Well, it seems retirement is going to keep me busy and there will be no room for just wasting the days I can now claim as my own. My own because I no longer have an employer that I am answerable to and that is a good thing. I started the week with a morningContinue reading “A busy, dizzy week”
Category Archives: Symptoms
A word with my GP
As a follow-up from a previous post about my lack of contact with my Neurologist, I thought I would make a comment and update where I am now. So, my husband and I went to the Doctor yesterday, so I could talk to him about a number of things which may be Parkies related andContinue reading “A word with my GP”
A ‘wee’ bit of feedback
Every now and again when I am writing this blog, I make a comment or tell a story about something that has happened or is happening in my life which seems to generate a lot of feedback and discussion. A recent post I made about continence has been one of those. When I had postedContinue reading “A ‘wee’ bit of feedback”
Let’s get a ‘wee’ bit personal…
Even when you are a bit of an open book, as I try to be in this blog, there are some things that are more difficult to talk about. I find it interesting too – as a side note – that when I sit in front of a doctor – others of you may identifyContinue reading “Let’s get a ‘wee’ bit personal…”
Off my game… does that mean?
So today I went to play bowls as I have been doing for a few months now. Tuesdays and Saturdays and it’s a great way to get exercise and socialise with others and have a good afternoon out. It is interesting to note that on Tuesday when I played I had two really good games.Continue reading “Off my game… does that mean?”
Is it tiredness or something more…
We are currently in Wellington with soon and daughter in law and their three busy boys. I got up at 5am as I couldn’t get back to sleep. Throughout the day I noticed that I had trouble finding words and some big pauses while I tried to find the words. Did I detect a look,Continue reading “Is it tiredness or something more…”
How are you doing?
For those of us that have a diagnosis of Parkinson’s, I hope that for the most part we are supported by our GP’s, our specialists and other health professionals we are involved with. We need to have our medications reviewed from time to time and ensure that as we progress we have all that weContinue reading “How are you doing?”
Responding to need
I have read many posts on a Facebook page that I belong to about how to get help for a family member with Parkinson’s. The first thing to do is make sure that the person with Parkinson’s or PWP goes to see their GP, discuss what the person’s challenges are and request an assessment toContinue reading “Responding to need”
Support Groups… we all need different things!
Tonight, my husband and I attended the monthly support group that we have at a local bar. We have been going for a while now and it is nice to know that it is a safe group to talk about our diagnosis and other things in our lives. Many of the group are still working,Continue reading “Support Groups… we all need different things!”
Learning to bowl… with a Parkies brain
A good example of how slowed processing in my Parkies brain, can make things more challenging than for the average person. Too much information, from too many people, in a short space of time just ends up a confusing jumble in my mind. So I wrote this poem… Learning to bowlWhich side is the bais,Continue reading “Learning to bowl… with a Parkies brain”
My journey with Parkinsons 