People are constantly saying to be grateful for this life that we have been given; this life is a fleeting gift and we need to make the most of every moment. I am a positive person, and always believe that it is important to look for the good, even if it is the tinniest thing […] Read more…
Chronic Fatigue Syndrome
It has been four years…
This week marks 4 years since I stopped working as a nurse. I remember a doctor telling me a little while before that it would be ideal to have at least 6 months off to deal with my health. I drove to my parents’ house and burst into tears to Mum, thinking how on earth […] Read more…
Goal setting with chronic illness
The hype of the New Year (“New Year, New You” and all that) can be motivating and refreshing. It can also cause alarm and self-deprecation. While one person may be swearing off chocolate and lacing up their shoes ready for a 10 km run, you may be reaching for the sweets jar and curling up […] Read more…
Living a satisfying life (even when unwell) & changing your expectations
As of today, I have been unable to work for three years. Wow. That is a long time. It took me that long to get my degree for the career I loved! On the day that I had been unable to work for a year, I had a group of friends over with my family, […] Read more…
An Autoimmune Protocol update
The Autoimmune Protocol (AIP) is a diet which focuses on foods that have been shown to either cause or worsen autoimmune conditions. I have written about what I have learned about AIP, recipe ideas, and my experiences in these posts: Beginning AIP Week one of AIP Week two of AIP Week three of AIP Week four of […] Read more…
You look good
Among the community of people with chronic illnesses, a common topic of contention is the grey area of receiving a compliment – a particular compliment, that is. The compliment in question? “You look good.” It seems harmless. It is a mostly well intentioned statement, offered up as a token gesture of good will and care. […] Read more…
Glimpse into learning to live with chronic illness
Now and again, someone stumbles across my blog who is new to dealing with chronic fatigue, or a friend of a friend points them in my direction for advice. This has made me think that it is time to do a summary post about some of what I have learned about dealing with certain issues […] Read more…
Glimpse into my atricle contribution for Your Zen Life!….ME/CFS International Awareness Day – May 12th
I wrote an article for International Awareness Day for the Your Zen Life website, and it was published last week! If you are interested in reading it, it is on the website at http://www.yourzenlife.com/post/me-cfs-international-awareness-day-may-12th, or read below. Did you know that May 12th is International Awareness Day for Chronic Immunological and Neurological Diseases? One of these […] Read more…
Glimpse into a day in the life of a sufferer of Myalgic Encephalomyeltis/Chronic Fatigue Syndrome
As part of raising awareness of Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) leading up to the International Awareness Day on May 12th, I decided that I would document an average day for me, a sufferer of ME/CFS. Wednesday April 30th, 2014: 11am: I wake up just after 11am, feeling groggy and tired. I lie there for […] Read more…
Glimpse into part two: things to do when your body doesn’t want to play ball -Wellness Wednesday week 16
Last Wellness Wednesday, I blogged 5 ideas for things to do when you are chronically unwell, to keep yourself entertained and happy. You can read them here. This week, I bring you five more ideas! 1. Do a chore. I know, I know, I said that these ideas would entertain you and make you happy! […] Read more…