And here's what's going on in our life. (I'm adding more detail than some of you need, but I have lots of new readers!)
Glen: Glen is keeping busy with his "regular" job (recruiting adjunct faculty for IWU), teaching (in adult learning programs with IWU), and working on his second masters degree (Liberty University). And of course, the current politics have him on pins and needles. I think he'll miss it, though, when it's all said and done. :-) And he's singing in a quartet this Sunday evening, and he recently had a solo backed by the choir, band and flute. It was absolutely gorgeous, and of course, I'm so proud!
Pam: I've been enjoying every spare minute with my little girls, although those are more rare than a few weeks ago. I'm deep into a Strategic Planning course, one of the core courses for my BSA program. I'm ready to get out of this class and move on to accounting (I think advanced accounting). I'm a gal that really needs her sleep, and between the schoolwork, house work, taking care of my little ones, and especially Maddy's last cath around 12:30 or 1, I've been averaging about 6 hours of sleep at night. I know, I know. At least Maddy sleeps through the night, and I don't have to get up in the night to feed the baby, like most mommys, but most days I feel on the edge of exhaustion.
I am participating in a young mom's Bible study, and we are currently using the book Power of a Praying Parent. I've really benefited from this focus a lot, and it's made a real difference in the way I pray for my children.
I have an exciting weekend ahead! Thursday night, I am joining my Aunt Pam and cousin Melanie for a fun evening at a Taste of Home show. And then Marcia Carnes from church is hosting a young moms sleepover. She's had it on her heart for some time to open her home and heart to us. (As a side note, my mom and grandma would love Marcia--she uses her good dishes every day and sets a beautiful table!! ) Sounds like I'm taking Maddy with me, since Glen is rather panicked about learning to cath her and keep up her routine of feedings and medicine, etc. Marcia suggested it, and I'm just hoping the other ladies don't mind. Fortunately, she's a very good baby, and I imagine I would have really missed her. So for two evenings anyway, I'm going to pretend that I have no schoolwork or housework that needs attention!!!!
Carli: Carli is still loving school. She's stayed on green (good behavior) every day so far, and she loves telling me this every day when she comes home. Today she had an all day field trip to the pumpkin patch, and I was so bummed that I couldn't go along, due to some previously scheduled doctor appointments for Madeline. She is reading more and more every day. Her recent list of words included a lot of color words, and she's gotten to where I can just spell it (rather than showing her the words), and she can tell me what word it is. She sounded out "Little House in the Big Woods" the other day (did I already tell you this??). I've enjoyed going into the classroom to read to the children as often as possible.
Olivia: Where do I even start with Olivia. She cracks us up. I don't remember hanging on to Carli's every word like we do with Olivia (that's a bit of hyperbole for you). Maybe it's because she started talking so much later, but I love listening to her. Yesterday morning she crawled into bed with Glen for a few minutes (I think he was blissfully unaware--dead to the world), and then she came out with eyes gleaming and said, "I sept lith Daddy...isss morning!" I about died laughing at her. She paused before saying "iss morning" (this morning) like she was going to try out this new phrase to see how it sounded. She spends a lot of time making messes while mommy tries to clean or do schoolwork or feed Maddy. (Anyone with ideas on teaching a two year old how to get only one toy or set of toys out at a time, please let me know. Oh, and the plan will be useless to me if it means that I have to have her pick up every five minutes. I don't have the time!!)
Madeline: Madeline continues to delight my heart. She's in that really adorable stage when she just looks around at everything. She's starting to give the slightest hint at a smile. Like Olivia talking, we've been watching with baited breath for the smiles since they've been slow in coming. A very sneaky and absolutely wonderful lady from church put some money in my diaper bag tonight to buy a wrap, and I can't wait to use it, especially here at home. She's my first cuddler, and I love every minute of rocking her.
We continue to struggle to put weight on Maddy. She's only gained one pound since birth. The doctors haven't swept it under the rug, so to speak, but one of the best doctors that I have has said that we can't expect her to be in the middle of the chart with everything she has going on. She did refer me to a GI doctor for a possible swallow study (she still chokes quite a bit when eating and has pretty bad reflux), and she mentioned that the next step would be a feeding tube through the side to the stomach that would allow her to get more calories while still getting the benefit of breastfeeding without the risk of choking on fortified milk in the bottle. Obviously we would rather her just gain weight the normal way, but we're open to this option if necessary. What's interesting, though, is the same day I heard this, I met a lady at Chick-fil-a whose grandson has CP. She told me a bit about the spine surgery that he had, probably similar to what Maddy will have eventually, and also that the feeding tube that he had placed was the best decision they'd made. She told me this without me even starting to get into Maddy's story, so she had no way of knowing that this was something that had been mentioned. I'm sure that his will be more permanent, given his condition, but I've been told this wouldn't have to be a permanent situation for Maddy. Of course, I have yet to see the GI doctor, and he may have a different ideas. Please pray that we'll know what to do. Oh, and for those who have been wondering, until the reflux issue is resolved (Zantec didn't seem to make much of a difference, so we're trying Prilosec), we will not be taking Maddy off of oxygen.
Madeline had her first developmental therapy session last week. She seemed to really enjoy the one-on-one time with Erynn, who'd I already met a few months ago. Erynn also has a son with spina bifida, and she was so excited to add a baby with SB to her caseload. We start occupational therapy in a couple of weeks.
Ok, here's some pictures!
Erynn (DT) working with Maddy in the Bumbo seat
(Please excuse all the cords. We have a lot due to oxygen and monitor)
Maddy trying to figure out what Oliva's doing
Maddy after bath. You can see the pretty severe curvature
(kyphosis) on her lower back
Maddy after bath. You can see the pretty severe curvature
(kyphosis) on her lower back
1 comment:
I love having the conversation about the "first real smiles" with first time parents. It is a feeling that cannot be described accurately.
The only feeling that compares is when they reach up for you to pick them up for the first time with both arms.
I know you already know these things, but they are what brings me joy.
It sounds like you are adjusting well to all of the changes.
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