Cure MAPT FTD: MAPT Families Fighting for a Future

We are aware of the burden of this disease on patients and families and the lack of resources to efficiently diagnose and treat FTD. We are working collaboratively with other genetic FTD organizations and institutions to further reach MAPT families in an international effort to provide support for MAPT families and gene carriers, identify areas for advocacy, promote research, and to contribute to future therapeutics. Fueled by the past trauma of watching loved ones succumb to FTD, terrified of how FTD will dictate the future, and fighting for those whose minds are currently failing them.