PD Protocol is for people living with Parkinson’s disease, those newly diagnosed, care partners, and family members who want a clearer, more organized understanding of the condition. It’s especially helpful for anyone feeling overwhelmed by conflicting information or unsure where to start.

PD Protocol is built from lived experience, research, and real-world application. It’s not written to sell a single solution or philosophy. Instead, it focuses on clarity, context, and practical understanding—helping readers navigate Parkinson’s disease with more confidence and less noise.

No. PD Protocol is not medical advice and is not a replacement for care from a qualified healthcare professional. It’s an educational resource designed to help people better understand Parkinson’s disease, organize information, and feel more informed when having conversations with their care team.

You can reach me by emailing hello@rekajanisse.com. While I’m not able to offer individual medical guidance, I do read messages and appreciate hearing from members of the Parkinson’s community, care partners, and collaborators.

The pricing reflects the format and depth of each version. The Gumroad version includes an additional PDF format, rich images, and Protocol Plus content — including curated podcasts, favorite products, and favorite supplements. It’s designed as a more interactive, reference-style experience. The Amazon version is a streamlined Kindle eBook intended for simple, portable reading. Both contain the same core educational content, but are priced based on how they’re designed to be used.