My Nonprofit Reviews

I lost a grandson to Full T18 and I have an 8 year old granddaughter that has Partial T18. My daughter was/is mother to both. Being a part of this group allows me to share my experience, as well as, encourage others who are going through their journey. It’s a great resource to have considering there is not much info on the internet.

Having the Facebook page support group has proven to be very beneficial to a lot of families. Mainly, those who have lost a child, or, experiencing grim hope for a future for their bundles of joy. It allows families to reach out to others that have gone through(or experiencing) the same thing. What better way to help with healing. My granddaughter, A’Shana, has Partial Trisomy 18. She’s 7 years old. She has a lot of issues but stable for her condition. In November 2014, my grandson, her brother, A’Meir, was born sleeping. This was a difficult time for me. Being able to read other people’s posts, let me know that I wasn’t alone. I realize that some see Trisomy information as outdated. I disagree. I feel that it’s because there’s not enough money for the proper research to be done. This is why I try to take up donations(started last year), and send to the foundation. It may or may not help A’Shana, but, prayerfully, one day, thousands of children will be saved.