Call an expert helpline, explore the latest dementia research, and get the support you need.

SUPPORT & RESOURCES

You don’t need to go through it alone. Get advice, guidance and support from the many organizations ready to help you find the answers you need.

EXPLORE WIDER RESOURCES

Many organizations are doing important work in this space and offer great starting points for anyone navigating dementia. Some provide direct support and guidance, others lead cutting-edge research and clinical trials, and all offer a wealth of trusted information to help you better understand the disease.

The latest in studies and clinical trials, and how to get involved.

Cure MAPT FTD is a nonprofit dedicated to advancing research and awareness for frontotemporal dementia caused by MAPT gene mutations.

Cure MAPT FTD is a nonprofit dedicated to advancing research and awareness for frontotemporal dementia caused by MAPT gene mutations.

Cure MAPT FTD is a nonprofit dedicated to advancing research and awareness for frontotemporal dementia caused by MAPT gene mutations.

Cure MAPT FTD is a nonprofit dedicated to advancing research and awareness for frontotemporal dementia caused by MAPT gene mutations.

Cure MAPT FTD is a nonprofit dedicated to advancing research and awareness for frontotemporal dementia caused by MAPT gene mutations.

Cure MAPT FTD is a nonprofit dedicated to advancing research and awareness for frontotemporal dementia caused by MAPT gene mutations.

GENFI is an international study that tracks families with inherited FTD to understand disease progression and guide treatment discovery.

GENFI is an international study that tracks families with inherited FTD to understand disease progression and guide treatment discovery.

GENFI is an international study that tracks families with inherited FTD to understand disease progression and guide treatment discovery.

GENFI is an international study that tracks families with inherited FTD to understand disease progression and guide treatment discovery.

GENFI is an international study that tracks families with inherited FTD to understand disease progression and guide treatment discovery.

GENFI is an international study that tracks families with inherited FTD to understand disease progression and guide treatment discovery.

The 10,000 Brains Project is a philanthropic initiative that uses artificial intelligence to accelerate research and treatment of neurodegenerative diseases.

The 10,000 Brains Project is a philanthropic initiative that uses artificial intelligence to accelerate research and treatment of neurodegenerative diseases.

The 10,000 Brains Project is a philanthropic initiative that uses artificial intelligence to accelerate research and treatment of neurodegenerative diseases.

The 10,000 Brains Project is a philanthropic initiative that uses artificial intelligence to accelerate research and treatment of neurodegenerative diseases.

The 10,000 Brains Project is a philanthropic initiative that uses artificial intelligence to accelerate research and treatment of neurodegenerative diseases.

The 10,000 Brains Project is a philanthropic initiative that uses artificial intelligence to accelerate research and treatment of neurodegenerative diseases.

AFTD is a nonprofit that provides information and support to families affected by FTD, funds scientific research, and advocates to raise awareness of the disease.

AFTD is a nonprofit that provides information and support to families affected by FTD, funds scientific research, and advocates to raise awareness of the disease.

AFTD is a nonprofit that provides information and support to families affected by FTD, funds scientific research, and advocates to raise awareness of the disease.

AFTD is a nonprofit that provides information and support to families affected by FTD, funds scientific research, and advocates to raise awareness of the disease.

AFTD is a nonprofit that provides information and support to families affected by FTD, funds scientific research, and advocates to raise awareness of the disease.

AFTD is a nonprofit that provides information and support to families affected by FTD, funds scientific research, and advocates to raise awareness of the disease.

LBDA is a nonprofit organization dedicated to raising awareness of the Lewy body dementias (LBD), supporting people with LBD, their families and caregivers, and promoting scientific advances.

LBDA is a nonprofit organization dedicated to raising awareness of the Lewy body dementias (LBD), supporting people with LBD, their families and caregivers, and promoting scientific advances.

LBDA is a nonprofit organization dedicated to raising awareness of the Lewy body dementias (LBD), supporting people with LBD, their families and caregivers, and promoting scientific advances.

LBDA is a nonprofit organization dedicated to raising awareness of the Lewy body dementias (LBD), supporting people with LBD, their families and caregivers, and promoting scientific advances.

LBDA is a nonprofit organization dedicated to raising awareness of the Lewy body dementias (LBD), supporting people with LBD, their families and caregivers, and promoting scientific advances.

LBDA is a nonprofit organization dedicated to raising awareness of the Lewy body dementias (LBD), supporting people with LBD, their families and caregivers, and promoting scientific advances.

Everything ALS is a nonprofit that connects patients, researchers, and technology partners to accelerate ALS research and clinical trials.

Everything ALS is a nonprofit that connects patients, researchers, and technology partners to accelerate ALS research and clinical trials.

Everything ALS is a nonprofit that connects patients, researchers, and technology partners to accelerate ALS research and clinical trials.

Everything ALS is a nonprofit that connects patients, researchers, and technology partners to accelerate ALS research and clinical trials.

Everything ALS is a nonprofit that connects patients, researchers, and technology partners to accelerate ALS research and clinical trials.

Everything ALS is a nonprofit that connects patients, researchers, and technology partners to accelerate ALS research and clinical trials.

Beyond Memory — initiated by the Kissick Family Foundation, 2025

The content on this website is for informational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment.