Do my father’s memory problems prevent him from writing a legally binding Will?

For any will to be legally binding, its author must have (or be deemed to have had) the ability to understand the nature and effect of their will at the time of it’s writing. The capacity to understand the nature and effect of a will at the time of writing is referred to as ‘Testamentary Capacity’.

The same applies where an individual is looking to amend an existing will. He or she must be deemed to have testamentary capacity in order to make such changes in a legally binding manner.

Testamentary capacity is therefore determined by an individual’s ability to understand the nature and the effect of their will at the time that the will is made.  In the vast majority of cases where the integrity of brain function is not in question, there is no need for an individual to undergo formal assessment of their testamentary capacity.  However, where further evaluation is required in order to establish testamentary capacity, Clinical Neuropsychologists are arguably best placed of all clinicians to perform this type of evaluation and to provide expert opinion.

Having a diagnosis of dementia or any other condition affecting your thinking ability does not automatically negate your ability to write a legally binding will.  The testamentary capacity of an individual with dementia will depend on a number of matters including:

  • How long they have suffered with dementia.
  • The severity of their cognitive losses.
  • The type of thinking difficulties they experience (i.e. whether these relate to memory or language function).
  • The level of complexity of their estate.

In some cases, it may be possible to facilitate the testamentary capacity of an individual via the adoption of strategies to support their function in the affected area of thinking.

Some people get help from friends or family or simply write their will themselves.  The advantage of seeking professional advice is that a proper capacity assessment can be undertaken at or close to the time that the will is written, forming a safeguard against any future challenges on grounds of incapacity.

Where wills are challenged on grounds of an absence of testamentary capacity, Clinical Neuropsychologists may be called upon to provide an expert opinion on a retrospective basis.  In such cases, Clinical Neuropsychologists integrate specialist knowledge of the symptoms and course of brain diseases with details / circumstances of their client, to infer the likelihood of testamentary capacity at the time the will was written.

Living with Aging: Alzheimer’s, the Disease of Our Time

This interesting presentation is from TED, a nonprofit organization devoted to Ideas Worth Spreading.

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When George Perry began studying Alzheimer’s disease less than 30 years ago, few scientists knew of the condition, let alone the public, which now cannot have a day pass without new revelations in the press.

What is this disease that so closely touches all our lives and seems so intractable to treatment? Is the heightened awareness due to our increased longevity, or its incidence?

While most therapeutics are directed to the effects of the disease, the future lies in modifying responses to aging to maintain normal function throughout our lifespan.

Dr. Perry is Dean and Professor of Biology, University of Texas-San Antonio, joining the UTSA faculty in 2006 from Case Western Reserve University where he was Professor of Pathology and Neurosciences and Chair of the Department of Pathology. He is also distinguished as one of the top 20 Alzheimer’s disease researchers with over 800 publications; one of the top 100 most-cited scientists in neuroscience and behavior research; and one of the top 25 scientists in free radical research. He is Past President for the American Association of Neuropathologists, on the editorial board of over 60 journals, and is Editor-in-Chief of Journal of Alzheimer’s Disease.

*About TEDx, x = independently organized event

In the spirit of ideas worth spreading, TEDx is a program of local, self-organized events that bring people together to share a TED-like experience. At a TEDx event, TEDTalks video and live speakers combine to spark deep discussion and connection in a small group. These local, self-organized events are branded TEDx, where x = independently organized TED event. The TED Conference provides general guidance for the TEDx program, but individual TEDx events are self-organized. (Subject to certain rules and regulations.)

About TED

TED is a nonprofit organization devoted to Ideas Worth Spreading. Started as a four-day conference in California 25 years ago, TED has grown to support those world-changing ideas with multiple initiatives. The annual TED Conference invites the world’s leading thinkers and doers to speak for 18 minutes. Their talks are then made available, free, at TED.com. TED speakers have included Bill Gates, Al Gore, Jane Goodall, Elizabeth Gilbert, Sir Richard Branson, Nandan Nilekani, Philippe Starck, Ngozi Okonjo-Iweala, Isabel Allende and UK Prime Minister Gordon Brown. The annual TED Conference takes place in Long Beach, California, with simulcast in Palm Springs; TEDGlobal is held each year in Oxford, UK. TED’s media initiatives include TED.com, where new TEDTalks are posted daily, and the Open Translation Project, which provides subtitles and interactive transcripts as well as the ability for any TEDTalk to be translated by volunteers worldwide. TED has established the annual TED Prize, where exceptional individuals with a wish to change the world are given the opportunity to put their wishes into action; TEDx, which offers individuals or groups a way to host local, self-organized events around the world, and the TEDFellows program, helping world-changing innovators from around the globe to become part of the TED community and, with its help, amplify the impact of their remarkable projects and activities.

Mum and me

Filmmaker Sue Bourne’s mother has Alzheimer’s and now lives in a nursing home in Scotland. For the last three years Sue, and her daughter Holly, have been filming with Sue’s mother. Their film is a funny, charming, quirky and sometimes harrowing record of how the family have fumbled along trying to make sense of the disease.

Ethel Bourne passed away in 2011 – her obituary can be found here

NB: The film will play after a short advertisement.

Play Film PART – 1

Play Film PART – 2