LIFELYME
(A non-profit 501(c)3 charity organization)
An Educational Resource for Lyme Disease and Related Diseases


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    NEWS UPDATE

Minnesota has a NEW BILL to protect Physicians treating Lyme Disease Click Here!


Connecticut Attorney General Charges IDSA with Violating Lyme Antitrust . Click here for more info!


Lyme Disease Review Panel Hearing WEBCAST
The Infectious Disease Society of America (IDSA) Lyme Disease Review Panel hosted an all-day hearing as an opportunity for patients, physicians and scientists to present information relevant to the 2006 IDSA Lyme Disease Guidelines. Click here!


UAB's Whitley Installed as President of Infectious Diseases Society

12/11/2009
Richard Whitley, MD, director of the University of Alabama at Birmingham (UAB) Division of Pediatric Infectious Diseases and a renowned researcher on antiviral therapies designed to fight infections in children and adults, has been installed as president of the Infectious Diseases Society of America (IDSA).

IDSA represents more than 9,000 physicians, scientists and other health-care professionals who specialize in infectious diseases. The society helps establish practice guidelines for the treatment and prevention of infections, promotes the development of new antimicrobials to treat drug-resistant infections and works to ensure a robust and appropriate response to public-health threats such as pandemic influenza.

Whitley is on the Advisory Council for the National Institute of Allergy and Infectious Diseases, one of the National Institutes of Health. He also is on the 2009 H1N1 Influenza Working Group of the President’s Council of Advisors on Science and Technology (PCAST). The group is providing recommendations to U.S. President Barack Obama on needed federal responses to pandemic flu.

A distinguished professor of pediatrics, microbiology, medicine and neurosurgery, Whitley is vice chair of UAB’s Department of Pediatrics and co-director of UAB’s Center for Emerging Infections and Emergency Preparedness. He will serve a one-year term with ISDA that ends November 2010.

Whitley is credited with helping to develop vidarabine, the first drug to treat encephalitis caused by the herpes simplex virus. The vidarabine breakthrough more than 30 years ago opened the door to an entire field of antiviral therapy now crucial for the treatment of influenza, human immunodeficiency virus (HIV) and other infections.

His research also is focused on using a genetically engineered version of herpes simplex virus to fight cancer. Studies show that this enhanced virus, rendered incapable of spreading the herpes virus, enters tumors and attacks cancer-cell biology to stop tumor growth.


After musician Steve Cole was diagnosed with Lyme disease in 2007, he and his wife, Julie, set upon a path of educating others on the debilitating disease. And Steve has even recorded a CD of contemplative music to help fund research and treatment. Cole’s CD, “Angel’s Wing” is available online.

To contact Julie Cole to arrange a speaking engagement, call 850-892-9837. More information about the work of the Lanford Foundation is available at the www.lifelyme.org

To read Steve's story click here.


Klimas Clinic now open in Miami, FL
The time has finally arrived ! Dr. Nancy Klimas opened the new Chronic Fatigue & Immune Disorders Research and Treatment Center in December. Located in Kendall at 8720 N. Kendall Drive, Suite 108, Miami, FL 33176, the clinic will begin seeing patient on Friday, December 4th. Clinic days will be Mondays and Fridays for the near future. The clinic is a private fee-for-service clinic, meaning full payment will be requested at the time of service. Forms will be given to you to submit to yur own insurance provider.

Labs will be drawn at the clinic but will be billed directly through your insurance provider. For more information, visit the website at www.cfsclinic.com. If you have any questions or want to make an appointment , email the clinic at info@cfsclinic.com or call 305-595.4300.


UNDER OUR SKIN DOCUMENTARY ON SHORT LIST FOR BEING NOMINATED FOR THE OSCAR ! Lyme documentary

A gripping tale of micobes, medicine and money UNDER OUR SKIN investigates the untold story of Lyme disease, an emerging epidemic larger than AIDS. Each year thousands go undiagnosed or misdiagnosed, often told that their symmptoms are "all in their head." Following the storeis of patients and physicians fighting the disease, the film brings into focus a hounting picture of the health care system and a medical establishment all too willing to put profits ahead of patients.

New DVD of UOS Available at the website, check it out. http://www.underourskin.com/

Don't miss this film. Under Our Skin has won 7 top film awards. Besides the highly acclaimed Tribeca Award, the most recent film was the "Best Feature Film - Silver Award", at the International Health Film Festival in Greece


Fall 2009

The 'Turn the Corner Foundation' will hold their Annual Gala "UNMASK THE CURE" Thursday Evening at the Edison Hotel, Ballroom in New York, New York. Several of members of LIFELYME will be attending the event.


Summer 2009

NEUROENDOCRINE IMMUNE CENTER will be dedicated to ME/CFS, fibromyalgia, Lyme disease, GWS, MCS, and other related illnesses.

Sat., Jun 27, 2009, via the Co-Cure Listserv: Fantastic news! The New Jersey Assembly has unanimously passed Assembly Resolution 202 to fund a Center of Excellence in New Jersey for Chronic Neuroendocrine Immune Disorders - which include CFS, FM, Persistent Lyme Disease, and related illnesses. The Assembly voted unanimously for the passage of this legislation. Presently, THE LANFORD FOUNDATION - Lifelyme, Inc. and PANDORA, Inc. are drawing up a separate NEI Corporation for the Center, and proceeding with the planning for the housing for the facility in New Jersey. We are on track in the development of our Corporation Business Plan and a committee composed of over 30 volunteers has been organized. We are all very excited about the support we have received from a multitude of top NJ officials interested in promoting our project. ( More info below )

GOLF FUND RAISING TOURNAMENT IN BUFFALO

The 'FIRST ANNUAL CWA GOLF TOURNAMENT FOR CHARITY' was held at the Chestnut Hill Golf Club on September 13th in the Buffalo area. The weather was perfect, and a great time was enjoyed by all. Pictures have been posted on Lori Lawhead's Facebook page. Our thanks to John and all the wonderful people who made this event memoriable. Plans are already being made for the 'SECOND ANNUAL CWA GOLF TOURNAMENT' for Spring, 2010.


On the NEI Center

*The NEI Neuroendocrineimmune Disorder Research Center

The Lanford Foundation - LIFELYME, Inc. first conference "Similarities and Paradoxes in Chronic Illnesses" hosted last January 2008 at the Vinoy Resort in St. Petersburg, Florida was a notable event because it brought together speakers from both the Chronic Fatigue/Fibromyalgia, Gulf War Syndrome and Multiple Chemical Sensitivity community and the Lyme community. The sharing and resulting merging of information on chronic illnesses presented at this conference was a eye opener for the medical professionals who attended the event. As a result of the success of the conference, P.A.N.D.O.R.A., Inc., a CFS/ME organization in Miami, Florida invited us to partner with them on the establishment of a NEI Reseach Center. Presently we are working together towards this goal.


MEETING THE CHALLENGES OF LYME DISEASES AND OTHER CHRONIC ILLNESSES

The Lifelyme foundation understands the similarities and paradoxes that exist between all Neuroendocrine Immune Disorders. These illnesses include Lyme Disease ( Borreliosis Complexes). Chronic fatigue Syndrome, Fibromyalgia, Gulf War Syndrome, Multiple Chemical Sensitivities, Autism, Alzheimer's and autoimmune disease like MS, Lupus, RA, ALS, and Parkinson's. The need for better testing, diagnosing and treatment of NEID patients has created new challenges for researchers, physicians and the resulting pressure for better patient care in our society.

In November, 2008, in an effort to help meet these new challenges, THE LANFORD FOUNDATION, Lifelyme, Inc. and P.A.N.D.O.R.A., Inc. decided to collaborate our resources. P.A.N.D.O.R.A. is a non-profit CFS/ME/CFIDS foundation located in Miami, FL. The partnership between Lifelyme and P.A.N.D.O.R.A. was notable as it brought together for the first time advocates from the Lyme disease community and the CFS/ME?CFIDS community. This merge resulted in P.A.N.D.O.R.A. Inc. embracing Lyme disease as one of the diseases under the P.A.N.D.O.R.A. umbrella. Our collaboration also developed into the forming of a grass roots initative to establish a Neuroendocrine Immune Center at a Medical Ccllege in the Northeast. Once the NEI Center is in full operation it is our vision to setup satelite NEI Centers in other states.

The idea for these NEI Centers is based on the philosophy that the similarities in the symptoms of Neuroendocrine Immune Disorders are the human bodies response to similarities in the underlying pathophysiologies that cause Neuroendocrineimmune Disorder illnesses. Neurological and psychiatric problems and autoimmune diseases are implicated in patients diagnosed with NEIDs. Research is connecting Lyme Disease, Autism, Alzheimer's, MS, Parkinson's, Lupus and other immune dysfunction. Immune deficiency in cancer patients is well documented, and tumor cells have developed a variety of cellular, and molecular mechanisms to avoid anti-tumor immune responses. Accordingly the cornerstone of the NEIDs research mission is that discoveries and advances made in any one of the NEIDs will be beneficial to other chronic illnesses.


 

All Lifelyme advocates are volunteers. Lifelyme's Board members are professional, dedicated and passionate people giving 100% of their time and energy towards the mission of the foundation.

We are doing our part - Please won't you do yours?

Mail donations to:

NEI CENTER

c/o THE LANFORD FOUNDATION - LIFELYME, INC.

1400 VILLAGE SQUARE BLVD.

SUITE 3-241

TALLAHASSE, FL 32312


Thank you for your support.

Donations can be made by check or thru Paypal - click on Donations in left-hand column on this page.

 

 

Disclaimer: The mission of "THE LANFORD FOUNDATION - LIFELYME, INC." is to provide educational information for anyone interested in tick-borne diseases, neuroendocrine immune disorders, and related illnesses. Information presented is intended only for educational purposes. The purpose of the information offered by Lifelyme is not mean't to provide medical advice for anyone. Anyone suffering from a neuroendocrine immune disorder or related illness should contact a qualified physician for diagnosis and treatment.
We respect your right to privacy - view our policy. Website was created and is maintained by M.C.C.C., LLC
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Copyright © 2009 THE LANFORD FOUNDATION - LIFELYME, INC,.pending.