The Younger Years Part 2

(Sorry it's a long one!)

Everybody has bowel motions.  It is part of life. Growing up, I just seemed to have alot more than 'normal' people.  Mum tried all things holistic-naturopaths, different food diets, dieticians, oh and the potions!!...I recall a family holiday to Yeppoon and amongst snorkeling and boom-netting, we also visited an iridologist.  She sent us home with a HUGE bottle of aloe vera juice and chlorophyll! As a 10 year old trying to stomach this was just awful! 

It wasn’t long after this that I had my first Endoscopy and Colonoscopy.  I can vividly remember as a 10-11 year old driving with Mum to Buderim to have something unknown and slightly scary done to me.  The 'preparation' is something you never forget and never gets better, no matter how many times you have one...starting a few days before, with a low fibre diet and then the day before…drinking about 3 litres of Fleet…a liquid that can only be described as tasting like goat spit and makes you gag with each swallow! 
I recall sitting in the waiting area with my hospital gown on, the ones that tie up at the back, no undies on, feeling very vulnerable. The rest is a blur.

I was diagnosed with Ulcerative Colitis.  An inflammatory bowel disease that affects the lining of the bowel wall and rectum.  I was started straight away on a high dose Prednisone (a type of steroid that quickly attacks inflammation) and salazopyrin (which belongs to the anti-inflammatory group of drugs).

As a child all you want is to fit in and be ‘normal’ but there was no chance of this now.  One of the side effects of Prednisone is fluid retention and weight gain.  I went from being a scrawny kid to feeling like a puffer fish.

Being such a naïve child I guess I didn’t really know what all this meant-Ulcerative Colitis (UC).

I knew I had to take tablets everyday and supplements that mum felt may help and that if I started going to the bathroom too often then I would be put back on the stuff that made my face fat.

I hit high school and loved it. I had a lot of friends and remember flitting around different groups of people at lunch.  I met my husband and some very wonderful people still in my life today there.  I graduated having been Vice-Captain and my best friend as School Captain.

I think for most of the time the UC remained fairly controlled. I had flares up I don’t really remember it having much impact on my life.  I danced, played softball, learnt the organ/piano, got my first job at the local newsagent and really enjoyed my school days. 

It was around the age of 15-16 that I was referred on from my specialist based at Buderim to the Irritable Bowel Disease (IBD) team at the RBWH in Brisbane.  The specialist there had treated my Nana and another family member for their IBD.

I wasn’t responding to my medication anymore and after more colonoscopies, it showed that the inflammation was no longer just affecting the lining of the bowel,  but the thickness of the bowel wall too…I now had Crohn’s disease.

Me (with my big bro) just before UC diagnosis

And after UC diagnosis, on Prednisone

Until next time.... xo

The Younger Years - Part 1

I have very fond memories of my childhood.  Growing up, we lived out of town on 10 acres.  My older brother and I spent days swimming in the dam, setting traps for lobbys and enjoying as much of the outdoors as we could. 

When I sat down to right this post, so many little memories came popping back.  
I remember sneaking to the fridge to scrape the fresh cream off the bucket of milk that Dad had gotten from our cow Goldie.  I remember not caring if chook poop squished between my toes as I did my afternoon chores of collecting the eggs.  I realise how lucky I was to have so many rich experiences.  We never visited a petting zoo-we practically had one at home.  From seeing a calf being pushed into this world, wet and gooey and watch it take its first incredibly wobbly steps to helping chicks peck their way out of their eggs and feel their soft fluffiness on my cheek. I can also tell you that chooks really CAN run around headless!!! We grew up knowing bon-fires, camping, fishing, wading in flood waters as the weir overflowed, catching tadpoles, freedom and respect for our parents. So many of these things I want for our son.

When it came to school I loved it. Our primary school was small. About 60 kids all up and everybody knew everybody. We would ride our bikes down to the corner and leave them in the gutter while we waited for the bus.  Winter and rainy days were the worst-not because of the cold or rain, but because of the leeches that flicked up off the road! I made my first friend on that bus.  She had the longest hair I had ever seen, a thick fringe cut to her eyebrows and as I recently told her-she is my oldest friend!

As much as I had such a wonderful childhood, there were other bits that certainly weren't as fun.  Constant trips to the bathroom, diarrhea, stomach pains coupled with my Mum's quest to find out what was 'wrong' with her daughter….

Until next time, take care x

I'm Blogging!

It seems everyone is doing it these day, whether it's as a 'release', an outlet, for therapy, for exposure or just because. So here I am. I'm blogging! I have no idea how to add details in the 'About Me' tab or what these gadgets or widgets mean but I'm sure I will work it out along the way!


During a lazy lunch with some beautiful friends in which I was re-telling the details of my latest flare (more on that later), it was put to me that it might be time to 'sexy-up' Crohn's and start a blog! So here it is. I want this blog to be a place to tell my personal journey, a place for me to talk about me and my experience with Crohn's Disease and most importantly get the message out there that it is ok to talk about inflammatory bowel disease and not something that needs to be swept under the carpet.


I have Ileocolonic and perianal Crohnn's Disease. A chronic inflammatory bowel disease. It primarily causes abdominal pain, diarrhoea (which may be bloody if inflammation is at its worst), vomiting and weight loss. It may also cause complications outside the gastrointestinal tract such as skin rashes, arthritis, inflammation of the eye, tiredness, and lack of concentration.
This is a disease that cannot be made 'prety' with pink ribbon, breasts, bras or butterflies, but it is real and affects males and females at a rate of 5 in 100,000 people.  Occasionally it can affect more than one member of a family.  Both adults and children may have Crohn's disease, but there are peaks of incidence around 25 and 65 years of age.
 Talk to any mum of a child in nappies and they will be able to re-tell all the in's and outs of their little ones bowel movements from the moment they were born.  For some reason society can accept this kind of conversation but is completely repulsed by any sort of talk about their own bowel habits.  We are extremely embarrassed by something that is firstly out of our control and secondly done by every single person (including the Queen!) on this earth! I'm not saying that we all need to divulge these details to each other on a regular basis but to know that it is ok to discuss these issues with with supportive friends or family if you need to. Nobody should suffer in silence.


I have lived with Crohn's most of my life and will continue to post about my journey and current  prognosis.  My goal is to get awareness out there about the disease. Early detection means getting the treatment and support you need.


Until next time...


Jem xo