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Better Together for Healthy Bone Marrow

rare revolution magazine
community members' stories


Rare Revolution Magazine Articles

During 2024 and 2025, some of our amazing community members shared their stories with Rare Revolution Magazine…


Click here to access the Rare Revolution article titled "one in a million", a story shared by Claire who has aplastic anaemia

Click here to access the Rare Revolution article titled "a day in the life: living with sickle cell anaemia - Naomi's story"

Click here to access the Rare Revolution article titled "a day in the life: living with dyskeratosis congenita - Paula's story"

Click here to access the Rare Revolution article titled  "a day in the life: being diagnosed with Fanconi anaemia as a child and as an adult - what are the differences?"

Click here to access the Rare Revolution titled "living rare in your twenties" by Jovi and Virginia who both have PNH

Click here to access the Rare Revolution article titled: "having SDS shouldn't hold you back, it shouldn't define who you are"

This project is supported by The National Lottery Community Fund – thanks to players of The National Lottery.
Super Rare – But not alone

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