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Re: Crichton

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Hi Lovette,

that is an excellent tactic, addressing people affliated with ALDF and giving

them some food for thought. I am sure they will be very interested in hearing

what people with lyme disease have to say about these quacks.

We should be doing that more often. If ALDF starts losing credibility and

funds, they won't be able to wage their falsehoods about lyme disease and

short term antibiotic treatment.

Way to go, Lovette! i hope you are feeling a little better

relizabeth

<<

This is my official response at Crichton's website to his

affiliation with the June 1st " gala " ALDF Event:

I read that you will be attending a Lyme disease " gala " which the ALDF

is sponsoring on June 1st. Why are you attending this event? Are you

aware that ALL patient advocacy and support groups view this group as

inbred, greedy, and completely opposed to helping Lyme disease victims?

The common perception in the Lyme community is that their board members

work for insurance companies who seek to deny Lyme victims much-needed

antibiotics, and that they are harassing our Lyme literate doctors by

filing complaints against them with licensing boards for overuse of

antibiotics.

Please reconsider your association with this group. There is nothing

to be " festive " about at a gala dance when Lyme disease victims are in

wheelchairs, and have neurotoxins clouding their brains and destroying

their lives. I was an attorney for 17 years, as well as a 4th year

Seminary student when Lyme disease incapacitated me, and my entire

family, in August of 1998. My husband and daughter are now asymptomatic

after 9 months of long-term antibiotics, but my 14 year old son, who

used to be in the gifted program in school is now failing and needs to

be on long-term antibiotics but his doctor's license was revoked for

treating Lyme patients with long-term antibiotics. My son's life and my

life are ruined, and yet the ALDF believes there is something to

celebrate! I simply cannot fathom this - would there be a gala event,

and dance with festivities for polio victims, or AIDS victims? I hardly

think so.

I trust that you will make the right decision and end your

affiliation with this event. I have read all of your books, but

unfortunately, I can no longer read because of this illness, and I must

wear sunglasses indoors due to light sensitivity. I cannot integrate

letters into a Scrabble Board - this is an absolutely devastating

disease, and certainly not one to be celebrated! I am happy to discuss

this further with you if you are interested.

Lovette Mott, Esquire

2389 Chambersburg Road

Biglerville, PA 17307

(717) 334-6339

smott@...

>>

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In a message dated 4/25/00 3:09:16 AM Central Daylight Time, smott@...

writes:

<< I simply cannot fathom this - would there be a gala event,

and dance with festivities for polio victims, or AIDS victims? I hardly

think so. >>

I agree with the general tone of your letter...but there are fundraisers all

the time for diseases. You have to have an event the rich want to attend in

a tuxedo and cocktail dress to mingle with other celebrities in order to get

their money. Spend money to make money.

I am completely behind the work of the LDF and believe their message is far

more accurate than that of the ALDF. But, I am somewhat surprised the LDF

has never had a gala...or I just haven't heard of it. Their approach is more

low-key whereas the ALDF has gone the big PR route.

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Hey! Let's do something on the west coast. I can wish can't I? Seriously,

with the power and exposure of California, the entire country would be

sandwiched in. We even have a Lyme law on the books (though it could be

better). With the glitz of southern California, what hasn't there been a

gala affair? I didn't know that there were to philosophical approaches. Can

anyone confirm whether there has or has not been such an event?

California dreamin'

Annie

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