How Can Patients Contribute to Lyme Research?
The last National Institute of Health treatment trial for Lyme recruited over 15 years ago. Yet at least 300,000 people in the US contract Lyme each year.
Thankfully, there's good news: MyLymeData lets patients record their symptoms and experiences. How does it work? A Lyme patient can simply visit MyLymeData to privately record their symptoms.
If you're a Lymie, take your first survey to help this amazing cause. You should be able to complete it within 30 minutes. You can take a break and come back to it if you need to. After the first one, they will send you additional surveys (about quarterly) to track your progress. They will let you know the patterns, findings and discoveries from their collective data.
The more patients that participate in this study, the better!