To recommend thrift to the poor is both grotesque and insulting. It is like advising a man who is starving to eat less.
-Oscar Wilde, The Soul of Man under Socialism
I guess that I am fortunate that my doctor as a teen was the local well-respected expert on developmental disorders and who certainly isn't in it for the money, he's simply a wonderful doctor.
I have the same temperature thing, my normal temperature is about the same as yours.
To recommend thrift to the poor is both grotesque and insulting. It is like advising a man who is starving to eat less.
-Oscar Wilde, The Soul of Man under Socialism
Yes, and it's crap. maybe people would work on preventing the sensory overload that leads to autistic meltdowns instead of turning us into Zombies?
The only medication that I have seen that consistently helps those of us cope with neurotypical society is Ritalin. In my case it reduces my sensory sensitivities and helps with my executive system dysfunction.
To recommend thrift to the poor is both grotesque and insulting. It is like advising a man who is starving to eat less.
-Oscar Wilde, The Soul of Man under Socialism
"Qu'est-ce que c'est que cela, la loi ? On peut donc être dehors. Je ne comprends pas. Quant à moi, suis-je dans la loi ? suis-je hors la loi ? Je n'en sais rien. Mourir de faim, est-ce être dans la loi ?" -- Tellmarch
"Человек не может снять с себя ответственности за свои поступки." - L. Tolstoy
"[it] is no doubt obvious, the cult of the experts is both self-serving, for those who propound it, and fraudulent." - Noam Chomsky
I'm thinking that by the time this is over people who live in Arkansas could end up with a free blow job on the moon.
"Jan, cut the crap."
"It's just a donut."
I heard one grumble about the FDA a while back from some natural healing folk in the martial arts and new age occult communities. There are a large number of traditional herbal remedies that have been used for quite some time. Being natural substances, they cannot be copyrighted, trademarked or otherwise owned by corporate entities. However, there is an alleged Evil Conspiracy that prevents such substances to become FDA Approved.
On the other hand, allegedly at least, the drug companies will commonly study natural herbal remedies, isolated the active ingredient, learn how to synthesize something nigh on identical to the active ingredient, and then copyright the synthetic.
Now, medicine isn't my field. I just Googled some appropriate keywords. Others might do the same. There are lots of opinions on the subject out there. Among other things, The Establishment will warn that plants vary, and preparation will vary. Even if one understands what a natural drug can do, it is often hard to hit a given dosage reliably.
But, yes, there are a number of people who smell something fishy in the FDA. They are too much in bed with the industries they are supposed to be managing and regulating. At least some of the new age freaks and traditional herbalists are grumbling.
To recommend thrift to the poor is both grotesque and insulting. It is like advising a man who is starving to eat less.
-Oscar Wilde, The Soul of Man under Socialism
This makes sense if the objective of the system is to maximize profits for the companies while minimizing competition from natural alternatives. It makes less sense if the objective is affordable health care.
How absurdly expensive is the testing? Could a university looking for research projects manage it, or is the bar set so high that only a major for profit corporation would be able to clear it?
I am imagining a UC Berkeley project to get FDA approval for using Marijuana for pain relief. ™
http://www.bg-medicine.com/content/n...r/news/q/id/24
It takes about eight years per test, 90% of drugs fail testing, and its estimated that this ends up costing around $800 million per new drug approved. Do you know how many people with borderline and off-label symptoms you'd have to sell to just to break even?
Of course, if you're actually reading FDA reports on new drugs, you'll almost always find the following lines somewhere: "The mode of action [of drug] is unknown," and "This is not a cure." Most of the testing is designed to ensure it does what it says it does, without causing short-term consequences worse than the original symptoms. For long term medications, patient = lab rat.
Well now, that's just illegal outright. Doctors and researchers can't just pick up the most effective medical plants we know of (cannabis, opium, coca) and start doing "experiments" with them. That would be crazy. Instead, they'd have to apply for a limited number of federal licenses for study, and those have only been opened up in the last few years. If you're interested in this line of study, you'll need to buy a Senator or two first.
Welcome to the American regulatory regime? The bold part could be applied to medicine, inter-generational entertainment copyrights, most stock market regulations [that are actively enforced], big-farm subsidies...
About 75% of drugs are still actually extracts from a naturally occurring plant, but here's how it goes. They find something that is used in traditional medicine somewhere, then try to isolate the most active chemical. The process of isolating the single chemical is often patentable, so they have the single chemical tested under the FDA rules rather than the entire plant. Alternatively, they might find a different starter chemical that can be manipulated until it matches the original plant source.
In the other cases, they'll tweak the chemicals with a few reactions, ie: turning opium into morphine or heroin.
A major problem arises in not studying how the other chemicals effect our biology. IE: Cannabis has dozens of active chemicals, but Marinol only includes one or two of them. Patients say it just isn't as effective, and the Marinol pill can actually deliver a lethal dose where smoking the plant itself can't.
The only botanical mixture currently approved by the FDA is actually an ointment made from green tea, the same chemicals they came out loudly decrying just years before:
Amazingly though, the FDA still doesn't recognize a single health benefit of actually drinking green tea, but they'll approve a prescription ointment to put on your junk."FDA concludes that there is no credible evidence to support qualified health claims for green tea consumption and a reduced risk of gastric, lung, colon/rectal, esophageal, pancreatic, ovarian, and combined cancers. Thus, FDA is denying these claims. However, FDA concludes that there is very limited credible evidence for qualified health claims specifically for green tea and breast cancer and for green tea and prostate cancer, provided that the qualified claims are appropriately worded so as to not mislead consumers." On May 9, 2006, in response to "Green Tea and Reduced Risk of Cardiovascular Disease", the FDA concluded "there is no credible evidence to support qualified health claims for green tea or green tea extract and a reduction of a number of risk factors associated with CVD."
However in October 2006, the FDA approved an ointment based on green tea. New Drug Application (NDA) number N021902, for kunecatechins ointment 15% (proprietary name Veregen) was approved on October 31, 2006, and added to the "Prescription Drug Product List" in October 2006. Kunecatechins ointment is indicated for the topical treatment of external genital and perianal warts.
I would literally not trust American medicine until I was on my death bed. Then I'd say: "Experiment away! I've got nothing left to lose."
Last edited by independent; 11-01-2009 at 09:41 AM.
'82 iNTp
"Sometimes it is said that man cannot be trusted with the government of himself. Can he, then, be trusted with the government of others? Or have we found angels in the form of kings to govern him? Let history answer this question." -Jefferson
http://online.wsj.com/article/SB125694764832619997.html
A report issued by the nonpartisan Congressional Budget Office highlights faults with both sides of the argument to create a public health-insurance plan...
The House's public plan would save money by having lower administrative costs than private plans, according to the CBO's findings. But several other factors would drive up its costs, the report said... The CBO says its findings aren't conclusive.
-Please keep in mind that the CBO has a long track record of underestimating the cost of government programs.
---
-So cry many Boomers like Haymarket & Playwrite whenever they fail to explain their hypocritical self-justifications, their double-standards, and their double-think forays into evil. Perhaps their consciences bother them, perhaps not. Who knows.
To recommend thrift to the poor is both grotesque and insulting. It is like advising a man who is starving to eat less.
-Oscar Wilde, The Soul of Man under Socialism
"Qu'est-ce que c'est que cela, la loi ? On peut donc être dehors. Je ne comprends pas. Quant à moi, suis-je dans la loi ? suis-je hors la loi ? Je n'en sais rien. Mourir de faim, est-ce être dans la loi ?" -- Tellmarch
"Человек не может снять с себя ответственности за свои поступки." - L. Tolstoy
"[it] is no doubt obvious, the cult of the experts is both self-serving, for those who propound it, and fraudulent." - Noam Chomsky
Actually, I have read that in people with ADHD and many on the autism spectrum Ritalin and other stimulants (like caffeine) have almost the opposite effect to what they do with "normal" individuals. I have noticed this myself, caffeine actually calms me and can even make me a little sleepy. Which is why the people that get Ritalin illegally to use thinking it will help them study are morons, it will just make them hyper.
Just to nitpick, Ritalin is an amphetamine derivative, but it is not nearly as powerful as meth.
To recommend thrift to the poor is both grotesque and insulting. It is like advising a man who is starving to eat less.
-Oscar Wilde, The Soul of Man under Socialism
Hey - if it worked for him?
We had a local case in which a woman had a nasty physical condition that was being relieved by a medication - that she was suddenly deprived of because it "hadn't been proven to work." On being told that it worked for her, she was told "Anecdotal evidence isn't clinical proof."
Well, for mass distribution, no. OF course not. But for a case in which is HAS been proven to work?
We're only at the very edge of individualized medications, probably with a genetic base. So one person's crap is another person's cure and vice versa.
How to spot a shill, by John Michael Greer: "What you watch for is (a) a brand new commenter who (b) has nothing to say about the topic under discussion but (c) trots out a smoothly written opinion piece that (d) hits all the standard talking points currently being used by a specific political or corporate interest, while (e) avoiding any other points anyone else has made on that subject."
"If the shoe fits..." The Grey Badger.
Listen, I know several people with ADHD with that experience, it's NOT an urban myth.
To recommend thrift to the poor is both grotesque and insulting. It is like advising a man who is starving to eat less.
-Oscar Wilde, The Soul of Man under Socialism
I don't think a patent like that would be valid. A valid patent has to be a new thing. Suppose a company went to the effort to show that a medicinal plant works and patented the plant,
Such a patent likely would not withstand challenge because knowledge that the plant had medicinal properties was previously known to practitioners of traditional medicine.
Why don't you explain what you're talking about? As far as I know you're the only doctor in the house and that's even your specialty, so I assume you know what you're talking about and we could all benefit from your knowledge, but it's not reasonable to expect people to take your word for things without at least explaining.
Odin reported personal experiences with stimulant drugs that seem to support the idea of the inverse effect; what do you know that refutes this idea? I'm asking because I'm genuinely curious. What is the effect that leads Odin to believe he's being slowed down by stims?
"And what rough beast, its hour come round at last, slouches toward Bethlehem to be born?"
My blog: https://brianrushwriter.wordpress.com/
The Order Master (volume one of Refuge), a science fantasy. Amazon link: http://www.amazon.com/dp/B00GZZWEAS
Smashwords link: https://www.smashwords.com/books/view/382903
That's not exactly correct. About 75% of medicines are compounds or derivatives of compounds found in naturally occurring plants or fungi. For example penicillin is an antibiotic produced by bread mold. Penicillin is produced at a big scale today (50,000 tons annually), all of it from penicillium fungal strains derived from an original isolate obtained from a rotten cantaloupe in a Peoria farmer's market during WW II.
Few new drugs are obtained in this way today. Some have tried, but they have not been very successful.but here's how it goes. They find something that is used in traditional medicine somewhere, then try to isolate the most active chemical.
Splitting hairs? If you go in to a pharmacy, the majority of the chemicals inside those pills (or the precursers to them) can also be found in naturally occurring plants, fungi, etc.. I think we agree on that plus or minus the specificity of the language.
And while the pharma companies don't necessarily own patents on the chemical itself, they can patent methods for synthesizing or extracting those chemicals. Since the plant itself isn't tested for medical efficacy (no profit incentive), you have to go through the doctor and the patent to get the chemical you could have grown in the backyard. And with genetically modified crops as a precedent, what is stopping pharma from teaming up with Monsanto in creating and patenting a plant strain that boosts output of a particular active chemical?
Now, as far as penicillin goes, maybe the fact that we've pumped the whole population up with the extract of a single strain has something to do with why the antibiotic doesn't really work anymore? Maybe there are other chemicals in the mold that would suppress bacterial evolution, maybe allowing penicillium to evolve on its own would leave it more effective in the long run: but there's no financial incentive to ever find out.
Few new drugs are found today at all. Placebos have become so effective that its hard to get anything past late stage trials. Some of the most popular prescriptions (Prozac) probably couldn't get past FDA evaluation if they were introduced today.
Faith in a pill, faith in a god, faith in acupuncture, whatever. Its been my anecdotal experience that those with the highest faith in pills have the worst chronic medical conditions.
'82 iNTp
"Sometimes it is said that man cannot be trusted with the government of himself. Can he, then, be trusted with the government of others? Or have we found angels in the form of kings to govern him? Let history answer this question." -Jefferson
It's expensive because the era of magic bullets is gone. Consider antibiotics and chemotherapy drugs. One of the first of these drugs was penicillin. Penicillin was strikingly effective. When given to people with bacterial infections almost all of them were quickly rid of the bacteria, that is, they were cured.
One of the reasons why this happened was that people sometimes cure themselves of bacterial infections. That is, their immune systems can destroy bacteria when present in manageable numbers. What an antibiotic does is kill the vast majority of bacteria, reducing their numbers to a manageable level that the immune system cas finish off. Another reason the antibacterials worked was that bacteria are so different from humans that compounds that wreck havok with their physiology often left ours untouched. This allowed lethal levels (to the bacteria) of antibiotics to be used.
In cancer, the bad guys are the patient's own cells gone rogue. They are still human cells and have human cellular physiology. Anything poisonous to them is going to be poisonous to the patient. The doctor cannot use lethal levels of anti-cancer drugs because they will will the patient too. Similarly, because the cancer cells are part of the body, they will not draw the same vigorous immune response as an utterly foreign agent like a bacteria.
What this means is it is much much more difficult to wipe out a cancer incursion with chemotherapy than it is a bacterial incursion with antibacterials. Thus, standard cancer therapy involves mechanical removal of as large a fraction of the cancer cells as possible, followed by (if necessary) cell-killing treatments (radiation, chemotherapy) designed to preferentially kill cancer cells over normal cells.
For example, my wife had stage I grade 2 endometrial cancer 11 years ago. She had a TAHBSO (Total Abdominal Hysterectomy and Bilateral Salpingo-Oophorectomy) and that was that. With stage I, about 90-95% of the time, the cancer has not yet escaped from the uterus. Removal of the uterus intact achieves mechanical removal of 100% of the cancerous cells and the patient is "cured"--although one cannot know this is the case for many years afterward, if ever. On other hand, if cancer cells are found outside the uterus, in the lymph nodes (stage III) or elsewhere (stage IV) the prognosis is worse or much worse. This is because they are (or were in 1998 at least) no really effective radiative or chemotherapies for endometrial cancer.
On the other hand, breast cancer is a cancer with a reasonably good prognosis (as cancers go) even though surgery fairly often does not remove all of the cancer. Radiative and chemotherapies are more effective for this cancer.
It's not like there was some "penicillin" for breast cancer. There will proably never been anything as effective against cancers as pencillin was against susceptible bacteria. Various new compounds were developed over time that had a modest improvement in efficacy or were better tolerated or had fewer side effects and doctors gained more things to try.
Since the improvements at each step were marginal at best, one has to test in lots of patients to see if a real improvement exists. Such large scale studies are expensive.
I recall a cancer drug at phase II trial about which there was a lot of excitment. One of the patients, who was terminal, got dramatically better, and ended up apparently "cured". But during phase three trial it simply was not sufficiently better than the control therapy and was dropped.
Our drug was markedly better than the standard drug for that one guy, but is was not better for most guys. And you have to consider the reverse, that for some other guy the standard drug might be markedly better and it would be bad if he got our drug instead.
It's not easy.