Patients are coming together to have an impact and create change in Lyme disease policy.
By Phyllis Mervine
The purpose of having balance Lyme disease stories from Lyme patients is to provide some human interest to incentivize Congress to fund Lyme disease research.
By Phyllis Mervine
Members of the Tick-Borne Diseases Working Group share their feelings about what being a part of the process has meant to them.
By Phyllis Mervine
LymeDisease.org’s Lorraine Johnson gave the following verbal comments during the Tick-Borne Disease Working Group’s June 21 meeting.
By Lorraine Johnson, JD, MBA
You don’t have to be an “anti-vaxxer” in order to raise questions about the safety and efficacy of a Lyme disease vaccine.
By Phyllis Mervine