Little baby in her princess towel
Nicholas is starting to love Ella more and more...except when she flails her arms and legs and accidentally hits him
The kids' stockings are ready for St. Nick to fill them on Christmas Eve

Nicholas has been feeling so much better since we started him on a new amino acid diet last Thursday. He gets juiced fruits and veggies with his AA formula and gets pumped breast milk at nap time now. He is sleeping better, his stats are higher, he is talking more, and moving his hands and fingers more. His old formula was just too difficult for his body to break down and digest so we are relived to find a better diet for him!
Here he is holding his "wand" and a new ping-pong ball. They are among his new favorite toys!
I mentioned in a previous post how much Nicholas loves watching Finding Nemo and my friend, Catie, took note. She sent Nicholas this faux aquarium which he enjoys watching while he falls asleep.
Catie also sent Ella a lot of clothes that her daughter has outgrown so now Ella's closet is packed full of adorable outfits. Thanks, Catie for thinking of our kiddos!
My two precious children
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Tuesday, December 14, 2010
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Information about Spinal Muscular Atrophy (SMA)
Click HERE to learn about Spinal Muscular Atrophy.
About Me
- Jessica
- Washington, United States
- We are the Gustafsons: Daddy Jeff, Mommy Jessica, Big Brother Nicholas and Little Sister Elizabeth. We started our blog in 2008 when our son was born as a way to document our life. Jeff and I feel so blessed to be parents to two amazing kids. Our oldest, Nicholas, was diagnosed with a terminal condition called Spinal Muscular Atrophy. We are praying for a cure for Nicholas and all children who suffer from this physically limiting diagnosis. We are also parents to a little girl who who brings us sunshine and laughter everyday. We treasure every moment with our sweet kiddos. Please let us know you visited our blog by leaving us comment. May God bless you today and always.
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Falling In Love
Our Wedding Day
Brother & Sister Love
Motherhood
Nicholas's Story
Click HERE to read Nicholas's story from birth to his diagnosis with SMA at 10 months-old.
All About Nicholas
sweet. easy-going. smiley. happy. fighter. playful. courageous. loving. joyful. amazing. gift. wise. strong. handsome. kind. brave. Heaven-sent.
Nicholas's Birthday
Nicholas at 1 Year
Nicholas at 2 Years
Nicholas at 3 Years
Nicholas at 4 Years
Nicholas at 5 Years
Nicholas at 6 Years
All About Ella
loving. cuddly. toddler. curious. explorer. walker. silly. happy. sleeper. blessing. fearless. adventurous. kisser. sassy. dancing queen. spirited.
Ity Bitty Baby Ella
Ella at 1 Year
Ella at 2 Years
Ella at 3 Years
Ella at 4 Years
Ella at 5 Years
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December
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- Family Lunch
- 2010: A Year in Review
- Christmas 2010 {Part 4: Stockings}
- Christmas 2010 {Part 3: Christmas Day}
- Christmas 2010 {Part 2: Christmas Eve}
- Christmas 2010 {Part 1: December 24th}
- Let's Try This Again, Santa
- No Santa Visit This Year
- Ella is 3 Months
- This and That
- Family Photos
- Christmas Tree
- Movin' and Shakin'
- This is SMA Video
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3 comments:
They are really cute stockings! Your kids are really cute! Nicholas looks so strong. Is he type 2? Have you done testing on Ella to see if she's SMA free? I hope you guys have a Merry Christmas.
Nicholas was diagnosed as a weak type 2 because he could sit up for short periods of time around 8 months to 1.5 years-old. He cannot sit up anymore though so I think he is considered a strong type 1/weak type 2. We did prenatal testing with Ella at 12 weeks and she does not have SMA and isn't a carrier of the disease. Genetics are so strange that way...we have two kids and both on opposite ends of the spectrum. Merry Christmas to you and your adorable family!
I love all the pictures--especially the last one. I like how they're both smiling at each other. What sweethearts! Nicholas has such a cute smile. Glad to read that he is responding well to his new diet.
As a complete stranger, I am so touched by each of your posts and photos. I continue to pray for Nicholas!
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