My Nonprofit Reviews

We had a little girl with Trisomy 18 who lived for 13 months. This group was so supportive, from sending a sweet gift upon registration to providing connections with other parents who shared similar struggles with their child. So often, I found that the best advice or recommendations came not from the doctors but from these parents who had been there, done that, and knew what to suggest. Our family is so grateful for the Trisomy 18 Foundation!