A diagnosis of aplastic anaemia is scary. But you are not alone. You can join our community today and make sense of your diagnosis and what lies ahead. It's some 800 members strong - this is people like you, who've been diagnosed with aplastic anaemia or another rare bone marrow failure, such as paroxysmal nocturnal haemoglobinuria (PNH) or dyskeratosis congenita.

On this site you will find lots of inspiring stories from people just like you, so read on.

Join our vibrant member-only Facebook group

Our closed Facebook group is now nearly 1,300 member strong and growing. Here, you can safely discuss anything that is playing on your mind - whether it's your diagnosis of aplastic anaemia, a bone marrow transplant or journey to recovery. Here you will also find like-minded people actively blogging about bone marrow transplant and practical discussions about travel insurance, sharing of stories. It's the sort of community where the only silly question is the one unasked!

This is a wonderful support site...the more people we have the more information we have. I'm often blown away by the knowledge on here. It's so helpful. It's great to help people struggling. It's also wonderful to hear people's stories further down the line: babies being born, people going on to uni, good luck!

Please get in touch if you'd like to join the community and share your story.