Victoria is doing so many things now. She definitely is not limited physically when it comes to her gross motor skills. She is everywhere, doing everything! The only thing that limits her with her fine motor skills is her impatience with sitting still to do a task for more than 5 minutes at a time. But, we believe that will improve as she gets older.

Victoria’s heart repair is still doing wonderfully, as reported by her cardiologist at her recent checkup at his office. We feel so thankful that he believes that she will never have to undergo any other open-heart surgeries EVER!

Victoria is really beginning to “communicate” so much now. Though she speaks “gibberish” most of the time, I can understand a few words she speaks from time to time. She takes after her mother in that she likes to “talk” with her hands! Sometimes, she speaks “gibberish” and moves her hands all over the place. I know she is trying to tell me something really important and I sure wish I knew what it was! I’m just glad that she is “trying” to communicate now.

Victoria will discontinue receiving therapy services from Early Intervention on March 10th and the public school system will take that over. Her new therapists will begin seeing her at the Mom’s Day Out program that she is enrolled in. We decided to wait to start her in 3K until the fall, although she could go immediately when she turns 3. Victoria is so small yet and we want her to have a little more time to mature before starting school.

There are so many other things our little girl is accomplishing and we just feel thankful to witness little miracles every day! There is no doubt in our minds that we have, as a family, been given a gift. Living life with a special needs child is, indeed, very special. As a friend recently told me, “Anyone can have a ‘normal’ baby any day. But, we won the lottery! We were given a special child!”

For some reason God chose our family to receive this special gift and we live in wonder of His faithfulness to us!