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 Re: Under Our Skin comes to PBS
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     The Bakers Dozen & the Lunatic Fringe
The Bakers Dozen & the Lunatic Fringe: Has Junk Science Shifted the Lyme Disease Paradigm? by PJ Langhoff  Includes key evidence from the historic CT Attorney General investigation into the IDSA clinical practice guidelines for Lyme disease.


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     * From: cherryrudkin
     On: 05-08-2012
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Re: "the Jemsek Diaries"
     * From: dixie
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Re: ""
     * From: dixie
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Re: ""
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Re: "Reflection on my past 9 years."
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Re: "Reflection on my past 9 years."
     * From: dixie
     On: 03-20-2012
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     On: 03-20-2012
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 By: chris9282
On: 03-20-2012
   "Telling your friends"
 By: chris9282
On: 03-15-2012
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 By: chris9282
On: 03-13-2012
   "Reflection on my past 9 years."
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On: 02-24-2012
   "lyme still sucks"
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On: 02-01-2012
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   "DAMN MY LIFE"
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On: 08-20-2011
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     DIAGNOSIS AND TREATMENT GUIDLINES
ADVANCED TOPICS IN LYME DISEASE
Guidelines by JOSEPH J. BURRASCANO JR., M.D.
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ILADS Evidence-based Lyme Treatment Guidelines
International Lyme and Associated Diseases Society
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     Obituaries
·Remembering Leslie Wermers. One year ago today.2009-11-02 20:10:50
·Lyme disease patients mourn passing of well known doctor2009-07-01 04:00:00
·All she lost: My sister's battle with Lyme disease2009-05-19 04:00:00
·Laura Treanor, 19, Lyme disease not ruled as cause of death2009-05-07 04:00:00
·Lila Star Smith Harms, 25, dies from complications of Lyme disease2009-05-05 04:00:00
·Lyme Disease Patients Loses a Hero and Friend2008-11-16 19:57:38
·Nancy L. (Scully) Strayer: March 20, 1946 - March 12, 20082008-04-12 04:00:00
·Bite from tick on holiday led to death leap2008-04-11 06:49:39
·Rugby great, Mike Gregory, loses his battle with Lyme disease2007-11-24 23:51:00
·Missouri teen, 15, dies from Ehrlichiosis2007-09-04 04:00:00
·Steven F. Wells, 45, dies after battle with Lyme disease and ALS2007-08-14 07:03:39
·Bruno C. Malvezzi2007-07-31 21:06:47
·In loving memory of Dr. Edward McNeil2007-07-24 19:45:00
·Lyme disease is a growing problem, Britteny Gallgher, Kansas City, MO2007-05-24 04:10:00
·Lyme Disease Skyrockets In Maryland2007-05-23 04:00:00
·C. Peter Thomas, 46; Sound Engineer2007-05-21 04:00:00
·Jimmy Duarte, gifted musician, charismatic islander, dies at 702007-05-17 15:12:03
·Obituary: Lyme Disease Advocate Karen Johnson ''Rose'' Rose, 1947 - 20072007-04-30 22:50:17
·BETH'S QUEST: Family crusades against Lyme disease2007-04-29 04:00:00
·Tick kit distribution aimed at heading off Lyme disease2007-04-28 12:40:00
·Letter to the Editor: In Memory of Lyme Advocate ''Rose''2007-04-26 11:00:03
·Lyme Advocate ''Rose'' Succumbs to Lyme Disease2007-04-19 18:25:19
·Body of Missing Woman with Lyme Disease Found2007-04-14 21:46:32
·Michael Coers won Pulitzer Prize2007-03-21 10:00:43
·E STREETER IN LYME 'SUICIDE'2007-03-19 12:33:30
·Lost to Lyme Lyme disease facts2007-03-19 04:00:00
·Musician remembered as battler against Lyme disease2007-03-19 04:05:00
·Maine Musician Bill Chinnock Dies2007-03-08 13:45:18
·Obituary - Eric von Schmidt - Singer and painter was in Dylan's circle2007-02-27 11:00:00
·JAMES P. KOCH2007-02-22 00:53:49
·Andrew Spielman, 76, Expert on Insect-Borne Diseases, Dies2006-12-26 04:00:00
·Martin Frank Dumke2006-11-29 04:00:00
·Bill Reynolds: For QB Coen, tragedy lies beneath the surface2006-10-29 04:05:00
·Coen plays on without No. 1 fan2006-10-17 04:00:00
·Librarian was dedicated to students, family2006-09-19 17:02:58
·TORMENT OF BRAIN BUG PROF - Alasdair Crockett2006-09-19 13:43:35
·Widow of Lyme disease victim appeals for help2006-09-18 22:44:57
·Professor commits suicide after catching dementia from tick bite2006-09-17 22:17:12
·Tick talk: Family blames member's death on tickborne illness2006-08-21 04:00:00
·Death of York PA area doctor due to Lyme and ALS2006-04-29 20:40:02
·Emmy-winner Scott Brazil dies of ALS and Lyme disease at 502006-04-22 11:37:59
·Kym Cooper- Dead Woman's Own Letter Tells Her Lyme Disease Story2006-02-05 14:08:53
·Kym Cooper - Worn down by Lyme2006-01-22 01:56:26
·Kym Cooper, 1968-2006, After long battle with Lyme disease2006-01-19 13:51:02
·Tribe leader Francis mourned2006-01-14 18:22:58
·Easton mourns former selectman after fatal accident2005-12-17 13:04:17
·Educator, union leader dies from complications of Lyme disease2005-12-08 09:25:32
·'A TERRIBLE WAY TO GO'2005-10-22 14:39:56
·Leo Bogart, R.I.P. (1921-2005)2005-10-21 15:55:28
·Leo Bogart, 84, Sociologist Who Studied Role of Media in Culture, Is Dead2005-10-21 15:46:44
·Passages: Pat Pepper2005-10-10 01:11:11
·Man loses battle with Lyme disease2005-10-09 10:37:43

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· Report on the IOM Meeting Regarding Lyme Disease[ 0 comments - 1469 reads ]
· Under Our Skin comes to PBS[ 2 comments - 8440 reads ]
· National Museum of Women in the Arts honors Susan Swartz[ 0 comments - 1394 reads ]
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Talk Back to ABC News about Reforming U.S. Healthcare

ABC's Good Morning America wants to know what problems-- or solutions-- you may have for the U.S. healthcare system.  Click Here
 
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Featured Blog of the Day


 By: chris9282 (Click Here to read all of chris9282's Blogs) On: 03-20-2012
Title "Telling your friends" (Click Here to read this Blog)
Click here to view all LymeBlog Blogs
Hello again everyone, its Chris. i will soon be going in for another lengthy appointment with my doctor to have another round of testing done. YIPPY!!! id like to touch how to tell your friends about your Lyme disease. lets admit it, Lyme is scary. especially to people who have no clue what it is. the best way to help your friends and in term help them help you is to answer questions. make it less scary for them. they want to help you. they really do. but you need to tell them how. they do not want you going through this alone. they are you friends after all. you need to help them help you. give them the tools websites they can learn about lyme from. give them the opportunity to help you. helping them at the same time  Psychologically helps you come to terms with it and help you become less scared of it. some will not understand as quickly what you are going through. in that case just let them ask you questions. let them pick at your brain get some answers to what they want to know. lets be honest it cant hurt. if your memory is effected by Lyme like mine is. it can drill it in there and help you remember it!!! less stress and a larger support group can reduce your mental recovery time. i wont put any numbers on that but it really does help. in previous journal entries i stated that Lyme is a mind game. and the best way to defeat it is to accept it and accept that you are not broken. but in turn you have hit an hurtle. the difficult part is jumping over the hurtle. the harder part is figuring out what direction to take after you jump it. it will sound strange to hear it after suffering from Lyme but the hard part isnt the sickness during the treatment. the hard part is figuring out what way to go while recovering. you have choices. move forward with your life get active and live life. or let it swallow you. yes i know its hard to move and be active after all that. but thats the mind game. you then have to take it and run with it. prove to yourself and the world that you will not let it stop you. if i have learned anything from Lyme its that i am so much stronger then i know. i am spiritually stronger, emotionally strong physically stronger. believe me you can do it. i KNOW you can do it. you have the tools. you have the strength emotionally and physically. get up move be happy! take my advice for what its worth. get up, take a walk, get out from under the rain clouds. its sunny out here.  todays preventative tip for avoiding Lyme is PERMETHRIN SPRAY! here is the website comparing DEET vs. Permethrin http://www.lymeneteurope.org/info/deet-versus-permethrin-as-a-tick-repellent again i say this for your benefit. preventative measures can help you avoid multiple exposures to Lyme disease. help yourself and others with knowledge. do routine tick checks! treat your pants with permethrin if you so choose to do. wear light colored clothing that ticks will be more visible on. above all EDUCATE YOURSELF! take the initiative. better yourself and those around you. 
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Last 20 Blogs


 By: chris9282 On: 03-20-2012    "Telling your friends"   1 reads
 By: chris9282 On: 03-15-2012    "Parents of children with Lyme"   1 reads
 By: chris9282 On: 03-13-2012    "Reflection on my past 9 years."   1 reads
 By: carold On: 02-24-2012    "lyme still sucks"   3 reads
 By: ksnew2005 On: 02-01-2012    "Looking for Lyme Doctor in Midwest"   1 reads
 By: ILoveLyme On: 01-22-2012    "DAMN MY LIFE"   2 reads
 By: Shadow On: 08-20-2011    "Cruise Blues"   4 reads
 By: shadow On: 08-14-2011    "Can someone please explain to me . . ."   481 reads
 By: Shadow On: 08-11-2011    "Expecto Patronum"   536 reads
 By: map On: 07-13-2011    "Have any of you had this happen?"   317 reads
 By: Shadow On: 07-02-2011    "Lemonade - Part 2"   582 reads
 By: Shadow On: 07-02-2011    "Lemonade - Part 1"   564 reads
 By: map On: 06-28-2011    "Babeasia"   586 reads
 By: map On: 06-28-2011    "Dr. Rhett Burgeron "   578 reads
 By: Shadow On: 06-22-2011    "The Depths of Darkness and Despair"   773 reads
 By: Tia On: 06-21-2011    "Hello there!"   697 reads
 By: lillylumberlady On: 06-17-2011    "New Info on Natural Healing"   709 reads
 By: Shadow On: 06-17-2011    "Process of Transformation"   691 reads
 By: lillylumberlady On: 06-15-2011    "I'm still here!"   671 reads
 By: Shadow On: 06-14-2011    "Posted some pictures of my new IV line on blog"   679 reads
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Featured Blog Comments of the Day


From: cherryrudkin On: 05-08-2012   To ticktoon Re: "the Jemsek Diaries"
When the world'shp pavilion dv6000 dvd drive leading search engine went public eight years ago, it was hoping to price its new offering as high as $135 a share. It had to settle for $85 in a nervous market, but it's never really looked back. The stock now fetches more than $650, and there are no indications that it plans on introducing its first stock split anytime soon. There are now dozens of popular companies hp pavilion dv6500 dvd drivetrading in the triple digits. One of them
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From: dixie On: 04-13-2012   To Re: ""
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From: dixie On: 04-13-2012   To Re: ""
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From: gogirl On: 03-23-2012   To chris9282 Re: "Reflection on my past 9 years."
Hi Chris,I have Lyme, and so does my 14 year old son. The remark that 'fear' drove you really got my attention. That was the case for me also. The treatments can be hard on people and I see why younger adults would not want to spend all the time and money working toward their health.....but I'm glad you have! Fear finally challenged me, too. We will continue getting better and then we can look forward to the day the doctor want us on a maintenance plan! Whoot! 
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From: dixie On: 03-21-2012   To Re: ""
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Lyme disease in the News

                                                   

 Report on the IOM Meeting Regarding Lyme Disease

Opinion / Editorial
“Medical progress should no longer be impeded by the polarizing controversy that has characterized Lyme disease research in the past. The dialogue must continue and encourage mutually respectful collaboration across scientific disciplines and among researchers, clinicians and patients, even when view points differ, if we are to make progress.”
(Gregg Skall, Womble Carlyle Sandridge & Rice, PLLC)


Report on the IOM Meeting Regarding Lyme Disease

LymeBlog News
Lexington, KY USA
From: National Capital Lyme & Tick-Borne Disease Association
www.natcaplyme.org
natcaplyme@natcaplyme.org
Phone & fax: 703-821-8833

Washington, DC – Thursday, April 21, 2011.  The Institute of Medicine (IOM) released their report on April 20, 2011, on “The Critical Needs and Gaps in Understanding Prevention, Amelioration and Resolution of Lyme and Other Tick-Borne Diseases.” The report confirmed what Lyme patients have known for years – that Lyme disease is a serious illness, and significant gaps remain in our understanding of the disease.

At the request of the National Institute of Allergy and Infectious Diseases (NIAID), the IOM was entrusted to plan and hold a two-day workshop to assess the state of the science of Lyme and other tick-borne diseases.  A committee was formed, which provided a forum for broad scientific and public input, and produced a summary report on the critical needs and gaps in research.

Although we share the concern with many in the Lyme community that treatment was not included in this workshop, we are pleased that other critical themes were addressed. The National Capital Lyme Disease Association (NatCapLyme) would like to thank the IOM for completing this arduous task with integrity within the guidelines they were charged to respect.

Pamela Weintraub’s powerful presentation at the IOM workshop last October made a notable impression on the IOM Committee.  In its preface, the IOM Committee wrote: “Pamela Weintraub spoke eloquently about her personal experience and her family’s challenges with Lyme Disease.” Echoing Pamela Weintraub’s call for research, the IOM report states that “a new environment of trust and a better environment for more constructive dialogue [is required] to help focus research needs and achieve better outcomes.”

We commend the IOM for so effectively establishing the convergence of science with real-life situations and highlighting both the need for more scientific knowledge and the serious societal challenges that need to be addressed. 

Importantly, the IOM Committee noted that “the burden of disease is a growing concern.” The Committee recognized that “tick-borne diseases (TBDs) represent some of the world’s most rapidly expanding arthropod-borne infectious diseases, yet significant gaps remain in our understanding and knowledge about them.”  Some of the themes discussed in the IOM report suggesting greater emphasis and more research are:

        ·  A national integrated research plan for advancing the science on tick-borne diseases;

        ·  A long-term study of Lyme disease and other TBD patients; Educational programs for the public;

        ·  The current status of diagnostic tests and biomarkers for tick-borne diseases;

        ·  Biorepositories for tick-borne diseases; Biological understanding of persistent symptoms;

        ·  The impact of coinfection in severity of human TBDs;

        ·  The role of immune response to tick-borne infection and its effect on bacterial load and disease manifestations;

        ·  Animal models that explore mechanisms of pathogen persistence following antibiotic treatment.

A diverse group of scientists and physicians with expertise in tick-borne infections discussed a breadth of scientific topics. Some profound insights shared by several of these presenters include:

        ·  “Science is not belief, but the will to find out” (Benjamin J. Luft, M.D.)

        ·  “Everyone is studying the early stage of this infection, no one is studying the persistent phase of this infection.”  (Stephen Barthold, D.V.M., Ph.D.)

        ·  “You do not require an antibody response to develop this disease”  (Janis J.Weis, Ph.D.)

        ·  “Treat the patient, not the test”  (Juan Olano, M.D.)

        ·  “[For the child] long-term effects last 50-70 years”  (Richard F. Jacobs, M.D.)

        ·  “…the poor understanding of the true incidence and geographical distribution…I don’t think we have a clue”  (Richard F. Jacobs, M.D.)

        ·  “How can you say, ‘I’ve treated you for four weeks and therefore you no longer have Lyme disease.’ The fact is, we don’t know!” (Sam T. Donta, M.D.)

        ·  “Under-powered studies which purport to demonstrate universal efficacy need to be viewed with circumspection”  (Sam T. Donta, M.D.)

        ·  “All that shouting drowns out all the complexity and the nuance and the work that needs to be done”  (Pamela Weintraub, senior editor at Discover magazine, and author of Cure Unknown: Inside the Lyme Epidemic)

In addition to thanking all the presenters, we want to express our gratitude to the Lyme community for supporting our effort to see this workshop through.  The thousands of Lyme patients who responded to our surveys and allowed their stories to be shared in “The Human Dimension of Lyme and Other Tick-Borne Diseases: The Patient’s Perspective,” the NatCapLyme paper commissioned by the IOM, provided a valuable contribution to the IOM workshop and report.http://www.iom.edu/Reports/2011/Critical-Needs-and-Gaps-in-Understanding-Prevention-Amelioration-and-Resolution-of-Lyme-and-Other-Tick-Borne-Diseases.aspx (p. A-67)

We strongly urge each of you to continue the process that IOM initiated by reading the IOM report so that you can extract from these works what is beneficial to your specific case in your quest to achieve wellness and to overcome the negative effects of Lyme disease. http://www.iom.edu/Reports/2011/Critical-Needs-and-Gaps-in-Understanding-Prevention-Amelioration-and-Resolution-of-Lyme-and-Other-Tick-Borne-Diseases.aspx

The IOM workshop brings us another step closer to improving the lives of Lyme patients and their families who have been profoundly impacted by tick-borne infections, and who have been caught in the crossfire of opposing views for such a long time.  The next logical step is collaboration between all stake holders to fill in the gaps uncovered in this workshop concerning diagnosis, addressing the topic of treatment, and the need for a consistency of language in discussing Lyme disease. “Medical progress should no longer be impeded by the polarizing controversy that has characterized Lyme disease research in the past. The dialogue must continue and encourage mutually respectful collaboration across scientific disciplines and among researchers, clinicians and patients, even when view points differ, if we are to make progress.” (Gregg Skall, Womble Carlyle Sandridge & Rice, PLLC)

We implore Congress to fund and the IOM to convene a second workshop that would address research needs for effective treatment for persistent Lyme disease. 

National Capital Lyme & Tick-Borne Disease Association
P.O. Box 8211 · McLean VA 22106-8211 · Phone & Fax 703-821-8822
NatCapLyme@natcaplyme.org · http://www.natcaplyme.org

Posted by Editor on Friday, April 22 @ 21:11:45 EDT (1469 reads)
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 LymeBlog News: Under Our Skin comes to PBS

Lyme In The NewsUnder Our Skin comes to PBS
LymeBlog News
Lexington, KY USA
By LymeBlog News Staff

The award-winning Lyme documentary “Under Our Skin” will air nationally on Public Television stations during Lyme Disease Awareness Month, May 2011. This has the potential of reaching millions of homes across the country. The film will be shown through NETA (the National Educational Telecommunications Association), which is offering the film free-of-charge to the PBS network.Call your local PBS station and encourage that “Under Our Skin” is placed on the calendar for the month of May, 2011. It’s free!Check to see if the film is scheduled to show in your area. If your local PBS station has not scheduled the film, please contact them and ask them to show it. Many of the stations that are broadcasting UNDER OUR SKIN agreed to schedule it after receiving a handful of calls from viewers in the community.
 
For local PBS station contact information, go to www.pbs.org/stationfinder

Questions contact info@openeyepictures.com
 

Posted by Editor on Saturday, April 16 @ 15:34:00 EDT (8440 reads)
(Read More... | 2198 bytes more | 2 comments | LymeBlog News | Score: 5)

 People with Lyme: National Museum of Women in the Arts honors Susan Swartz

People with LymeNational Museum of Women in the Arts honors Susan Swartz
ParkRecord.com
By Scott Iwasaki, Of the Record staff


"My husband and I co-produced a couple of documentary films with Impact Partners," she said. "One deals with mercury poisoning ('Mercury Rising') and another with Lyme disease ('Under Our Skin')."

A decade ago, artist Susan Swartz was diagnosed with mercury poisoning from eating fish from contaminated waters. Six years ago, she contracted Lyme disease.

In both instances, Swartz, who splits her time between Martha's Vineyard and Park City, nearly died, but they also gave her a new perspective about her art. "My paintings have become more bold as a result of those experiences," Swartz told The Park Record during an interview. "In this world where commerce and technology seem to influence so many people, I think I want my message to take on the real beauty that is in our natural surroundings. If any of my paintings take people away from those other distractions, even for a few minutes, then they are succeeding in conveying what God gave us naturally.
Swartz's paintings will have the chance to reach new audiences when the National Museum of Women in the Arts in Washington, D.C., honors the artist with a special exhibit, "Susan Swartz: Seasons of the Soul." The exhibit will run June 17 through Oct. 2  

(Photo courtesy the Bishopric Agency)











"This is really a big deal for me and I'm so excited," Swartz said. "The museum staff has been talking to me for about a year and half. I got word of a commitment date two days before Christmas last year and what a nice Christmas present for me." Swartz said the NMWA, founded by Wilhelmina Cole Holladay, was the first organization to give equal footing to female artists. "I can't think of any organization that has done more for women artists in our country than NMWA," she said. "Ever since I attended a function years ago, I have dreamed about my work hanging there, so it is an incredible privilege, now, to show my works at this institution."
The exhibit will feature 13 compositions, all of which show her keen eye for the environment, which has developed over the past 40 years.
"I am in what I would call my impressionist/expressionist stage right now," Swartz explained. "I feel like I've gone trough my portraits, my small animals my flower stage and my barn stage and my scuba-diving stage. Now I'm completely into nature.
"In the summer I'm on the East Coast and do a lot of water scenes with water lilies and that sort of stuff," she said. "When I come back to Park City, I paint my trees and landscapes again."
Having recovered from illnesses that were environmental in origin, Swartz became an environmental activist and she believes her art is the perfect vehicle to spread those messages.
"Everyone has a talent that I think they can apply to a greater good," Swartz said. "I think I'm most happy when my work inspires others to make a difference in our environment."
However, she knows that her art is only part of ...

Posted by Editor on Wednesday, April 13 @ 22:11:23 EDT (1394 reads)
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 Latest News: Review: The Poison Plum by Les Roberts

Lyme In The News
Review: The Poison Plum by Les Roberts  
by Lydia Niederwerfer, Lydia's Blog, Lyme-Aware.org
 
 


Less Roberts, author of "The Poison Plum" I found it intriguing, imaginative and worth reading. It held me spellbound while at the same time left me unsettled and distressed because if you take the time to do more research on the plight of those that suffer with Lyme Disease right now you will find that this book in its underlying facts is so close to true life.
Critics and reviews have stated that Les Roberts’ book, The Poison Plumis by some too over the top in expressing the views of "fundamentalist Christians" and political enthusiasts who think outside the norm. It goes way beyond inconceivable; others had nothing but praise for the book.
 
Originally, I had written a review that follows in the same format of others. A freak accident wiped out my entire’s week work which included the review of Les Roberts’ book. Although I feel the original review was adequate, after re-reading the reviews that were already out there, I reconsidered a different perspective from the first.
 
Each and every one of us has different tastes and interests when it comes to reading books. As we all have difference of opinions on how much government involvement should be allowed in our personal lives. For example, right now, those that oppose the increase of Government and want to uphold the Constitution are considered radicals and trouble makers.
 
I love to read all types of books and watch all types of movies: suspense, thriller, autobiographies, educational, fluff, feel good, romance, comedy and spiritual. It all depends on what is happening in my own life. Books and movies are used to escape or expand on what is happening in real life. We have the choice on what we would like to read and what we would like to watch. If you don’t want to read a particular book: don’t; if you don’t agree with a particular movie: don’t watch it. End of story.
 
Connie Strasheim did an excellent job of concisely describing The Poison Plum. “Paradoxically, life's greatest truths are often found in fiction, and nowhere has the truth about Lyme, the fastest-growing infectious disease in the United States, been so accurately revealed as in this powerful, gripping story about a congressman and his quest for justice, a woman's desire for her son's healing from Lyme disease, and the powers that oppose them.”
 
I, too, like others was captivated and disconcerted with the underlying truth of the basis of the book. Often I found that I had to set it aside to calm down. You see, within this work of fiction, Roberts does a thorough job on intertwining fact within fiction.
 
In the beginning, the reader is presented with the infamous works of the Government’s Tuskegee Syphilis Experiment in Alabama in the 1940’s where approximately 400 African Americans were used as human guinea pigs. Some may think, that was decades ago. Surely, the Government has come a long way since then; however, there are several concerns and conjectures on where the 2001-2002 West Nile virus became such a problem and why. If you ask those that are struggling with chronic Lyme Disease, there are those that feel the particular strain of Lyme Disease that becomes chronic is a form of a “bio warfare” defense. With all these examples, if you take the necessary time to research, you will find supporting evidence.
 
No sooner are you shown the horrors of what the Government is capable of, then you are thrust into the present. A tragedy at the hand of a beloved, honored and Congressional Medal Honor recipient at Plum Island, one of the most inconsolable experiences that we have been exposed to over and over only to be left asking: Why?
 
In the reader’s journey to find out, you are led through a single mother’s quest to find a cure for her son’s illness, that physician upon physician has a different idea as to what could be the problem. She then finds out that the answer may be at her job with the Government at the biological research laboratory. This thrusts her into a world of deception, government corruption, and the political injustices in search of the truth. Only to end with a major twist of turn of events.
 
This book is not for the faint of heart or those that choose to see the world through rose-colored glasses. It is also not for those that are firm believers that the Government is only looking for the best interest of the people and has no underlying motives of its own.
 
"... painted with imagination, clarity, intricate description and exceptional pacing--well, not only does it entertain, but it also immerses the reader in its world, captivating the soul from page one until the very end. ~ Connie Strasheim, Author/Medical Researcher of Insights Into Lyme Disease Treatment: Thirteen Lyme-Literate Health Care Practitioners Share Their Healing Strategies
 
"This book encompasses many aspects of what is really taking place in our world and I think we need to heed the author's warnings. The Poison Plum is very well written and includes all the essential elements of a spellbinding thriller." ~ Marjorie Tietjen, Freelance investigative journalist 
 
"This is one for the record books! This one will change the way you think, open your eyes and leave you speechless. This is one book you will never, ever forget! Les Roberts has knocked it out of the ball park with his creative genius. Get it!" ~ Laura Z.  
 


Posted by editor on Thursday, March 24 @ 22:15:44 EDT (1524 reads)
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 Opinion / Editorial: Will false claims by Lyme disease associations backfire?

Opinion / EditorialLymeBlog News
Lexington, KY USA
By Mac McDonald, Editor, LymeBlog News

An anatomy of misinformation and Internet harassment by Lyme disease associations
Although researching organizations and Action Alerts is not an easy task, we all need to check the facts before firing off phone calls, faxes and emails to politicians

I would hope that everyone reading this article would know by now that when they receive emails containing false information that they have not really won the Nigerian Lottery, that Microsoft will not really send them thousands of dollars if they forward an email to 8 people, and that the little boy who is dying will not really receive money if they forward the email to everyone they know.  Most of these misinformation emails are familiar to all of us.  These emails are worded in such a way as to motivate the reader to action out of hope of personal gain or a desire to help someone.  The old saying is, "When something sounds too good to be true it usually is."

Recently there has been a rash of misinformation email and Internet campaigns with various political agendas spread by persons representing major political parties.  Unlike the notices above, these email campaigns contain information meant to enrage the reader and motivate them to take action.  These online, political, misinformation campaigns often sound "too bad to be true", but they must be.  How else could someone put them on the Internet? 

There must be laws which require that information on the Internet be factual, right?  Wouldn't someone who spread false information harm their own credibility and, therefore, hurt their own cause?

What follows is this journalist's attempt at dissecting the anatomy of just one such case of a false information campaign: spread using the Internet to one small, special interest group of followers and resulting in well meaning people harassing politicians and spreading a false rumor to everyone they know.

In my opinion, this particular misinformation campaign has damaged the credibility of the perpetrators rather than helping their cause.
In the age of the Internet anyone can claim to be an authority on a subject and quickly spread false rumors to thousands of people
I think I see a formula in most political disinformation campaigns on the Internet:

  • Step 1 of a disinformation campaign: Claim to be speaking for a large number of people.
  • Step 2 of a disinformation campaign: Issue a public statement, press release, media interview or letter that contains false, inflammatory, statements or true statements, intended to be inflammatory, which are not relevant to the subject being discussed.
  • Step 3 of a disinformation campaign: Express indignation and spread emails or Internet announcements, again with false statements or true statements which are not relevant, and ask others to join your fight and spread the word.
  • Step 4 of a disinformation campaign: Use words and terms in your documents that will incite outrage in your Internet audience with false statements or true statements which are not relevant.
  • Step 5 of a disinformation campaign: Keep your attacks simple and include very little, or no, actual explanation of your position. 
  • Step 6 of a disinformation campaign: Make it necessary for the object of your attack to make lengthy, complicated responses or explanations which most people will not understand.
  • Step 7 of a disinformation campaign: If the object of your misinformation campaign: responds, escalate your attack.  Keep repeating the false statements or true statements which are not relevant.
We are looking at an "Action Alert" from someone claiming to represent a national organization.  If the communication contains inflammatory wording and logical accusations the reader is motivated to spread the word to everyone they know and, in the Internet age, that requires little more than clicking on FORWARD in their email program.

If the false "Action Alert" calls for the reader to contact a politician and includes suggested wording for an email, fax, or telephone call it makes that action that much easier.  If the names, phone numbers, fax numbers, and email addresses of the politicians are included it makes it almost an effortless task on the part of the reader to take action.

What if the false information comes from someone who claims to speak for anywhere from 4 to 35 organizations depending on to whom they are making the claim?

SR-133 in New Jersey and Lyme disease:

When New Jersey State Senator Christopher “Kip” Bateman (R-16) decided to sponsor a resolution to urge the Governor to encourage a private business to locate their research center, dedicated to chronic neuroendocrine immune disorders or NEIDs (Senate Resolution no. 133) in the State of New Jersey he must have thought it would be a "slam dunk".

Senator Bateman is a conservative, “Taxpayer Champion” who does not shy away from expressing his opinion on controversial issues.  He has 15 years experience in state government.

But this resolution should not be a controversial issue.  This should not require a lot of the Senator's time or staff resources.  After all, his co-sponsor is from the other side of the aisle, Senator Loretta Weinberg (D-37), so there should not be opposition along party lines.  There should not be any opposition from the federal government, both the National Institute of Health and the Centers for Disease Control and Prevention approve of the research center.  Patient advocate groups should be supportive, after all, the more research into their ailments the better.  Easy job, write the resolution, get it through committee and get a vote to pass it.

Beside, this is not like a bill, this is not trying to pass a law, this is basically asking the Governor to encourage a private industry to locate in the Garden State.  It is good for the economy which is good for his constituents.

I can only imagine the Senator's surprise when he received a letter dated October 6, 2009, from a person claiming to be the president of the "national Lyme Disease Association" (note that national is not capitalized in the letter therefore is not part of the official name of the organization).  This letter is supposedly representing the views of 35 affiliate organizations.  The letter is signed by Patricia V. Smith, President, Lyme Disease Association, Inc.
  • Step 1 of a disinformation campaign: Claim to be speaking for a large number of people.
Smith includes a list of 33 organizations with the name of the ...

Posted by Editor on Tuesday, December 07 @ 03:00:00 EST (3321 reads)
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