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Chelsea M.
Frazier
Tuolumne County, California
Total cost:
$1,365
Number of family members with LD: 4
Lost work/school:
Number of years sick: 9 months
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My third and
youngest child to contract Lyme disease was my daughter, Chelsea.
She was seven years old at the time of the tick bite. It occurred
in March of 1996 while we were hiking a couple miles from our
home located in Sonora, CA. It was in her posterior neck and
wasn't discovered until it was engorged the following day. Her
local physician treated her with liquid erythromycin for ten
days. On May 26, 1996 she acquired yet another tick bite while
visiting her Grandfather's ranch in Hollister, CA. I sent this
tick in for Borrelia burgdorferi culturing but was told
it was negative. It had been over 2.5 months since the first
bite and it was at this time that she began experiencing symptoms.
They occurred despite the short course of antibiotics she had.
She developed chest pains, stomach aches, and felt poorly. Her
physician felt she probably had an allergy to milk and had me
remove it from her diet and observe her. I did this for several
weeks and continued to watch her suffer from the stomach aches
and chest pains. She was also beginning to lose her reading and
math skills and becoming forgetful. She returned to her doctor
in late August and I requested she have an ELISA, and Western
blot both IGG and IGM. Her physician knew our family history
which included three other members with it. He still felt it
was highly unlikely that she had it too. The first tests were
performed a little over five months after the initial exposure
and proved to be equivocal. Her serology was 1.15 and her Western
blots both showed suspicious reactivity to 39. 41. and 93 kDa
proteins. Her physician elected to wait four to six weeks and
then retest her. These second two Western blots both IGG and
IGM now met all the criteria required by Centers of Disease Control.
She has two of the three required bands on her IGM and five of
ten required on her IGG. There is a small window of opportunity
to catch such a striking lab profile as this. Now nearly seven
months into the disease she could finally begin treatment. She
took a six month course of Biaxin during which time I spent months
fighting my insurance for coverage. They said, "Our review
of current literature, Rahn et al., (Annal of Internal Medicine 1991:114:472), and Tierney et al.:
Current Medical
Diagnosis and Treatment 1997
edition does
not support the efficacy of using antibiotics beyond 30 days
for the treatment of Lyme disease". In order for them to
approve the continuation of antibiotics I had to do extensive
research and send them copies of peer-reviewed studies which
documented improved outcome with chronic (i.e. >30 days) Biaxin.
I did this which I shouldn't have had to! I knew that it had
already been proven, why should I have to show them this proof?
It's their responsibility to know the facts, not just pretend
to with a lot of academic lingo.
The outcome
of Chelsea's story is a good one, but only because I knew the
disease parameters and how they can manifest. I knew from the
first presenting symptom of chest pains (70% of children with
Lyme disease have chest pains) that she very likely had contracted
Lyme disease. But months went by and a lot of expense had to
be incurred prior to treating her. She has been off the antibiotics
now for seven months and has remained symptom free. |