Such long days

A carer's day can be so very long. Mine starts early, getting up before everyone else just to get my own head straight, and try and make sure I have done what I need in order to get through work ok. Then the little things that are so essential to helping ease her into a sense of being functional. Nice pot of tea, and the teacosy on, a gentle call  that it's morning again. Listening so carefully to gauge from her muffled voice her state of mind, without needing to ask and cause stresses. Trying to get her own mind round to being able to express in her usual specific and exacting manner  exactly how she is feeling can be overwhelming. Once overwhelmed, there can be no going back, and potentially a whole day wasted.  It's not so likely these days, but the threat is ever-present. So, like a bomb-disposal expert, I listen intently. And I don't ask how she is.

"Shall I bring your cup of tea up, or shall I leave it on the coffee table?" The gentle cajoling needs to to take different forms, but should come reasonably regularly as she loses track of time. But they can't keep on or mention that, as she can start to dwell on what she finds difficult nowadays, or how much it can all seem, which then slows things down even more. I NEED to get to work, and it is so much easier if she does make the bus in time, but she can't be made to feel the urgency as then frustration or guilt slows her down more, and the downward spiral begins.

Many times, this spiral is only one way. And eventually the whole day is given up on. But the decision to stop is put off as hour after hour she tries and fails to get started.

It's nearly midnight. She's been in bed for an hour or so, her tablets have helped her drift off, and I've managed to secretly catch up on some of the work I should have completed. But she is sleeping, and so I've helped her though another day. And I can't think anymore, so have to give up on mine too. Until tomorrow comes and we start yet again.