Contact us

We want to hear from you!

Maybe you have story you'd like to share, want to let us know about some press or fundraising you are doing or would like us to come and give a talk. Please get in touch.

Don't forget to check out our FAQs at the bottom of the page. If you can't find the answer to your question, please contact us by filling in the form below or emailing

Did you know you can join our mailing list too?

General Enquiries

Find Us

Level 3, Barclay House
37 Queen Square

Get Directions

Google Maps | Citymapper


+44 (0) 20 7831 0883


Get in touch

Other Enquiries


With our colleagues in the Genetic Alliance UK policy team, we want to make sure that voices of SWAN UK families are heard by policy makers across the UK. If you would like to raise a policy issue with our team, or to ask us any questions, please get in contact at


Our research team specialises in studying the experiences of patients and families affected by genetic conditions, including undiagnosed conditions. If you would like to contact us to ask about a research project, or have other questions about research, then please contact us at


Membership of SWAN UK is free to any parent of a child or young adult affected by a syndrome without a name living in the UK. All you need to do is complete and return our registration form which you can download and email back to or print and post it us. 

Find out more about joining us


Our Big Ambition here at SWAN UK is that all families of children and young adults affected by a syndrome without a name have the support they need, when they need it. You can help us achieve this ambition by fundraising for us. We'd love to hear from you!

Visit our Get Involved page to find out more about how you can support us or email


I’m a professional, can I join SWAN UK?

Membership of SWAN UK is only open to parents of children or young adults affected by a syndrome without a name. You can keep up to date with us, however, by joining our mailing list

Does SWAN UK support families of adults affected by a syndrome without a name?

At present we are only funded to support families of children and young adults aged 025. However, if you are the parent of an adult affected by a syndrome without a name who needs support please get in touch and we will see how we can help.

My child has a diagnosed rare disease/condition, can I join SWAN UK?

The aim of SWAN UK is to support families who are affected by undiagnosed genetic conditions. Within our community we also have some members whose children have been diagnosed with a very rare genetic condition for which no other support exists. Some families join our community after receiving a very rare diagnosis from genetic sequencing.

If your child has a diagnosed rare disease or genetic condition for which an established support group already exists, you will not be able to join SWAN UK.

What happens if my child gets a diagnosis, do I have to leave SWAN UK?

We recognise that getting a diagnosis can be a very stressful and emotional time for families and they often need our continued support to make sense of the diagnosis. We will work with families to identify their needs and see how these can best be met – sometimes this will involve signposting them, if relevant, but often the diagnosis is very rare and no other support exists so for now they remain part of our community. We never ask anyone to leave and will continue providing support as long as the family feels they need it.


As a result of genetic sequencing, more children are being diagnosed with very rare conditions, such as single-gene disorders where they may be one of only a few cases known worldwide. We have a specific forum for members whose children have been diagnosed called our ‘graduates group’ where they can discuss issues resulting from their new diagnosis and we are working with them as a group to identify the support they require.


Join our community of families

Join us