Family, Personal Journey Series, Success, Treatment
Caroline’s Story (Syndactyly and Polydactyly)
We are Caroline and Justin Hughes, a couple living in England, with a son called Kaiden, who was born with Syndactyly and Polydactyly. Our journey started…
Read MoreFamily, Personal Journey Series, Success, Treatment
Alisha’s Story (Complete Complex Syndactyly)
Throughout my pregnancy everything was going great; our baby was perfect! We had a few ultrasounds done and everything seemed just fine. We went in for…
Read MoreFamily, Research, Treatment
Our Opinion of Second Opinions
Being comfortable with your treatment plan is the most important aspect of syndactyly treatment. If you have questions about your doctor’s recommendations or are just curious,…
Read MoreFamily, Patient, Success
Surgical Treatment
“Most children treated for syndactyly have a wonderful outcome with normal finger motion and good maintenance of the reconstructed web space. Some, but not all, rotation…
Read MoreFamily, Fundraising, Research, Scientific
Caps For Kids With Syndactyly
Show your support for children effected by Syndactyly by purchasing an official NFS ball cap for $20.00. All proceeds go towards the Foundation’s continuous research efforts…
Read More