On Thursday i had two occupational therapists come and see me in view of having some equipment in the house to help keep me safe. Annemarie who i see monthly and she is my voice of reason. She is the voice in my head if i know i do too much 😊 And Angela. Angela is someone i used to work with when i was a nurse on the intermediate care team. But there is no other person i trust more, in fact i would trust all i worked with to look after me.

It took a lots of guts last year to get a walking stick that i use when i get wobbly. Pride got in the way a bit and i was worried how people might perceive me. I know!!! But when you are young and used to being independent, its hard. But i bit the bullet and now i have a collapsible walking stick in my handbag, like a fashion icon!! Lol

The same regarding having equipment in my house. The thought upsets me greatly, and i having been shedding a few tears of late. I feel like i am 47 going on 80. Which i know is ridiculous but its something i just have to get my head around, accept and know I am safe and still independent. Once they are fixed and i have used them a few times , like my stick i wont notice them.

My stairs are very steep so when i am tired its hard work climbing them so i am having a secondary rail put on the wall so i will have two banisters. Which will probably be helpful.

Climbing into my bath / shower is hard with perception and balance so i am getting rails on the wall and a bath board which should help hugely.

I am confiding these things to you so that if you need equipment, get it. How does the saying go Pride comes before a fall? I would rather be safe then end up in hospital because my pride got the better of me 💖

My Alien

Dementia is a funny thing. One can’t see it or feel it. And you really wouldn’t know you had it until something happens out of the ordinary and then you know.

I call my dementia the alien sometimes or the black entity other times. You know the horror film when you don’t want to go into the cellar in case the black mass gets you, well that is how I see my dementia.

Most times I forget I have it, and then most times when I feel tired I know but ignore it. I feel its waiting to say, ‘Im Here’ horrid thing.

Changes that happen are subtle as if my alien does things that I wouldn’t realise but I know. I know my body and mind.

I have eaten apples every day for 20 years, loved them. Gala Apples are my favourite as they are crisp and juicy. Now I don’t like them – strange I know. I don’t like biting into them, the texture against my mouth, the crunch I don’t like. I buy them out of habit and then they go off. If I cut them into wedges and into smaller amounts then that is fine.

There is a poem called ‘Apples’ in the book ‘To Forget With Grace’ by Jacqui Peedell and Jo Davies. Jacqui lives very well with her dementia and wrote this book of poems which I bought from her when we met at the Alzheimer’s Show. I understand where she is coming from, when I read her poems. Her book is available on Amazon on 20th June.

The same with carrots. I used to love raw carrots but against don’t like them now and if I cook them they have to be really cooked whereas in the old days I used to like a bit of crunch to them cooked.

I don’t like the smell of raw meat now. Last time I did a chicken casserole, I felt sick preparing it. Never had that problem before. After I cooked it, I threw most of it away as the smell was still up my nose.

Colours are getting more and more confusing. If I am playing a game against the computer where you shoot the balloons down, colours change in front of my eyes and its frustrating to say the least. I have just found out that I can change the colour of the keyboard on my phone. So it’s now blue with white letters and I can see it better.

I have also taken the predictive text off the phone and I am less stressed now, which is strange cause I used to love the predictive text before the alien took over my brain. Words get muddly as it is without adding to it. I get frustrated when the grammer police get on my case whether a word is spelt correctly, or the right or wrong word is used in the right category. Does it matter?

The English language is complex as it is. Which, witch, bare, bear, i before e except after c is the only thing I remember. Those versus they. I always think its a bit like the French language, la versus le, is something feminine over masculine. What makes a book le livre masculine. Yet La Chemise – feminine. Language is complex indeed.

No wonder we have trouble with our speech and language. When we have dementia.

Yet, despite all the weirdness my alien tries to fool me with I love my life. So I obviously am still beating that little horror. Every day is a blessing

Pilot Decision Making Tool for GP’s (UK)

I got word recently that there is a pilot decision making tool for GP’s in the UK going out this year. This is to aid Dr’s to make a diagnosis in dementia in younger people. I have looked at a copy of the tool in question and its amazing.

I think back to how I got diagnosed and what a fight I had to get anyone to believe that there was anything wrong because of my age at that time. 45 …… Stress and depression were bantered about and although I was under stress with my job I knew my signs and symptoms weren’t caused by stress.

This tool is a long time in coming and I am glad its here to help new patients my age. Hopefully it will help Dr’s not put everything in a box as well.

At the moment if I have to see my Dr and I do try not to, the first thing they say is ” How do you know what you have is nothing to do with your dementia?” As if to say, now when you have anything wrong its the dementia’s fault and we can’t help you!!!

This response is very frustrating and it takes all my effort not to walk out and never go back for this is what I really want to do. Last time I went, they blamed the symptoms of my menopause on the dementia!!! What!! Lol!! Then they took note when I told them what my symptoms were.

I have to say on a positive note that the nurses and nurse practitioner are fantastic and I usually see Sue over the Dr’s any day. Sue always asks how I am coping with my dementia after i have spoken to her about whatever I have gone there for which shows she cares.

Hopefully this new tool will help my GP’s as well.

(The link to the tool is here

There is a feedback survey too on the webpage & all comments would be gratefully appreciated so the final version of the tool can be made the best it possibly can be)

Arts and Dementia Conference

On the 9th March 2017 I went to London with a fellow friend Dianne and our lovely student Kristina (I usually call her Katrina so I hope I got it right) to the 1st International Arts and Dementia Research Conference.

I was dreading going 1) because it was going to be a really long day and I get tired quickly 2) the trains being as busy as there are that time of morning and 3) people being as busy as they are in London. Lol!!

I got up at 5.45am and had already booked a taxi the night before to take me down to the station as no buses run that early. Managed to get seats on the way to London, once there we went on the Tube which I hate. Not because I have dementia, I would have hated it before as well. All those people squashed together like sardines, we really couldn’t get on the first two trains and then Kristina grabbed my hand and got me onto the third train, standing, squashed and bless she was really good. Kept asking if I was okay. If she hadn’t had pulled me on, I would still be waiting I think!!!! Lol!!

We got to Portland Place on time just a little before 9am, so that was good as I hate being late for anything. There was coffee, tea, water and juice, with biscuits on arrival and we had to register and was given a name badge. Then we were told that we had to choose a room to sit and then stay in that room all day, so we weren’t too happy about that. We got sent a programme, beforehand, of different talks that were happening and we marked down what ones that interested us and they were all in different rooms. So, we thought that was bad planning on their part for not making it clearer. However, in the introduction speech we were told we could go to whatever talks we wanted to, space allowing, so that made things easier.

Portland Place dates back to 1775 and is a beautiful historic building. I wanted to take some pictures of the ceilings to show you but it was really hard to do it discreetly. There were large chandeliers hanging from the ceilings, showing beautiful colours when the sun shone on them. There were five different rooms all with different décor and just stunning. We went into 4 of them, Heggie, Sainsbury, Harben and Founders.

We started off in the Sainsbury Room where we were welcomed, followed by a talk by Anne Basting, an American professor from Wisconsin – Milwaukee. And I liked her talk very much. And she was my favourite speaker of all I think. Probably because she proactive in bringing positivity about dementia. She has written a few books ‘Forget Memory: Creating Better Lives for People with Dementia’ is one.

Anne has also completed numerous projects including The Penelope Project which focuses on Homers Odyssey and was based at Luther Manor Retirement Community. There are about 700 residents and they all got involved somehow and when it suited them, which is nice cause they had the choice.

This is Anne’s site if anyone wants to look up any more of her projects. All of her projects encouraged interaction from others living with dementia and I like that a lot. The thing I remember more about what she said was “Your Story is my story” and “beautiful questions” meaning all questions which are asked to others which are open are beautiful cause they encourage a person to open up about themselves whether it’s a little or lot. All her projects have positive impact on others.

We had a coffee break and then we went to the Heggie Room. The talks were 1) about ‘play’ and people living with dementia, about them living in the here and now, living in the moment. 2) Remembrance Dance, something that is happening that encourages good quality of life for people living in nursing homes with dementia by the power of dance. They said that in Denmark, all children learn dancing at an early age and these dance skills can be recognised even if nothing else is. The body remembers what the mind has forgotten. Then someone from the Aged Exchange spoke about improving the wellbeing of people with dementia. All easy to follow and understand and I felt at ease then. I wrote simple notes to remind me of different things. The speakers were from USA, Netherlands, Denmark and UK.

Then we had lunch which was provided. A choice between hot and cold and there were gluten free choices as well. Plenty of fluids were provided as it was a beautiful day outside and hot inside.

In the afternoon, we split up and went to different talks but it got more complex as it was more research based stuff in the afternoon. Someone told me to let it wash over me if I didn’t understand it which helped me a lot. The only talk I was interested in was Creative stimulation: Living with dementia and I was a little bit disappointed as again the ethos was concentrating on the elderly population living with dementia. The whole day was centred round it to be quite honest and us, young ones living with dementia got forgotten.

We had one more talk to go to and then we ended on a hour long discussion which was a bit complex and Dianne and I looked at each other numerous times and we got lost. But my ears picked up something that was said about carers and nursing, then I joined in the conversation and it felt fine.

We had an evaluation form to fill out. It’s a shame only Dianne and I went as those living with dementia. The conference was open to all. It was quite nice to network and we got chatting to someone who found it interesting that we did talks to post diagnostic groups. My bugbear was that it centred on the elderly over young. I have also suggested that it would be nice to have a speaker who lives with dementia who is involved in something creative. Next time Dianne and I said we would stay in London and go to the second day as well as that looked interesting.

All in all, it was a really good and interesting day and I was pleased I went in the end. I got home at 20.40 in the end. Today is a restful day.

New Research Project

Yesterday, a few of us went to a meeting at our local health centre. We met a young researcher from Oxford who was collating research on how to make travelling on public transport better for everyone, especially those living with dementia.

It was interesting cause she listened to our experiences when we use buses or trains.

Like I always have to sit near a bell on the bus, but then so does a few of us. Or how complex it is catching a train, especially going to London where it’s so busy and manic. She was interested in what sort of technology we use to help us in getting through life. For me, i use Google Maps a lot, my calendar on my phone is my lifeline and I use Google a lot, How do I……… is typed a lot as have no clue otherwise.

This researcher and others are trying to devise a device or app that will help us use public transport in the future. So it’s a case of watching this space. We said we didn’t mind trialing it when it did come out.

I like anything that is positive and this is hugely positive 💖

Talk about Living Well with Dementia

Yesterday, I did my first talk of the year. I always get nervous beforehand and I always feel relieved when it’s over and I have no mishaps. I never know how the talk will go and what I talk about until I do it as I like to change it about a bit.

The microphone was a bit hit and miss as usual!! 😂 😂 I have yet to give a talk where the microphone works really well. But it’s all experience!!! 😜

I just advise people that they can live well with dementia. Never to give up, Adapt and always retain a sense of humour. I don’t suffer with dementia, I live with it. It’s a matter of perception.

I recited one of my poems and sold a few of my books. I am in awe that people want to read and buy my books, and that people want me to sign them which I find strange but nice as well.

The Three P’s – Positivity, Perseverance and Patience

We are all capable of doing great things. Its just a matter of mind set. I understand or know that for some people its really hard to look beyond what is wrong with them and see the positive over the negative. We are all different, unique beings.

I came across this quote today and thought it was apt in this place and time. It’s by Francis of Assisi

“Start by doing what is necessary; then do what is possible, and suddenly you are doing the impossible”

So for me for example, I did what I had to do when I first got my diagnosis, retired from my job, stopped driving and looked into how I could fill my time, and worked on old skills that were hard to do. Like computer skills, cooking skills etc.

I joined groups, started to write in a way to make my brain work, in a way to stop me forgetting words, and I still hand write after a fashion so to keep the skill going.

I join groups to speak and meet others, my speech and thought processes work hand in hand and sometimes I forget what words I need to say but I work through it. Perseverance for me is the key, no matter what.

Now I have written a book which for me I did the impossible, and used my own photos in the mix. Double Whammy!! Might not be brilliant in some peoples eyes, but it doesn’t matter as words are just used to help my brain. And if it encourages others to keep going, so be it.

Remember we are all capable ~ Positivity, Perseverance and Patience (lots of that) ♥

Be your Own Fighter

Today which is Thursday, I went to CST in the morning and we did quizzes. You always think that you don’t know anything, but we know a lot more and it always surprises me.

Like What is the largest ocean? What is the capital of Greece? We remembered all the answers to those sort of questions. Amazing what our brain can retain and keep. I just wish I could retain others things apart from general knowledge.

Then this afternoon we went to a Dementia Action Alliance meeting in Hythe, at Age UK. It was mostly talk about getting businesses to become dementia friendly which is really important. I like going to these meetings as getting used to seeing people I know and meeting new people. And although they are all professionals, they listen to what we have to say. And listen to our point of view what is important and means a lot.

Out of the blue I was asked to do a book signing at a dementia Awareness day on 20th May in Hythe, I feel a bit strange that people want to read my book and get to know me, but at the same time I also feel excited and pleased as well. It’s a point that I want to get across that we are all special in our own way.

Life is hard sometimes, but we all have to find our own niche in a way to survive. This is my way of fighting against the alien in my brain 💖

Acceptance is the key

I am usually okay with my dementia. I have accepted it a long time ago, and if people don’t get it then its their problem. But what I don’t like is when someone makes me feel stupid because I just don’t remember. It’s not my fault. Yes, I am young, yes I have got something wrong with my brain, yes I do have dementia.

I had to catch a train this morning. I didn’t have to go too far, two stops and I was there. I get nervous getting trains. The stations are usually very hustle and bustle, too many people. I got my tickets and then couldn’t remember what to do with them and the ticket gate. Do they go through the top hole or the bottom hole? I felt myself getting hot as this meant I would have to ask someone.

Perceptions are a funny thing. We are all human beings and make snap judgements without realising we do it. The man at the gate who worked at the station, did just that. I could see it in his eyes, and the way he smirked when I asked him which way my ticket went. I patiently explained that I had dementia and just couldn’t remember. No big deal. But instead of just telling me and thats that. I took my ticket from me, sighed and did it for me.

I wanted to ask him if he had had training about dementia and dealing with someone with dementia. But was more worried about catching my train. In the UK, the government is very hot about rolling out dementia training for everyone in business.

I just felt frustrated today by the whole experience.

Never give up on dreams

i-am-still-me-bookWell, my book has come out today on Amazon and Authorhouse. I feel so proud of myself. I never, in a millions years, thought I would write a book of poems when I first got diagnosed with dementia. It’s a book of poetry some pertaining to my dementia, but most about life in general or nature. There are about 20 photos in the book as well. I chose the cover because I love nature and trees, and the trees losing their leaves remind me of my brain. I want to tell people never to give up, on anything 💖