Hartford (WTNH) - Connecticut has long been known as ground zero for Lyme Disease.
Now, state lawmakers are taking the controversy surrounding Lyme
Disease treatment head on.
Over the years there has been a lot of debate over how patients
are diagnosed and treated for Lyme Disease. A bill to protect
doctors and help patients could ease that frustration driving many
out of state for treatment.
Many are ticked off, banding together, to educate and raise
awareness about the tick-borne disease.
When it comes to treatment, some patients go out of state.
Andrew Hancock and his mother drove from Brookfield, CT to New
York for their first visit with Dr. Daniel Cameron who specializes
in Lyme Disease.
"It's a bit of a hassle," said Andrew. "I wish it was different
in Connecticut but it's not, so we're here."
"We haven't really seen anybody who specializes in Lyme, which
is pretty ironic considering we live in Connecticut," said Laura
Hancock, Andrew's mother.
Waiting patiently is Erin Morrissey and her mother from
Glastonbury.
"She wasn't being diagnosed in Connecticut," said Erin's mother
Betty. "I was very worried about her. She has been very sick."
"I'm doing better, it's a slow process," Erin said. "Week by
week, I see improvement so it makes me happy but it's been
frustrating."
Connecticut families like the Morrisseys and Hancocks make up
about 10 percent of Dr. Cameron's practice. That's because in the
state of New York, he is able to diagnose and treat without fear of
retribution.
"As a doctor, I can't rely on just the test. I can't rely just
on the rash. I need to look at the whole symptom pattern," Dr.
Cameron said. "I need to be able to take my patients, diagnose them
and treat them based on what I learned in medical school."
The medical community is at odds as to whether chronic Lyme
Disease exists and over long term treatment, which includes
intravenous antibiotics.
In Connecticut, supporters say doctors who choose the latter,
are haunted by past threats of losing their license.
"That perception has really turned into a tangible reality,"
said Rep. Kim Fawcett. "[A perception] that a lot of doctors out
there maybe just think, Lyme Disease, I don't want to get involved
in it. So what they do is deflect to their patients, 'I can't
really treat you here, you have to find a specialist.'"
That's why State Representatives Kim Fawcett and Jason Bartlett
are leading the change behind a bill to protect Connecticut
physicians.
"Our legislation doesn't say what they do. It just gives them
the freedom to diagnose clinically and treat how they see fit,"
said Rep. Fawcett.
But the Department of Public Health disagrees and sent testimony
against house bill 6200.
"We oppose any bill that would prescribe or limit any particular
kinds of treatment," said Dr. Robert Galvin, CT Public Health
Commissioner.
However, activists say the department is behind much of the
scrutiny doctors are feeling.
"The department does not hunt down physicians and try to
impose regulations on them. We do respond to complaints which may
reach us from hospitals, from families and from other physicians
and when that happens we investigate the complaints," said Dr.
Galvin.
To encourage doctors, the Connecticut State Medical Society
is in support of the bill.
"There is a perception in the community that there are
physicians who are reluctant to treat patients particularly in Lyme
Disease because of some fear that there might be retribution
because of that treatment," said Dr. William Handleman, President
of CT State Medical Society.
The bill would help families like the Hancocks stay closer to
home, getting relief from a debilitating disease.
The joint committee on public health voted unanimously in
support of the bill. Now supporters will push for a vote before the
House and Senate during this session. A similar bill was passed in
Rhode Island.
Visit
Lyme Rights or
Lyme Disease Association for more
information.