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…
Myalgic Encephalmyelitis
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…
Tai chi
When I had better health than I do now, I loved to be active. I have never been particularly good at sports, but I was always doing something – softball, hockey, gymnastics, rowing, cricket, swimming, gym classes, dancing, hiking, cycling – I enjoyed the outdoors, and fun, high-energy activity. My Mum has learned and then […] 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…
Glimpse into International Awareness Day May 12th ~ countdown…13 days
Glimpse into things to do when your body doesn’t want to play ball -Wellness Wednesday week 15
A common question I see popping up in forums and groups for people with chronic health issues is “how do I stop myself from going crazy with boredom/frustration/loneliness/anger/sadness?” It can be a problematic issue, and it is a catch 22 situation. You feel so unwell because your body is sick, so you inevitably miss out […] Read more…
Glimpse into body image with chronic conditions (i.e. wanting to look and feel great!) Wellness Wednesday week 15
Something that I do not see written about much in relation to Chronic Fatigue Syndrome (CFS), Postural Orthostatic Tachycardia Syndrome (POTS) and other chronic illnesses, is body image and getting fit. Obviously, it is not the highest priority when you are struggling to gain a good quality of life, so it doesn’t feature so much in […] Read more…