Welcome to the new blog series: Wellness Wednesday! Exercise is a scary word for people with Chronic Fatigue Syndrome/Myalgic Encephalomyelitis (CFS/ME), and other chronic issues. I know I struggle with balancing the desire to get back to my active self, and the fear of causing yet another relapse due to even light exercise. So this […] Read more…
Long term illness
Glimpse into Motivation Monday – week 7 2014
Welcome to the new blog series… Motivation Mondays! To get things started, here is an idea to think about this week…. “Do not wait until the conditions are perfect to begin. Beginning makes the conditions perfect.” A big part of having a chronic illness is waiting. Waiting for answers, waiting for results, waiting for improvements. […] Read more…
Glimpse into a community for health and happiness
I would love this blog to be a hub for a community of kindred spirits, coming together in the interest of their health, to find motivation, ideas, and inspiration. Whether it be due to CFS/ME, or other types of chronic illness, food intolerances, or healthy eating and a willingness to improve your well being that […] Read more…
Glimpse into a misunderstood illness; Chronic Fatigue Syndome/Myalgic Encephalmyelitis
Having a chronic health problem is frustrating and horrible. Having a chronic health problem which is yet to be fully understood by medical and scientific explanations is like slamming your head against a wall of nails. The sheer arrogance, ignorance, insensitivity and degradation put towards people with these illnesses is mind boggling. I recently had […] Read more…
Glimpse into the New Year
Today is New Year’s Day. A day typically dedicated to reflection and statements of intentions. Every New Year for the past 3 years, I have made New Year’s resolutions. These have all revolved around my health and improving its state of deterioration, which had begun to speed up between 2008 and 2010. Each year, I felt more determined […] Read more…
Glimpse into brain fog
Something that a lot of people ask me about or don’t understand, is the feeling of “brain fog”, which is so prevalent in conditions like Myalgic Encephalmyeltis. Obviously, brain fog is not a scientific term, but it so clearly depicts the feeling. Pic taken from here Your mind is blanketed with London-like, pea soup fog; […] Read more…
Glimpse into my thoughts about chronic illness
I have chosen to write 5 things I hate about having a chronic illness, 5 things that help put a positive spin on chronic illness, and 5 things I still need to learn from or about living with chronic illness. I hope this helps people feel less alone, get some ideas, or understand other people’s situation… […] Read more…
Glimpse into Chronic Fatigue Syndrome
A couple of weeks ago, I went to see my doctor, and came out feeling like we had had a break though. I have been seeing him for close to a year now, and he has tested me for so many conditions in an attempt to explain my symptoms. I have had several tests come […] Read more…
Glimpse into defining ourselves through illness
I read some advice recently about not letting your illness define you. This initially sounded logical, and quite a basic instinct. However upon mulling it over, I started questioning the feasibility of this concept, when you are deep in the throws of a chronic condition. If being defined means to describe the nature or basic qualities […] Read more…
Glimpse into the misconceptions surrounding pushing through chronic illness
This morning, my mum and I were talking about people’s perceptions of you when you have a chronic health problem. I know that I have touched on this before, but when you are living with an ongoing issue, it is tough enough without having to deal with people’s misconceptions and judgements. We came to the […] Read more…