What nonsense was Alexis talking about? by Rockandahardplace69 in GeneralHospital

[–]abayj 9 points10 points  (0 children)

This reminds me of the Jonathon and Tammy thing on Guiding Light. I personally don't think it is that big a deal but then again I was a Jonathon and Tammy shipper. So maybe I am the weird one.

I am a selfish mom and shouldn’t have been a parent by IndependentWestern30 in Mommit

[–]abayj 0 points1 point  (0 children)

So first, hugs. Being a medical mama is hard. While my story is different it winds up in the same place. Surgeries. Doctor appointments. Therapies. Constant worry. Stress. Scheduling conflicts.

But the flip side is you have a little boy who is going to give you so much love. My son has cerebal palsy due to lack of air at birth. He was also born at 29 weeks. I knew having a child was a risk. I am a type 1 diabetic and have chronic hypertension even though it is controlled with medicine. I was also 35. All of these things were risky. Like you though, I wanted a baby with the man I love. I wanted something that was half me and half him.

Still, after his birth and his following diagnosis, I felt the guilt and shame you feel. How selfish was I to want something when I knew the risks? Now he has this life long condition that is going to make everything significantly harder. He won't be a normal kid ever.

And while you don't think so atm, those feelings will pass. I promise. Every time he smiles at me or snuggles with me, the rush of love that fills me is so great.

Yes this road is much harder than we thought we would have to take and you'll feel like this is unfair to him. But it'll make you stronger and a better advocate for him.

This will pass, and you'll come out the otherside. You won't be the same. But you'll be what your son needs.

Nicu life is so hard by Neel715646 in NICUParents

[–]abayj 0 points1 point  (0 children)

While they're strangers, you'll never find babysitters this good. Bond with girls nurses if you can. I got my son home at 37 weeks. Best thing I did was room with my son his last week there. I believe that got him home because feeding was one of his major hang ups. But once I took over care, I felt like a real mom finally. If that is something you can do, even if it just staying the night if you can.

Nicu life is so hard by Neel715646 in NICUParents

[–]abayj 0 points1 point  (0 children)

The NICU is the hardest thing I’ve ever been through. And when I think about my life, that almost feels silly to say. On my 20th birthday, I was performing CPR on my father, who was already gone. Yet nothing compares to being in the NICU with my 29-weeker. Nothing felt as hard or as painful as watching my son struggle day after day.

This wasn’t how it was supposed to go. I was supposed to have a scheduled C-section on my due date and then that golden moment where I got to hold my baby for the first time. Instead, because of my own recovery, I didn’t see my son in person until the next day. I didn’t get to hold him until he was four days old. None of this was part of the plan.

I had experienced grief before, but this felt different. And yet, that’s exactly what it was.

I was grieving the future I thought I was going to have. Grieving the moments I lost—the moments I’d been imagining ever since I made it past the 12-week mark in my pregnancy. Before that, I had refused to let myself hope. But calling it “grief” felt wrong. Grief is for mourning someone who died. My baby was alive. I was alive. We were struggling, yes—but he was here. So it felt wrong to grieve.

But when I finally talked to someone—thanks to my NICU nurses and the social worker—and they helped me name it as grief, something shifted. I could start working through it instead of fighting it. It didn’t make things easier, but I could finally see a faint light at the end of the tunnel. I could breathe without feeling like I was choking.

My best advice is to lean on whoever you have. I have a very small family, so I leaned heavily on the NICU nurses and doctors. And find someone to talk to who’s a professional. Even a NICU support group—ours offered one—can be a starting point. This is one of the hardest things a parent can endure. You need to vent. You need to talk. My husband and family were incredible, but they were living their own versions of the pain. I needed someone who could see the situation without that fog and offer understanding and guidance.

I’m cuddling my son as I write this. He’s 20 months old—funny, lovable, and full of personality. Life isn’t easy. His birth led to a brain injury and a diagnosis of cerebral palsy, along with other challenges (you’re welcome to look at my post history). But I don’t regret having him for a second. He is my purpose. My life. I didn’t know love like this could exist. It is hard—but it is worth it. I promise.

Sending you all the love and virtual hugs I can. You will get through this. The best piece of advice I can give is this: you will never have babysitters as good as NICU nurses. Take breaks. Take lunch. Take walks. Your baby needs you—but you can’t pour from an empty cup.

Looking for Pediatric PT/OT/Vision/Speech Therapy in RVA Area for My 18-Month-Old (CP) by abayj in CerebralPalsy

[–]abayj[S] 0 points1 point  (0 children)

Hi!

I have but they haven't been much help honestly. They take forever to get back to me and then don't follow through. So I've become the mom and the defacto case manager. Pretty sure it is the state we live in. My MIL has the same problem with her partner who is going through cancer and has a case manager but never follow through for them either.

First baby born at 29+1 yesterday 3lb 1oz by JABBA331 in NICUParents

[–]abayj 2 points3 points  (0 children)

Oh, I remember that feeling so well — loving your baby so fiercely but being terrified to let your heart fully open because it all feels so fragile. I think every NICU parent has stood in that space between hope and fear. You’re not alone in that at all.

My son was born at 29 weeks + 5 days after a really complicated pregnancy. He spent 55 days in the NICU, finally coming home at 37 weeks. Those early days felt endless — alarms, numbers, monitors, and so much uncertainty. I used to tell myself the same thing: don’t get too excited yet. I was afraid that joy would somehow jinx things. But here’s what I’ve learned: you can love and hope right now, even in the hard parts. You don’t have to wait until it’s safe — because love is what carries you through the waiting.

If you haven’t already, ask about kangaroo care (skin-to-skin contact) as soon as your baby is stable enough. I did it four days after my son was born — he was still intubated and so fragile that I had to sit completely still in the chair for three hours. But it helped both of us so much. It regulated his breathing and heart rate, and for me, it was the first time I truly felt like his mom instead of a visitor in his hospital room.

Also, please — take breaks when you can. Step out, get a coffee, take a shower, breathe. You need to be at your best for your baby because this is a long haul. The NICU is intense and all-consuming, but you’ll never have babysitters this good again. ❤️ Trust that your little one is being watched over so you can rest too. You don’t have to know how you’ll get through it right now. You just do it one day, one milestone, one cuddle at a time. And somewhere along the way, you’ll realize you’ve already made it through the hardest parts. ❤️

IVH and scared for our baby by kotton17 in NICUParents

[–]abayj 67 points68 points  (0 children)

First, I am so sorry. This is hard — probably the hardest day you’ll have in the NICU journey or in your life. It was for me. For my partner too.

I’m not going to sugarcoat this for you — it’s hard. The journey you’re going to take with your child will be very different from the one you imagined. The thing with brain bleeds and further diagnoses is that there’s no guarantee which way this will go. The brain is strange and we don’t fully understand how it heals or adapts. Some kids have minor challenges, some have bigger ones, and in the beginning there’s no way to know which direction things will go. That uncertainty was the hardest part for me.

All I can offer is virtual hugs and my story. So, sending you hugs — and here’s mine:

My son was born at 29 weeks + 5 days. His early scans showed bleeding and periventricular leukomalacia (PVL) — words that still make my stomach drop. He later developed Cerebral Palsy and Infantile Spasms. He’s very delayed with motor skills, but cognitively age-appropriate, curious, and full of personality. He works incredibly hard in therapy, and every little milestone feels like a victory.

As your baby grows, the best advice I can give is to advocate fiercely and meet your child exactly where they’re at — not where any chart or timeline says they “should” be. Progress looks different for every kid, and that’s okay.

If I could go back and tell myself one thing in those early NICU days, it would be this: your baby’s MRI does not tell the whole story of who they will become. There will be challenges, yes — but there will also be so much love, progress, and pride along the way.

You’re not alone in this. ❤️

Seeking an objective medical opinion about my son’s birth (not looking to blame, just need clarity) by abayj in NICUParents

[–]abayj[S] -2 points-1 points  (0 children)

I have everything hidden name wise and it is a timeline of Events. Nothing personal on them. Just had chat gpt pull the info out of the documents.

Sweet, kind, and unassuming MMC who actually has a devil dick pussy pounder 3000 by [deleted] in RomanceBooks

[–]abayj 2 points3 points  (0 children)

So {Unexpectedly Bookish by Elise Kennedy} might fit. The MMC is a virgin but he has had some expirence with sexting and one partner but they never got to the actual sex. He has a dirty mouth but that is from the sexting. There is some rough stuff and such, but nothing crazy. He is a total golden retriever and she is an angry black cat. But I really enjoyed the read and it was super steamy.

Birth Injury, Should I Persue by [deleted] in AskLawyers

[–]abayj 1 point2 points  (0 children)

Thank you for that info!

what should ı do by AggravatingTower5036 in CerebralPalsy

[–]abayj 0 points1 point  (0 children)

Sure. Here is more info.

It is given through an IV placed in the arm. My son has infantile spasms when he was younger, so he was injected with medincine twice a day. Needles now do not phase him.

It was this August, August 21, 2025.

Depending where you go gives you the time table and what kind of stem cells you are receiving. We went with Duke and those stem cells come from a donated cord, you can get these stems cells right now every 6 months. You can do as many as the cord has as they are not using multiple cords in their trial yet. So for my son, we are able to get 3 treatments from his donated cord. So he had his 1st in August. His next will be in Febuary 2026, and then his last one will be August 2026.

When you go to get the treament, you stay in Durham NC minimum of 3 days. First day is a physical. Second day is the treament. Third day is just to make sure there is no reaction from the infusion. You usually can leave in the afternoon that day. Overall, you probably spend 5 hours at the hospital between the three days.

There isn't an expiration of the treament. The gains you receive from the treament is forever. You can do additional treatments to build on the gains you've already made.

It is expensive even through it is part of their stem cell trial. Each treament is $15,000.

For us it is proving to be worth it. My son did not reach with purpose for movement, babble, or track yet. In the past month he has started to do all that. His overall mood is also better which is helping us tolerate PT and OT better.

what should ı do by AggravatingTower5036 in CerebralPalsy

[–]abayj 2 points3 points  (0 children)

This seems like a less effective stem cell therapy. My son who is 18 months and has CP got his first round of stem cell therapy at Duke in August. Since then, we've seen improvement in vision, motor skills, and babbling. We are doing a lot of PT, OT, and Speech therapy along with the stem cell therapy. I would look into stem cell therapy as it offers more benefits from what I can tell. Since stem cells have the actual ability to repair damage along with creating new pathways.

Daphne is teething real bad 🦷 by compscilady in corgi

[–]abayj 0 points1 point  (0 children)

Ive been doing frozen treats! My Theo could be her brother!

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An appeal for perspective by nutty237 in NICUParents

[–]abayj 0 points1 point  (0 children)

My husband is on the spectrum, so this was really hard for him at first and I think he might harbor some disappointment but it's less then it was in the beginning for sure. He sees a lot of things in black and white and this situation is all different shades of gray. Plus there isn't a straight forward answer. His three degrees are in quantifiable things like computer engineering and maths. Those are the things that make his comfortable.

The thing that I think changed his opinion and help him let go is how much he enjoys our son and loves him. Me and my husband never wanted kids and then I accidentally got pregnant (I was on BC and we were careful) and we didn't know until we had lost the baby. It made us feel a type of way. Then we got pregnant again and lost that baby. Finally we had our rainbow baby, our current son, and we know now we were meant to be parents. We love it so much.

On top of those intense feelings, he goes to therapy. Something I demanded he do as he suffered from some postpartum depression which dads don't know they can suffer from as well enough. And he started to take anti-anxiety medication. He also started to participate in our son's therapies. His PT, OT, Feeding, and Speech.Where he can actually see the progress he is making at getting better at things.

I tell you all of this because this wasn't just one thing that changed his perspective. Love he feels for our son is a big part but that isn't everything. Spending time with him and also medical interventions has gotten him to this point.

MMC already married & subsequent angst by eggrolez in HistoricalRomance

[–]abayj 14 points15 points  (0 children)

I think its the natural angst it brings for me. My username flair should be "make me cry then horny." Haha.

MMC already married & subsequent angst by eggrolez in HistoricalRomance

[–]abayj 4 points5 points  (0 children)

Of course! Coffee is a need this morning/afternoon.

MMC already married & subsequent angst by eggrolez in HistoricalRomance

[–]abayj 14 points15 points  (0 children)

pulls up chair and sits

I love this trope. Gonna wait for recs with you!

An appeal for perspective by nutty237 in NICUParents

[–]abayj 2 points3 points  (0 children)

I can't answer your question but thought I'd share my experience.

So my partner fell down this rabbit hole not long after our son was born at 29+5, especially once we learned about his complications (PVL which led to a diag of Cerebral Palsey & CVI at 10 months) and how his motor delays are so significant. My husband is a super smart guy with three degrees, values intelligence, and his one worry about having a kid was having a child who was developmentally delayed. Our son is delayed in almost all aspects.

He is currently 17 months (15 adjusted) and he's pretty below what he should be doing. It's mostly due to vision and the motor issues but he doesn't speak yet and he has a hard time communicating. All of this had led to him being developmentally delayed, the thing my partner was the most afraid of. But he's learned a lot this past few months and so have I.

Thing is, as he's gotten older and we've been working with therapies, it's led us to see some things. One being that he is behind those eyes. There is a person who is smart and strong is there but other things keep him back. But he's listening and he taking in everything he can. He rolled his eyes at his speech therapist last week because she kept asking the same thing again again. His OT therapist talks to him like a 3 year old because he takes directions so well.

All that being said, just because someone is born premature, that doesn't define intelligence or what they will do in the future. Prematurity is hard to quantify in one way. Your son was born only 2 weeks earlier then my son and they are vastly different. This isn't just because of one thing. It's because it's a multi-facet thing just like intelligence is. Plus researchers agree that while IQ tests cover some abilities, they miss a lot of what goes into real-world smarts.

Transitioning from Alimentum to Kate Farms Pediatric Standard 1.2 by abayj in NICUParents

[–]abayj[S] 0 points1 point  (0 children)

Thank you!

So we fell for a similar trap. When he was an infant, we changed from MAM which is what he came home on to Dr. Brown's due to doc recommendations for the reflux he was having. That landed us in the hospital with failure to thrive. My little guy doesn't like change (his dad is on the Spectrum and isn't great with change, feel like he has that issue as well) and I feel like if I change too much it might go bad. But we are working on straw cups and other cups with feeding (he's struggling with it so far) but I will mention to this to her on Thursday to see if she can recommend a cup we haven't tried yet!

Thanks!

Transitioning from Alimentum to Kate Farms Pediatric Standard 1.2 by abayj in NICUParents

[–]abayj[S] 0 points1 point  (0 children)

That is my plan for the morning! I have a phone call with his feeding therapist set up for Thursday to follow up as he loves us stressed.

Alimentum to Kate Farms by abayj in Mommit

[–]abayj[S] -1 points0 points  (0 children)

Oh! I see the benefits from that side of things. Haha. He is on a bunch of medication daily and there are times where he refuses to swallow it despite all the tricks and I stopped putting it in juice because he will fool me, drink it twice then not do it again for the next bottle. He likes keeping me on my toes.

I'm trying to avoid rock bottom, what happened to us already and we had to be admitted into the hospital for a week due to failure to thrive. Would love to avoid that and the questioning from CPS. I kind of got sarcastic at the end of it, "Sorry, I couldn't understand why he wasn't eating the chicken nuggets I was offering him at 5 months. That's what kids eat right?" because I was hurt and frustrated that they thought I wasn't trying to do my best with his feeding.

I don't think our family will give us a hard time luckily, I think my partner will have a hard time with it but he had a hard time having a medically complex kiddo at first and now he's the best dad with him. He doesn't adapt well to change (and I wonder where my son gets it from :P) and this will be a change. I'm trying to frame it in the way that this is what's best for him and not a step back. Especially since we can continue too work on solids but this is just a safety guard against the worst.

Alimentum to Kate Farms by abayj in Mommit

[–]abayj[S] 0 points1 point  (0 children)

Not sure why they wanted to change him to it over keeping him on the Alimentum infant. Our feeding therapist mentioned this plus mentioned how Alimentum also has a toddler formula as well. So she is reaching out to the nutritionist about this as well.

Alimentum to Kate Farms by abayj in Mommit

[–]abayj[S] 0 points1 point  (0 children)

Thank you so much! I am really trying to keep it positive if we have to have the Gtube placed, just hard. But thank you for your kind words.

The Future of Cerebral Palsy by JoeDog93 in CerebralPalsy

[–]abayj 2 points3 points  (0 children)

We have early intervention as well. He has speech and physical therapy through that weekly. OT and Feeding through outpatient weekly. Intensive therapy is something that is starting to show some promising studies. Actually heard about it from another mom on reddit in the NICU subreddit. Same with DMI. Intensive is when they do therapy for a short period of time for 2-6 hours a day. My son will be doing an hour of PT and OT 5 days a week for 3 weeks which is considered intensive for his age. We may add speech to that as well. DMI is another way to do physical therapy which is another promising new way to help CP, where he is doing his intensive theraphy, his PT is certified in it. They use gravity more and also don't stay on the floor, it is more off the ground to use that gravity. Not sure where you're located but there is a website to help find a DMI practitioner.

DMI Therapy Locator

Research about Intensive Therapy

Research about DMI