I decided to write this thread in honour and remembrance of my beautifully brave baby boy, Junior, if anybody finds them self in a similar situation and just wants somewhere to write for support, share stories or just to remember their child, I thought it would be a nice place to do so.
My son was diagnosed with Edwards syndrome when I was 17 weeks pregnant as I had an amniocentesis, he fought harder than i expected and made it through the pregnancy. He was delivered via c-section and was the sweetest little boy I ever laid eyes on. He changed my perception completely about Edwards syndrome, he was tiny yet so strong and alert. He breastfed, he responded to my voice and to his musical toys and he had 5 amazing love filled days with us. His death has effected me more than I actually thought it would but I’m determined to still be a mummy to him and to make sure he’s remembered. I just wanted to dedicate a place where I can talk freely about him and others can too if they are in a similar situation.
Please or to access all these features
Please
or
to access all these features
Get updates on how your baby develops, your body changes, and what you can expect during each week of your pregnancy by signing up to the Mumsnet Pregnancy Newsletters.
Antenatal tests
Support for parents of baby with Edwards syndrome
52 replies
Georgia1512 · 09/10/2019 14:56
OP posts:
Whensitbedtime ·
10/12/2019 05:30
This reply has been deleted
Message withdrawn at poster's request.
Please create an account
To comment on this thread you need to create a Mumsnet account.