Sally’s fund was created when our daughter, Sally, was diagnosed with lyme disease. We found this diagnosis to be a very difficult and lonely journey. Our daughter wanted to make sure that no one else would have to go through what she endured. This fund was established to provide education, information, assistance, and support for those suffering with lyme disease and other tick borne illnesses. Since Sally’s diagnosis, we are now a family with lyme disease, for Sally’s father and little sister have lyme disease, as well.
DISCLAIMER: This information is for educational purposes only. We are not doctors. It is not intended nor implied to be a substitute for professional medical advice. The reader should always consult his or her healthcare provider to determine the appropriateness of the information for their own situation or if they have any questions regarding a medical condition or treatment plan.