My Nonprofit Reviews
Review for Williams Syndrome Association, Troy, MI, USA
When my granddaughter was diagnosed at birth, I felt so clueless, helpless and scared. I started researching and the association provided a lot of information. When my son and daughter-in-law went to at conference, I was able to go. It was a tremendous experience where I was able to learn a lot and meet a lot of WS families. When I found that Emma would not need open heart surgery, I cried for hours. I love getting posts on Facebook, especially from families who have just got the diagnosis and need a hug and a kiss. Meanwhile my Emma is now 4. She has overcome a lot of hurdles. She brings such joy and love to our family. I donate every year and buy lots of stuff on Amazon smiles. Thank you WSA for all you do! Here is a picture of my beautiful Emma.