Leave a gift in your Will

Create a lasting legacy for people affected by axial SpA.

A gift in your Will is not about loss – it’s about life. It’s the final chapter of your story, one that keeps helping others long into the future. Without the generosity of people leaving a gift in their Will, much of our work would be impossible.

Danny has pledged to leave a gift in his Will to NASS.

“Being a genetic condition, my axial SpA could easily be passed down to at least one or both of my children. I want to make sure that NASS is around forever to support them.”

Produced by Stepping Stone Media 

Your Support in Action

“Since axial SpA is genetic, my children could suffer as I did. By leaving a gift to NASS, I hope they – and future generations – have access to better care and support.” – Danny, NASS supporter

Thanks to people like Danny, NASS is reducing the average 8.5-year delay to diagnosis, training health professionals, and providing ongoing support for people with axial SpA.

NASS is the only charity in the UK dedicated to transforming the lives of people with axial SpA. We receive no government funding, so every step forward is thanks to the generosity of people like you. It is not uncommon for around 40% of our income to come from gifts in Wills – helping us provide vital support and information, reduce the time to diagnosis and campaign for change.

Why Include NASS in Your Will?

  • It’s impactful. Every gift, large or small, helps future generations affected by axial SpA to receive the care, information, and support that they need.
  • It’s tax-efficient. Gifts to charity are exempt from Inheritance Tax, reducing the tax burden on your estate.
  • It’s flexible. You can leave a percentage of your estate (residuary gift), a fixed sum (pecuniary gift), or a specific item such as jewellery or shares.
  • It’s established. Many of our supporters choose to remember NASS in their Will. It’s a way of preserving your values and making a difference for years to come.

How to Leave a Gift to NASS:

Use our official details:

· Name: National Axial Spondyloarthritis Society

· Charity numbers: England & Wales (1183175) | Scotland (049746)

· Address: Ground Floor, Unit 6, Cambridge Court, 210 Shepherds Bush Road, London W6 7NJ

If you already have a Will:

You can add NASS using a simple document called a codicil. A solicitor can advise you on this.

If you need a new or updated Will:

We’re part of the National Free Wills Network, offering a simple Will for free. There’s no obligation to include NASS, but we hope you’ll consider it once your loved ones are cared for – even 1% of what’s left can change lives. Fill out the form below to register your interest and get started with the National Free Wills Network:

 

NASS is a member of the National Free Wills Network, which means that our Members and supporters can meet with a local solicitor and have a simple Will made, or updated, for free.

Pledge to leave a gift via the National Free Wills Network

Fill in the form below and we will securely pass on the contact details you provide to the National Free Wills Network. You will also receive a NASS legacy giving brochure to download (if you'd like to receive a printed copy, please email fundraising@nass.co.uk to request your copy). Within 3-4 weeks, you will receive a welcome pack from the National Free Wills Network with details of all local solicitors participating in the scheme. If you'd like to receive your welcome pack via email, please provide your email address. If you'd like to receive your welcome pack via post, you only need to provide your address. Then, you can contact your chosen solicitor, and mention the National Free Will Network. The solicitor will draw up your simple Will, and NASS will cover the cost at a special discounted rate. There is no obligation to remember NASS in your Will when you use this service, although we hope you choose to do so. Thank you for considering pledging to leave a gift in your will to NASS.

    We'd love to keep in touch to tell you about our work, our fundraising activities and other ways you can get involved. You can change your mind any time. If you already hear from us, we will continue to contact you in the same way. If you don't already hear from us, please tick the box next to your communication preferences.

Frequently Asked Questions

Does the size of my gift matter?

Absolutely not. Every gift, large or small, makes a difference.

What if I change my mind?

You can amend your Will or withdraw your pledge at any time.

Do I need to tell NASS I’ve left a gift?

You don’t have to — but letting us know means we can say thank you, plan ahead, and keep you connected to our work.

 

Ready to Take the Next Step?

  • Download our Gift in Wills Guide: [ https://nass.co.uk/wp-content/uploads/2024/04/FINAL-BROCHURE.pdf ] your essential guide to legacy giving with NASS.
  • Complete our Legacy Pledge Form: [https://nass.co.uk/wp-content/uploads/2024/04/FINAL-BROCHURE.pdf] to let us know confidentially if you’ve included NASS in your Will.
  • Find a solicitor and get help writing your Will through the National Free Wills Network.
  • Or speak directly to Paul for a confidential chat: fundraising@nass.co.uk | 020 8741 1515 (option 2)

The future is built on the generosity of people like you. People who believe in hope, support, and a life well lived.

Leaving a gift in your Will is one of the most powerful ways to help ensure that NASS can continue raising awareness, improving lives, and providing essential support for people affected by axial SpA for many years to come.

Your kindness today creates lasting change for tomorrow.

Get in touch

If you have any questions about leaving a gift in your Will to NASS, please email fundraising@nass.co.uk or call 020 8741 1515 and press option 2.

Contact the fundraising team

Other ways to fundraise

  • 220k

    Adults in the UK

    1 in 200 of the adult population in the UK have axial SpA (AS). That's twice as many as multiple sclerosis and Parkinson's disease.

  • 26

    Average age

    Axial SpA (AS) is a condition that affects young people. Symptoms start late teens to early twenties, with the average age of onset being 26.

  • 8.5

    Years to diagnosis

    The current average delay to diagnosis from when symptoms start is 8.5 years, by which irreversible damage to the spine may have occurred.

  • 59%

    Mental health

    59% of people with axial SpA (AS) report experiencing mental health problems compared to 25% of those with musculoskeletal conditions overall.