Andrea Roseman is the mother of an Alpha-gal Syndrome patient and an advocate for those with tick-borne illnesses.
She represented the Alpha-gal Syndrome Community before the 2020 Tick-Borne Disease Working Group (TBDWG) in Washington, DC. She discussed the need for the following:
- Patient information and handouts on tick-borne diseases in medical offices;
- Significantly more education of medical professionals regarding tick-borne illnesses;
- Enhanced food labeling to identify and communicate which products contain meat-based ingredients.
You can view Andrea’s presentation by clicking the video link below.
Tick-Borne Conditions United is a registered 501 (c)3 non-profit organization. Your support goes to fund education, research, and advocacy to help those with tick-borne conditions.