17/06/2026
I live in Staffordshire and for the first few years after diagnosis I received prescriptions to help with staple gluten-free foods, but that eventually stopped.
As a family of 5, our food bill is huge. I often hear parents on the school run talking about the rising cost of food, and although I completely understand, I usually stay quiet because I would love our shopping bill to be that low.
The reality is that a gluten-free food shop is incredibly expensive. Bread alone for packed lunches is an essential in our house and costs so much more. If I’m honest, I try not to look too closely at the total when I get to the till! 🙈
Does anyone else feel the same? How much extra do you think being gluten free adds to your weekly food shop? 🛒
Imagine being diagnosed with coeliac disease in Wales today.
You could receive a prepaid gluten free food card to help cover the extra cost of gluten free staples.
Meanwhile, many people in England have seen gluten free prescriptions reduced or removed altogether.
Same condition.
Same medical need.
Very different support.
It’s brilliant to see Wales recognising that a gluten free diet isn’t a lifestyle choice. It’s treatment.
But it does raise a question…
Should support for people with coeliac disease depend on your postcode?
Tell us where you’re from and whether your area offers any help with gluten free food.
👇 We’d love to hear your experience.