Community Achievement Award 2017…This one is for Dad

OMG!….Am blown away today…..I have just found out that I am a semi finalist in the SA Community Achievement Awards 2017 – ‘Carers SA Carer Achievement Award’.

I am really humbled and proud to be nominated and be amongst the finalists for the last round of judging happening real soon. This award is dedicated to my dad who inspired me for a lifetime.

Whilst ‘Dementia Downunder’ is not about awards and accolades, the real reward for me is sharing your stories, removing the stigma about dementia and creating culture change.

Awards dinners are fantastic opportunities to spread the good word about ‘DD’ and get dementia care back on the agenda!

Time to get the best available care for our most vulnerable members of our community.

Bring it on!

#SACAA

Consumer Guidelines Video ….Out Now!

Very proud of Louise Heuzenroeder and her work with the consumer guidelines. Louise has created a video and a valuable document that makes things easier for consumers to navigate the care of a person with dementia.

The consumer companion guide entitled – ‘Diagnosis, treatment and care for people with dementia: A consumer companion guide’ has been developed for members of the public to complement the Clinical Practice Guidelines and Principles of Care for People with Dementia.

The pic above features Dementia Champion Louise Heuzenroeder and Dementia Advocate Ian Gladstone.

Click the link below to view the video (it may be slow to load). ‘Dementia Downunder’ is represented at the end of the video.

http://sydney.edu.au/…/cd…/resources/dementia-guidelines.php

Dementia Care 2017 & Beyond…..My Blueprint for Positive Change

*Warning – The following post contains my own personal opinions on dementia care in 2017 and beyond. It is not intended to be disrespectful to anyone but more so spark ideas and some action in the community. Is this post emotional and created without complete knowledge of the politics and every single aspect?…Absolutely!…. Dementia is important…Dementia is different….and with me….. “It’s Personal!”.

The Blueprint:

• Government to acknowledge and address the growing tsunami of people with dementia and allocate adequate funding and resources to match.

• All hospitals to consider new pathways into the ED (Emergency Dept in Hospital) for older persons and especially those with dementia. Lighting, sound, environment, staff training all to be considered.

• Set up a Dementia Taskforce in each state to plan for the future, and have strategies and initiatives being discussed NOW.

• Have strategies to reduce ‘Code Blacks’ and have restraint as a last option, not a first option.

• Create purpose built dementia related facilities to cater for people with BPSD and other difficult conditions that cannot be handled by aged care facilities. (similar to Ward 18 and GEM units)

• Research for a cure is really important but so is managing the 400,000+ people already with dementia in Australia. Maybe the funding allocation for caring versus research should be reviewed? (I am not across the %’s here)

• Acknowledge and start genuinely caring for people under 65 of years age with dementia (younger onset dementia) and have age appropriate facilities for them in a central location (in four directions may be a bit unrealistic at this stage). The facility environment should be conducive to younger people and the person with dementia be considered with every single decision. No more people under 65 with dementia being placed in nursing homes.

• Aged care facilities to allocate their most passionate and best qualified carers to the people with dementia requiring the most care. Eg BPSD, Stage 5,6,7, and those in Memory Support Units. These people are so vulnerable and need the best care we can provide from those who want to be caring in that space.

• Media is to be encouraged to no longer promote false hope for families and stop writing about snake oil cures and listing off things that ‘may’ help with dementia. If there is no actual proof that something works, then it is not news.
• Encourage real life stories and personal accounts to be published in the media to create awareness. The ‘lived experience’ is really powerful and cuts through as it is genuine and sincere and demonstrates the hardship on a grass roots level.

• Our security teams in hospitals and dementia related facilities to have extensive ‘dementia specific’ training and formulate a different protocol for handling people with dementia.

• Stricter rules on ‘driving with dementia’ – The declines can happen rapidly and someone who is driving ok this week can end up driving through a shop window the next. This could save lives.

• Disabled toilets and bathrooms to cater for ‘people with dementia’ (and their caregivers) equally to other disabilities. Eg. space & equipment for carers within bathroom, appropriate and dignified signage etc

• Public spaces eg parks/playgrounds could all become ‘Care Parks/Playgrounds’ (or something similar) and facilitate everyone with a disability or cognitive impairment. One standard policy that covers everyone. We should all be considered and treated equally.

• Dementia will eventually be the no.1 leading cause of death in Australia (currently 2nd)….We need to prepare NOW.

Outdated Disability Signage….A Sign of The Times?

I have been thinking about current signage for people with disabilities and I believe it’s about time for a review or better still an overhaul. Our airports, shopping centres and the like use ‘the wheelchair’ as a generic symbol to represent disability.

My point is that ‘not all disabilities are visible’ and is the wheelchair symbol relevant in our complex and diverse modern world? What about people with cancer, down syndrome, diabetes, dementia and the list goes on. I certainly am not downplaying or discriminating against people in wheelchairs but moreso calling for a positive and unified NATIONAL SYMBOL that encompasses anyone requiring ‘extra assistance’.

While we are at it….. the word ‘disability’ is so condescending and immediately puts people on a lower rung. We must treat everyone with respect and dignity, and here would be a great place to start.

I remember in the 80’s when businesses were rapidly installing the long overdue wheelchair access ramps and rails etc, but times have changed and so have the requirements. The amount of people with dementia is rapidly rising and with no cure and constantly diminishing funding something is going to give.

Wouldn’t it be great if our councils, charities and service providers could work together towards common goals such as parks and playgrounds that combine relevant equipment, signage, fencing, pathways and most importantly bathroom facilities. Perhaps we should call them ‘Care Playgrounds’ and ‘Care Parks’ and have an ‘all inclusive’ mindset where all people are considered in the planning? Combine funding to build better quality facilities and get better results may be a better option also?

I have heard about some airports calling their disabled toilets ‘Accessible Toilets’ which is a positive step forward in the interim…but can we do better than this?

Our airports now offer ‘prayer rooms’, wouldn’t it be great to have several accessible ‘quiet rooms’ for whoever needs them? Knowing the requirements of people with dementia this would certainly be a better use of resources amongst a busy and confusing environment, and once again be ‘all inclusive’.

Brisbane airport is leading the charge with training programs, signage changes, and more overall awareness. Let’s hope we can extend the push into other areas and start looking after everyone equally. The Hills Councils, Community and Dementia Workgroup are working on a Dementia Friendly Park in Mt Barker as well.

Something to certainly ponder….

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Muffin Robbery Causes Chaos at Men’s Group

An incident occurred today at Men’s group which could have had catastrophic consequences. Feisty Fred the grumpy 95 yo resident had dozed off while painting one of the indoor golf boxes today. Fred had been unable to hold his paintbrush due to his self confessed condition of being “almost dead”, and proceeded to tell me he “couldn’t give a stuff!” then nodded off.

Nifty Neville the 70 year old resident (a former doctor) saw an opportunity to reach across and steal his muffin. I watched the theft take place and decided to keep the peace by not declaring that I saw him take it. Seconds later Fred woke up, looked at Neville (who was grinning like a cheshire cat) and noticed crumbs on his chin. Fred then let out an an almighty spray aimed at me. He said “Why don’t you go and punch this bastard in the the nose, he just stole my muffin!”. He then said “If you don’t belt him I will, I wanted that muffin!”.

I decided to leap into action and promised Fred I will source him a brand new ‘extra fresh’ muffin just for him. I ran to the kitchen but no-one was there, the morning tea trolley had left so I was forced to run to another wing of the aged care facility and beg for a muffin. Luckily they complied and I raced the muffin back to Fred.

Fred moved his new muffin to a safe place on the table before devouring it. He did zero painting today but I guess he was engaged in the group indirectly and a brawl was averted…..This is Dementia

Magical Moment at Memorial

Last weekend would have been Bob’s (dad) birthday weekend so as a family we had a private memorial for him, complete with a Skype linkup via laptop with my brother’s family who are currently in Bali.

The memorial was absolutely amazing in more ways than one. My Mum (Jan) arranged for all the grandchildren to release a white balloon each in honour of Bob.

What happened next was bizarre….

After we all released our balloons we counted them in the sky and watched them all float away together until they could no longer be seen.

We started playing tennis about 20 minutes later and were having some family fun when we all noticed one of the white balloons had returned and was floating around the backyard.

How could this be when all the balloons had literally travelled kilometres?

I don’t normally believe in ‘signs’ from above’ but it was certainly a magical moment that made our day😀

Secret Men’s Business…Uncovered

Men’s Group brings me new challenges each week and I guess that is why I like it so much. I wanted to share another dynamic that comes with Men’s Group and that is ‘interacting new residents into a group’.

This week I had a new resident come and join us, his name is Harry and he is an absolute gentleman. He reminded me of my Dad in the way he dressed, and the way he communicated. I go and collect him from his room and introduce myself, and at this point I am rapidly assessing his capabilities. I shake hands with Harry and ask a few ‘safe’ but searching questions. I only have a few seconds to determine the following:

• Can he communicate ok?
• What is his level of cognition?
• Is he agitated or aggressive at all?
• Can he understand what I am saying to him?
• Does he have insight to where he is at with his dementia?
• Do I need to bring anything he might need or want? Eg a jacket or comfort item.

As I walked Harry over to the group we would talk casually about sports and his business life. Straight away he tells me is a member of a golf club. I then list off other sports and he said he used to play football. Instantly we have common ground and we are reminiscing. He is happy to be with me as the conversation is in ‘his world’.

I offer to play some indoor golf with him. He refuses and makes up an excuse. (This is common behaviour in a new group). I then set up the golf box and clubs and get Harry to help me carry the clubs. I set up balls on the ground and hand him a club, he once again refuses. I then realise that Harry recognises the game but is probably worried he will play it wrong or embarrass himself. I then arranged another resident to putt some balls in front of Harry so he can re-connect with the skills required.

I gently pass the club to Harry again and ask him “you sure you don’t want just one go?”. He refuses again politely and gives me an excuse. I then decide to start putting some balls into the golf box. Harry gets all excited when a ball goes in and he congratulates me. It happens again and he starts cheering and telling others. He is now engaged in the game. I then make an excuse to do something else and I ask Harry if he would mind holding the club while I attend to something else. (I have already laid out the balls on the floor). As I go to walk off I say to Harry “you may as well have a quick hit while you are there holding the club?”. He then putts and the ball goes in the hole. The group erupts and cheers. He putts again with same result. He is now on a ‘hat trick’ and once again he gets the ball in the hole. Everyone cheers , we make a huge fuss of Harry and feels part of the group.

As we were doing painting as well yesterday I tried to get Harry involved with this. Once again more refusals and excuses. We then agreed that he could just observe today so he politely agreed to sit at the table and chat with all of us. The conversations were fantastic and was a ‘huge win’ as even if the man does not do the activity we are interacting with each other and chatting about memories. The group also changes and becomes more interesting. I purposely placed paint and a brush in front of him should I get the chance to get him to try painting. I offered him the brush once again he refused. I have worked out that the key is to be side on to the men and act as casually as possible. My body language is always making the resident feel in charge and I am trying to be ‘one of the lads’. I then ask Harry if he could hold the box for me while I paint . He jumps at the chance to help me and does a great job of steadying the box. He compliments me on my painting skills and he has a smile on his face.

The message I wanted to share today was that in lifestyle activities it is possibly best not to give up when a resident rejects an activity. We need to delve into how they are feeling and determine why they are refusing. The key I have found is to be subtle and allow the resident to be in control. Almost tempt them into participating with strategically placed items and allow then to never fail. We need to set them up for success each and every time. Once again I am blown away with how people interact and engage. What an amazing classroom we have ?:)

‘Team DD’…Take a Bow!

I just wanted to take this opportunity to thank all of our fabulous ‘DD’ members for your input, support and stories, and for just being an integral part of our amazing community.

The ‘magic’ of Dementia Downunder cannot happen without such a positive and supportive mindset, and without such a sincere and caring environment.

I often get asked what makes Dementia Downunder different?… I tell people that we are initiating conversations that were previously stigmatized, taboo or swept under the carpet. There are not many groups having the raw and sensitive conversations we have across such a diverse range of people, professions and sectors. We are also creating collaborative solutions to problems that have been around (and many ignored) for decades.

This myriad of perspectives, shared feelings, feedback and information is actually ‘bridging the gaps’ in our under-resourced health care/aged care systems. Our ‘people helping people’ philosophy continues to defy the odds when so many situations are ‘road-blocked’ due to lack of funding.

I also wanted to share that I am involved with some proactive working groups now that are making some big changes to the way we care for our older people, and those with dementia. I want to thank my mentors, close friends and associates (you all know who you are and I can’t name you all as I don’t want to miss anyone) who all have helped ‘Team DD’ make a difference.

Thank you!….

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

No-One Should Have No-One

Today the very ‘glamorous’ Linda Booth and Brett Partington presented at the Loneliness & Social Isolation Symposium at Morphettville Racecourse’s Phar Lap Room.

We both put ourselves out there once again with our ‘heart on our sleeve’ speaking styles. There was a big crowd of 160 very receptive people.

‘Blinged Up’ Linda Booth was the hit of the day with her generous offer to give out free hugs to everyone in the room. (with a gentle push from me and a very big cardboard sign)

Thanks to the very innovative and professional Judith Gooden for inviting us to present. It was a fabulous opportunity to promote the benefits of ‘Dementia Downunder’ and share our stories about dementia to reduce loneliness and social isolation.

Congratulations to all the other fabulous presenters who gave up their time to speak today.

Welcome to all the brand new members who have joined ‘DD’ today from the Symposium.

Overall – a great initiative from SA Collaborative Projects.

PS – Thank you Linda for allocating me to receive above the regulation amount of your famous hugs.

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