Getting diagnosed is a journey in itself! I hadn't even heard of
Coeliac Disease when I got diagnosed, so there was no way I would have been in a position to push the GP for tests - I'm just extremely fortunate that my GP was being so thorough.
Did you know that
Coeliac Disesase is the most under diagnosed disease in Australia? The stats are astounding. 1 in 100 people are affected by
Coeliac Disease in this country, but less than 75% of us know that we have it. Check out
http://www.coeliacsociety.com.au/I was well, very well, prior to having my little girl Lucy. I had an extremely busy job (averaging 50 - 60 hour weeks) managing a team of 10, in a start up that was growing so fast we hardly knew how to keep up, and was running at least 4 - 5 times a week, with regular half marathons and 10
kms races keeping my weekends busy. Then I found out I was pregnant....WOW! How exciting!!
The first 25 weeks of the pregnancy were horrible (sorry Lucy!) to say the least....throwing up most mornings, and chronic stomach pains....obviously I constantly feared the worst. But I got through it, and eventually felt better. On December 4
th 2007 Lucy joined my husband and I. I have to say, it was the most amazing moment of my life. She was (and is) perfect.
Welcoming a new born into my world was fabulous, and extremely challenging. After my standard 6 weeks post birth check up, I went back to exercise....I joined a fab, fab group in
Collaroy (northern beaches,
NSW) called Step into Life, and inducted myself back into the world of sport. It all started really well....for a few months, I was energised and feeling great. But slowly, slowly over time, I stopped feeling that endorphin rush we sport junkies love. I thought "oh get over it, you've been up half the night with a small child, of course you're a bit tired" but as time went on, and Lucy slept more, I just felt that I had less and less to give. I remember at one point looking at the training and saying "I haven't got anything to give you today".
I was also craving crap food! I wanted muffins, biscuits, chocolate....you name the sweet thing, I wanted it, especially in the afternoon.
Every time I saw my GP, I'd say to her "I just don't feel right". No stomach cramps, no upset tummy, no rash, no nothing to show for it, I just felt extremely tired, and just didn't feel right. I know that sounds so cliched, but at the time, I couldn't articulate what the problem was. I just didn't feel right.
I had restless legs at night, I couldn't sleep (even though I was becoming more and more tired as
time went on)....I was SO frustrated. And my hubby got to the point where he stopped asking how I was "I'm tired, just SO tired" was the standard response as I was lying on the sofa looking at Lucy wondering just when she'd go to sleep.
My GP started some blood tests. The first lot came back that my iron was a bit low (normal post birth anyway) and my thyroid a bit
under active, but neither thing so bad that it would be making me feel as tired as I was. The second round of blood tests were taken, and to my surprise, she called me at 9pm about a week later. God, I was thinking, "please, please don't be ringing me to say I'm pregnant!" - I couldn't have coped. She told me my blood was showing
Coeliac antibodies. I had to keep eating gluten (never, ever stop eating gluten until you've had an endoscopy - a small intestine biopsy, otherwise you might get a false negative for
Coeliac Disease) and I went in for a biopsy a few weeks later.
The
anesthetic was amazing! I was gutted when they woke me up, it was the best sleep I'd had in 8 months!
The following week, I was in Melbourne, at a client meeting, eating my
turkish bread sandwich, and I got the call. "Zoe, you are
Coeliac. You need to go onto a gluten free diet for the rest of your life". I hung up the call, finished the sandwich and got on with the meeting. That was a Thursday I think. I spent the rest of the week ordering pizza, eating pasta, getting as much bread into me as physically possible. I weighed 66
kgs the week I was diagnosed. I now weigh 62
kgs. I'll explain how I managed that without even trying in another post.
I didn't have any classic symptoms of being a
Coeliac. Except being very fatigued. I didn't show any signs of irritable bowl syndrome, I didn't get
dermatitis (a skin condition that many
coeliacs get)...I was just bloody tired all the time. The danger of not getting diagnosed is serious - osteoporosis and bowl cancer being two big ones. I've had a
Dexa scan on my bones - unfortunately they are already showing a less than normal range for my age, so I feel blessed that I'm diagnosed now and can do something about it (
incidentally my Mum has severe osteoporosis - she hasn't been tested for
coeliac.....
hmmmm).
Don't let anyone tell you to go gluten free before you have a biopsy. It's extremely important you keep eating gluten before you go in. Also, a blood test IS NOT a final diagnosis of
Coeliac Disease - it is only an indication. The only true way to diagnose is through biopsy (which by the way, doesn't hurt at all - you get to have a nice sleep for half and hour and wake up with no pain at all). There is also a gene test now, so after you've been diagnosed, you can send your immediate family (kids, mum, dad and siblings) off to have a small swab from their mouth. If they have the gene, they need to be monitored. If they don't, they never have to worry about it!
Don't be afraid of being diagnosed either. I can assure you, that despite being gutted about having to give up bread, pasta etc, I have found ways around it, and I now feel absolutely amazing - probably the best I have done in years. I'll share some of my other thoughts on living a gluten free life soon.
Ps - I honestly used to think people with food
intolerance's were making it all up! How wrong I was....I am eating my words now!