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Hear Our Community Voices – Marfan Awareness Month 2026

Hear Our Community Voices – Marfan Awareness Month 2026

Marfan Awareness Month. Community Member: Sally Ferguson.   Part of our 'Community Voices' Series. At CTDNA, we believe there is power in sharing stories. Our Community Voices series, gives a platform to individuals living with heritable connective tissue...

Hear Our Community Voices

Hear Our Community Voices

Hear Our Community Voices. Community Member: Jennifer Hillier.   Our 'Community Voices' Series. At CTDNA, we believe there is power in sharing stories. Our Community Voices series, gives a platform to individuals living with heritable connective tissue disorders...

Research Update

Research Update

New Global Research Confirms What We Already Knew: The Burden of hEDS and HSD is Heavy.   A major new international study has highlighted the realities of living with hypermobile Ehlers-Danlos syndrome (hEDS) and hypermobility spectrum disorders (HSD). Despite...

Hear Our Community Voices

Hear Our Community Voices

Hear Our Community Voices. Community Member: Rebecca Peiper.   Introducing Our 'Community Voices' Series. At CTDNA, we believe there is power in sharing stories. Our Community Voices series, gives a platform to individuals living with heritable connective tissue...

The Little Mouse that Sparked the Loudest Voice

The Little Mouse that Sparked the Loudest Voice

The Little Mouse that Sparked the Loudest Voice in an Aussie Country Town   In January 2021, Rhianna Cunningham lost her battle with Vascular Ehlers-Danlos Syndrome (vEDS), a rare genetic disorder characterised by fragile blood vessels and skin that bruises and...

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