OK, just the blog is moving. Fabricio set it up for me 3 years ago under his info, and since I can never remember his username/password I decided it was time to start a new one. Kind of fitting since tomorrow is Camila's 3rd birthday, right? Let's just hope we always live in Minnesota, otherwise I'll have to come up with a new URL. :)
http://nunezfamilyinmn.blogspot.com/
Friday, October 15, 2010
Thursday, September 30, 2010
State Fair
So we went from not knowing if we were going to go to the Fair this year (nap schedules, tantrums, and so on) but we ended up going twice! Fabricio and I have never been to the State Fair twice in any given year, so this was a first for us. Camila loved it, and keeps talking about going back. I told her it was done for the summer, that it was going to be too cold, etc., but that backfired b/c now that we're having this amazing fall weather she thinks the Fair is open again. She still loves the carusel, but she also had a blast on this mini tilt-a-whirl car thing. And of course, the cotton candy was a great treat. Amelia had a great time looking at all the things around her, and she did great missing her morning nap (until it was time to leave, which made the ride home a little noisy until she crashed.)
Good news!
Yeah! I finally heard back from the ortho, and they say that Amelia's scoliosis is actually just "positional". I need to call them to confirm (it was a voice mail) but my understanding is that the curvature was just from the way she was positioned during the x-ray. (Try getting a ticked off 10 month old to lie absolutely still.) Although I wish we hadn't spent the last week worrying, I'm surprised and relieved that everything is ok.
On another note, Amelia started crawling 2 weeks ago. She is slowing building up speed, but she's already getting into trouble. For example, Camila has a table fan sitting on her floor. (I only plug it in during naptime/sleeptime.) Amelia tried pulling the cord out of the wall to get the fan into her lap, and almost succeeded. But we're willing to put up with all the trouble-making since the crawling is doing great things for her tilt! She is building up neck/trunk muscle strength so quickly. She is getting 2 more teeth and has the worst cold she's ever had, and her tilt is not regressing! It's never been like that. All summer, it seemed like that tilt would be more pronouced (it never went away completely) whenever she would even sneeze. I'm excited to see what a few more weeks of crawling will do!
On another note, Amelia started crawling 2 weeks ago. She is slowing building up speed, but she's already getting into trouble. For example, Camila has a table fan sitting on her floor. (I only plug it in during naptime/sleeptime.) Amelia tried pulling the cord out of the wall to get the fan into her lap, and almost succeeded. But we're willing to put up with all the trouble-making since the crawling is doing great things for her tilt! She is building up neck/trunk muscle strength so quickly. She is getting 2 more teeth and has the worst cold she's ever had, and her tilt is not regressing! It's never been like that. All summer, it seemed like that tilt would be more pronouced (it never went away completely) whenever she would even sneeze. I'm excited to see what a few more weeks of crawling will do!
Thursday, September 23, 2010
Amelia update part II
Just a quick update --
We heard back from Gilette's this morning, and found out that the x-rays we had done at the beginning of Sept show that Amelia has scoliosis. It appears to be mild, a 16 degree curvature in her upper lumbar, but I'm now waiting to hear from the ortho team as to our next steps. Infant scoliosis is very rare, so I'm really not sure what they'll want to do. I'm assuming they'll want to follow/observe her for a while to make sure it doesn't get worse. Although depending on my conversation with them, we may end up scheduling an appt with them at our Nov follow-up for her tort.
The nurse couldn't tell me much about it, such as if the tort and scoliosis were related or not and if that's why her tort is so persistent, but it feels like we have one more thing to worry about. Maybe best case scenario is that the scoliosis is making her tort look worse than it really is, and she wouldn't need the neck surgery after Nov but would have to wear a back brace instead? I'm just not sure what to think at this point. I'll post again when we know more.
Thursday, September 16, 2010
SMA Fundraising Update (Baby June)
A couple of weeks ago I posted about a fundraising effort I'm part of: Molly's Mommy Friends. We are trying to raise $10,000 towards SMA research in honor of Molly's baby, June. I wanted to post an update for those of you that follow my blog (as quiet as it's been these past few months) but also for those of you that may pop over here from time to time. If you haven't donated, please consider it. If you're considering it, please take that next step and donate. Thanks!
In the few weeks we have been active, Molly’s Mommy Friends has raised over $2,000 for the Gwendolyn Strong Foundation. Good Job Mommies! We still have a ways to go to reach our goal of $10,000 by October 5th. Please continue to get to the word out. Here are a few ideas on how:
1. Send an e-mail request with a link to the donation page.
2. Have a blog? Post the link for your followers to see.
3. Are you on Facebook? You can post the fundraising link to your page. You can Twitter it too (say that really fast 3 times.)
4. Prefer pen and paper? Mail letters to friends and family with the page link or request a check (we can send checks to GSF.)
5. Get your children involved, and make flyers to pass out in your neighborhood.
6. Visit your local businesses and ask them if they would be willing to donate a portion of the sale of something to GSF on behalf of Molly’s Mommy Friends.
7. Have a party and charge admission with a portion going to GSF.
8. Have a tag sale and donate the proceeds.
The possibilities are endless. If you ask ten people to donate $10 that’s $100. If ten Mommy friends do this it's $1,000. Small steps (or in this case, small donations) can add up to something significant.
Thanks again for helping with this special cause and for honoring June, our SMA angel.
http://www.firstgiving.com/juneangelbaby
In the few weeks we have been active, Molly’s Mommy Friends has raised over $2,000 for the Gwendolyn Strong Foundation. Good Job Mommies! We still have a ways to go to reach our goal of $10,000 by October 5th. Please continue to get to the word out. Here are a few ideas on how:
1. Send an e-mail request with a link to the donation page.
2. Have a blog? Post the link for your followers to see.
3. Are you on Facebook? You can post the fundraising link to your page. You can Twitter it too (say that really fast 3 times.)
4. Prefer pen and paper? Mail letters to friends and family with the page link or request a check (we can send checks to GSF.)
5. Get your children involved, and make flyers to pass out in your neighborhood.
6. Visit your local businesses and ask them if they would be willing to donate a portion of the sale of something to GSF on behalf of Molly’s Mommy Friends.
7. Have a party and charge admission with a portion going to GSF.
8. Have a tag sale and donate the proceeds.
The possibilities are endless. If you ask ten people to donate $10 that’s $100. If ten Mommy friends do this it's $1,000. Small steps (or in this case, small donations) can add up to something significant.
Thanks again for helping with this special cause and for honoring June, our SMA angel.
http://www.firstgiving.com/juneangelbaby
Tuesday, September 14, 2010
Amelia & torticollis update
After talking to her pediatrician and PT, we decided to take her to a neurologist and an opthamalogist to rule out other things that may be a factor in her persistent torticollis. Setting up that neuro appt was the scariest thing we've had to do. It's terrifying to think that your baby may have some neurological impairment. Fabricio set up the appt b/c I couldn't even bring myself to make the phone call.
We had her neuro appt last week, and fortunately everything looks fine. We then had her eye appt today, and everything looks fine there too. So, while that's great news in general, it's also frustrating b/c we still don't know what's causing this darn tilt to be so stubborn. We also took her in for a 2nd opinion with a different children's craniofacial team, and this doctor wants us to continue PT for 2 months, then come back for a follow-up. Next step with him will be surgery to release her SCM muscle. We would then be back at square one with her, and doing another 6 months or more of PT.
When Amelia was diagonosed at 2 months, we NEVER thought we'd be still doing therapy at 18 months (which is what will be the case if we have to do surgery.) Thank God Fabricio has good insurance. And thank God I was able to leave my job, as I'm not sure how we ever would have made this work with both of us working full-time. And I doubt she'd get much home therapy at daycare, as no matter how great daycare is, it's hard enough for me to do as much as we need to. There's no chance a daycare provider would have enough time. As it is, I feel like we're doing exercises ALL THE TIME. I never get to just sit and enjoy playing with her. I'm always trying to get her to look a certain way, use a certain hand, put weight on a certain leg, practice standing, practice crawling, doing quad play, doing tripod play, practing sitting to stand, practing elevated sitting to stand. And whatver else PT wants me focusing on this week. You get the point.... And yet she still tilts and we may be looking at surgery in a few months. We'll continue doing weekly PT until then, as much home therapy as possible, and pray that we'll make enough progress by November.
There's one thing that this experience has taught us, however, and that's just how true the cliche "it can always be worse" really is. While I wish to God Amelia didn't have such severe torticollis, I've seen other babies/kids at the Rehab center, at the neuro, and at the opthamalogist that make me realize that we're lucky that she "only" has torticollis. I've seen children fighting cancer, children who are partially blind, children who are unable walk, and a child who is unable to breathe on his own and his mom has to pull/push a portable ventilator in a wagon.
So, if more PT or even surgery is what it takes to help Amelia hold her head correctly, avoid future vision impairment, and not develop a learning disability, then that's what we'll do.
Thursday, September 2, 2010
In Memory of Baby June
You may have clicked on the blog I follow, BABY BABY, and know that my friend Molly lost her baby June to Spinal Muscular Atrophy (SMA) after only being with her a few weeks. It was a devasting loss, as they did not know they were carriers until Baby June was born.
I am participating in an online fundraising effort through the Gwendolyn Strong Foundation for SMA. We are trying to raise $10,000 by June's birthdate, October 5. If you have been touched by Molly's story, please consider making a donation in June's name. Here is the link:
http://www.firstgiving.com/juneangelbaby
I am participating in an online fundraising effort through the Gwendolyn Strong Foundation for SMA. We are trying to raise $10,000 by June's birthdate, October 5. If you have been touched by Molly's story, please consider making a donation in June's name. Here is the link:
http://www.firstgiving.com/juneangelbaby
Friday, June 25, 2010
Amelia's Baptism
We had Amelia baptized this Wed, since Fabricio's brothers Chino and Fausto are visiting. As expected, Amelia didn't make a peep, didn't care when the pastor held her or poured the batismal water on her head. Camila on the other hand didn't make it past the opening prayer. We were prepared, and had a Grandpa get her a snack. As you can see from the picture below, she's still eating her Cheerios. :)
Wednesday, June 16, 2010
Teeth and potty training
I forgot to add last night - Amelia has her first tooth (got it May 18) and her 2nd one is popping through just today. She's rolling over great to her left, and just started rolling over to her right this morning. The right is her weaker side, so this is a big deal. She's also sitting up on her own for 1+ minutes, and her PT is really happy with her progress. Some times she still regresses, but overall she's doing great.
Camila is now fully potty trained (except for overnight.) It was so much easier than I thought. For some reason she just "got" it. We experimented with the potty chair a few times, and then on May 1 I went hard core and asked her often during the day if she needed the potty. A sticker and chocolate chip were enough motivation for her. She was down to 1 accident per day within 10 days, and by June 1 she was out of diapers. At least that was one battle I didn't have to fight with her, since we're constantly fighting temper tantrums, etc. :)
Tuesday, June 15, 2010
Couple more pics
Just some random pictures of the girls. You can't tell from the pictures below, but I've been having a really difficult time with Camila lately. She pushes her limits and my limits as far and as often as she can. She laughs when I put her into time out. She screams at the top of her lungs when we're on playdates, in public, wherever. Just this past week I've had to give her first time out at Target, and one at Amelia's PT appt. I am trying to be as consistent as I can so she knows what the limits are and what will happen when she misbehaves and doesn't listen, but boy, is she a challenging girl!
Amelia on the other hand couldn't be a more easy-going girl. She sleeps a ton over the night hours (7:15 pm-8:30am, sometimes later, getting up once to eat around 6:30.) She then needs to take a nap by 10:30, and sleeps for 2 hours. Her afternoon nap is a bit more erratic. She loves her puffs, and Camila loves feeding them to her. I've started making Amelia's food, but we'll see if this is a short-lived interest.
Fortunately, Camila adores Amelia, and vice versa. Even when Camila is in her worst mood, I only have to mention something about Amelia and she stops crying to ask me to repeat it. She loves playing with her, feeding her puffs, watching me change her diaper, giving her hugs and kisses. Amelia will strain her head as far as she can to see Camila every chance she can. They "talk" to each other at dinner (Amelia cooing at Camila and Camila laughing at her). It's been so much fun to watch them interact (and reminds me that as challenging as Camila is, she's still a good girl at heart.)
Wednesday, May 19, 2010
Amelia meltdown
Sunday, April 11, 2010
Amelia - 4 1/2 months
Some pictures of Amelia and Camila. Amelia is now 4 1/2 months, chatting up a storm. She's really mellow, but is getting pretty vocal. She rarely complains, but when we don't pay attention to her cues when she's getting tired or hungry, she'll drop off the edge and have an "Amelia meltdown".
She's grabbing at toys with both hands, and rolling over to her left side. She rolled from tummy to back on March 28, but it was only once. Camila didn't roll until she was 4 1/2 months, and the PT warned us that Amelia could have some milestone delays b/c of her torticollis, so we're not worrying about it too much yet. We're still in PT once per week, and will likely keep that frequency for another 3 months before dropping to once every other week for another 3 months or so.
Amelia continues to be an amazing sleeper. She goes to bed by 8:00, wakes up once to eat around 6:00, and is back to sleep until 8:00. Well, I should say that this is most of the time. The first few nights after I stopped working she was getting up 3 times per night. It was super annoying! I remember that Camila did the same thing at 4 1/2 months. Fortunately, she seems to have gotten over that spell. The best part is that I'm able to put her in bed awake, and she'll fall asleep on her own. Sometimes naps are tougher, but in general she is a fantastic sleeper. (Much better than Camila!!)
As you can tell from the pictures, she smiles all the time. She is always in a good mood! It almost seems like she flirting, because she will often twist to the side and give a little side smile. She also laughs/giggles a lot. She's just so much fun! Camila is still in absolute love with her sister. Amelia spends a lot of her time watching Camila, smiling at her, and giggling when her big sister is acting goofy.
As a side note, Camila has been making slow but steady progress on potty training. She's used her potty chair each morning these past 3 days. Although I can't get her to use it any other time of the day, I'm glad that we're having some success.
Easter
A few pictures from Easter. Amelia did great, and Camila had a blast "playing bubbles". It's amazing how easy Amelia is compared to Camila. When she was ready for a nap, I just put her down on a blanket and shut the door and she fell asleep. When Camila was this age, she never napped anywhere but home (or daycare). I completely understand what people mean when they say they have an easy baby, because (knock on wood), we have one. On the other hand, Camila is still a handful, as always. :)
Tuesday, March 16, 2010
Amelia's 4 month stats
We just had Amelia's 4 month appt today. She weighs 14 lbs (yeah, I'm not sure that weight is entirely accurate....) and is 25 inches long. She's in the 60% for weight but 90% for height. Hmmmm.... I was a little concerned that she's only gained 3 lbs since birth, but the Pedi assured us that it's normal for her to be leveling off already. (We never expected her to always be such a big baby.) :)
Her Pedi checked for flat spots, and he's very happy with her skull. Unless she develops a significant flat spot, he says there's no need for a cranial cap/helmet. Also, he was very impressed with the progress she's made in PT, and said that the way she looks right now, he'd have a difficult time diagnosing her with torticollis. (Her therapist also told me this morning that while she started at a 17 degree tilt, she's now around a 3-5% tilt.)
So, overall a very good appt! :)
Tuesday, March 9, 2010
Amelia pics
So, I've been very delinquent in posting pictures of the girls, particularly of Amelia. So, below is a download of pictures I've taken these past few weeks.
Amelia is in PT once per week with Children's Rehab for her torticollis. We've been seeing progress every week, which has been such a relief. She'll still have facial assemetry until she's a year old (and potentially a little after that) and we need to keep a close eye on any flat spots (very common for tort kids). In the next month or so we'll work with her therapist to determine if she needs to be reevaluated by the craniofacial team at Children's and potentially get fitted for a cranial cap. She doesn't have any significant flat spots yet, so that's a relief. We're happy that her range of motion is significantly improved, and she's slowly gaining strength in her right neck muscles.
Amelia is a polar opposite of Camila - she is such an easy going baby! We can just look at her and she gives us a big grin and squirms around. Below I've tried to capture the many different faces she gives us. She's also obsessed with her hands at the moment, and is constantly with one if not both hands in her mouth. She's also quite the drooler, which gets a little messy at times! :)
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