Jeremy Murphree wrote a new post 1 week, 5 days ago
Donated to Morgellons.org After 2012? You Might Be Owed Money—Here’s Why
Jeremy Murphree wrote a new post 1 month, 2 weeks ago
Lymeapalooza: The Festival with Heart
Jeremy Murphree wrote a new post 4 months, 1 week ago
Anger, Rage, Obsession, and Impulsion: Why People Think Lyme Disease is a Factor in the Luigi Mangione Case
Jeremy Murphree wrote a new post 8 months ago
The Devil's In The Details
Jeremy Murphree wrote a new post 9 months ago
When the Person You Love has Lyme, with Fred Diamond
Jeremy Murphree wrote a new post 9 months, 2 weeks ago
Officials are Downplaying Lyme Disease, it Needlessly Contributes to Death
The numbers are staggering and deeply concerning – Lyme disease cases have skyrocketed in recent years, posing a grave threat to public health that demands urgent attention. According to the latest data, the number of reported Lyme disease cases in the US has more than doubled over the past decade, reaching record highs that show no signs of slowing down. What was once a relatively obscure illness is now a full-blown epidemic, with devastating consequences. Lyme disease mortality rates have climbed steadily, robbing families of their loved ones and leaving communities in mourning. The true scale of this crisis is likely even worse, as many cases go undiagnosed or unreported. The time for complacency has long passed. We must act now to confront this alarming public health emergency head-on. Increased funding for research, education, and prevention programs is crucial to turning the tide against Lyme disease. The health and wellbeing of millions hang in the balance – we cannot afford to let this crisis spiral further out of control. How Government Officials are Minimizing the Severity of Lyme Disease Government officials have long downplayed the severity and prevalence of Lyme disease, leading to widespread underreporting and misdiagnosis. Despite overwhelming evidence of the growing Lyme epidemic, many authorities continue to deny the scale of the problem, hampering efforts to raise awareness and provide proper treatment. Lyme disease is often misdiagnosed due to the complex, multi-symptom nature of the illness, and the failure of standard testing methods to reliably detect the infection. Yet government agencies persist in promoting the idea that Lyme is easily diagnosed and treated, even as patients struggle to find competent medical care. This pattern of denial and obfuscation has serious consequences, leaving countless individuals to suffer the debilitating effects of Lyme without access to the support and resources they desperately need. It is time for our elected leaders to acknowledge the reality of this public health crisis and take decisive action to improve Lyme disease awareness, diagnosis, and treatment across the country. The Deadly Toll of Lyme Disease Denial and Dismissal Lyme disease is a devastating illness that, if left untreated, can lead to life-threatening complications and even death. Yet, far too often, the severity of this disease is dismissed or downplayed, with devastating consequences. The long-term effects of untreated or undertreated Lyme can be truly horrific. Chronic Lyme can cause debilitating neurological issues, cardiovascular problems, and a host of other debilitating symptoms that can be fatal if not properly addressed. Tragically, many patients struggle for years to get the care they desperately need, only to succumb to the ravages of this insidious disease. Black Individuals More Likely to Experience Inequities in Early Diagnosis and Treatment of Lyme Disease, New Research Shows | Johns Hopkins Medicine The data on Lyme disease fatalities is deeply alarming. Studies have shown that the mortality rate for those with disseminated or chronic Lyme can be as high as 15-20%. These are not mere statistics – these are human lives cut tragically short due to a lack of understanding and urgency around this illness. It’s time to take the threat of Lyme disease seriously. Dismissing patients’ symptoms or failing to provide appropriate long-term treatment is nothing short of medical negligence. We must demand better education, research funding, and compassionate care for all those affected by this devastating condition. The lives of countless individuals depend on it. Holding Authorities Accountable and Demanding Urgent Action The time for complacency on Lyme disease is over. As cases continue to rise and the medical establishment fails to adequately address this crisis, it is imperative that we hold authorities accountable and demand urgent action. Lyme disease advocacy must shift into high gear. We need to pressure lawmakers to increase research funding, strengthen prevention efforts, and protect the rights of Lyme patients. The status quo is unacceptable when thousands suffer needlessly due to medical neglect and misinformation. It’s time to get loud and get results. Through coordinated Lyme disease activism, we can force meaningful policy changes and shine a spotlight on this devastating illness. The stakes are too high to sit idly by – the health and wellbeing of our communities depends on the urgent reforms we fight for today. Taking a Stand: How You Can Help Expose the Lyme Disease Crisis It’s time to shed light on the Lyme disease crisis and demand better care for those suffering. As an insidious, often misunderstood illness, Lyme has devastated countless lives, leaving patients to navigate a complex and frustrating healthcare system. But we can change this. By sharing our stories, educating our communities, and rallying for policy reform, we can expose the realities of Lyme disease and push for the resources and treatment options patients desperately need. Political Action related to Lyme Disease Start by joining a local Lyme disease support group. Here, you can connect with others who understand the daily challenges you face. Together, you can brainstorm impactful awareness campaigns to amplify patient voices. Lyme Disease Patient Education | Lyme Disease Resources (globallymealliance.org) Next, be proactive about Lyme disease education. Volunteer to speak at schools, community centers, or healthcare facilities. Equip people with the facts about transmission, symptoms, and prevention. The more informed our society becomes, the better we can protect ourselves and our loved ones. Events by the Center for Lyme Action – Center for Lyme Action Finally, reach out to your elected representatives. Urge them to increase funding for Lyme research, improve diagnostic testing, and mandate insurance coverage for long-term treatment. With persistence and passion, we can drive the policy changes that save lives. The Lyme disease crisis demands our attention. ByRead more
Jeremy Murphree wrote a new post 1 year ago
Jeremy Murphree Shares His Firsthand Account of Living with the Mysterious Morgellons Disease
What is Morgellons Disease and Why is it So Controversial? Morgellons disease is a highly controversial and much-debated condition that has left the medical community puzzled. This unexplained skin condition is characterized by the presence of strange, colored fibers emerging from the skin, along with other unsettling symptoms. The very existence of Morgellons is a point of contention, with some medical professionals dismissing it as a delusional disorder, while others believe it to be a real and perplexing physical ailment. Patients who claim to suffer from Morgellons often describe a range of symptoms, including crawling sensations under the skin, fatigue, joint pain, and neurological issues. The fibers found in Morgellons lesions have been the subject of intense scrutiny, with some researchers suggesting they are merely textile fibers from the environment, while others argue they are of unknown biological origin. This lack of consensus has fueled the controversy surrounding Morgellons, leaving those affected feeling misunderstood and frustrated. Despite the ongoing debate, the experiences of Morgellons patients cannot be ignored. Whether it is a distinct medical condition or a manifestation of something else, the suffering and distress experienced by those affected deserves attention and further investigation. Jeremy Murphree’s Personal Struggle with the Debilitating Effects of Morgellons Jeremy Murphree has been living with the debilitating effects of Morgellons disease for over a decade. In this candid Zoom interview, he shares his personal struggle and the daily challenges he faces. Morgellons is a controversial and poorly understood condition that causes a range of distressing symptoms, including crawling sensations under the skin, strange fibers emerging from the body, and chronic fatigue. For Jeremy, the physical and emotional toll has been immense. “It’s a lot to manage,” Jeremy admits. He describes how Morgellons has impacted every aspect of his life, from his work to his relationships. Despite the lack of medical consensus around Morgellons, Jeremy is determined to share his story and connect with others going through similar experiences. “It’s a horrible scenario, the tests for Lyme disease are not accurate and the treatment is not reliable for about 20% of those diagnosed with it. If you do manage to find a doctor who can produce legitimate evidence you’re infected – good luck getting anybody to understand what that means. People just don’t want to talk about Lyme disease… or believe it could ever affect them.” Living with Morgellons disease is no easy feat, but Jeremy is here to share his story of hope and resilience. As a Morgellons patient advocate, Jeremy knows firsthand the challenges of coping with this complex condition. In his own words, Jeremy candidly discusses the ups and downs of his journey, offering guidance and support to others who may be struggling. He emphasizes the importance of self-care, community, and never giving up in the face of adversity. The Charles E. Holman Morgellons Disease Foundation https://thecehf.org Justin Begaye Interviews Jeremy Murphree for Upcoming #MorgellonsBook #LymeDisease #Marijuana Prof Eva Sapi: The Potential Connection of Borrelia Infection and Breast Cancer https://www.youtube.com/watch?v=csUtZ9plgVs A chemical imbalance doesn’t explain depression. So what does? https://www.sciencenews.org/article/chemical-imbalance-explain-depression Depression is likely not caused by a chemical imbalance in the brain, study says https://thehill.com/changing-america/well-being/mental-health/3569506-depression-is-likely-not-caused-by-a-chemical-imbalance-in-the-brain-study-says/ Study finds depression is not likely caused by a chemical imbalance or low serotonin levels https://www.fox5atlanta.com/news/study-finds-depression-is-not-likely-caused-by-a-chemical-imbalance-or-low-serotonin-levels Microbes and Mental Illness: Past, Present, and Future https://www.mdpi.com/2227-9032/12/1/83 Lyme Disease Increases Risk for Mental Illness https://psychnews.psychiatryonline.org/doi/full/10.1176/appi.pn.2021.10.7 https://www.morgellons.ioThe New Morgellons Movement https://www.morgellonssurvey.orgMorgellons Survey Quality of Life and Morgellons, Treatment Considerations with Dr. Steven Feldmanhttps://www.youtube.com/watch?v=EFHT5InHuGQ Interview with Skin Deep Star, Dr. Steve Feldman MD, PHDhttps://www.youtube.com/watch?v=7mkqnzRz1Ko How to Have a Better Experience at Your Doctor Visit: Steven R. Feldman, MDhttps://www.youtube.com/watch?v=bsiS2hxOW2k&list=PL3nII97JiwYtI5_rhr3BXL2eg7O6E2nOH&index=6 Interview with Morgellons Expert, Dr. Ginger Savely DNP – YouTube Interview with Morgellons Expert, Dr. Ginger Savely (youtube.com) Morgellons Patient Accused of Injecting Fibers Into Their Skin Livestream event with Special Guest, Gregory Smith M.D. FAAP (youtube.com) Special Interview with Lyme Expert, Dr. Robert C. Bransfield (youtube.com) The Case for the Entourage Effect and Conventional Breeding of Clinical Cannabis: No “Strain,” No Gain – PubMed (nih.gov) The Grass Might Be Greener: Medical Marijuana Patients Exhibit Altered Brain Activity and Improved Executive Function after 3 Months of Treatment https://www.frontiersin.org/journals/pharmacology/articles/10.3389/fphar.2017.00983/full Is CBD the future of antipsychotic drugs? A new global study investigates https://wellcome.org/news/cbd-future-antipsychotic-drugs-new-global-study-investigates Cannabidiol versus placebo as adjunctive treatment in early psychosis: study protocol for randomized controlled trial https://trialsjournal.biomedcentral.com/articles/10.1186/s13063-023-07789-w Cannabidiol (CBD) as a novel treatment in the early phases of psychosis https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9110455/ Major trials to test effectiveness of cannabidiol on psychosis https://www.psych.ox.ac.uk/news/major-trials-to-test-effectiveness-of-cannabidiol-on-psychosis Recreational cannabis use hRead more
Jeremy Murphree wrote a new post 1 year, 1 month ago
First Interview with Dr. Courtney Day Plagued by Strange Technical Glitches
Can you tell us about the history of your interest in medicine and what led you to specialize in Lyme Disease and Morgellons? How do you approach the diagnosis and treatment of these complex conditions? Can you walk us through your methodology? What are some of the key environmental factors that contribute to the development of Lyme Disease, Morgellons, and other similar illnesses? To what extent do you believe stressful and emotionally toxic environments contribute to the progression and persistence of diseases? In your experience, what holistic, natural, or alternative therapies have shown promising results in treating bacterial, fungal, viral, and parasitic infections associated with these illnesses? Does medical marijuana have a place in treating Morgellons? Are there any therapies which Morgellons patients should avoid? How does diet factor into a patient’s treatment and what considerations do you feel help in this regard? Is genetic testing beneficial towards treatment? What challenges do patients with Lyme Disease or Morgellons typically face during their treatment journey, and how do you support them through these challenges? Have you ever encountered a patient who believed they had Morgellons, but upon examination, it became evident that they did not? How did you explain the absence of symptoms to them? What are some of the most fascinating symptoms of Morgellons that have particularly piqued your interest? What is your experience with parasites and what can you tell us about leishmaniasis? Is it associated with Morgellons? Where should the research on Morgellons go next? Are there any specific areas that you feel require attention? Can you share a success story from one of your patients who had a particularly challenging case of Morgellons? Do you have pets? What can people do if they would like to see you for their cRead moreJeremy Murphree wrote a new post 1 year, 2 months ago
Michelle McKeon, "The Lyme Specialist" Livestream Event
Jeremy Murphree wrote a new post 1 year, 3 months ago
Live Interview with Dr. Omar Morales of The Lyme Mexico Clinic, 11AM EST Feb 1 2024
Jeremy Murphree wrote a new post 1 year, 4 months ago
Understanding the Rabbit Hole: Exploring How Trauma Bonding Leads to Confusion in Morgellons Groups
Jeremy Murphree wrote a new post 1 year, 8 months ago
Skin Deep: The Battle Over Morgellons is FREE on YouTube – Finally!!
Jeremy Murphree wrote a new post 1 year, 8 months ago
Debunking the Myth: Morgellons is not Associated with Fungus or Mold
Jeremy Murphree wrote a new post 1 year, 8 months ago
Redefining Morgellons: Exposing the Exploitation and Addressing Hurt Feelings
Jeremy Murphree wrote a new post 1 year, 9 months ago
Key Strategies for Discussing Morgellons so that People Will Want to Listen
Jeremy Murphree wrote a new post 1 year, 9 months ago
Stigma: Why Friends and Family Struggle to Openly Discuss Morgellons
Jeremy Murphree wrote a new post 1 year, 9 months ago
Why Morgellons Research Stumps Many Doctors: Unraveling the Complexity of this Controversial Condition
Jeremy Murphree wrote a new post 2 years ago
Morgellons Disease: A Closer Look at the New Mayo Clinic Study and How it Fails to Understand the Literature
Jeremy Murphree wrote a new post 2 years ago
Lyme Movie: New Film Shines a Light on Patients' Ongoing Struggle with the Medical Community
Jeremy Murphree wrote a new post 2 years ago
Lyme Literacy, Understanding Lyme & How to Make Sure Your Doctors are Well-Informed
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