Tuesday, August 11, 2026

Tomorrows


 

I know I don't write like I used to. But I saw this quote not long ago and it's been stewing and sitting in my head since and I wanted to reflect on it. 


Gosh. I miss him. His weight. His smell. His smile. All of him. 

We are closing in on the 2-year anniversary of his death in a couple months and I've been thinking of him more the closer we get. I finally sat down and watched the hour-long video that we had playing at his funeral. I cried and laughed. So many pictures I actually don't even remember picking out in honor of him. 

Sometimes I wonder if I gave him everything that we could give him. Looking at those photos made me see the things we gifted him with. He was far from a typical child, but I see now that we gave him a life worth living. 

While we did spend so much time in doctor's offices and hospitals and therapies and he had some rough days that didn't allow us to even leave the house due to his health or just his grumpy moods (shout out to Kyle for explaining to the lady cutting his hair YEARSSSS ago that our lives revolved around his brother's moods), I was so happy to see the smiles on his face for other things we were able to go enjoy. 

For a while, we did regular photography sessions with him, marking each year he got older, and then photos of him and Kyle together when we had him. I noticed how easy his blue eyes were to capture. 
Eventually, his dad learned the ins and outs of photography to capture the boys together, due to never knowing how David's behavior was going to be that day. Most of our photo sessions were literally planned the morning of with whatever clothes the boys had in their closets.

We went on vacation almost every single year despite how hard that could sometimes be to plan. It was almost always to South Carolina. But I have so many pictures of him there in the ocean, on the beach & in the pool. He was almost all smiles. We did Disney World one year with Grandma and Grandpa and he hated it. Loved it the first day but was miserable the rest of the day unless he was riding the monorail or in our hotel room.  It was quite the adventure to make that drive with a 10-year-old and almost 4-year-old, but we did it. Changed diapers in the van, fed him on the move, cleaned up the aftereffects of car sickness. While we never went back to Disney, we still didn't let those troubles almost every year keep us from our South Carolina trips. 

David was the oldest grandchild on my side of the family, and he was integrated so well, that I'm not sure any of his cousins would even think twice about his disabilities. Many of them knew how to use the gtube and loved playing with him. I think his first best friend was Mikel Jr, and his other cousins just became extra best friends as they came along. We spent so much time with family at the lake every summer, and as he grew older, he didn't get in the lake as much but enjoyed laying on a blanket down in the grass near us and occasionally we would see him "running" through the yard-AKA scooting as fast as he could through the grass away from us. He loved a good fire pit at the lake with grandparents and cousins. He loved the golf cart rides he got out at his grandparents with his cousins, but quite possibly, loved the one where Logan took off driving with him unsupervised by an adult while they were both very young the best. 

We did holidays and seasonal things every single year. He didn't understand why but he was always included and with us. Halloween was probably the most confusing of all for him. I saw pictures of  Scooby-Doo, a frog, a lion, Elmo, Peter Pan, army guy, Woody, superman, spider man and a doctor (probably my favorite costume for him ever) all in that slide show. He looked happy in the pictures, but I know I remember the look of disdain on his face when I’d put the costumes on him. He saw Santa, had a stocking, and presents under the Christmas tree. Which were always as many hats, mirrors and chew toys I could find. I used to buy him lots of fun tshirts, until he started ripping them to shreds and preferring to be naked from the waist up. He attempted to dig the guts out of a pumpkin at Halloween (hated it), dye Easter eggs (scared me he was gonna spill all the cups of dye), got an Easter basket every year. We enjoyed pumpkin patches in the fall and I even manhandled his wheelchair over hiking trails in the spring. He got to go boating once in a while in the summers. He loved watching bubbles and one year, his bubble machine was the hit of his Easter basket. We weren’t fans of winter stuff. It was like wrestling an elephant into a pair of pantyhose to get a winter coat on him and made it so hard to carry him to the van. Snow and wheelchairs aren’t a great mix either.  But I still did it and took a few falls while doing it. 

He got to go to school. Starting at 3. They didn’t quite know what to do with him, but as time went on, every teacher he had came to love him probably almost as much as we did. He made friends (his best friend, Megan, beat him to heaven and they’re probably dancing up there now). He went to grade school, middle school & high school. He had school pictures and school IDs. He rode the bus. He went on field trips. He walked across the stage with the help of his brother and graduated. He had highs and lows at school just like other kids. I went to countless IEP meetings and eligibility meetings. I fought to have certain things in his IEP’s and was taught other things to ask for over the years. 

His sibling relationship wasn’t like others. He and Kyle played sometimes, and other times Kyle also ignored him like most brothers 6 years apart would do. We called Kyle “The Little Big Brother” because let’s face it, there was never any acting younger than David, even as an infant. In the end, Kyle was the one on the other side of him, holding his hand when he died. In that moment I watched the hardest thing in my entire life-losing my oldest child and watching the youngest one lose his only sibling. 

He had a good life. Yes, it was hard a lot too. But he was so strong. We took him to restaurants, where we allowed him to steal the cloth napkins and he was famous at Hooters for a while. We decorated his wheelchair for holidays and seasons, wrapping different colored garlands around the handles and giving him his own license plate when he turned 16. He got the chance to "walk" in a gait trainer and scoot on a scooter around the gym while his peers were roller skating. We went to zoos he clearly didn't care much about, drove in the mountains and got him out to enjoy the views. He made giant messes in his room with his toys, dumping out his laundry baskets that were filled to the tops only to play with something he already had out. He was able to move freely around his safe space in his bedroom. 

Making the final decision to let him go was for someone much stronger than I am, even though ultimately, I had to pretend I was indeed strong enough. I think if I had been alone, he probably would have lived a little longer (possibly years, but quite possibly only days…we will never know). But having someone with me who listened to me talk about David as she and I both kept trying to put our fingers on what was going on with him before he went drastically downhill guided me in making the best decision in a moment of pure fear and panic, was what made me see that we probably would never get the days back that David had in the past and deserved to be had in the future. He would have had to be hooked to a feeding machine for many hours of the day instead of scooting and playing. He would have been miserable like that. I knew God was going to let him in. I prayed for that so much as he was growing up. 

Looking back on the video slide show made me see that I gave him a good life. Most of the time a great life. I gave him all I had and doing that for so many years has left me drained in such a way that I am actually still recovering from it. I truly loved him like there was no tomorrow and saw in the end that there would be no more tomorrows like he had in the past. 


All I can tell you is that I loved him from the moment he was born to the moment he took his last breath and I will never regret any second of that. It's a love you never recover from. 






I wish I could put that video up on this blog for anyone who would like to see it, but it exceeds the limit for size and I don't know how to make it smaller. It's so worth the watch. 






Friday, January 2, 2026

Grief. Grit. Grace. Grief.


 It’s a cycle. Grief is a cycle that spins around and around and around. You wait for it to stop in one spot but it never does. 

I’ve been trying to not write only about grief. But it is what I currently (and forever will) know. So I feel like I’m qualified to speak about it. And if someone doesn’t wanna read it-that’s great. Just close the tab and keep on scrolling 😀

I’m forever learning in this new space I’ve been in. He’s been gone for 445 days and there isn’t a day where I don’t think about him. I think about his smiles. His laughter. His crying. His sounds. His weight. His crooked pinkies. His webbed toes. His cowlicks. His blue eyes. His life. 

Grit is a big part of grief. If someone says “you have a lot of grit”, it’s because I do. And I know I do. Because I keep showing up day after day after day for the people still in my physical life when some days all I can think about is the one I miss that’s in his eternal life. 

I still have a child here on earth. And I am so incredibly proud of him. He may be an adult now, but you never stop taking care of your kids right? He will always need me-even though he thinks he already doesn’t. I drive him crazy. But I know he loves me and I hope one day he will appreciate the fight I fought for him and David the last 7 years. That was grit as well. I tried my best and I KNOW I didn’t leave my kids, I didn’t try to have zero physical custody, I didn’t only see them 3-4 days a month. 

Grit is also fighting through that bitterness. There are things I will never forgive people for in the last several weeks of his life. And I can’t change it. But. I can try my best to recognize it and deal with it in a healthy way. Some days that requires a deep dig of the heels into the dirt to stop myself from letting that bitterness overshadow me, but it’s getting easier. 

And that’s where the grace (and a great therapist) comes in. I held David 95% of the 9,003 days he lived in this world. I felt his weight. I heard his laughs. I changed his diapers and I made sure he was fed. I loved him. Every. Single. Day. I showed up for him. I know twenty-four years old is no longer a baby or a child. But in our case, David was mentally 6-9 months old. So he WAS indeed a baby. Do you remember the years your children were little? Sometimes not sleeping well? On a schedule? Needed fed? Your life revolved around them and not yourself? Eventually they grew out of that and became more independent.  I never got that. I assumed I would spend the rest of my life caring for my infant adult and not knowing life  beyond that much. Imagine that. To have that yanked from you within hours one night. After seeing improvements and then your loved is is just…..…gone. 

My grace has become knowing that I can have joy even when I feel sorrow. It often goes hand in hand. Family get togethers-I’m happy, but I’m sad David isn’t there. Christmas-gift giving is one of my favorite things, and I love it, but David should have new hats and mirrors to play with. Some days I just give myself the grace to just feel the hurt. The weight on my heart is heavy with longing for him. I cry because occasionally I question if he was even real. And it’s only been just over a year. I feel guilty for that. For maybe thinking he was a dream. I’ve allowed myself the grace to know it’s OKAY to have the feelings of anger. Of sadness. And that bitterness. There is no specific time limit there. But I am not allowed to set up camp there indefinitely either. I feel. I talk about it. And then I try to climb from that hole and get back on solid ground. 

I’m trying to “do for myself”. I really am. I struggle leaving my safe zone of my house but I am going to try better. Get a little healthier and maybe eat a little better. Try to just LIVE. (I’m taking a trip to see my mom soon. It’s the first time I’ve flown without Moe or one of my sisters in a while….I’ll have to be responsible for getting to where I’m going instead of just following him or them trustfully around the airport knowing I’ll get where I’m going because they don’t let me down. LOL)  I’m still trying to figure out where I “fit in” in this world without the identity I knew for my entire adult life. I still feel like a special needs parent. But I don’t know where that fits without the special needs child physically here. 

I will never stop grieving him. I’m really only surviving because I don’t have a choice. I have David sized holes inside of me and I won’t ever fill those. 

It’s ok to always have grief. It’s really all about the grit and grace grief requires.