Welcome to our site about our son Brodie Dick who will join our family on August 8, 2011 at 8:00. At 22 weeks we went in to find out if we were having a boy or a girl and we found out that we were having a boy but that he may have a birth defect. After an agonizing week we found out that our son had CDH (Congenital Diaphragmatic Hernia). CDH occurs when the diaphragm fails to fully form, allowing the abdominal organs into the chest cavity and preventing lung growth. CDH occurs in 1 of every 2500 births and a baby with CDH is born every 10 minutes. 50% of babies diagnosed with CDH do not survive. The cause is not known. This will be a journal of our journey and will allow our family and friends to keep up to date on what is happening with us and our son Brodie. Thanks for your prayers and support!


Wednesday, August 10, 2011

Day 3 Morning ECMO Day 2


This is Brodie's home.  You can see his bed behind one of the machines.  As you can see he is hooked up to a lot of machines and there is very little room in there for anything else.  Since he first started ECMO his numbers have been good.  We hesitate to say that he is doing good because he is still so ill but he is at least trending in the right direction.  The good news is that he is starting to have some of his medications decreased and we may lose one machine in the next few hours.  They have scheduled the surgery to repair his diaphragm for tomorrow morning.  His doctor was not sure he was stable enough so he said that the surgeons could schedule it but that if he did not show some improvement they will have to wait.  If you already haven't figured it out anything can change at any moment.  Just when you hear something good you then hear something to take the wind out of your sails and vice versa.  As strange as this sounds I think that this has helped us because we don't get too happy with the good news or too sad on the bad news.  I will say that yesterday was a tough day because there was just too much bad news for one day.  LaVona is not feeling as good today because she pushed herself a little too much yesterday but she plans to get plenty of rest today.  It looks as though we will be in the hospital another night in these luxurious accommodations.  Just please know this his condition is still not good so we need your continued prayers and are thankful for everything.   I will also post a picture of Brodie so that you can see where the ECMO machine goes into his neck.  It pains us to see that he has to go through this so early in life.  One line is in his juglar vein adn the other is in the carotid artery.  He will actually lose this carotid artery and be left with just one.  This could cause development issues and we will for sure have increased follow up due to ECMO.  There will hopefully be not much news until later today.  We think that we have reach the point where no news is good news.  Feel free to ask us any questions on here. 

3 comments:

Sonny and Bernadette said...

Todd and LaVona please let us know if there is anything we can do for you guys. Your Devon family is lifting up Brodie and your entire family in prayers. If Brodie does have surgery tomorrow, please let us know in the post what time the surgery will be. We would like to be specifically praying for him when he is in surgery. Give LaVona a big hug for me...and send her my love.

Linda LaRoque said...

Praying for Brodie and you all.

Jenny said...

Todd & LaVona,
I know what you and Brodie need most right now is prayer, so know that we are lifting all of you up to our Loving and Sovreign God....but I'd really love to be there to give you a big hug right now! How is LaVona doing? Is she recovering from labor alright?
-Jenny (& Erin)