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Lyme disease often misdiagnosed
Jeremy Herb
The Daily Journal

San Mateo, CA
August 22, 2006

Denise Huajardo Springer started losing vision in her left eye in 2001 and began suffering from bouts of extreme fatigue. The San Mateo resident had to put medical school on hold as her health deteriorated.

Her doctors said she had Multiple Sclerosis. Her doctors were wrong.

Springer had Lyme disease, contracted from tick bites, despite three doctors who told her otherwise. When her son developed his speech slower than normal, Springer learned that her 2-year-old also had Lyme.

She had herself tested and found out her incorrect MS diagnosis was really Lyme, and she passed it onto her son when he was born.

"One doctor told me I needed to come to grips with the fact I had MS," Springer said. "Something all along told me I didn't have MS."

Now, Springer's health has improved after undergoing long-term treatment, which includes injections, acupuncture, supplements and antibiotics she continues to take. Her son's health also improved, and Huajardo-Springer said he started "talking up a storm" two weeks after he began taking antibiotics.

Her story is one of many highlighting a growing controversy in the medical community over diagnosing and treating the most common vector-borne disease in the United States.

Lyme disease is a bacterial disease contracted most commonly from a deer tick bite. The classic sign of the disease is a bull's eye rash around a tick bite, but many patients don't get the rash, including Springer.

Initially, the disease causes flu-like symptoms, but long-term effects, including severe fatigue, muscle and joint pains, numbness and other symptoms, can persist past the four-week treatment recommended by the Center for Disease Control and Prevention.

Chronic treatment contested

Most patients can be cured with a few weeks of antibiotics taken by mouth, according to the CDC Web site. For those who continue to have symptoms, the CDC says longer courses of treatment are not beneficial, and have been linked to serious complications, including death.

Phyllis Holm said long-term treatment is what helped her daughter Megan recover from Lyme, after wading through 23 doctors over a three-year span to get it diagnosed.

Holm said she was told repeatedly her daughter was undergoing stress, and her symptoms of extreme fatigue were psychological.

When she was finally diagnosed, Megan had to go on oral antibiotics for a year and a half, followed by eight months of IV treatment, which is what finally improved her condition.

Holm and Lyme-literate doctors say Megan had Chronic Lyme, which is what also plagued Huajardo-Springer.

Chronic patients have recurring symptoms that can return after being dormant for months or years, and Lyme-literate doctors say long-term treatment is needed.

The mainstream medical community, however, has not embraced long-term treatment. San Mateo County Health Officer Dr. Scott Morrow said this is because there isn't peer-reviewed science that provides evidence for Chronic Lyme.

One Lyme specialist even ran into legal troubles for providing long-term care in North Carolina.

The North Carolina Medical Board suspended Dr. Joseph Jemsek's medical license for one year last month. The board said Jemsek, who has about 400 Lyme patients nationwide, including California, strayed too far from standard treatment methods, and did not properly inform patients his treatment was considered unorthodox.

Jemsek can continue to practice medicine during the year, as the suspension resembles a probationary period.

In California, there are laws that allow doctors to prescribe long-term treatment - so long as they make it clear to patients it is not the standard treatment. California is one of only a handful of states to make this distinction.

Medical bills point upwards

The debate over Chronic Lyme runs deep into patients' pocketbooks.

Holm said she spent over $100,000 out of pocket for her daughter's treatment. The medical bills aren't going to stop soon, either, with antibiotics still needed for her daughter.

Treating Chronic Lyme can be a lengthy and expensive process, with multiple medications that can be necessary for years. Holm said even with "relatively good" medical insurance, her bills went skyward, and most patients face the same costly situation.

It took Melanie Reber more than 15 years to learn she had Lyme, after suffering from migraines, numbness, various rashes and other mysterious symptoms.

After doing her own research and finding a local doctor to diagnose her with the disease, her condition worsened after seven months of oral antibiotics, likely due to the co-infections she had, which are additional diseases ticks carry along with Lyme that can potentially complicate treatment and prolong symptoms.

She sought a specialist to treat it aggressively, and her health improved after an additional 15 months of antibiotics through an IV, followed by more oral medicine.

"It really affects your life in every way: financially, physically, mentally, spiritually," Reber said. "It robs you of you. All you know. All you are sure of."

The 19 prescriptions she had to pay for also robbed her of her savings.

Reber said her insurance coverage maxed out at $500 per year, when just one of her numerous medications costs $200 every day.

"I had to use a stove timer for my medications," Reber said. "In the morning, I'd set out pills in a clock shape. I'd take the 12 O'clock, set the timer, then two hours later take the 1 O'clock, and so on."

Support groups ease pain, find doctors

Holm said one of the biggest assets during her daughter's battle with Lyme was the support group they attended.

"The support group has been invaluable," Holm said. "It's a place to learn. Everyone shares their secrets and tips on how to deal with the little things that come along."

Holm said there are about 80 to 100 people in San Mateo County who are in the group, and about 20 attend meetings.

The California Lyme Disease Association also provides help, sponsoring a support group online that has more than 300 members and provides contacts for doctors who will diagnose Lyme.

"You can't get medical help - that's why the support group is important," Holm said. "We know we're sick and not crazy, even if the mainstream doesn't see it that way."

Morrow said many doctors do not treat Lyme, sometimes because they don't think the disease is prevalent in California. He estimated there are less than five doctors in the Bay Area who will provide treatment.

One of the reasons the number is so small is the difficulty in diagnosing Lyme. The ELISA test is used to screen patients who show symptoms, but according to the International Lyme and Associated Diseases Society Web site, this gives a false negative 35 percent of the time.

Further complicating diagnosis are the wide range of symptoms associated with the disease. Many cases end up like Springer, where doctors suggest other illnesses instead of Lyme.

In addition, many patients don't recall a tick bite or the rash that comes with the disease, which makes it even less likely that Lyme will be suggested.

When Lyme is treated quickly, the symptoms are generally eliminated quickly with oral antibiotics. But when it takes months or years before the disease is diagnosed and treated, it can eat away at a patient's health and cost thousands of dollars.

CALDA President Phyllis Mervine set out to find how common it was for doctors to overlook Lyme. She said she surveyed 50 people in Ukiah who showed similar symptoms to the disease. Out of the 50 patients, only two said doctors suggested testing for Lyme.

Mervine said she hopes to change this statistic, and may get some help from new state legislation. This is the first year in California that Lyme is a lab reportable disease. Last year, 24 cases of Lyme were reported, but there have already been 87 cases reported this year through May.

Educating people - in both the medical community and the general public - is the key to advancing Lyme research and awareness, Morrow said.

"If we truly only have three cases (in San Mateo), it's very different in the physician's mind versus 100," Morrow said. "It's a big difference in public perception and in the medical community."

How can I protect myself from Lyme disease?

Whenever possible, avoid entering areas that are likely to be infested with ticks, particularly in spring and summer when ticks feed.

If in an area with ticks, wear light-colored clothing so ticks can be spotted more easily and removed before becoming attached.

If in an area with ticks, wear long-sleeved shirts and tuck pants into socks.

Application of insect repellents containing DEET to clothes and exposed skin, and permethrin (which kills ticks on contact) to clothes, can help reduce the risk of tick attachment. DEET can be used safely on children and adults but should be applied according to Environmental Protection Agency guidelines to reduce the possibility of toxicity.

Check for ticks daily and remove them promptly. Embedded ticks should be removed by using fine-tipped tweezers. Cleanse the area with an antiseptic.

You can reduce the number of ticks around your home by removing leaf litter and brush and woodpiles around your house and at the edge of your yard. By clearing trees and brush in your yard, you can reduce the likelihood that deer, rodents, and ticks will live there.

Source: CDC

 

 

Health Official: Coming Months Are High Season For Ticks
Bay City News Wire - CBS5

San Francisco, Oakland, San Jose, California
October 25, 2006

October begins the season in California most likely to bring out  bloodthirsty ticks, a public health official warns, including those capable of transmitting Lyme disease.

"Although most people associate ticks with summertime outdoor activities, adult western black-legged ticks are more likely to be encountered in late fall and winter,'' Mark Horton, California's top public health officer, said this week. "With California's temperate climate, adult ticks are abundant throughout the cooler months between late October and March.''

Ticks are slow, flightless arachnids that often cling to tall grass or to low bushes in naturally vegetated areas.

While many species of ticks can be found, the carrier species for Lyme disease is the western black-legged tick, which is mostly reddish brown in color and about the size of the tip of a match stick. It can be found in most California counties but primarily in humid northwestern coastal areas and the western slopes of the northern Sierra Nevada, health officials said.

Typically an animal or human brushes past natural vegetation and a waiting tick comes aboard for a meal.

Ticks dig their mouthparts inside their host and stay there until fully engorged with blood, which can take days, health officials said. By then Lyme disease, Rocky Mountain spotted fever, anaplasmosis, ehrlichiosis and babesiosis can be transmitted.

The best ways to avoid ticks are avoiding the edges of trails, grassy areas and brush. It is easier to notice a tick on light-colored clothing and health officials advise periodically inspecting yourself and others, especially in the scalp and hairline areas.

Long pants and shirts make it harder for ticks to get beneath clothing, particularly if tucked in, and applied repellents containing DEET are considered helpful.

A tick bite can appear like a mosquito bite but more often has a "bull's eye'' of inflamed tissue or redness surrounding the bite in the first 24 hours after the bite. Symptoms of Lyme's disease include a spreading rash accompanied by flu-like symptoms such as fever and body aches.

If you find a tick attached to yourself or someone, use tweezers to grasp the tick close to the skin, and steadily pull up. Wash your hands and apply some antiseptic to the spot of the bite. Consult a doctor if symptoms develop.

 

 

Tick-borne Relapsing Fever: A Tahoe Tale
Dr. Jason Eberhart-Phillips, MD
El Dorado Hills Telegraph

Folsom, CA
August 23, 2006
Opinion/Editorials

Steve Fernald knew something was amiss when he conked out on the living room sofa one Friday evening in June.

The 53-year-old culinary arts instructor at Lake Tahoe Community College was taking a moment to rest his feet at home during his daughter's graduation party. He had done all the cooking for the party and had spent much of the evening climbing up and down stairs to serve his guests.

When he awoke later on the sofa he felt unusually weak and quite chilly. Not one to spoil a party, he said good night and headed off to bed.

A survivor of two heart attacks, Steve doesn't usually get too bothered when he isn't feeling right. "I'm a bulldozer kind of guy," he says, when it comes to minor illnesses.

But by the next morning his illness was anything but minor. His temperature was 102 degrees and rising. "I felt punk," he said. When his fever reached 104.5 degrees, his wife Madeline brought him to the local emergency room."It was like being in another realm. It was out of my control. I was just praying for survival. There was not a lot I could do," he said.

What Steve had was tick-borne relapsing fever (TBRF), a bacterial infection caused by the seemingly innocuous bite of a soft-bodied tick.

Lucky for him, Steve's emergency room doctor recognized his illness and confirmed it with a simple blood test. The doctor himself had suffered from TBRF the previous summer. He gave Steve an antibiotic and kept him in the hospital until the worst symptoms resolved.

"It was very scary, believe me," Madeline said. "We had no idea these little critters even existed."

She was referring to the reclusive soft-bodied ticks that transmit this disease. Unlike the more familiar hard-bodied ticks - like the ones dogs get or those that pass on Lyme disease - these ticks feed at night, when their victims are sleeping. Their bite is painless and they drop off after 15 to 20 minutes.

Most people never know they were bitten.

That was the case for Steve. A week before he became ill, he and his wife were sleeping in a Tahoe-area summer home where they serve as caretakers. Some time while they slept a tick had a late-night snack on Steve's blood, which gave him the infection.

Soft-bodied ticks usually feed on mice, rats, chipmunks and other small animals. These creatures are the natural hosts for the bacteria that cause TBRF. Humans only get infected by accident, when a hungry tick can't find one of its usual furry victims.

Fortunately, TBRF is rare, with only a few dozen cases reported each year in the 14 western states where it occurs.

But the Tahoe basin is becoming a hotbed for this disease, with five cases reported there last year, in addition to Steve's case last month. Incidence peaks during the summer.

Most cases occur when summer visitors come to the mountains and sleep in cabins or vacation homes where rodents had made their nests during the colder months. An inspection of the old, rambling home where the Fernalds were staying found ample evidence of rodent infestation. In fact, a dead mouse was lying in a trap right under the bed where Steve slept.

Preventing TBRF is a matter of eliminating the breeding and nesting places of rodents in and around cabins and vacation homes in wooded, mountainous areas like Lake Tahoe. This means removing rubbish, including excess firewood and building materials, from areas near the home.

It also means rodent-proofing buildings, to prevent easy access to the inside of the house. All holes in a building's exterior should be sealed, including openings around pipes and conduits.

Any existing rodent nests should be removed from walls, ceilings and floors, and fumigants should be used to eradicate ticks.

Bottom line: If you aren't sure that your vacation retreat hasn't got a rodent problem, don't sleep there.

It's been a month since Steve became ill, and now his health is back to normal. During that time he has been doing a lot of reading about ticks and tick-borne diseases, including TBRF. He is glad his story will be told, if it helps others avoid becoming sick.

"This was a big surprise. I really wasn't aware of this disease before," he said.

Dr. Ebert-Phillips is the El Dorado County Health Officer
http://www.edhtelegraph.com/articles/2006/08/23/opinion/editorials/01

Courtesy: www.lymeinfo.net
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                                  © 2006 The National Lyme Disease Memorial Park Project