• Managing severe symptoms & consequences of mental illness

    Dad suffered with severe agitated depression for many years. His illness responded to medication but his symptoms worsened from time to time, with high levels of agitation, severe feelings of depression and anxiety, poor appetite and sleep, and often telling us that life was not worth living, feeling hopelessness about getting better or that anyone could help.

    Mum was his full-time carer and was amazing with him but, when we all felt that the consequences of his illness were too difficult for her, the only available option was for him to go into private psychiatric hospital.

    He would often be in hospital for a number of weeks up to a few months. Mum would still spend most of the day with him in hospital, as she was uneasy about others looking after him, particularly as he was often alone, reporting he had not seen anyone that day. He never attended therapy groups, as there were often younger clients that he didn’t relate to, and he couldn’t sit still for long.

    We came across Claimont following a recommendation by a friend when we were at the point of re-admitting him to hospital, as he was once more very needy and getting worse.

    Claimont requested previous psychiatric notes and a Claimont nurse assessed my father, spoke to us, my mother and father’s psychiatrist, and suggested a plan before we agreed to go ahead with a trial of the service.

    Three nurses rotated to provide live-in care over a period of a few weeks, liaising with the psychiatrist, helping to review his regular medication, offering him as-required medication when very agitated or to help him sleep, and distracting him when he was preoccupied. In fact, he received the same care as when he was in hospital, except he was at home surrounded by his family and belongings, and he had the same staff dedicated to him.

    Perhaps the most notable outcome was that Claimont staff undertook a carer’s assessment for mum, which highlighted quite how overwhelming it was for her to look after dad, and how difficult it was for her to ask for help. We held a family meeting where mum stressed she wanted to continue caring for dad. However, she agreed a plan to have more breaks to see her friends and family, go to the theatre, and have peace of mind that dad was being looked after.

    We continued to use Claimont to provide home visits to give mum breaks and live-in care during times when his symptoms became worse or she needed respite.

Community support

Across all disciplines – residential and supported living – CareTech’s ethos is to empower each individual to maintain existing contacts with the community and explore new opportunities for growth and development.

Each person’s needs are different; some are self-sufficient, with the capacity to make their own decisions and live a semi-independent life, whilst others require continuous care and support. We want our service users – whatever their abilities or challenges – to get involved and become part of their wider community. This provides them with the best opportunities to lead an independent life, enabling them to experience everything their community has to offer, whether this is attending college, following interests and hobbies or simply meeting new people and making friends.

Young people and adults are supported as they access the local community, find employment or education, and develop friendships, with the aim of gradually reducing the level of support and building independence skills, including travel training and assessing risk.

Our core values are to respect, support and promote the dignity, rights and self-determination of each person. Our community support is an integral part of our service, with staff enabling, empowering and supporting them as they live life as a valuable member of society.

Community support – Case study

Supporting Shehnaz

Names have been changed to protect identities.

Shehnaz is 43 years old and has ASD and moderate Learning Disabilities. She lives on her own in a residential home and has done so for the past 5 years.

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