Friday, November 25, 2011

Rosie is 15 months old!

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She loves to play with leaves! She can sign train, please, banana, cracker and probably other ones too but I can’t think of them. She can say Daddy (according to Marc) definitely da da and ma ma and na na (for banana). She is talking all the time even though we generally don’t know what she is saying. When she is sitting in her high chair she signs please repeatedly hoping for something more tasty. She doesn’t know the signs for all the different foods (neither do I) so she goes with please.

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She had her 15 month check up today and got three shots. She handles them quite well. Her height is 28 1/2 inches (5-10%) and her weight is 15.2 (1%) and her head is 17 3/8 (10%).

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She holds her own like nobody’s business. She will flail her limbs and throw her head back if she doesn’t get her way. It has led her to many head bumps on the floor and wall. She’s so incredible feisty.

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She just got her third tooth. It’s on the top. She loves dance parties and her brother and sister.

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She loves to swing. In fact, when Isa and Jimmy went to the leaf pile to play with Daddy, she bee-lined to the swing set to get the swings all to herself.

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She missed out on some good fun.

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She didn’t care!

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She will swing any way you let her!

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Rosie laid down on the ground and Jimmy decided to join her. They smiled and talked to one another. They still share their food and drinks with one another and love to splash around in the bath tub.

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Rosie’s thinking, I got you right where I want you…in the palm of my hand.

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2 comments:

  1. Wow already? Cute fall photos!

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  2. hello, what a beautiful family you have there.
    My name is Kim, my husband and I have 5 children, our youngest has down syndrome. He was also born with complex heart defects
    I am always searching for childre, who like my sonhave DS and a single ventricle heart defect.
    I found your blog through another blog, Bobbie (thisbobbieridesagain. I have been attempting to reach his mothers, as my son has the same heart defect and it is very rare among children with Down Syndrome
    I have left them a comment, however, it looks like they only blogged during his surgery and recovery.
    Anyway, I noticed you commented several times and hoped you may know them personally. If so can you please pass on my email to them,
    kknipp@kc.rr.com or they can read about my son at www.carepages.com page name HeWill
    My son had the same first two surgeries as Bobbie and was slated to also have the fontan, however, his cardiologist failed to tell us, the fontan was onlu short term solution due to the fact that kids with DS develop pulmonary hypertention with this cardiac formation. The plan was to start him on viagra, just as Bobbie. However viagra is very damaging to the liver and no child with DS and fontan (and on viagra) has lived into the teen years.
    We were devastated and then another mom found us via internet, whose son has same defect, ds, had fontan and on viagra. She found a surgeon in Boston (#1) who specialized in these kids and does VENTRICLE GROWTH procedures to give these kiddos full hearts. I know sounds crazy, and when she contacted me, I thought she was nuts. But God worked on my gut, until I couldnt stand it and I emailed this surgeon and sought out the truth myself.
    I could write a long story, but short, sweet and simple is...not crazy, truth, six months later, our son had the surgery. it is 3 years later and he is a healthy and happy and has a four chambered heart, a walking miracle....please share our story with Bobbies moms...thanks

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