Reflections on the 10th UK Dementia Congress

Last Tuesday morning I excitedly boarded the train to begin my journey to the 10th UK Dementia Congress in Telford. I was looking forward to diving into the Dementia world, meeting new people as well as those I have connected with on Twitter. The programme looked fantastic and it was the first residential conference I have attended – expectations were high!

On Thursday evening I boarded the train home – flagging and exhausted, with a lot to process! My feelings during the week were so mixed.  At times I felt the buzz of enthusiasm, of future prospects; at other times I felt the despair and struggles still going on all around us in dementia care – not to mention to the health and social care systems as a whole!

A question

The Congress opened with a debate, the subject in question: has dementia care improved in the last 10 years?
Despite the immense challenges still ahead of us, it is clear that times have changed since 2005. With the rise of dementia awareness, and increased funding into research, times are set to continue changing – it’s safe to say I’m excited to be a part of it!

Reflections

I have tried to summarize my reflections in 4 points:

  1. We were given a statistic that 80% of people living with dementia live at home – I wonder why, then, the vast majority of the talks and groups at this conference focused on long term care and acute hospitals?
  2. There appeared a distinct lack of recognition of Occupational Therapy and the multi-disciplinary team. One presentation in particular boasted of multi-disciplinary involvement in looking at nutrition and dementia on a hospital ward – need I explain my indignation at OTs NOT being involved in the MDT list provided?! Aaaand breathe…
  3. There seemed to be limited focus on understanding eating and drinking difficulties in dementia, and little research about it – something that definitely encouraged me to continue with my research, of course.
  4. A positive – it was really great to see and hear about small projects springing up around the country: wards and A&E departments being renovated to be dementia friendly, a dementia home treatment team being set up and projects to make the care provided in care homes more person-centred. Another of my favourites – an excellent research project on how to use gardens in a therapeutic way, to improve the quality of lives for people living in care homes.
    Despite the sparseness of outcomes or evidence presented in some of these, what excites me is the fact that things like this weren’t happening 10 years ago. Who knows how much further these will have developed in the next 10 years, becoming so much more wide-spread?

Look to the future!

So… I encourage everyone reading this to look forward with anticipation towards the next 10 years. Sadly, the prevalence of dementia is currently on the rise, but with a continued fervour for research and an ever-increasing awareness of it, there is strong hope for improved quality of care and dignity for people with dementia… perhaps even a cure.

Reaching a phd milestone is a good time to look back

PhD Progress and Academic Advice – What I learned in my first PhD milestones

It has been a while since I last posted so I thought I would update you on my progress. The last couple of months have been primarily spent working on my 2nd milestone – the initial literature review.

What does this involve?

A lot of searching databases, a lot of reading, and a lot of learning! My conclusion: confirmation of my belief that dementia care in acute hospitals, more specifically during meal times, is a much needed and relevant research topic.

So, despite ups and downs, despair and breakthrough: the times I wanted to give up and the times I may have lost my passion and direction, I am (for now) ready to soldier on!

Relief is the best way to describe how it feels to finally submit this milestone. Pulling all the work together, and realising my final conclusion, has lifted me back up to carry on. On top of this, a reflection on the last 9 months has given me the little boost I needed.

Reflecting…

Having started in February of this year, I missed the initial research modules provided to the new starters of last October; therefore, I found myself, this October, in the ‘research training’ with a group of amazing enthusiasts ready to start their own Masters and PhD programmes. In addition to the valuable teaching from the module I began to realise something else – I actually have made progress personally, professionally and academically in the last 9 months! Being able to answer some of the worries and concerns these people felt as they entered the unknown instilled some self-confidence, in that I have the answers to SOME of the questions.

Some practical tips!

In light of my experience so far I will leave with a little advice for anyone embarking on this journey (or thinking about it):

1. There will be good times and bad, and you will not always feel positive but keep your eye on the goal and keep hold of why you chose to take this path.

2. Right from the beginning keep a record of your search strategy and reading – this will save a lot of time!

3. Use each other for support, meeting up for coffee is not a waste of time (unless it’s too often!). Often talking through and encouraging each other can give you the boost you need!

4. Value your clinical work, don’t lose focus on the reason for choosing a clinical academic pathway.

5. Finally… this advice from Dame Jessica Corner: “the first step to changing the world is to believe what you are doing is important.”

Should Clinical Practice have to be secondary to Academic Research?

The Clinical Academic pathway I am undertaking involves splitting my time, 60% academic and 40% clinical – this is often a tough ask. Priorities must be balanced and schedules carefully managed. With this split, the question often raised is this: during my PhD, is my clinical work secondary to my academic?

I would argue no!

Of course, research is important – why else would I have chosen to commit the next 4 years of my life to it? Research is essential for developing innovation, knowledge and understanding, consequently responding better to an evolving healthcare system. Undertaking the PhD will enhance understanding in how to apply research in clinical settings and to ensure evidence-based practice.

  1. I consider attaining my PhD in the next 4 years as the key to my future – so why is my clinical time just as important?
    Clinical work is what originally drew me to become an Occupational Therapist (OT) and has driven me to continue: this compassion for vulnerable individuals, and the fulfilment and satisfaction of making a difference in people’s lives. Without clinical practice I could never experience the precious moments where a distressed and agitated person connects through a calm smile, where a piece of music brings a withdrawn person to laugh, sing and dance for a few minutes. These interactions cannot be felt from the “ivory tower” of academia.
    Working effectively and compassionately with patients who have dementia is a highly-skilled role. There is no comparison to clinical practice when developing face-to-face skills and maintaining a passion for giving these people quality of life. 
  2. Clinical practice, as an OT in my case, provides a plethora of skills which pure academia could not. My current role, though not exclusively working with people with severe dementia, is still extremely beneficial. The role enables me to develop my understanding and practice of the complex needs that older people have. In order to maintain functional independence for as long as possible, someone with dementia may also require specialist seating, complex moving and handling care plans, pressure relieving equipment, mobility and functional assessments and much more. These care plans are formed and prescribed using skills which OTs need to develop in practice – not just to read about.
    Without the clinical knowledge that I have developed so far – skills that I will continue to learn and develop – I will not become an accomplished, reliable and effective leader in my clinical field.

Without the clinical knowledge that I have developed so far I will not become an accomplished, reliable and effective leader in my clinical field.
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The clinical academic route can be a lonely one, not belonging fully in either camp, and it is not without its challenges. Without doubt it takes both time management and discipline to fully commit to both, but there are so many benefits to continuing development in both fields. I am confident that through this course I will be able to contribute to the care of people with dementia in a way that is unique and makes a significant, lasting, difference.

 

Can phd change the world? Occupational Therapist mug says yes!

Ready to change the world – challenging nutritional care in acute hospitals

On overhearing a 3rd year PhD student saying that “when you start your PhD you think you will change the world but you very quickly learn otherwise, realising your work will be of little significance”, I was horrified and disappointed – what is the point of what I’m about to embark on? Why spend 4 years of my life working towards something which will not have any impact?

Perhaps with the naivity of a new starter, I fought the idea of my PhD being insignificant. Perhaps it is the naivity of a new starter which continues to drive my fight against the disappointment of not being able to change the world, but an inspiring talk from Dame Jessica Corner*, at the Faculty of Health Sciences Post Graduate Conference last week, reassured me I need not be disappointed – that I have started a journey which will create impact on the world to a lesser or greater extent. Dame Jessica advised us that the 1st step to changing the world is to “believe what you are doing is important” and that is certainly something I can acclaim to! My PhD is just a baby step, I am still right at the beginning, but I am confident that Occupational Therapy, Dementia care and reducing malnutrition are all important enough to invest time, money and effort into. There are still plenty of opportunities for my research to fill some gaps and change practice and guidelines for care!

Here are two reasons why I believe what I am doing is important:

  1. We need to listen to those in our care

So far I have found plenty of research on how to improve meal time experiences in long term care settings – environmental changes and strategies to improve social interaction at meal times, for example. There are observations and concerns about insufficient assistance while eating and drinking, and meal times being a task rather than an engaging activity in both long term and acute care. But what about the views of those who, for one reason or another, are malnourished?

What about asking and observing those with dementia in our acute hospitals to really explore and discover the reasons behind not eating and drinking? What about examining the reasons for aversive behaviours at meal times instead of brushing someone off because of their “challenging behaviour” and therefore minimising their independence.

  1. Occupational Therapy skills and the importance of a multidisciplinary approach are not being recognised for their potential impact

After hearing a talk from Dr Tara Sims** at the PGR conference and reading the papers referenced below, I have felt a renewed enthusiasm for being an OT, the impact the skills of an OT can have in care, and especially in challenging poor nutritional care. Occupational Therapists have the skills to assess and evaluate the eating process, as a vital activity of daily living, and can make significant contributions to individualised care plans. Using a holistic approach and activity analysis, we can assess the cognitive, mental, physical, social, sensory and environmental factors around a meal time experience, working with other professions to inform care.

Imagine the impact if OTs, Dietitians, Speech and Language Therapists, Nurses, Doctors and Physiotherapists all combined their extensive skills to comprehensively evaluate malnutrition and dehydration in acute hospital care – I think it’s safe to say we could change the world!

 

* Dean of Faculty of Health Sciences, University of Southampton
**Senior Lecturer in Occupational Therapy, London Southbank University

References

American Journal of Occupational Therapy (2007) Specialized Knowledge and Skills in Feeding, Eating and Swallowing for Occupational Therapy Practice. American Journal of Occupational Therapy 61(6): 686-700

Paul, S. and D’Amico, M. (2013). The role of occupational therapy in the management of feeding and swallowing disorders. New Zealand Journal of Occupational Therapy 62(2): 27-31.

Clinical Academic Research – Dementia PhD

As I approach the first milestone of my PhD – the formulation of a research question – I felt it would be good to start a record of my studies, to share some of the interesting finds and information that I come across during my time as a doctoral fellow.

So who am I?

Naomi Gallant: newly married and recently embarked on a Clinical Academic PhD with the University of Southampton. As a doctoral fellow in the Wessex CLAHRC, my research is focusing on improving quality of fundamental care for people with dementia in acute hospitals, specifically reducing the risk of malnutrition and dehydration. I’m a qualified Occupational Therapist (OT), graduating from University of Southampton in 2011, since when I have held several OT roles ranging across physical and mental health settings. Not wanting to lose these clinical skills, and realising the importance of research influencing care at the point of delivery, I have chosen to follow a clinical academic route with the aim of collaborating research and practice.

So why dementia?

There is a significant need in our society for an increase in dementia awareness. As the Department of Health (2013) highlights, society is not geared up for the increase in the condition, with avoidance being a common reaction – something which needs to be challenged. Conversations with those outside of the clinical or academic world only serve to emphasize the need for dementia awareness in people who have not experienced it within their own spheres. Comments such as “can someone with dementia really use Twitter?” and “the government have spoken a lot about dementia, it must be a real problem?” have fuelled my desire to spread the ‘Dementia word’.

So why me?

Since 2011 I have worked in a variety of settings, both as an OT and a Health Care Assistant (HCA). My time as an HCA in 2 different dementia care homes initiated my passion for ensuring optimum quality of life for people who are unable to express their needs due to severe cognitive impairment. My experience of seeing people, bed bound, in advanced stages of dementia furthered my realisation of a need for better understanding of, compassion for, and care towards these people.

As an OT I have worked in acute dementia wards, community care teams, and general hospital medical and rehabilitation wards. Despite the variation from specific dementia care settings, and despite a lot of wonderful, compassionate nursing staff, I have seen a need for improved dementia care in all of these places. The need seems especially acute on hospital wards where the environment, staff training and resources are primarily ill-equipped to face the challenge of a growing dementia population.

With all these factors combined, the opportunity to undertake this research – which could in small or large part contribute to future policy making – was one which I could not let pass me by. I hope you enjoy the insight this blog aims to bring into my journey.