John Z
John, age 71, is a retired divisional fire commander. He is white British, married, with one adult child.
John’s wife was a fit and healthy young woman when they married in 1963. From 1973 onwards she was occasionally unwell but with nothing serious and nothing significant.’ In 1974, on one occasion, she found that she could not write her name to sign a cheque. This led to a medical consultation but no conclusive outcome. She appeared to recover fully. Over the next few years, periods of non-specific symptoms continued to recur and in 1976 she experienced impaired speech and mobility which John thought was a stroke. The doctor reassured him that it wasn’t a stroke and that she would get better, which she did. About nine months later the same thing happened again and this time John’s wife was treated with 3 monthly injections. She improved, though certainly wasn’t the person’ she had been. She regained her mobility, but decided to stop driving.
In 1984 the same thing happened again and, in a different medical practice, the doctor said, it was time to put the cards on the table,’ and told John and his wife that she had MS. John thinks that although the medical authorities had known about the diagnosis for some time, they had not disclosed it because it would have an adverse effect on life.’ John is not critical of this but, looking back, he doesn’t think they would have lived their lives any differently had they known that she had MS.
In 1987 they moved again, back to their original medical practice and, this time, also under the care of a consultant. John’s wife continued to deteriorate, whatever treatment was prescribed, and began to experience severe pain in her lower back and buttocks, particularly when sitting down. She needed to have very strong, narcotic painkillers to control this pain and eventually needed to see a pain specialist. But, ultimately, the pain remained.
In 1992 John retired from work and looked after his wife at home, with the help of special equipment and, eventually, visits from district nurses. John advises that equipment such as stair lifts and adapted vehicles are bought earlier than you think you might need them. By the time they had a stair lift installed her ability to go upstairs at all had declined and they only used it for six weeks before adapting a downstairs room for her.
In 2002 John’s own health began to deteriorate and, although he hadn’t considered the possibility that his wife would go into full time residential care (she did go for respite care) he was strongly advised by the doctor, after being particularly unwell one weekend, that he should let her go to live in a nursing home. John’s wife has lived in a nearby nursing home since 2003.
Over the past five years her condition has deteriorated markedly and she is now bedfast, doubly incontinent and without speech. John visits his wife every day to feed her and, although she can’t communicate with him, he is sure that she knows he is there. Occasionally, she will smile at him. John takes some comfort from his observations that she does not seem to be distressed but, nevertheless, he acknowledges that it all takes some coping with.’