My son got his diagnosis for cystic hygroma at 19 weeks, although the fluid had been thick since 10 weeks. I know it's probably not 'special needs' but I am really interested in meeting other moms who have kids with this condition. It's so rare and I haven't been able to go to anyone for support. I'm currently 33 weeks along and his CH is there and seems like it will be staying there. Not huge but will definitely be part of his life.
If anyone has experience with this or can link me to someone, that'd be amazing.
Im so sorry :(
You might find this thread helpful
Quoting Marbles.:" Im so sorry :( You might find this thread helpful http://forum.baby-gaga.com/about2175592.html"
Thank you for sharing that with me, I will check it out.
And it's quite alright, he is perfect to me no matter what, and we've made it through some of the hardest parts already. I'm excited to have him and I know he'll get through whatever happens(: