A CH sufferer serendipitously discovered that using LSD recreationally stopped his pain. Word quickly spread among CH sufferers, but as you can imagine, they were worried about being busted by the man who wears the badge.
A medical researcher got wind of this and did some rudimentary research on a drug that is chemically similar to LSD, but does not cause a "high"; in other words, it has no abuse potential. He made a remarkable discovery: many of the patients he studied reported that taking just THREE DOSES PER YEAR stopped the pain.
The problem then, is that the illness is rare enough that you could never make back $2.5 billion dollars selling three pills per year to patients, so no big pharma company would want to go thru all the red tape to get it approved by the FDA. As a result, there remains no effective FDA-approved treatment for CH.
Many of these patients continue to self-medicate with old-fashioned LSD while looking over their shoulder for "The Man". How sad....
Profit indeed comes before people, but I had no idea how abusive the system could be. And for the record, I do not have CH.
Call me picky, but as far as I am concerned, any discernible input latency is completely unacceptable. I can't believe that people actually save their old CRTs to play Guitar Hero because the new ones tend to be so laggy.
I've been working as a contract software developer for a few years now. I feel like I get a out of working on different projects. I meet smart people who have stayed in the same place for years. They definitely have the advantage of deep knowledge of the environment, but I find that they often lack breadth of knowledge sometimes.
Before the fedgov got involved, it was freely available. The companies that have owned the patent have done NOTHING ZERO ZIP NADA except act as monopoly suppliers of the drug. A pharmacist who shares my point of view says that it costs pennies per dose to manufacture. But through careful manipulation of the legal and insurance systems, they are able to collect over ONE BILLION DOLLARS PER YEAR for this drug.
You are absolutely correct to point out that most patients pay only a very small co-payment. Jazz Pharmaceuticals, the company that currently owns the patent, knows this. They know that they can't charge $12,000 per month if a patient with a 10% copay is on the hook for $1,200 per month. They will simply collect $10,800 per month from insurance and write off the remaining $1,200 (because they are so nice, ya know).
Seriously, these people are evil geniuses. They are gaming the system, preventing sick people from receiving medication that they did absolutely nothing to develop.
Oh, and they are notorious for parking their money overseas to avoid paying taxes, just like Apple has been criticized for. At least Apple researches and develops useful products that people want to buy.
Come to think of it, Jazz is sort of like SCO could be if they had one their LINUX lawsuit and been able to demand $699 license fees from LINUX users for a product they did not create.
Oh, and to make matters worse, the fedgov refused to approve the drug for more uses, not because they thought it wasn't effective. No, they want to keep it from being used for more common illnesses because it is a drug of abuse, you see. They have to protect us from ourselves. I'm sure you understand this, given your
Having seen how people are affected by what they do, that people who need the drug can't get it because of the cost, I wanted to spread this knowledge far and wide so that people can know what the government is doing to sick people in their own name.
"Money is the root of all money." -- the moving finger