Receiving the Diagnosis
It is one of the hardest things to hear – that your bundle of joy has been diagnosed with an extremely rare genetic syndrome that you probably never heard of before. We are here to help. You will find resources for you and your family to help you cope with Prader-Willi.
MakING a Donation
100% of your tax-deductible donation to the New Mexico Chapter of the Prader-Willi Syndrome Association will remain in New Mexico, helping individuals and families in our state who are coping with Prader-Willi.
What we do
Help Individuals & Families
Advocate for Change
Educate Healthcare Providers
What Drives Us
The New Mexico chapter of the Prader-Willi Syndrome Association (USA) is an organization of families and professionals working together to raise awareness, offer support, provide education and advocacy, and promote and fund research to enhance the quality of life of those affected by Prader-Willi syndrome in New Mexico. We will be a self-sustaining organization, empowering those affected with Prader-Willi syndrome to enjoy a productive life in an informed and accepting community.
There are many ways you can get involved in helping the Prader-Willi Syndrome Association (USA) locally and globally. With our many On The Move Walks and online fundraisers such as eWalk, we have something available for everyone. We welcome you into our amazing community! Let’s Save and Transform Lives together!
May 28 - Axes For Hope
Noon – 5pm Throw Axes and Support People Living with Prader-Willi Syndrome.