Caring, Sharing & Preparing for Cognitive Impairment (inc Dementia)

‘Caring, Sharing & Preparing for Cognitive Impairment Conference’ – NRAH – 9/3/18

This presentation was one I took very seriously. There was 200 Doctors, Nurses and Medical Professionals in the room. The Conference was all about getting the 3 health networks from SA together to share information.

My presentation is 11 minutes long and there is a small glitch at 3.09 secs into the video where an incoming call stopped the recording. (Only 10 seconds was missed).

I felt privileged to be able to deliver this presentation on behalf of the families and also people with dementia. Lets hope the messages get through. (fingers crossed)

Thank you also to Ian Gladstone for his terrific presentation which had the crowd roaring with laughter. Can’t wait to interview him next weekend. Bravo

 

The Drama Queen With A Caring Heart (Dementia Story)


Here it is everyone,

Grab a coffee and a couple of Tim Tams as you prepare to listen to Linda Booth open her world to us. Linda simply ‘keeps things real…’.

Upon hearing the interview back I realized how many valuable tips and scenarios Linda actually mentioned.

Linda’s story has a ‘little bit of everything’ and in true Dutch style she refuses to ‘sugar-coat’ issues. I feel privileged to hear her talk about her thoughts and feelings at times of great stress. This interview has some nerves at the start and gets better and better with a very confronting final story.

So sit back and relax and get ready for

‘The Drama Queen with a Caring Heart’….Linda Booth

*Thanks to Zak Partington for voiceover, editing and technical assistance

Discussions in Dementia – *Coming Soon

Discussions in Dementia

Welcome to the innovative new podcast series that delves into the highs and lows of caring for people of all ages who are battling dementia.

Tune in to me chatting with everyday Australians as they navigate the ever changing landscape of dementia.

I will be talking with family caregivers, paid carers, nurses, doctors, dementia trainers & people with dementia. Each person will have a unique and different story to tell as they candidly discuss all things dementia.

Why do a podcast? …

To give people an inside look into the lives of Australians from all walks of life impacted by dementia across  ‘tell all’ 30 minute segments. You will be able to click on a link and play each interview at your leisure. All podcasts will be placed on the Dementia Downunder (DD) website for easy reference under the ‘podcast’ tab.

What is different about the podcasts?

They allow the ‘real stories’ behind dementia to come to the surface. There is so much stigma associated with dementia and these podcasts will weave across many relevant topics and even dip into some ‘taboo’ topics and traditional ‘no-go zones’.  The interview format is really informal and is pretty much a couch chat over a coffee.

Conversations are recorded at our Woodside Studio and are a great way to discover how to positively overcome the challenges facing Australian families.You can even listen to them as you drive to or from work.

SUBSCRIBE NOW! – To receive the first podcast in your ‘inbox’ when released in late January.

 

 

Diffusing Anger in Dementia Care

This post is probably not what you expect.

Am Totally Humbled…..Thankyou Dementia Australia!

Today I was honoured to be part of the launch for the new name and branding for Alzheimer’s Australia – which is now Dementia Australia.

I was able to be on stage at the national conference with executives including an idol of mine Christine Bryden (advocate). I am also on the plaque which will be featured in every Dementia Australia office in each state.

I am proud of this as it is a legacy of my Dad’s battle with Dementia and the ceremony was very touching with Prof Graeme Samuel becoming emotional on the microphone and saying to me “Your Dad would be so proud of you”. I almost lost it at this point and it was truly a magical moment in my life.

I met so many people today,learnt heaps and was able to mingle with the’ big hitters’ in Australian Dementia Care.

An exhausting but fabulous first day!

What will tomorrow bring????

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Dementia in Prison

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Dementia is really difficult… full stop. Imagine you were in prison and not only trying to survive amongst a very tough culture, but having to deal with the symptoms of dementia as well?

Dealing with Death & Dementia

Hi Everyone,

Yesterday my uncle sadly passed away from Parkinson’s Disease. I wanted to share his family story because I feel that whilst their situation is unusual, it is not unique. I also believe we can learn some things in the process in how to handle grief.

My uncle and his wife live in a country based aged care facility in a double room. The complication is that my aunty has dementia (stage 4/5), and relied on her husband to do most of their ‘thinking and remembering’. My aunty was the ‘doer’ and did all the cooking, cleaning and almost everything else, so I guess they balanced each other out. As a couple they were inseparable. The other complication is all immediate family live interstate.


My initial concern was for the welfare of my aunty and how she will cope with the loss of her husband, how she will cope day to day and her overall well-being. I decided to reach out to our fabulous ‘dementia whisperers’ ( Jane Doolette and Sue-ellen Taormina) for some valuable advice and tips. I am sure they won’t mind me sharing these tips to our DD community as it certainly is a great learning opportunity that can help families.


**Please be aware there are many different ways to handle dementia and it really depends on the individual and where they are at with their dementia. Following are some great ideas to consider but seek further advice to tailor to your individual needs:


THE IMMEDIATE (Jane):


Your aunty needs to be validated that he is gone and allowed to cry if she is upset. She needs someone (that understands dementia) to sit with her and gently (re) tell her. She needs to be part of the arrangements, seek her ‘advice’ or approval on decisions made. It’s so easy for her to get lost in the busyness of arrangements and all the people involved.

If possible she needs to go to the funeral with someone who cares and loves her and hold her hand – probably it would be too overwhelming to go back to the ‘wake’ etc unless she wants and I’d suggest no longer than half an hour and then quietly take her home.


Make sure she had the funeral card with his photo on it (perhaps 2) so that it can be put on her bedside table and that she is allowed to talk about him. It’ll be hard immediately with the empty bed and perhaps the curtains around that bed could be pulled for scheduled parts of the day.


LATER ON (Jane):


I imagine she may get moved to a single room, hopefully it’d be after the funeral but I somehow doubt that. ($ and beds). When she moves it’s really important that the new room is set up as much as possible to a smaller version of what they shared.
If she has something of his (chair or something he cherished) have that in her new space. I think that it’s important over the next 6 weeks (somewhat is considered ‘normal’ grieving time) that this grieving rituals are acknowledged with and for her.
Follow her cues but if possible talk about him, people often think that those with dementia don’t grieve or miss.


Around that time, it’s time to move forward slightly- for example, move the funeral card from the bedside to on the wall so that he is remembered but add the happy photos of him, probably when they were younger.


If/when she asks where her husband is, it is advisable to say ‘he’s not here’ (Some staff may sometimes say that her husband has passed away, whilst factual may upset the person with dementia) and try to steer the conversation to the good times eg ‘john loved his golf didn’t he?….etc


THE IMMEDIATE (Sue-ellen):


There are a couple of ways to handle the death of a spouse depending on the stage of dementia! I think in the beginning we owe it to person with dementia to clarify if your aunt will respond better to the truth or whether it would be in her best interest to just offer lots of loving support and blitz her world with lots of visuals of her husband and constant reminisce.


Sometimes it is cruel to let the person with dementia relive the shock and pain of losing their spouse, if we remind them when they forget … having said that at a stage four using the same language ie when asked “where is my husband?” staff respond truthfully – but use the same words and offer physical comfort and reminisce to help her remember.


Putting a new resident in the room with her is not a good idea either … it will make her anxious. In the past I have told the person ‘the truth’ (about the death) and gauged their reaction and then set up the way to go forward based on that reaction.


LATER ON (Sue-ellen):


It goes without saying that ongoing care and emotional support is paramount. Keeping her busy will also help with the process so she does not miss his company so much.


She would have spent most of her time with him also so fostering new relationships will be important – maybe another lady with the same interest?


Getting lifestyle staff involved can also help your aunt feel valued and not so alone.
A reminisce Book is also a good tool to help your aunt remember good times.


*Thank you for these expert insights Sue-ellen and Jane and I really appreciate your input.

Special thoughts to all my extended family at this sad time

What ‘Dignity with Dementia’ Looks Like To Me…

 

Allowing people with dementia to finish their sentences

Calling people by their name

When getting ready for the day, encouraging them to do as much as they are possibly capable

Knocking on the door…calling their name…waiting for a response…respecting their privacy

Placing yourself in their shoes ALL the time

Taking the blame for EVERYTHING

Caring for them, no matter how difficult they are

Covering them up as quickly as possible when they are naked

Respecting their feelings at ALL times

Taking the time to find out their history and triggers

Learning to read their body language

Being genuine and sincere

If they make a mistake, NOT letting them know

Protecting them at ALL times

Being there when they need you

Treating them as normal as possible

The Dementia Rollercoaster – Who’s With Me?

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The Dementia Rollercoaster is certainly not one for the faint hearted. Sometimes it’s scary, sometimes it’s not that bad. You never know what’s around the corner unless you ride it regularly. The more you take on the twists and turns the better you get at handling them. There are times of exhilaration and absolute joy but can soon be followed by terror and breathtaking moments.

Everyone is scared of a new rollercoaster, as fear of the unknown is a powerful concept. You will be proud that you had the courage to get on board, and feel good that you have made a difference to someone else.

What I have learnt over the last few years is that on the Dementia Rollercoaster you just need to strap in, hang on, and do the best you can. When you get time for a breather, tell others about your experience so they won’t be as scared.

The Dementia Rollercoaster is open to all riders, does not discriminate and the queues are getting longer each day. (Written by Brett Partington)