Whether you are a new family with a loved one just diagnosed with Ring Chromosome 20 Syndrome seeking information, an existing member seeking support, a healthcare professional with a new r(20) patient, or you want to get in touch to help with fundraising – whatever your reason, we’re here to help.
We are a small team of volunteers so if we don’t respond to you immediately, you understand why. However we do try to respond in a timely manner to all enquiries.