Abe Saves
Our Life After Loss
October 15, 2014
Aware
September 24, 2012
Five
I'm angry. I'm angry that I have no idea what a five year old likes. I'm angry that I find myself looking at clothes, wondering what size he would be in. I'm angry that I worry about Judson being an "only child" when in fact he is not. I'm angry that he has to carry around a picture of his brother, cause that's all he has. I want my first born. I want Judson to have his brother. I want the impossible.
Instead we make trinkets to take to his grave. We make cupcakes that we think he'd like. We sing "Happy Birthday" through tears. We will let his little brother blow out his candles and eat his cake. We do our best to hold onto our fading memory. It's hard to celebrate a life that is no longer.
I love you sweet boy. The love you brought to our hearts carries us through. We will forever honor and cherish this day. Love and miss you to the moon and back.
October 05, 2011
Unwrap It Up
October is SIDS/Infant Loss Awareness month. I've made a decision to do my part in participating any way that I can. I've wanted to get something out there for a while now, but I've recently befriended a great source of inspiration. I've realized that the silence of this dis-ease is, by it's very nature, a true cancer. I've been quiet about my experience for 3 years, humbly suppressing any gained wisdom or knowledge. Maybe I thought it was just something we had to go through, as we were so often told. Maybe I thought with enough passage of time some sort of understanding would unfold. Maybe I thought ample therapy could help. But I still wake up every single morning with a gnawing reality; I lost my son, he is never coming back. Sometimes my dreams will momentarily stun me into believing this isn't true, but I quickly regain equilibrium. I am a bereaved father, in love with a bereaved mother. My unsuspecting mantra. Who would have guessed?
It's difficult to define SIDS awareness. It's an oxymoron, really, because SIDS by definition means unawareness. Unaware of any explicable cause of death. This is a frustrating conclusion for a parent to face, and an even more frustrating causation for a death certificate. SIDS has morphed into fear mongering over suffocation, leaving our babies to lie alone in cribs on their backs with no blankets and barely any clothing, crying out for their mother's soothing affection. I've been there, I've seen it elsewhere. It is truly revolting. One mistake Jamie and I will never make again as parents is buying into the debilitating hype that SIDS is preventable by certain pacifiers and sleeping behavior. This is simply not true. SIDS has become one more way to dupe parents into thinking they have control over something they don't. Oh, and you can make profits galore. Pick up any baby product these days and there will be something about SIDS. "This 'product' helps reduce the risk of SIDS". It's all done to profit off of your fears and insecurities, and it should be stopped.
I could go off on that forever, so I'll spare you my own opinions about it. I realize every parent needs to do what makes them feel comfortable and safe. Increasingly, however, I've become more sensitive to the propaganda and shear nerve of the medical community with regards to SIDS. Their definition is very slippery. They continue to call suffocation SIDS and thus perpetuate the lack of information parents receive. If you are reading this and you are a parent then I challenge you to define it for yourself right now. What is SIDS? What do I think I'm doing to prevent it? Chances are you're doing (or have already done) what the medical professionals tell you, which is nothing more than not allowing your baby to suffocate. Yes, we need to be aware of our babies environments and the implications of possible hazards, but SIDS is not suffocation! It's a tortuous stigma for a parent to have to carry, one that is grossly misrepresented and one that I find terribly offensive. I do have a sense of peace knowing that I had nothing to do with Abe's death, but there is something else that haunts me. Thousands of babies will continue to die from this unknown on/off switch hidden inside the human brain if we don't address it head on. Bad statistics and egregious nohow will only heighten our unawareness and stifle any possible cure. We need leadership, we need research, and we need it now!
So this is my contribution to the cause. I lost my son to SIDS. It's not something I will ever feel OK about. It's a wound as raw as time, and time never ceases. But in the spirit of this month of awareness I really wanted to push myself to word vomit all that I know about the issue, which is more than just an issue, it's my life. My intent isn't to make anyone feel uncomfortable or alienated. Quite the opposite, really. Very few dip their toes into our water, but we are eager and ready to share. I think people would be surprised at our willingness to talk about our son, his death, our grief and the absurdity of SIDS propaganda. Indeed, talking about Abram is the only thing that lets the voice out of our hearts. He holds an indefinite claim deep down inside of us and we can be content with that. Our biggest fear, however, is that Abram will become forgotten to the world. It's a fear that every grieving parent feels. Judson has a brother, and he deserves to know his brother. Abram's memory is something we are obligated to fuel as part of the engine in our family. If we let our hearts close up to the pain that's in tandem with our joy, our family will suffer terribly. The realism of this loss is something that we will never evade. So I'm just gonna throw it all out into the blogosphere, all in good time, and y'all can digest or refuse as you wish.
This is my awareness.
May 25, 2011
Our Rainbow Baby
May 02, 2011
Angel Day, Part 3
At times it is hard to believe that it's been three years since losing our son. Most of the time it feels like it's been longer, because everyday is a struggle. I try not to think about that day because it was the most difficult day of my life thus far, but I also try and hold onto it because it was the last time I held him, nursed him. Even holding his lifeless body is something that I try and remember clearly and hold dear in my heart. Josh and I have said so many times that we truly feel fortunate to have lost our son the way that we did. Other circumstances that may have been surrounded by guilt or blame our unfathomable to us. We never had any of that and feel heartache for those that have experienced loss in that way. Loss is never easy and we have so much love for those that experienced our loss with us. Tonya, we love you more than we can say.
April 03, 2011
Who's counting!?
March 14, 2011
Good Tidings!




