Newsgroup Leader Katheen
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Joined: 20 Jan 2006
Posts: 654
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 Posted: Sat Jul 08, 2006 9:02 am Post subject:
Connecticut's Numerous Stupid Whores and Children with Lyme Disease
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From: Kathleen Dickson <kmdickson0308@yahoo.com>
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To: Kathleen Dickson <kmdickson0308@yahoo.com>,
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Subject: LDA collecting Lyme in Children Abuse data
Date: Saturday, July 08, 2006 05:01:18 [View Source]
When my kids were kidnapped by DCF they were taken to
an 80 soomething year old "doctor" who wrote Diane's
notes in Lara's chart (my kids are not stupid- they
watched her), and the moron MD hired by DCF told my
kids they do not have Lyme disease.
http://www.actionlyme.org/Schoen.htm
Lara had 7 CDC bands at age 25 months and is
congenitally infected.
DCF hores moron MDs to see the kidnapped kids. This
we also know from Dennis Long at Gales Ferry
Pediatrics not reporting the multiple genital injuries
to not only the Inkel children, but yet another baby.
http://www.actionlyme.org/INKEL_MOTION_APPREARANCE_21_JUNE_06.htm
DCF hires morom MDs who find what DCF tells them to
find. The best example is Laura Lustig, but the same
is true for the perjurers Vladimir Coric (whose father
was penalized for fraud and has the same name),
Christopher Gottshalk, James Phillips, DMHAS'
Elizabeth Byron, and Kenneth Marcus- ALL PERJURERS-
Whores for the State.
I already proved they perjured themselves in my
federal lawsuit. These are the worst kind of sluts
because Lyme is an international problem and this is
Corrupticut.
Diane also tests positive for Ehrlichiosis.
Kathleen
From: b
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To: SpinLyme@yahoogroups.com
Subject: [SpinLyme] LDA needs lyme patient statements
ASAP
Date: Friday, July 07, 2006 11:41:56 [View Source]
| Quote: | From Pat Smith, President
Lyme Disease Association |
=======
The LDA needs statements by July 8, 2006 from Lyme
patients for a
very important meeting. Patients (or parents) can
write if they meet
any of the following criteria:
They (or children) must have been denied a diagnosis
and/or
treatment/reimburse ment at some point in their
disease due to the
fact they do not meet CDC surveillance criteria (CDC
criteria = EM
rash OR positive ELISA followed by positive Western
Blot plus major
system involvement) and/or They (or children) have
been denied
treatment based on IDSA (Infectious Diseases Society
of America)
Guidelines which only address short term treatment
and/or They (or
children) have seen a large number of doctors to get a
correct
diagnosis and treatment (state approx. number over
what time period)
and/or They must travel two or more hours (one way) to
get Lyme
treatment (include how many hours, travel to another
state, fly
there, stay overnight)
Please include
1. Information about how the above situation(s)
applies to you (or
children).
2. Misdiagnosed as _________disease.
3. Permission to LDA to use and share the material for
its purposes
(You must include this).
4. Letter writer's name, address, state, email (no
need to name
anyone else)
5. The entire statement in ONE page.
6. By July 8, preferably email back to Lymeliter@aol.
com in a clean
email, DO NOT HIT REPLY BUTTON, send clean new email
only.
7. Or fax to the LDA at 732 938 7215.
DO NOT include doctor names. Do not write your entire
story. This
will not help us.
Sample of type of content
I have probably had Lyme disease for 10 years. I
traveled to 10
doctors for the first five years to try and get a
proper diagnosis.
I was told I did not have Lyme disease because I had a
negative
test, although I did have many symptoms. I did not
have the bull's
eye rash either. They did not know what I had but they
said it was
not Lyme. I finally found a doctor who is 300 miles
away in a
different state. That is ten hours I need to be driven
by someone
else to get treatment for Lyme, since I cannot drive
that long.
He diagnosed me clinically and I have been on
treatment and my
symptoms improved greatly. He also diagnosed me with
several co-
infections. No one even mentioned them before.
Unfortunately, my
insurance company often refuses to pay for my
treatments because I
don't meet the criteria for Lyme disease.
If I cannot continue treatment, I may lose my job and
have to go on
disability. I do not want that to happen. Now my child
has been
bitten. She needs to see a doctor but there are even
less doctors
for children. Someone needs to help Lyme patients.
John Doe
000 Second Street
Anywhere, State
johndoe@email. com
(or fax number if you fax the letter)
Thanks everyone.
Now! Register for the LDA conference on October 20,
2006 in
Philadelphia. Go to www.LymeDiseaseAsso Philadelphia.
Go to www
Pat Smith, President
Lyme Disease Association, Inc.
PO Box 1438
Jackson, NJ 08527
888-366-6611 information line
732 938-7215 fax
www.LymeDiseaseAsso www.LymeDi
[Non-text portions of this message have been removed]
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