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 wheat intolerances. Show all posts
Showing posts with label wheat intolerances. Show all posts

Wednesday, October 3, 2012

The 7 Stages of My Gluten Grief


I think that loss is one of the hardest things in life to deal with. Whether it’s the loss of a loved one, a limb, or a lifestyle enjoyed for decades, one is faced with an array of emotions as they adjust to the changes in their life. 

Monday, July 23, 2012

A Prescription for Persistence


I can’t say that my getting to the bottom of my illnesses came about because I was so clever or smart, because I spent a long time floundering in the world of information overload. I can’t give my doctor credit for it either, because she and the other doctors in the medical practice misdiagnosed me. 

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.