TOUCHED BY LYME: California Lyme cases “don’t get no respect”
There’s a troubling statement about Lyme disease on the CDC website which is widely cited in the media: “This disease does not occur nationwide.” (Editor’s note: Since this blog was published, the CDC has deleted this line from its website.)
What in the world does that sentence mean?
Even using the CDC’s own highly restrictive Lyme surveillance criteria, there are cases on the east coast, cases on the west coast, and cases in the middle. So, what about that scenario is NOT “nationwide”?
The CDC emphasizes that virtually all US cases of Lyme disease occur in only 14 states: Connecticut, Delaware, Maine, Maryland, Massachusetts, Minnesota, New Hampshire, New Jersey, New York, Pennsylvania, Rhode Island, Vermont, Virginia, Wisconsin.
And the website strongly implies that if you haven’t spent time in one of those states, your chance of contracting Lyme is pretty much nil.
But as my colleague Lorraine Johnson recently pointed out in her blog the Lyme Policy Wonk, those numbers don’t jibe with data from other sources. (Why Doesn’t the CDC Count Lyme Disease Cases in the South and the West? Everybody Else Does.)
It is true that Lyme-infected people in the remaining 36 states often have a devil of a time getting properly diagnosed and treated for the illness—which can result in fewer cases being submitted to the CDC’s reporting system. But the problem is deeper than that.
A case in point—my home state of California. During my 12 years of Lyme advocacy, I’ve personally heard from hundreds if not thousands of Lyme-infected people who have been told by medical professionals, “You can’t have Lyme disease, because there’s no Lyme in California.”
A recent article from KQED public media in San Francisco spells out the conundrum of Lyme in this state. As one tick expert explains it:
“There are definitely patches in California where the risk is just as high as the East –it’s just not the same spatial extent.”
In other words, the risk isn’t spread out evenly. The article goes on to say:
Hikers can move from high-risk area to a low-risk area and never know it….One moment you’re strolling through redwood forests, the next through oak forests, and a couple of hours later you may come across scenic chaparral. While on this iconic hike, you probably don’t realize that you’ve moved through both high- and low-risk Lyme disease areas. The question is, do you know where you are most at risk? The answer is in the oak forest where layers of rich leaf litter are a kind of Club Med for ticks.
But you know what? While oak forest with layers of leaf litter may indeed be Club Med for ticks, plenty of ticks hang out in what might be considered the YMCA—ordinary spots like a backyard garden, a wooden picnic table , or an outcropping of rocks.
It all depends on where the garden, the picnic table, and the rocks are located! You do not have to be in an oak forest to get nailed by an infected tick in California.
The article goes on to say:
Part of what puts Californians at risk is a lack of awareness — among the public and even among doctors. Much of the research and public health information is based on East Coast ecology and may not apply to the West.
For many Californian physicians, Lyme disease is just not on the radar, even though …Lyme-infected ticks have been located in 42 of California’s 58 counties. About 100 cases of Lyme disease are reported in California each year, but according to Supervising Public Health Biologist Kerry Padgett of the state Department of Public Health, the disease is likely more widespread. “There is an under-diagnosis and under-reporting of Lyme disease in California,” says Padgett.
Well, there’s an understatement!
What KQED’s article fails to point out is that the words “100 reported cases” mean something very different to the CDC and state health officials than to the average person.
A more accurate way of putting it would be: Every year, about 100 cases make it through the meat-grinder that is the CDC’s labyrinthine Lyme disease reporting process. You start with thousands of people who go to their doctors with undiagnosed Lyme disease. Throw out all the ones who are misdiagnosed with something else. (“No Lyme in California,” remember, so the diagnosis isn’t even considered.)
Of the ones where Lyme is at least thought about, take all the positive lab tests that are reported (by law) to the state. Send those cases to the county health departments of the patients’ place of residence.
The county health department is now supposed to take those positive Lyme cases and investigate each one individually, to make sure it precisely fits the CDC’s rigorous surveillance criteria. This sometimes involves contacting the patient and/or the doctor (a time-consuming and resource-intensive undertaking).
And of course, most California counties, like their counterparts in other states, are under-funded and under-staffed. Is it any wonder that many Lyme cases just seem to fall off the end of the turnip truck, never to be heard from again? Only thoroughly vetted cases are sent on to state health officials, who double-check to make sure each one meets the CDC’s tough requirements in order to be counted, and then forward them on to the federal agency.
A few cases survive that winnowing process. Voilà: 100 reported cases of Lyme in California. The rest are left in the dust somewhere.
Under-diagnosed and under-reported, indeed.
TOUCHED BY LYME is written by Dorothy Kupcha Leland, LymeDisease.org’s VP for Education and Outreach. She is co-author of When Your Child Has Lyme Disease: A Parent’s Survival Guide. Contact her at firstname.lastname@example.org
- August 7, 2017 at 9:27 am
Dorothy – nailed it. “Club med for ticks.” You kill me. You bring up some very important points that entomologists, health professionals, epidemiologists and researchers need to be aware of, particularly the diversity of terrain in CA. Thanks for your spot-on article.
- August 7, 2017 at 1:32 pm
As I have already pointed out…. if the true understanding of the extent of this pandemic were accepted reality by society as a whole (~20% of the adult population nationwide) look to who would take the biggest financial hit.
The number one suspect for suppressing the true Lyme Pandemic numbers are undoubtedly 3rd party payers. They have the most to loose financially and the government right behind them.
Without a big mega corporation with something to sell, the player becomes those who have something to loose.
This is a crime against humanity.
- August 10, 2017 at 3:26 pm
Thank you for writing about this issue. I would like to add that it is not just under-funding that inhibits proper procedure in case counting. My county, Sonoma, deliberately throws out all lab reports from Igenex without ever attempting to follow up as they are required to do. They also refuse to respond to Tick Borne Disease Advisory Group requests to tell us how many lab reports they have thrown out. Furthermore, I have been told that they pre-select the number of cases they will confirm per year. I have the Deputy Public Health Officer Karen Holbrook recorded saying “We plan to continue counting 8-10 cases per year.” And now, with a new more restrictive case definition it will be even fewer. Or perhaps they will stay with their pre-selected number.
- August 12, 2017 at 3:26 pm
Can’t even tell you how many times in the last 45+ years a Doctor has said, “You can’t have Lyme Disease, it’s not in California!” Even this year, w/below low levels WBC my Infectious Disease doc said you must be coming down with a cold, same statement from other Docs. It’s hard not to be sarcastic! So this must be why the Oncologist needs blood tests every 3 months, maybe to see if I’ve recovered from my cold? This same I.D. doc also told said, “Igenex is a phony lab!” Kaiser Dr.’s computers are linked so they can see what test & what Doctors you’ve have had in the past so it’s not like they can’t read what’s going on.
After receiving prism glasses, the O.D. said, “now you can tell your Kaiser I.D. Dr. it was all in your head.” These glasses help the neurons to reconnect properly, what a difference the made with fatigue.
So glad to have found a group of Doctors that have Lyme Disease that are helping me get back on the road to recovery, w/o antibiotics(which was only temporary 2 wk fix anyway). Plus, thanks to my Kaiser GP she has help get the lab work done.
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