It shouldn't be this hard…to access allergy care because of where I live.

It shouldn’t be this hard. Children’s allergy care and access to life-changing treatments shouldn’t be limited because of where they live or how much they can afford to pay.

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Why Natasha's Story Matters.

Natasha’s story matters because we don’t want any more families to suffer as we have done. It matters because people should not live in fear of their food allergies as we did.

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Every Child Deserves to BE Included

When we met the staff, we knew we could make this work because they asked US what THEY could do to make sure they were INCLUSIVE whilst keeping Natasha safe from harm!

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She Speaks in Colours - Ellen's Gift of Hope

When you lose a child, people often send you cards that say “There are no words.” Well, Thea found the words, and each one was carefully chosen and full of thought and meaning. It’s a powerful and poignant song, it’s sorrow & joy wrapped up together. It’s the soundtrack to our grief and the hope at the end of the rainbow.

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Gaining Independence with Food Allergies

"I’m 15 years old and I’ve been severely allergic to nearly all tree nuts since I was 2 years old. Throughout my childhood, my mum has been there for me during every allergic reaction I’ve had, but last winter, in the run-up to Christmas, I had to go it alone for the first time without my mum.”

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It's the most wonder/anxious time of the year...

If you have food allergies, as the Christmas celebrations and parties begin, you can find yourself filled with anxieties about how to keep safe.

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