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 www.chromosome18.org
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
