Hi Reader,
Today is HUGE! The documentary, The Quiet Epidemic was just released globally and is now available for streaming on Apple TV, Amazon Prime and Vimeo on demand.
I had the privilege of interviewing the co-directors of this film, Lindsay Keys and Winslow Crane-Murdoch. The back story on how they met and how and why they created this impactful film is a healing story all its own. Personal passion is miraculous and having passion makes the impossible …. POSSIBLE.
I have to say, even though my family has recovered from Lyme and PANS, I felt another layer of healing just by watching this film. It’s incredibly validating and demonstrates just how controversial this disease really is. (At one point in the film, the CDC called a father because the family was receiving media attention for seeking answers about their daughter’s debilitating illness.) Talk about controversial. The Quiet Epidemic a must watch.
Listen to this inspiring interview or watch it on YouTube which includes captions for accessibility. Be part of this important movement and share this film with your community, your physicians, your school, family and friends.
| Listen Here |
Coffee Talk is On-Demand
If you missed my last Coffee Talk with Debbie Kimberg of Hijacked Brains you can watch the recording right here.
This conversation is all about Testing! Lyme tests, PANS test, Mold testing, deficiencies and so much more.
Our next coffee talk is happening May 23, at 1 pm ET / noon CT. We are still floating topics so if there is a topic weighing on you let us know. You can simply email me back or send me a message on Instagram.
Last Call for Your Gratitude Hat
It’s not too late to order your Gratitude Hat. They are adorable. When you wear this hat you remind yourself and the people around you that Gratitude is everything. It’s what got me through the darkest days. All proceeds are donated to The LymeLight Foundation. I am so grateful for the fans who have already purchased one. Shop Here and grab yours. THANK YOU!
Until next time, Happy Day!
Liza
Hi Reader, Want to know the three things that changed the course of my life? Number one (without a doubt) LYME DISEASE! We received the diagnosis for my kids in February 2020, right before the world shut down. Like most families, my kids were struggling long before the diagnosis, which was just the tip of the iceberg. Awareness is crucial and no better time than right now! Be tick aware my friend. May is Lyme Awareness Month. If you do find a tick, here is a resource you need to save. Second...
Hi Reader, Just a quick note to let you know that I am having an online conversation with The LymeLight Foundation tomorrow - Wednesday, April 26 at 12 noon ET / 11 am CT / 9 am PT. During this Instagram LIVE we will discuss: Best practices to apply for a Grant through The LymeLight Foundation. Why starting a Fundraiser is both healing and purposeful for our kids. Examples of how families use their Grant money. Success stories of LymeLight Foundation Families. Join the Conversation Feel free...
Hi Reader, What if our suffering is actually happening for us? That’s the message of my latest podcast guest, Bianca Michele, and she just wrote the book on it! Bianca Michele suffered for six years battling an extensive list of complex conditions including chronic Lyme disease, mold, Mast Cell Activation Syndrome (MCAS), as well as Chronic Inflammatory Response Syndrome (CIRS) – all while her Australian doctors misdiagnosed her and called her a ‘mystery case.’ To heal her body and her...