Svetlana Arandjelovic

Will you support my Live Fearless Challenge?

I’m taking on the Live Fearless Challenge this September for the 2nd year in a row to raise awareness and funds for the almost 180,000 Australians living with Crohn’s disease and ulcerative colitis. Money raised through fundraisers like this is literally why I’m alive, walking around and functioning the way I am today. The new research and drugs that have become available to me in the last year has meant this year has looked very different for me than what last year did. 

IBD is one of the most misunderstood chronic health conditions. There is currently no cure, it is significantly underfunded, and is the only major chronic condition in Australia without dedicated government funding for patient support.

Yet people living with Crohn’s disease and ulcerative colitis are ‘frequent flyers’ of the hospital system. It strips away income, disrupts education, work, relationships and travel, and can have a significant impact on both physical and mental health.

Flares can last anywhere from weeks to months if you’re ‘lucky’, or years like my most recent flare. Trying to find a treatment that works for me and controls my disease after failing so many drugs including three biologics, is painful and exhausting, both physically and mentally. Infusions, self injections, dozens of tablets a day, steroids - I’ve been through it all. Last year, surgery to remove part of my colon and have a colostomy bag was a very real possibility and I’ve never been so scared in my life. Some days are better than others but some days are full of pain, tears and mental defeat but through all of it we have no choice but to go on with our days, silently suffering and our bodies in survival mode 24/7.

Trying to explain to people why you can’t eat is exhausting. Trying to explain to people why you can’t leave the house because you’re bed ridden for weeks/months at a time is exhausting. Trying to explain why you can’t do certain things is exhausting. Trying to get people to understand that just because you look fine does not by any way mean that you are anywhere near well - justifying this invisible illness is SO HARD. I lose 10kg at a time when I get really sick, and I don’t have that weight to begin with. Then I have to deal with the insensitive comments about my weight loss on top of everything else, when putting on and maintaining a healthy weight is all I ever dream of. Then there’s the other side effects to these chemo based treatments, like chronic fatigue, brain fog, severe whole body eczema, severe hair loss, and other adverse side effects that result in ambulance trips to emergency. Over the last 10 and a bit years I’ve missed out on so many opportunities and general enjoyment because of this disease taking over my life. 

That’s why I’m getting active (or as active as I can) this September for the second year in a row. Every movement is for the thousands of people living with IBD who face this in silence. Last year i was the second highest fund raiser in Australia, raising $17,000!!! Let’s see how much we can do this year. 

Your donation will help fund critical research, patient support, education and advocacy - because no one should have to manage this disease on their own. Though God is always with me. Bless everyone who donates - I appreciate it more than words 💜

All donations over $2 are tax-deductible (you’ll receive a receipt straight to your inbox).