How shall I put this?
*Baby #5 is on the way.
*We're trying to catch up to the Duggars.
*We've jumped on the baby bandwagon. (It would be more appropriate to say we've been thrown under the wheels of the bandwagon.)
We got a HUGE shock recently when we found out we are expecting again. Whoa. I posted recently about Mallory's obsession of getting a new baby. Elizabeth joined in on the requests as well. After being told countless times, "No, we're done." she took matters into her own hands and began praying... for twins. Well, apparently her prayers have been answered. But so have Edward's because the ultrasound only revealed one. New baby is due December 15th.
Surprisingly, I'm not feeling as sick as I normally do. This is a completely new concept for me. It's strange not to have to be confined to the house for fear of V.A.A.A. (that would be Vomiting Anytime and Anywhere). I do feel nauseous in the evenings, but I am grateful that it isn't so severe. It's starting to subside some as I am nearing the end of my first trimester.
It has taken a while for this to sink in. The other kids were all invited to join our family. This one is definitely making a surprise appearance. I truly believe he/she is meant to be here as Edward and I were taking the necessary steps to prevent an expansion in the family.
Monday, May 17, 2010
This Is What Happens When You Get Rid Of All Of Your Baby Gear
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Thursday, May 6, 2010
Braggy Mom Post
One Friday a few weeks ago, Elizabeth told me, "Mom, I have some of my artwork in an art show. It's tomorrow at ________ (our local community college)." In the midst of my mom duties I muttered something like, "Oh, that's nice, Honey." The next day Elizabeth said to me, "Are you ready to go to the art show?" "Uhh... sure." It wouldn't be completely dishonest of me to say I forgot about it. The girl and I freshened up and headed out the door. I expected to see a nice little display of elementary schoolers' artwork. When we walked in the door, I saw this:

We searched and searched and searched until we found Elizabeth's. We were thrilled when we saw a third place ribbon on her 3-dimensional mask! The crazy thing is that when Elizabeth's art teacher gave her a note telling her she submitted this mask made at the beginning of the year, Elizabeth couldn't even remember what she was talking about. After a while it dawned on her what her teacher was referring to. And her teacher later told me that she realized that she didn't have any artwork to submit for the design category so she went through her stash to see what she could find. She came across this piece that was in the back of a closet. She decided to submit it, and we're glad she did!
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Tuesday, April 27, 2010
Birthday Girl

Our sweet little Mallory turned three! She brings such joy into our family and is every one's toy. She is a very obedient child, and she is eager to help others. She is such a sweet girl.
She likes for me to carry her around. Obviously at three years old, she's getting a little too big (even though she is a very tiny thing) for me to do this. For the last few weeks I've told her that when she turns three I'll hold her on my lap as much as she wants, but she will have to walk when ever we go somewhere. So she's been taking full advantage of it this last week. Last week as we were running errands, I would get her out of the van and put her down. She would immediately raise her arms to me and say, "I'm still two, you know." She's pretty hard to resist. She has been doing a great job walking by herself now that she is three. This morning, I carried her out of bed to drop the kids off at school, and she was still in her jammies and bare feet. When we got home, I just carried her into the house so her little feet didn't get cold on the garage floor. She looked confused and stated, "I'm three now." Obviously I was breaking my own rules.


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Friday, April 16, 2010
2010 Walk to Cure Diabetes
Saturday, April 10 was a beautiful day for a Walk to Cure Diabetes! It was a special treat for us as this walk was held in our small town. About 40 people joined our team, Ross's Gator Crusaders. Again, we were humbled by the support we received from family and friends. Our small diabetes support group worked with the organizers of the event, a young lady named Brianna (diagnosed at age 7) and her mother, Becky. They originally hoped to have 100 walkers take part and to raise $1,500. An estimated 500 walkers were in attendance and $15,000 was raised for JDRF! As a family that is affected by type 1 diabetes, we can't even begin to say how important this is! This money will be used to make life easier and more comfortable for Ross and will put a cure within our reach!
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Monday, April 5, 2010
Thursday, April 1, 2010
March 32nd
...or in other words, APRIL FOOL'S DAY! Ahhh, one of my favorite days of the year. As I've said before, I don't like the mean-spirited tricks when victims feel bad. But come on, who doesn't like a good gag! I've participated in April Fool's Day over the years, and my family still keeps me around. I've spent the last few nights getting some ideas off the Internet. This was the first year Edward pulled some of his own. Man I'm a lucky gal! First of all, I invited my old pal Jose over to welcome everyone to the breakfast table. Jose came to be from old Halloween gear from the basement.



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Sunday, March 28, 2010
The McDorklesons
Every time we go into a shoe store Elizabeth always smuggles home a few of those nylon stockings people can use when they try on shoes. She smuggles them home for the sole (heehee) purpose of putting them on her head. All six of us traipsed over every inch of the mall last night to look for shoes for Ross. And I should have known that the nylons would appear in our house today. And this is what we did with them....




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Sunday, March 14, 2010
Chicken Terror
This weekend we tagged along with Edward on a business trip to Branson. Edward's district manager organized a group outing to Dixie Stampede Saturday night. The Dixie Stampede Dinner and Show involves live animals, acting, stunts, lighting, sound and pyrotechnics. It was a lot of fun, and the dinner was ENORMOUS. No silverware is allowed, so the kids thought it was wonderful! At one point during the show, the waiters put huge, hot Cornish hens on each plate. I leaned over to Drew, and while reaching for his hen, I started to say, "Here. Let me open up your chicken so it can start to cool." But before I could finish the sentence, Drew nearly flew into my lap and screamed, "NO! Don't! It's too scary!!!!" I was a bit stunned, and it took me a minute to figure out what he was even doing. I thought he was joking at first, but it was soon evident that he was scared to death. I tried to get him to calm down, and he finally explained that he was too scared to see the "chicken's insides." I got it out of him that he was scared to look at it's skeleton. You would have thought someone was chasing after that boy with a chainsaw!
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Tuesday, March 9, 2010
This Kid Can't Catch a Break! Except He Kind of Did.
This is almost getting comical. It was off to the doctor again today with Ross. This time, the diagnosis is a fractured thumb. At baseball practice last night, he took a hit right on the knuckle. It was the very last thing he did at practice, and he toughed it out as we left. We put ice on it before bed, just thinking it was just smashed. I got a call from the school nurse this morning telling me she suggested we get it checked out. I ran him over to our beloved family practice physician where she splinted him and sent us over to the hospital for x-rays, just to be on the safe side we thought. We left the hospital a half-hour later, and we were told our doctor would probably call us in the morning with results. Another half-hour later our doctor's receptionist called to let us know his thumb was indeed fractured. I must have sounded like a total moron when I very exaggeratedly (made up word, I know) kept saying, "IT IS?!?!" Next stop is ortho in the morning. To be continued.... As Ross was walking down the hall at school this morning, sporting an ice pack, a girl that has a crush on him stopped him and asked him all about it. When he told her he got hit with a baseball at practice, she told him, "Oh, you're SO tough!" For those that know Ross can just see him rolling his eyes as she said that! :)
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Thursday, March 4, 2010
Cute Question of the Day
This morning Mallory asked me, "Do grandmas have mommies?" I love how two-year-old's brains work! It reminded me of some of Elizabeth's questions at that age. I vividly remember her asking, "Do chickens have lips?" and "Do cats have hineys?" I love it.
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Wednesday, February 24, 2010
We're Gonna PUMP... You Up!
Something exciting is going on at the Felker house, and it's called an insulin pump! Hooray! We are all very excited. We've heard nothing but positivity from people who have pumps. I've been ready to get one as soon as possible, but when we were initially diagnosed, our endocrinologist said he kind of likes to wait until a patient is about a year out of diagnosis so we can learn the ropes of diabetes, so to speak. We work REALLY hard to keep Ross's blood sugar under control. At the end of last year we ran into a really rough patch. Ross would go to bed within normal range (80 - 150), would sleep all night without getting a snack of course, and wake up in the 300-400's. It was very frustrating. Our nurse practitioner suggested getting started on a pump, and I think we were all more than ready. After trying something new in the mean time, we got over that hurdle of highs.
We attended a pump class at the hospital in January to familiarize ourselves a little more with how pumps work. They are pretty awesome. It's kind of similar to an IV that will be hooked up to him pretty much 24/7. He will remove it to shower and to play full-contact sports. He can leave it unhooked for up to an hour. If he needs to have it removed for a longer period, say for swimming, he would just hook it back on, enter a dose, and remove it again. The actual pump houses the insulin that travels through a tube (similar to an IV) to a patch on his skin. He can wear this patch on his stomach, legs, or arms. The outside of the patch will have a clip type of mechanism that actually attaches to the tubing. On the side of the patch that will stick to his skin will be a very tiny cannula that will go through his skin about a fourth of an inch to his fatty tissue. This cannula looks like a small spider leg to me. It is about the width of a couple of strands of hair. He will rotate sites where the patch attaches every three days. He will have a little insertion device that will "punch" the patch into place. It isn't nearly as bad as it sounds. Most people say that the finger sticks are much worse than attaching a patch. Ross even had one attached at the pump class, and he said you couldn't really feel it.
In addition to having a pump, we are also getting a continuous glucose monitor (CGM). He will have a second patch, or sensor, on the opposite side his pump is attached (other side of the stomach, other arm, other leg). This is a tubeless system. A handheld device (to me it kind of looks like one of those electronic 20Q games) will be able to tell us where his blood sugar is at all times without having to prick his fingers. He will have to prick his finger twice a day to calibrate the device, or make sure it is reading his blood sugar correctly. It will be able to tell us how he is trending. If we take a BG (blood glucose or blood sugar) reading and it says 100, that sounds good to us. But is he dropping rapidly from a 250 to a 100? Will he continue to go down? That is a big benefit of a CGM. Those kind of things will help us have a little more peace of mind when it comes to sports. To us, one of the biggest benefits of the CGM is that we can set an alarm to sound anytime he drops below a certain number or rises above a certain number. After the episode that landed us in the hospital and another scary situation in January, that gives us a lot of comfort! Unfortunately, the device only registers up to five feet away. Edward and I wish we could keep the device miles away to see what his BG is any time! :)
We made a decision on our pump, and it arrived last week. We go back up to his hospital next Monday to get started. And, we've been bugged for months by this 10 year-old boy for a cell phone, and he's been repeatedly told, "No way, no how." Well guess what? This pump that we chose came with a smartphone that houses the control center for the pump! So, he got his phone after all. I was telling a friend about this situation, and she told me something I hadn't really thought of. She said, "After everything that boy has been through, that's just fine! That's the least that can be done for him." And she's right. Ross says, "I'll be the only kid in my whole school that can have his phone out at school!!!" I don't know if he's more excited about the pump or the phone!
Exciting times here!
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Friday, February 19, 2010
Desperate Times Call For Desperate Measures
Mallory has changed her tune from wanting a kitten to wanting a baby. That is her new obsession. I hear, "I want a baby" several times a day. My reply is always, "You'll have to talk to Daddy about that. He doesn't want to have another baby." She knows she's not getting him to budge at this point. So her little brain has been hatching a plan. She informed me earlier this week that, "Since we can't have a baby, we will just steal one from some people." She told me this with a straight face and an earnest heart. She is completely serious. I told her, "Oh my! We could never do that." She simply and sincerely asked, "Why?" I told her if we stole a baby from people, they would be very, very sad. I asked her if she would be sad if we had a baby and someone stole it from us. She barely shook her head yes. And then said, "We can still steal one." She's getting desperate.
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Thursday, February 11, 2010
Ross Keeps Us On Our Toes
I do believe Ross has his holidays mixed up. Halloween is the holiday that you are suppose to scare everyone, not Valentine's Day.
I was murmuring about a snow day on Thursday when I got the text Wednesday night that school would be cancelled the following day. By early Thursday morning, I was grateful he was home with me, not in his homeroom.
The kids all slept on the floor together in Mallory's room Wednesday night. Sometime during the night, Drew had a bad dream and came to sleep on my floor. Grateful for the chance to sleep in, I dozed in and out of sleep in my comfy bed Thursday morning while I listened to Mallory, Elizabeth, and Ross playing in her room. Elizabeth came in screaming something about Ross shaking and she couldn't wake him up. I don't exactly remember what she said, but I know I was running down the hall before she could finish telling me. I found Ross on the floor, face-down, partially under the bed convulsing. I rolled him over to find his eyes closed, his body rigid, and his lips blue while he twitched and labored to breathe. He was making very scary, almost gurgling noises. I began shouting his name and rubbing his chest with my knuckles, trying to stimulate him. Within a few seconds color returned to his lips as his tongue moved enough to allow the air to reach his throat. He stopped convulsing just a second later. I presumed it was his diabetes, so I pulled out his glucose monitor to test his blood. I'm beating myself up now because I should have given him an injection of his emergency glucogon. It is a special syringe and vial that he carries with him at all times to be used if he is ever unconscious. Anyway, as I tested his blood, it was 140 which is completely normal. That is why I didn't use the glucogon - because his blood sugar was normal. Anyway, I held a glucose tablet (rapid sugar tablet) to his lips to see if he could lick it, but he could not. I then had Elizabeth go get some juice. I squirted a few drops into his mouth and he began to swallow a little. He slowly began to take in a little more. Within five minutes he was awake and reactive and taking in juice on his own. I tested his blood, and he was already at 245. I was grateful it was rising. He was very upset to learn what had just happened. He had no recollection of even waking up that morning, even though he had already been awake for at least a half an hour. According to Elizabeth, they played for about a half-hour. Ross was sitting up on the bed, watching the girls play on the floor beneath him. She said he sat straight up and just dropped to the side and began convulsing and making "funny"noises. He then fell to the floor, and she thought he was joking. She kept calling his name and tried to tickle him. When he didn't respond, she came to get me.
After I felt Ross was stable, I called his endocrine team at Cardinal Glennon Children's Hospital to tell them about the episode. They suspected his 24 hour insulin (He takes a dose of Lantus at bedtime.) needed to be reduced from 20 units to 18. The nurse thought that possibly he had a seizure because he was hypoglycemic, or low, and when I began to stimulate him, his blood sugar rapidly rose. That didn't sound so feasible to me because everything happened within about three minutes. But... who am I to question an endocrine nurse?
He very shortly began complaining of a severe headache. He was just writhing in pain, trying to get comfortable. I gave him a dose of ibuprofen, but it didn't touch the headache. An hour-and-a-half later I gave him a dose of Tylenol. He begged me to call the hospital back. I said maybe we should give the Tylenol a half-hour to work. If it didn't then I would call. Well, it didn't, so I called the nurse back. I told her I was very concerned about the headache. She told me she wanted to check with his endocrinologist and stepped away from the phone for a few minutes. She got back on and said Dr. Dempsher thought perhaps this was not diabetes related and wanted me to take him to our ER since we are an hour away from the children's hospital. I called my mom/neighbor to come up with the other children, and we were at the ER in five minutes. He already began feeling a little better at that point. When we got to the ER, they took blood tests, performed an EKG, and a CT scan. The first two were fine, but the doctor said he saw some swelling on his brain. I was a little concerned at that point, but not too much because he had no fever and his white blood counts were normal. He wanted us to be taken by ambulance to Cardinal Glennon. I was glad to go. By the time we got there, Ross was pretty much feeling just fine.
Lots of waiting and lots more questions in the Cardinal Glennon ER. I felt a lot of relief when the neurologist said she saw no sign of swelling on the CT scan. She said when people aren't use to reading pediatric scans, they can mistake a child's brain as being swollen when actually it's just kind of "crowded" into the skull. Our beloved diabetes nurse heard the crazy news and came to find us. He did not think any of it sounded diabetes related. A few minutes later a diabetes nurse practitioner came in to get the history. She did think it was diabetes related. Shortly after that we were told we were being admitted for more testing.
We got comfortable in our room and tried to settle in for the night. Ross continued to feel fantastic and has continued to. We woke up this morning to waiting, testing, waiting, testing, and more waiting. He had a MRI and an EEG. All were clear as expected.
Basically, the diagnosis is this was just a random thing. The neurologist told us that as kids are growing and developing, and their brains are continuing to grow, sometimes an electrical misfire occurs and can cause this. He said chances are 70% to 80% that he will never have another episode again. If he would have another seizure, technically it will be considered epilepsy, and he will have to go on medication. Right now, there really isn't anything to treat.
Edward and I are a little divided on this. I believe this was not diabetes related because I tested his blood within three minutes of the seizure, and he was in normal range. On a side note, had I given the glucogon, it wouldn't have helped, but I'm still kicking myself over it. It wouldn't have hurt anything if I'd given it to him. Anyway, Edward feels it was diabetes related. He believes his blood sugar was low but as he began seizing, his liver produced a natural glucogon (which we all have) which rapidly raised his blood sugar. We'll never really know, I suppose.
We feel grateful for the love and concern we've received. I continue to have the word GRATEFUL in my mind today. I'm grateful Ross is well. Grateful for modern medicine. Grateful for my family. Grateful for the peace I feel. Grateful.
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Friday, February 5, 2010
Our Trip to Nauvoo
I keep forgetting to post about our trip to Nauvoo, IL. We travelled to this historic little town in late October. It's a sweet little place that takes you back into the mid 1800's. This website provides a little more information. "Historic Nauvoo is located in Western Illinois, bordered on three sides by a bend of the mighty Mississippi River. The restored homes, mercantile establishments and community buildings maintain the charm of what once was a beautiful, industrious city. Today, Nauvoo provides an opportunity to experience the people and times of the past."



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