Hello whoever might be reading this! I haven't posted in so long!! Miss being on here and I've decided I'm going to try to get back into the swing of things!

 
I'm currently 31 weeks pregnant with our 
baby boy, Samuel. At our 29 week check-up my OB had me 
get an ultrasound to measure babies growth, and in that appointment they
 found some abnormalities with his umbilical cord. An "umbilical vein 
varix" is what they called it. Essentially they explained to me it meant 
there was a dilation (enlargement) in part of his umbilical cord right 
in his abdomen. I was immediately moved to the status of a "high risk 
pregnancy" and sent to a perinatologist (a doctor who follows women who 
have high risk pregnancies, I'm sure for multiple reasons, including 
the diagnosis they had just informed me of with our son). I remember my 
OB sharing vaguely in the appointment why I needed to see the specialist, 
but for some reason it didn't register with me immediately that what she
 was sharing was potentially scary, even life threatening stuff in 
regards to Sam's well-being and the rest of my pregnancy.
Once
 I digested what she told me, did a little googling (never a good 
idea!) and I then messaged her on myChart and asked a few more solidly formed 
questions. Her nurse messaged me back shortly after and simply stated 
that the doctor would call me directly to address the questions; which 
she did not long after. Basically she explained to me that when they see
 this UVV (umbilical vein varix) in babies cords it can mean a lot, it 
could be nothing, or it could lead to something really very serious. It 
was just the facts she shared, and regardless of how ambiguous the 
explanation felt, it was just the truth.
She said when 
she sees this condition along with other factors, it could point to 
genetic abnormalities or chromosomal abnormalities in baby, it could 
point to the baby becoming anemic because of the malfunction in the cord, not
 giving baby the nutrients he needs to thrive, and in the worst case it 
could cause things as scary as death in the womb before birth or 
stillbirth. She then reassured me that Sam's growth has been perfect up 
till now, and she's had absolutely no other reason to be concerned for 
his well-being, and that there have been no other signs of chromosomal 
or growth abnormalities in him. However, watching the cord was extremely 
important, because if it continues to dilate it could cause blood clots to 
form ultimately which could lead to him being still born.
I
 waited patiently for about 5 more days when I was scheduled to see the 
specialist, at which appointment they did confirm the UVV and also 
echoed essentially all that my OB said in that there were no further 
reasons to worry or be concerned about Sam's well being/development as 
of right now. Just that he wanted to see me on a weekly basis from now 
until delivery to monitor the cord and make sure it doesn't do anything 
we wouldn't want it to do (grow), and that baby did continue to do what 
he needs to do (grow!)
So, we're definitely playing the
 waiting game right now. My husband and I opted against genetic 
screening for our various reasons, and ultimately as strong believers in
 God and in His plans for our lives, we know that however our child is 
born (whether a baby with some type of syndrome or abnormality, or a 
baby who is born developmentally "normal" having no special needs) we 
would feel blessed and know Sam is meant to be ours forever, and we love
 him so beyond unconditionally regardless of any of that. The waiting 
game for me feels like watching this cord in his belly, making sure our 
boy is growing and thriving in the womb, and trusting the care of the 
Doctors in our lives for the next 9 weeks, and trusting God to nudge 
them if he needs to come sooner than his due date, and just for Him to 
give my mind and body peace so the little one isn't feeling my stress 
and concern for him as we go through this last leg of pregnancy.
I
 wanted to blog about it for 2 reasons. Reason 1, it's healthy for me. 
It's a space to process and lay my thoughts, fears and anxieties 
down, regarding all of this-- and to leave it here and not in my head. Reason 
2, as horrible as it is to search google when any medical condition is 
involved, I know I do it, and I also know a million other people do to! 
Ultimately I know people are looking for answers, reassurance, or just 
someone to commiserate with when tough times come; and the only things 
online I could find regarding ANY of this were old (like 10+ years old) 
case studies done, and a few threads between Mamma's on the Baby Center 
web site.
So, I thought, if anything, I could fill the 
gap for one of those reasons for some Mom out there, who is pregnant 
with her little love and facing this challenge. I feel you sister!! It's
 stressful!! It's a lot of uncertainty. And my hope is to just update 
periodically as I continue my weekly appointments with the specialist 
and OB, and obviously I want to be optimistic that at the end of all of 
this, I'll be sharing a photo of our beautiful, healthy and perfect baby
 boy! I know not everyone who has dealt with this has had a happy 
outcome, and while I'm believing that 100% for our little Sam, the truth
 is I don't know what the outcome will be. No one ever can know. That's 
literally just life. But, I'm hoping to be a beacon of hope to someone 
out there who needs it, whether it's today, or if someone googles and 
finds this post in the year 2029. (Although by then I think there'll be a
 lot more medical technology/information and maybe this won't be a 
concern to anyone then! Ha!) but, you know what I'm saying.
Our
 sweet boy is due to come between now and December 23rd! And I 
absolutely cannot wait to snuggle this beautiful boy & introduce him
 to the best big sister he'll ever know and welcome him into our home!
We love you so much little guy!!