Showing posts with label NILMDTS. Show all posts
Showing posts with label NILMDTS. Show all posts

Sunday, January 4, 2015

(Even the Littlest) People Matter.

I feel like I need to talk about other things than potty training and my naughty toddler. As a quick update, the toddler is still naughty, but he's totally potty trained for day and naps and it really was fine and good after five days. We're now on day 13 of zero diapers and totally set. We're about to throw his butt in pull-ups for nights though because Mama needs to sleep and do less laundry, but anyway. We have two living children and that's all that really matters.

We'll be celebrating our daughter's first birthday exactly 10 days from today. In six days, about 40 people will cram into our home to witness her baptism and first birthday festivities. Four days later (on her actual birthday!), we will be flying to Whistler for skiing, spa indulgences and fun with our good friends and fellow babyloss family who are also parents to Jack, Grace & Piper. Jack's fourth birthday was on New Year's Day. Who would've thought we'd be renting a ski condo in Canada with friends who also have a dead son, four years later? If you asked me on December 4, 2010, I would've called you a lunatic. But we're so grateful to have such close friends who literally carried us through some tough days in those first months of loss and still have so much support to offer.

Just a few days before Christmas, Andrew's print arrived in the mail. We decided on a professional pencil sketch for his 4th birthday. Like so many of our babyloss friends, we wanted something to display in our homes that would show the true beauty of our children while still keeping them sacred and protected from gawking and ill responses. We first caught a glimpse when I was sent the initial sketch two days after his birthday. I was so happy to receive this during his birth month.

When it first arrived in my inbox, I was underwhelmed. It was stunning and drawn with such care, but it wasn't the boy I held in that hospital room-- nothing one dimensional could possibly contain all that he was in our arms that evening. There were tiny changes I requested she make (space between fingers as I remember & skinnier nostril cartilage). It was beautiful, but I found myself underwhelmed because it wasn't really him, as if what I expected was to have him back in our arms for the cost of a pencil sketch. We will never have more of him and never another portrait or photograph or experience with him. This was it.

This was shared on her facebook page, and now here. Andrew, spitting image of Claire. 
                                                 
After a day or so, I kept staring at his portrait and just fell in love with it. We received the professional copy just a week or so later and had it professionally framed. We picked up the framed piece two days before Christmas and it now has a place among our family photos. It is a cherished piece. We also ordered four copies that will be given to our families when they arrive this week.

Now four years after losing Andrew, we're still trying to find our place in this mess of babyloss. We want to contribute and help others. In many ways, we've already done that. My husband has recently signed up to help as a liaison for NILMDTS. My friend Brooke (who is basically a babyloss celebrity and contributing author to Three Minus One and I've had many meals with her and she slept in my house! Are you jealous?) blogged about a company called Sevenly recently. One of their recent campaigns supported Now I Lay Me Down To Sleep. I bought up two shirts immediately and posted a picture of one of them on Instagram. They still have some available in four different prints, so check them out! They've raised over $19,000 in shirt sales for NILMDTS, donating $7 from each shirt to the organization.

We're just so passionate about supporting them and ones like it because it normalizes loss for everyone. It makes losing a child more bearable, less embarrassing and more accepted. It makes families like us feel like human beings with hearts and not looked at like charity cases and lepers. We gifted some local NILMDTS photographers gift cards during the holidays to encourage their efforts and thank them sincerely for all they have done for us and other families. I attempted and successfully managed to use my grant-writing skills to send $1k their way. We shop on Amazon Smile with with 0.5% of purchases going to the organization that is the sole reason we have images of our firstborn son and proof that he was real, ours, and is adored. 

If we ever get the guts, we'll use a NILMDTS photographer to shoot family pictures. We're not ready. Four years and two kids after losing our firstborn child, we still haven't had another professional photo shoot. He's always missing. It still hurts and there's still a void.

I'm considering another volunteer opportunity (because I really do need more to gab about than potty trianing, amiright?), but that's just being discussed and nothing concrete yet. It will probably take a village and in an effort to keep Andrew's memory alive and well within me, it's something I'm seriously considering.

People are still losing babies. I can't do anything about that (and neither can they, sadly), but it's something that hits me hard and something no one should go at alone. 

Monday, October 13, 2014

NILMDTS Featured!

I wrote back in August about winning $1,000 for an organization near and dear to our hearts and the reason we have beautiful photos of our Andrew, NILMDTS.

Well, they're featured this week! It's Pregnancy and Infant Loss Awareness Day on Wednesday and it's timely to have them at the top of the website with a beautiful photo.

Check it out!

Monday, August 18, 2014

Grant Writing... and Winning!

As summer comes to a close and school starts up soon (Benjamin tomorrow! Eeek!), I am once again reminded of how much I miss the classroom. I miss the freshness of new kids coming in, organizing, planning for instruction, and what I miss the very most, teaching. I just love watching my own kids grow everyday, but I do excitedly dream of heading back to the classroom in the future.

During my teaching years, I wrote a lot of grants. In fact, I was one of the main writers on our team to win our school the California Distinguished Schools Award for the first time. Many veteran teachers had been on the committee before and the school never won after years of trying. They said it couldn't be done. Everyone was discouraged. If you know me, you know I'm fairly determined and not willing to take no for an answer if what I want is something I'm passionate about. Well, we did it. In addition, I won a series of grants through Mobil to be the only classroom on our campus with a SmartBoard, EXPO document camera, students response systems and a variety of other teaching tools, many related to technology. I love writing grants. Maybe it's my journalism background that just gets fired up. Or maybe it's the competition of it all.

Well, it's been a few years. A month or two ago, I randomly saw a program online by JOLLY TIME Pop Corn called the Kernals of Kindess awards program. They were selecting individuals or organizations that "pop up" and make a difference in other peoples' lives. They were giving away 100 grants of $1,000 to keep doing great work in honor of JOLLY TIME's 100th anniversary (of being a 5th generation family-run company... how cool is that?). When I saw this, I immediately thought of Now I Lay Me Down To Sleep and the impact they made on us as a family, giving us the precious gift of Andrew's only photos. Those photos mean more to us than any other gift because that is all we have of our son. We're just so grateful. And we didn't pay a dime for those photos or the 1 a.m. session of that photographer coming into our hospital room and facing us at our worst time. I wanted to support this amazing non-profit and give it a go! I had nothing to lose and only about 15 minutes of my time to sacrifice-- a lot less time than that photographer spent with us that night.

I put my fingers to work and filled out the application, nominating NILMDTS. I don't remember what I wrote, but wish I remembered! I randomly checked my junk mail box last night to find an email announcing I won one of the 100 grants.

Out of 6,620 entries!

The story of NILMDTS will be featured in October and I can't wait to link you all to that when it comes around. Aside from the monetary gift, they are receiving so much publicity that is much-needed for the fantastic non-profit that they run. Conveniently, as my friend Caroline pointed out, they will be featuring the story during the Pregnancy and Infant Loss Awareness week in October. I don't know if that's just coincidental, but it's fantastic.

While it's just a snippet, just look up at the header of my blog to see some of the art of a fantastic NILMDTS volunteer photographer to know why I am indebted to their kindness and work on behalf of grieving families.

Sunday, September 16, 2012

Grief Revisited

The calendar pages are thinning out again. We're closer to him.

I'd be lying if I said it wasn't easier anticipating his birthday this year than it was last year. There's just something so definite about 1 year. It seems so monumental in so many ways, including personal relationships. At the 1 year point, things always started to get real. We were engaged just weeks after our first year of dating was up. Now that he's nearing the age where babies aren't referred to in terms of months but in terms of years, it feels different. But it doesn't change that he's gone. Or how much we crave to have him here, in our arms to hug, love and watch grow.

But two years? I'm not as anxious, and maybe Benjamin is in part to thank for that, but I guess I just don't know what to think anymore. We had a long talk the other night about Andrew and how we're dealing. It's not that this is a closed chapter of our lives. We'll forever be damaged and changed. We talked about how we're just worse people for losing him. That it caused us to be more guarded and scared. That we're more angry and still question why our family was crushed.

The jealousy is still harbored when we pass another family with two beautiful children in tow. When we learn of a firstborn being welcomed into someone's home. When a two-year-old boy is in our presence.

I told my husband the other night that I'm glad we're still broken. That I hope we're always broken and lack acceptance when it comes to losing Andrew. I don't want to accept that our son had to tragically die when he was supposed to be welcomed into our home at any moment. I don't want to accept that we'll forever memorialize him and speak to his sibling(s) in past tense, because they will never have a chance to meet him face-to-face. I'm sad for us, but I'm immeasurably sad for them.

We sat last week in our formal living room that doesn't have a whole lot of living in it at all. It's where Andrew's urn is and all of our tangible memories we display of him. It's also where we keep the photobook of his entire life, all in about 40 pages. It displays pictures of my entire pregnancy and how excited we were to be growing a son. Our son. Our firstborn. And now? It's so difficult to see those photos of our smug, innocent, naive selves; so difficult that we skip straight to the back for pictures of him. Just reliving the pregnancy in pictures, though wonderful as it was, makes me weak in the knees. I become nervous, sad, and angry when I see us in that state. It's like were were a ticking time bomb just waiting to explode. Every single picture framed in our home aside from the few of Benjamin were from before we became the people we are today. We were happily hopeful and lived in the world where babies didn't die. I'm jealous and frustrated looking at all of those photos. Seeing blog posts from our former selves is just so hard for me to read, because I was different and... better.

We talked through our tears about how the greater part of our lives will be lived in this broken state and world where babies and innocent people die terrible, horrible, and unfortunate deaths and it's just sad. Sure, there's beauty and will always be beauty, but it's always going to be less beautiful and less good. And that sucks. There's just no way around it.

My husband used to work for a company in LA that handled all the back-end work for professional photographers. He met some incredibly talented people there. It's LA, after all... but when you pair up photography with hip individuals and young, free spirits, you get a pretty nice mix of people. One of those amazing people shot our wedding.

In our broken state on December 5th of 2010, an equally talented and selfless person stepped into our newly broken lives and took photos of our deceased son for us as a volunteer for NILMDTS. He didn't have to come into such a vulnerable situation, find parking at a hospital in the middle of the night and meet our dead son and his broken parents. But he did. Those photos are absolutely the most valuable we have and we cherish them. This week, Ray wrote a note on the forums of his former photography company to thank and encourage those photographers who volunteer their time and resources (and emotions!) to do such good for families like us. We know it's not exactly easy. As we approach the two year mark, Ray decided to reach out again in admiration for those who humble themselves to do such remarkable deeds. They deserve all the recognition; it's because of them that we have photos of our firstborn and those just cannot be more important to us. As Ray wrote in his letter, ..."because of you, {Benjamin} will get to "meet" his older brother through the most beautiful photos..."

If you're a volunteering photographer reading this, we thank you. So many of us loss families just cannot even begin to thank you enough.

Today we prepare for a playdate at our home with some families in our area that we've grown to consider as part of our own family. It's a beautiful day, the sun is shining, the beer is cold, the new toys are ready, our second son is growing and learning, and we're thankful. In a good, but not ever as good as it could have been way, like it was before our worlds changed. We miss you Andrew. We miss who you were, would be now, and would be tomorrow. We miss all of the memories we'll never get to create with you. It doesn't have to be the 5th or your birthday for us to think of you or mutter those words. We think them every single day we live.

Monday, May 9, 2011

The Most Wonderful Gift

I'd like to think I showed progress today, but it's probably just the grief train going easy on me right now, in this very moment. I'm not counting my chickens, however, because we all know it changes like the wind.

Today our NILMDTS photos arrived in our brand new mailbox. {My husband is quite handy.}

Breathtaking. 

My heart was beating out of my chest as I clicked the CD into my laptop this afternoon. I propped the Kleenex right next to me knowing that at any moment I might burst into hysterics. But you know what?

I didn't. I was just in awe of what incredible beauty he was. He is. For the first time since he was born, I was proud. Up until now I've been ashamed, frustrated, angry, embarrassed. But today, seeing those photos made me incredibly proud to be the mother of that little boy.

These photos are 5 months, 4 days old, and the same age our Andrew would be if he were here with us today. I have been on pins and needles hoping to receive them since at least January. Finally, they're here. He looks nothing like a dead baby-- but a newborn (as he was). The photographer did an incredible job capturing his gorgeous features. They look no different than a photo shoot of a living child. Perhaps a discerning eye could tell, but to me, they're perfect.

I guess my only sadness is knowing that this is it. There are no more special Andrew photos making their appearance any time, ever again. This is all we've got. About 5 of our own images, roughly 30 printed copies of poor quality from the hospital, and 17 from the professional photographer. Just about 50 photos of my child. I have more photos of him inside my body than I do on the outside and there is no turning back. No more photos are there to take. No body present to be photographed. I suppose those photos are even more precious as all of them were taken when he had life in his body. He was breathing. He was growing. Those are my happy memories.

I hesitate to share these. I don't believe this is the forum, though I know others might disagree. Because he is our only child and only 3 people besides the hospital staff and our photographer have seen any photos of Andrew at all, it feels sacred. He is sacred to me. His body, his photos. While I would be willing to share with people, I don't feel it belongs broadcast on the blog. I want to have the opportunity to share them with people I know, love, and respect. I know, love, and respect many of you who read, but there are many people I don't know that in cases of stillbirth, (still) do not fully understand how important it is for our children to be treated as something beautiful rather than diseased. I refuse to allow a single scoff at the sight of my child. I can't control that via the internet. My son deserves protection from his mother and I'm proud to protect him.

Maternal instinct kicking in? I guess. I'm still not sure what that's like if I'm being really honest.

But this boy... he's beautiful. Downright gorgeous. I hope Andrew's future brothers/sisters have some of his features. I'd love a piece of him carried on through our family in the flesh.