We are a group of families from Minnesota and the surrounding states living with galactosemia. We were founded in 1998.
One in 80,000 children will be born with galactosemia. The purpose of GFMN is three fold:
We hold two meetings yearly - usually one in the spring and one in the fall. Meetings are held at various locations around the state. All those interested in learning more about galactosemia are welcome to attend.