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!
Monday, September 17, 2012
Bronchoscopy Went Well
The bronchoscopy went well today and the ENT said that the airway and vocal chords look great. There was some granulated tissue from suctioning that he removed but other than that it went as expected. They told us that they wanted to move forward with taking out the trach. They admitted him and just let him rest today. It has been a little stressful because after he woke up from the procedure his saturation was staying between 90-93. We can't seem to figure out why he isn't doing as well as normal. It has been a long time since we just sat and stared at a monitor praying that the number will go up. They wanted him to be 92 or better to try and cap him and in true Brodie fashion, about an hour and a half before they were supposed to do it he suddenly went up and stayed at 93 or 94. They decided to cap him and when they did he stayed at 94. I guess we figured he would go down and kept waiting for it to, but he just stayed the same. He has been doing great since and the ENT said he will come by at 6 in the morning and see how he did. If he does well then they will take it out and monitor him all day. As I type this I keep hearing little noises coming from his bed and realized that it was Brodie. He can now make noise since capping the trach is like not having a trach at all. We will see how tonight goes and let everyone know how things are progressing.
Friday, September 14, 2012
Could Brodie be Trach Free Soon?
As I look back on the last 13 months I can definitely see that we have had some difficult times but now I can honestly say that we have made it through the tough times and are happier than ever. We are blessed to have Brodie and are still thankful every day that things worked out the way they did. Here is an update on what has been going on with us. We took the boys out to Disneland all of last week and had a great time. It was great to get away with just the four of us. We had such a wonderful time and for that week life just seemed "normal". Brodie did great on the plane and he even rode all the rides that he was tall enough to ride. He not only went to Disneyland but he also went to the beach, Sea World, and his first baseball game. He laughed and smiled most of the trip and only cried we he got near the Disney characters. Who would have thought that after all he went through that he would have been taking a trip at 13 months. We have been waiting to hear from the doctors about what we are going to about the trach. We finally got the call yesterday that if there are no obstructions found during the bronchoscopy on Monday that they will take out the trach, monitor him overnight and send him home Tuesday trach free. I can't tell you how happy that this makes us. It will not only allow us to get back to a more normal life but we think it will definitely help him out developmentally. If it comes out it is going to be crazy to be able to see his whole neck and always hear him talk, laugh and cry. He has been really progressing lately and the therapists said that they think he will be walking by Christmas. He is showing more of his personality every day and keeps us laughing all the time. We will update you next week on how thing go on Monday and Tuesday. Thanks so much for all of the prayers and we know that without all of you that he never would have made it this far.
Monday, August 27, 2012
Brodie is ONE!!!!
I am sorry that I have not posted since Brodie's birthday. Brodie has been amazing us daily and we are so thankful that we made it to a year. We had such a great party and thanks to all of you that came to support Brodie and our family. Once Brodie came off the ventilator and oxygen he never looked back. For the past two months he hasn't made much progress but the last couple of weeks he decided it was time to get on the move. He now goes from sitting to his stomach, from lying down to sitting and he has even started to do the military crawl. We are so happy that he is on the move and can't wait to see what he has in store for the next couple of months. If you were to see him you would not know that he had a rough start to his life and that he has had a stroke. Once he gets the trach out he will look like a normal little boy. We have a bronchoscopy scheduled for September 17th and if everything looks good they will possibly take the trach out. We feel that he is ready and would have no problems if they took it out. It sure would be nice to get back to more of a normal life. If he does not get it out then we will have to wait until March or April. If it does not come out now that will be OK too because we never dreamed that he would be where he is right now. We are constantly reminded of what a miracle we have and feel so blessed to have him in our life. I can't imagine what our life would have been like if we would have lost him. He brings so much happiness and joy to our lives and although it has been a tough year we can honestly say that it has been the best. There are so many families of CDH babies that don't get to bring their babies home so we never want to forget how blessed we are. Below I will post a link to the pictures from Brodie's birthday party. I know there are alot but I hope that if you were not able to make it that you will enjoy the pictures. I will let everyone know what we find out about the trach and again we thank each of you for everything you have done for us this past year.
http://www.claytonwallace.com/mp_client/pictures.asp?eventid=0&groupid=225
The password is Todd
If you would like one of the pictures let us know. We will have a cd and be able to print them out.
http://www.claytonwallace.com/mp_client/pictures.asp?eventid=0&groupid=225
The password is Todd
If you would like one of the pictures let us know. We will have a cd and be able to print them out.
Monday, June 11, 2012
Brodie 10 Months and No More Vent
Brodie has reached the 10 month milestone and is improving daily. What this means for our family is that we are finally getting back to a more normal life. The picture above is Brodie at the Jimmy Buffet concert. We are fully aware that this is probably not the best concert for his first concert but he had a great time. I can't believe that back in September we were not sure that we would ever bring him home and then eight months later I would have him sitting between my legs rocking back and forth to Jimmy Buffett. We are amazed daily at his progress and are so blessed to have such a special boy in our lives. I can't say that it has been easy but the rewards far outweigh the hard times. As of this morning Brodie is officially off the ventilator. We went to the Pulmonolgist a couple of weeks ago and he was so amazed at Brodie's progress that he decided to be more aggressive with the vent wean. He came up with a 12 day plan to get him off the vent and Brodie breezed right through. We go in for a blood gas in a few days and hopefully that will look great as well. He told us if he was off the vent and did not need the trach for ventilation then there was no need for the trach anymore. He said that he could possibly get the trach out this summer. Although this is great news we are thinking that it won't happen based on previous conversation but we will just take whatever comes our way. Brodie looks great and that is all that matters to us. We have offically decided today that we will be having Brodie's 1st birthday party on Aug 11, 2012 from 11:30 to 3:30 in The Woodlands. We would LOVE for everyone that would like to come to be there. We would like to not only celebrate Brodie's first year of life but also for everyone that would like to meet him to come out. Whether you are are family, a good friend, medical staff or someone that we have never met that has followed his story we would be honored to have you. The only thing we ask is that you let us know so that we know how much food to get. There will be a splash pad, bounce house, playground, food and fun. You can email us at vonasteward@msn.com. Also, if you would like an invitation please give us your address. Thanks again for everything that all of you have done and hopefully we will get to personally thank you in August.
Saturday, May 12, 2012
Brodie 9 Months
It is hard to believe that Brodie turned 9 months on Tuesday. Time has flown by and it blows our mind that in 3 months he will be one. I can't tell you how proud of Brodie we are right now and how thankful we are that he has made so much progress. He looks really good and is such a happy baby. He has now been off oxygen for over a month and it looks like we will get the trach out maybe next April. That seems like a long way off but it is definitely something to look forward to. Brodie is sitting up by himself, clapping and even says mama and dada. We never dreamed that he would progress as well as he has but we are so pleased. He still has a tough time being on his tummy and when we put him on all fours his right side is too weak to keep him up. These are the first signs of the effects of the stroke that we have seen. Hopefully with all of the therapy that he gets he can overcome these deficits. He had a developmental appointment on Thursday and they were amazed at his progress. They put him at 7-9 months and said he has caught up on quite a few things. Life for us is still busy but it is very rewarding to see how far he has come and we know he will continue amazing us daily. Tomorrow our church is doing their baby dedication so Brodie will be a part of that. If any of you would like to watch it you can go to this link at 11:30 tomorrow and watch it live http://live.woodlandschurch.tv/. We are so thankful to all of you a for everything you have done for us and hope that you are as proud of Brodie as we are. I am also going to post a recent picture of our two boys as well so look for that. Hope everyone has a wonderful Mother's Day and I know this one will certainly be special for LaVona.
Wednesday, April 11, 2012
Brodie Eight Month Birthday
Sorry that I have not posted in some time. We have been very busy and I keep saying I will do it tomorrow and tomorrow never gets here so I decided to do it today. We can't say enough great things about how Brodie has been doing. He has exceeded our expectations and continues to amaze us daily. We went to the pulmonologist the other day and when he walked in he was amazed at how well he was going. He was off oxygen and smiling at him when he walked in. This doctor remembers the Brodie that "may not have enough blood vessels going to the lungs to sustain life." He gave us the go ahead to keep him off oxygen as long as his saturation stayed above 94. We have kept him on and off of oxygen but I am proud to report that he has not had oxygen since Thursday of last week and shows no signs of needing it. This is far quicker than we thought based on the requirements of almost four months ago. The pulmonologist said he hoped to have him off oxygen all together before he turns 1 and then get the trach out after RSV season next year. That would mean that he will have the trach another year. I think that he will be completely off oxygen soon and hopefully we can talk them into taking the trach out before he turns 1. We will see and we are pleased with either of those options but Brodie has shown us time and time again that he surprises us. His latest trick is sitting up all by himself. They set that a a goal for him but I don't think they ever thought he would do it so quick. He is grabbing for toys, putting them in his mouth and even has his two bottom teeth. The only thing that he is struggling with is tummy time. They would like for him to be able to do 5 minutes and he can hardly do 1 minute. Would you want to get on your tummy with a trach? We are working on that and rolling over so hopefully he will be doing that soon. Currently he is sick with something and not himself. He has about 8-10 bowel movements a day and has a lot more secretions. Hopefully he will be over this soon because he has not been as happy the last few days. Thanks so much for the continued support and prayers. We can't thank everyone enough for the help we have received over the last eight months and it has been exactly a year since went to the ultrasound and found out the news of Brodie's CDH. We however have been blessed with an amazing boy that continues to prove that he is a fighter and has reminded us what life is all about. Each of you has helped us in some way along our journey and I hope that Brodie's life has helped you in some way. Again, I am sorry for not posting in a while and keep this updated more often now that everything is slowing down. IMMEDIATELY after posting this I will post pictures (sorry for that too). Hope all is well with everyone and have a great week!
Wednesday, March 7, 2012
Brodie 7 Months
It is hard to believe it but Brodie is turning 7 months old tomorrow. Things have still been hectic but we are doing well. Brodie has been doing great. He recovered from his surgery and has yet to vomit since he got the fundo. The only bad thing about it is that he gags alot but nothing comes out. This can be very tough to watch but I think it will get better with time. He has been progressing and has physical therapy every Tuesday and Thursday and occupational therapy every Monday and Wednesday. He is grabbing toys with both hands and he even sat unassisted last night for about 5 seconds. He has two teeth coming in and just loves to show them off when he smiles. Overall he is healthy but it wouldn't be Brodie if he didn't have some issues. Sunday night we had to go up quite a bit on his oxygen and when we would take his oxygen off his numbers would go down in a hurry. We were pretty worried about him but he has since gotten back to where he was before. The neurologist was concerned about his head size since it has gone from 25% to 50% to 75% on the growth chart since he was born. We had a follow up MRI and they said that he had benign hydrocephalus. I am not sure that I even understand fully what this is but I understand it to be excess fluid in the brain but not enough to worry about right now. We have to go back in for another MRI in 6 months. We are so proud of how far he has come and are amazed by him daily. This past Saturday I took him off of oxygen for two hours and he stayed above 95 the whole time. Yes, our little Brodie was breathing on his own for 2 hours with no problems. We are so encouraged and it seemed like for that small amount of time that a little bit of light peeked through the end of the tunnel. We know we have a long way to go but it is nice to know that he can do it on his own for a significant amount of time. Bradie turned 3 on Monday and it is scary how fast time goes by. Even though times are a bit difficult right now, my fear is that the time goes by too fast and that we are too busy to enjoy the early years of Brodie. We can't thank all of you enough for all of your help, support and prayers. I wish each one of you could meet him and see one of God's little miracles. I promise that I will put up pictures soon. We got both the boys pictures done last week and they turned out great. Hope everyone has a great week!
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