Lyme disease, often misunderstood and overlooked, can have significant impacts on one's health and well-being. In this journey, I want to share my story of discovering I have Lyme disease, shedding light on the complexities of diagnosis, treatment, and living with this condition.
This blog is my first “report”, so to speak, about my journey, and I’ll share with you how I discovered I have Lyme Disease and what my next steps will be.
What is Lyme Disease?
Lyme disease is a bacterial infection transmitted to humans through the bite of infected black-legged ticks, also known as deer ticks. The bacteria responsible for Lyme disease is called Borrelia burgdorferi. While not all tick bites result in Lyme disease, those infected may experience a range of symptoms, including fever, headache, fatigue, and a characteristic bull's-eye rash.
If left untreated, Lyme disease can lead to more severe complications, affecting the joints, heart, and nervous system (just to name a few). Early detection and treatment with antibiotics are crucial for managing Lyme disease effectively. However, due to its varied symptoms and the limitations of current diagnostic methods, Lyme disease is often underdiagnosed and can pose challenges for individuals seeking proper care.
Discovering I have Lyme Disease
My journey with Lyme disease began unexpectedly. Despite years of focusing on my health and addressing various issues, Lyme disease was not something I had ever considered.
When my doctor initially suggested testing for it, I hesitated. I couldn't recall being bitten by a tick or experiencing the classic bull's-eye rash associated with Lyme disease. However, I learned that not everyone presents with these symptoms; in fact, only 60% to 80% of individuals do.
Ultimately, my decision to undergo testing was influenced by another health issue: mycotoxin illness. After testing positive for mold exposure, which often correlates with Lyme disease, I reconsidered the importance of exploring this possibility further. The test results confirmed my suspicions—I had Lyme disease.
While my diagnosis wasn't the most severe case, it still marked the beginning of a new chapter in my health journey. Lyme disease can manifest differently in each individual, affecting various bodily systems such as the heart, joints, nervous system, and more. For me, it primarily impacted my energy levels and digestive health, adding to the list of symptoms I had been grappling with for years.
Next Steps with my Lyme Disease Diagnosis
Navigating life with Lyme disease requires patience, resilience, and access to proper healthcare. Unfortunately, Lyme disease often flies under the radar in mainstream medicine, leading to underdiagnoses and inadequate treatment. Many individuals, like myself, face challenges in accessing timely and comprehensive care.
As I embark on this journey, I am committed to sharing my experiences, insights, and resources with others who may be facing similar struggles. From discussing treatment options to advocating for improved testing protocols and healthcare accessibility, I aim to empower others to take charge of their health.
While my journey with Lyme disease is just beginning, I am hopeful that by raising awareness and sharing information, we can foster a community of support and understanding. Together, we can challenge misconceptions, break down barriers to care, and strive for better outcomes for all those affected by Lyme disease.
Discovering I have Lyme disease was a surprising and challenging moment in my life. However, it has also inspired me to advocate for greater awareness and accessibility in healthcare. By sharing my story and journeying alongside others, I hope to make a positive impact and contribute to a brighter future for those living with Lyme disease.
As I continue to navigate this path, I invite you to join me, share your experiences, and together, let's shine a light on Lyme disease and empower each other towards healing and wellness.
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