Tomorrow is the day. Liam must be at Children's tomorrow no later than 7am for his scope and possible relocation of his gtube. We have to leave at 5:30a to make sure we get there on time. I'm nervous that Liam is going under and nervous that he's most likely going to have to have another hole cut into him. We need to do whatever we have to to stop the pain he's having now though. We also need to be able to use the feeding pump again at night. It's that moment of complete and utter "my hands are tied and there's nothing I can do" kind of situation. To top it off his allergies are bonkers again causing his asthma to act up. Please pray for Liam and pray that the doctors make the right decisions. Thank you ❤️❤️❤️ #cdh #cdhsucks #surgery #gtube #tubie #spoonie #feedingtubeawareness
This isn't a fairy tale. Our lives have been forever changed by Congenital Diaphragmatic Hernia. We're just trying to find a way to make it work.
Thursday, February 26, 2015
Surgery Tomorrow
Thursday, July 24, 2014
1 day post op: medi port removal
To catch up: yesterday Liam had his mediport taken out!! He did amazing and the surgery went beautifully. No complications what so ever. He came out of anesthesia a acting normal. The nurses commented on how he behaved like he never had surgery and that it was amazing as well as a breath of fresh air for then to witness. My son is a fighter and a miracle and he always amazes me as well. The best surprise of all was that they did NOT have to use a breathing tube for him while under!!! That's a first ever for our miracle!!
Today:
Liam had a great night last night. Slept all night long and slept in until 9am. That's unusually for him but he needed the sleep. He's playing and laughing and acting normal this morning. Again as if he never had surgery. I admire his resilience and his strength tremendously. I am basking in my sons laughter and happiness today knowing that this is what I waited so long to hear after he was born, knowing that this is how it's supposed to be. To the eye he is just a normal little boy who loves to play and laugh and have fun. His Gtube and scars are the only reminders he isn't a normal boy. But who needs normal and what is normal anyway? Normal is just over-rated. Why be like everyone else when you can be you? I love the little boy he's turned out to be. I live that I can breathe easier knowing they mediport is gone and that I no longer and to retrain him, pole a needle into him and flush it every month. I love that a fever is just a fever now. That his ailments are just simple ailments. So what if he has some GI and lung issues. He's overcoming them everyday. So what if he's small. He will get there when he's ready. That's the one thing about Liam, he does things on his own timeline. So to my little boy, you've grown, you've overcame. Don't ever be afraid to be who you are. Don't ever feel embarrassed or ashamed of your scars for they tell a story of your strength and your will to fight and survive. Your earned this life so make the best of it and enjoy every minute!!
Pics from yesterday:
Liam's monkey toes picking up my necklace yesterday before surgery just laughing away.Saturday, November 17, 2012
Hectic Crazy Busy Life
Last Sunday November 11th Liam's Jport on his button litterally broke completely out. I had to rush him to Children's where he was admitted since he had to undergo surgery.
This time last year:
Liam weighed 10 lbs 4 oz. As of his last weight he was around 25 pounds. Last year he wasn't even on the chart. This year he's in the 10th percentile. He's come a long way.
Even Justin has changed. Though he's making a huge effort to do it purposely. He's lost alot of weight and started builting mucsle. I have to say Im jealous that I cant seem to find the energry to work out when everything is said and done.
Oh and Liam got another hair cut. After that IV in his head we had no choice.
Sunday, July 22, 2012
Looking Back 7/22/11
Liam was slowly being weined from the paralytic and finnaly was allowed to wake up and open his eyes for us. I remember sitting there stairing at him when the nurse said he was being allowed to wake up. Admittedly, I cried when I saw his beautiful eyes.
Saturday, July 21, 2012
Miracles
| A year ago today I was sitting in NICU when our primary Sue got the call that that the surgical staff was on their way up. It was time, liam was getting repair surgery that would safe his life and put him on the road to recouvery. I was all alone, Justin was on the road on his way to us. We had all hoped hed make it before surgery. Unfortunately he didnt so I spent a very long 45min in the parents kitchen waiting before the surgeon came in. Justin didnt make it untill 3 hours later. Liams repair surgery being done on my birthday was the best gift I have ever or wilk ever recieve. Now a year later I am reliving the anxiety, the pain and the elation. A year ago today we were blessed to meet little Lulani and her parents. Happy Birthday miss Lulu. We pray you have a special day. Sent from Yahoo! Mail on Android |


































