~About Us~
We are a non profit organization that provides Support and
Education for those with Lyme Disease in the state of Indiana and the surrounding areas.
This organization was founded by two Best Friends who wanted
to be able to provide help to others who were struggling with Chronic Illnesses
just like them.
They did this with the hope
that this Support Group and Web Site would be helpful
not only for those with Lyme Disease, but also for their
Families and Friends who may want to find out more about Lyme.
Crissy Cardone, diagnosed with Lyme Disease in 1994 serves as
the Indiana Contact Person and can be contacted directly at:
Lori Leary, diagnosed with Lyme Disease and Fibromyalgia in 1998, serves as the
Pennsylvania Contact Person and can be contacted directly at:
General email, questions, comments, and requests for a Free Lyme
Disease package and/or test kit can be directed to:
DISCLAIMER: This site is for informational
purposes only and is not to be considered a substitute for professional medical
advice, examination, diagnosis or treatment. Always seek the advice of your
physician or other qualified health professional before starting any new
treatment or making any changes to existing treatment. Do not delay seeking or
disregard medical advice based on information on this site. Medical information
changes rapidly and while efforts will be made to update the content on this
site, some information may be out of date.