The Alabama Lyme Disease Association is a non-profit501(c)(3) that serves the community in Alabama (and beyond) through awareness, education, outreach and research.
As the central voice for patients affected by Lyme disease and other tick-borne illnesses in Alabama, it is our mission to educate those affected by tick-borne diseases, Caregivers, Healthcare Professionals and the General Public. We have partnered, and will continue to partner, with researchers, legislative partners and medical providers to provide a voice for those affected through advocacy, education, science-based research, legislative change and patient/caregiver support.
The Central Voice for Lyme in Alabama
The information provided by Alabama Lyme Disease is for informative purposes and to facilitate communication. We strive to update our Facebook page and website often, however, please be advised that new scientific discoveries emerge all the time and we, therefore, cannot guarantee that this information reflects all of the most recent scientific data. Links and/or addresses that are displayed on our website are provided as a courtesy to Facebook page and website visitors and The Alabama Lyme Disease Association is not responsible for the content of or actions taken due to the opinions and information provided on this or any other website to which we post a link. It is the responsibility of each individual to personally ascertain what is accurate, complete and beneficial from any informational source you find on the Internet or elsewhere. Additionally, the information found on the Alabama Lyme Disease Facebook page and website, or provided by its associates, is not intended to be a substitute for medical advice and/or care, nor is it meant to diagnose and/or treat any medical condition, including, but not limited to, Lyme disease and other tick-borne illnesses. If you suspect you, a friend or a family member may have Lyme disease or any other tick-borne illness, it is important to seek immediate professional medical advice and treatment.