We went to London to campaign against the new NIPT test with Don’t Screen Us out! If you want to learn more or haven’t heard of them then please visit their website http://www.dontscreenusout.org
We had a brilliant time!
Rebecca
Xx
We went to London to campaign against the new NIPT test with Don’t Screen Us out! If you want to learn more or haven’t heard of them then please visit their website http://www.dontscreenusout.org
We had a brilliant time!
Rebecca
Xx
These are flowers. Imagine if the yellow flower was your unborn baby that had a prenatal diagnosis of Down syndrome and the blue flowers are all the other babies that don’t. Continue reading “Just a little flower”
For these reasons I thought it would be a cool idea not to just use my reasons but reasons from other people from the Facebook group, Future of Downs. This is a community that is amazing for people who have someone with Down Syndrome in their life or even have Ds themselves. Continue reading “Reasons loving someone with Down Syndrome is amazing!”
To lots of people it is just the 1st of October but to us it means that it’s the first day of Down Syndrome Awareness month. Throughout the month I will be writing post all about Ds and how it affects us and what we have been through. Continue reading “It’s the first of October…”
It’s like being a school, I need an excuse and I need to explain. That and the fact that I’m so bloody excited! Continue reading “Why there will no blog on the 11th October!!”
Last week we got a call from a lovely lady at a huge uk magazine Continue reading “BIG RORY NEWS!!!”
Some people might already know all about Rory but I’ve had messages asking for a blog about him. So this post is a brilliant opportunity to raise awareness for Rory’s conditions. Continue reading “Time to meet our little Rory”