MS and How Drug Companies Can Profit from Outdated Counts


A Fairy holding a Wolf puppy

My kind of Tooth Fairy!

     Visa recently commissioned a study to find out just how much parents where giving their young children for each baby tooth that they lost? It turns out, quite a bit. On average each child was receiving $3.19 per tooth. That in it self kind of blew me away because I think fifty some odd years ago I was getting a dime to maybe a quarter per tooth. Times certainly have changed.

     Now you’re probably asking yourself, what does the Tooth Fairy have to do with multiple sclerosis? And truth be told, very darn little actually. However there is one big irony that I have discussed before in a couple of my posts here regarding, MS by the numbers, and how these numbers just do not add up. 

     It seems strange to me that Visa would spend money commissioning a survey, or study about baby teeth, but large corporate drug companies seem to have little if any interest in finding out just how many people in America and around the globe really have multiple sclerosis? Let’s face it, these corporate drug giants are raking in hundreds of millions, perhaps billons, of dollars on these horrifically expensive drugs so you would think it would be to their advantage to know just where the incidence and higher numbers of MS patients are around the world and where their future profits might lie?

     Apparently though, they are satisfied in using numbers that were collected some twenty to thirty years ago, and they are still quoting those numbers today, as I have read recent drug company pamphlets where these very same numbers are still being used. If you don’t recall, those numbers were something like 450,000 people in the U.S with perhaps two to three million people worldwide having multiple sclerosis, which I believe to be a huge undercount of what the real numbers truly are. But since these numbers were taken so long ago, who knows what they actually are today?

     It makes one wonder why drug companies would not want to update these numbers in light of the possible increased sales potential around the world? Unfortunately, there is a possible financial motive for drug companies to stay with these decades old smaller numbers. If they used larger numbers they fear that this would actually decrease their profits on these drugs because they would have to produce larger batches driving down the overall cost because of the larger patient base that might use them. And because most industrialized nations outside of the U.S. control drug costs at much lower prices then what these drug behemoths want to sell them for. But by keeping the smaller numbers, remember it’s a supply and demand kind of thing, and because of how ridiculously expensive these drugs are, especially in America, drug companies can actually justify making more of these drugs then are really needed and then letting them reach their expiration dates so they can destroy whole batches and claim large tax write offs against what they do sell, increasing their profits on the back end as well.

     Greed in its truest form, they got you coming, and going. And the saddest part of all, the insurance industry probably knows that they do this and says nothing about it to protect their own bottom line, because drug companies are probably heavily invested in them as well!  

8 thoughts on “MS and How Drug Companies Can Profit from Outdated Counts

  1. Terrie Raiter

    Thank you for exposing the drug companies. I always thought that the number of people with MS was so much higher than I have read. I also think that all of the med prices for MS is ridiculously high. I know for a fact how much cheaper they are in Canada, Hungary and Germany. I have family in those countries that have checked it out for me. We have a voice but who will listen? The drug companies are all connected to the politicians. Most of us are not even aware that our candidates are being paid under the table for ‘special favors’. I think that this a problem with no solution. Thank you. I enjoyed your article.

  2. Lynnie Heal

    Billions upon billions has been made out of MS patients via MS drugs and even MS societys also who have all promoted them and even MS researchers . Its so sick to the core its SICK


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