Skip to content

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.

Share Your Alpha-gal Experiences. Take the Survey!

Please click here to begin survey.

Filter by Topic:

Alpha-gal Syndrome
Back To Top