THE BEST NEWS WE COULD HAVE EVER RECEIVED

My future's so bright I gotta wear shades!

My future’s so bright I gotta wear shades!

Chris and I just received an email from Killian’s doctor, Ali. This email wasn’t just any email to tell us that Killi is doing good or that we need to work on things to help him do better. This email is so special because of all of the hard work our son, his doctor, his teachers, Odie, and Chris and I have put in for the past year is all worth it.

God has given us a great gift of the right people being put in  our lives at the perfect moment to help our son.

God has provided for our every need. We can’t thank HIM enough for this blessing. 

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A Little Boy Making Big Progress

King of the road!

King of the road!

As you know Killi has completed his first term of therapy, we are now in the second term and hopefully when he has finished this round he will be ready for school in September. Since Killi has improved greatly on his social skills we are focusing more on the speech. It’s pretty exciting as a parent when your kid, who was almost completely nonverbal, is now blabbering on all the time. I just wanted to share with you some of the new words that he is saying.

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Our Next Big Adventure

killi pic

Our Wild Man

We are moving forward in the next phase of working on Killian’s delays.  Like I mentioned in a previous post, we went to a specialist at the hospital that told us he was delayed and kept saying, with her sweet Thai smile “o no good.”  I have tried to implement every recommendation that she gave us.  She assured me that I would not be able to find a speech therapist that speaks English and I was Killian’s best option. After a month and half, my son has become a little more social with improvements with his eye contact but his speech has not.  It does not matter what I do to change this, he is simply choosing not to talk to us with words we can understand.  He does currently have a special language that he uses.

We have decided that we are not the best teachers for Killian in helping him to speak.  I started to search out different options for help with developmental delays in Bangkok. Yesterday I visited the Reed Institute in Bangkok.  I met with the director and explained everything that has happened with Killi. How he was talking, went mute when we moved to Bangkok, our disgruntled nanny that was clearly affecting him, our new nanny that he loves and the progress he has made in the last two months with his babbling.

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Special Needs

first time he has intentionally looked at the camera and said cheese!

first time he has intentionally looked at the camera and said cheese!

We all have needs, some more than others. I didn’t really want to write about this but then again I think that it is important to share how we are adjusting with anyone else that might be an expat or a parent going through the same thing, it’s always nice to know you aren’t alone.

As a parent it is extremely hard not to compare your child to the kids you see around. When at different playgroups I think “well Timmy can do this but Killi can’t or Jenny can do that but why can’t Killian…?” Everyone says that children develop at their own speed and on their own time and I know that this is true but as a parent it is hard not to worry and think about if your kid is falling behind. You wonder if your child is actually falling behind or are you blowing it out of proportion. Everyone is eager to give their two cents on when their kid started talking or in an attempt to help you not worry about it down play the situation but in all reality that doesn’t help put a parents mind at ease, nothing will at this point.

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