If your child has been recently diagnosed with a food allergy, or you are feeling overwhelmed by a new stage in allergy management, please register your interest for this presentation being held in Melbourne.
Doctors and specialists are great at diagnosing and prescribing medication for the allergies we have. However, when our son was first diagnosed with multiple food allergies, including anaphylaxis, there was little support for the every day challenges we would encounter. Over the years we have gathered plenty of information, talked to many many other allergy families, and of course we have done the hard yards of learning things as we go.
It is my hope, to equip and enable parents who are feeling overwhelmed by the challenges of food allergies.
By providing practical information and emotional support, we can enable each other to enjoy the fullness of life again, albeit in a slightly different manner. Please register your interest via email or phone. If you are not able to attend this specific date, please feel free to contact us for upcoming events and opportunities.
Thursday, September 15, 2016
Saturday, April 23, 2016
Monday, April 18, 2016
Multicultural Allergy awareness is crucial for the lives of our little ones. Here is a message from one of our Allergy Mums - PLEASE share this message for others to read on Facebook, Pinterest... anywhere and everywhere you can.
This is just a request to spread the word about anaphylaxis (life threatening allergies). Yesterday my 2 year old son was in hospital for an anaphylactic reaction after another mum gave him a biscuit. I needed to administer his epipen and call an ambulance as his legs stopped working, he vomited and developed hives. The epipen did it's job as he could still breath.
The other mum didn't speak English so there was a language barrier there. I was sitting right there when I saw her offer it to him. I said 'no thanks, he has allergies'. It turns out she had already offered him one and he took it and ate it (he's 2) but I didn't see because his back was towards me; I was responding to the second offer....
I'm not blaming that other mum as the onus was on me to keep an eye on him - I guess I dropped the ball there.
I would encourage people to spread the word, especially to translate this to their non English speaking family and friends. It's a huge cultural thing to share food and it's an easy and generous thing to do without knowing about anaphylaxis.
I know allergies are on the rise and that some people may find other kids/people with allergies an inconvenience to their lunchbox and eating experience. I have attached a picture of this inconvenience, who also happens to be the light of my life.
Share toys, not food.