Is there such a thing as an “allergy to wifi”? Lots of people claim there is; science, not so much.
I debated about writing about this topic, given that I just wrote about it last week on my not-so-super-secret other blog. However, as I thought about it during the weekend, I realized that the tragic story that so saddened and disturbed me to prod me to discuss so-called “electromagnetic hypersensitivity” or “electro-hypersensitivity” (EHS) was so horrific that a more detailed, SBM-level discussion was indicated, particularly in light of a similar case electromagnetic hypersensitivity that didn’t end so tragically discussed by Harriet Hall in September. I’m referring, of course, to the case of Jenny Fry, a British teen who hanged herself in June and whose mother has been claiming that her “allergy to wifi” was what drove her to suicide. So, while there will be some overlap with my previous discussion, I will try to step back and take a broader view of the evidence regarding the fake diagnosis of EHS, interspersed with examples (hopefully) illustrating my point. Think of this as the post I wished I had written the first time around but, due to time constraints, couldn’t.
Bogus science and lawsuits over EHS
By way of background, it’s worth briefly revisiting the case that Harriet discussed. Indeed, if you Google “lawsuit” and “electromagnetic hypersensitivity” and “wifi” the first two pages of results consist mostly of articles discussing it. That’s probably because this is just the latest lawsuit that made the news. It happened in Massachusetts, where the parents of a 12-year-old boy (designated “G” in court records) who was attending Fay School in Massachusetts alleged that the school violated his rights under the Americans with Disabilities Act by failing to make accommodations to protect G from electromagnetic radiation from the school’s wifi routers. From the complaint’s summary statement:
One topic that keeps recurring and obligating me to write about it consists of critically analyzing stories of children with cancer whose parents, either on their own or at the behest of their child, stop or refuse chemotherapy or other treatment. It is, sadly, a topic that I’ve been discussing for nearly a decade now, starting first on my not-so-super-secret other blog and continuing both there and here. Indeed, the first post I wrote about this problem was in November 2005, a fact that depressed me when I went back through the archives to find it because so little has changed since that time.
I was painfully reminded of this last week when stories started circulating in the media about the death of Makayla Sault, an Ojibwe girl and member of the New Credit First Nation in Ontario:
The entire community of New Credit is in mourning today, following the news of the passing of 11 year old Makayla Sault.
The child suffered a stroke on Sunday morning and was unable to recover. Friends and family from across the province travelled to New Credit First Nation today to offer condolences, share tears and pay their respects.
Time and time again, we’ve seen it. When pseudoscientists and quacks can’t persuade the scientific and medical community of the validity of their claims, they go to the law to try to gain the legitimacy that their claims can’t garner through proving themselves by the scientific method. True, purveyors of pseudoscience and unscientifically-derived medical practices do crave the respectability of science. That’s why they try so hard to take on the trappings of science. The problem is that they just can’t do it right, try as they might, or when they do it right their methods are shown to be no more effective than a placebo, aside from the occasional seeming “positive” results that would be expected based on random chance alone. However, failing to achieve the respectability that the mantle of science provides, practitioners and advocates of pseudoscience frequently try to codify their woo into the law.
The reason that they would do this is not too hard to discern. Few legislators and politicians are scientists, and even fewer are scientifically inclined. Back when I still lived in New Jersey, I may have been lucky enough to have had a Congressional Representative who really was a rocket scientist (well, a physicist, actually), but now that I live in Michigan I’ve gone from having a scientifically inclined Congressional representative to having one of the dimmest bulbs in Congress representing me. What that means is that it’s far easier to persuade politicians that this woo or that woo deserves to be permitted or even licensed. That’s how we now have many states licensing acupuncturists, naturopaths, and even “homeopathic physicians,” as Arizona does. The pressure for this sort of acceptance of unscientific medical modalities is building, as well, as Kimball Atwood has documented. Another example is the Dietary Supplement Health and Education Act (DSHEA), which was passed in 1994 and in essence ties the FDA’s hands when it comes to regulating most supplements. Indeed, the very existence of the National Center for Complementary and Alternative Medicine (NCCAM) is a testament to the success of this approach, as a powerful Senator (Tom Harkin, D-IA) almost single-handedly foisted this scientific atrocity on the NIH against the desires of scientists. The results have included a $30 million scientific boondoggle of a trial to test chelation therapy and a profoundly unethical trial of Dr. Nicholas Gonzalez’s “protocol” for pancreatic cancer patients that a recent clinical trial has shown to be worse than useless. The most recent example of this trend is the way that CAM supporters have tried to hijack President Obama’s health insurance reform initiative to insert coverage for everything from any licensed “alternative medicine” practitioner to Christian Science prayer healing.
Recently, two new fronts have been opened up in this battle. One is disturbingly close to me, as it involves the Canadian province of Ontario whose north shore on the Detroit River is less than two and a half miles from my office, the other in Oregon, which, although it’s happening nearly 2,000 miles away from where I live and practice, could portend a new and disturbing tactic of the anti-vaccine movement to do what various other purveyors of pseudoscience have done before and try to win in state legislatures where they can’t win in science or the courts. Of course, in a democratic republic, it is the right of everyone, even supporters of quackery, to try to petition his or her legislators, but it is equally the responsibility of those of us supporting science-based medicine to try to educate legislators why allowing them to alter the law to protect their pseudoscience has the potential to result in great harm.