An illness transmitted by a tick, Lyme disease is found in all 50 of the United States and many countries worldwide. sometimes the term "Lyme Disease" is used to indicate a complex illness that includes other diseases transmitted by ticks, such as Ehrlichia, Bartonella, Babesia, Rocky Mountain Spotted Fever, and others.

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FREE! Lyme Disease Education Seminar with Carolyn B Welcome, PA-C

Lyme Disease Conference- Chico,CA

Carolyn B. Welcome, PA-C, will be the Keynote Speaker, raising awareness about Lyme disease early detection and prevention. Her clinical specialty is Lyme disease and related infections. She learned from Dr. Bernard Raxlen that treating complex chronic illness requires a working “knowledge of neurology, psychiatry, rheumatology, ophthalmology, gastroenterology, gynecology, endocrinology” as well as the ability to listen with compassion. Carolyn’s time working with the practitioners at Gordon Medical has added a new array of tools in her arsenal of options to treat Lyme disease.

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Catching Up with Dr. Elizabeth Large, N.D.

By Carolyn B. Welcome, PA-C

Dr. Elizabeth Large divides her time between GMA’s main office in Santa Rosa and its new waterfront location in San Rafael. Among the many tools in her toolbox, this naturopathic physician offers expertise in Methyl Genetic Nutrition Analysis (MGNA), a program that provides in-depth interpretation of data from 23andMe genetic testing. This method has allowed her to home in on her patients’ individual needs.  Dr. Large’s toolbox also includes Chinese and Western plant-based treatments, Low Dose Immunotherapy (LDI),* oral and intravenous antibiotics, IV therapy and hormones.

“Natural medicine is not one size fits all,” she notes.

Eric Gordon, MD and Elizabeth Large, ND at GMA - Maggie Perkins 2017

Eric Gordon, MD and Elizabeth Large, ND at GMA – Maggie Perkins 2017

Thanks to the information given by MGNA, Dr. Large is seeing fast and quite amazing results in patients who have had health problems for most of their lives.

“When you see a lot of variants in one area – histamines, for example,” she explains, “it might help to explain unresolved issues.” [Read more…]

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Join Wayne Anderson, ND FREE on Monday to learn about Lyme disease!

Online FREE from
June 19-26, 2017

The Chronic Lyme Disease Summit 2 starts on June 19th, and tens of thousands will learn from the expert protocols that could radically improve the life of someone with Lyme disease.

Will you be there? I will be speaking on June 19 (Day One), so be sure to get registered now! I will discuss the different types of Borrelia, the Renaissance of Lyme disease treatment, and challenge versus treatment protocols. You can also purchase the full Summit to watch at your own pace. See the link below to find a package that works best for you.

Chronic Lyme Disease Summit 2 [Read more…]

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Elizabeth Large Featured in Press Democrat Article on Lyme Disease

Lucia Montiel, 9, uses a wheelchair to move around her Sonoma coast home since being diagnosed with Lyme disease (John Burgess/The Press Democrat)

Lucia Montiel, 9, uses a wheelchair to move around her Sonoma coast home since being diagnosed with Lyme disease (John Burgess/The Press Democrat)

Lyme disease leaves victims frustrated, searching for answers

Excerpted from an article by MARTIN ESPINOZA
THE PRESS DEMOCRAT | May 18, 2017

Treating these infections is like working in the dark,” said Large, adding that ticks can cause multiple infections. “You’re looking to find the light switch. Hopefully, the more you treat, you start to get a clearer picture of the infections the patient has.

Although tick activity is high in the spring and early summer, ticks are active yearlong, [Read more…]

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“Look of Lyme” Video Channel Launch at Under Our Skin

Look of Lyme
From Under Our Skin

What Does Your Lyme Look Like?

Look of Lyme is a new initiative by the makers of UNDER OUR SKIN to bring your personal stories of suffering and courage into the limelight. While the Internet and social media have exploded with personal videos, there is no place that serves as a repository and archive of the ever changing and growing landscape of Lyme disease. Look of Lyme changes that, offering a way to make the personal political by harnessing the power of crowdsourcing and media. Our individual stories create a collective story that cannot be dismissed! Also, as we begin to develop a third film in the UNDER OUR SKIN collection, Look of Lyme is a way we can screen for possible film subjects. After receiving your videos and possibly editing them for brevity, consistency and branding, we’ll present them on a new YouTube channel accessible to millions worldwide.

Go to the Look of Lyme webpage to get guidlines on how to film and submit your video.

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Wayne Anderson, ND at the Chronic Lyme Disease Summit 2

Online FREE from
June 19-26, 2017

Join Wayne Anderson, ND

online at the Chronic Lyme Disease Summit 2

June 19-26, 2017! – Webinar – Register for Free Now!

*more information on the summit available soon

Dr. Anderson will be speaking on Day 1, June 19. Don’t miss this opportunity to hear him speak about his unique understanding of treatment for Lyme disease and the coinfections seen with it.

A curious and dedicated clinician, Dr. Anderson is committed to the ongoing process of learning and teaching. In addition to his clinical practice, Dr. Anderson maintained his initial focus on teaching. For over 20 years he taught medical students at Touro Osteopathic Medical School, and supervised residents from Sutter Hospital and interns from the Physician Assistant programs in the clinic setting. He is also a popular speaker on the topics of Lyme disease and neurotoxin illness. He has spoken at conferences for the International Lyme and Associated Diseases Society (ILADS), the American College for Advancement in Medicine (ACAM),  Orthomolecular Health Medicine (OHM), and Lyme Induced Autism (LIA), as well as select private symposiums on CFIDS, Lyme, and Autism.

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Update on SISOH Metabolomics Research 4/6/17

Eric Gordon MD and Wayne Anderson ND at SISOH

Eric Gordon MD and Wayne Anderson ND – photo courtesy of the Press Democrat, Christopher Chung

From Eric Gordon, MD

Many of you are probably wondering where we are with the SISOH research. Good news is that Kelly Fox, previously one of the Medical Assistants at GMA, has come on as a full-time Research Coordinator! Kelly is very experienced in working with chronically ill patients, and we think you will find her a delight to work with.

Our ongoing CFS/ME studies are group studies working to develop an accepted group of biomarkers to define people with CFS/ME. We have enrolled all the patients in the replication study with Dr. Cheney, and hope to publish that in fall of 2017. [Read more…]

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GMA Welcomes Elizabeth Large, ND Back to Our Offices!

Elizabeth Large, NDBy Elizabeth Large, ND

Gordon Medical is delighted to have Elizabeth Large, ND back in our offices! Dr. Large is a board-certified Naturopathic doctor with 15 years clinical experience treating complex illness. She is trained as a primary doctor but her clinical emphasis is focused on treating complex disorders that might encompass the following: Chronic Lyme disease or infection, digestive disorders, chronic fatigue, mood disorders, allergies and endocrine imbalances. If you have seen numerous doctors for your medical condition without benefit, you are in the right place.

After many years of practice, Dr. Large began seeing patterns emerge among her patients, both pediatric and adult. Her patient population exhibited similar symptoms such as chronic fatigue, anxiety, depression, chronic digestive issues, high reactivity to foods and medications and other unusual symptoms. She discovered that many of her patients were suffering from chronic infections or neurotoxic illnesses such as Lyme disease, co-infections, mold and/or heavy metal toxicity. [Read more…]

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Help Set the Lyme Research Agenda with Lymedisease.org Survey

Lyme Research AgendaToday, LymeDisease.org launches a survey of 25 research questions for the community to vote on and prioritize. The answers will be used to develop a research agenda for the Lyme community which will be publicized and used as a tool to give patients a voice in the funding of research. The ultimate goal is to ensure that research that matters to patients is funded.

Take the Survey

Read more at Lyme Policy Wonk

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MyLymeData 3-month follow-up survey launched

MyLymeData

From Lorraine Johnson, JD, MBA at LYMEPOLICYWONK

Originally published on LymePolicyWonk on November 15, 2017

Last year, LymeDisease.org launched MyLymeData–a national patient-centered big data project. Today it is the largest study of Lyme patients ever conducted, with over 6,000 currently enrolled. Our goal is 10,000 participants. MyLymeData allows patients to pool their data to help find a cure.

This week we are rolling out MyLymeData’s three-month follow-up survey, which tracks patient symptoms, treatments, treatment response, and functional status on a quarterly basis. This survey holds the key to questions patients care about. What treatments work? Why do they work for some people and not others? [Read more…]