The last few days have been difficult ones as I unfortunately managed to get some kind of stomach bug. I have had three days of changing symptoms, all of which seemed like classic COVID symptoms. However, I have tested myself 3 x and have been clear. So the first day, I just felt really rottenContinue reading “Medications and sickness”
Author Archives: kiwipommysue
Being honest and not always positive!
I read today another PD person’s Blog about feeling less than positive and her symptoms getting on top of her for the last few days or so. She is usually a very positive person, but she is having a bad run of it at present and she was apologising for writing a less than positiveContinue reading “Being honest and not always positive!”
Do unto others…
Being raised a Catholic – one very lapsed Catholic I might add – there is a prayer somewhere that goes ‘Do unto others as you would like them to do unto you’. I think that is something that we should all keep in mind as we go through life. As much as possible I tryContinue reading “Do unto others…”
Just because life is not all about Parkinson’s
A poem I wrote over 20 years ago after meeting my wonderful husband online. I always say he is the best internet shopping bargain I’ve ever had. A wee bit of Friday Fun! Ode to Shopping for Shoes and finding a mateBeen sitting here thinking and considered with careAnd now here’s my thoughts that I’dContinue reading “Just because life is not all about Parkinson’s”
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….”
I’ll keep you in my mirror Layla…
Inspired by a bike ride with my grand-daughter today. Also, a metaphor for watching over her as she grows. I’ll keep you in my mirror Layla I’ll keep you in my mirror Layla and watch you as you ride I’ll keep you in my mirror, till we are side by side I’ll keep you inContinue reading “I’ll keep you in my mirror Layla…”
Sleep …Zzzzzz
I don’t know whether it is just a natural part of the ageing process, but I find that I can’t seem to go to bed early these days. It may be part of Parkinson’s perhaps, but I find if I go to bed before about 11.00pm I stay awake for much longer. It also helpsContinue reading “Sleep …Zzzzzz”
If you care, will you go into care?
I was reading a post by someone on a Facebook Page for people with Parkinson’s and their carers tonight. It was posted by the daughter of someone who has Parkinson’s and whose husband has become her carer. Both parents are in their 80’s. Doctors have recommended that the Mother with Parkinson’s needs to go intoContinue reading “If you care, will you go into care?”
Freedom
What does freedom mean to me? It is the ability to do what I want and be who I want. To be able to make my own decisions. It is about being able to do things for myself and to gain satisfaction in doing so. It is also about being able to go where IContinue reading “Freedom”
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?”
My journey with Parkinsons 