|
Explains that she just accepted the diagnosis even though it was clear that she would not be able to continue with quite a lot of activities.
|
|
|
And how did you feel when you realised what had happened?
Well, you just accept it. It has affected your speech and your memory, everything's affected by it and also your mobility. I mean, I drove a car, I, you know, I was a member of the, you know, all different associations. That all goes by the book, I mean, you lose all that, which is a pity. |
|
|
|
She lost peripheral vision on the right and sometimes has to turn her head to see things on the right of the television screen. She also see some shadows in her vision.
|
|
|
Can you describe to me what, what's the problem then?
Well, the, the right side was affected and although I can see, but I also see shadows as well with this eye, you know, which is a nuisance but I suppose that's just par for the course really.
How does it affect sort of watching the television or …
No, I'm, I'm fine because with one eye, I mean, you're, you've got perfect vision and with the other eye you've partial vision with that eye, so I can look at the television. Sometimes if there's something on the programme and you're supposed to look at the right side and you've to turn your head to look at it because you can't use your eye to, to look at it. That's the only thing but that's not difficult. |
|
|
|
A carer helps her to get in and out of the bath and puts her support stocking on but she still feels a bit independent because she can bath herself.
|
|
|
And what about in the bathroom? Have you had any changes in there?
Yes. I've got a special seat in the bath and I am helped, every morning I get, somebody is here to help me to get in the bath and I can sit and shower myself and it makes me feel independent as well because I can do that myself. And as long as she's there to help me and help me in and help me out and she also, while I'm in the bathroom, she does my breakfast, so when I come out, I've got my breakfast all ready as well [laughs].
And how has that worked out having a carer?
It's worked out very well. That really has worked.
And do you always have the same person coming in?
Well, usually, there, they come for quite a while and, unless they go on holiday, then get somebody else but, I've known quite a few of them and they're all, they're all, they all know their jobs and that's very good. I've been very lucky.
So you just mentioned there that you have some special stockings that you have to wear since the stroke?
Yes. These are what they call elastic stockings and they are to support… they are support, they are support stockings.
And how do you find putting those on?
Well a nurse comes in the morn, every morning to put them on, to help, to put, well, she does put them on and I can take them off myself at night. |
|
|
|
Try to do as much as you can for yourself and don't rely on other people or you'll lose your independence.
|
|
|
Well, to try and do as much for yourself as you can and not rely on other people all the time and I think a lot of people just, you know... I think they just sit back and let other people help them too much and I think that way, you lose your independence. Maybe I'm wrong but it's the way I think, I feel about it. |
