2025

It is 5:59pm on Wednesday, December 31, 2025. Another year about to be finished that Sonzee never lived. Oh, how my heart still hurts the same as it did back in 2021, after the first year that came and went without her physically present. If only that could change somehow. Just a little something to remove the sharpness would be nice.

2025 was a year that I wrote my fewest blog posts to date, capping it off at a whopping 5. It isn't that I didn't have anything to write, it is more that the redundancy makes me hesitate. The knowledge gained over the years means I am acutely aware of what sitting down to honor my feelings will do. The same pit in my stomach, the same heaviness settling in my chest, the same tears that will flood my eyes, the same pain that I try so hard to keep at bay to continue to be able to function, in similar words of Sonzee's older brother, "it hurts to [write] about her, why would I want to do that?" Fair point sir. 

2025 finished with my 801st blog post being written. I suppose I could celebrate that.

2025 brought another travel hockey season and a pause but restart in competitive gymnastics for Sonzee's siblings. To watch them do what they love but face the challenges they deal with while doing so breaks my heart. There is a plan to it all, sure, but I wish they didn't have to struggle or be dealt with anything negative after all they have had to deal with in their short lives. Sonzee's oldest sister took up band and is playing the guitar. Her little brother is still figuring out if he wants to play ice hockey or soccer. 

2025 brought ant colonies and 2 chickens into the Zaila household. A new renovation (that is still not fully completed), but maybe by the next new years eve blog it will be. 

2025 brought the acceptance of Sonzee's twin girl being accepted to a study abroad program for this spring semester, starting in just 19 days. The concept of going from 5 kids to 4 kids to 3 kids actively living in the house for such a lengthy amount of time has not fully been processed. 

2025 was the year I visited Sonzee the least but spoke to her the most. It was the year she was given the least number of painted rocks, but the year I thought about painting them but not doing them the most. (The thought for sure counts more.) It was the year I still struggled to accurately communicate how many children I have but decided on using -ish if I cared to talk more about her. 

2025 was the year Sonzee turned 10 but will forever be 4 years 11 months and 24 days. 

2025 was the year that Sonzee's death outlived her life. I often wonder how I have to live longer experiencing grieving her than I did at her living her life with her. That won't ever make sense. 

Since I don't have any positive way to finish 2025, I will repost an excerpt from my 2024 New Year's Eve post.

In 2024, I accepted that there’s no "fixing" grief. I came to terms with this in the same way I had to accept that a cure would never make Sonzee an active participant in her own life. I accept grief for what it is: permanent, ever-changing, and woven into the fabric of my existence. I accept that it will influence everything I do, every day. I accept that others, even family members, may never fully grasp the depth of grief’s impact. And I accept that there will always be a void—one that nothing can fill. It’s larger than everything else, and though it sometimes shrinks, it is never gone. It can swell at any moment, without warning, and consume everything. I accept grief, but I don’t like it.

If happy ever did exist...

Hi baby girl. 

How are you doing? What have you been up to? I can almost hear you teasing me, “You know how death is, Ema, I’m really busy.” I know I don’t need a reason to write to you, but you probably already know there is one. My brain has been stuck on repeat these past two weeks, and yesterday it all came crashing down. So, I decided it was time to write you a letter.

When you were born, you spent eight days in the NICU. While I was there, I received a gift package filled with thoughtful items from a mom who had lived the NICU life herself, someone deeply woven into the special needs community.

A few weeks later, when we were admitted to the PEMU room at PCH for monitoring, we had our first visitor. It was her, the same mom who sent that package. She came in with so much warmth and understanding. I remember getting up to use the bathroom, and she held you close so I could take that short break without panicking. Just before leaving, she held you near her face and whispered, “Do something, or cut this shit.” And no sooner had she walked out before the door even closed, I pulled the seizure alarm cord for the first time. That was when we finally had confirmation.

In the weeks that followed, I remember so many phone calls and texts with her, her optimism ringing through my fear. “At least it’s seizures,” she’d say. “You can treat seizures.” She was the one who understood, who always had words when I couldn’t find my own.

And then, the day you left me, I left that world. Partly by choice, partly because those still living that life don’t really want someone like me in it. I became the mirror no one wants to look into...the living reminder of what could happen. And for me, they became the reminder of everything I lost. It’s mutual, really. Too painful for both sides.

Five years, eight months, and twenty-five days after your journey began, she has now joined mine. My heart feels shattered for her, for us, for me, all over again.

Because this is what happens, every single time.

People who haven’t lived this life say how sad it is. They say they “can’t imagine,” because truly, they don’t want to, it’s too much to even picture. They’ll grieve for a bit; they’ll be sad for a while… and then life will go back to normal for them. Their children are still alive. Their homes are still full.

But for us, the ones who carry this forever, there is no going back. We cry in the shower. We hide our tears from the others. We wake up every day under the weight on our chest. We argue silently with ourselves about whether to help another parent, knowing the emotional toll it takes. We debate medication just to get through the day. We live life divided into “before” and “after.”

We try to figure out how to live again. How to find meaning. How to feel anything that resembles whole. We take family photos that include a grave. We'll make every song relate to you in some way. We list your age as if you’re still here, just to avoid awkward silence. We don't always mention that we are part of a secret club and sometimes that leads to horrible guilt, but the alternative requires energy we just don't always have. We imagine what you might be doing in a place no living person can ever understand. And every time another child dies, we lose you all over again.

So, here I am. Back in the hole I was just attempting to crawl out of after a challenging 3 weeks, sitting with you to hopefully allow you to help pull me back out. I still don't know how it works, but please go look for Avi and show him the ropes. He's a lot older than you, but you have more experience in his new world. Tomorrow he'll become a close neighbor to you. Aba will go and see you; I am sorry I just can't go sit under that pavilion. I love you baby girl!

"If "Happy Ever After" did exist
I would still be holding you like this                                                All those fairy tales are full of shit"

Until next time. 

Love always and forever, 

Ema

Coming to a head

Dear Sonzee, 

Hi baby girl! How are you? I am sitting on the porch facing the lake in VV, for another summer without you. I was (as usual) holding everything together. Keeping myself (physically and emotionally) occupied to prevent the whispers of grief that I have kept at bay in that locked space. While I know 2 things can exist, I can enjoy my summer and I can miss you; I can continue to live life without you, and I can also miss you so terribly I want to be with you. The 2 existing things are coming to a head. 

Last weekend (as you probably know because Gan Eden surely got more crowded) a flash flood went through a river in Texas, where a lot of summer camps were located. The impact was deadly with an entire bunk of 8/9 year old girls and their counselors swept away; some of their bodies still have yet to be located. While the news of the reality of that situation was spreading across the US, your sisters were participating in a camp marathon where they chose to run in honor of you. Again 2 truths existing together colliding in my heart and head. 

Any loss of a child sits heavy beyond belief in my core. I know what these parents are feeling, the panic, absence, anger, confusion, intense pain, all with the added challenge that those who have never experience their child's death are saying how they are heartbroken (and while that may be true, they have no idea). They get to wake up to their children. They have them still, here. They are heartbroken at the potential of their loss, but they are unable to truly grasp the new reality of these newly bereaved parents. The ones I will soon see popping up in the online bereaved mom/parent support groups. The ones who now know the pain of everything they have always been subconsciously afraid of experiencing. 

The black hole of grief has opened up and swallowed me. I dislike this hole, despite the fact that my therapist would tell me (and after 5 years I know) that 2 things can exist, I can sit in the hole, I can give the grief time to sit with me, AND I can climb out of the hole. (For the record, I prefer to stay out of the hole and not even entertain it, because as your brother Tzvi would say, "why would I want to think about it when it's too painful") After 5 years I have almost mastered the ability of skipping over the holes, or so I have thought. Because always, when I think I have, and it has been a decent amount of time since the last "oops I feel into the hole I was avoiding moment", I inevitably find myself back at the bottom of the Alice in Wonderland hole. I guess maybe I believe my therapist a bit more about 2 things being able to exist. I can sit here in this horrible pitch-black hole filled with your absence and excruciating pain, AND I know that I will be able to survive the depths of what I have fallen into. 

I just wish these 2 things didn't have to co-exist.

 

2 boys and 2 girls

We never learned the gender for our children prior to their birth. With Sonzee being the 4th Sam had actually wanted to know, but because for the previous 3 he didn't want us to find out, I decided we should stick with our pattern. We already had a girl, then a boy, and then a girl, in my mind of course baby #4 would be a boy. How could it not be? Me an (at the time) very much type A person, there would be no doubt, no question, we would have 2 boys and 2 girls. The perfect family. Afterall, we were evening out the odd number of children, so there wasn't a way we could have an odd number of girls to an odd number of a boy. 3 weeks prior to baby #4's arrival I had a panic attack. We have a boy's room and a girl's room, BUT, what. if. baby. #4. is. a. girl? How would that work? You can't have 3 girls in one room. It didn't make sense. And then....Sonzee was born. A "healthy baby girl" as Sam would write on our social media announcement. I cringed. I asked him why on earth he'd write that. Was he challenging Hashem?? 4 (very long) weeks later, we would learn she had epilepsy, so I guess he was. Within 2 months my perfect image of what our perfect family was going to be, was no longer (but hey, she did have blue eyes so there was always that). 

This year for Passover we traveled to Florida. We took a day trip to Key Largo today to go on Jet skis. Our initial plan was 3 jetskis, Sam with our oldest boy, the 2 girls together, and me with our youngest. Then (as most of my planning goes these day) Hashem said, nah, let's do 2 jetskis, all 6 people can fit on 3, so we will do one for the boys and one for the girls. And so we did. Almost 2 hours into our ride and on the return after so much laughter, speed, and smiles we were idling under a bridge and a nearby boat (aptly named: "This is the Way") and a person on the boat waved to me and as I waved back my inner dialogue took over. 

"Oh wow, 2 jetskis, one that has the boys with the father and one with the girls with the mother, that's even, that's perfect, what a perfect family, 2 and 2"

"But no, there is another, she just isn't on the jetski's, because she is dead, and even if she were alive, she wouldn't be on the jetskis, in fact, would we even be on this trip? What would we have done? What would we have done for the last 5 years? Not all of these #lifeexperiences" 

The heavy hit of grief smacking me in the face, almost cringeworthy to say it was similar to the wind and saltwater doing that simultaneously. Ironic I was on a jetski in an ocean with waves when the grief hit. Another memory a video about grief related to waves. Eventually the grief settles, similar to the waves, but you really don't know when, or how high the waves will be. You know after 5+ years there will be more waves, but you also know they aren't as insurmountable as they once felt, there is a break between them where you can actually breathe, and you can actually see the beauty that is all around you. You know, or rather I'd say you can acknowledge that even though you are no longer whole, you are no longer that unit of perfection that wasn't but was, you still have the perfect family; 2 living boys and 2 living girls, and from the view of others, and in reality, it is actually perfect, but it's always going to be missing the 3rd jetski. 

Five years

Dear Sonzee, 

It officially happened. You have been absent from our physical presence for more than 5 years. I still cannot wrap my head around this. It seems impossible, yet at the same time it makes perfect sense. After all, so much has happened since you left us. There is truth to the whole concept of life stands still after your child dies, but it seems to only affect the parents, because for everyone else, life just continues. There was a definite divide of life before your death and life since. Life since seems to go by at the speed of light but yet in a slow motion form. It really doesn't make sense when I try to assign the motion words. Maybe if you could imagine the blurred images of a slow motion movie but the background is going a million miles a minute with streaks of light. 

Somehow we ended up 5 years post your death. I just cannot comprehend it. I thought I had this whole grief thing figured out somewhere between year 3-4, but Mrs. Penny reassured me after my last mini break down that that won't even come into the discussion until maybe year 8. Life wiithout you has certainly changed, but it is not any easier. I have just managed to figure out how (althought sometimes I doubt it) to wake up every day and plaster a happy smile across my face and act like I am just the jolliest human around. I probably fool 90% of the people I come in contact with that my life is perfect. That I am lucky, because I have 2 boys and 2 girls. That we are fortunate because we can afford to have our kids in all of these extracurricular activities. That aba and I have this perfect marriage that didn't almost fall apart because of having a child with complex needs who physically up and left us. That we get to travel and take amazing family pictures. But, anyone who actually knows us knows that all of these statements couldn't be further from the truth, but 5 years post your death and we have a certain rhythm that makes us look like "we've got this" (we don't).

Year 5 brought less people (thankfully) sending the once a year text saying they were thinking about me. In fact, the same people who reached out to me today reach out to me constantly through the year. It makes me feel less angry to be honest. Morah Zupnick texted me, "Sending you lots of love and protection from the stupid idiots who are going to text you when they haven't in a year". Maybe year 5 finally has weeded those people out. The ones who I know mean well, but yet frustrate me because why only think about me today? Why not realize I am feeling the same horrific pain and loss during every. other. single, day. of. the. damn. year????? Today is just an in our face reminder of the obvious fact that you are physically missing from our lives. Whether today happened or not we would still feel your absence, and we do. A LOT. The same will hold true for Thursday when we have to do this dreaded day again for the 8 of Shvat, but even worse because people will undoubtedly send me birthday wishes as well for my hebrew birthday (as if that's what I want to think about on that day!!!??). I can't say these thoughts directly to people, but hopefully they read this and feel less insulted at my stance? Hopefully they can appreciate the mixture of emotions that I struggle with on the daily. The ones where I put my feelings aside to make others feel less awkward or better about their wishful attempts of being sincere. I know, it's both an issme and a personal problem, but I am working on it.

This whole year 5 of your absence has finished out with a lot of change that I am not ready to share just yet, but it added a nice extra knife twist to your absence. It no doubt came from you, but it isn't 100% easy for me to accept just yet, but like all else, in time it will be. 

I hope you like all of your new rocks and the new setup of your stepping stones. Hard to even fathom that next week you will be turning ten. I am working on your present currently and I hope you like all of the changes and organizing I have done with your space. You are so very missed baby girl. I know you visited Nurse paige, and if you are ever so inclined, I'd love to have a glimpse of your new life. Or you could just let me know a little about it, like who your friends are, any drama you have experienced, the milestones you have achieved. I would take whatever it is you could share with me. 

But until then and until next time. 

I love you baby girl!

Love always, 

Ema