Birth To Three Years

This section will focus on the needs of the young child. There are so many changes that take place during the first several years of a child’s life and that doesn’t change just because your child has Prader-Willi syndrome. While easier said than done, it is important to try not to compare your child to the standard measures of what a child “should” be doing at any given stage of development. Children with PWS are typically delayed achieving their milestones, but with therapy these skills will come in time. Parents of a child with PWS learn to celebrate each milestone, big or small, and gain a true appreciation of the hard work that goes into mastering each new skill. Explore the links above for more information on the topics that are relevant to these young years.

Make Connections | Get Support

PWCF has a host of parents to support and help guide you, in-person share and support groups, and links to online support groups. Click Here for Individual Support and Support Group information. You never need to feel alone.

Additional Resources:

Physician’s Note Symptom & Treatment Checklist to help you document the need for supports and services

When Your Baby is in the NICU

Health Care Providers Referral List