Showing posts with label surgery. Show all posts
Showing posts with label surgery. Show all posts

Thursday, February 26, 2015

Surgery Tomorrow

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 


Taken last night when Liam woke up crying in pain saying "my belly button hurts". Breaks my heart 

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. 

Seriously my favorite pre-op pic!! He's just simply sitting there, happily playing a Thomas the train learning game on his Mickey Mouse innotab. 

Another lovely pre-op pic. Liam decided he wanted to walk into OR and he would do so holding the hands of not one but two beautiful nurses and flirt with everyone he saw along the way. These two nurses where amazed and flattered. Aparently they don't see too many willing and happily walking themselves to the OR. Everyone stopped to get a look and commented on how adorable and sweet he is. Yes ladies I know you love him but he's my baby forever and always. I know he was in great hands. 

Post OP cuddles. Liam tried to hide his beautiful smile from the camera. He was still tired here as this was very soon after waking up. 

At home just 2 hours later he's munching on French fries and playing a game. Liam was extremely active yesterday and wanted to eat the whole house up. He was treated with French fries because well because because. He simply just had to ask and I would jump yesterday. No naps for this little guy at all yesterday. He powered through it and enjoyed the day for everything it offered. 

He did however go to bed at 8pm, fell asleep around 9pm and slept until 9am this morning. And again he's having a great day acting as if yesterday never happened. 



Saturday, November 17, 2012

Hectic Crazy Busy Life

Sorry for Lacking on the post. Alot as been going on and I've got my hands full. Ill try to get you cought up:



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.
 
He had surgery monday afternoon then was released at 9:15pm. The GI who did the surgery said that his tube was completely clogged up so I have to clean it once a week using soda. YES SODA, i.e. pepsi or coke.
Liam also has to be put on the surgical roster to have his tube repleced every 2 to 3 months routinely since theyve had to do emergency surgery 3 times since August.
He also has to have a mediport put in before his next surgery and to do that he has to be perfectly healthy, which brings be to my next update.
 
Today is day #3 of Liam having a snotty nose, cough and congestion.
Everyday it gets worse but we're thinking it's due to the weather flip flopping. Atleast we're hoping.
He goes to his Ped on wednesday so we will know more then.
Im praying he didn't catch RSV, he doesnt get his first centages until wednesday,
 
During PT we talked about how Liam's right foot turns outward. We're going to work on manualy turning it inward. When she comes back in 2 weeks shes going to bring these strap things thatll prevent him feet from going outward. She said this could also be a cause for him not being able to stand on his own yet. We're also working on getting Liam to be able to move from say the couch to say his play table by turning around and steping away from the couch toward the table.
It's all part of catching him up really.
 
On the eating by mouth front, he still only hold interest for suckers.
He will bite on a baby rice cake or numnum but wont eat it.
No liquids by mouth yet either.
He's still on baby formula because we havent figured out why he doesnt tollerate concentrated formulas and all Junior formulas are concentrated apparently.
You can touch his mouth withou him gagging now.
Thats a HUGE step.
You still cant put anything in his mouth though.
 
 
 
 
Lanie has been a loving, doting big sister.
She spends most of her days playing with Liam.
She uses his blocks to build tall towers and Liam pulls a Godzilla by destroying them. They just laugh and laugh.
Infact she does alot to make him laugh and no one can make him laugh like she can. We're very proud of her handling everything so well.
With all Liam's needs we dont get to spend as much time just being with her or even buying things for her.
She understands that brother needs things and even helps.
We cant go into a store without her saying "Oh this would be perfect for Liam".
It's enough to bring me to my knees sometimes.
Shes so giving and loving.
Most people dont get to see that part of her.
I wish there were more hours in the day to do whatever she wanted with her.
 
I find myself looking at Liam during med time or feed time and thinking "Why cant he just be normal?". I feel guilty because to me its like wanting to change him and I love him, his personality is amazing. But Id love to spend less time being a nurse and more time being their mom.

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.

This time last year Liam had gotten his first Gtube. We all thought he's have it out within the year. Now he has a GJtube and we know for a fact that he will have to have it for atleast 3 to 4 more years :(
 
This time last year Liam fit so perfectly in my arms. He wasn't happy unless he was being held.
Now...
Liam barely likes to be cuddled unless he doesnt feel good. He is so much taller and he's so heavy its hard for me to hold him for long.
 
This time last year Lanie was shorter and chubby. Her hair was barely below her shoulders.
 
This year, her hair cascades down to the middle of her back.
Her personality, and attitude have tripped.
Shes taller, leaner.
And funnier.
 
Ive changed too.
Even after the time in NICU and the 2 hospital stays I was still happy.
My hair was still long, to my lower back. I looked alittle tired but I hadnt aged too much.
 
Now... Ive chopped my hair off. Put on 5 pounds.
I am constantly tired. Sometimes I put effort into trying to hide the circles, the exhaustion, the stress with makeup and clothes, like above. But even then I look like Ive aged a good 10 years in 1 year. (below was begining of October this year)

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.
Last pic of Liam with hair
 
"No Dad I dont want my hair cut"
 
Even bald he's a cuttie :)
 
Ive also posted a few new videos on YouTube.
You can check them out on my channel "BuggiesMommy"
 
 


 

Sunday, July 22, 2012

Looking Back 7/22/11

A year ago today my little lamb was 1 day post-op from repair surgery. He survived the repair and began healing.


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.



Liam threw his first fit.

So Lanie sang to him "Go to sleep little liam"

And he calmed right down.





Fast forward: 7/22/12











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.

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