Contact Us

Contacting Chromosome 18 Europe

Any questions, please email the co-founder of the charity, Bonnie McKerracher.

If you need to communicate in any language other than English, please let us know and we will put locate a translator.

For information about particular syndromes, go to

Hope to hear from you soon!

Facebook – Chromosome 18 Registry and Research Society Facebook Page.

The parent, global Chromosome 18 Website.

Other Resources

Unique – The Rare Chromosome Disorder Support Group.

A Different Kind Of Normal – 18q- Website.

Rare Connect – Membership website; Connecting rare disease patients globally