To all you ‘carers’ out there…

Before I get into this post, let me say that I have a degree of reluctance to label those that support us as ‘carers’. To me, this takes away from the person’s identity as a husband, wife, partner or other family member who cares about us, but not necessarily identifies with the role of ‘carer’. IContinue reading “To all you ‘carers’ out there…”

Carers views vs PWP

This journey of ours that we travel on with Parkinson’s is a challenging one. There is no denying that. If we have family who support us or partners that live with us, it is a joint experience and each affects the other as we learn what Parkinson’s means for us all. I was reading a post inContinue reading “Carers views vs PWP”

No-one can help me till I help myself!

I have frankly admitted in recent times that life has been more than a bit of a struggle at the moment. Health issues – not related to Parkies – especially the dreaded knee, have been getting on top of me. While I don’t consider myself controlling, I do like to be in control of myContinue reading “No-one can help me till I help myself!”

Being alone doesn’t have to = being lonely

Over the years with my husband I have learned that at times he needs to do his own thing and I do mine. Having lived in a very controlling relationship in my second marriage, this is a refreshing change. Now my husband works shift work there are often weekends where I spend a lot ofContinue reading “Being alone doesn’t have to = being lonely”