Dancing in the Lyme Light

4 years ago I travelled to Exmouth for a work trip and was bitten by an insect that left me with debilitating symptoms. Ive lost over 10kgs, suffered from extreme muscle and nerve pain, fatigue, hair loss, seizures, brain inflammation, insomnia, sensitivity to light and sound. I can no longer work, drive, get groceries, clean my house, garden and barely leave the house.

Recently I was diagnosed with Lyme disease and a range of Co infections. Think of the last time you felt so sick you could barely get out of bed. Now times that by about 100 and you might begin to understand what it feels like to have Lyme.

What’s worse is Lyme disease is not recognised in Australia. There are little to no treatment options and Drs are in fear of losing their ability to practice. But there are some lovely souls who are trying to help us fight the battle of our lives.

There is no government support. I’ve been rejected by Centrelink 8 times and NDIS 3. Now I’ve received a tax bill for at least $6k even though I’m unemployed. You wouldn’t expect treatment like this in what’s supposed to be a first world country. But my story sadly is not uncommon.

I went from being a happy, healthy 33 year old to some days barely able to move. It’s agony and what saddens me is there are so many of us suffering in silence.

We all go through challenges in life that shape us. Hopefully one day I’ll be strong enough to help others like me who are doing it alone. I’m asking for your help something I rarely do. But unfortunately I have no choice.

Please help me fund my medical treatment and donate to my cause. Every little bit helps. If you are doing it tough and can’t spare any money, please share my story to help spread awareness about Lyme disease in Australia.

Love and light xx