I’ve always been a firm believer in trusting one’s gut
instinct. I taught The Apprentice and Junior Accountant, when they were young
girls, that if something doesn’t feel right, it probably isn’t, and I’ve
started teaching the younger three the same thing.
Fed up with ongoing illness and dissatisfied with the experts’ opinions, I started my own research for answers. My desire for an exact diagnosis and treatment turned into a journey of discovery and the start of a new way of life, not just for me, but for my family too.
Pages
Star:
1. any heavenly body.2. a person's destiny, temperament, etc.
www.dictionary.com
Whether you’re reading this because you’re gluten intolerant, suffer from PVFS or CFS, are starting to grow your own veggies, embracing natural and/or alternative remedies, or just want to enjoy the journey with us, please remember I’m not a medical expert, nor am I here to debate global warming. Being diagnosed with a life-changing illness, looking for answers or changing the way one lives can all be overwhelming events, so I hope that by sharing the triumphs and tragedies, you too will benefit in some way from our journey.
I hope you enjoy the journey and if you leave this blog having learnt only one new recipe or started to think about finding your star, then this blog’s purpose has been served.
My two favourite sayings:
Pondering the choices we make at the crossroads is like revision in the school of life. Regretting the mistakes or taking for granted the successes means we have learnt nought.
An attentive student will gain wisdom from the mistakes and joy from the successes. Cartillyer – 2008
'Strength does not come from physical capacity. It comes from an indomitable will.' Mohandas Gandhi
Showing posts with label chronic fatigue syndrome. Show all posts
Showing posts with label chronic fatigue syndrome. Show all posts
Wednesday, July 11, 2012
Wednesday, June 27, 2012
The Specialness of Specialists
(Try saying the title of this post three times really fast.)
I visited specialist doctor rooms a couple of times as a
child. The quietness of the rooms was unnerving, the many empty chairs gave me
the distinct impression that no one liked going there, and the cold, meticulous
manner in which the specialist dealt with his patients, i.e. me, convinced me
he was the reason people stayed away.
Tuesday, June 5, 2012
Time To Change Doctors
When our doctor slammed the door shut on our three-week plan to help us live with my post-viral fatigue, I started thinking about our doctor’s abilities.
Saturday, May 19, 2012
Our PVFS Three-week Plan
The thought of having post-viral fatigue syndrome (PVFS) for
six months depressed me. I already felt useless as a wife and mother and I
struggled to continue with my online studies. I had heard of chronic fatigue
syndrome (CFS), so when I started researching PVFS I soon discovered that PVFS, CFS, myalgic encephalomyelitis (ME) and Fibromyalgia shared similar symptoms.
The thing that scared me the most was how long some people had suffered from
debilitating fatigue.
Sunday, May 6, 2012
It Began With a Virus
For anyone who has been diagnosed with post-viral fatigue syndrome (PVFS), chronic fatigue syndrome (CFS), or myalgic encephalomyelitis (ME), and refuses to accept the diagnosis, this post is for you.
I first discovered that something wasn’t right with my body in April 2010 when I fell very ill with a virus. My entire body ached for two weeks – my muscles, my bones, everything from the top of my head to the tips of my toes. I couldn’t stand to be touched. It was like the all-over ache people get with the flu, but a hundred times worse. The only fever was on the first day and I didn’t have any other symptoms, except for extreme fatigue.
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