Well done Raita, and thanks for the great interest you have been showing in helping PNG. All the best in you pHD and studies. Would be good to get a glimse of the documentry.
Keep up the great job.
.................................................
On the foreign affairs issue.....absolutely disgraceful, and I do not have to tell my experienc as I am sure we all have our own stroies to tell about the rot that is happening there. It must stop, and yes the good people must stand up and say enough is enough!!! For God's sake how long are we going to keep travelling down this same road. Though I get frustrated about the system, I do not know what to do. It will take a coordinated strategic action from a mass of likeminded "righteous" people in order to change things. One off protests and complaints will not achieve much. The
righteous/good must show solidarity against these evil force - I do not mean to sound too philosophical but if we do not show this solidarity these evil people/force will continue to push us around and we'll continue to here case of the poor journolist being attcked!!!!
Regards olgeta!!
Raita <raitainpng@...> wrote:
Hi guys,
Sorry to reply late for your celebration, and thank you very much.
Now I am in Japan to re-start PhD course in
neuropharmacology, which I left without degree before JICA volunteer in Manus. Also I will join a diploma course in the tropical medicine in Nagasaki, for only 3 months (June-Aug.). Contact me if you have a plan to come to Nagasaki while I am there, or Tokyo after Aug.
By the way, I will be on TV about PNG HIV/AIDS documentary. as a interpreter, not a presenter though. TV crew went to Wewak, Mt Hagen and POM last month. to have interviewed some doctors and Health ministar etc. It will be worth while watching if you are in Japan. I am sure it will raise tremendous fund through UNICEF in PNG. 28-29 / May / 2007, 8am-10am, Fuji TV
thanks for the infor
--- mol william <w_mol2003@...> wrote:
>
> Raita Tamaki,
>
>
> wanted me to post this message to the forum but
> somehow he couldn't so he asked me to post it for
> him. Below is the message.
>
> Hi guys,
>
> Sorry to reply late for your celebration, and thank
> you very much.
>
> Now I am in Japan to re-start PhD course in
> neuropharmacology,
> which I left without degree before JICA volunteer in
> Manus.
> Also I will join a diploma course in the tropical
> medicine in Nagasaki,
> for only 3 months (June-Aug.).
> Contact me if you have a plan to come to Nagasaki
> while I am there,
> or Tokyo after Aug.
>
> By the way, I will be on TV about PNG HIV/AIDS
> documentary.
> as a interpreter, not a presenter though.
> TV crew went to Wewak, Mt Hagen and POM last month.
> to have interviewed some doctors and Health ministar
> etc.
> It will be worth while watching if you are in Japan.
> I am sure it will raise tremendous fund through
> UNICEF in PNG.
> 28-29 / May / 2007, 8am-10am, Fuji TV
>
> TOKSAVE tasol!
>
> Mail: rt173cm67kg@...
> Mobile: 090-9847-0987
> Mobile mail¡§tamakiraita@...
>
>
>
>
> ---------------------------------
> Easy + Joy + Powerful = Yahoo! Bookmarks x Toolbar
>
Rodney Itaki
___________________________________________________________
The all-new Yahoo! Mail goes wherever you go - free your email address from your
Internet provider. http://uk.docs.yahoo.com/nowyoucan.html
wanted me to post this message to the forum but somehow he couldn't so he asked me to post it for him. Below is the message.
Hi guys,
Sorry to reply late for your celebration, and thank you very much.
Now I am in Japan to re-start PhD course in neuropharmacology,
which I left without degree before JICA volunteer in Manus.
Also I will join a diploma course in the tropical medicine in Nagasaki,
for only 3 months (June-Aug.).
Contact me if you have a plan to come to Nagasaki while I am there,
or Tokyo after Aug.
By the way, I will be on TV about PNG HIV/AIDS documentary.
as a interpreter, not a presenter though.
TV crew went to Wewak, Mt Hagen and POM last month.
to have interviewed some doctors and Health ministar etc.
It will be worth while watching if you are in Japan.
I am sure it will raise tremendous fund through UNICEF in PNG.
28-29 / May / 2007, 8am-10am, Fuji TV
Hi guys,
Sorry to reply late for your celebration, and thank you very much.
Now I am in Japan to re-start PhD course in neuropharmacology,
which I left without degree before JICA volunteer in Manus.
Also I will join a diploma course in the tropical medicine in Nagasaki,
for only 3 months (June-Aug.).
Contact me if you have a plan to come to Nagasaki while I am there,
or Tokyo after Aug.
By the way, I will be on TV about PNG HIV/AIDS documentary.
as a interpreter, not a presenter though.
TV crew went to Wewak, Mt Hagen and POM last month.
to have interviewed some doctors and Health ministar etc.
It will be worth while watching if you are in Japan.
I am sure it will raise tremendous fund through UNICEF in PNG.
28-29 / May / 2007, 8am-10am, Fuji TV
TOKSAVE tasol!
Mail: rt173cm67kg@...
Mobile: 090-9847-0987
Mobile mail¡§tamakiraita@...
--------------------------------------
Easy + Joy + Powerful = Yahoo! Bookmarks x Toolbar
http://pr.mail.yahoo.co.jp/toolbar/
I totally agree with Poyap and Willie, however in order for one to act ( action ) a thought has to generated first...A THOUGHT PRECEEDS AN ACTION...
Well folks, Iam out of here,
Cheers
Moses
mol william <w_mol2003@...> wrote:
Valid point Poyap,
Somebody told me, 'everything one can think of can be achieved or be done, if not now later'.
Many years ago
somebody said, 'we could go to the moon' and pople thought he was a psycho. Now it is possible.
Many things Leonardo da Vinci thought of & drew are now being invented. For example, he thought of the principles of vertical take-off & landing aircraft; the helicopter, in 1493 (See picture of airscrew below). In 14th September 1939 (446 years later), Igor Sikorsky (see photo below), successfully built & flew the first helicopter. He named it, Vought-Sikorsky 300 (see picture below).
In this world, In regards to thought, I think we can simply classify people into 4 groups:
1. People who don't think & don't do anything 2. People who don't think but do things 3. People who think but don't do things 4. People who think & do things
Valid point Poyap,
Somebody told me, 'everything one can think of can be
achieved or be done, if not now later'.
Many years ago somebody said, 'we could go to the moon'
and pople thought he was a psycho. Now it is possible.
Many things Leonardo da Vinci thought of & drew are now
being invented. For example, he thought of the principles
of vertical take-off & landing aircraft; the helicopter,
in 1493 (See picture of airscrew below). In 14th September
1939 (446 years later), Igor Sikorsky (see photo below),
successfully built & flew the first helicopter. He named
it,
Vought-Sikorsky 300 (see picture below).
In this world, In regards to thought, I think we can
simply classify people into 4 groups:
1. People who don't think & don't do anything
2. People who don't think but do things
3. People who think but don't do things
4. People who think & do things
Which one are you? Think!
William
--------------------------------------
Easy + Joy + Powerful = Yahoo! Bookmarks x Toolbar
http://pr.mail.yahoo.co.jp/toolbar/
The main reference for mercury was from Tietz;s Textbook of clinical Biochemistry plus reference articles from that textbook. - A bit of plagerism but for the skae of distributing info.
Poyap James Rooney <pojaroo@...> wrote:
Actually Moses who you "thought" gave that comment on technicality was infact willie and not me. This is a clear example of how "mass thought" can get derailled and a false believe, disillusion perpetuated, how the original thought can get twisted, modified from one individual to
another and at the end the the original idea, thought is unrecognisable from the original, just like mercury.
Anyway, ...... Noken tingting tumas....JUST DO IT!! as in the Nike Ad. Enjoy you thoughts!!, but don't dwell in thought for too long without doing something, a good mix of thought and ACTION is health, too much of one and not the other is not good.
poyap
moses wiau <mouwiau04@yahoo.com.au> wrote:
Poyap,
As technical as one would get, where did one obtain the thought of being technical? Is not thought the very essence that drives the greatest computer- brain,etc...which controls our very being like emotions;relatioships;intelligence;etc..These are the inherent qualities that
define what/who we are as humans...
Well, it was nice to gauge constructive views. Hope to discuss further stimulating topic on the forum.
Cheers
Moses mol william <w_mol2003@yahoo.co.jp> wrote:
Poyap! that's a great & complete summary on lead. May help as a reference.
Moses, yeah! as you know very well I am more technical then you. That is simply because thought is a very complex & abstract topic.
Actually Moses who you "thought" gave that comment on technicality was infact willie and not me. This is a clear example of how "mass thought" can get derailled and a false believe, disillusion perpetuated, how the original thought can get twisted, modified from one individual to another and at the end the the original idea, thought is unrecognisable from the original, just like mercury.
Anyway, ...... Noken tingting tumas....JUST DO IT!! as in the Nike Ad. Enjoy you thoughts!!, but don't dwell in thought for too long without doing something, a good mix of thought and ACTION is health, too much of one and not the other is not good.
poyap
moses wiau <mouwiau04@...> wrote:
Poyap,
As technical as one would get, where did one obtain the thought of being technical? Is not thought the very essence that drives the greatest computer- brain,etc...which controls our very being like emotions;relatioships;intelligence;etc..These are the inherent qualities that define what/who we are as humans...
Well, it was nice to gauge constructive views. Hope to discuss further stimulating topic on the forum.
Cheers
Moses mol william <w_mol2003@yahoo.co.jp> wrote:
Poyap! that's a great & complete summary on lead. May help as a reference.
Moses, yeah! as you know very well I am more technical then you. That is simply because thought is a very complex & abstract topic.
As technical as one would get, where did one obtain the thought of being technical? Is not thought the very essence that drives the greatest computer- brain,etc...which controls our very being like emotions;relatioships;intelligence;etc..These are the inherent qualities that define what/who we are as humans...
Well, it was nice to gauge constructive views. Hope to discuss further stimulating topic on the forum.
Cheers
Moses mol william <w_mol2003@...> wrote:
Poyap! that's a great & complete summary on lead. May help as a reference.
Moses, yeah! as you know very well I am more technical then you. That is simply because thought is a very complex & abstract topic.
Poyap! that's a great & complete summary on lead. May help
as a reference.
Moses, yeah! as you know very well I am more technical
then you. That is simply because thought is a very complex
& abstract topic.
Cheers!
William
--------------------------------------
Easy + Joy + Powerful = Yahoo! Bookmarks x Toolbar
http://pr.mail.yahoo.co.jp/toolbar/
Moses thanks for your lightning fast, breakneck pace response!!!. What is your learned opinion on the mercury induced psycosis, would it have a characteristic and recognisable psychotic manifestation or would it follow a nonspecific organic psycosis.
moses wiau <mouwiau04@...> wrote:
Hi Pou,
Good to know about Mercury...
I hope you are fine in Melbourne.
Cheers
Moses
Poyap <pojaroo@yahoo.com.au> wrote:
Hi all - here is a liklik story about Mercury, hope you can get through it in one sitting.
Mercury is a very interesting substance. I remeber as a kid finding a small bottle of mercury in an old workshop and finding myself facinated by it. It was like water yet very heavy, it shined like the other metals I was familiar with but flowed. I use to play around with it in may hands, rolled it around on the floor, pick it up with a magnet and did many other things to satisfy my curiousity. Little did I know the potential danger I was exposing myself to, and may it did affect me somehow, who knows??
Anually, the atmosphere and surface of the earth is exposed to about 36,000 tonns of mercury.
The single largest source of mercury is the natural outgassing from granite rock (about 30,000 tonns)-not too sure about this process, if our mining collegue can enlighten us. The metal fillings used in dentistry is made of mixtures of metals containing mercury (amalgam). Some studies have shown high levels of mercury in the blood of people with amalgam dental fillings, but the general consensus is that they are safe.
The mining industry uses mercury to extract gold and other minerals from the raw material as outline beautifully by VB. Great effort should be made to dispose of the waste products of mineral extraction. When this is not done mercury and other toxic substance can pollute and contaminate the environment and cause serious health problems in animals and humans.
Mercury can take different forms each having a different level of toxicity. Basically there are three different forms as outline belowed
in order of toxicity:
1) Elemental ("natural") mercury (Hg 0) - this is essentially non toxic,this what we find in the dental amalgams.
2) When exposed to other modifying (oxidising) chemicals elemental mercury (Hg 0) can be ionised to Hg2+ --> this is more toxic then Hg 0.
3) Further modification forms the very toxic forms (the alkyl Hg).
SO HOW DOES THE INOCENT ELEMENTAL MERCURY Hg 0 GET CORRUPTED??
a) In industry, the chemical modification of Hg 0 to Hg 2+ is frequently accomplished by exposing Hg 0 to a strong oxidants such as chlorine.
b) Hg 0 can also be bioconverted to both Hg2+ and alkyl Hg by microorganism that exist in the human gut and in the bottom sediments of rivers and lakes.
These modified and now toxic forms of mercury accumulate in the acquatic food chain and reach their highest concentration in the large fish. Humans in turn acquire them by eating these
fish.
HOW DOES MERCURY AFFECT HUMAN HEALTH??
Mercury toxicity can be expressed in three ways.
1) Mercury changes the structure of many essential proteins in the body, from collagen in skin to important enzymes for normal functioning of the body, this change in protein structure render these proteins dysfunctional and incabale of doing their jobs (detail are beyond the scope of this summary).
2) Protein structure modification makes them suseptable to autoimmune destruction as the bodies immune system no longer recognised them as self, and mounts an attack against them.
3) The most toxic form of mercury the alkyl mercuries can easily penetrate into the central nervous system causing brain damage. Unborn children are also affected as mercury freely passes from the mother to the fetus.
TOUGH LESSONS THE WORLD HAS LEARNT ABOUT MERCURY. Much of what is known about the health effects of mercury has
been gained from investigations of the 1951 to 1963 industrial dumping of Hg waste into the Minamata Bay, Japan. Fish in Minamata bay became heavily ladened with Hg and humans around the area who relied on these fish for protein in turn became intoxicated. The symptoms and signs of heavy mercury intoxication included:
Ataxia - unsteady gait impaired speech - slurred visual field contriction hearing loss psychotic changes
Collectively, these symptoms have become to be known as Minamata disease.
THE ANALYSIS OF MERCURY. The analysis of blood, urine and hair for mercury levels is used to determine exposure. Blood and urine levels correlate well with the degree of toxicity.
Significant exposure is indicated when blood mercury levels > 50micrograms (if exposure is the the alkyl mercuries) > 200micrograms (if exposure is to Hg 2+ form).
THE WHO SAFTY STANDARD FOR DAILY EXPOSURE OF Hg
IS 45Micrograms PER DAY WITH A DAILY URINARY EXCRETION EXCEEDING 50Micrograms/DAY INDICATING SIGNIFICANT EXPOSURE>>>>.
Treatment of mercury includes the administration of penicilamine which binds mercury and mobilises it for quicker excretion. Treatment is monitored by urinary mercury excretion.
We should continue to educate ourselve and the public regarding the issue of toxic metals in relation to the mining industry
The points I want to stress here are:
1) We need to know what form of mercury are our people exposed to in order to stratify them into appropriate risk levels, and determine wheather or not treatment is needed.
2) To determine this, samples need to be taken from fish and other aquatic animals in the area.
3) If it is found that levels of alkyl mercury in
these fish are high it would indicate the same in humans and would further suggest that the general exposure of the environment has been going for some time.
4) If the people around the area are intoxicated ((Minamata disease), do they deserve treatment and if so who is to pay for their treatment.
Cheers poyap
How would you spend $50,000 to create a more sustainable environment in Australia? Go to Yahoo!7 Answers and share your idea.
How would you spend $50,000 to create a more sustainable environment in Australia? Go to Yahoo!7 Answers and share your idea.
Hi all - here is a liklik story about Mercury, hope you can get through it in one sitting.
Mercury is a very interesting substance. I remeber as a kid finding a small bottle of mercury in an old workshop and finding myself facinated by it. It was like
water yet very heavy, it shined like the other metals I was familiar with but flowed. I use to play around with it in may hands, rolled it around on the floor, pick it up with a magnet and did many other things to satisfy my curiousity. Little did I know the potential danger I was exposing myself to, and may it did affect me somehow, who knows??
Anually, the atmosphere and surface of the earth is exposed to about 36,000 tonns of mercury. The single largest source of mercury is the natural outgassing from granite rock (about 30,000 tonns)-not too sure about this process, if our mining collegue can enlighten us. The metal fillings used in dentistry is made of mixtures of metals containing mercury (amalgam). Some studies have shown high levels of mercury in the blood of people with amalgam dental fillings, but the general consensus is that they are safe.
The mining industry uses mercury to extract gold and other
minerals from the raw material as outline beautifully by VB. Great effort should be made to dispose of the waste products of mineral extraction. When this is not done mercury and other toxic substance can pollute and contaminate the environment and cause serious health problems in animals and humans.
Mercury can take different forms each having a different level of toxicity. Basically there are three different forms as outline belowed in order of toxicity:
1) Elemental ("natural") mercury (Hg 0) - this is essentially non toxic,this what we find in the dental amalgams.
2) When exposed to other modifying (oxidising) chemicals elemental mercury (Hg 0) can be ionised to Hg2+ --> this is more toxic then Hg 0.
3) Further modification forms the very toxic forms (the alkyl Hg).
SO HOW DOES THE INOCENT ELEMENTAL MERCURY Hg 0 GET CORRUPTED??
a) In industry, the chemical modification of Hg 0 to Hg 2+
is frequently accomplished by exposing Hg 0 to a strong oxidants such as chlorine.
b) Hg 0 can also be bioconverted to both Hg2+ and alkyl Hg by microorganism that exist in the human gut and in the bottom sediments of rivers and lakes.
These modified and now toxic forms of mercury accumulate in the acquatic food chain and reach their highest concentration in the large fish. Humans in turn acquire them by eating these fish.
HOW DOES MERCURY AFFECT HUMAN HEALTH??
Mercury toxicity can be expressed in three ways.
1) Mercury changes the structure of many essential proteins in the body, from collagen in skin to important enzymes for normal functioning of the body, this change in protein structure render these proteins dysfunctional and incabale of doing their jobs (detail are beyond the scope of this summary).
2) Protein structure modification makes them suseptable to autoimmune destruction as
the bodies immune system no longer recognised them as self, and mounts an attack against them.
3) The most toxic form of mercury the alkyl mercuries can easily penetrate into the central nervous system causing brain damage. Unborn children are also affected as mercury freely passes from the mother to the fetus.
TOUGH LESSONS THE WORLD HAS LEARNT ABOUT MERCURY. Much of what is known about the health effects of mercury has been gained from investigations of the 1951 to 1963 industrial dumping of Hg waste into the Minamata Bay, Japan. Fish in Minamata bay became heavily ladened with Hg and humans around the area who relied on these fish for protein in turn became intoxicated. The symptoms and signs of heavy mercury intoxication included:
Ataxia - unsteady gait impaired speech - slurred visual field contriction hearing loss psychotic changes
Collectively, these symptoms have become to be known as
Minamata disease.
THE ANALYSIS OF MERCURY. The analysis of blood, urine and hair for mercury levels is used to determine exposure. Blood and urine levels correlate well with the degree of toxicity.
Significant exposure is indicated when blood mercury levels > 50micrograms (if exposure is the the alkyl mercuries) > 200micrograms (if exposure is to Hg 2+ form).
THE WHO SAFTY STANDARD FOR DAILY EXPOSURE OF Hg IS 45Micrograms PER DAY WITH A DAILY URINARY EXCRETION EXCEEDING 50Micrograms/DAY INDICATING SIGNIFICANT EXPOSURE>>>>.
Treatment of mercury includes the administration of penicilamine which binds mercury and mobilises it for quicker excretion. Treatment is monitored by urinary mercury excretion.
We should continue to educate ourselve and the public regarding
the issue of toxic metals in relation to the mining industry
The points I want to stress here are:
1) We need to know what form of mercury are our people exposed to in order to stratify them into appropriate risk levels, and determine wheather or not treatment is needed.
2) To determine this, samples need to be taken from fish and other aquatic animals in the area.
3) If it is found that levels of alkyl mercury in these fish are high it would indicate the same in humans and would further suggest that the general exposure of the environment has been going for some time.
4) If the people around the area are intoxicated ((Minamata disease), do they deserve treatment and if so who is to pay for their treatment.
Cheers poyap
How would you spend $50,000 to create a more sustainable environment in Australia? Go to Yahoo!7 Answers and share your idea.
Hi all - here is a liklik story about Mercury, hope you can get
through it in one sitting.
Mercury is a very interesting substance. I remeber as a kid finding
a small bottle of mercury in an old workshop and finding myself
facinated by it. It was like water yet very heavy, it shined like
the other metals I was familiar with but flowed. I use to play around
with it in may hands, rolled it around on the floor, pick it up with
a magnet and did many other things to satisfy my curiousity. Little
did I know the potential danger I was exposing myself to, and may it
did affect me somehow, who knows??
Anually, the atmosphere and surface of the earth is exposed to about
36,000 tonns of mercury. The single largest source of mercury is the
natural outgassing from granite rock (about 30,000 tonns)-not too
sure about this process, if our mining collegue can enlighten us.
The metal fillings used in dentistry is made of mixtures of metals
containing mercury (amalgam). Some studies have shown high levels of
mercury in the blood of people with amalgam dental fillings, but the
general consensus is that they are safe.
The mining industry uses mercury to extract gold and other minerals
from the raw material as outline beautifully by VB. Great effort
should be made to dispose of the waste products of mineral
extraction. When this is not done mercury and other toxic substance
can pollute and contaminate the environment and cause serious health
problems in animals and humans.
Mercury can take different forms each having a different level of
toxicity. Basically there are three different forms as outline
belowed in order of toxicity:
1) Elemental ("natural") mercury (Hg 0) - this is essentially non
toxic,this what we find in the dental amalgams.
2) When exposed to other modifying (oxidising) chemicals elemental
mercury (Hg 0) can be ionised to Hg2+ --> this is more toxic then
Hg 0.
3) Further modification forms the very toxic forms (the alkyl Hg).
SO HOW DOES THE INOCENT ELEMENTAL MERCURY Hg 0 GET CORRUPTED??
a) In industry, the chemical modification of Hg 0 to Hg 2+ is
frequently accomplished by exposing Hg 0 to a strong oxidants
such as chlorine.
b) Hg 0 can also be bioconverted to both Hg2+ and alkyl Hg by
microorganism that exist in the human gut and in the bottom
sediments of rivers and lakes.
These modified and now toxic forms of mercury accumulate in the
acquatic food chain and reach their highest concentration in the
large fish. Humans in turn acquire them by eating these fish.
HOW DOES MERCURY AFFECT HUMAN HEALTH??
Mercury toxicity can be expressed in three ways.
1) Mercury changes the structure of many essential proteins in the
body, from collagen in skin to important enzymes for normal
functioning of the body, this change in protein structure render
these proteins dysfunctional and incabale of doing their jobs
(detail are beyond the scope of this summary).
2) Protein structure modification makes them suseptable to
autoimmune destruction as the bodies immune system no longer
recognised them as self, and mounts an attack against them.
3) The most toxic form of mercury the alkyl mercuries can easily
penetrate into the central nervous system causing brain damage.
Unborn children are also affected as mercury freely passes from
the mother to the fetus.
TOUGH LESSONS THE WORLD HAS LEARNT ABOUT MERCURY.
Much of what is known about the health effects of mercury has been
gained from investigations of the 1951 to 1963 industrial dumping of
Hg waste into the Minamata Bay, Japan. Fish in Minamata bay became
heavily ladened with Hg and humans around the area who relied on
these fish for protein in turn became intoxicated. The symptoms and
signs of heavy mercury intoxication included:
Ataxia - unsteady gait
impaired speech - slurred
visual field contriction
hearing loss
psychotic changes
Collectively, these symptoms have become to be known as Minamata
disease.
THE ANALYSIS OF MERCURY.
The analysis of blood, urine and hair for mercury levels is used to
determine exposure. Blood and urine levels correlate well with the
degree of toxicity.
Significant exposure is indicated when blood mercury levels
> 50micrograms (if exposure is the the alkyl mercuries)
> 200micrograms (if exposure is to Hg 2+ form).
THE WHO SAFTY STANDARD FOR DAILY EXPOSURE OF Hg IS 45Micrograms PER
DAY WITH A DAILY URINARY EXCRETION EXCEEDING 50Micrograms/DAY
INDICATING SIGNIFICANT EXPOSURE>>>>.
Treatment of mercury includes the administration of penicilamine
which binds mercury and mobilises it for quicker excretion.
Treatment is monitored by urinary mercury excretion.
......................................................................
We should continue to educate ourselve and the public regarding the
issue of toxic metals in relation to the mining industry
The points I want to stress here are:
1) We need to know what form of mercury are our people exposed to in
order to stratify them into appropriate risk levels, and
determine wheather or not treatment is needed.
2) To determine this, samples need to be taken from fish and other
aquatic animals in the area.
3) If it is found that levels of alkyl mercury in these fish are
high it would indicate the same in humans and would further
suggest that the general exposure of the environment has been
going for some time.
4) If the people around the area are intoxicated ((Minamata
disease), do they deserve treatment and if so who is to pay for
their treatment.
Cheers
poyap
"In what clinical situation can a localised/specific
iron chelation be utalised Willie."
Well, Poyap, that is something to think about! I mean
something that is given systemically but can act more
locally where the inflammation is to inhibit the
availabillity of iron. I guess it is a problem of drug
design & delievery systems-a problem for the
pharmacologists
Good analagee,... but the 'country's innocent, citizens
may also be starved to death' because of the generalized
anemia, especially as you know if there are other medical
problems, especially cardio-respiratory conditions etc.
As I know innate immunity is the frontline line, mainly
nonspecific defence against invaders.
Probably, we could say, that this system protects from
further infection & also to suppress the growth of already
invading bugs. But not totally effective in completely
clearing the bugs.
Dendritic cells are also component of the innate immunty.
As I have mentioned several times before, OK-432 or killed
bacteria have been used to activate them to keep them more
alert than usual to effectively & quickly attack any bugs
& even cancer cells. It is said, that they have a certain
degree of specificity too. Hepcidin system is another
component of the innate immunity that tries to minimise
infection.
Broadly speaking, is it the innate immunity or the
adaptive (more specific & effective, but slower) immunity
we should utillize to control infection? That means
specific vaccines/vacination.
Any other views?
William
--------------------------------------
Easy + Joy + Powerful = Yahoo! Bookmarks x Toolbar
http://pr.mail.yahoo.co.jp/toolbar/
In what clinical situation can a localised/specific iron chelation be utalised Willie. Just wondering!!.
The postualtion being put forward (in regards to hepcidin) is of iron restriction as a general "inate" immune mechanism. (I know you know Willie but just trying to reiterate the point maybe to others. If I can use the following analagee...
If the whole body was like a country that had stocked up its food (iron) during a drought. Suddenly this country is invaded by some outsiders who are looking to take this stock of food supply, grow in numbers and eventually take over the country (body). The country, as part of it security system has a special intelligence officer (hepcidin), who when detects the presence of these invaders (the signal for hepcidin being - TNF-alpha, IL6 and other cytokine produced by hepcidin's central
intelligence agency (CIA) collegues..the macrophages), sends the following message..the fellow looking after the food supply.
"We are being invade by an enemy force, make sure all the food supply doors are closed tight and do not let any of the food out of our stock pile, the "task force" ie the neutrophiles, lymphocytes (The acquired, specific immune system) are doing their best to rid our country of the enemy, once they have done so, I will let you know when we get open the doors to the food supply again"
Clinically the above analagee can be seen with the typical changes that can be seen with iron studies during and inflamation ie there is an increase in the storage form of iron and decrease iron availability.
Ferritin(iron storage protein) goes up
Transferrin saturation goes down
Serum iron decreases
Less iron is
released from macrophages.
Willie I just remember a talk at a conference I attended last year about some new research looking at specific or localised iron "starvation" (if i can use that word) being looked at in tumours, whereby the restriction of tumour cells to iron is being looked at as a possible mode of treatment....I really can't tell you anymore detail then that(can't remeber), but its interesting.
ciao
poyap
"hope you like the analagee"
mol william <w_mol2003@...> wrote:
I have found a paper regarding the inhibiton of bacterial growth by iron starvation in vitro (attached file).
A study done in Sydney, Australia, using the bacteria, Helicobacter pylori & published in Nov. 2003.
Iron starvation inhibits growth in the 'exponential' growth phase but not in the 'stationary' growth phase.
Does this mean that iron depletion is more effective in acute infection when growth of bacteria is high (exponential phase)?
I think iron chelators that work specifically & locally may be more beneficial than hepcidin or its analogues that inhibits absorption of iron from the guts.
I have found a paper regarding the inhibiton of bacterial
growth by iron starvation in vitro (attached file).
A study done in Sydney, Australia, using the bacteria,
Helicobacter pylori & published in Nov. 2003.
Iron starvation inhibits growth in the 'exponential'
growth phase but not in the 'stationary' growth phase.
Does this mean that iron depletion is more effective in
acute infection when growth of bacteria is high
(exponential phase)?
I think iron chelators that work specifically & locally
may be more beneficial than hepcidin or its analogues that
inhibits absorption of iron from the guts.
Any other ideas?
Thanks!
William
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Thanks Willie, I haven't come across any papers demonstrating the affectivness of iron depletion in controlling microorganisms - in vitro, but I am pretty sure someone has done such work.
Hepcidin was first isolated by Park et al - "Hepcidin, a urinary antimicrobial peptide synthesised in the liver. J Biol Chem. 2001; 9:397-403. During studies of antimicrobial properties of various human body fluids. In the course of their study one of their urine donors developed systemic infection and it was observed then that the hepcidin concentration increased X100 fold. This and subsequent studies have clearly demonstrated hepcidins role in "inflammtion".
Hepcidin or the lack of it's functionality also plays an important role in the developement of hemachromatosis, it has been shown that hepcidin knock out mice develope severe hemachromatosis, which is a disease charcterised by iron
overload.
Of relevance to our previous discussion on toxic metals, Lead poisoning mainly causes peripheral neuropathy, abdominal pain, anemia and encephalopathy. Lead inhibits many enzyme systems, and effects several stages of haem biosynthesis including the final step of incorporating iron into the protoporphorin ring, hence leading to a decreased capacity of haem to carry out its important function of carrying around oxygen.
Tests that may be helpful in demonstraing lead toxicity:
1. Tests demonstrating the presence of excess lead: Blood lead, chelatable lead excretion, urinary lead.
2. Tests demonstrating the toxic effects of lead....(maybe for our people up at Tolakuma, we should do this, ...or maybe it has been done all
ready, prehaps Sylvester can clarify). If we do this we confirm that not only are the levels of lead in the water system and blood samples are high, but they are also afecting the health of those exposed people.
These tests include:
PBG synthase activity
Urinary ALA and coprporphyrin
Zinc protoporphyrin.
These can be done as a follow up study, , ...next step.. (if not already done).
Sampla ting ting.
On another note but related, I still disagree that we should wait till afetr the. I don't believe evrything should come to a standing halt just because of the elections. mol william <w_mol2003@...> wrote:
Poyap, interesting topic & good summary there.
We have discussed it briefly before. Anyway, I would like to ask: as you said, it is one of the body's defence mechanisms to rid or at least control the growth of invading pathogens. In chronic infections despite all these mechanisms, the infection still persists. So my question is; how effective is this 'anemia' in controlling infection. Have you come across some papers that prove clearly using in vitro experiments, its effectiveness.
Infact, it would be possible to do
such experiment in vitro. Culture, say any pathogen (TB bacteria etc.) & apply different amount of iron & also deplete iron & study the bugs' growth patterns. I know there are some culture medium rich in blood or iron (blood agar etc.).
The value of hepcidin agonists as a therapy is very interesting, but what do you think about the non-specificness. I mean hepacidin agonist would reduce iron absorption from the gut so the entire body is depleted of iron & not only the invading bugs.
Poyap, interesting topic & good summary there.
We have discussed it briefly before. Anyway, I would like
to ask: as you said, it is one of the body's defence
mechanisms to rid or at least control the growth of
invading pathogens. In chronic infections despite all
these mechanisms, the infection still persists. So my
question is; how effective is this 'anemia' in controlling
infection. Have you come across some papers that prove
clearly using in vitro experiments, its effectiveness.
Infact, it would be possible to do such experiment in
vitro. Culture, say any pathogen (TB bacteria etc.) &
apply different amount of iron & also deplete iron & study
the bugs' growth patterns. I know there are some culture
medium rich in blood or iron (blood agar etc.).
The value of hepcidin agonists as a therapy is very
interesting, but what do you think about the
non-specificness. I mean hepacidin agonist would reduce
iron absorption from the gut so the entire body is
depleted of iron & not only the invading bugs.
Any other thoughts on this interesting topic?
William
--------------------------------------
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Hello friends,
Just tok save ken olsem PNG.j.sci.technol.eng is accepting manuscripts.
The journal scope is very broad covering life sciences (including
clinical medicine), physical sciences, social sciences, technology and
engineering.
I have created a blog - http://pngjscitech.wordpress.com/ to publish
the abstracts. This blog is to fascilitate discussion between readers
and authors of articles published by the journal. Some of the titles
recieved so far have been put up so visit the journal blog and have a
look.
So askim i go out ken lon supportim journal and submit a manuscript.
Original research, reviews on current topics, book reviews, comments
and letters are welcomed.
regards
ri
Ensure delivery by adding ECGCase@... to your address book.
Please click here if you are unable to access the diagnosis page.
BACKGROUND
A 66-year-old man presents to the Emergency Department (ED) with chest pain and shortness of breath that started several hours ago as he was cleaning his porch. His chest pain is dull in quality and radiates to his neck and arms, and when asked to rate the severity of the pain, he indicates a 5 in a range from 1 to 10 (with 10 being the worst). The chest pain is not associated with diaphoresis, nausea, or vomiting. The patient also had exertional weakness for 4 days. He denies having dizziness, lightheadedness, or loss of consciousness.
The patient underwent a 3-vessel coronary artery bypass 8 years ago. Since then, he has had stable angina that occurs approximately once a month. His medical history is also clinically significant for hyperlipidemia, hypertension, and poorly controlled insulin-dependent diabetes mellitus. His medication regimen includes hydrochlorothiazide, insulin, isosorbide dinitrate, simvastatin, aspirin, and
sublingual nitroglycerin as needed. The patient smokes 2 packs of cigarettes per day. The review of systems yields unremarkable findings.
The patient is afebrile but appears uncomfortable. The cardiovascular examination reveals bradycardia. His heart rate is 39 bpm and regular, his blood pressure is 130/53 mm Hg, and his respiratory rate is 18 breaths per minute. His first and second heart sounds are normal. No murmur or gallop is present. Except for evidence of his previous surgery, his other physical findings are normal.
The patient’s laboratory results are normal except for mildly elevated troponin I levels. An ECG is obtained (see Image 1).
Authors: Salyka Sengsayadeth, Resident, Internal Medicine, Vanderbilt University
Ehab S. Kasasbeh, MD, Resident, Department of Internal
Medicine, James H. Quillen College of Medicine, East Tennessee State University
Ryland P. Byrd, Jr, MD, Chief of Pulmonary Medicine, Medical Director of Respiratory Therapy, Quillen Mountain Home Veterans Affairs Medical Center, Professor, Department of Internal Medicine, Division of Pulmonary Diseases and Critical Care Medicine, James H. Quillen College of Medicine, East Tennessee State University
eMedicine Editors: Erik D. Schraga, MD, Department of Emergency Medicine, Kaiser Permanente, Santa Clara Medical Center, Calif
Rick G. Kulkarni, MD, Assistant Professor, Yale School of Medicine, Section of Emergency Medicine, Department of Surgery, Attending Physician, Medical Director, Department of Emergency Services, Yale-New Haven Hospital, Conn
Sorry, Rodney, didn't seem to realize. Just copy & pasted,
if you don't mind.
Thanks! Helen,
for the update & guidlines, will consider it. There is an
interesting point, I would like to bring up!
As we know, the incidence & prevelance of cancer in
developed countries are higher than in underdeveloped
countries. Infectious diseases are the exact opposite. In
normal, healthy persons a certain amount of exposure to
bacteria etc. (pathogens) don't exactly make us sick but
activate our innate immunity or keeps it alert & active.
Innate immunity is nonspecific but the frontline battlers,
while adaptive immunity comes later on and are more
specific in attacking a certain pathogen.
Certain cells within the Innate immunity who has the
potential to quickly recognise pathogens as well as
deformed body cells (that have the potential to turn into
cancer cells), surveillance our system, regularly &
removes them. Thus, the thoery is that if you have a real
active innate immunty, then your chances of cancer
developement is low. (well, there are other factors also).
The Japanese has gone 1 step further. OK-432 or Picibanil
is prepared from bacteria that resides in our pharynx
(throat) by treating them with heat & penicillin (Chugai
pharmaceuticals) . The cells are dead but their structures
are intact. It is then injected intravenously, into
terminal cancer patients. Research has found that it has
prolonged their survival compared to control groups.
There are other uses of OK-432 but won't mention it now.
So if our inert immunity is active then the chances of
developing cancer is low (I haven't come accross any
research that has proven this theory yet. The above use is
not prevention but a kind of treatment).
Finally, remember THIS IS ONLY A THEORY!
William
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No idea yet! But Rodney, probably around that time
(September 10). Soon they will call for papers via their
home page.
Anyone know the contacts of the organising committee?
William
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Great idea PJ,
JT
>>> "Poyap" <pojaroo@...> 05/04/2007 5:23 pm >>>
Thanks John, I think just as nearly all the other problems being
faced by PNG right now, the answer is for us PNGeans, to SAY NO!!!!,
this is not good enough for me, this is not good enough for my
children and my people and stop compromising. "Evil prospers when
good people do nothing".....bible verse don't know where exactly but
some of you may know. It is about time the "GOOD PEOPLE" stop hiding
in their shells, get out, and do something....
On this particular issue, I think that it should come from the fifth,
the imeptus should come from the RMO themselve and the fifthyear
medical students, they should get together form an association, the
Medical Students already have one and that should continue to the RMO
years...they should push for NO RMO to start work until all the
beuracratic red tape is finalised and they are on the payroll, only
then should they start.. we should encourage them to do just that.
.....
..
.
..
Apinun now
Poyap
--- In pngdoctors-cme@yahoogroups.com, moses taram <mtaram_76@...>
wrote:
>
> Thanks John for raising this issue of concern.
> This chronic problem has been experienced also by resident
medical imaging technologist, laboratory technologists, dental
therapists, and pharmacists for over 10 years now.
> As the saying goes, one can learn from a mistake, but the
greatest mistake one can make is not learning from it.. What is
happening to NDOH - HR, or the government?
> Mi lusim olsem long yupla..
> Moses Taram..
>
> John Tonar <John.Tonar@...> wrote:
> Ladies and Gentleman,
>
> I failed to understand year after year, residents were left to fan
for themselves when they resume their residency training. They do not
need a protest or strike to let Dr Mann come down to address them.
>
> When I started my residency on the 6th Jan 1997 in Lae, we went
without pay for 6-8 weeks. DOH gave the same old reason. We (Manape,
Urakoko, A. Ame) had to physically called into personel officer - to
get some attention.
>
> That was 10 years ago!...system failure?
>
> DOH : Resident Doctors Scenario
>
> You plant a geniune apple seed, got the plant up. sunshine, water
etc. Saw the first fruit on its way to maturity. Instead of continued
care to obtain the ultimum content; energy and sweetness, instead you
grab a bush knife and slash it in half.
>
> This is unthinkable.
>
> I sympathised with our RMO in PNG...I was given the same plate 10
years ago.
>
> Just a concern only.
>
> Is there any way we can discuss to improve this scenario? over to
the forum
>
> JT
>
>
>
>
>
>
> Send instant messages to your online friends
http://au.messenger.yahoo.com
>
Thanks John, I think just as nearly all the other problems being
faced by PNG right now, the answer is for us PNGeans, to SAY NO!!!!,
this is not good enough for me, this is not good enough for my
children and my people and stop compromising. "Evil prospers when
good people do nothing".....bible verse don't know where exactly but
some of you may know. It is about time the "GOOD PEOPLE" stop hiding
in their shells, get out, and do something....
On this particular issue, I think that it should come from the fifth,
the imeptus should come from the RMO themselve and the fifthyear
medical students, they should get together form an association, the
Medical Students already have one and that should continue to the RMO
years...they should push for NO RMO to start work until all the
beuracratic red tape is finalised and they are on the payroll, only
then should they start.. we should encourage them to do just that.
.....
..
.
..
Apinun now
Poyap
--- In pngdoctors-cme@yahoogroups.com, moses taram <mtaram_76@...>
wrote:
>
> Thanks John for raising this issue of concern.
> This chronic problem has been experienced also by resident
medical imaging technologist, laboratory technologists, dental
therapists, and pharmacists for over 10 years now.
> As the saying goes, one can learn from a mistake, but the
greatest mistake one can make is not learning from it.. What is
happening to NDOH - HR, or the government?
> Mi lusim olsem long yupla..
> Moses Taram..
>
> John Tonar <John.Tonar@...> wrote:
> Ladies and Gentleman,
>
> I failed to understand year after year, residents were left to fan
for themselves when they resume their residency training. They do not
need a protest or strike to let Dr Mann come down to address them.
>
> When I started my residency on the 6th Jan 1997 in Lae, we went
without pay for 6-8 weeks. DOH gave the same old reason. We (Manape,
Urakoko, A. Ame) had to physically called into personel officer - to
get some attention.
>
> That was 10 years ago!...system failure?
>
> DOH : Resident Doctors Scenario
>
> You plant a geniune apple seed, got the plant up. sunshine, water
etc. Saw the first fruit on its way to maturity. Instead of continued
care to obtain the ultimum content; energy and sweetness, instead you
grab a bush knife and slash it in half.
>
> This is unthinkable.
>
> I sympathised with our RMO in PNG...I was given the same plate 10
years ago.
>
> Just a concern only.
>
> Is there any way we can discuss to improve this scenario? over to
the forum
>
> JT
>
>
>
>
>
>
> Send instant messages to your online friends
http://au.messenger.yahoo.com
>
This chronic problem has been experienced also by resident medical imaging technologist, laboratory technologists, dental therapists, and pharmacists for over 10 years now.
As the saying goes, one can learn from a mistake, but the greatest mistake one can make is not learning from it.. What is happening to NDOH - HR, or the government?
Mi lusim olsem long yupla..
Moses Taram..
John Tonar <John.Tonar@...> wrote:
Ladies and Gentleman,
I failed to understand year after year, residents were left to fan for themselves when they resume their residency training. They do not need a protest or strike to let Dr Mann come down to address them.
When I started my residency on the 6th Jan 1997 in Lae, we went without pay for 6-8 weeks. DOH gave the same old reason. We (Manape, Urakoko, A. Ame) had to physically called into personel officer - to get some attention.
That was 10 years ago!...system failure?
DOH : Resident Doctors Scenario
You plant a geniune apple seed, got the plant up. sunshine, water etc. Saw the first fruit on its way to maturity. Instead of continued care to obtain the ultimum content; energy and sweetness, instead you grab a bush knife and slash it in half.
This is unthinkable.
I sympathised with our RMO in PNG...I was given the same plate 10 years ago.
Just a concern only.
Is there any way we can discuss
to improve this scenario? over to the forum
JT
Send instant messages to your online friends http://au.messenger.yahoo.com
JT, thank you for bringing this up.
We had the same problem too.
Something is DEFINITLY WRONG here. I do not have much
information on the process of getting new RMO on the
payroll.
If anyone know, lets discuss this issue.
ri
--- John Tonar <John.Tonar@...>
wrote:
> Ladies and Gentleman,
>
> I failed to understand year after year, residents
> were left to fan for themselves when they resume
> their residency training. They do not need a protest
> or strike to let Dr Mann come down to address them.
>
> When I started my residency on the 6th Jan 1997 in
> Lae, we went without pay for 6-8 weeks. DOH gave the
> same old reason. We (Manape, Urakoko, A. Ame) had to
> physically called into personel officer - to get
> some attention.
>
> That was 10 years ago!...system failure?
>
> DOH : Resident Doctors Scenario
>
> You plant a geniune apple seed, got the plant up.
> sunshine, water etc. Saw the first fruit on its way
> to maturity. Instead of continued care to obtain the
> ultimum content; energy and sweetness, instead you
> grab a bush knife and slash it in half.
>
> This is unthinkable.
>
> I sympathised with our RMO in PNG...I was given the
> same plate 10 years ago.
>
> Just a concern only.
>
> Is there any way we can discuss to improve this
> scenario? over to the forum
>
> JT
>
>
>
___________________________________________________________
The all-new Yahoo! Mail goes wherever you go - free your email address from your
Internet provider. http://uk.docs.yahoo.com/nowyoucan.html
Ladies and Gentleman,
I failed to understand year after year, residents were left to fan for
themselves when they resume their residency training. They do not need a protest
or strike to let Dr Mann come down to address them.
When I started my residency on the 6th Jan 1997 in Lae, we went without pay for
6-8 weeks. DOH gave the same old reason. We (Manape, Urakoko, A. Ame) had to
physically called into personel officer - to get some attention.
That was 10 years ago!...system failure?
DOH : Resident Doctors Scenario
You plant a geniune apple seed, got the plant up. sunshine, water etc. Saw the
first fruit on its way to maturity. Instead of continued care to obtain the
ultimum content; energy and sweetness, instead you grab a bush knife and slash
it in half.
This is unthinkable.
I sympathised with our RMO in PNG...I was given the same plate 10 years ago.
Just a concern only.
Is there any way we can discuss to improve this scenario? over to the forum
JT
Guys, you all remember Dr Udayan Ray, who once the chemical patholoy
lecture at UPNG. He is now the clinicl chemistry director at Hobart.
PJ, is that correct?
He has kindly agreed to be an editor and reviewer for the PNG JSTE.
Willie has also kindly accepted the invitation to a reviewer as well.
If any of you guys are interested, let me know.
ri