Afghanistan is looming…

Well, the time is drawing near…we’re down to about 2–3 weeks. The original departure date was around August 1–5 but Tom has said that it might be a few days later. As far as I’m concerned, they can just as easily say it will be a few days earlier so I take every piece of news with a grain of salt.

That said, right now, the plan is for Tom to be gone about eight months. I still can’t believe I have two kids this time around. Looking back, 13 months by myself was a piece of cake compared to what I have in front of me this time (believe me, even though I’m glad it’s only eight and not 12 or 13 months…it will still feel like a LOOOONG time). Of course there is a SLIGHT chance he could be home earlier—but he’ll have no idea until after he gets there and things start moving along. I’m keeping my fingers crossed that he’ll be home by Owen’s fifth birthday (February 2) but of course (!) I don’t plan on it. There’s that grain of salt thing again. (Also, return dates as early as December have been tossed around but I have ZERO hope of those happening. I take that one with a salt shaker’s worth of salt.)

Owen still seems to be doing okay. Every once in awhile he’ll say he doesn’t want daddy to go away and that he’ll miss him. I tell him I will miss him, too—and that daddy will definitely miss us. I asked if he wanted to see on a map where daddy would be and he said yes—but didn’t really seem that interested (though I’m really thinking he just couldn’t comprehend it). We’ll keep trying. We also have a big calendar to X off each day—since you can’t really expect him to understand MONTHS of time.

I do have Tom’s actual address already and will be emailing it to family but will post it on the Afghanistan Info page (linked in the static menu bar above) once he actually arrives there. There is also a new Goodies page and a USPS Shipping page linked as well.

Genetic Testing Results

Today we went to UNC Chapel Hill to the Pediatric Genetics clinic to get the results of Owen’s (and Tom’s) genetic tests explained to us. (This was from when Owen had his blood drawn back in April—it takes a month or so to get the results, and then Tom and I had to get ours done and wait another month, and then it took a few months to get into the specialist.)

Previously, all we had been able to tell from the greek-to-us multi-page results was that both Owen and Tom had the exact same markers (Owen’s and mine didn’t match at all so I basically got no results for me). But the thing with genetic testing (that our developmental pediatrician told us) is that there are MILLIONS of combinations of things and the science is still so new that they maybe only know what (for example) 50,000 of the possible five million results mean. So while they can tell you something isn’t right, they can’t tell you exactly what effect that might have.

So today we got to talk with a genetic counselor who gave us more information. She still couldn’t really give us any more information on what effect the gene mutation has (like if it’s the direct cause of his autism or autistic tendencies) but she was able to tell us enough about the mutation that we can pretty much rule out it being anything serious.

Let’s see if I can explain this.

Basically, the part of the gene that has the mutation is in the middle of the chain—which is better than at either end where two chains connect (if it was at either end, it would definitely cause much more noticeable issues). So my brain worked it out as “It would be like origination and destination points of your trip are set in stone, but the route is variable. If either end changes, the whole thing changes, but if the route changes, it’s not a big deal.” She agreed it was an apt correlation.

Also, the other good point is that he isn’t MISSING anything on the strand—he actually has an extra set of something (his own plus the double set from Tom for a total of three instead of the normal two). And the set of three is fine—if there were four sets it would be a major problem. And lastly, since Tom has the identical genetic mutation and had absolutely no issues growing up (or today), it’s very unlikely (statistically impossible) that it is causing Owen’s issues.

So taking that and all his background (and our family’s backgrounds) into consideration, she didn’t see any reason to think this mutation was the cause of the autism and said we really don’t have anything to worry about. She will research it more to see if she can find anything, but she doesn’t expect to find much. She said the only time we will likely need to think about it again is when he hits the teenage years and/or wants to have kids—in case they have come up with a defining characteristic of that specific mutation or if it will have any effect on his own kids. We were told not to worry about getting Katie tested at all unless we started to notice any issues.

So basically everything scientifically is good…now I just have to get the in-home therapy started so we can work on his minor issues.

The last payment!

I just made the last payment on our only credit card that was carrying a balance—so we are officially done with credit card debt!! And amazingly…done mostly since I’ve stopped working (which of course makes me wonder just what the hell we were doing with my salary the whole time I was working)!

Of course, we still have the mortgage and two cars and Tom’s student loans…but the original debt is gone!

In an ironic side note, the amount we made at our garage sale was just about the exact last payment ($539 vs. $534). I guess it was meant to be.

Update your bookmarks!

If you bookmarked the blog since it’s been revamped, you might have a link that includes a bunch of numbers and a strange userid (the address I needed to use until all the background stuff was taken care of). It will still get you to the same spot, but if you want to change it, it actually appears as www.hudson2001.com now!

Email notifications FYI

If you sign(ed) up for email notifications (I can’t tell), I just wanted to let you know that if you opted for immediate notification (instead of once a day or whatever) you might not be seeing the entire post. I often make changes right away (I blame mommy brain, often forgetting all that I wanted to say) but the notification has already been sent out. So I recommend either clicking the link and reading it on the website or opting for the once a day notifications.

Happy birthday to me!

Well, it’s been a long and tedious road, but the day is finally here: my blogs have been migrated, completely revamped with new themes and widgets, and now live at the main website—www.hudson2001.com—instead of a specific blog address (so change your bookmarks!). All of the content is the same, though the Blather and Owen/Katie blogs have been merged! And I’ve even added a lot from the pages that were on the website before (like Tom’s writings and photos from Iraq and our “new” house stories). However, one slight change with content is that the Recipes blog is currently locked. Long story…but they may be going away now that technology will let me compile and access them in a better fashion.

I have to give mad props to my friend, Tori, who basically did all the heavy lifting on this project—and I can honestly say it would NEVER have gotten done if it weren’t for her. Migration sounds easy, but is a total pain in the ass. That said, this blogging platform (WordPress) is a lot more involved and easier to use (behind the scenes—not for you!) so my life just got a lot easier.

Since the blogs were out of commission for about three weeks, I had A LOT of posting to do in the past two days…but I think I got completely caught up. Thanks to Tom for keeping an eye on the kids all day for almost two days so I could knock it out. There is still some tweaking going on behind the scenes, but nothing you should really notice. Let me know if you run across anything really weird or glitchy.

If you want to get emails when new posts are made, you will need to enter your address over there to the right—your old subscriptions from the old blog are no longer valid.

Enjoy!

😀

Warning: Under Renovation

My blogs are undergoing renovation right now…

You might have noticed that the Owen & Katie blog has changed (and most of the kinks have been worked out) and just tonight I changed this one (though the kinks are giving me more grief)…so if you notice anything wonky, please know that I’m working on it.

Also…major major changes might be in the near future, though hopefully you won’t notice too much aside from everything just looking different (the big changes will be on the backend in stuff you can’t see).

NHCL welcomes newborns with sweet salutes

The Camp Lejeune Globe published this story on Facebook today:

You only get one chance to make a first impression, and Marine Corps Base Camp Lejeune’s newest family members are doing it in style.

When the double ring of bells toll over the intercoms, attention is assumed on the decks of Naval Hospital Camp Lejeune.

“Announcing the arrival of baby girl (or boy), United States Marine Corps,” a voice echoes through the facility, followed by the familiar notes of the lullaby “Twinkle, Twinkle Little Star.”

I posted on their Facebook page that I just delivered on 7/10 and we didn’t hear anything…though maybe I wasn’t paying attention or maybe they don’t do it at 3:29am. 🙂

They responded:

Congratulations Jennifer Hudson! That’s quite a way to start your day! According to Capt. Lane, babies born very late in the evening or very early in the morning are all announced at 8 a.m. out of respect for other patients who have the luxury of sleeping during normal hours. Hopefully you were catching a few winks when the bells tolled. You deserve it!

I probably was sleeping—or otherwise occupied—but it would have been really cool to hear it (i.e. know about it in advance).

OB Appointment…guess what happened?

Short story?

Unless something happens on its own this weekend, I’ll be induced Monday night…

Long story?

My blood pressure was high at the appointment so the doctor was concerned that it might be pre-eclampsia (it hasn’t been high for a few months, but since I’m near the end, it was a worry). She also wanted an ultrasound to measure the baby (something I was apparently supposed to be having done every so often—NOT the fetal monitoring I’ve been doing, but an additional ultrasound—but hadn’t had in a while) so she walked me across the hall for that since she had an opening right then. On the way I told her that I was concerned that the last doc mentioned stripping my membranes today and possibly inducing labor next week and she said she wouldn’t do that unless it was medically necessary—so that made me feel better. Everything with the baby measured just fine (head, length, amniotic fluid, etc.) but the doc still sent me off for lab work to rule out or diagnose the pre-eclampsia. (On a sidenote, the tech guessed that the baby was about 8.5# but the doc said “Oh, the +/- on that is about a pound…” |-| So why even give a guesstimate that could be so far off?)

The lab work actually went amazingly well, considering I have the worst veins on the planet and it usually takes three techs and four pokes to hit a vein—the girl got it on the first attempt! Everything was marked STAT so I knew I’d have results fairly soon.

So, up in Labor & Delivery Triage, they hooked me up to the monitors (like I’ve been doing at my weekly appointments, just with another nurse) and my BP was fine and the baby’s movements were fine—and most of the lab work came back just fine…except the protein in my urine was __fill in the blank with whatever number was high enough to cause more tests but not high enough to be severely concerned__ and the midwife wanted me to do a 24-hour urine test. Uh, yuck. No thanks. Especially when she said that if the protein marker results were __whatever number high enough__ I would be admitted RIGHT THEN. As in tomorrow afternoon! So I half-jokingly said “Can’t I just skip it and agree to come in and be induced Monday?” And she was fine with that!!! So that’s the plan…unless, of course, something happens before then or I have any strange symptoms that might be cause for alarm.

So, no, I didn’t initially want to be induced…but since things went a little awry, it did seem like the best option. Especially since if things go according to plan…I’ll have Katie on her namesake’s birthday: July 10! (I’ll be admitted for induction at 6pm on Monday night the 9th and will likely have her sometime after midnight on Tuesday the 10th!) 🙂

School screenings findings meeting

Long story short, the school didn’t really seem to think Owen was in dire need of any special education—which, yes, is a good thing—but they did notice some areas in which he was on the lower end of normal (some language and social stuff)…but still normal (and said he was actually quite advanced on a lot of language stuff).

That said, we were able to request a more formal language evaluation (since that’s what we’re most concerned with) and classroom observation (his speech issues we’re concerned with might be better observed—or negated—by seeing him interact with kids for a longer time period)…so we are waiting to schedule those. Best case scenario, we are hoping that we can get him into a social situation (preschool) with other kids which will improve certain aspects of his language skills because he will learn from the other kids and also have to use his language to communicate with them (instead of with us who already understand him pretty well).

As a sidenote, these findings have NO effect on our ability to get the ABA (applied behavioral analysis) Therapy benefits through the military, so even if we don’t qualify for any special education programs through the school district, we will still get the one-on-one therapy.

Chromosome test results

I just technically got Owen’s chromosome test results. I say technically because the pediatrician read them to me over the phone—and of course it’s all Greek—he wasn’t even familiar with the exact result so he said he has to read up on it. I can’t even tell you what the exact findings were until I go pick up a copy of the report (it was too complex to write down over the phone).

That said, apparently it was recommended that Tom and I get tested, too. I’m assuming it’s so we know if we need to 1) watch Katie for signs and/or 2) get her tested early. If we’re clear, the mutation starts with Owen; if one of us (or both) have the anomaly, she’ll need to be checked because we will likely pass it down again.

For some reason, this is more disturbing to me than the initial autism diagnosis, even though it technically doesn’t change anything and there’s nothing we can do about it either way…it’s just knowledge.

Just a note about the blog…

I try to always post things in order (which is why I often get behind) but I sometimes miss something I meant to post… so the best thing for you to do is always scroll down just a bit to see if there’s something you might have missed. For instance, I had already posted about something that happened on 4/13 but just today (4/22) realized I had some posts that belonged on 4/12 so if you didn’t scroll down, you might miss them. It doesn’t happen all the time, but in case it does, a quick scroll will show it to you!

Welcome to autism.

So we finally had Owen’s appointment with the developmental pediatrician to check into his speech delays. We’ve actually been a little concerned since about 18-24 months, but figured he was steadily progressing, so we weren’t THAT worried—and our pediatrician wasn’t super worried, either. But at his 36 month appointment, I finally just bit the bullet and asked the pediatrician for a referral to get Owen checked out—if for nothing else to just ease our minds (if nothing was wrong) or worst case, get started on an action plan (if something was wrong).

Well, we have good news and bad news. I always like the bad new first, so here goes:

The bad news? Owen was diagnosed with autism.
The good news? It’s a very mild form.

Even though I had a tiny inkling in the back of my head going into the appointment…it was still a shock to hear and my head was just spinning from everything the doctor was throwing at me (websites, studies, possible tests, results, terminology, insurance issues, second opinions, yada yada yada). So, really, even now a day later I don’t have a lot of details…

Some points, however (which I’ll probably still muddle, but you’ll get the gist):

The doc said Owen is very intelligent (the tests he took scored him in the normal/average to slightly above average on knowledge), he just has some language issues (things like pointing at what he wants vs. asking for what he wants in a sentence) and possibly even ADHD (how busy he is all the time and his ability to play/play without other interaction).

The doc wants to run a chromosome test (basically just for us to have the knowledge) but he doesn’t anticipate anything horrible since right now, Owen doesn’t fit the profile for any of the severe instances (where he would require more tests).

The official diagnosis is High Functioning Autism. I can (and will) schedule an appointment for a second opinion with a civilian doctor in town, even though I trust and have faith in the doctor we saw. I’ve already started the process to get him enrolled in the EFMP (Exceptional Family Member Program) on base, which qualifies us for additional assistance programs (such as in-home therapy, parenting programs, etc).

The Exceptional Family Member Program (EFMP) is a mandatory enrollment program for all active duty personnel with family members with special needs. The goal of EFMP is to assist military families in managing the dual demands of a Marine Corps career and the special needs of a family member. An exceptional family member includes a family member enrolled in DEERS and MCTFS who possesses a diagnosed physical, intellectual or emotional need that requires specialized medical or educational services. Enrollment in the EFMP program is designed to assist the sponsor with assignment to a duty station where appropriate services necessary to support the family member(s) are available. Installation EFMP Specialists are available to assist sponsors and their family members with the enrollment process, resource, referral, and support before, during and after Permanent Change of Station transitions. Specialists also serve as advocates for EFMP families to ensure access to vital medical, educational and community services. For more information about the EFMP program please contact your installation office.

I’ll have to visit the local elementary school to get him evaluated for an IEP…which, fingers crossed, will allow him to attend preschool there (five minutes from our house). I need to start researching therapists because there’s a waiting list. And I’m sure about a thousand other things I’m forgetting or haven’t thought of/learned yet.

The good thing, however, is that the pediatrician said I’m doing everything right with him (just from watching us interact during the appointment)—so that’s positive at least—and I can just keep keeping on at home.

I have shared the diagnosis with my family and friends and they have all been amazingly supportive. In fact, the comments two friends made really stand out and I want to share them here, so I will remember them forever (and maybe someday I can read them without crying like an emotional pregnant woman):

  • Aaron: Here’s the thing to remember—a diagnosis doesn’t change who Owen is. All it does is attach a label to a collection of his behaviors so that you can get the appropriate assistance to help him continue to develop. He’s still the same child that you’ve been playing with and taking pictures of and sharing stories about that he’s always been.
  • David: That just means he’s even more special!

So, this is sure to be an interesting, frustrating, and eventually rewarding journey… Stay tuned!

And now, for a bit of backstory…

Or, why I haven’t been posting much.

We found out I was pregnant on November 13, then called the hospital to see what I had to do to come in and get bloodwork to confirm it. I was told if I had a positive urine test that I could come in. So I waited a few days until it was convenient, and—

** INSERT LONG AND FRUSTRATING STORY WITH THE NAVAL HOSPITAL **

Ugh.

So we made it on base a little before 9am. And since they’re doing construction, one entire parking lot is gone, which means I had to park in the very last row about 200 yards from the hospital. Not a big deal in the grand scheme of things, but super annoying.

So apparently I’m in the Red group, but there’s nothing anywhere noting which section is Red and which is Blue, so I stop at the first Family Practice I see—assuming they’ll tell me if I need to go elsewhere or whatever. So I say I’m there for walk-in bloodwork for a pregnancy and she says “Have you had two positive urine tests here?” Um, no. I told her when I called the appointment line, I was specifically told that as long as I had a positive urine test at home, I could get the bloodwork. She says she’s sorry, but that’s NOT their policy, but they can do a urine test for me. Of course I was pissed. I tried not to be too bitchy, but I asked if there wasn’t anything they could do since 1) I was told something else on the phone and 2) I wanted to get OB involved ASAP since I’ve had a problem pregnancy before and wanted them to do whatever they could to make sure this one worked (and couldn’t they check my records?). (As a sidenote, as I’m talking to her, a coworker was calling [whoever] to tell them about the screw up with the appointment line rep to make sure it didn’t happen again.) So the lady asks if I’m high risk and I say actually, I probably am—they considered me high risk when I had [him] because of my age and thyroid issues, and I’m older now, so…I’m likely to be high risk again. So she doesn’t say anything but makes some motion which TO ME says she’s going to bypass it and let me get the bloodwork. She prints me something and directs me to the lab. I didn’t even think to look at the sheet.

So I get to the lab, take my numbers, and wait. I finally get called, hand him the paperwork, and he asks if I’m prepared to give a urine sample. Wait, what? No. I tell him it’s supposed to be bloodwork. Then I read the sheet and it clearly says urinalysis. Ugh. So the lady apparently led me to believe she was giving me bloodwork but gave me urinalysis and didn’t. even. tell. me. (No, she didn’t specifically tell me I was getting bloodwork, but after the entire discussion about my past and being high-risk, I assumed I was getting bloodwork—and she didn’t say either way.) So I tell him I’ve got to go back. Luckily Owen is a little rock star and just keeps playing with his cars and my phone.

So I go back to the first place and it’s the other girl (who has been making the phone call) and I say “Remember me? I thought this was supposed to be an order for bloodwork.” And then she’s all “Well this isn’t even YOUR clinic. You’re Red. This is Blue.” I ask where the signs are and how I’m supposed to tell—did I miss something?” No, she tells me, we were just doing you a favor so you didn’t have to [go 20 yards farther down the hall to your correct clinic]. Like I was putting her out or something. So off we went.

So we get to the correct RED clinic and have to start from scratch with this lady. I retell the ENTIRE story (Blue clinic visit, appointment phone call, bloodwork that was really urinalysis, failed pregnancy, high risk) and all I get is “Well, our policies are two in-house positive urine tests before bloodwork.” I just wanted to scream HAVE YOU HEARD ANYTHING I’VE BEEN SAYING? To her credit, she said she’d ask a nurse. So I waited and waited. Then she came back and said a nurse should be up in a minute.

In the meantime I asked if I could make an appointment for Owen since he missed his 30-month well-visit and I was pretty sure he needed some vaccine updates. So she tells me he shouldn’t need anything until he’s FOUR and throws a sheet of paper at me with their vaccine schedule. So as I’m trying to read his vaccine chart (via Dropbox on my phone so it’s super tiny and I’m not even sure what I’m looking for!), she says “How about Monday, November 21 at 11?” So she caught me off guard by wanting to make an appointment before I was sure he needed one, then she was all “You’ll have to call to cancel if he doesn’t need it.” And I said, surprised, “Did you schedule it already? I’m still looking to see if he needs it.” And she said No, I’m just waiting on you. All snotty. SERIOUSLY? I finally found that all he needs is a flu shot, so I told her that, thinking I could either take that appointment or they might be able to do it right then. Yeah, no. She tells me they can’t do flu shots until he’s four…but I can go out in town and get one. What? WHAT THE HELL? A military hospital can’t give a toddler a flu shot? If there was some other extenuating circumstance, they certainly didn’t tell me. So now I’m pissed about that on top of everything else.

So then the nurse comes out and signs the form giving me the okay for bloodwork and the snotty lady enters it into the computer and you can tell she’s rolling her eyes while doing it. REALLY? The little old grandma-like lady was a bitch.

The rest of the time there was just fine—the lab techs (who were awesome to Owen) and even waiting for Tom’s scripts. But I am sure my blood pressure was SKY HIGH anyway. (And we were leaving the hospital parking lot 2 1/2 hours after we got there. Ugh.)

And THIS is why I wanted an in-town doctor for both of us. Because I >:XX hate the hospital. Something always pisses me off when I have to go there.

** END OF LONG AND FRUSTRATING STORY WITH THE NAVAL HOSPITAL **

—the following day I got a call that yes, I was pregnant—due July 24, 2012.

So, we had plans for lots of family to be visiting over the upcoming month, but kind of wanted to not tell them because 1) it was still REALLY early (only five weeks) and 2) we wanted to surprise them with the news when we came up for Christmas.

But…my mom and David were the first to visit (the few days before Thanksgiving, on their way to Atlanta to see the Filipeks) and…HOW COULD I NOT TELL MY MOM? 88| So we told them and they were super excited. Unfortunately, after they left and Tom’s mom and brother arrived, I started feeling crappy. Like, seriously crappy. I tried to hide it for a few days—but then it just kept getting worse, so we finally broke down and told them, too. By the end of their week-long visit, I was in pretty bad shape. Incapacitated, even.

I call it the Yucks™ (I suppose it’s morning sickness—which is realy all-day sickness—without any barfing). I had it with Owen, but not nearly this bad or this early. The best I can describe it is that all at once and all day long you feel like:

  1. You just ate a too-big meal.
  2. You are a little hungry.
  3. You have a big ball of nervousness weighing on your chest.
  4. You have a hangover.
  5. You are mentally exhausted.
  6. You are physically exhausted.

I seriously just sat on the couch or in bed like a zombie and wished someone would knock me out until July. Nothing I ate (or didn’t eat) made any difference. No amount of sleep made any difference. I had no energy to do anything simple like post to my blogs, let alone cook or pick up the house. I lost about 8# during the two worst weeks. Thankfully, my dad and Linda were total rock stars, playing with and taking care of Owen, helping put up Christmas decorations, and taking care of laundry, cleaning, and meal prep for the two weeks they were here. I did help out the few hours and or random day when I felt better (YucksLite™ ) but it was few and far between.

We actually momentarily debated NOT going to Michigan for Christmas because I felt so bad…but figured I might as well feel bad where there were other people to help out with Owen. 🙂 I’m so glad we did go, because Owen had a great time staying at Gramma Jean and Grandpa David’s house, visiting with the Len cousins and Schwalm cousins (he now knows the word COUSINS!), and seeing Grandma Marsha and Uncle Rob (Grob) for a bit. I did have a few decent days, but for the most part, I was still dealing with the Yucks™.

So, at this point, seven weeks after we found out…I still feel like crap. Needless to say it’s been a LONG seven months weeks and there have been many, many times I’ve just felt like crying because I’m SO tired of feeling this way. The first trimester is almost over, and I’m keeping my fingers crossed that most of this goes away. Of course, then other fun stuff is bound to appear (like I’m already experiencing gas, bloating, burping, and minor reflux in addition to the Yucks™ ). Of course, my friends all say that being this sick means it’s either a girl—or twins. I’ve disowned the people that have mentioned twins.

Oh! I almost forgot! Another lovely naval hospital story… |-|

After a two-day wait for the general practice office to offically refer me to OB, I had to call and schedule the first ultrasound appointment pretty quickly. Easy, right? The first opening they had was like December 21. I told her that there was a 99% chance we’d be on vacation then, so if there was ANY way to get it even a few days earlier, that would be great. Nothing doing, no way no how, that’s the absolute earliest you can come in. Now, I understand they have to wait a certain number of weeks to be able to get a heartbeat, but I really don’t think a few days earlier would be the breaking point (it wasn’t like I was asking for two weeks early or something). But she does tell me that if I do find out for sure that we aren’t going to be here, to call back and they will try to get me in earlier. Wait, what? Just a minute ago it was no way, no how…but now you’re telling me to call back and you’ll try to get me in? Ugh. So, fine. So when we had decided we were going to Michigan (granted, only about a week before the scheduled appointment), I called and told the lady what I wanted (and I know it was the same lady—I recognized the voice) she immediately became snotty and said “WHO TOLD YOU THAT?” I wanted to say “It was you—I remember you” but I didn’t. Yeah, they can’t get me in that soon at all and wouldn’t even take my name down for a cancellation. The next available appointment was almost three weeks later. Really? Oh, and they’re only in the morning. And I can’t bring Owen with me. And suddenly she tells me that I need to be prepared to be there for 2-3 hours for labwork and a visit with the nurse. WHAT? Since when? You’d think they’d tell me all this the FIRST time I called to schedule the appointment. Breathe. Breathe. Breathe. So I had no ultrasound to show anyone at Christmas. And I’m keeping my fingers crossed that everything goes well Friday…though it’s the naval hospital, so I’m sure something will piss me off.

So…thus far…this hasn’t been an enjoyable or exciting experience for me. I’m really hoping things get better.

At daddy’s softball game!

Well, actually it was softball… Tom called to tell me he was in a pickup softball game if we wanted to come. It was a gorgeous day and Owen was up from his nap, so off we went. And Owen was REALLY excited about the whole thing—he just kept hopping around saying BASEBALL! BASEBALL! BASEBALL! and was ever MORE excited when someone handed him an actual softball to carry around! Of course I didn’t capture the best parts, but I did get some to give you an idea.

And then running the bases with daddy after the game!

Smart kid!

Typically in the morning, we give Owen a snack (granola bar) and a juice, then we eat breakfast an hour to an hour and a half after he gets up. Sometimes (rarely) we just skip the snack and eat breakfast a bit earlier. We just used to give him the snack, but lately he’s started asking for it.

So this morning, I decide we will eat breakfast early, and this is what happened:

Owen: Snacks! Snacks!
Me: No, it’s time for breakfast.
Owen: SNACKS! SNACKS!
Me: Okay. [Hand him a granola bar.]
Owen: [Finishes the bar in about two minutes.] Breakfast!

Scammer. 🙂

Going Away Picnic

We wanted to have a picnic like last year…perfect weather, fun for Owen in the pool, a bunch of friends over, some good food, and a new family photo. Unfortunately, the weather didn’t cooperate…and neither did Owen. We got a decent photo out of the 25 attempts…

But it doesn’t even come close to the apparently once-in-a-lifetime shot we got last year (one of two attempts).

But he was super cute the morning of the picnic when he discovered he could climb up onto the bay window ledge in the living room. What fun!

And he loved Gramma Jean’s mower…when it was turned off. She turned it on to give him a ride and it was “NOISY!”

Then Tom helped him pick a flower for me—my first flower! Sigh. :heart:

And last but not least…Gramma Jean got Owen a pop-up tube/tent contraption…which he LOVED. I’m not sure where it’s going to fit in either house, but we’ll have to find a place.