Monday, February 25, 2013

Sharing the Love

Looms of Love is an awesome page that provides children and babies on a health journey with knitted hats free of charge. They are making one for our little lamb Liam and sending it to him. Please go like their Facebook Page and let them know Liam Michael Bryant sent you.

 
***********************************************
My Prayer Warriors have been praying for Liam as well as many may others. Please go check ourt their Facebook Page and let them know Liam Michael Bryant sent you.
 
************************************************
Super Skylars Prayer Warriors: This little boy Skylar was born with Craniosynotosis, 14q23.2 duplication with normal karyotype 46,XY. Please keep this sweet little guy in your prayers and go like his Facebook page.
 
***************************************************
I've been follow Sir Isaac for about a year now. He was born with CDH like Liam. He has a feeding tube and a trach. We love this little guy and pray you will all go and follow his progress.
 
 

Auction is LIVE!!

The auction for CDH Research is live!! If you all could head on over and check out the auction items and share the auction with others that would be awesome! 100% of the proceedes go to CDH research via Breath Of Hope! Lets make this auction successful and help put an end to the suffering CDH causes

http://www.facebook.com/ShootingForLiam






These items and more are in the auction!
 

Tuesday, February 19, 2013

S4L Auction for CDH Research

We're in the process of putting together  a auction to raise money for CDH Research. ALL proceedes from this auction will be donated to Breath Of Hope for Research. We are currently looking for donations for this auction. If you are willing to donate please contact us on our Facebook Page http://www.facebook.com/ShootingForLiam

Now for a sneak peak at whats going to be in the auction and the vendors who have donated!!

******************************
Cecile with UpperCase Living has donated a beautiful frame that is sure to brighten up your home for Spring. Please go Like her Facebook Page to show her love for helping us raise money for CDH Research as well as help us spread awareness by creating some awesome CDH UpperCase Living Items. http://www.facebook.com/UppercaseLivingByCecile
 
 


*************************

Megan Hansen, A Independant Consultant for Sentsy has donated 6 Baby Scentsy Buddys. Please visit her Consultant page if your interested in purchasing Scentsy products
https://meganhansen.scentsy.us

All baby Scentsy Buddies come with 1 scent and will  be sent to you directly from the Scentsy Warehouse. These are a $20 value.







 
*****************************************
 
Megan at Miss Bella's Closet has donated $150 worth of Gift Certificate's. 2 $25 gift certificates and 2 $50. Please go like her Facebook Page to tell her thank you for helping us raise CDH Awareness and money for CDH Research http://www.facebook.com/MissBellasCloset
 
 
 
****************************
 
 Remember, the money raised goes to CDH Research so please bid with your hearts <3 <3 <3
 
 

S4L CDH Awareness Balloon Release

Unfortunately with the information I gained talking to Parks and Rec, our CDH Awareness Balloon Release isn't going to be as big as I'd hoped for. They want $210 for the only available arbor, a $100 deposit on top of that, we need to purchase insurance and we have to go through a special events committee that takes 60 days to get through. We don't have 60 days, we have 39, nor do we have the funds. So our event has been downsized. There will be no vendors. We will however be meeting at the Sports Park in Visalia at 1pm by the Playground wearing our teal and turquiose. We will do our best to spread awareness to those around us, and we will be releasing balloons. We are going to get as many balloons as we can, especially for those of you comming from out of town. Balloons will cost $2 and the money will be donated to Breath of Hope for CDH Research. You are also welcome to bring your own balloons, just be sure they are laytex because its illegal to release mylar balloons. Make sure to Like our Facebook page to stay current on all our events. http://www.facebook.com/ShootingForLiam

Tuesday, February 12, 2013

Ask Me

 


Feeding Tube Awareness Week might have ended yesterday but that doesn't mean we have to stop spreading awareness or knowledge. Feeding tubes are somewhat of an unknown to the majority of people. There are alot of missunderstandings and wrong information floating around out there and S4L wants to help fix that. Liam has been on a feeding tube for quiet some time now and has had 3 different types of tubes. Go ahead and ask any questions or state any concerns you have and we will be happy to answer. Comments are welcome. If you want to stay annonymous just email me at shootingforliam@yahoo.com You can also post questions at http://www.facebook.com/ShootingForLiam
 
Liam after Gtube and Nissin Fundo Surgery. October 2011

Here's some Questions we got on Liam's FB page:

Q: I have been following Liam's journey since my son was diagnosed with CDH inutero in Dec 2011. I have followed your ups and downs with Liam's feeding and am pretty worried we are gonne be on the same journey. We have a GJtube placed tomarrow at 9a instead of his Gtube. I would like any advice on how to care for a GJ that you could give me.

A: Feeding tubes can be over whelming at first. When Liam came out of surgery for a Gtube I was petrified to hold him because I thought Id hurt him. It took me weeks to realize I could hold him like a normal baby. And when it came time he did pull out the tube, he acted like nothing happened.

*As for care: keep the site cleam. Use a wet wash cloth to clean the area and keep it as dry as you can. Our medical supply CO provides us with split 2x2 guaze to use around the tube but I found that they don't work very well. They didn't soak up all the leaking fluid and the pad itself would be drenched in no time. The guaze had to be changed every few hours or they would just contribute to irritating the skin. I ordered a few Gtube pads a few weeks ago and within 2 days I saw a HUGE improvement. Check out Sew Amazing Creations. She makes really awesome tube pads at the cheapest price on the market. Only $1 per pad! http://www.facebook.com/SewAmazingCreations

*The most imortant thing with a GJtube is that you do NOT want it to spin. If it spins the J port could back out of the intestines into the stomach defeating the purpose of the GJ. Again the best thing I found to keep this from happening is the Gtube pads.

*Keeping your child from pulling out tube is a challenge but it is possible. We used to think a onsie would prevent Liam from pulling out his tube but last August we learned how very wrong we were. He was able to pull it out right with no problem whatsoever. Tummy belts work really well because the child cannot grab ahold of the tube with their hands and yank on it. I have this problem with Liam. There are many places online where you can order these but they are costly. Decorative yes but I know I cant afford $20 to $40 for one. Cherubim has a inexpensive tummy belt that works really well. Its stretchy and has built in velcro that makes it super easy to get on your child. They run $8. http://cherubim.storenvy.com  You can also use an ace bandage. The extensions are another issue. We use POSEY's (those things the hospital uses to strap on your little ones Pulse Ox) to strap the extensions to Liam's leg. It requies two now that he's bigger. When he was shorter and skinnier we were able to use one and strap them to his ankle. Works like a charm. We also thread his enstensions through his pant legs so it hides them from him.

*Pump feeding and mobility are a daily issue when you have an active one like Liam who just cant sit still. We figured out that we can put the pump and bag into its portable backpack and strap it to his walker allowing him to roam the house at his pleasure. Allowing him to free roam and crawl around without getting too far away from the pump is an issue. We have to just watch him and keep him near the pump or follow him around with the pump. As he's getting older we've noticed that he somtimes listens when we tell him to stop as he's crawling too far away but he also loves to ignore people. The other thing we've notices that when he's getting too far away and it pulls the tube just slightly he feels it and stops himself from going further away. He knows he doesnt like the pain. I think that as they get older it gets easier on everyone.

Q: My son has had a Gtube since July. We have had nothing but problems with it since his 6 week post op appointment. It has leaked, his skin is being eaten. They want to put in a GJ in cause he's throwing up past his Nissin and is failure to thrive.

A: Thats how Liam is. His tube leaks all the time. The Gtube pads are the best thing Ive found. They are thick so they pull the tube taunt against the inside preventing fluid from leaking through. Thats something the guaze doesn't do. We've tried all kinds of creams the GI prescribed but the best thing was to keep it dry.

Q: What problems have you had with the GJtube?

A: The main issue is that for some reason his GJtube actually desinigrates. The ports pop out because of this and his J port line has gotten clogged many times. We're not sure if its Liam or the way these tubes are made. Theres nothing we can do to prevent the tube system from falling apart but we can prevent it from getting clogged. Once a week we have to use soda, we use Pepsi but you can use Coke, to clean the Jport. We use 6 to 8 mls of soda, inject it into the J extension then let it set for atleast 15 to 20 minutes. Then we can go back to using it as normal. These are orders via our GI. Because its such a small amount it won't hurt him. And Ive monitored him after and theres no hyperness are anything else we've noticed after the soda gets into his system.



Liam's first feeding tube was an NG tube in the NICU. Because of the Cpap machine they have to put it in through the mouth. The second time he got his NGtube was in September of 2011.

GJtube Button

 

Sunday, February 10, 2013

Princess Alexandria Update

If you've all been keeping up on Facebook you know that Princess Alexandria got sick and ended up in the ICU on bipap. They said she'd be there for several weeks. She finally got out of ICU and onto the regular floor on just oxygen. Everyday she was getting better and stronger. Today mom posted that Alexandria might get released tomarrow. Make sure you don't say it outloud so that Alexandria cant hear you because these CDH babies have a communication line going. As soon as its said that they might go home, they tend to pull tricks that ends up in more time at "club med". We're praying for you Princess and can't wait to read the post that says your home <3 <3 <3

Feeding Tube Awareness Week


It's feeding tube awareness week again. Time to spread awareness as well as facts. Time to break the stereotypes.

What do I hate most about the feeding tube?
The stares I get from strangers when I take my son out in public while on his feed. He's only 18 months now but soon he will be old enough to recognize the looks of strangers and those looks are going to make him feel different, out of place, and maybe even like a "freak". As it is I get glares, questioning looks, and looks of distaste from strangers who see Liam on a feeding tube. No child, or parent should have to deal with this stress.

Commonly asked questions:

Why does your child need a feeding tube?
The requirement of feeding tubes can vary from a medical condition, failure to thrive or many other reasons. In Liam's case he was Failure To Thrive (FTT). He couldn't eat enough orally to keep up with the additional calories his body required to grow and thrive. He would get tired halfway through a feeding, be breathing fast and just fall asleep on me. This is the case for many infants with or even without other medical conditions.

How long will your child be on a feeding tube?
This is a question I get asked a lot. Its hard to say how long a child will require a feeding tube as it depends on the child. Every child is different and has different needs. In Liam's case it started out with the doctors thinking he would only need his feeding tube for a year. Then the time line changed to possibly age 2 when he got his Gtube. Now that he has a GJtube and has a oral aversion to food theyre thinking he will need it 4 more years. When I get asked this question I simply respond "He will need the feeding tube until he is able to eat by mouth and gain weight without using the tube." There is no set timeline as to how long a child will need a feeding tube.

How many types of feeding tubes are there?
NG
G
NJ
ND
GJ
J
TPN
(Click here to find out more about these)

The Feeding Tube Awareness Foundation offers a lot of information about feeding tubes and spreading awareness.

Lets use this week and spread awareness any way we can. Post on Facebook or Tumblr. Tweet about it, post pics on instagram about spreading awareness. Examples of hashtags you can use: #feedingtubeawareness #i<3atubie #tubielove

If you have any tips on how to prevent feeding tubes from being pulled out, how to keep an active child near their pump or any other tips please share with us. You can post in comments, email us your tips or post on our Facebook page.


NG (Naso Gastric): Runs from the nose to the stomach