Awareness Day 2023

...now and in the lead up to June 22nd (and beyond!) …..and this one has been designed for use on Instagram or Twitter (from a PC, just right click to...

Annual Reports

...from whom we raise and spend the funds we receive as well as some information on our future plans to continue to develop the charity. Annual Report and Accounts 2022...

Families

Unique's Funday Friday | 19th June 2020

...Facebook from 14th June 2020) and banner. Unique’s Funday Friday Facebook Banner Unique’s Funday Friday Facebook profile photo frame – available on Facebook from 14th June. Unique’s Funday Friday Instagram...

Mental health & wellbeing

...email our Family Support Officer, Marion Mitchell at marion@rarechromo.org. NEW for 2022: Health and Wellbeing Information Guide Click here to read and download our brand new guide to Mental Health and...

Where can I get help and support when the Unique team is not available?

...have a list of other crisis services here: https://www.mind.org.uk/information-support/guides-to-support-and-services/crisis-services/helplines-listening-services/ You may also find Unique’s practical support guides helpful, in particular, our Carers Wellbeing and Self-Isolation guides: https://www.rarechromo.org/practical-guides-for-families/ NEW for 2022:...

Our History

...more charities competing for the same grants. Please help us with donations and fundraising so that we can continue our essential work. Last edited by Craig Mitchell, 21st April 2022...

How genomics helped get a diagnosis

NHS England Genomic Medicine Service supported Unique’s Rare Chromosome & Gene Disorder Awareness Day in June 2022 by sharing information and family stories; highlighting the role genomics and the National...

What is an Array-CGH?

...CGH and how does it help? For Rare Chromosome and Gene Disorder Awareness Day 2022, we’re launching the first in a series of animations to help families better understand key...

New Adult Sibling Research Opportunity

**UPDATE 31st October 2022: This research is now closed for recruitment** One of our Information Officers at Unique, Francesca Wicks, is launching a new research project focusing on understanding the experiences...

Martina & Lucy

Meet Lucy and her Mum, Martina! Lucy has a 10q26.3 deletion and 2q35 duplication. Martina says, “Lucy is an absolute joy. She is a wonderful little girl. She is so...

10q25 And 10q26 Deletions

5q Duplications

15q25 deletions

5q14 duplications

15q14 deletions

GRIN2B-related neurodevelopmental disorder

Wolf-Hirschhorn Syndrome (4p16.3 deletions)

3p25 Deletions

MPPH Syndrome

SETD5 Spanish