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Two Decades of Dedication
Celebrating Gill and Gordon Parry’s Fundraising
by Despina Dinca & Ginger Irvine

Gill and Gordon ParryFor more than twenty years, the village of Hawarden and the surrounding North Wales community have come together in support of NA research, thanks to the remarkable dedication of Gill and Gordon Parry. 

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Introducing Citizen Health
Building the Foundations of a Global NA Registry
by Dave Asinger & Despina Dinca

Citizen health logo

We are pleased to share an important step forward in our long‑term goal of building a robust, secure, and patient‑centred registry for VPS13A and XK diseases. 

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A Family’s Story
Living With VPS13A and Navigating a System Not Built for Ultra Rare Conditions
by Huma Baig

This spring, we were contacted by Huma Baig, one of six siblings from a close‑knit family living in the UK.

Three of the siblings, Somara, Javad, and Khurram, have been diagnosed with VPS13A disease. Their story is one of resilience, love, and unwavering determination in the face of challenges that no family should have to face alone. 

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Veronica's Story
Finding Joy in the Everyday
by Veronica Thomson & Kim Thomson

Veronica, Regina and Mark Thomson

Veronica Thomson is a VPS13A diagnosed patient who lives in the USA with her beautiful family. This is her story. 

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News from NA-USA
Funding Research and More
by Joy Willard-Williford

Joy Willard-WillifordNeuroacanthocytosis Advocacy USA, Inc. has a lot of news to report. Read on and learn more.

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Sheila’s Open Garden Fundraiser
Over a Decade of Creativity, Community, and NA Advocacy
by Ginger Irvine & Despina Dinca

Sheila Averbuch

Sheila Averbuch’s Mercat Cottage Garden has long been more than a beautiful space; it has been a place where creativity, generosity and advocacy meet. 

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Supporting Research and Diagnosis
Renewed Grants for VPS13A and XK Progress
by Despina Dinca

Research we fund - NA Advocacy & NA |Advocacy USA

This year, the NA Advocacy and NA Advocacy USA are proud to continue funding two important projects that reflect our long‑term commitment to both scientific discovery and practical diagnostic support for VPS13A and XK diseases.  

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Creating a Legacy of Hope for Neuroacanthocytosis Patients
The Gift That Keeps Giving: How Planned Giving Creates a Legacy for Generations
by Roxanne Lestrange

Roxanne Lestrange, Director of Philanthropy and Operations for the Community Foundation of Brevard in Melbourne, Florida, offers a Planned Giving 101 tutorial. Please note that the article is written from an American perspective, but most of the concepts presented are universal. As always, consult your own financial advisor or attorney on these matters. We encourage you to keep The Advocacy for Neuroacanthocytosis Patients (based in London) and Neuroacanthocytosis Advocacy USA, Inc. in mind when creating your legacy.

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25th VPS13 Forum Report
New Clinical Developments
by Despina Dinca

Report - 25th VPS13 Forum - New clinical developments - 27 April 2026The 25th VPS13 Forum took place on 27 April 2026, moderated by Dr Kevin Peikert along with Professor Ruth Walker and Professor Adrian Danek.

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Understanding Emerging Therapies
PART 1 - Genetic Approaches – A Long-term Path
by Ruth Walker, Kevin Peikert & Despina Dinca

Understanding emerging therapiesWe are starting a series of articles designed to support our readers in understand what is going on as new therapies emerge in the research world. 

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In this issue
At a Glance
Two Decades of Dedication
Introducing Citizen Health
A Family’s Story
Veronica's Story
News from NA-USA
Sheila’s Open Garden Fundraiser
Supporting Research and Diagnosis
Creating a Legacy of Hope for Neuroacanthocytosis Patients
25th VPS13 Forum Report
Understanding Emerging Therapies
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