Dan Salkeld, PhD, Bay Area Lyme Scientific Advisory Board member, is a Research Scientist in the Department of Biology at Colorado State University, and tick researcher extraordinaire. He discusses the ecology and epidemiology of Lyme and other emerging tick-borne pathogens such as Borrelia miyamotoi. Ticktective Video and Podcast Editor: Kiva Schweig.
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Bay Area Lyme Foundation Partners with American Junior Golf Association to Provide Critical Education About Tick-borne Disease
Golf is Estimated to Be Among the Highest Risk Sports for Contracting Lyme and Other Tick-borne Diseases
Portola Valley, CA, July 15, 2021 — Bay Area Lyme Foundation, a leading sponsor of Lyme disease research in the US, and the American Junior Golf Association have announced a new partnership aimed at educating young golfers about Lyme disease and providing tips for preventing tick bites. For this partnership, Bay Area Lyme Foundation will provide prevention materials, tick removal keys, Tick Tock Naturals® organic tick repellent and Sawyer® picaridin lotion to all AJGA members. In addition, Bay Area Lyme Foundation will become a Leadership Links charity partner, and two tournaments will be named for the Foundation by the end of 2023.
“As former AJGA and Harvard Division 1 golfers, my brother and I wish we had been educated on the risks associated with Lyme disease and the prevalence of ticks throughout the U.S., and ways to prevent being bitten,” said Nina Fairbairn (AJGA ’13, Harvard ’17), an investment partner who volunteers for Bay Area Lyme Foundation as an Advisory Board member and is spearheading this partnership for the Foundation. “Few golfers seem aware of the risks and even fewer take precautions, and it’s imperative for us to change this.”
Golf courses are a hotbed for ticks that can carry Lyme disease. Ticks flourish in areas between woods and open spaces, which is the exact terrain of golf courses, and live on the small forest animals that often occupy golf courses. Lyme disease is the most common vector borne illness in the United States with at least 476,000 new cases each year.
Col. Nicole Malachowski, first female Thunderbird pilot, National Women’s Hall of Famer, and Former Deputy Director for US Air Force Readiness and Training for the Office of the Under Secretary of Defense for Personnel and Readiness, and Bay Area Lyme Foundation Ambassador shares her challenging journey from military fighter to Lyme warrior. Ticktective Video and Podcast Editor: Kiva Schweig.
Written by: Christina P. Kantzavelos
Driven by a desire to create a centralized resource and supportive community for those impacted by Lyme and tick-borne disease, the San Diego Lyme Alliance (SDLA) was formed as an affiliate of the Bay Area Lyme Foundation in 2019. The challenges of navigating Lyme disease are vast and need not be faced alone. So following in the footsteps of past and existing local Lyme support groups, SDLA established three regional “Circle of Support” group meetings in Carlsbad, Scripps Ranch and La Jolla. Creating this safe space for open dialogue enabled Lyme patients, family and caregivers to build meaningful connections, feel supported and stay informed.
In March 2020, life changed abruptly. COVID-19 demonstrated the importance of human communication and connectedness, with a rise in feelings of isolation, depression and anxiety. While the pandemic presented the challenges of isolation, it also provided the opportunity to explore new ways of interacting and building meaningful connections. Quick to adapt to the online virtual world via Zoom, the “Empowerment Circle” (EC) was born in June 2020. Initially facilitated by Mark Guay, Christina P. Kantzavelos and Patricia Cosulich have joined as co-facilitators to round out the EC Team. Over time our group has brought together participants from San Diego and beyond, including San Francisco, the east coast, and even Canada. The pandemic presented an unexpected opportunity to bring people together more effectively, transcending time, geographical separation and physical limitations.
Monica Embers, PhD, Associate Professor of Microbiology and Immunology at the Tulane National Primate Research Center and Bay Area Lyme Scientific Advisory Board member discusses xenodiagnosis, Borrelia persistence, and her ongoing research in non-human primates. Ticktective Video and Podcast Editor: Kiva Schweig.
Wendy Adams, MBA, Bay Area Lyme Advisory Board Member and Research Grant Director, discusses Lyme research, Lyme persistence studies, and the reality of Lyme rashes. Ticktective Video and Podcast Editor: Kiva Schweig.
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Bay Area Lyme Foundation Announces Call for Entries for the 2021 Emerging Leader Awards
Grant aims to inspire new research toward overcoming the challenges of Lyme disease
PORTOLA VALLEY, Calif., November 17, 2020—Bay Area Lyme Foundation, a leading sponsor of Lyme disease research in the US, is announcing a call for entries for their 2021 Emerging Leader Awards (ELA), which are designed to encourage scientists who embody the future of Lyme disease research leadership in the US. This year, two grants, $250,000, and $100,000 will be awarded. Recipients will be researchers from academia or the private sector in the US. who have not necessarily conducted previous research in tick-borne diseases. All applicants are encouraged to bring learnings from other therapeutic areas to their research projects. Their proposal must have a defined scientific approach and rationale that can advance diagnostics or treatments for Lyme disease. Applications will be accepted through February 15, 2021, at midnight pacific. The full criteria and application for this award can be found here.
“This year has given us all the opportunity to consider the great importance of medical research and the devastation that can arise when a pathogen is not well-understood by the medical and scientific community,” said Wendy Adams, research grant director, Bay Area Lyme Foundation. “We clearly need novel approaches to make Lyme disease easy to diagnose and simple to cure, and we hope these awards offer the support that innovative researchers require.”
Many experts agree that if you are a patient being treated for chronic Lyme disease, but are not getting better, underlying mold toxicity could be at fault. Mold illnesses and Lyme Disease share many symptoms and if all treatments have been exhausted for Lyme with no result, mold could be the hidden offender. According to the book New Paradigms in Lyme Disease Treatment, “mold toxicity causes patients to develop symptoms from Lyme infections and vice versa, and people with weakened immune systems are far more susceptible to sickness from mold…and doctors are just beginning to understand and explore it, and like Lyme disease, many conventional physicians are not even aware of it.”
Many people know that black mold poses a huge threat, but are unfamiliar with other types of mold causing health issues. Mold illness causes extreme inflammation, called chronic inflammatory response syndrome (CIRS) and when coupled with Lyme disease, symptoms such as fever, headache, and fatigue are exacerbated. Often, mold-related allergies are misdiagnosed or worse, many doctors assume the problems are psychosomatic. Because of this, many people are not aware they are suffering from CIRS plus Lyme disease simultaneously.
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Bay Area Lyme Foundation Launches Ticktective™ Podcast
PORTOLA VALLEY, Calif., September 30, 2020 — Bay Area Lyme Foundation, a leading sponsor of Lyme disease research in the US, announces the launch of the Ticktective podcast and video series. Ticktective is a Bay Area Lyme Foundation program designed to investigate the latest scientific knowledge and advances in Lyme and tick-borne diseases. The podcast offers insightful discussion with researchers, physicians, patients, and thought leaders in the field.
“Because the science surrounding tick-borne disease is so complex and there are so many unanswered questions, Ticktective aims to share firsthand perspectives about the challenges of Lyme in ways that will intrigue more scientists, physicians and patients to join our battle towards making Lyme disease easy to diagnose and simple to cure,” said Linda Giampa, executive director, Bay Area Lyme Foundation.
There are more than 400,000 people diagnosed with Lyme disease each year in the US, and millions of Americans live with persistent Lyme disease (PLD) caused by an ongoing bacterial infection. The current “gold standard” diagnostic for Lyme disease misses up to 60% of cases of early stage Lyme disease, and if not treated promptly, Lyme may progress to a debilitating stage, becoming difficult, or impossible, to cure. Bay Area Lyme Foundation has funded over 100 research projects at 37 institutions across the US in a mission to find solutions for these patients.
Bay Area Lyme Foundation Advisory Board Member, “Chronic” co-author and SonyATV singer/songwriter, Dana Parish, shares her perspective on chronic diseases, autoimmunity, COVID-19, and speaking out in the face of adversity. “Chronic: The Hidden Cause of the Autoimmune Pandemic and How to Get Healthy Again” is available for purchase on Amazon here. Ticktective Video and Podcast Editor: Kiva Schweig.
