Gayle
 
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Lily

 

A little about me

  • My age: I am 30yrs old
  • Where I live: In Australia with my Fiance Andrew and our baby son Logan.
  • Latest developments in my life: Our baby son Logan arrived into the world on Friday the 19th of September 2003.
  • My main interests: Taking care of Logan, creating and learning how to build websites, scrapbooking and managing my forum.
  • My other interests: Going out for coffee, picnics, long scenic drives, going to the movies, listening to music, interneting and spending time with Andrew and Logan.
  • How can you contact me: Email me at: snowcherub3@yahoo.com
  • ICQ: 93559219 , MSN: snowbeauty73@hotmail.com.

How I became sick with ME/CFS

I first became sick in 1990, at the age of 16 when I was hit with a barrage of chronic secondary viral infections which lasted for 1 and a half years, I took anti biotic after anti biotic because I had too , yet the infections persisted.
Throughout that time I managed to work full-time for 12 months as a pharmacy assistant and then start a 12 month diploma in theatrical makeup (not a beautician!) under the teaching of Dawn Swane at "The Art and Technology of Makeup College" in Chippendale, Sydney. Life was going pretty well and I had my future and career mapped out...then in March of that year (1992) I contracted another virus, yet this time it was very severe and left me incredibly sick and completely exhausted and unable to continue on with my studies. I then decided to defer them to the following year.

12 months on and I still was no where near well enough to study, let alone travel the 3 hrs a day to get to Sydney then back home!, it was then evident that my body just wasn't doing what my mind was telling it to do!, I then started to get worried that something was more wrong than just a severe virus and went to see some specialists, a few gallons of blood and lots of other tests later , I was diagnosed with M.E/CFS .....what an exciting life for a 20 yr old I thought, this was not my plan for my life and I refused to believe in my mind that I would be sick for much longer!, and so began my mission to find a cure.....

11yrs on and the ME/CFS is still as persistant as ever, despite having tried everything and done everything from spending $1000 on 3 different forms of natural therapies, to positive thinking, special diets, exercise, and gamaglobulin injections to get my system well again but to no avail.
I find this incredibly frustrating especially because I have no control over it, it's not like I can do a course to get better or win lotto or something it's completely out of my hands, and beyond comprehension not only to myself but to everyone around me.

In January 2000 when I contracted glandular fever (the first dose!) I finally excepted that continually bashing myself up emotionally, and saying to myself and everyone else "when I get better" , was only placing enormous amounts of stress on myself, which inturn would not help me get better!......I finally found peace with the disease and it felt good.

As anyone with M.E./CFS knows, it's a long hard and often very lonely road, we not only have to cope with the effects of the illness, but also other people's ignorance which at times can be worse, not to mention very damaging, my hope for the future is that as sufferers of this disease we will be taken seriously and treated with the respect we deserve.

Gayle

Life is mostly froth and bubble;
Two things stand like stone:—
Kindness in another’s trouble,
Courage in our own.

Adam Lindsay Gordon

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