weekly wrap upIt’s already Friday? How’d that happen?

Kathryn’s school week…
We’re doing Winter Promise’s picture studies, which have been going fine but so far Kathryn is not excited by paintings depicting the American Revolution. I know we’ll have to give this a few more weeks before I can decide if this is working for us or not, but I’m not that excited about it yet either.

We added another project to Kathryn’s composer lapbook. I’ll post more about this soon.

I am really liking our Christian Character Traits for Kids workbook. Each week has several sections: Character Trait (explains what this trait is); American Hero (a historical figure who exemplified this trait); Biblical Truth (she reads a Bible passage and answers a few questions); and Building Your Character (considering how she can implement this character trait in her own life). It’s really a devotional that uses American history to teach Biblical truths. So far, Kathryn and I both give this a “thumbs up.” You can, by the way, order this devotion even if you don’t use the rest of the Winter Promise curriculum. It’s available here.

We are continuing our chronological daily Bible readings, and each week, Kathryn is expected to make at least one page to add to her Bible Portfolio.

Each week Kathryn colors a U.S state map and fills in a notebook page with facts about the state. This is part of WP, but also available separately from Homeschool in the Woods; it’s the Olde World Style United States Maps set, available for download or on CD here. She likes this kind of geography study. This week was Massachusetts.

In math, Kathryn is working on the following skills: multiplication properties, making change, estimating money, place value, division, prime numbers, mystery numbers, and subtracting 5-digit numbers.

Sea Monster Pop-UpKathryn’s history studies on Early Explorers involved reading about John Cabot, Amerigo Vespucci, Ponce de Leon, Magellan, Cortez, and others. We added those figures to her timeline book, and she made a sea monster pop-up — because in those days many sailors believed in sea monsters!

In learning about the early Americans, she is still reading Naya Nuki, began The Tinker’s Daughter, and we learned about Life in a Pueblo. Of her own accord, Kathryn is re-reading The Diary of Remember Patience Whipple. This is how I often see Kathryn, with her nose behind a book…

Kathryn behind book

Both girls…
Two evenings this week, we all watched Incredible Creatures That Defy Evolution, parts one and two. We loved these videos and highly recommend them! One of the animals featured in part one was the platypus, which went right along with Kathryn’s biology study of mammals, specifically marsupials and monotremes. Then we found a fascinating series of short videos on YouTube about two little joey kangaroos (so cute!), and their development from birth to independence: Kangaroo Joeys.

We realized this week that something BOTH girls need to work on is paying closer attention to written directions, in math problems, or their vocabulary workbooks, for instance.

Lindsey’s week…
I am so thankful that Ken has taken a more active role in our homeschool this year. It’s been absolutely necessary with Lindsey’s schoolwork; he is great at math, and life is much better if he helps Lindsey with her math work (rather than me). This year’s Physical Science is rather math-heavy, too, so while I’m pretty good with Biology and such, Lindsey’s science this year makes my brain spin. I could do it, but Ken’s much better with it, so he has taken that upon himself. He’s such a good dad.

ColorGuard practice has been challenging this week, as the girls are learning new routines, and new moves and footwork to go with the routines they already know. Last Saturday, they had an extra five-hour practice. I’m proud of Lindsey for sticking with it and doing a great job.

Even though she didn’t do as well on a few tests as she would have liked, I think Lindsey is getting more comfortable with her classes at the homeschool academy. There were some school years early on when she missed more school days than you can imagine, but the public school system moved her up to the next grade in spite of all she missed. This created some serious gaps in her education. This academy is definitely a challenging workload for her, but we have a couple of tutors who are helping to fill in the gaps she has from all those turbulent school years. I honestly don’t care what her “grades” are, but I want her to know the material, and I want her to do her very best. She is a smart girl who is capable of so much, and I know that as we help her get caught up, she will really soar.


Jamie
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Sep 022010

hospitalAfter weeks of testing followed by a ten-day stay in the hospital, my dad was finally given a diagnosis for his condition: central pontine myelinolysis. (No, I’d never heard of it before this either.)

What happened? Last April, my dad had a little virus and got dehydrated. Because the medicine he is suppose to take for his low-functioning pituitary gland was out of whack, this dehydration quickly became bad and his sodium level dropped dramatically. This is called hyponatremia. In cases as extreme as his was, hyponatremia often causes death. He was taken to the hospital, where they brought his sodium levels back up to the normal range. When levels drop too low, and then are brought up too quickly — as in Dad’s case — this can result in central pontine myelinolysis.

When these sodium levels rise too quickly, it pulls water from brain cells. “Through a mechanism that is only partly understood, the shift in water and brain molecules leads to the destruction of myelin, a substance that surrounds and protects nerve fibers. Nerve cells (neurons) can also be damaged. Certain areas of the brain are particularly susceptible to myelinolysis, especially the part of the brainstem called the pons.” [quoted from here]

The most frequently noticed symptoms are impaired speech and difficulty swallowing. We did notice the impaired speech a little bit last year but it never seemed to get worse, and my dad didn’t seem to notice. Within the couple of months, however, it got significantly worse and his swallowing began to be severely impaired. He could not swallow well enough to eat or drink properly, which led to his getting dehydrated again (because hypopituitary medicines were still not being taken correctly). He lost a significant amount of weight, and at one point, my six-foot-tall father weighed just 126 pounds.

In the hospital this time around, they closely monitored Dad’s electrolyte and sodium levels, straightened out his medications, had him on an IV for fluids, and pureed all of his food to make it easier to swallow. They also did CT scans, MRI’s, EMG’s, barium swallow, and all sorts of blood work. After ruling out stroke, ALS (Lou Gerhig’s disease) and several other diseases, they were finally able to diagnose him.

epiglottisThe muscles in Dad’s throat are so weak and slow that the flap in the back of his throat that is suppose to cover the windpipe when he swallows is not able to do it’s job. As a result, he cannot drink liquids because he risks aspirating which would cause instant pneumonia. If his food is pureed, he is able to swallow it, so my sister found a great little food processor that does the job well. The doctors at the hospital want him to agree to have a feeding tube for liquids because it is unlikely that he can maintain a proper hydration level simply by what he eats. Dad really doesn’t want the feeding tube. As it is, he is embarrassed about his speech, and feels like he can never go out to eat again or sit at Waffle House sipping coffee with his buddies. I think a feeding tube would feel like the last straw in attempting to maintain his dignity. The hospital did release him, but with very strong cautions. He is being diligent about keeping up with how much liquid he is getting throughout the day, and will also have follow-ups with his doctors to make sure his medications are properly monitored.

I’ve realized once again that I take so many things for granted. Like swallowing, for instance. I sit here sipping tea as I type this. What if I could never again drink tea? Or a pumpkin spice latte on a chilly fall day. Or a cool gulp of water after working outside in the summer. What about tea parties to celebrate birthdays, or a cup of coffee with a girlfriend? And talking: I do a lot of that. What if everyone suddenly had a hard time understanding me?

It is not very likely that Dad’s condition will improve, but it is possible. I’d appreciate continued prayers for his physical health to improve, but also for him emotionally. This is nowhere near as bad as it could have been, but it still may be hard for him as this has changed his life in some fairly dramatic ways.


Jamie
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Sarah's Family

(Wow! Thanks to Sarah — who is also an adoption coach — for sharing her family’s dramatic adoption story in today’s Guest Post! Look for positive adoption stories like this here on my blog most weeks, and please “grab” this button to put on your own blog and share the inspiration!) ____________________________________ My husband and [. . . continue reading]

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Aug 312010
blog award

Recently I’ve realized, I blog differently nowadays. When I began blogging 2 1/2 years ago, I wrote mostly about homeschooling. But since that time, my life has become more {searching for a word} complex. Right now I simply have less time to just ponder. Right now… …I’m still learning how to be mom to a [. . . continue reading]

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Practicing Gratitude: Gifts #326-350

Listing more of my one-thousand gifts… 326) talking more with my sister lately 327) sleeping late with my hubby on his birthday 328) Kathryn moved to a chess class at a more convenient time 329) a couple of good visits with my dad 330) laughter 331) Ken having time to help with homeschool this week [. . . continue reading]

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It’s just over a month until the first Blogographers’ Meet-Up, so I’d better get busy in letting y’all know some details! So here’s the scoop in a nutshell: Who: Blogographers (anyone who loves blogging) Date: Saturday, October 2, 2010 Time: 10AM -  2PM Location: Marietta Square We’ll meet near the fountain in the middle of [. . . continue reading]

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Weekly Wrap-Up: Week 2

So this was the week when my dad was in the hospital with a mystery illness. The super-frustrating part is he still has no answers, no diagnosis. I think I’m going to have to get rather insistent with someone at the hospital to tell us what is going on. They are talking about discharging him, [. . . continue reading]

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