Question Time for Carers... Week 2...Only 1 Question?

NotTooLate

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Jun 10, 2017
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Hi @Lizbuff

A retired teacher, you didn’t say. A very undervalued profession. So many finding out now that it is not that easy. They should all be paid double and given a house by the sea on retirement! By the way, did I say I was a retired teacher too!? :rolleyes:

Interesting about the loss of skills using things like the printer and PC. I find sometimes I sit here and for a while I can not for the life of me think how to do things. It is usually programs that I have been using for years. I write notes a lot now as prompts.

It seems that she was very active, but slowly she stop doing the things she liked doing. I can only assume that she found it harder and harder to do those things?

I think there is a point where decline becomes a one way journey. The problem is we can’t really say when that is, but that is why I think it is important to recognise and get help as soon as possible, but doctors seem too quick to dismiss any idea of dementia.

The final point you make, hit a chord with me and I had to stop writing for a bit; ‘She isn’t a child, but she is as emotionally and physically vulnerable!’

I hear a lot of how harsh, changed, hurtful and different we are, but inside we are all, emotionally and physically vulnerable too!

I hate what I’m becoming, but I feel it all!

Stay safe and keep well!

Richard
 

NotTooLate

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Jun 10, 2017
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Hi @countyboy

At 77 you seem to be doing well and that certainly gives me hope!

Do you think there was anything different between you being diagnosed with Alzheimer’s and then FTD, I take it you still had the same treatment?

I’ve just been looking at you first post, where you mention the obvious factors taken into consideration when diagnosing dementia.

Your age. They will tell you again and again, dementia is not related to age, but we all know that it is, otherwise why is this a factor?

2. Type of dementia. Ok, if you have symptoms that can be classified as a certain type, does that help? Is the treatment different? Is one more important, or devastating than another?

3. Underlaying illness related to dementia, What and how does this help?

4. Other health, or medical issues. This is the one area that I think has less attention, but is one of the main areas that could have a positive impact. I think the dementia symptoms are by their very nature symptomatic of another health, or medical issue.

I agree that these, as you state are used in the diagnosis, but you have to ask why?

Your post certainly give me hope that statistically I don’t have to worry so much! ?

Stay safe and keep well!

Richard
 

NotTooLate

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Jun 10, 2017
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Hi @Wifenotcarer

Like the name!

So, was there anything before the signs of short term memory loss, such as illness, depression, drink, drugs, accident, injury, or fall etc?

I’m sure the fall didn’t help. Another one of those things you hear again and again; someone has a fall and demential symptoms get worse.

Interesting about the stroke thing… so you and the doctor thought it was a stroke. Did he show signs of a stroke, face down one side, slurred speech etc?

So, what did they say cause the onset of the disability problems that followed?

How are you both coping now?

Stay safe and keep well?

Richard
 

NotTooLate

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Jun 10, 2017
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Hi @Dimpsy

Isolation and loneliness, bad thing when you are not use to it! This together with an active life, with work and friends and teaching many crafts, the change must be so much to deal with. Do you think Mum became depressed? Did the doctor help in any way?

It is such a shame when you seem to have nothing to carry on for. Dad dying must have been the final blow. It does seem that moving in with you has had a major impact on her life for the good. I’m on Donepezil too, but not sure what it does, as for your Mum, I think being with you has given her the contentment she needs.

I believe that physical and mental issues earlier in life can be a trigger to later dementia symptoms and think this is what you are clearly saying too. I just wish more was put into research for this.

Stay safe and keep well!

Richard
 

NotTooLate

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Jun 10, 2017
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toolate.blog
Hi @annielou

You say your Mum was lonely and a bit depressed, but you don’t think this could have been a possible cause? Was your Mum on any medication?

I’m also interested in the symptoms were noticed after the cataracts. Did she have any operations?

Normal ageing, is one of those things they will say has no real bearing on dementia symptoms, but we all know they do, in part that is.

Stay safe and keep well!

Richard
 

NotTooLate

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Jun 10, 2017
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Hi @Sam Luvit

No apology necessary!

I believe whole heartedly that every close family member of anyone suffering the symptoms of dementia, should have full access at all times!

This is not a question of law, this is a question of morality!

I’m afraid that it seems that once a, ‘Care Home,’ or institution takes over, then they acquire all rights, or that is what they think.

For the loved ones being removed into an alien environment, I should imagine the shock is devastating and would certainly make any problems far worse. If those that are close and have always been there, are now replaced by unknowns, that have no connection, then hell must ensue.

I’m hanging on, but if I was suddenly to wake alone, helpless and lost, I wouldn’t be able to cope, but the main thing is…. I wouldn’t want to cope!

Stay safe and keep well!

Richard
 

Dimpsy

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Sep 2, 2019
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Hi @Dimpsy

Isolation and loneliness, bad thing when you are not use to it! This together with an active life, with work and friends and teaching many crafts, the change must be so much to deal with. Do you think Mum became depressed? Did the doctor help in any way?

It is such a shame when you seem to have nothing to carry on for. Dad dying must have been the final blow. It does seem that moving in with you has had a major impact on her life for the good. I’m on Donepezil too, but not sure what it does, as for your Mum, I think being with you has given her the contentment she needs.

I believe that physical and mental issues earlier in life can be a trigger to later dementia symptoms and think this is what you are clearly saying too. I just wish more was put into research for this.

Stay safe and keep well!

Richard

I think you are right, loneliness can lead to all sorts of mental problems and I'm positive mum was depressed by the time dad died. Her attorney at that time showed no interest in mum's welfare and deliberately ignored any suggestions from me to seek medical help.
When mum moved, she was having major panic attacks and nightmares, but over time they have faded and she has stayed mentally stable, apart from a chest infection at Christmas which knocked out the memory of how to shower herself.
What I have picked up on from this website is how quickly some people go downhill, whereas for others it's a slow fade to grey and I wonder why that is. I know the time will come when we see a decline but in her 90th year mum is holding her own.
Best wishes to you and thank you for raising such an interesting topic.
 

NotTooLate

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Jun 10, 2017
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Hi @Dimpsy

Progress of dementia symptoms is dependent on a few things, but others may say there is a whole lot more. Dementia is related to the death of brain cells. As more brain cells die, the symptoms develop. When you end up having too few brain cells remaining to keep your mind and body functioning, then rapid decline follows, Along with this is what damage there is in the brain and what parts are affected. This means that the effects can vary in both duration and signs and symptoms.

They can categories types of dementia, or change, add, or amend a diagnosis on how your symptoms change, the change in scans and how the dementia is progressing.

I think your description is so apt! Some go quickly downhill, while others fade to grey!

Some like me, plan to stay in the light as long as we can!

All my Blog Post are here....
 

annielou

Registered User
Sep 27, 2019
1,917
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Yorkshire
Hi @annielou

You say your Mum was lonely and a bit depressed, but you don’t think this could have been a possible cause? Was your Mum on any medication?

I’m also interested in the symptoms were noticed after the cataracts. Did she have any operations?

Normal ageing, is one of those things they will say has no real bearing on dementia symptoms, but we all know they do, in part that is.

Stay safe and keep well!

Richard
Short answers
Mum said for a long time that anything she forgot or mixed up was because she was old and lonely and when first diagnosed she would say that is reason she got dementia. She did spend a lot of time on her own and was quite lonely and did used to get quite down about it. She wasn't on any medication
It was after she went for eye appointment but before any actual operations for her catarracts that I realised memory not what was.
For a bit before that she would, like lot of people, forget names or other things sometimes and used to constantly say I'm 70 you know as an explanation. We thought yes and she doesn't do a lot with other people or need to remember things as much so probably just normal and nothing to worry about.

Long answers if have hours to spare
Mum lived on her own (still does) and didn't see many people, about 5 years ago she fell out with my aunt who lived on same row who she saw a lot of and then over time she also drifted a bit from her other friend she used to see regularly from where she had lived previously and by 2017 wasn't seeing her much at all. I saw mum one day in week, usually on Wednesday, we'd either meet in town about 12 o'clock or I'd go to her house or she'd come to mine and then hubby would come home from work about 6, we'd all have dinner together and then around half seven we'd either take mum home or we'd go home from mums. We also saw her similar amount of time on Saturdays and Sundays. I rang her every day at 5 for between 1/2 and 1 hour and after she'd stopped seeing my aunt I'd started ringing her on a morning about 11 too. She would often say she was bored and lonely and wished she had a friend to do things with. As the last couple of years went on mum would call me during the day and in evening wanting someone to talk to as she was bored and asking me to go over on days I didn't normally. It got to around 20 plus calls a day besides the twice I rang her and by end of last summer I was going over for part of every day. Then as her confusion and anxiety got really bad I lived with her for 3 months and now go over every day for about 8/9 hours apart from 2 afternoons a week when carers come.
Towards end of 2016 she got new glasses but not long after she kept complaining about them saying they were annoying her and didn't seem right and she wanted her eyes retesting. She had worked for a glasses making company a few years before and knew that modern places like where she went made them on machines and sometimes got them wrong and kept saying hers were but she wouldn't make an appointment to go back. During 2017 I tried lots of times to make her appointment to go back for a retest. Sometimes she'd say we'll go in opticians while we're in town next Wednesday but then she would change her mind. A couple of times I made appointment online for her while we were at my house but then once on day before and once on day of appointment she changed her mind and I had to cancel. We eventually went late october 2017 after she kept saying things looked wobbly and blobby and she couldn't read writing on tv properly. Thats when they referred her to hospital as they saw dark spots on her eye. She was diagnosed at hospital with full macular hole in left, part macular hole in right and catarracts in both eyes. She didn't want macular hole op on left eye as would have to go to city hospital a bit away and said she didn't like it there but agreed to have catarracts done which she did in 2018. It was while going back to hospital for appointments I noticed she was struggling to remember what had been said, when appointments were, why we were there and forgetting about how eye felt when she looked out of it. When she had catarracts done she needed reminding what to do when bathing and putting drops in, first one she wasn't too bad but by 2nd a few month later she had more or less completely forgot procedure and what to do and was quite grumpy about it.
Mum used to go stay at my sisters for a week or two a few times a year, on a few occassions during 2017 mum would say she wanted to go stay at my sisters as she was bored and lonely and fancied a change of scene but then when sis and I would talk about dates to take her and fetch her back she'd change her mind and actually went less that year than previous years. She stayed for 2 weeks in the summer with teenage nephews while sis was on cruise. She wasn't well while there and a few times when I rang her she would tell me something then next time I rang tell me something different, I put it down to her not being well at time. Afterwards mum said kids were getting older now and didn't need her looking after then and she felt like two weeks were too long up there on her own. Sis said yes they could probably mange alone now so if mum preferred to just go up when sis was there she could just do that in future which mum said she did. Hubby I and mum were going up for weekend later that year and mum said she didn't want to go as journey too long, She did go next time we went for a weekend near end of year and in spring 2018 when my niece had her baby we all went again but not long after that mum said she wasn't going anymore. She said my sister had told her the kids said they didn't want nannan to go anymore which wasn't true. Who said and exactly what was said changed a few times over coming year but the basic reason was Mum said sis and kids didn't want her there. No matter what sis or I said she wouldn't go, not even with us, she hasn't been since and neither have we. My sister now has to come down to stay here.
Mum used to catch buses to my house on her own some wednesdays , in the summer of 2017 we had road works for a few months in village just before my house and bus driver told them one day it would be better to get off and walk if only going to top of my street as it'd be quicker than waiting in lights on bus for ages. Mum though she was closer than she was to mine I actually live near bottom of long road. Mum got off and it took about 1/4 of an hour to walk to mine and she said she felt like she was bit lost and maybe on wrong road at one point. Its just one long road from where she got off to mine and we travelled on it constantly so I wasn't sure why she hadn't know where to go and how long would take walking but she said it was cos driver made it sound like he wasn't coming down road and it threw her. She refused to come over on bus on her own after that and so after that I would either go to hers or meet her in town and we'd come to mine together. She'd always been nervous about going on buses and not knowing when to get off so I wasn't that surprised. Afterwards I did wonder about her thinking she was going wrong way and feeling bit lost being a bit odd and maybe memory related.
She would change her mind a lot too, sometimes she'd have a bit of tummy trouble and say not to go over she'd be ok on own and didn't want company and wanted to lay down and be on her own, but an hour or two later would ring and ask us to go over. Sometimes if we'd planned to go somewhere that day she'd say you and hubby go I don't want you to miss out but then later she'd ask why we didn't take her and seem surprised or annoyed we'd been without her and sometimes said we were lying and didn't want her to go. We put it down to her being a bit grumpy or wishing she'd gone but afterwards as things have progressed she did it more and more and realised she had forgot what said.
There were lots of little things we just didn't think about but as time wore on they got more and more noticeable and after eye problem in late 2017 I was thinking they were memory related and possibly some sort of dementia. It took till september 2019 before mum said I could make appointment with gp (which she later denied) we saw gp in october then memory clinic came out and we got diagnosis from memory clininc in november of alzheimers.
Hope I didn't send you to sleep with my rambling x
 
Last edited:

Lizbuff

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Apr 9, 2019
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Hi @Lizbuff

A retired teacher, you didn’t say. A very undervalued profession. So many finding out now that it is not that easy. They should all be paid double and given a house by the sea on retirement! By the way, did I say I was a retired teacher too!? :rolleyes:

Interesting about the loss of skills using things like the printer and PC. I find sometimes I sit here and for a while I can not for the life of me think how to do things. It is usually programs that I have been using for years. I write notes a lot now as prompts.

It seems that she was very active, but slowly she stop doing the things she liked doing. I can only assume that she found it harder and harder to do those things?

I think there is a point where decline becomes a one way journey. The problem is we can’t really say when that is, but that is why I think it is important to recognise and get help as soon as possible, but doctors seem too quick to dismiss any idea of dementia.

The final point you make, hit a chord with me and I had to stop writing for a bit; ‘She isn’t a child, but she is as emotionally and physically vulnerable!’

I hear a lot of how harsh, changed, hurtful and different we are, but inside we are all, emotionally and physically vulnerable too!

I hate what I’m becoming, but I feel it all!

Stay safe and keep well!

Richard

Hi Richard

So you are a retired teacher too? What did you teach (other than children!?). Mum taught reception & absolutely loved it. I couldn't agree more with your suggestions regarding salary & seaside houses!

Keeping notes is a great idea - I worked with lots of programmes too in my job & couldn't have got by without the process documents we put together as a team, even having done the processes loads of times.

Mum really was active - I think it was losing interest rather than anything else, but I could be wrong. She was increasingly ashamed at any hint of memory loss or need for assistance & still is. I'm still 'not allowed ' to tell her friends (several have guessed, which makes things a little awkward for me as they want updates & she's usually in earshot). This saddens me greatly - I have often told her it's nothing to be ashamed of & isn't at all her fault. Easy to say, I guess.

I think diagnosis was tricky because, as I've read a lot on here, she was very good at hiding how bad things actually were. A testament to her intelligence I guess!

I hope I didn't upset you with my last comment. It makes me so angry & sad that there seems sometimes to be so little compassion, generally, when it comes to dementia. Don't get me wrong, I love children & babies, but when I see how much specialist care & attention they receive, how much money is donated to child health charities & so on, I wish the same care & concern existed for those living with dementia, particularly when it comes to inpatient hospital care. I now point blank refuse to leave my mum when she doesn't understand where or why she is. I was made to leave one particular night - when I arrived in the morning she burst into tears saying "I didn't know who had put me here, why I was here or if you were ever coming back for me again." I must admit I joined in with her tears on that occasion & have fought many a scary nurse to stay with her since.

Your last few comments struck a cord with me too - I know only too well that it's tricky to adjust to mood swings, lack of empathy & so on, but fron what mum has said it must be so scary feeling unsure all the time. She came in to me this morning & said "what am I supposed to be doing?" & she hates the thought that she's somehow doing the wrong thing or is in the wrong place.

I don't know what to say that might be of use or support to you, but please know that reading your posts & hearing about your research is a great joy to me - there is hope! In the meanwhile know that you are very much not alone.
Sending very best wishes to you - please continue to stay safe x
 

NotTooLate

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Jun 10, 2017
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Alvechurch
toolate.blog
Good Morning Liz!

Primary Teacher and being male, I seem to end end up most of my time with Year 6, the lovely 10 and 11 year olds, but I have taught everything from Nursery up to YR6. All of the years are unique! It is an amazing vocation where you have a child for 12 months and can change their whole life!

Being ashamed of not being yourself is understandable. When you go from being someone that was central and valued, to someone that is cared for is so frustrating! I know that sometimes I appear lost to my daughter and son. They will tell me I seem distant, detached and unresponsive, but the strange thing is, I’m not sure I realise this until I’m told. I then feel ashamed of my behaviour that I have no control over.

I don’t know what you mean about hiding things, I would never do such things! I did not want a diagnosis. I didn’t want a label. I didn’t want a death sentence, so I did everything I could to fight against it and still am!

Your comment did upset me, but not in a bad way, if that makes sense. It is out of frustration. Since my diagnosis, I seem to be seen as different, a non entirety almost. There isn’t anything really that can be done, so you end up being seen as a manakin. Something that can be moved, placed and controlled at will. The thought that a there is something going on inside my mind, that becomes a secondary consideration. The medical profession knows best is the mantra, but something I don’t whole heartedly agree with!

I’ve told my family, that if I get to a point where I’m not in this world, then put me in a home, but really, deep down inside, I’m dreading that ever happening, because I hear so much from carers that say the love ones seems to know. I fear this locked in state, where to the outside world, I’m not here, but I there looking out and seeing, hearing and feeling it all! But, I will never express this to my own. They have a life to live too and that is important to me!

This idea that, I should be doing something, is another something that I to go through. I’m constantly worried about wasting time. I should be doing something, I’m sure today I should be…. and that is as far as I get. I just go around in circles, doing the wrong thing at the wrong time.

I will never stop, while I am able to string two thoughts together. I can’t, I’ve got too much to loose!

You stay safe and keep well…

Richard
 

NotTooLate

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Jun 10, 2017
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Alvechurch
toolate.blog
Good Morning @annielou

I was amazed to read that your Mum is still on her own. I take it she likes her independence and I can understand that. The loneliness and mental problems associated with this are insidious and slow. It’s not that case that everyone will go through this. Many thrive on being alone, but when something happens, like your Mum falling out with her sister, it can be the trigger that sets depression off.

When you say about your Mum changing her mind a lot, wanting to be on her own and making excuses to do so and then later asking if you would be coming over, is something I go through a lot. I want my kids to get on with their lives and not be tied to me. I don’t want to be a burden. Then, I miss them and I usually text and say, ‘If you want to come over anytime you can!?’ I know it must be frustrating for them.

Changes are slow and all our lives appear to move at a snails pace and it is only when we look back and compare that we realise how much time as flown and how things have changed. I know I am not the me I was and when I look in the mirror, it is definitely not the same me that’s in my head!

I don’t mind your ramblings, I’m guilty too, but I think it helps!

Stay safe and keep well!

Richard
 

NotTooLate

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Jun 10, 2017
301
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Alvechurch
toolate.blog
Seizure2
Fall6
Blow to the head4
Accident
loss of a loved one3
Illness1
Heart Attack3
Mental illness
Drugs issue
Drink issue
Depression5
None 4
Infection 1
Stroke3
Severe Pain1
nearly 88% of repossess noted events prior to the first signs, or symptoms of dementia.
 

annielou

Registered User
Sep 27, 2019
1,917
0
Yorkshire
Good Morning @annielou

I was amazed to read that your Mum is still on her own. I take it she likes her independence and I can understand that. The loneliness and mental problems associated with this are insidious and slow. It’s not that case that everyone will go through this. Many thrive on being alone, but when something happens, like your Mum falling out with her sister, it can be the trigger that sets depression off.

When you say about your Mum changing her mind a lot, wanting to be on her own and making excuses to do so and then later asking if you would be coming over, is something I go through a lot. I want my kids to get on with their lives and not be tied to me. I don’t want to be a burden. Then, I miss them and I usually text and say, ‘If you want to come over anytime you can!?’ I know it must be frustrating for them.

Changes are slow and all our lives appear to move at a snails pace and it is only when we look back and compare that we realise how much time as flown and how things have changed. I know I am not the me I was and when I look in the mirror, it is definitely not the same me that’s in my head!

I don’t mind your ramblings, I’m guilty too, but I think it helps!

Stay safe and keep well!

Richard
Thanks x
My mums changing mind was similar, but also she had often forgot what she had said earlier and she would often ring and ask why we hadn't been when we should have, then when I said I'd not gone because she said not to, she'd cover up and say oh did I, well I was just ringing to see if you fancied coming now. It progressed over time to her getting quite upset about us doing things without her when she'd told us to and her accussing us of not wanting to see her and lying including on quite a few occassions ringing while I was out somewhere and screaming down the phone that I didn't care about her as she was home alone and she'd been sat waiting for me and I'd just swanned off.
I have sometimes wondered if falling out with my aunt contributed to it, it was my dads sister, she had been friends for a few years living near by and they saw each other every day but then there was quite a bit of manipulating by aunt then her dropping mum when it suited and a bit of bullying in my opinion so not the best relationship and eventually after a silly thing they fell out and mum decided enough was enough and she wasn't going to go to aunt and make friends again. But she did miss her and was lonely on her own.
My mum in one way wants to be independent, likes to be in charge, always has. Over the years if I ever treated her like we're equal and I have as much right to be right and decide something as her then she would quickly remind me I'm her daughter and her child and children should do as their parents tell them and respect them. The parent has the last word always. She would make me feel like to have a different opinion to her meant I wasn't a good daughter. She would sulk for hours or days ignoring my calls or attempts to make friends until she decided she thought I'd had enough and then she would answer me and act like nothing had happened. Believe me I have never shown disrespect to my mum I love her to bits but she hasn't always been right and over the years as a married woman with a husband house and job of my own I did feel I could have my own opinion as an adult. She has loved to give me her opinion on every aspect of what I do and mostly I'm happy to receive it if not always take it, but although she asks my opinion frequently she has never been fond of me offering a different opinion to her. But on the other hand for quite a lot of years, over 20, I have been the person she has asked to go with her to appointments, ring and arrange workmen, talk to banks, SS, anything official. I was the one who did the leg and phone work to arrange her moving house the last twice. When she had to have an operation years ago she didn't want me to stay with her when she came out of hospital but wanted hubby to take me there on his way to work at 7 the next morning and stay till bed time for a few days which I did willingly.
Currently she lives alone but to be honest I don't think she manages very well. I stayed with her for 3 months from october last year as she was so confused and scared because she couldn't remember things but then she was prescribed sertraline for her anxiety and agitation and aggression and she was a lot calmer and I tried going home overnight. I now go over each day between 10 and half past and leave between 7 and half past but she has gone back to often ringing on an evening mixed up so I'm not sure how long she is going to be ok on her own.
I feel quite selfish not staying with her now really, but her home is a one bedroom bungalow and when I stayed I had to sleep on a fold up bed in living room, putting it up and down every day, there was nowhere to keep my things and I had to use a suit carrier to hang a few days clothes at a time up in her hallway and keep my toiletries etc in a carrier as she didn't want them in her bedroom or the living room. My husband used to come and see me every day after work to have his dinner with us and sit with me and mum for a few hours. I would take mum to my house a few times in week if I could to do my housework and washing etc. It was an awful situation and I don't think I could do it long term, plus mums bungalow is supposed to be for single people and I really shouldn't have been staying there.
We have considered mum staying here which at times she has said she'd like to but mainly says she wouldn't. We have stairs and when mum comes in day I follow her up and down as she is bit wobbly on them so over night I worry she may wander and fall down them. When she stayed at christmas she kept wanting to go home, although that was pre sertraline days so may not be same now but when she's here in day as it gets later she gets confused about where she lives, who I am etc and that could be worse when here than in her own home, although she does it there too. I'm not sure if hubby, or me could cope with looking after mum 24 hours a day again, I feel so bad for admitting that and I feel like I will end up doing it again soon but don't know how I am going to cope so basically I think I'm just putting it off and hoping for best when i go home from mums on a night which makes me feel awful. But I was physically and mentally exhausted when staying with mum as I got hardly any sleep and no breaks and at the moment I'm just about hanging on by sleeping in my own bed with hubby. I feel so sad for my mum and so sorry as she never gets a break from her dementia and I feel guilty for wanting one for myself when I come home.
Gosh thats more of a ramble than before sorry I maybe shoud come back and edit that later, sorry for hogging your post x
 

Fitzalan

Registered User
Apr 25, 2020
33
0
No significant event. Mum did have a couple of minor strokes after she was diagnosed, and of course it's always possible she had some that went undiagnosed before.
 

Countryboy

Registered User
Mar 17, 2005
1,680
0
South West
Hi @countyboy

At 77 you seem to be doing well and that certainly gives me hope!

Do you think there was anything different between you being diagnosed with Alzheimer’s and then FTD, I take it you still had the same treatment?

I’ve just been looking at you first post, where you mention the obvious factors taken into consideration when diagnosing dementia.

Your age. They will tell you again and again, dementia is not related to age, but we all know that it is, otherwise why is this a factor?

2. Type of dementia. Ok, if you have symptoms that can be classified as a certain type, does that help? Is the treatment different? Is one more important, or devastating than another?

3. Underlaying illness related to dementia, What and how does this help?

4. Other health, or medical issues. This is the one area that I think has less attention, but is one of the main areas that could have a positive impact. I think the dementia symptoms are by their very nature symptomatic of another health, or medical issue.

I agree that these, as you state are used in the diagnosis, but you have to ask why?

Your post certainly give me hope that statistically I don’t have to worry so much! ?

Stay safe and keep well!

Richard
Hi Richard first of all you appear to be looking at Dementia Positively that’s good it’s very important that you stay in control of you own future Do Not let bureaucrats take over , hopefully you have a supportive family.



Just to give a brief history of my Diagnoses

I July 1999 I visited a GP with chest pain this lead to my being asked if I would see a consultant in Old age Psychiatry in October after an examination and several mental tests November 1999 I was diagnosed with Alzheimer’s disease and was asked if I would be prepared to take a “new drug Aricept” obviously because was still in the trail stage in UK Aricept could only be prescribed by the Consultant therefor I had to visit the Memory Clinic every moth for prescription I was also assigned an Occupational Therapist’s set up monthly meetings with my employer and unison union representatives etc to enable continue to working with reasonable predictable structure.

In 2001 my Consultant moved to another location and I was assigned a younger Consultant with all the fresh ideas and the first thing I was told I had to inform the DVLA obviously I did and was annoyed when my driving licence was issued for one year this is when the Red mist came down I was raging :mad::mad:after that and tended to argue with the Consultant about my diagnoses this went on for a couple of years and in February 2003 the scan have a PET Single Photon Emission Tomography Brain Scan at Hospital in next County the scan identified frontal lobe brain damage, a second SPECT scan was carried in April 2004 to confirm the illness.

However with the support of the Occupational therapist I continued to working until my retirement in 2008 at the age 65:):)
 

TNJJ

Registered User
May 7, 2019
2,967
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cornwall
Hi. We held an 80th birthday for dad at a local hotel. We first noticed the signs when he went the wrong way into the hotel and had got confused (we had been before). Then the walking . Very slow and unsteady. He is now 86 and was diagnosed in 2015 with Vascular Dementia. He only walks with a gutter frame now after having several strokes.First in 2015.
 

Wakky

Registered User
Jan 5, 2020
54
0
My mother had AD and died 5 years after diagnosis. There was no significant event prior to developing this horror.
My husband was diagnosed with AD in September 2019. There was no significant event prior to this. I had noticed changes in him about 18 months to 2 years prior to the diagnosis and it was me who persuaded him to see the Gp - and I went with him. We were told he is in the early stages of AD. Knowing how my mum was, I dread the future and pray I don't have to cope with years and years of him getting worse.
 

NotTooLate

Registered User
Jun 10, 2017
301
0
Alvechurch
toolate.blog
Hi @TNJJ

Quick Question: You say your Dad had his first stroke in 2015 and this was the same year he was diagnosed?

Do you think he may have had a stroke before this time?

Stay Safe and Keep Well!

Richard
 

TNJJ

Registered User
May 7, 2019
2,967
0
cornwall
Hi @TNJJ

Quick Question: You say your Dad had his first stroke in 2015 and this was the same year he was diagnosed?

Do you think he may have had a stroke before this time?

Stay Safe and Keep Well!

Richard
Yes I do . But I think they were small TIA’s so nobody noticed.He has heart failure as well as declining kidney function so I think it could be tied in all together. Yes it was 2015 when diagnosed after his stroke.
 

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