That is what I tell them, when I hug them at the same time. She's going to kindergarten soon, and he is just reaching each milestone at a superhuman speed. I love the chaos. The mornings. She's been at my side, home, home with me, always a few steps away if not climbing on me for what seems like all my life. I feel like my life started when I met my hubby, and life made sense when she came to join us. She's changed so much, she is a little girl now. And she loves to learn, and dance, she's not shy at all. And is eager to be on her way to all-day school. It's me that has the problem with that. I heard the only thing sadder than watching them grow up is not. And that is 100% true, but there's this ache it causes to clingy mommies still. At least I've got the rest of this school year to enjoy the way things have always been, and prepare myself for the new status quo. And this is me on the verge of kindergarten, imagine when she's off to college. I know how it feels for her to move inside my stomach, and her chubby cheeks and pigtails, my first look at that exquisite little face when she entered this world. I think that's what I'll always see when I look at her.
Tuesday, October 6, 2015
Wednesday, September 30, 2015
Our CDH survivor story. Cami's story.
I remember picking out paint for the nursery. It was a light grey. It was going to be a shared nursery and I was so excited we finally owned our own home and I was going to design the most darling shared nursery of my dreams. I was nesting and excited. Her name would be Cameran and we would call her Cami. My little Cami Cottontail. Then one night I had a preterm labor scare. Everything had been normal. They stopped the contractions but there was a mass on ultrasound. Her heart was out of place. It was her lung, a mass on her lung. It was a CCAM they said, the better option. We'd watch it and not worry. Long story short through many follow ups with a perinatologist we determined it was Congenital Diaphragmatic Hernia. I could spell it in my sleep. CDH. My heart broke, my blood ran ice cold, and I started to sweat. I remember going home and wrapping myself in the warmest blanket I could. I was so cold, yet sweaty and I had never felt that sensation before. I knew this disease from research. My days until delivery day were tough. Enough tears and enough tense worry that tested my sanity. This was my third pregnancy and it was supposed to be perfect. And it wasn't. I used to stand in my yard in beautiful Hawaii and look up at the sky. I felt safe there. I knew someday this would be over and I'd look up at the sky and be safe again. I just needed this little girl to be safe. I needed this little girl to be playing by the ocean, dresssed in pink, with pigtails in her hair. I needed to be strong. Luckily the wonderful man I married was strong when I couldn't be.
This is a CDH survivor story and I'm writing that for those parents out there that desperately need me to tell you her story. Your searching about ECMO, lung to head ratio, and all these syndromes. Ultrasounds are intense, and you don't know how you'll get through your baby shower. Would you rather have a good lung to head ratio? In the words of our surgeon HELL YES!!! Does it make any guarantees? No. So inform yourself and understand and at a certain point my advice is to get the hell off the internet. Things got scary three days after she was born, after the repair. The worst two weeks of my life. She was out in six. They go through so much and sometimes they have bad days. Their body is trying to heal in multiple areas and they have setbacks. It's not the birth story we dream of. But it's still our story. And we're still able to send them love and be present even though we can't touch them sometimes. You will know that bastard called pulmonary hypertension and you just need to stay the course mom. They in that little body are engaged in a war and they look so alone. Well they are not. They have an army around them at all times. They have angelic beings we call NICU nurses and gentle doctors, or very clinical doctors fighting along side them.. I found they all gave comfort in different ways. Cami was out in 6 weeks and did not need ECMO. Now they call is a mild CDH story. Isn't that funny. Mild. I hope this finds whoever needs this story the way I did. Because let's be honest, CDH research is depressing business a lot of the time. That is because survivors move on. They are out there, a lot of them. I'm sorry i'm 3 years late writing to you, I searched desperatly too. Cami is a handful and I've been so busy, a wild child with a rebel heart. I really hope tonight you have a peaceful night of sleep mom. You do your part til delivery day, that's all we can do. I wish you the best of luck and keep dreaming. Take those maternity pictures. My biggest regret is not. I also had another baby, our 4th. Pregnancy and delivery was smooth sailing.
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