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BBC to Air Documentary on Former Rugby Player with Motor Neuron Disease 

The British Broadcasting Corporation (BBC) is set to air a documentary that highlights the experiences of a former professional rugby player who was diagnosed with motor neuron disease (MND).   Rob...

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AFTD Advisor M.-Marsel Mesulam Appears in Podcast to Discuss Recent PPA Study 

Medical Advisory Council member M.-Marsel Mesulam, MD, recently appeared in an episode of The Brain Podcast to discuss a recent study on primary progressive aphasia (PPA) and offer insights on the...

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“Forget Me Not Village” Aims to Bring Dementia Village Model to Rural U.S. 

A recent article in The News Review spotlighted the founder of “Forget Me Not Village,” a care facility that uses a “dementia village” model to give residents significant freedom in a comfortable,...

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ADDF Chief Executive and Chief Science Officers Discuss Advancing Dementia...

Alzheimer’s Drug Discovery Foundation (ADDF) Chief Executive Officer Mark Roithmayr and co-founder and Chief Science Officer Howard Fillit, MD, discussed advances in diagnostic methods for Alzheimer’s...

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Pilot Study Looks into Benefits of Therapeutic Exercise for People with PSP 

A study published in Frontiers in Neurology investigates the benefits of a tailored, therapeutic exercise program for people with progressive supranuclear palsy (PSP).   PSP falls into the category of...

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Study Describes Motor Sign Phenotypes of People with Genetic FTD 

A study published in the journal Neurology sets out to describe observable attributes and patterns in motor signs (known as motor sign phenotypes) associated with genetic FTD, and to investigate their...

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Researchers Identify Key Proteins Involved with Development of FTD 

Researchers at the VIB-KU Leuven Center in Belgium have identified proteins involved in the development and progression of FTD and amyotrophic lateral sclerosis (ALS).   The researchers hoped to...

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Veteran Reporter Writes About Living with Primary Progressive Aphasia and...

Ian Black, a former editor and reporter for The Guardian, recently wrote an article for the newspaper sharing his experiences getting a diagnosis for and living with primary progressive aphasia (PPA)...

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National Family Caregiver Month: AFTD Comstock Respite Grants and Self-Care

FTD can be exhausting for people with a diagnosis and care partners alike. The around-the-clock work of caring for someone with FTD can lead care partners to neglect their own needs, leading to...

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Support AFTD’s Mission with a Year-End Gift

AFTD was founded 20 years ago with a single donation. Since then, the dedication and generosity of our volunteers, donors, and partners has enabled our growth to better meet the needs of all who face...

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