My Nonprofit Reviews

I've been aware of this nonprofit since December of 2009. My daughter was diagnosed by a physician at Harvard in April of 2009. I contacted the founder Diana Pohlman with a few questions and she was hugely supportive. My husband and I both immediately trusted her. I've seen this nonprofit grow organically over the past 14 years. We donate to PN because we know the funds will directly benefit further research or efforts that will generate funds for further research.

Pandas Network is phenomenal. There were the true pioneer when it comes to support for parents whose children have Autoimmune Encephalitis or PANDAS which was the original name. Their website offered the most up to date list of practitioners which happen to be very difficult to find. Without the help of the founder in 2008 and her insight, I would have lost my daughter. We now have her back and she is a thriving adult after IVIg and Augmentin.