A Lyme disease diagnosis can feel overwhelming. No matter how long you’ve been sick, you're not alone on this journey. With knowledge and support, you can tackle this. So, in this blog post I’m sharing some crucial steps to take following a Lyme disease diagnosis.

Justin Bieber's diagnosis of Ramsay Hunt Syndrome inspired me to share my experiences with the viral co-infections, and syndrome diagnoses that often come along with late-stage Lyme disease.

Whether you’re a fan or not I bet you’ve heard, that Justin Bieber has canceled his upcoming tour due to facial paralysis. The pop star recently released a live video sharing his symptoms and his latest diagnosis of Ramsay Hunt Syndrome associated with an active varicella-zoster (VZV) infection. VZV causes shingles and chickenpox but in rare cases causes more severe illness, especially in those with a compromised immune system.

Getting a thoughtful and useful gift for your loved ones can be a challenge, and even more so if they’re dealing with a chronic illness! You might be wondering what to get someone who is dealing with debilitating symptoms, well, wonder no more! I’ve created a list of my favorite supportive gift ideas, to provide comfort all year long!

The Tick-Borne Disease Working Group (TBDWG) has announced its first public 2021 meeting!

In this short blog post, you’ll find the links and information you need to register for the meeting and apply to comment to the TBDWG - you can submit either a written or verbal statement.

High attendance and personal accounts sharing our struggles getting proper testing and treatment will show Congress that Lyme disease research and funding are critical to the American people.

Registration closes 8/17/21

Part 2 of my research, experience, and opinion around the Covid-19 vaccine and chronic Lyme disease. Like many with chronic Lyme disease, I felt fearful about getting this new vaccine. So like everything I do I researched the absolute hell out of it. In this video, I share what I learned, and my experiences with the second Covid-19 vaccine.

My research, experience, and opinion around the Covid-19 vaccine and chronic Lyme disease. Like many with chronic Lyme disease, I felt fearful about getting this new vaccine. So like everything I do I researched the absolute hell out of it.

I know this is a hot button issue, please no nasty comments. This is not medical advice, nor is it a political statement. I am simply sharing my research and thought processes around how I made this personal health decision.

This week I had the opportunity to speak with members of congress during the Lyme Fly-in event. They offered us so much training, it really inspired me to create this week’s video with Lyme disease advocacy tips to show you how to become a Lyme disease advocate.

Check it out to learn how you and your loved ones can easily become Lyme disease advocates, and why it's important!

Light therapy I use in my Lyme disease recovery! In this video, I share the health benefits of UV exposure, SAD lamps, infrared light, blue-light blocking glasses.

PUFAS Polyunsaturated Fatty Acids: How My Favorite Snack was Keeping Me Sick! "Good fats" have been a big part of my anti-inflammatory/paleo diet, until I started reading up on PUFAS.

In this week's video, I share what I've learned about polyunsaturated fatty acids, and how my favorite snack was keeping me sick!