- 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- Julia Segal: Unpublished papers available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?
Category Archives: carers
The Trouble with Illness: How Illness and Disability Affect Relationships is being published by Jessica Kingsley on 21st Jun 2017. I spent the last summer writing it, discovering files which were dated 2007 in the process; at last it’s coming … Continue reading →
Caring, like loving, can be very satisfying and fulfilling, but it can also be very painful. If we care, we allow our feelings to depend on the behaviour and feelings of others, not just ourselves. Caring can affect others’ feelings … Continue reading →
– when everyone would rather it didn’t. Children need parents, when it would be much easier if they didn’t. Children may have to think about their parents in ways nobody wants. Parents may have to think about their children in … Continue reading →
We want the NHS to be an Ideal Carer (see previous blog). The Francis Report into the failure of care at the Mid-Staffordshire NHS Foundation Trust stated that ‘patient care is at the very centre of the NHS, and no … Continue reading →
The idea of what a carer (or partner or parent or child) of an ill person should be is powerful. It embodies an ideal which people want to live up to. It sets standards against which others may be judged. … Continue reading →
I think my husband may have this could you offer any advice to me please, especially how to react to it and how to get him some help. This came as a comment but I think it deserves a new … Continue reading →
I wish it was all over I wish everything was back as it used to be. I want them to live for ever I hate this situation I wish they were dead I am a monster to feel like this … Continue reading →