LymeNet Home LymeNet Home Page LymeNet Flash Discussion LymeNet Support Group Database LymeNet Literature Library LymeNet Legal Resources LymeNet Medical & Scientific Abstract Database LymeNet Newsletter Home Page LymeNet Recommended Books LymeNet Tick Pictures Search The LymeNet Site LymeNet Links LymeNet Frequently Asked Questions About The Lyme Disease Network LymeNet Menu

LymeNet on Facebook

LymeNet on Twitter




The Lyme Disease Network receives a commission from Amazon.com for each purchase originating from this site.

When purchasing from Amazon.com, please
click here first.

Thank you.

LymeNet Flash Discussion
Dedicated to the Bachmann Family

LymeNet needs your help:
LymeNet 2020 fund drive


The Lyme Disease Network is a non-profit organization funded by individual donations.

LymeNet Flash Post New Topic  New Poll  Post A Reply
my profile | directory login | register | search | faq | forum home

  next oldest topic   next newest topic
» LymeNet Flash » Questions and Discussion » Activism » Alec Baldwin Gets Lyme Disease &our people talk about it

 - UBBFriend: Email this page to someone!    
Author Topic: Alec Baldwin Gets Lyme Disease &our people talk about it
treepatrol
Honored Contributor (10K+ posts)
Member # 4117

Icon 4 posted      Profile for treepatrol     Send New Private Message       Edit/Delete Post   Reply With Quote 
Link

http://www.cinemablend.com/new/Alec-Baldwin-Gets-Lyme-Disease-8052.html

Alec Baldwin Gets Lyme Disease

By Ed Perkis: 2008-03-04 18:56:41

If you're like me, you probably think there haven't been enough independent
comedies about Lyme disease. I can only think of 10 or 15 off the top of my
head. Alec Baldwin agrees with us and is going to produce and star in the
movie, Lymelife, about what happens when deer ticks go bad.

Actually, according to Variety, Lymelife is about more than Lyme disease. It
is described as a "dramedy" set in Long Island suburbia in the 1970's. The
Lyme disease combines with relationship and real estate problems to come
between two families. Baldwin will be joined in the cast by Emma Roberts
(recently of Nancy Drew), Cynthia Nixon, Rory Culkin, Kieran Culkin, Jill
Hennessy and Timothy Hutton. I liked this movie better when it was called
The Ice Storm. Hopefully we will not be subjected to another key party.

The co-writers and directors of Lymelife are Derick and Steven Martini. I
have never heard of them, but they wrote and starred in an indie film called
Smiling Fish and Goat on Fire about eight or nine years ago. They also have
a few other scripts in development. This will be their first directing
experience. Hopefully they are ready, since filming will begin in New Jersey
next week.

RELATED: alec baldwin, lyme disease

Reader Comments:

1.. Betty , IOWA LYME ACTIVIST Says:
March 5th, 2008 at 17:41
To Martin Scorsese and Alec Baldwin,

I hope you will use FACTUAL info about CHRONIC LYME disease patients in
this lyme story of Alex getting lyme disease.

I do hope this movie will show this as CHRONIC lyme, and not a tick bite
embedded or a bulls-eye rash where the patient is lucky enough to get to a
LYME LITERATE MD PROMPTLY and cured!

I've had chroinc lyme disease for 38 years; 34 years MISDIAGNOSED by 40-50
drs. I have many other complications since I believed every drs. OTHER
diagnosis they gave me for 34 years.

In my case, it was a tick off my folk's LIVE CHRISTMAS tree that bite me
1969! I was able to track this back using my journal diaries! It was
sub-zero Iowa weather so I wasn't outside gardening; I had no pets and
neither did my roommates. All normal ways of getting bitten were NOT
present.

I hope most of all that Martin's movie will get into the LYME
CONTROVERSAY!!

Our good LLMD, lyme literate MDs from ILADS, International Lyme Associated
Disease Society vs. the bad drs., IDSA, Infection Disease Society of
America, who do NOT believe in CHRONIC LYME.

The IDSA drs. treat for UNDER 30 DAYS! They proclaim the patient, CURED OF
LYME! NO WAY JOSE! HOG WASH !! The IDSA drs. are responsible for us being in
such bad shape as we are, and of the MANY LYME DEATHS due to other
complications of chronic lyme.

Martin, I do hope you will get Wisc. author, PJ L, recent 2-08
lyme series books, "IT'S ALL IN YOUR HEAD". Book 2 has 80 lyme patients
internationally in it; I'm in this one.

Book 1 has the basics of lyme disease, and 8 other lyme patient stories
including of 2 patient's lyme deaths, and part of PJ's continuing lyme story
with the 12 year COURT system in trying to get her 2 children back from her
ex-husband.

Book 3 will cover other things including controversial lyme subjects!

Martin, I have respected your work for decades, and I hope you will get
our CHRONIC LYME DISEASE story across where our family, friends, co-workers
turn their backs on us since we do NOT have a VISIBLE illness; it's all
INVISIBLE!

Martin, I enjoyed them recently honoring you for your work!! Kudos Martin
to a very deserving man.

I also hope you touch on this: the high costs of finding a LLMD/lyme
literate MD to treat us who will NOT TAKE INSURANCE; the health insurance
companies refusing to pay ANY LYME RELATED EXENSES; the loss of jobs, a
spouse, your children, your home, bankruptcy, and being homeless!

How our veterans do NOT receive help from our US govt. on paying any of
their lyme expenses when they were BITTEN WHILE IN SERVICE!

Looking forward to a 1st class chronic lyme movie! Thank you all!

1.. Diane J. Says:
March 5th, 2008 at 23:08
Over the years, Martin Scorsese has "gone places" with his honesty in
movies.

So very many citizens in the US suffer from chronic Lyme disease, a very
painful and disabling disease that wrecks lives, divides families and very
often causes financial disaster. The overwhelming majority of doctors ignore
us--by belittling us.

Chronic Lyme disease is defined as a brain infection of the Lyme pathogen:
neuroborreliosis, a neurological disease.

About half who get Lyme disease are children. Often they can't go to
school and can't participate in life with their friends. It can hurt to
think. 90% of kids with Lyme have bad head pain. But will these kids (and
adults) get the antibiotic treatment they need to help them?

The infectious disease doctors in the US (IDSA) lie by saying chronic Lyme
disease does not exist. They do the bidding of many for-profit health
insurance companies that don't pay for treatment.

It is profits over patients.

Who else profits? The painkiller, statin and antidepressant
superindustries. Follow the money.

The overwhelming majority of people with wrecked lives caused by Lyme
don't know that Lyme is the name for their illness. It's the magic keyword
on the Internet to connect with others.

We'v been ignored for decades.

Except by ILADS (International Lyme and Associated Diseases Society)
physicians--our hero doctors!

However, some of our hero doctors have had to fight legal battles for all
of the above reasons.

And I wonder, where has America gone?

I refer readers of my comments to PJ Ls 2 new books of a 3 book
series, "It's All In Your Head." These contain Lyme patient stories. My
story is in there.

As are stories from around the world. Ticks with Lyme can't read road
signs!

I look forward and am grateful for Mr. Scorsese and Alec Balwin's efforts
in the upcoming movie, Lymelife.

Diane J.

1.. Jennifer Says:
March 12th, 2008 at 15:37
You have GOT to be kidding. A movie about the disease that has brought
nothing but heartache and suffering to my family including my 3 year old who
was born with it. I'm so not happy about this

[ 24. March 2008, 06:58 AM: Message edited by: treepatrol ]

--------------------
Do unto others as you would have them do unto you.
Remember Iam not a Doctor Just someone struggling like you with Tick Borne Diseases.

Newbie Links

Posts: 10564 | From PA Where the Creeks are Red | Registered: Jun 2003  |  IP: Logged | Report this post to a Moderator
bettyg
Unregistered


Icon 10 posted            Edit/Delete Post   Reply With Quote 
hi tree,
I thought this heading looked familiar ... wonder why since I replied to it! neuro lyme mind [lol] [Big Grin]

1 more reply over there now...

George Howell Says:
March 21st, 2008 at 14:33

This idea is controversial, but then "Lyme" is controversial.

"Lyme" beyond the acute stage is really a "Th1 inflammation".

The bacterium that causes "Lyme" is one of fifty-three known bacterium that causes the "The inflammation", and is the reason that sooo many people cannot get tested Positive for "Lyme", but yet seem to have the illness.

For more information, go to www.autoimmunityresearch.org or www.bacteriality.com,

and read the articles that are linked in the right hand column.

The truth is that the IDSA docs do not know what chronic "Lyme" is, and the ILADS docs only know the answer partially.

IP: Logged | Report this post to a Moderator
adamm
Unregistered


Icon 1 posted            Edit/Delete Post   Reply With Quote 
I'm convinced that the IDSA docs know much better than the

ILADS docs what chronic Lyme is, but are simply lying through their

teeth--Check out Borrelia's history as a weapon and google

operation paperclip. [Eek!] [dizzy]

IP: Logged | Report this post to a Moderator
lymie tony z
Frequent Contributor (1K+ posts)
Member # 5130

Icon 1 posted      Profile for lymie tony z     Send New Private Message       Edit/Delete Post   Reply With Quote 
Well now isn't that special Adam....

seeee....alll folks can agree on SOMETHING!

Although I am not partial to the bio-weapon theory... I am convinced the IDSA is lieing about chronic lyme disease...

for purely financial reasons....follow the money!

zman

--------------------
I am not a doctor...opinions expressed are from personal experiences only and should never be viewed as coming from a healthcare provider. zman

Posts: 2527 | From safety harbor florida(origin Cleve., Ohio | Registered: Jan 2004  |  IP: Logged | Report this post to a Moderator
   

Quick Reply
Message:

HTML is not enabled.
UBB Code� is enabled.

Instant Graemlins
   


Post New Topic  New Poll  Post A Reply Close Topic   Feature Topic   Move Topic   Delete Topic next oldest topic   next newest topic
 - Printer-friendly view of this topic
Hop To:


Contact Us | LymeNet home page | Privacy Statement

Powered by UBB.classic™ 6.7.3


The Lyme Disease Network is a non-profit organization funded by individual donations. If you would like to support the Network and the LymeNet system of Web services, please send your donations to:

The Lyme Disease Network of New Jersey
907 Pebble Creek Court, Pennington, NJ 08534 USA


| Flash Discussion | Support Groups | On-Line Library
Legal Resources | Medical Abstracts | Newsletter | Books
Pictures | Site Search | Links | Help/Questions
About LymeNet | Contact Us

© 1993-2020 The Lyme Disease Network of New Jersey, Inc.
All Rights Reserved.
Use of the LymeNet Site is subject to Terms and Conditions.