Parkies …. it’s no joke!

I was reading a post on a Parkinson’s Facebook page I belong to. It was on the subject of people making jokes about Parkinson’s. They said, “Recently Wendy asked a question about how to handle a thoughtless comment making fun of someone with PD in her presence when she has been recently diagnosed.” Sometimes itContinue reading “Parkies …. it’s no joke!”

Please don’t disable me before my time….

I was having lunch the other day with some of my colleagues and I was talking about how my husband caught me climbing on a ladder in the garden. I had looked up while putting some netting on my cherry tree, when I saw him looking through the window in our bedroom. When I wentContinue reading “Please don’t disable me before my time….”

A sense of urgency perhaps?

This diagnosis has changed my thinking in so many ways. I think deeper and feel deeper than I ever have. I analyze my life and my decisions are informed in many ways on an emotional level much more than previously. There is obviously a good deal of practical thinking in my decision-making processes, but theContinue reading “A sense of urgency perhaps?”

Sing like no-one is listening…

Last night I was in my kitchen cooking and my husband was in the lounge watching television. I love to cook and also listening to music while I cook. Usually something upbeat that I can sing along to. I love to sing along to songs I know – sometimes I may not absolutely know allContinue reading “Sing like no-one is listening…”

What would I tell my newly diagnosed self…

I am a member of a Parkinson’s Facebook group and find it very helpful hearing from others with this condition. It is a very positive group and they have themes on it like ‘Talent Tuesday’ where you are encouraged to share a skill or talent you have. Other days have other themes, but always youContinue reading “What would I tell my newly diagnosed self…”

I’ve borrowed an idea…

I was reading another person’s Blog the other day and I liked what I read and thought I might borrow the idea she talked about. Check it out yourself on Parkinsonscare at https://parkinsonscaregivernet.wordpress.com/ She talked about having a word for the year and her word was ‘adventure’. Finding ways to put some adventure into herContinue reading “I’ve borrowed an idea…”

Medication Management

Ever since going on to medication as soon as I was diagnosed, I feel I have managed things quite well. Sure, there have been the odd occasions where I have forgotten to take my meds in the evening. Or perhaps the lunch time meds get taken at 3.00pm. Or the dinnertime meds have turned intoContinue reading “Medication Management”

Another year draws to a close…

Here it is the 18th of December 2022 as another year draws to a close.  I have to say that this past year has been a good one.  On the 21st of December last year we moved into our new home, into a single storey home that is much more sensible for someone navigating theirContinue reading “Another year draws to a close…”

My Anniversary of two years since diagnosis… 15/12/22

This year seems to have flown by and so too has the time from my diagnosis two years ago tomorrow. As I did on my 1st Anniversary I like to stop and take some time to think about how this year has been for me. I have just had a brief look over my postContinue reading “My Anniversary of two years since diagnosis… 15/12/22”