Mike Adams seems to view me this way. It started out funny, but isn’t so funny any more. Of course, Galadriel was offered The One Ring and its great power, but declined it because she was afraid of what she would become. Maybe I am like Galadriel after all.
I decided to write this post for Science-Based Medicine because I’ve taken notice of recent posts Mike Adams has written about me, mainly because they are riddled with misinformation, fabrications, and lies. Even though at least two of his claims about me made me laugh out loud because of their utter ridiculousness, much of the rest of his recent writing about me has been downright defamatory, libelous even.
The stupid stuff
Before I get into the really nasty stuff, let’s look at the stupid stuff. It’s not that the nasty stuff isn’t also stupid, but here I arbitrarily decide to divide the discussion into parts about when Adams amuses me and when he disgusts me. If there’s one lesson I’ve learned from Adams’ attacks on me, it’s that, apparently, I have incredible power—possibly even superhuman! I mean, seriously. Adams really does seem to think that I have massive power over what Wikipedia does and does not publish about vaccines and medicine! Indeed, as I thought last night about what to write and even ended up staying up until 2 AM to do so (mainly because I was so exhausted after a day in the operating room that I crashed on the couch between 8 and 11 PM), I was half-tempted not to disabuse him of his apparent delusions about my overwhelming power. After all, if Adams really does think that I have so much power, why would I want to reveal to him the truth that I do not? On the other hand, far less amusing are Adams’ attempts to link Karmanos Cancer Center and me to the criminal Dr. Farid Fata, a lie by insinuation that is despicable even by his low standards. What should I expect, though, from someone who’s been running scams since Y2K and posting threats against GMO scientists?
Of course, I am not naïve enough to believe that Adams doesn’t actually know damned well that I don’t have that level of influence on Wikipedia. Rather, it’s all a sham, a con man’s patter, to convince his readers that I’m a major player in a conspiracy to manipulate health articles on Wikipedia from behind the scenes. He uses such fabricated stories as tools to fire up his gullible and stupid followers. Does Adams even realize how ridiculous his articles come across with their overwrought language? In fact, I laughed out loud when I read that Arianna Huffington and I “are not directly murdering children, but they are doing everything in their power to kill any truthful discussion about vaccine damage (that might save children)” and then this:
Dying of cancer can be a horrible way to go, but as a cancer specialist I sometimes forget that there are diseases that are equally, if not more, horrible. One that always comes to mind is amyotropic lateral sclerosis (ALS), more commonly known as Lou Gehrig’s disease. It is a motor neuron disease whose clinical course is characterized by progressive weakness, muscle atrophy and spasticity, with ultimate progression to respiratory muscles leading to difficulty breathing and speaking (dysarthria) and to the muscles controlling swallowing. The rate of clinical course is variable, often beginning with muscle twitching in an arm or a leg or slurring of speech. Ultimately, however, ALS progresses to the loss of ability to move, speak, eat, or breathe. The most common cause of death is from respiratory failure, usually within three to five years after diagnosis, although there is the occasional outlier with a less malignant form of the disease with a slower course of progression who can live a long time, such as Steven Hawking.
In other words, ALS is a lot like cancer in some ways. It is a progressive, fatal disease that usually kills within a few years at most. On the other hand, it is different from cancer in that, at least for many cancers we actually do have effective treatments that prolong life, in some cases indefinitely. In contrast the most effective treatment we currently have for ALS is a drug (riluzole) that is not particularly effective—it prolongs life by months—and can be best described as better than nothing, but not by a whole lot. So it is not surprising that ALS patients, like cancer patients, become desperate and willing to try anything. This is completely understandable, but sometimes this desperation leads to activities that are far more likely to do harm than good. I was reminded of this when I came across a post in the antivaccine propaganda blog, Age of Autism, referring to an article in The Scientist entitled Medical Mavericks. The fortuitous posting of this story, which was apparently designed to try to show that it’s not as crazy as critics have said to be treating autistic children with “Miracle Mineral Solution” (MMS) (which is a bleach) given that the introduction explicitly mentioned Kerri Rivera and the patient described in the article used sodium chlorite to treat his ALS, provided me the opening to discuss a group whose existence and advocacy brings up a complex tangle of issues that boil down to questions of how far patient autonomy should be allowed to go. I’m referring to a company, PatientsLikeMe, which describes itself thusly: