Saturday, July 3, 2010

The gift of blogs

Wow, yesterday was a tough day. Today has been rough too, as I sift through all the wonderful heartfelt messages we've received from those touched by Kaia's story. Thank you all for lighting candles and sharing the night with thoughts of her. It means so much to us!


I received a wonderful gift in my email yesterday. A good friend of mine has been behind the scenes, working on getting our story on a big-time mom blog site. I'm not sure if the person who posted this blog realized that she posted it right in time for Kaia's angelversary, but she did. And what a wonderful surprise that totally made my day! I can visualize CHD awareness as a light that is spreading and shining brighter and brighter and brighter! It's amazing! Also, YOU CAN WIN a totally free piece from LLD. To win LLD's signature "Little Lion" (CHD warrior!), just go to the blog and leave a comment. You could be chosen! The blog is located here, and is called "A Mother's Grief Transformed: The moving story of Stephanie Urban and Little Lion Designs.

That blog post sort of snowballed into another one by a fellow local crafter, who was touched by Kaia's story and reposted it here.

And to top it off, the monsterbites365.com blog is still up and you can still with a Little Lion by commenting on that one too. Two chances to win in only one week. I love it! Please click here to go to the monsterbites blog and enter to win.

I didn't choose for this week to be the week of give-a-ways or contests or anything. But I think it's a great way to honor our little warriors. And I am so proud and honored to have two of my pieces be gifted into your homes, as a reminder of how precious life is, how amazing children are, and how one person can change lives for the better.

Live in love,
Steph

Friday, July 2, 2010

Dear Kaia, Today is your one-year angelversary

Two days ago, I was driving your little brother or sister to St. John's for his/her 33 week check-up. As I was nearing the hospital, I heard an ambulance siren. I looked in my rearview, and there were the lights. An ambulance was going to the same hospital that I was. This is the hospital where you were born. All of a sudden, this wave of emotion came over me. The last time I was here and heard ambulance sirens, it was your ambulance transferring you to Rainbow Babies. The hospital wouldn't let me ride in the same ambulance with you because I was a "different patient" and we were going to two different units of the hospital. I laid in that ambulance and strained to watch your ambulance the entire way. Our ambulances rode side by side the entire way. Twenty minutes felt like a lifetime. I couldn't stand to be separated from you like that. It wasn't fair. I cried and cried, only to get there to find you laughing and giggling.


It was midnight, and I still couldn't sleep. So many nights with no sleep, and I was so tired. But I could never sleep when I knew something was wrong with your heart. It wasn't until the next morning that they told us you had Hypoplastic Left Heart Syndrome. The whole next week we spent with you in the NICU. You smiled every day and would stare at us the entire day, until your eyes got so tired, they had to rest. June 9th, you laughed and giggled all the way to surgery. You always made mommy feel okay about what you were about to face. Your attitude was so light. I lost family members trying to keep you that way that day of your surgery. And I don't regret it. Your happiness and lightness was and is my only concern.
It wasn't until two days before you passed onto your new life, that I saw you laugh and giggle again. The pain was too big for you to laugh through. I understand. 

On this day, one year ago, at 10:02 pm, you looked me in the eyes and told me you were leaving. I didn't believe you. I wish I had believed you because I would never have left that room. I want you to know it's one of my biggest regrets. The next time I saw you, you were gone. I held your body and screamed that it wasn't so. I wouldn't let you go until you were cold and stiff. To this day, I can't watch the videos of you yet. Someday I will be able to. I hope. This doesn't mean I don't love you. It means I'm a human who longs to be able to hold you and watch you grow as a human. Instead, I watch you grow as a soul....a divine spirit that envelopes our family and continues to reach families across the world. I talk to you and you use my hands to do the work that requires hands, and you take care of the rest. This is your first angelversary, and I remember you for all that you were, but also, for all that you continue to be as you grow in ways that are larger than inches.


I want you to know that I see you. When I think of you, I see you laughing and picture you playing with butterflies. I know you. I know your soul was/is pure and true and good. You are very much around. I feel you. I know you show yourself to me in more ways than I actually recognize. But you are everywhere and in everything. There's rarely a day that goes by that I don't tell your story. Just yesterday, I was at the store when a woman asked if this is my first baby. When I said "no", she asked (just like everyone does) how old you are. My answer is "ageless", and then I tell your story. I've gotten it down to a short version, so as not to drown people in sorrow. I don't believe your story should be one of sorrow, even though you make me cry often. I want the light that is you to always come through. After I told your story, the woman said, "I have goosebumps. That is so amazing." And I say, "I know". Because I do know. You ARE amazing. Someone once told me that goosebumps are a sign that those who have passed are right next to you. Each time I tell your story, the person says "I have goosebumps." I take that as one sure sign that you are there, telling your story through me.

As the days go by, you don't diminish. You seem to grow bigger and greater with every person I meet and every woman, man and child that has come into our new path. Your story has raised a good chunk of money for research, so far. You have changed lives emotionally, physically and mentally. I know how proud I am to call you "daughter". And, even though I will never understand fully why you had to go, I do see how powerful and completing your life is since you have moved on. Maybe it was the only way to finish your life's work.

As long as I live, I will never stop living with you and beside you. You guide us in your light. And we know God will take good care of you until we can be fully reunited again. We are a family of four, and we are on a beautiful path, of which you built.

All my love,
Mommy

Tuesday, June 29, 2010

testing 123

new commenting system test.

Monday, June 28, 2010

updates


Well, it's been awhile since I've updated about Eric and I and baby Urban. I just finished this piece for someone, and it reminded me of our family. I can't believe we'll be a family of 4! Kaia might not be physically here, but she's definitely here!

It's summer, and we've been really working hard to prepare for our new addition. Baby Urban is growing very well. In my last post about us, we had to have a repeat anatomy ultrasound at 26 weeks to make sure the baby wasn't dropping off in size anymore. The little bean is supposedly 13 days behind, gestationally, which caused major alarms to go off for the doctors. But after a long fetal echo, the baby's heart looks healthy. The doctors wanted us back about a dozen more times before we gave birth to this one, so they could continue to monitor the growth. However, after the stress of two level 2 ultrasounds and a very long fetal echo (6 ultrasounds later), we decided to ride this pregnancy out on faith and leave it at that. We haven't had an ultrasound since week 26, and we will not be having any more. My belly measurements have been right on track, and keeping me stress-free will help baby to grow to be the correct size. I was under a HUGE amount of stress in my early pregnancy due to issues in our lives that I've since overcome, and the doctors think that could be a reason for the size. So, the less stress, the less ultrasounds, the less worry....the healthier the baby. And our main goal is to keep this baby healthy as can be, no matter what the cost!

So, with no further ultrasounds, I have no more pictures to share. I can say that my weight gain is right on track to where I was with Kaia. And with only 7 weeks to go, I'm definitely feeling ready. I feel like I was just here with Kaia, and it's so exciting and bittersweet to be going through it again. On one hand, I want Kaia to be here. But if she were here, this little one would not be. So, her life helped create this new life, and we celebrate every minute we have in this fabulous life we are given! I can't believe it's been almost a year since Kaia's passing, almost a year since our marriage....and this baby is almost here too. We feel so blessed to be given such love and joy in our lives.

It's been hot hot hot here. So, I've been couped up in my little studio with my little air conditioner, pumping out all the orders I have had. I think some pieces have come out so nicely. I just finished one that I'm so proud of. It's for a girlfriend of mine and her son. She wanted a piece to celebrate her son and whatever dreams he might have for his life. Here it is:
"A Dream For Liam"
16 x 20

Hear Us Roar!

Win win win!!!! Did I get your attention? You can win a Little Lion piece! How? Well, I'll tell ya! It's super simple. Just go to the fabulous monsterbites365.com website and read this blog "Hear Us Roar!" (click to be taken directly there). All you have to do is follow the link and comment on that blog post by telling them what animal you associate with a specific personality trait – Little Lion Designs is named after Kaia’s courage, etc. While you're there, make sure to subscribe to their blog. Lots of amazing goodies on there weekly.

Sunday, June 20, 2010

New art for adults are up!

Hey all! I've been truckin' along with art and wanted to share some adult pieces I have done recently.
Visit my etsy site (click here) to purchase available art or to special order a piece.

Sunday, June 13, 2010

hmmmm

Does anyone have issues with some spammer out there trying to post comments on your blog that's a bunch of Chinese lettering, which is a link to something? I've never clicked on it because I don't want to know what that link leads to. But I have to monitor all my comments, and I require a captcha. So, it's an actual person putting them up, which I just keep rejecting. But they are insistent. And now they come under different names, several times for each blog entry. It's annoying, and I'm not sure how to get it to stop. Anyone have this issue with blogging and know how to avoid it?

Tuesday, June 8, 2010

new pieces, new pieces


New pieces are up at www.facebook.com/littleliondesigns and www.littleliondesigns.etsy.com. They're also on my website at www.littleliondesigns.com. 

Reminder that my show is running all of June at Bela Dubby. Bela Dubby hours and location are located here.

Saturday, June 5, 2010

HoPE

I'd like to take a minute to ask for some prayers for a very special mom, Jenna Evans. I don't know her, but I do know her story through some heart moms. Jenna lost her daughter, Bentley on April 6th of this year. Bentley had Holoprosencephaly and lived only 4 months. Bentley had an older sister named Hailey, Jenna's other daughter. Hailey passed away just yesterday from meningitis, completely unrelated to Bentley's condition. She lost both of her children in only two months. Knowing how difficult it was to lose one child, I cannot imagine what she is going through at this time. It's an unbearable pain, and the ONLY thing that gets you through is support and lots of it, constantly....for months. Please keep Jenna in your prayers, not just today, but for the weeks and months to come. The pain doesn't go away, but I know with prayers, it will become somewhat liveable. There is a facebook support group where you can go and offer her words of kindess and support. Click here to visit.

Thursday, June 3, 2010

Show is up!

Well, it's officially up! My first big show is now up at Bela Dubby in Lakewood. Bela Dubby is located at 13321 Madison Ave, Lakewood, OH. I have 21 pieces up there now and am bringing in 2 more over the weekend. This Saturday there is a big arts and crafts exhibit there. It's on Saturday the 5th from 12-??. It would be a great time to go shopping for local art. :) Be sure to pick up a CHD fact flyer (hanging on the wall in a fabric pouch with all the business cards and such) and bring it into Planet Green in Rocky River for 10% off anything in the store.

Everyone is officially invited to the opening party, as well. It will be on June 12 from 5-8 pm. Lots of veggie and vegan fare, cookies, coffee, beer, etc. will be available.

Thank you all for supporting local art and helping me raise awareness and funding for the research/prevention (and one day cure!) for congenital heart defects.

click image to enlarge.


Click here to visit little lion designs official website. Sales and contact info are located in the "contact" section.