Race Benefits: Alabama Lyme Disease (ALDA)
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.
