Hi folks. I am on my 3rd pregnancy, first pregnancy ended in missed miscarriage, second is my son who has spina bifida and now I am after finding out at my 12 week scan that this baby has a cystic hygroma.
Everything else is looking fine, no signs of cleft lip/palette, brain looks good, measuring exactly with dates etc but my consultant said there is about an 80% chance that baby has a chromosomal disorder (downs, Noonans, pataus, or Edwards). It is also possible that it is caused by a heart defect but its too early to properly check the heart yet.
Next step is to get either a CVS or an amnio test done- i think I'll wait and do the amnio because the risk is lower but means it will be a bit longer before I have some answers.
Honestly, so long as it isn't fatal I don't really mind. We have been through a lot with our son already and are used to the life of being 'special needs' parents (hate the term special needs). It is also still possible that it will turn out to be nothing and the fluid will correct itself, which is obviously the best case scenario!
Everything else is looking fine, no signs of cleft lip/palette, brain looks good, measuring exactly with dates etc but my consultant said there is about an 80% chance that baby has a chromosomal disorder (downs, Noonans, pataus, or Edwards). It is also possible that it is caused by a heart defect but its too early to properly check the heart yet.
Next step is to get either a CVS or an amnio test done- i think I'll wait and do the amnio because the risk is lower but means it will be a bit longer before I have some answers.
Honestly, so long as it isn't fatal I don't really mind. We have been through a lot with our son already and are used to the life of being 'special needs' parents (hate the term special needs). It is also still possible that it will turn out to be nothing and the fluid will correct itself, which is obviously the best case scenario!