Hello, and welcome to the GANES website!
My name is Angie Forsyth, and I am the founder and current president of GANES - the Galactosemia Association of the North Eastern States. I am also the mom of a 6 year old son with classic galactosemia and would like to take this opportunity to tell you about our group!
By forming GANES, we are looking forward to being able to serve individuals and families in need, establish a more localized support network, and provide opportunities to become involved in supporting our mission:
...creating and strengthening opportunities for networking among individuals and families affected by galactosemia and medical providers, and to support education and research related to the study, treatment, management , and a cure of the disease.
Please take a look through our brand new website courtesy of our volunteers, David Reid and his company NYLI for designing the site Patrick Fernstrom for hosting the site. See how you can make GANES yours!
Galactosemia Resources
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PLEASE NOTE: This website is intended to provide general information only. Always seek the advice of your physician or other qualified health professional for medical advice, examination, diagnosis, and treatment.