Do you feel you know why you have had a difficult experience?

I do not have a life, no social life of my own. I bring her to the centre at the moment. I cannot leave her at a daycentre on her own because they will not accept her. I can only leave her at home if there is someone with her. I do not have a social life, it’s a 24 hour job. I have come now but my son is at home and will go to work at 1.30 pm then its alright, but if he had gone to work then I would have had to bring her with me.

No, I cannot see anything good for me at all but I cannot say it in front of her. I know it inside. My children know it that dad does not have a life. My children last week, took me to see Liverpool play a match. I had to keep my Mrs at my brother’s for one night. They say to me daddy get out, have a holiday, go and do this and that they say, but I do not feel like doing anything.

Why not?

If I go and if something happens to her, then I will have to do the running around. Its better then to keep things as they are instead of having to run around if I keep her at someone’s else house. If something happens to her health it will be me doing the running around. So from inside I do not feel like going.

In that I had never really sat at home, as a man. And sitting at home, not able to do much in the house. Watching T.V and sitting all day at home talking-the quarrels started to increase between two people. She was in depression and I did not know the reason that she was the way she is because of depression. I used to feel she is not working in the home and she wants (needs) to go out. And having left work, it takes time to settle things financially and so we rowed much during this time.

We did not get any help from anywhere at the time.

Where did you hope to get help from?

We did not know, we did not have hope that we will get help not heard anything about depression. Not heard anything about depression or epileptic not heard anything. No help and we had not heard about this at all. All we did was go to the doctor and doctor writes us prescription and we come back home and back again. That’s all.

So afterwards?

So after these specialists came and we were sent to them and brain scans were done. They told us that these epileptic fits are happening due to depression. Then they sent us to a psychologist and then we got to know a lot more. Five years later we got to know that this is due to depression.

Regarding the caring that you provide can you describe a typical day to me? What is a typical day like for you?

My typical day if we sit the two of us at home, then both of us will argue about something or another. There is nothing worth arguing about, it’s nothing in it. It’s usually about eating. She has diabetes but will not like to eat. Instead of getting up at 6 am, today she got up at 5.30 in the morning and she kept working and at 9 am she had an appointment for her diabetes. She did not worry about the time but starting arguing. To get my Mrs out of the house there are arguments and to get her back into the house there are arguments. If someone came and sat in the house then she does not worry.

So how do you have to help?

I have to keep reminding and nag her. If I keep doing the nagging then she gets depressed, she starts crying and her mind does not work. I have to say gently that, ‘I am not telling you off but I am telling you about the time. I tell her, ‘Look at the time. We can come back and do the housework when we get back. I do not want you doing the work. We can do the housework when we get back. When I say that she says no you do not need to do the work I have to do the work. If we do not go out of the house then its sayonara [everything is ok].

In that when we go to the doctor, we talk to the doctor. The doctor should listen to what we say, if the doctor explains to her and to us, then its feels good. If the doctor tells her something but does not listen us then it does feel not right. If we go to the consultant at the hospital, then the doctor talks to her and if we explain to her, and so we understand a lot about some things. But if they talk on medical grounds then we don’t understand.

If they explained to you would that be better for you?

Then it would be good, good. What it is about whatever, interview dates or appointment. If you can talk to that person, if they give us a letter and we can show that letter then it is better. If it’s not in writing and we there will be some words we don’t understand. So we get confused at those times.

If you had the chance or the opportunity to change things to improve them, how would you do it? Can you explain to me again?

I would like it, I do not want an interpreter, but the conversation that takes place there, if it was in writing and you can get it, then we can keep it and talk to somebody about it. If someone, asks me, that you went today, diabetes nurse’s appointment. She talked to me face to face. It wasn’t such a big point that we didn’t understand. My Mrs right now has a bladder weakness and she cannot control urine. She wets herself. So they are going to put a pelvis ring inside. Somebody asked me, what is it? So I said they are going put a ring but we do not understand the word pelvis. If they send us a letter on the doctor’s report, and if they give to us, then we can keep it on our records and try and understand a bit.

What about your friends or family or anyone else?

No. My wife’s friend is Chinese she lives next door to us. She is elderly. We got a lot of support from her.

In what way?

She used to come our home everyday, and sit and talk with us. My Mrs is a people’s person and she like people a lot. If anyone comes to our home she is happy. She forgets to argue and forgets her illness and she gets entertained by people. She loves to feed and give refreshments to people. She [the neighbour] used to come home everyday and sit with her. My Mrs has a habit of drinking a lot of tea, in a day she will drink at least 20-30 cups of tea. When the Chinese woman came she got my Mrs to stop drinking tea. She got her to drink hot water. Once before, when before I stopped working, the Chinese woman came when my Mrs had fallen. She got her spare key and she got the neighbours together and opened the door and she pressed the panic button.

When you got her support, how did you feel?

In my heart I felt there is someone nearby and felt if something happened there is nothing to worry about or if I wanted to go out then I will get support. If I tell her that I am going out, she will phone or will come into the home, sit with her or take her out for a walk for a bit.

So did you get some relief from that?

Yes, some relief, that someone is nearby, that not alone.

We come to the community centre here and near us there is a group for ladies only near our home, she goes twice a week, and it’s for ladies only. I do go with her but drop her off in the morning at 11-30 am and pick her up at 1pm every Tuesday. They do light exercise with them. She goes on Friday at 12 noon and finishes and 3pm. Once I have dropped her off I have to sit in the house, cannot go out because if her health gets back, they phone and I have to go back and pick her up. If she goes far from me, then I cannot go far. She goes to cancer research every Tuesday after 1 pm. At this place they said because it’s a ladies group, I sit in the car or walk around nearby. After one to one and half hours I go and pick her up.

If you look back and think back about caring what would you say to someone?

In this country you get a lot of government support there is no need to suffer about what to do or what will happen. For resources, if we sit at home, nobody is going to come and help you. We have to get out and ask someone, but our people are shy (reluctant) to discuss things openly what is happening in our homes. But it’s necessary because only when we talk to someone will we get help without that we will not find a solution.

In that there is one big problem. In NHS the doctors, the psychiatric doctor, every few months they keep changing. They are on this training course or that one. They keep changing. So far, my Mrs has had a change of three to four psychiatrists. The last appointment the psychiatrist I am going someone new will be coming. So if a new one comes, he will work in a new way, so it keeps changing a lot. If it stayed with consultant psychiatrist then it would be better. The changing of psychiatrists and the appointment that they give is time limited. If they spent a lot more time only then can they understand about their mental health and about their mind. They give just 10-15 minutes appointment how are they going to know anything?

So you want more time?

Want more time and the same consultant all the time would be good.

Anything else?

The other thing is the medicine that they give, the capsules. In some things, my Mrs has metformin, a diabetes medicine, it comes in a packet and a bottle. If it comes in a packet she will say that this medicine is different. So if the same packaging every time- what has happened is that in their mind is that the medicine has changed. Often her capsules that come, the colour is different so she will say they have given the wrong medicine. So the if the same package came continuously, that would be good too.

Let me see, what I can tell you is from what I have done. I have one older son. He went to London to study and when they were younger children and went to school, my wife was in hospital and I would come from work and go to school to pick up the children. Sometimes, I would be too late, my boy would cry, then I would be unhappy thinking what is going to happen to the children, what are we going to do? Wife’s health was not too good. Financially, I was not strong so I could stop my work right away. I did not know about whether I would get benefits or not. Inside, I would be upset and unhappy (confused) how are we going to do things? Like pay the mortgage. My wife’s health was getting worse.

At that time what did you feel?

At that time, I did not think too deeply otherwise, thinking about the house, thinking (worried) about money. At the time I had bought a house, about two years. There was lot of confusion did not know what to do- no solutions, what can I say, felt stressed.

Is it different now?

The children are older now and the wife’s illness has been long now so I know what to do and what not to do, so things are falling into place now slowly.

If someone had taken care of her, then I would not have known what was going on in my own home but because I am at home, with her for 24 hours a lot more, we get to know a lot more about things.

In this experience, through your life, have you lost or gained opportunities?

I have not lost opportunities it is the way it is.

Some people who have the responsibility for caring say we gained opportunities in different ways to others, how do you feel? Do you see it as an opportunity or loss?

Not an opportunity lost but a gain.

In what way?

Because I have come to know a lot more about the workings of my own home (sansar) since I am at home. Before I was at work for eight hours and at weekends going out, did not know what was going on at home. If we live at home continuously so I have had the opportunity how to live with your wife, how to take care of her, what to do, so now I have come to know. If someone like carers were taking care of her, and I would have worked, then she would not have improved.

So what was it like at first, in terms of your life story?

Simple, steady. There were difficulties but in everyone lives these come, that happens. It was nothing to worry about. When Mrs illness became worse and came out. If it was a medical illness then people can talk about it, but here it is mixed with medical so the difficulties got worse. But then as things happened, solutions then came, children were small and now they are bigger so the responsibilities started to lessen so now when I look back. I feel I am happier than before. Happier in the sense that I do not have to worry about money just to look after my Mrs’ health. I now know what her mood is and what she will do and if she does not have money with her she will become unhappy. If we give her money then she becomes happy. It does not matter if she spends it.

I will give you my own example, when my daughter was at university. When my Mrs health was bad, my daughter went to college/university in Wolverhampton. She had to come back home at the weekends because my wife’s health was so bad, sometimes in the evenings she had to come back from college. This was because she was the only woman and as a daughter she could understand her mother. So for her it was stressful with her education and she got behind. That was when support was needed but there was no support at that time here.

For the family?

For the family, for the children. My daughter was older, but if the children are in secondary and primary school, it is very stressful for them. I was at work, my children were at school and had to come home and have to do things.

What other ways did they have difficulties, your family?

In terms of difficulties; eating and drinking, because when they come from school they needed to eat. When my Mrs health was bad, there would be no food made. Her mind was such that she could not do any work only sleep. So when the children came home, their clothes were not organised to go to school. Because of depression from the beginning we had to do things from an early stage. So there were a lot of problems when they were small. As the children got older, slowly we got to know and things fell into place. But in the beginning there were a lot of problems.

When the benefit rates are increased, when the Carers allowance increases if you are getting income support then it gets deducted. So you get what you get, you do not get an increase. The costs carrying on are increasing, so if a Carer works then they will not get any financial benefits. If you think that Carers get ’48 carers allowance and then increase it by ‘2 per month to bring it up to ’50 then they cut that ‘2 from other benefits you get. So we do not benefit in any way. So we do not benefit financially. To look after the cared for person, there are expenses.

What kind of expenses?

To take them out there are expenses aren’t there? With some of them like my Mrs, if you leave her in the house she is got to get depressed. I have to take her out.