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So my yet to be born little girl may end up disabled in some way (upd: she's okay!)

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JoJo UK

Unconfirmed Member
OP I know right now you are most likely crawling the walls not knowing what to do or say and I hope it's all a worry over nothing.

If on Monday you get the news that there is some sort of physical condition my advice is don't worry, it's not the end of the world and 99% of the time the only people who will be worrying about it will be you and your partner. All you need to do is shower your (and your better half ;) ) with love.

Sorry gaf I don't care how soppy that sounds.

My wife has been a teacher in a special needs school (specifically working with children with physical special needs however the majority will have some sort of mental disability) for over 10 years. Up until 2 years ago (until she retired) my mother was a teacher in the same school for 25+ years.

My wife carries out an outreach program where she visits families and help them decide if their child should go to their school, a main stream school with help or another special needs school. No matter what harrowing stories she comes home with there is always one constant, if there is love (read support) in the home the kid is always happy.

I have helped out in the school since I was about 10 or so during summer schemes, holiday clubs, etc. I have a 13 year old son who also now helps out and when he was younger he would come in during school holidays to mess around and play.

What I'm trying to get at is one of the things I always see is kids don't see a disability, it really is just a label that adults use.

If you get news on Monday that you not sure how to process it please feel free to PM me the details, I can certainly run any information past my wife for her opinion (if you wish).

Best wishes OP.
 
I can relate in the smallest way as we had the extra fluid and tests though everything was OK. Before the results I had the kind of worry that is much more real for you. I'd say you just have to hope for the best and stay positive. Deal with the reality when you actually know what it is imo. Best of luck to you.
 

Fj0823

Member
OP I cant even imagine what youre going through right now.

The only thing I can say is that no matter what happens, your baby has one hell of a loving father. No matter what happens she is very blessed to have you.
 

RMI

Banned
Good luck OP. It's stressful enough to have a kid without any additional complications. I hope everything ends up OK.
 

Nista

Member
I hope everything turns out ok for you and your wife. I don't think I could have the patience and presence of mind to deal with a severely handicapped child, after seeing how hard it is on my mom's friend.

CMV is a odd one, I had it when I was a teenager, and it was basically like a bad case of mono, and they made me stay home from school for a week or two to not spread it to others. But it's one of those viruses you never really hear about.
 
I'm sorry to hear that OP. My brother was diagnosed with autism when my mom was pregnant and was recommended to abort but she thankfully refused and my brother came out fine. He's 18 now and is going to study computer science next semester with me. Don't lose hope and love your baby when he/she is here.
 
I'm picturing a baby wearing baby glasses looking at a newspaper and saying "I don't know, viciouskillersquirrel, with the way the real estate market is right now I don't think we can afford a doll house."
We didn't realise anything was wrong until he was around 18 months old and he started squinting at us with one eye. At first we thought it might've been a facial tic, but we followed up and it turns out he's far sighted in that eye. It's common in premie babies.

Getting him to wear the glasses took a lot of work, but he's four now and as far as he's concerned, they're just what he wears, like underwear or a shirt. The good news is that because we found it early, his eyesight in that eye is improving. Maybe when he's an adult, he'll be able to get corrective surgery or something, but for now, he'll just have to wander around looking like Harry Potter.

I am so grateful that Harry Potter wears glasses, by the way. Good role models for kids who wear glasses are so rare in media. So many kid characters who wear glasses are insufferable goobs, it's nice to see one who can be heroic.
 
We didn't realise anything was wrong until he was around 18 months old and he started squinting at us with one eye. At first we thought it might've been a facial tic, but we followed up and it turns out he's far sighted in that eye. It's common in premie babies.

Getting him to wear the glasses took a lot of work, but he's four now and as far as he's concerned, they're just what he wears, like underwear or a shirt. The good news is that because we found it early, his eyesight in that eye is improving. Maybe when he's an adult, he'll be able to get corrective surgery or something, but for now, he'll just have to wander around looking like Harry Potter.

I am so grateful that Harry Potter wears glasses, by the way. Good role models for kids who wear glasses are so rare in media. So many kid characters who wear glasses are insufferable goobs, it's nice to see one who can be heroic.

Growing up wearing glasses was rough. I guess Harry Potter becoming popular helped, but I never read the books or watched the movies
 
I'm sorry to hear that OP, can't really say much as I've never had children or anything but I just hope for the best and hope your baby is safe,
 

Oreoleo

Member
Possible to have an emergency C-section to prevent any/further complications? 8 months is pretty far along.

Love that kiddo with everything you've got and it'll all be okay, regardless of the outcome.

Edit: Brought it up to my mom who worked in the neonatal unit at Children's Hospital for like 40 years (though she was a nurse and not a doctor so take this with a grain of salt), she said everything is pretty much formed by 32 weeks and thinks any deformities would be unlikely. Though she's not super familiar with the virus, her experience with it was that it mostly manifested as liver issues that can result in hemorrhaging (ie, bruising). Hopefully that eases your concerns some instead of feeling like one more thing you have to be worried about. Good luck to you and your partner.
Editx2: She was thinking of a different virus >_< I guess being retired for like 5 years will do that to you. She corrected herself and said it can affect hearing and such but a lot of children born with CMV are completely asymptomatic. Keep your chin up bud.
 
Definitely unfortunate news, but I think at 8 months she'll be okay, though still sending positive vibes to you and your partner and wishing you all the best.

Regardless, I know you guys will love her unconditionally no matter what happens.
 

LosDaddie

Banned
Hey GAF, depressing post I know, but I wanted to vent/generally talk about this without having to resort to Facebook and in turn being bombarded with people I know IRL asking me "how things are" etc

My partner is 8 months pregnant, and on our 32 week scan, it was detected there was extra fluid in the womb - so she was asked to do a Glucose Intolerance test (so far, so normal - they're checking for Gestational Diabetes)

Anywho, missus has the test and then they call us the next day and say to her "There's something we found in your blood, you need to come in and see a consultant" At this point, alarm bells started ringing because they wouldn't tell us what they'd found, nor give a straight answer when asked "Is the baby okay?!"

Slightly panicked, we see the consultant the next day and are advised that baby has possibly contracted CMV (cytomegalovirus) - a piddly little virus that unfortunately can cause major damage, ranging from facial deformities, brain damage, blindness, deafness and everything in between.

We had the news today that the blood was tested further to determine if the CMV was a recent infection, and they've confirmed it is. Now we have to wait until Monday for another scan to determine if she's okay - at least physically. It's encouraging at least that up to the 32 week scan, all measurements of baby (arms/feet/legs/hands/organs/brain/skull) were normal - so I'm mostly confident she won't be disfigured or anything. (Christ even typing the words disfigured or braindamage makes me want to cry my eyes out)

I'll be honest and say we're feeling pretty devastated right now, but hopeful. Never been so scared in my life, but am maintaining total poker face for my partners benefit (she's been forbidden from googling the condition, as it does not make for pleasant reading).

Any parents of GAF ever encountered this virus when pregnant or have disabled children that can offer advice?

<3

ParentGAF checking in. I'm so sorry about the bad news.

While I don't have any advice for dealing with a special needs child, the best parenting advice I can give is to only worry about stuff you can control. There's going to be so many things regarding your child that will frustrate you that are out of your control. You'll have to learn to let go of trying to control life around your child, and focus on what you can control. Grind hard to set up your family for the best chance at success.

Hope all goes well with you and yours &#10084;&#65039;
 

Marvel

could never
I wish you and your family nothing but the best during this tough time. Do keep us posted.

Xx
 

op_ivy

Fallen Xbot (cannot continue gaining levels in this class)
Really sorry to hear that Sik. Stay strong, stay positive and hopeful.

I've never shared this outside of real life, but my family went through something similar when our 3rd child was born this last summer. Long story short, after 3 weeks in the nicu with a "failure to thrive" newborn with some fairly obvious issues, she was diagnosed with a life long, scary, genetic disorder. Doctors have always told us that there is a fairly wide range of lives people with this can have, largely dependent on how they are raised, but it was and still is scary as shit. But she's amazing and we love her. I'm not sure how similar our stories are, which ultimately is more severe, but stay hopeful. However she ends up, she'll be a daughter you love with all your heart.

Now I'm tearing up.
 
I wish you the best of luck and as other have said as she 32 Weeks in development already she should be fine . I had to be born at 32 weeks due to my mothers womb becoming toxic(Or something like that .) and I am fine so I would think that is a good sign for your child will be fine as well.
 
Our twin boys were born at 26 weeks, right on the cusp of viability outside the mother. We were matched with them as they were leaving the hospital after 3 months of NICU care and tricky surgeries. When we brought them home they were on oxygen tanks, meds, special feeding schedules, etc. and required many many many checkups.

It was hard to be sure (all parenting is hard!) but we never once loved our sons any less. Kids are super rewarding. As soon as they laugh at your goofy voice or fall asleep in your arms you understand why being a parent is so special.

Good luck!

You aren't kidding. I've had a pretty good life, but my son's first laugh surpassed all of it. I'm really, really looking forward to having a similar moment with my two week old daughter.

That said I was in a similar situation to you OP and after several months of emotional agony it turned out to be nothing. So don't dwell on the worst, just be excited about bringing your child into the world. If the worst happens you'll deal with it. Don't ruin this special time by overthinking things.
 

Plinko

Wildcard berths that can't beat teams without a winning record should have homefield advantage
Prayers for you, your partner, and daughter. Hope everything ends up well.
 
Sorry to hear it, OP. As a father of two, I know that our kids are everything to us.

Will be keeping you and your baby in my thoughts and hoping that this turns out as minor as possible.
 

Staccat0

Fail out bailed
OP I cried a little reading your post. Having a kid makes you feel everything so much more strongly in my experience.

I don't have any advice but my thoughts are with you. I actually read your post to my wife so I guess hers are too.

Will say though, with a kid comes a lot of things no matter what. One of them is usually being absolutely amazed at what you and your partner can handle and how much you love the baby. Obviously every kid deserves a healthy start and shit like this isn't fair, but if there is any silver lining it's that you'll be stronger when you meet the kid than you were 10 min before.
 
Thank you all - it really helps just reading the good vibes. I'll plonk a post in here late Monday after the scan with an update. Here's hoping for the best result possible!
 
I dont know what my issue was at birth, but my mother did have diabetes when she was pregnant with me and my sister. Also I was born really early, about a month and I was tiny. I have a learning disability and my hand writing is mostly shit, but I pulled through. I know I had some breathing issues as well and had to stay in the hospital for an extra few days but on the last day I past whatever test they gave me.

I hope everything turns out okay for you OP. I got a little choked up reading that and cant imagine what you are going through.
 

fallingdove

Member
My daughter was positive for every down syndrome test that doctors did during my wife's pregnancy so I can relate, in some small way, to the anxieties that a father can experience around health of their unborn child. In the end, my daughter was born without down syndrome but the concern that I had leading up to her birth really took its toll. keep your head up.
 
Mate, i really feel for you. You probably want to try and fix it but can't and it's a waiting game full of angst.

Having just had a son i understand the helplessness of not being able to help.

I have my fingers crossed for you and your girls. It will be ok am sure.
 

wachie

Member
Damn, my eyes are soaked reading the OP. I wish you and your partner the best and hope your little princess has zero affect from this. Thoughts and prayers, stay strong bud.
 

Oscar

Member
Knocked up a college gf back in 2009.

I still remember that awful feeling in the hospital, when the doctors were telling us that the heartbeat was too slow and there was an extremely low chance of survival. I was one of those who initially held the opinion of "If we find out something is wrong with it early, I hope my partner is ok with termination". But when I was actually in that position though, "I don't care if the baby is born with deformities/syndromes, I'll take care of him/her" is what I truly felt while in that waiting room.

She ended up miscarrying a few days later, we broke up within a year.

When my friends/peers who are all settled down stress about shit like the gender (OH GOD IT BETTER BE A BOY, BRO), I smh and tell them to just hope for a healthy baby.

My deepest condolences, OP. I hope everything works out for y'all.
 
More Parent GAF checking in. Really sorry to hear your sit, OP. I remember being beyond anxious for the results of the initial DS test. I can't imagine how much more stressful and worrying your sit it. As others have said, could turn out perfectly fine, and I'm crossing my fingers for a happy result. If you want to talk more about it, or see if any of the other parents/expecting GAF have more experience, come check out the Parent Thread. Lots of support and info in there.
 

JoeBoy101

Member
OP, You're going to have your daughter and you're going to love her. And she'll love you. There's nothing but time to remove the anxiety, but take comfort in that whatever happens, you'll get another wonderful girl in your life.
 
More Parent GAF checking in. Really sorry to hear your sit, OP. I remember being beyond anxious for the results of the initial DS test. I can't imagine how much more stressful and worrying your sit it. As others have said, could turn out perfectly fine, and I'm crossing my fingers for a happy result. If you want to talk more about it, or see if any of the other parents/expecting GAF have more experience, come check out the Parent Thread. Lots of support and info in there.

Thanks, and for the link to Parent GAF - I shall subscribe to the thread. :)
 
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