Skip to main content

It's POTTY Time!

At the end of August we began working on potty training/scheduling with Ethan. We weren't in a hurry to start working on this since Ethan can't tell us he needs to go and he can't walk to the potty, but since other kids in his preschool class were working on it, we decided it couldn't hurt to give it a try.




Ethan has really surprised us! Ethan's been using the potty at school and at home for about 2 months now. He averages about 50 to 75 percent success while he is awake, and is now wearing more pull-ups than diapers. He still can't tell us he needs to go, so it is more about scheduling and we give him the opportunity to try typically every two hours. When he is successful we cheer, sing, and celebrate! Ethan claps his hands and smiles. At this time he seems to really enjoy being successful and so we'll keep on taking him.




Since we have done a bit of traveling since Ethan started using the potty, we just take it with us -- have potty, will travel -- has become our motto. Although, we aren't exactly keeping track of all the places that Ethan has gone potty, we are excited that he seems to be pretty flexible and is still pretty successful even when we aren't home.



Comments

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. 

Here we go again!

Yesterday, our family got to take another trip to the ER. Just a little after 7am, after I had fed Ethan breakfast and gave him his morning medications, he and I came into the living room to play before we had to get ready to leave for school. Ethan had 5 seizures, each lasting 10 to 15 seconds, back to back. Jeff had not yet left for work so I had him get the Diazepam, Ethan's rescue medication, and we gave it to him. The Diazepam is supposed to stop the cluster seizures, but it didn't. The seizures continued and didn't show any signs of stopping so the three of us packed up and headed off to the ER. By the time we arrived at the ER the drowsiness that is a side effect of the Diazepam was very evident, and although Ethan wasn't sleeping, he was definitely out of it. He had another small seizure shortly after we got to the hospital while we were being checked in. Once again his vitals were monitored and blood taken. The doctor spoke on the phone with our neurologist...