Skip to main content

Reality - Part 2

So, I guess it was pretty obvious that Friday was a tough day. I have those from time to time, I think we all do.

Friday afternoon Ethan had his one year pictures taken and he did amazing! It seems like it has been months since he smiled for the professional pictures. He did so well it was really hard to pick which pictures NOT to get. LOL :) I can't wait for them to come in!

Today we spent the whole day together as a family. We ran errands in the afternoon - bank, the mall, Panera Bread for lunch, and then to Target before heading home. Ethan even sat in the shopping cart at Target like a "big boy." This is a very new thing for us - and while I still won't try putting him in the shopping cart if it is just him and I (if we have to run into a store just the two of us I always take the stroller) we are trying to do this when Jeff and I are together. Overall, I think Ethan enjoyes the new perspective, but since we have to make sure to put the belt around his chest instead of his waist, otherwise he'd topple forward, I'm not ready to do it when it is just me.

Being that today has been a better day, and almost "normal" day, I thought I'd write more about the "reality" I live in....

1. God is good all the time, and all the time God is good! I know and trust that Jesus loves Ethan even more than we do. That He has a plan for Ethan and for us.

2. Ethan is going to be 13 months old in a matter of days. A year ago we didn't know if we'd make it to six months. I am blessed to be able to hold and hug and kiss my little boy. While only the Lord knows the exact plans He has, as of today Ethan is overall medically stable and doing very well in light of his diagnosis. Ethan can roll like crazy and he enjoys playing with toys and interacting with people. He can sit without support and usually doesn't have to much trouble eating (pureed baby food) or taking his bottle.

3. I have an amazing husband who loves the Lord, loves me, and loves Ethan. Jeff works hard and helps at home. I am very blessed that I am able to stay home with Ethan. I can't imagine not being able to be here with him every day.

4. I have a whole new "family" that I would have never known if it wasn't for this diagnosis. My fellow PBD parents are amazing people. Some have kids in heaven already and others have little ones still fighting PBD but regardless of where along this journey someone is, this family is there for each other. I also have found a calling -- as the Family Registry and Support Group Coordinator for the GFPD --- I can help other families who are facing this diagnosis not feel so alone. Remember, PBDs are more than twice as rare as Cystic Fibrosis.

Here is my reality....




I never knew I could love anyone so much until I became a MOM!



Prayer Requests
  • Please pray for peace and comfort for all families impacted by PBDs. Pray that those who do know know Jesus as their personal Savior and Lord would open their hearts and minds to Him.
  • Pray for treatments and a cure! Pray that the doctors, researchers and therapists would be able to find new and better ways to help our children and increase their quality of life.
  • Pray for miracles! They happen! Pray that Ethan will grow and develop that he will stay healthy. Pray that he will learn to crawl, and walk, and talk. Pray that he will be healthy, strong and happy.
  • Pray that I will have more good days than tough days, and that I will be able to always seek the Lord and not ask why, but "How will you be glorified?"
  • Pray that our family and other families that are believers would be a witness to others about the hope that we have in Jesus Christ.

Comments

  1. That's an awfully cute little reality you have there! Thanks for sharing your joys and your struggles-we all have them and it makes us feel more connected when others are willing to share.

    ReplyDelete

Post a Comment

Popular posts from this blog

"God Chooses Mom for Disabled Child" by Erma Bombeck

I don't think this is exactly how it works, but I had to share anyway. I believe with all my heart that God does not make mistakes, and although I will fully admit that it hurts my heart that any child is born (or develops) disabilities and/or life threatening illness, I know that God is sovereign and that He has a divine plan (even when we don't understand it!). I believe that God brought Jeff and I together and that He knew Ethan even as he was growing inside of me. While this is not the journey we would have dreamed of or chosen, and there are going to be times (and have been already) when we struggle, stumble and fall  it is our hope that in the end that we will bring glory and honor to the Lord.  God Chooses Mom for Disabled Child Written by Erma Bombeck Published in the Today Newspaper Sept. 4th, 1993 Most women become mothers by accident, some by choice, a few by social pressures, and a couple by habit. This year, nearly 100,000 women will become mothe...

Faces of Peroxisomal Biogenesis Disorders

This Saturday we are hosting the first annual Pancakes for PBD benefit.  All the proceeds will go to the Global Foundation for Peroxisomal Disorders to help offset the costs for our family and others like us to attend this summer's 2012 Family Support Conference in Orlando, FL.  We hope that this will become an annual tradition and allow us to help raise awareness and money for peroxisomal biogenesis disorders. Here are just a few of the faces of PBD. 

Big Day - Field Trip to Bass Pro & Easter Seals Family Night at the Playhouse Children's Museum!

Ethan was so tired tonight. He had a busy day at school, which also included a field trip to Bass Pro to meet Santa and to go bowling, and then this evening we had our first visit to the Playhouse Children's Museum. More importantly though, here's a quick medical update: We are thankful to report that for the last two days no one has seen any seizures, so we are hoping and praying that this most recent increase in his medications might be making a difference. Our current neurologist (the one who is 2 hours away) called in a stronger dose for the diazepam. Ethan had been prescribed a 2.5 mg dose by the neurologist who saw him when he was hospitalized last month, but since it has not stopped the seizures the last 2 times it was administered, our neurologist calculated that a 7.5 mg dose is more appropriate for his weight.  So our hope is that the new dose will stop the cluster seizures, if they occur again. Obviously, the goal is to not have a need to use the...