin makapawala sa gana ug
makapaduka. Mas maung imnun lamang ang formula sa Dok Alternatibo tungod
kay tested na kini
3) Pakahuman ug inum sa Formula, mas mau nga maligo kamong duha sa medyo
init nga tubig aron painiton ang dugo ug ang mga kaunoran.
4) I-andam ang
adto kini himoon sa
5) Mas makatabang ang kandila, insenso, sexy music, massage oil,aron daw sagrado
kau ang dapit alang sa retwal sa pagpangita sa perlas—ang G-spot.
6) Pag sol-ob ug loag nga senina o bisan unsa nga komportable ka samtang
magpahigayon sa pagilok o ‘erotic massage’
7) Paningkamota nga matuman ang pagpangandam kay kausa ra kini himoon
–ang exploration sa G-spot. Mas rewarding ang epekto.
Sugod sa pagilok (5 – 7 minutes):
1) Imbitaha ang imong babaye sa balaang
iandam ang iyang emosyon sa
2) Samtang imu syang gipahigda sa
pagmahal, ang iyang kamahinungdanon, ug ang iyang pagtahan sa G-spot diin perlas
kini alang kanimu ug kaniya..
Pagmasahe (erotic massage) (30 minutes):
1) I-masahe ang imong partner, hinay nga pinagilok sa dapit sa dalungan, sa liog,
sa spine(likod), sa palibot sa totoy, sa tumoy sa tudlo sa kamot ug tiil lakip na
sa bugan. Take note, ayaw idoot, pagiloki lang sama rag ngapaspas ka gamit
ang balhibo sa manok Ayaw tumboka ang clitoris sa vagina pag ayo. Palabye lang
sa imung mga tudlo samtang galihok pataas-paubos sa iyang lawas.Gastohe ug
10 – 15 minutes .Mahinungdanon kini aron marelaxs imong partner. Ug magsugod
ug basa ang ngabil sa iyang vagina.
2) Mas maayong imong ipuli pagmasahe ang imong mga dila ilabi na sa liog, dungan
sabay ang paghunghung sa mga dirty words sa iyang dungan, sama sa ‘ lamia nimu
tilaan oy’ ‘kitkiton nako unya imong clitoris’, ug uban pa, Pinaage niini motaas
ang iyang kahinam. Timan I nga ang utok ug emoyion sa babaye mao ang ilang
pinakadako ug pinakaaktibo nga ‘sex organ’.
3) Timam I –wala pa kay adtoan, pagilok lang una, just enjoy samtang nag-enjoy
pud siya. gt agba
Pa w sa Gana (5-10 minutes):
1) Niini nga stage, narelax na kau ang babaye ug nagsugod na paguwa ang
iyang sexual hormones, dasiga siyang moreact sa imong mga pagilok in a
natural manner. Mamahimong idugang ang kissing, nipple sucking, yoni massage,
toe sucking, clitoral stimulation, etc. (I’m sure you get the idea : ) Ang puntos ani
mao nga wala nimu siya gidalidali hangtod nga mo-agulo siya pag ayo ug magpakilooy
nga sudlan na ang iyang kinatawo. Hinog na ang gana nga pwede na isulod nimu ang
imong tudlo alang wa sunod nga step.Usbon ko, nangita ka sa G-spot ug dili nimu
pwede sudlan sa imung kinatawo ang iyaha. Pasagdi sya nga maglimbag-limbag
sa kalami samtang nangalyupo nga ipasulod na imuha. Ayaw patintal!.
Pagtumbok sa G-Spot (10 minutes)
1) Niini nga stage, init na ug nagbasa na ang vagiuna sa imong partner. Nangamuyo na nga sudlan na ang iyahang kinatawo – WELL DONE! Kung wa pa makaabot nini nga period, balike ang naunang steps.
2) Posisyon para komportable mong duha! Niining puntoha, isulod mo na ang imong tudlo sa iyang ‘vagina’ samtang giduladula mo ang iyang clitoris. Pwede kang molingkod tapad niya o moluhod sa atbang sa iyang gabilangakad nga paa.
3) Pakigstorya sa iya kung komportable ba siya. Ayaw kaulaw o pagpanuko sa imong posisyon kay sa mosunod nga 20 minutos imong pagilokan sya pag ayo gamit ang iyang G-spot.
4) Hinayhinay nga imong isulod ang imong tudlo sa gabasa nga ‘vagina’ samtang imong gimasahe ang ilalom. Dulaa imong tudlo hulbot-sulod, pinatuyok sa ilalom ug bantaye kung wa ba siya sakite. Pangutana jud
kung giganahan ba siya o bantayan mo ang iyang tingog-agulo, gininhawa
ug iyang tibook body language.Enjoy!
5) BABAE. Importante nga niining puntoha, isulti mo kung giganahan ka
ba o wala..Kung gusto mo ba ang hinay nga pressure o kusog-kusog o kosgon pa.
Timan-I nga naghimu mo niini aron makat-on.
Ang pagpagilok sa G-Spot (15 - 20 minutes)
1) Karon, pagilok na sa G-spot! Isulod ang
2 inches pailalom, ug ikolitog. Salata sa ilalom sama ana sa picture sa itaas.
Gipalihok sama sa “come here” move gamit ang tudlo.Makaayo nga ihagkom
mo ang mga palad sa atubangan sa iyang ‘vagina’samtang ang imong
thumb (kumagko) nagduladula sa clitoris.
2) Niining bahina, pag-experimento sa nagkalain-laing pressure – hard,
soft, light, etc. Nadiskobre sa mga experto sa sexology (pagtoon sa sex),
maayong sugdan mo paglihok ang tudlo sama sa wiper sa sakyanan diin
pantay ang pressures.
3) [BABYE: Sultie ang imong partner kung giganahan ka ba o wala aron makabalo
siya unsaon ka niya pagmaniho sa kama.Maayo sab sulayan mo pag-ipit sa imong
paa aron sulayan kung ganahan kaba sa sensation niini.Just enjoy hangtod
15-20 minutos.]
4) Kung makakapa ka ug dapit nga medyo gaspang, o daw murag gabutoy,mao
na na ang imong gipangita-G-spot.Kung imo kining tandogon, ang G-spot
kasagaran mohubag og mo utog pag ayo. At this point, may mga babaye
nga gusto ug hard pressure, apan kasagaran gusto jud nila ang softer
pressure (baliktad sa pagpisil sa clitoris).
5) Kung nakaplagan mo na ang G-spot ug nag enjoy ang imong partner,
sabaye ug pagilok ang iyang clitoris pinadapat ang imong komagko.
6) Ang magic combination mao ang pagpagilok sa g-spot gamit ang
tudlo samtang ang kumagko sa cleto, mas mokurog sa kalami ang
imong pares. Di makapanangpit sa silingan!
7) Niini nga punto, ang babaye maglimbaglimbag na sa kalami Ayaw kabalaka,
walay daotan niana, relax lang ug ipadayon ug paabota nga mag
multiple orgasm siya.(magawsan nga dili lang kausa).Ohm kalami!
8) (Apan kung wala ka gawsi niining maong exercise, ayaw kabalaka tungod
kay may mga babaye gayod nga walay G-spot ug gikinahanglan sila ug
Nutritional Therapy. Usba sa gihapon ang maong proseso hangtod nga
makaplagan nimu ang G-spot sa sunod higayon. Ug matagbaw mo ang kinabuhing
magtiayon.)
9) [VARIATIONS: Pwede sab nga pagilokan mo ang G-spot samtang nagapadayon
ang orgasm o pagkahuman niini gamit ang nagkadaiyang pressure, strokes,
angles, etc.. sulaye sa
butangan nimu ug jerjer pillow o unlan nga gidesenyo jud para jerjer ang
ilalom sa iyang sampot aron mabag-o ang ‘angle’ sa tudlo ug sa ‘penetration’ niini].
Pwede pud magamit ang jerjer pillow sa mga sexual intercourse.
Panapos (5 minutes)
1) Niini nga higayon – humana ang orgasm – mapuypoy na ang energy
ug panahon na nga taposon ang exercise. Ibta na ang tudlo sa vagina ug
itapion kini sa ibabaw nga gakulob samtang ang
sa dughan samtang imong gitutokan ang iyang mga mata aron magpabilin
ang kainit sa ehersisyo.
2) Relax, ug sulod sa 5 minutos i-share ang inyong kasinatian samtang
nag-exercise kaganina kung asang bahina nga mas giganahan ang babaye o
asa ang wala aron maoy gamiton during sexual intercourse.Mas
maayo inyo unang estoryahan ang bahin nga gilamian ang babaye ug hunahunaon
kung unsa ang angayang himoon sa sunod exercise.
Mahitungod sa Tigsulat
Dok Edgar Delibo is a Doctor of Ministry in Alternative
Medicine graduated Cum Laude, a Filipino Inventor with Patent, a
DOST_SEI Scholar in his College Years at
Philippines
Natural Farming Technology. He is the Chairman of ALTERNATIVO
Multi-purpose Cooperatve, and Owner of Dok Alternatbo Herbal
Products with BFAD LTO. Registration RDI-RXI-FW_33.
He handles various radio programs Over
DXCP_Gensan (every
DXCO-Cagayan de
He maintains Clinics in different areas in Mindanao
DAVAO- Door 1 , Rebaja Bldg, Mc Arthur Highway, Matina, Tapad Bantay
Bata.( Note: Dili Kauban si Doc Laguit under question na karon sa BFAD, PRC,BIR), Beware!
DIGOS- Bonifacio Superhighway, Aplaya.Kada Domingo
,
POLOMOLOK- In-front Van Terminal.Kada-Martes
PANABO- Unahan sa NDC:
Note: Dok Alternatibo Clinic is Consists of Multiple Alternative
Medicine Doctors
Wednesday, February 27, 2008
Dok Edgar Delibo DMAM is the Inventor behind the Famous Fulvic Minerals
He is a bona fide member of Davao Inventors Association. with its main office located at Mac. Arthur H-Way Matina Davao City. you may call us at (082)297-1847 Or bayantel hot line (082)301-9587 or email us at dok_alternatibo@yahoo.com,inventorsnewscast@yahoo.com
What is Fulvic and what does it do for the body?
• Fulvic, a natural ionic molecule, is rapidly being recognized as one of the key elements in many scientific breakthroughs of the 21st century. It is one of the most crucial factors in the reversal and prevention of disease, as well as the maintenance of good health. Nature made fulvic abundantly obtainable, but like many things, man has interfered with this vital process and it is no longer available in adequate quantities in the foods we eat. You must provide your body with this essential element through supplementation.
What does fulvic do in the body?
l The fulvic molecule prepares nutrients to inter-react with each other.
When fulvic is present in the body, nutrients are dissolved into the simplest ionic form and disappear into the fulvic structure. Most of the benefits we receive from nutrients occur are due to their co-factor reactions with each other. Fulvic offers tremendous benefits because it enhances these reactions.
- Fulvic makes all nutrients more absorbable
- Fulvic transports nutrients right into the cells
It can often transport many times its weight in dissolved nutrients and elements. Fulvic is so powerful that one single fulvic molecule is capable of carrying 60 or more minerals and trace elements into the cells.
- Fulvic makes cell walls more permeable
It makes cell walls more permeable, so nutrients can more easily enter the cell, as well as allowing waste to leave the cells more readily. One of the strongest advantages of fulvic minerals is that absorption greatly exceeds traditional tablet supplements. As with any nutrient or supplement, the only way your body can benefit, is if it is absorbed. Fulvic enhances this process.
- Fulvic increases absorption of oxygen and decreases acidity
It quickly destroys acid in the body fluids which helps increase the amount of oxygen in the blood. A lack of blood oxygen is a major contributing factor for acidity. Excess body acidity is associated with virtually all degenerative diseases; including cancer, heart disease, osteoporosis, arthritis, kidney stones, tooth decay, sleep disturbances, depressive disorders, and more.
- Fulvic changes the pattern of metabolism of carbohydrates.
It also intensifies the metabolism of proteins, and has been shown to stimulate the immune system.
- Fulvic increases absorption of oxygen and decreases acidity
It quickly destroys acid in the body fluids which helps increase the amount of oxygen in the blood. A lack of blood oxygen is a major contributing factor for acidity. Excess body acidity is associated with virtually all degenerative diseases; including cancer, heart disease, osteoporosis, arthritis, kidney stones, tooth decay, sleep disturbances, depressive disorders, and more.
- Fulvic changes the pattern of metabolism of carbohydrates.
It also intensifies the metabolism of proteins, and has been shown to stimulate the immune system.
- Fulvic is a powerful de-toxer
Fulvic has the ability to complex and remove toxic heavy metals and other pollutants from the system. It can either alter them into useable compounds or eliminate them as waste. It detoxifies pollutants, including herbicides, radioactive elements, and toxic metals, by binding to these substances and flushing them out of the body, if unable to convert them.
- Fulvic has antibiotic properties
Although fulvics are not antibiotics in the technical sense of the word, as prescription drugs are, their antibiotic like effect is comparable to the power of penicillin in equally small amounts. Unlike antibiotics, fulvic can be used indefinitely without creating any antibiotic resistant strains of disease which are common problems with pharmaceutical drugs. People with healthy lifestyles and eating habits, who take fulvic on a consistent basis, report that they rarely get colds or the flu, and suffer very little from allergies.
- An extensive number of studies show that Humic extracts, specifically Fulvic, effectively and safely kill the HIV / Aids virus. In fact, one pharmaceutical company has patented a humic based drug that purifies blood for transfusions, killing the HIV virus without damaging blood cells.
Especially pleasing to the parents of asthmatic children is the powerful and immediate effect Fulvic therapy produces. New research by Dr. David L. Hahn of
- Fulvic’s function is to balance and energize all cell life and biological properties it comes in contact with.
Because fulvic carries both a negative and a positive charge, it energizes cells, and can behave as an electron donor or acceptor, depending on the need. If the individual cell is restored to its normal chemical balance and electrical potential, we have given cells life, where death and disintegration would normally occur. What if the newly energized cells belong to a liver, a heart, or a the thyroid? Those organs could have the potential to function at peak performance. Scientists believe disease is rampant today because people are so deficient in fulvic and the minerals, trace elements, and nutrients it contains.
- Although it isn’t advertised as a weight loss product, a great side benefit is that many people report losing excess weight after starting to take fulvic.
Although we don’t advertise it as a weight loss product, a great side benefit is that many people report losing excess weight after starting to take Fulvic. Body weight balances naturally because fulvic helps correct chemical and hormonal imbalances, assists the proper metabolism of food, and diminishes mineral deficiency cravings. When these changes occur, many people don’t have the desire to eat as much, and don’t crave breads, pastas, and sweets as much.
- More on heavy metal build-up...
Because fulvic minerals are organic, they will not build up in the body tissues, as do metallic and clay based minerals. When presented as organic fulvic complexes, cells have the ability to accept or reject minerals, including aluminum, lead, arsenic, mercury, etc., at their discretion. It should be considered though that these minerals may not necessarily be present to “nourish” cells, but are needed to act as “electrodes” in the fulvic electrolyte solution. In that capacity they are probably most essential for bio-reactions, electron transfer, catalytic reactions and transmutations.
- It is obvious that when metals, minerals and trace elements become complexed into fulvic, they take on an entirely new property of availability, unlike their original form. It is when fulvic is not present that one should seriously worry about toxic buildup from any source.
Where does fulvic come from?
- Fulvic is created by microbial activity at the roots of plants. Its function is to dissolve, and convert the metallic and clay based mineral molecules that are in soils, into a form that is usable by plants, animals and people. Once the minerals are dissolved, plants uptake, through their root system, the powerful fulvic substance that is loaded with dissolved minerals and trace elements. Supplements high in fulvic come from ancient deposits of lush plant matter that were buried millions of years ago before chemicals, pesticides, and other harmful substances ever existed. The fulvic strength of today’s plant derived mineral products depends on the fulvic concentration of its source. Fulvic content varies from deposit to deposit similar to the way minerals are found in veins throughout the world.
- Fulvic is no longer readily available in today’s plants
Because current farming practices use chemicals and pesticides that kill the microorganisms that creat fulvic, the essential natural process of converting metallic and clay minerals to a form that is usable by plants has basically stopped. When the fulvic microorganisms in soil are destroyed, plants are not able to take the undissolved metallic and clay minerals into their root systems. The minerals remain in their original inorganic form in the soil, and our plants become mineral deficient. To complicate matters, the mineral content of our soils is extremely low right now. Farm lands have been overused and minerals are not being replaced the way nature intended. Even organic foods can be deficient because of our depleted soils. Scientists feel this could account for the dramatic rise in health problems that plague our “fulvic starved” society. Foods with high fulvic content are very difficult to obtain, making it essential that we supplement our diets with this essential molecule.
- In summary...
fulvic is an immense arsenal pf powerful phytochemicals, biochemicals, supercharged antioxidants, free-radical scavengers, nutrients, enzymes, hormones, amino acids, antibiotics, antivirals, and antifungals. By adding this unique molecule to all our liquid products we have increased absorption and bio-availability, making them some of the most effective products on the market today.
Friday, February 15, 2008
The Real Story about the Florescent Lamp Invention And Its Inventor
What is a Fluorescent Lamp?
The history of the fluorescent lamp begins with early research into electrical phenomena. By the beginning of the 18th century, experimenters had observed a radiant glow emanating from partially evacuated glass vessels through which an electrical current passed. Little more could be done with this phenomenon until 1856 when a German glassblower named Heinrich Geissler (1815-1879) created a mercury vacuum pump that evacuated a glass tube to an extent not previously possible. When an electrical current passed through a Geissler tube, a strong green glow on the walls of the tube at the cathode end could be observed.
Because it produced some beautiful light effects, the Geissler tube was popular source of amusement. More important, however, was its contribution to scientific research. One of the first scientists to experiment with a Geissler tube was Julius Plücker (1801-1868) who in 1858 systematically described the luminescent effects that occurred in a Geissler tube. He also made the important observation that the glow in the tube shifted position when in proximity to an electromagnetic field.
Inquiries that began with the Geissler tube continued as even better vacuums were produced. The most famous was the evacuated tube used for scientific research by William Crookes (1832-1919). That tube was evacuated by the highly effective mercury vacuum pump created by Hermann Sprengel (1834-1906). Research conducted by Crookes and others ultimately led to the discovery of the electron in 1897 by J. J. Thomson (1856-1940). But the Crookes tube, as it came to be known, produced little light because the vacuum in it was too good and thus lacked the trace amounts of gas that are needed for electrically stimulated luminescence. An important stage on the long scientific path that lead to the fluorescent lamp was Alexandre Edmond Becquerel’s (1820-1891) observation in 1859 of the luminescence of certain substances when they were placed in a Geissler tube. He went on to apply thin coatings of luminescent materials to the surfaces of these tubes. Fluorescence occurred, but the tubes were very inefficient and had a short operating life. A few years earlier another scientist, George G. Stokes (1819-1903), had noted that ultraviolet light caused fluorspar to fluoresce, a property that would become critically important for the development of fluorescent lights many decades later.
While Becquerel was primarily interested in conducting scientific research into fluorescence, Thomas Edison (1847 – 1931) briefly pursued fluorescent lighting for its commercial potential. He invented a fluorescent lamp in 1896 which used a coating of calcium tungstate as the fluorescing substance, but although it received a patent in 1907, it was not put into production. As with a few other attempts to use Geissler tubes for illumination, it had a short operating life, and given the success of the incandescent light, Edison had little reason to pursue an alternative means of electrical illumination.
Although Edison lost interest in fluorescent lighting, one of his former employees was able to create a gas-based lamp that achieved a measure of commercial success. In 1895 Daniel McFarlan Moore (1869 - 1933) demonstrated electrically activated tubes 7 to 9 feet in length that used carbon dioxide or nitrogen to emit white or pink light, respectively. As with future fluorescent lamps, it was considerably more complicated than an incandescent bulb.
After years of work, Moore was able to extend the operating life of the lamps by inventing an electromagnetically controlled valve that maintained a constant gas pressure within the tube. Although Moore’s lamp was complicated, expensive to install, and required very high voltages, it was considerably more efficient than incandescent lamps, and it produced a more natural light than incandescents. From 1904 onwards Moore’s lighting system was installed in a number of stores and offices. Its success contributed to General Electric’s motivation to improve the incandescent lamp, especially its filament. GE’s efforts came to fruition with the invention of a tungsten-based filament. The extended lifespan of incandescent bulbs negated one of the key advantages of Moore’s lamp, but GE purchased the relevant patents in 1912. These patents and the inventive efforts that supported them were to be of considerable value when the firm took up fluorescent lighting more than two decades later.
At about the same time that Moore was developing his lighting system, another American was creating a means of illumination that also can be seen as a precursor to the modern fluorescent lamp. This was the mercury vapor lamp, invented by Peter Cooper Hewitt (1861-1921) and patented in 1901 (U.S. Pat. No. 889,692). As the name implies, Cooper-Hewitt’s lamp luminesced when an electric current was passed through mercury vapor at a low pressure. Unlike Moore’s lamps, those made by Cooper-Hewitt could be manufactured in standardized sizes and operated at low voltages. The mercury-vapor lamp was superior to the incandescent lamps of the time in terms of energy efficiency, but the blue-green light it produced limited its applications. It was, however, used for photography and some industrial processes.
Mercury vapor lamps continued to be developed at a slow pace, especially in Europe, and by the early 1930s they received limited use for large-scale illumination. Some of them employed fluorescent coatings, but these were primarily used for color correction and not for enhanced light output. Mercury vapor lamps also anticipated the fluorescent lamp in their incorporation of a ballast to maintain a constant flow of current.
Cooper-Hewitt had not been the first to use mercury vapor for illumination, as earlier efforts had been mounted by Way, Rapieff, Arons, and Bastian and Salisbury. Of particular importance was the mercury vapor lamp invented by Küch in Germany. This lamp used quartz in place of glass to allow higher operating temperatures, and hence greater efficiency. Although its light output relative to electrical consumption was better than other sources of light, the light it produced was similar to that of the Cooper-Hewitt lamp in that it lacked the red portion of the spectrum, making it unsuitable for ordinary lighting.
An electric current passing through a tube was the basis for another form of illumination, the neon light. While Moore used carbon dioxide, nitrogen, or atmospheric air to fill the tubes and Cooper-Hewitt and others employed mercury vapor, the next step in gas-based lighting took advantage of the luminescent qualities of neon, an inert gas that had been discovered in 1898. In 1909 Georges Claude (1870 – 1960), a French chemist, observed the red glow that was produced when running an electric current through a neon-filled tube. He also discovered that a blue glow resulted from the use of another inert gas, argon. The light could be used for general illumination, and in fact was used in France for this purpose beginning around 1930, but neon lighting was no more energy-efficient than conventional incandescent lighting, and it came to be used primarily for eye-catching signs and advertisements. Neon lighting was not irrelevant to the development of fluorescent lighting, however, as Claude’s improved electrode (patented in 1915) overcame “sputtering,” a major source of electrode degradation. Sputtering occurred when ionized particles struck an electrode and tore off bits of metal. Although Claude’s invention required electrodes with a lot of surface area, it showed that a major impediment to gas-based lighting could be overcome.
The development of the neon light also was significant for the last key element of the fluorescent lamp, its fluorescent coating. In 1926 Jacques Risler received a French patent for the application of fluorescent coatings to neon light tubes. The main use of these lamps, which can be considered the first commercially successful fluorescents, was for advertising, not general illumination. This, however, was not the first use of fluorescent coatings. As has been noted above, Edison used calcium tungstate for his unsuccessful lamp. Other efforts had been mounted, but all were plagued by low efficiency and various technical problems. Of particular importance for the story that was to follow was the invention in 1927 of a low-voltage “metal vapor lamp” by Friedrich Meyer, Hans-Joachim Spanner, and Edmund Germer, who at the time were employees of a German firm located in Berlin. A German patent was granted but the lamp never went into commercial production.
All the major features of fluorescent lighting were in place at the end of the 1920s. Decades of invention and development had provided the key components of fluorescent lamps: economically manufactured glass tubing, inert gases for filling the tubes, electrical ballasts, long-lasting electrodes, mercury vapor as a source of luminescence, effective means of producing a reliable electrical discharge, and fluorescent coatings that could be energized by ultraviolet light. At this point, intensive development was more important than basic research.
In 1934 Arthur Compton, a renowned physicist and GE consultant, sent a report to W.L. Enfield, manager of research and engineering at GE lamp department, outlining successful experiments with fluorescent lighting at the research laboratory of the General Electric Co., Ltd. in Great Britain (although it bore the GE moniker, this firm had no direct connection with General Electric in the United States). Stimulated by this report, and with all of the key elements available, a team led by George E. Inman built a prototype fluorescent lamp in 1934 at General Electric’s Nela Park (Ohio) engineering laboratory. This was not a trivial exercise; as noted by Arthur A. Bright, “A great deal of experimentation had to be done on lamp sizes and shapes, cathode construction, gas pressures of both argon and mercury vapor, colors of fluorescent powders, methods of attaching them to the inside of the tube, and other details of the lamp and its auxiliaries before the new device was ready for the public.”
In addition to having talented engineers and technicians along with excellent facilities for R&D work on fluorescents, General Electric controlled what it regarded as the key patents covering fluorescent lighting, including the patents originally issued to Cooper-Hewitt, Moore, and Küch. More important than these was a patent covering an electrode that did not disintegrate at the gas pressures that ultimately were employed in fluorescent lamps. This invention had been created by Albert W. Hull of GE’s Schenectady Research Laboratory, and was registered as U.S. Pat. No. 1,790,153.
While the Hull patent gave GE a basis for claiming legal rights over the fluorescent lamp, a few months after the lamp went into production the firm learned of a U.S. patent application had been filed in 1927 for the aforementioned “metal vapor lamp” invented in Germany by Meyer, Spanner, and Germer. The patent application indicated that the lamp had been created as a superior means of producing ultraviolet light, but the application also contained a few statements referring to fluorescent illumination. Efforts to obtain a U.S. patent had met with numerous delays, but were it to be granted, the patent might have caused serious difficulties for GE. At first, GE sought to block the issuance of a patent by claiming that priority should go to one of their employees, Leroy J. Buttolph, who according to their claim had invented a fluorescent lamp in 1919 and whose patent application was still pending. GE also had filed a patent application in 1936 in Inman’s name to cover the “improvements” wrought by his group. In 1939 GE decided that the claim of Meyer, Spanner, and Germer had some merit, and that in any event a long interference procedure was not in their best interest. They therefore dropped the Buttolph claim and paid $180,000 to acquire the Meyer, et al. application, which at that point was owned by a firm known as Electrons, Inc. The patent (U.S. Pat. No. 2,182,732) was duly awarded in December 1939. This patent, along with the Hull patent, put GE on what seemed to be firm legal ground, although it faced years of legal challenges from Sylvania Electric Products, Inc., which claimed infringement on patents that it held.
Even though the patent issue would not be completely resolved for many years, General Electric’s strength in manufacturing and marketing gave it a pre-eminent position in the emerging fluorescent light market. Sales of “fluorescent lumiline lamps” commenced in 1938 when four different sizes of tubes were put on the market. During the following year GE and Westinghouse publicized the new lights through exhibitions at the New York World’s Fair and the Golden Gate Exposition in San Francisco. Fluorescent lighting systems diffused rapidly during World War II as industrial manufacture, stimulated by wartime needs, gave rise to intensified lighting demands. The use of fluorescent lighting continued to spread in the years following the war, and by 1951 more light was produced in the United States by fluorescents than by incandescents.
What are the issues behind the Famous invention fluorescent Lamp?it is believed that a Filipino Inventor Agapito Flores invented the Fluorescent Lamp. but many controversies arises because of this renowned statements. according to research all the dates given are allegedly said to be wrong. How Did this Happen? Based on the history of the discovery of the fluorescent lamp the First discovery ways back into the 18th century where French physicist Alexandre E. Becquerel who had investigated the phenomena of fluorescence and phosphorescence, theorized about the building of fluorescent tubes similar to those made today.
2.merican, Peter Cooper Hewitt (1861-1921) patented (U.S. patent 889,692) the first mercury vapor lamp in 1901. The low pressure mercury arc lamp of Peter Cooper Hewitt is the very first prototype of today's modern fluorescent lights. 3. Edmund Germer (1901 - 1987) who invented a high pressure vapor lamp, also invented an improved fluorescent lamp. In 1927, Edmund Germer co-patented an experimental fluorescent lamp with Friedrich Meyer and Hans Spanner.
So What Is True About Agapito Flores?
Agapito Flores was born in Guiguinto, Bulacan, Philippines on September 28, 1897. He worked as an apprentice in a machine shop and later moved to Tondo, Manila where he trained at a vocational school to become an electrician.It has been reported that Agapito Flores received a French patent for a fluorescent bulb and that the General Electric Company bought Flores' patent rights and manufactured and sold his fluorescent bulb (making millions from it). However, all the inventors named above and more predate Agapito Flores' possible work on any fluorescent bulb.
According to Dr. Benito Vergara of the Philippine Science Heritage Center, "As far as I could learn, a certain Flores presented the idea of fluorescent light to Manuel Quezon when he became president. At that time, General Electric Co. had already presented the fluorescent light to the public."
Thursday, February 7, 2008
Tawa Tawa
"Tawa-tawa" has anti-viral and anti-bacterial components that can help cure even stage four of the dreaded dengue disease. not only that, lately tawa-tawa has been linked to cure cataract and other eye problems. a Filipino Inventor Dok. Edgar Delibo DMAM discovered an eye care using tawa-tawa extract as its main ingredients. the uniqueness of this product is that it is purely natural, its other active ingredients are isotonic solution and mineralized water. it may be used every day as an eye care solution for tired, weary eyes. it is very safe and no over dosage. this product is registered in the Bureau of Patents under Intellectual Property Office with the registration No. 000019 signed on February 2007 approved by Epifanio M. Evasco, the Director of Patents. this Product is Exclusively Distributed by Dok Alternatibo Herbal Products. This Patent Product is duly authorized by BFAD License To Operate No. RDI-RXI-FW-33. 
Dok Alternatibo's "Approved Patent Tawa-tawa eyedrops" contains tawa-tawa extracts which is believed to help cure corneal ulceration, a disease that causes inflammation of the cornea that leads to sore eyes, redness of the eyes etc. other components of this product such as isotonic solution (hydrochloric Acid) cleanses the eye and kills bacteria. another component is mineral water as its base ingredients all of this ingredients are mixed thoroughly and bottled. Its indications are for tired eyes, sore eyes, reading problems, blindness, cataract, far/near sightedness and other general eye problems. This eye drop is available in 15 ml bottle.
Dok Edgar Delibo DMAM is the Inventor behind the Famous Patent Tawa Tawa Eye Drop.
He is a bona fide member of Davao Inventors Association. with its main office located at Mac. Arthur H-Way Matina Davao City. you may call us at (082)297-1847 Or bayantell hot line (082)301-9587 or email us at dok_alternatibo@yahoo.com,inventorsnewscast@yahoo.com
What Doctors says (part 1)
What Doctors says (part 2)
Back pain
Muscle pain
Arthritis Pain
Carpal
OLEIA BALANCING OIL
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Simply apply a liberal amount of Oleia Oil around aching joints or sore muscles and experience liberation from pain in 15 minutes to 15 days. For chronic pain, apply oil 3 times a day. For those with hypertension, use 20 to 25ml of Oleia Oil for a light body massage.
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OLEIA Oil may help to:
- rebuild damaged joints and cartilage cells
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- act as an anti-inflammatory, as well as a lubricant for damaged joint.
OLEIA Oil is recommended for:
- people with the chronic painful conditions such as osteoarthritis, low back pain, rheumatoid arthritis, tennis elbow, recurrent pain due to sports injury etc.
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PSORIASIS/PSORIATIC ARTHRITIS "I have been suffering from psoriatic arthritis for 15 years now. I tried OLEIA OIL which my friend gave me one day. What a relief! OLEIA OIL has helped me to sleep soundly at night (because I have had no more joint pains) and has lessened the "itchiness" of my psoriasis." - Momoy Moreno, 50, Tahanang Walang Hagdan, Cainta, Rizal.
"OLEIA OIL is soothing to my skin. It has also lessened flare-ups of my psoriasis. I also apply OLEIA OIL on my tummy whenever I have hyperacidity, and I feel better faster." - Riza Lagunero, 40, Tahanang Walang Hagdan, Cainta, Rizal
SKIN RASHES/ALLERGIES “An apo ko, gumamit ng mamahaling ointment for rashes sa singit, kasi namamaga at hindi gumagaling. Sabi ko sa kanya, pahiran niya ng OLEIA OIL. Kinabukasan, sabi niya, hindi na raw makati at nawawala na ang rashes niya” - Paz Mediado, San Francisco, Iriga City
Ms. Sol works in the registrar's office of a university in Manila. She has had skin allergy, which kept coming back for one year. When she took OLEIA SOFTGELS, the skin allergy got healed, and it has never come back since.
STROKE Ms. Elen Pabillar had a stroke and was paralyzed from waist down to her left foot. She took four prescription drugs for more than one year until she complained of deafness. She switched to OLEIA SOFTGELS and she has now started to walk. Her hearing has also improved.
GOITER Ms. Iring tried OLEIA SOFTGELS for her goiter, since she did not want to undergo surgery. She is very thankful that the lump on her throat has started to shrink.
TUMORS/CANCERS After taking OLEIA SOFTGELS for almost three months, a lady had heavy vaginal discharge. She went to the doctor to have her check-up, and the doctor found out her myoma was gone. Her bleeding eventually stopped.
A woman from Baguio with breast cancer stage I had been taking OLEIA SOFTGEL and sodium ascorbate. She has been applying OLEIA OIL on the tumor for more than one month now. She has observed significant improvement in her condition.
A man in his 60's has prostate cancer and has had difficulty urinating. A few days after taking OLEIA SOFTGELS, he noticed better urination. He is continuously taking OLEIA SOFTGELS now and has noticed that his erectile dysfunction is no longer a problem.
Specific cases of patients who experienced symptomatic relief of inflammation after applying OLEIA Oil:
ARTHRITIS – case of a teacher in Don Mariano Marcos State University who cannot move her thumb without pain. 15 minutes after applying OLEIA Oil, naigalaw na niya ang kanyang daliri with no pain.
OLEIA helped a man from La Union who suffered stroke.
OLEIA helped an old lady who has gangrene due to diabetes.
OLEIA helped a man from Tubao, La Union with his psoriasis problem.
OLEIA helped a teacher from La Union with her frozen shoulder.
OLEIA helped a man with erectile dysfunction.
OLEIA relieves toothache.
OLEIA relieves dysmenorrhea pain
OLEIA helped a child from San Mateo, Rizal, who had cough, colds and flu.
5 days of OLEIA use relieved 70% of arthritis pain of a 69 yr-old man from San Fernando, Pampanga who has been suffering such pain for 30 years.
OLEIA helped teething problem of a toddler in Montalban.
OLEIA helped a 40 yr old lady from Angeles City with her wrinkle and fineline by making skin firmer and more hydrated.
OLEIA helped a lady from Marikina with her migraine, headache and sinusitis problem.
OLEIA helped a lady from Caloocan City with her back pain and frozen shoulder problem.
OLEIA helped a lady from Batangas City with her dysmenorrhea problem.
OLEIA helped a 55-yr old lady from Zambales with her varicose vein problem.
OLEIA helped a 70-yr old man from Olongapo City with his asthma/ emphysema problem.
OLEIA helped a teenager from Alabang, Muntinglupa in stopping SORE EYES.
OLEIA helped a woman from Tacloban City with her asthma problem.
OLEIA helped a woman from Leyte with her gastritis problem.
CONTACT US
Send a bottle of relief to your lolo, lola, tatay or nanay who may be suffering from pain due to arthritis, muscle pain, joint pain and other types of pain and inflammatory conditions.
Wednesday, February 6, 2008
Skin Detox Herbal Soap
Akapulko or Acapulco in English is a shrub found throughout the Philippines. A medicinal herb that contains chrysophanic acid, a fungicide used to treat fungal infections, like ringworms, scabies and eczema. Akapulko also contains saponin, a laxative that is useful in expelling intestinal parasites.
The extracts from the Akapulko plant is commonly used as an ingredient for lotions, soaps and shampoos.
Uses of Akapulko:
• Treatment of skin diseases:
Tinea infections, insect bites, ringworms, eczema, scabies and itchiness.
• Internal:
Expectorant for bronchitis and dyspnoea, mouthwash in stomatitis, alleviation of asthma symptoms, used as diuretic and purgative, for cough & fever, as a laxative to expel intestinal parasites and other stomach problems. A strong decoction of the leaves is an abortifacient.
Preparation:
• For external use, pound the leaves of the Akapulko plant, squeeze the juice and apply on affected areas.
• For internal use: cut the plant parts into a manageable size then soak and boil for 10 to 15 minutes let cool and use as soon as possible. Note: The decoction looses its potency if not used for a long time. Dispose leftovers after one day.
www.philherbalmedicine.com
About Virgin Coconut Oil (VCO)VCO is now getting global reputation as the healthiest and versatile oil in the world. The Philippines is one of the best sources of virgin coconut oil and it's popularity in the country is legendary. Although not an herb, we decided to make an article about VCO because of the growing interest on the oil and after receiving several inquiries from our visitors. Virgin coconut oil and regular coconut oil is rich in Lauric Acid, an essential fatty acid that is only found in high concentrations in mother's milk. When taken internally, Lauric Acid turns into a compound known as Monolaurin. It is this compound that is believed to fight viral pathogens that protects the body from bacteria, viruses and infections from parasites. Coconut oil also causes the metabolic rate to increase, hence helps reduce weight and is safe and beneficial for diabetics. For many years, coconut oil has been discredited (specially in the west) because of it's high saturated fat content. But recent studies have shown that not all saturated fats are the same. The medium chain triglycerides of which virgin coconut oil is classified, does not elevate LDL (the bad cholesterol) in our body compared to other polyunsaturated vegetable oils such as canola and sunflower oil which is widely produced in the west. How Virgin Coconut Oil (VCO) is MadeFirst, the husk and the shell is removed from fresh coconuts, then the meat of the coconut is shredded -a process called "Wet Milled", then the meat is "Cold Pressed" to get the coconut milk without any chemicals. The milk is then fermented in containers for a day or two. After which, oil is produced. This oil is carefully filtered and separated from the curd. You now have what is called, virgin coconut oil. A more modern way of separating the oil from the curd is through centrifugal force. The second method of producing virgin coconut oil (VCO) is using quick dried coconut meat and then processed in the same way. But the preferred manner by most is still the "Wet Milled" process. Difference between Virgin Coconut Oil (VCO) and Regular (RBD) Coconut OilRBD stands for Refined, Bleached, and Deodorized. Ordinary coconut oil usually comes from copra - coconut meat that is dried by either smoke, kiln or placing under the sun. Because the process itself is not sanitized, the oil must be further refined. To get more oil from copra, chemicals are usually used. RBD process is required to make the oil clear, odor free and tasteless. This procedure also removes the anti-oxidant and other properties of the oil. Some coconut oils are also hydrogenated which increases the serum cholesterol levels and thus is bad for the heart. While virgin coconut oil, being pure, unadulterated and unhydrogenated retains it's pleasant coconut taste, smell and all the health benefits of coconut oil. Much research still has to be done on the benefits of virgin coconut oil but preliminary findings and anecdotal reports are very promising. This may well be the much needed medicine to restore to health the ailing Philippine coconut industry. Benefits of VCO● A boost to the body's immune system ● A good source of saturated medium chain triglycerides ● VCO helps regulate blood sugar ● Lowers the viral load of AIDS patients. ● Has anti-viral & anti-microbial properties ● Helps hepatitis C, herpes patients ● Helps maintain healthy thyroid function ● Maintain LDL & HDL cholesterol levels ● Heals & nourishes the skin, hair & scalp from:www.googles.com
Dok Alternatibo presents its product "Skin Detox Herbal Soap" its main ingredients are Akapulko, Luba bark powder activated charcoal, Coustic soda, coco virgin oil & other essential oils. for best effect rub the soap into fine cloth and apply to affected area if you want to detoxify. | |
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Activated Charcoal
Activated Charcoal Fact Sheet
What is Activated Charcoal?
Activated charcoal is type of carbon made from wood, vegetables and other materials. It looks like a fine black powder. Activated charcoal is believed to have a large adsorptive capacity, making it able to bind with unwanted substances and toxins in the gut.Activated charcoal may help to lower cholesterol by interfering with enterohepatic circulation of bile acids. It has been found to lower total cholesterol and LDL cholesterol.
Why Do People Use Activated Charcoal?
DetoxificationBloating and gas
Malodorous gas
High cholesterol
Poisoning / overdose – under medical supervision. If poisoning or overdose is suspected, go immediately to the emergency department of a hospital.
Activated charcoal is also used in air and water filters.
Dosage Information
Activated charcoal is available in liquid or powder form.It is a popular ingredient in colon cleanse products.
Activated charcoal should be taken with plenty of water to avoid intestinal obstruction or constipation.
- Activated charcoal is estimated to reduce up to 60% of poisonous substances being absorbed.
- It works by adsorbing (soaking up) chemicals, thus reducing their toxicity (poisonous nature), through the entire length of the GI tract (stomach and small and large intestines).
- Activated charcoal itself is a fine, black powder that is odorless, tasteless, and nontoxic.
- Activated charcoal is often given after gastric lavage—the technique often called the stomach pump. Gastric lavage is only effective immediately after swallowing a toxic substance (within about one-half hour) and does not reach beyond the stomach as activated charcoal does.
Dok Alternatibo's presents its product. Dok A Activated Charcoal Capsule available in 100 milligrams and 100 grams. contains the same benefits as mention in the latter write ups. Dok A Activated Charcoal Capsule is best taken 1 hour before meals.
Turmeric ( Curcuma Longa)
Tumeric is one of the fastest growing ingredients in the natural channel reaching almost $4MM in sales. it is a common spice known mostly for its use in Indian dishes as a common ingredients in curries and other ethnic meals. turmeric has also been use in centuries in Ayurvedic Medicine. which integrates the medicinal properties of herbs with food. this extraordinary herb has found its ways into the spotlight in the west because of its wide range of medicinal benefits.
Turmeric is a potent antioxidant. Curcumin its main active constituent. is as powerful an antioxidant as vitamin C, E and beta carotene, making turmeric usage a consumer choice for cancer prevention, liver protection and premature aging. several published studies also shows that tumeric inhibits the growth of several different types of cancer cells.
in addition, turmeric is a powerful anti inflammatory, easing condition such as bursitis, arthritis and back pain. turmeric's anti inflammatory action is likely due to a combination of three different properties. first turmeric lowers the production of inflammation-inducing histamine. Secondly, it increases and prolongs the action of the body's natural anti inflammatory adrenal hormone, cortisol, and finally turmeric improves circulation, thereby flushing toxins out of small joints where cellular wastes and inflammatory compounds frequently are trapped.
Research has also confirmed the digestive benefits of turmeric. turmeric acts as cholagogue, stimulating bile production, thus, increasing the bodies ability to digest fats, improving digestion and eliminating toxins from the liver.
turmeric has also displayed anti ulcer activity. by reducing the amount of acid secreted. it helps to protect the linign of the stomach where peptic ulcer occur.
In the Ayurvedic medicine, turmeric is thought to have many medicinal properties and many in India use it as a readily available antiseptic for cuts and burns. Whenever there is a cut or a bruise, the home remedy is to reach for turmeric powder. Ayurvedic doctors say it has fluorideantibacterial agent. It is taken in some Asian countries as a dietary supplement, which allegedly helps with stomach problems and other ailments. It is popular as a tea in Okinawa, Japan. It is currently being investigated for possible benefits in Alzheimer's disease, cancer and liver disorders. Turmeric, under the name Avea, is becoming popular[citation needed] to treat depression. It is only in recent years that Western scientists have increasingly recognised the medicinal properties of turmeric. According to a 2005 article in the Wall Street Journal titled, "Common Indian Spice Stirs Hope," research activity into curcumin, the active ingredient in turmeric, is exploding. Two hundred and fifty-six curcumin papers were published in the past year according to a search of the U.S. National Library of Medicine. Supplement sales have increased 35% from 2004, and the U.S. National Institutes of Health has four clinical trials underway to study curcumin treatment for pancreatic cancer, multiple myeloma, Alzheimer's, and colorectal cancer. A 2004 UCLA-Veterans Affairs study involving genetically altered mice suggests that curcumin, the active ingredient in turmeric, might inhibit the accumulation of destructive beta amyloids in the brains of Alzheimer's disease patients and also break up existing plaques. "Curcumin has been used for thousands of years as a safe anti-inflammatory in a variety of ailments as part of Indian traditional medicine," Gregory Cole, Professor of medicine and neurology at the David Geffen School of Medicine at UCLA said. Another 2004 study conducted at Yale University involved oral administration of curcumin to mice homozygous for the most common allele implicated in cystic fibrosis. Treatment with curcumin restored physiologically-relevant levels of protein function. [1] Anti-tumoral effects against melanoma cells have been demonstrated.[2] Curry Pharmaceuticals, based in North Carolina, is studying the use of a curcumin cream for psoriasisbreast cancer into lungs and other body parts. Turmeric also enhances the effect of taxol in reducing metastasis of breast cancer. [3] Curcumin is thought to be a powerful antinociceptive (pain-relieving) agent. In the November 2006 issue of Arthritis & Rheumatism, a study was published that showed the effectiveness of turmeric in the reduction of joint inflammation, and recommended clinical trials as a possible treatment for the alleviation of arthritis symptoms.[4] It is thought to work as a natural inhibitor of the cox-2 enzyme, and has been shown effective in animal models for neuropathic pain secondary to diabetes, among others.[3]
www.google.com
Dok Alternatibo presents its product. Dok 1 a food supplement in a capsulated form its main ingredient is Curcumin Longa. 1 bottle contains 10 capsule 500 mg and is taken 3 times a day. Contraindicated to pregnant women.
Thursday, January 31, 2008
INTRODUCTION
If not because of some quarters maligning and discrediting the credibility and integrity of the man behind DOKTOR ALTERNATIBO and ALTERNATIVO MULTIPURPOSE COOPERATIVE, maybe we should not come up with this humble BIOGRAPHY of Dok ED. To GOD be the glory.
THE MAN BEHIND THE SUCCESS OF ALTERNATIVO COOPERATIVE
HIS EDUCATIONAL BACKGROUND
DOK EDGAR LOZADA DELIBO is the founder / organizer and currently the Chairman of ALTERNATIBO MULTIPURPOSE COOPERATIVE. He is a Doctor of Ministry in ALTERNATIVE MEDICINE confirmed by The OPEN SEMINARY on
THE GOVERNMENT RECOGNITION AND HIS ELIGIBILITY
After his graduation from college, the Civil Service Commission (CSC) granted him a Professional Career Eligibility without necessarily taking the CSC Prof exams as mandated by the Law. Then, due to poverty, he was not able to enroll a formal REVIEW but took the Licensure Examination for Teachers (LET) of the same year and passed. Subsequently, he took and passed the third, second and first class TESDA EXAMS and adjudge as the Best Trainer by TESDA PROVINCIAL Methodology Training Course.
HIS ADVOCACIES AND HEART FOR ALTERNATIVE MEDICINE
Because of his love for broadcast, in 1999 he volunteered as a Radio Anchor advocating Good Governance and practical Education over DXML Digos City while teaching at DIGOSTECH, Inc., By that year(1999), he was hired by ABS-CBN Davao as provincial Correspondent and weekly Program Host advocating Anti-corruption in the provinces which earned him a reputation of an anti-graft crusader with considerable enemies from those corrupt politicians in the government and unscrupulous businessmen. Soon, he was appointed as School Director of DIGOSTECH, the youngest at the age of 24. At the same time, he organized and led a Corruption Prevention Unit (CPU) named BANTAY KATAWHAN (with the reputable elders from Davao del Sur.) working with the office of the Ombudsman Mindanao. Three years after, he resigned as School Director and accept the offer of ABS-CBN DXAB as daily anchor of primetime BANTAY PATROL Radio Program popularizing the alternative medicine segment BANTAY PANGLAWAS. He was advocating natural treatment program due to his kidney stones and stomach disorders plus the health problems of his wife (myoma, toxic goiter, rheumatic heart, and migraine). He was the first who proved through broadcast that those illnesses can be cured effectively by natural treatment.
During that time, a board of Director from Department of Health (DOH)- Philippine Institute of Traditional and Alternative Health Care (PITACH) named ELIZABETH MICALLER Ph.D visited him as ‘guest on air’ and invited him to join a EUROPEAN IRIDOLOGY Class with basics of SCLEROLOGY. (She is being considered as the MOTHER OF IRIDOLOGY and SCLEROLOGY in the
While handling a radio program, he advocates livelihood trainings and seminars as well as free alternative medical missions. It was the moment of organizing the first batch of his Radio listeners and sympathizers organizing them into a cooperative.
Through series of meetings with Cooperative Development Authority officials, the cooperative was formally organized with CDA certification bearing the name ALTERNATIVO MULTIPURPOSE COOPERATIVE on June of 2006.
HIS AFFILATIONS AND OTHER ORGANIZATIONS
He is the man behind the progress of the cooperative who toil day and night in praying and working for its improvement. With his researches and experiments, he develop herbal formulations like Skin Detox, Gotukola Ointment, Liniment, Dok B Complex and most importantly, he invented an eye drop solution named as VISION tawa-tawa eye drops with patents from the Intellectual Property Office of the Philippines . He established a back up entity known as DOK ALTERNATIBO HERBAL PRODUCTS as A PRODUCER and distributor of Herbal Capsules like the popular unodostres, Naturesmed, and the like from the same producer MG HERBAL MANUFACTURING. To date we have more than 20 variety of products under our cooperative.
As a full-pledge inventor, he was admitted as a member of Davao Inventors Association (DIA) and become the Vice- President for National Advocacy of FILINFED or Filipino Inventors Federation Headed by Chairman Invertor PGonzalo Catan Jr. (owner MAPECON) and its President Inventor Vergilio Sangutan (owner MI HERBAL). He is the Auditor of IIPA or International Iridology Practitioner Association Davao City Chapter and attended various seminars both in local and national conventions. He has been invited as Guest speaker in various topics such as natural treatment for those so-called hopeless diseases such as diabetes, high blood pressure, Nervous Breakdown, Cancer and other chronic Diseases.
He handled various radio programs. DXCP at
We have 10 branches all-over region 11 and 12
1. GENSAN
2.
3.
4. CARMEN
5. TAGUM
6. MALITA
7. NABUNTURAN
8. POLOMOLOK
9. ALABEL
10. MAKILALA
BY/OF/FOR THE MEMBERS AND OFFICERS OF ALTERNATIVO MULTIPURPOSE COOPERATIVE
Tuesday, January 29, 2008
COMPANY PROFILE
Dok Alternatibo (D.A.) INVENTOR'S NEWSCAST is a duly recognized newspaper by the Department of Trade and Industry (DTI) with a Business Permit granted by the Local Government.
A unique newspaper which carries the well-research informations about Politics, Religions, Health, Entertainment, Current Events most importantly the promotions of Local and International Inventions that may probably help in solving current problems in our Society.
Edgar Delibo, the Publisher, is a bonafide inventor,the authorized (DIA) Spokesperson of Davao Inventor's Association and Mindanao Inventor's Federation incorporated (MIFI) and the Vice-President for National Advocacy of FILINFED.Known by honesty and integrity as an accredited KBP Broadcast-Journalist, he is employed by ABS-CBN DXAB DAVAO for 8 consecutive years till the present. In his radio program, he is known as DOK ALTERNATIBO for he is an Alternative Medicine Practitioner Aired over DXGM (4:30-5:00AM daily), DXOW (1:00-1:30PM daily) Davao City, HOT FM DIGOS (7:00-7:30AM daily) DXCP GENSAN (2:30-3:30PM daily) and DXAB ABS-CBN 1296 10-11:00AM every Saturday. He was then an Associate Publisher of Davao Sur Mantalaan, Digos City.
D.A. ALTERNATIBO NEWSCAST main office is located at Bonifacio Superhighway, Aplaya, Digos City, with annexes located at Mac Arthur highway, Matina, Davao City, with branches at LAGAO, GENSAN City, TAGUM City, PANABO City, MALITA, POLOMOLOK, ALABEL, and MAKILALA.
D.A. Inventors Newscast, a weekly Newspaper is the Sole Newspaper of Bonafide FILIPINO INVENTOR'S and their INVENTIONS duly recognized by Technology Advancement and Promotions Institute (TAPI) under the Department of Science and Technology (DOST).
Marcelo Suson Jr., a bonafide inventor of Davao Inventors Association, is the D.A. inventors Newscast, General Manager with vast knowledge and experience of Computer system analyst in Computer Programming business and marketing consultancy and newspaper concept and designs.
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