After years of collecting data, I compiled my Lyme Resource Guide to help patients and their families better understand the complex world of Lyme disease and give patients the tools to advocate for care.
I’ve been a medical detective for six years, and I want to bring what I’ve learned to those who can benefit.
If you would like a pdf version of the Lyme Resource Guide, please comment on this post and include your email, or reach out directly by email at: tmansolillo@gmail.com, and I’ll send it to you.
If you’re a Lyme patient, I’d love to hear from you and learn more about your experience with Lyme and tick-borne infections:
how long did it take to receive a diagnosis
how were you diagnosed
what do you wish your family and friends knew about your illness
what do you wish you knew BEFORE you became ill
When I’m not working as a Real Estate Agent or writing on Substack and Medium, I’m working on a book about my family’s journey through Lyme disease. My goal is to continue to raise awareness about Lyme and tick-borne infections so no other family experiences what we have.
The book will contain information for two groups of readers:
parents and young adults currently struggling with Lyme
those who know little about Lyme disease
Through my advocacy work, I speak with patients and their families all over the world, but I’d love to hear from you! I want to ensure the book covers the information that’s important to you or that you believe is currently lacking in the community.
Tracy, please send me the guide so I can share !
Yes, I would love it. Thanks Tracy YOu go girl!!