My baby girl was born with Cytomegalovirus (CMV). There is a wide range of symptoms and disabilities associated with CMV and I wanted to open this community for moms to connect and discuss their child's struggles and accomplishments. I feel that by coming together we can encourage one another and make more women aware of the dangers of CMV and prevention during pregnancy.
Hello everyone. I am new to all this. My baby is 6 monts, 3 months adjusted because she was premature of 27 weeks 4 days. She was diagnosed with CMV last week (6 months after...
Started by Maria on 12/20/2015 in Congenital CMV Moms
Last update on 12/20/2015 by Sarah
Just wanted to say how exciting it is to see that there are others 'out there' with the same or very similar stories to ours. So nice to now know that i'm not alone on this...
Started by Anthea on 10/18/2010 in Congenital CMV Moms
Last update on 12/20/2015 by Maria
I am hoping to hear from other moms about the struggles and joys they have with raising a child with CMV. I often feel alone as I look around to find something in common with...
Started by Calley on 04/27/2009 in Congenital CMV Moms
Last update on 08/16/2015 by Amanda
Hi everyone my name is Callie. I have a beautiful 7 month old son Andrew, who was born with congenital CMV. I am curious as to how long and how far delayed other children with...
Started by Callie on 07/30/2009 in Congenital CMV Moms
Last update on 02/12/2015 by Danny
Here is my story. I was diganosed with a primary CMV infection at 29 weeks pregnant. Only about 5% of the population has a primary infection as an adult. The chances of birth...
Started by Giedre on 01/31/2012 in Congenital CMV Moms
Last update on 11/12/2012 by Kristina
i have baby gal who is infected by CMV and now she refuse to drink milk we try to feed her with spoon n she will start to throw out everything. she is already 1 yr 3 mths old...
Started by Adeline on 03/24/2012 in Congenital CMV Moms
Last update on 03/24/2012 by Adeline
My baby was born on october 24th 2009. He has CMV. He has lost his hearing in his left ear and has had brain development issues. He is still in the hospital. Any advice?
Started by Jessi on 01/08/2010 in Congenital CMV Moms
Last update on 05/27/2011 by Elizabeth
I've been thinking about all the families out there with children affected by CMV. It breaks my heart knowing more babies are born all the time that will needlessly suffer and...
Started by Calley on 01/15/2011 in Congenital CMV Moms
Last update on 05/15/2011 by Elizabeth