- Being a carer isn’t easy
- People identify with those they care for
- Reading list: The Impact of Physical Illness on Professional Relationships
- Julia Segal Publications: books
- Julia Segal: Publications: Papers
- Julia Segal: Unpublished papers available
- Relationships in MS… Notes for a talk.
- Whose disability?
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Michael Rosen came to our house. He wasn’t visiting me but we met in the kitchen. My arms were full of a two year old son and I was drowning. He looked at me and asked how I was. I … Continue reading
It can be very hard to lean on others, especially when you know they have their own problems. Some people don’t want to be lent on, but others do. In Giri/Haji, there is a poignant moment when a dangerously drug … Continue reading
Worrying about worrying … The coronavirus is a real cause for worry. That is clear. But many people find themselves worrying in a way which doesn’t seem right. They are too worried, or worried about something which isn’t a real … Continue reading
16 March 2020There seems to be a real disconnect between people’s anxiety about health and their capacity to think or act. Perfectly intelligent people can be paralysed by panic: we know this in theory, but watching it in friends or … Continue reading
Hilary Mantel, The Princess Myth: ‘Mourning is work. It is not simply being sad. It is naming your pain. It is witnessing the sorrow of others, drawing out the shape of loss. It is natural and necessary and there is no … Continue reading
Using a stick (a cane, if you are American) outside for the first time is one of the harder transitions for someone with multiple sclerosis. There is a long period between needing a stick and actually buying one or accepting … Continue reading
I am writing a chapter about counselling people with mild cognitive impairments: Working with people with mild neurocognitive disorders (mild NCD) or mild cognitive impairments (MCI) for a book: Theory & Practice of psychoanalytic psychotherapy in dementia. Eds Sandra Evans, Jane … Continue reading