I don't often blog about diabetes anymore, I mean, there isn't much to say, highs, lows, shots and checks...life goes on. Anyway on the way to school today we were listening to a station we don't normally frequent (we usually listen to the Christian station) but we were half listening, kind of talking, dropped the big boys off (Thank goodness) and continued on to Ryan's school. The skit was some small character, it was strange...weird voice...whatever. He was talking about bad Christmas movies, the first one was rude but nothing tweaked my radar. The second one. oh my. "how do you know you're watching a bad Christmas movie? If Santa loses his foot because of diabetes it's a bad Christmas movie" Excuse me? seriously? I thank God that Lane Michael wasn't in the car, Ryan asked if that can happen...what do I say? I told him that if Lane Michael doesn't take care of himself then someday it can but not today. I'm angry. So I wrote to the radio station (I waited until I calmed down). I explained what happened, and how Lane Michael has a hard enough life and what they've just done is made him an easy target...made it cool for kids to joke about this...and told them how they've impacted my families life...I even explained how important ratings are, and I'm sure their concern is not my child but I just wanted them to know how they had effected us. they said the morning show is from Columbus Ohio and they'd address this as soon as possible. I hope they do.
Wednesday, March 26, 2014
Monday, June 3, 2013
Crap My Kids Do
This post is more for me and my memory - I want to remember someday all the funny things my kids are doing at this age. Ryan - age 3 - at the ball field yesterday he was talking to another child and his grandma. I wandered over to retrieve him and the Grandma said "oh Connor's fine, he's telling us that he's 5 and going to kindergarten in the fall" sigh. "Connor lies. his name is Ryan, he's 3 and he's not going to kindergarten" Girlfriend - age 2 - can't say booty. so singing "shake your booty" only ever comes out "shake your bobby" ha! She's also my little mini-me! This weekend I was finishing my dinner and she was standing next to me directing me "you not done mom! Eat you corn! you. are. not. done." So funny! She loves to be in my space and thinks she is big! wants to have coffee with the ladies and maybe even a cocktail! Not yet little girl! Little Miss - age 2 - Little Miss is a comedian - people smart, reads people well so I have no doubts I'll forget how funny she is but I want to remember this past weekend when we made huge strides in bonding with her (it's good for a child to bond to their caregiver - even if temporary - so that they know how to bond and will bond to future caregivers if not the same as current) anyway someone at church asked her if they could take her home with them (people always do this thinking its funny and it really bugs me on lots of levels) anyway for the rest of the day she was very clingy - in a constant state of a hug with me. she never left my side and sat on my lap as much as I'd allow her to. this is HUGE for Little Miss who before would welcome going with anyone, especially a man. and one more thing - Little Miss discovered swimming this weekend! She is fearless in the water! A true little water bug! She is jumping off the diving board at the pond, pops up and giggles! I bet she's swimming without a floaty by the summers end! Ethan - age 10 - right now Ethan is perpetual movement (unmedicated for the last week of school so he can enjoy all the food treats they give out) so yesterday when going up to bat he took a huge leap to get into the batter box - Rebecca called it his gallop...and later called him a gazelle because he takes such long strides on itty bitty legs - love this boy! he also has taken up snuggling with the chickens - like they're pets Lane Michael - age 10 - if I'm truly honest, Lane Michael isn't a funny kid. Lane Michael is serious and refined more than funny - his attempts at funny are usually awkward and sometimes inappropriate - but what I want to remember is that at the beginning of the 3rd grade he was figuring his own insulin. He can look at the box, measure out a serving and divide out how many units he needs for that serving and add to it any correction dose. He is simply amazing!
Posted by Unknown at 5:55 AM 0 comments
Labels: Ethan, Lane Michael, Ryan
Wednesday, April 3, 2013
The Best Kind of Friends
Ethan and Lane Michael had a chance this weekend to spend the night with my Mom and Step Dad, it was good for them. They had a great time. They didn't have school Monday so they stayed over Sunday night and hung out there on Monday. So since Mom had an early meeting, the boys all got to hang with their Grandpa Jack for the day...but we couldn't possibly leave Grandpa Jack with no cigarettes and 3 little boys (my nephew was there too). So after Todd and I took our little 3 home for bed, Mom headed to town for some smokes. Ethan decided he should ride along. Some of the best talks are had in the car. They started talking about friends and who was Ethan's friends and who did Lane Michael hang out with. Then Mom asked Ethan if he and Lane Michael are friends and without missing a beat Ethan said "we're the best kind of friends, we're soul mates."
Posted by Unknown at 11:07 AM 1 comments
Labels: Ethan, Lane Michael, twins
Friday, October 5, 2012
Boys of Fall
My Boys of Fall. Oh be still my heart! LITTLE MONSTER
Smart, funny, lives in his own show tune, this boy...my oh my! At football they call him Taco...we have no idea why. Lane plays first string on the line and is second string Center. And in recent practices he's been the Tackling Taco! Known to bring down the big boys during a scrimmage and very rarely sits the bench! It's such a big difference from last year when they only played a few plays during the last quarter. I'm sad to see football come to a close but so excited to get a good schedule going!
Posted by Unknown at 1:04 PM 0 comments
Labels: Ethan, Lane Michael
Thursday, March 15, 2012
Raising Brothers
Last night, I had the pleasure of witnessing one of my favorite things about brothers. Lane Michael was walking a few feet in front of us, he was unhappy because we had once again had to remind him that not every conversation (this one about downs syndrome) was about him. Ethan caught up to him and put his hand on Lane's back and was whispering something in his ear, I could hear him enough to know it was rapping/singing and occasionally Lane Michael would laugh at whatever Ethan had said. They walked like this for nearly a block before they saw Schneiders Market and took of running/racing to pick their treat for the night. such a special moment in their life, and I got to observe it.
Posted by Unknown at 10:56 AM 0 comments
Labels: Ethan, Lane Michael
Tuesday, September 13, 2011
Celiac Disease
Lane Michael's blood test came back (regarding celiac disease) and once again his markers are higher...we have an appointment on the 26th with GI at 3:15...she wants to look at growth, stomach issues (pain, constipation etc) and discuss his next biopsy and get that set up. The first year we faced this I was a nervous wreck, I didn't know how we'd make this life change, I didn't know what to feed him or how to take him to other people's house's, I cried, and I mourned, I know this disease isn't the end of the world...but it sure felt like it. The second year, I was ready, I thought we'd surely get a diagnosis, I just knew I could take this on, I could make this change and make it good. This would be ok. This year, I don't know how to feel. I don't want this. I've been thinking of all the changes we'll have to make. The foods we'll have to give up. All his favorite foods, like pancakes, donuts, spaghetti, lo mein...Lane Michael could live off lo mein. I'm sad again. I'm not ok with this. What would we feed him on vacations? Who could I trust to care for him in an emergency? Todd is saying that the change is too expensive for everyone to make, that we can get gluten free for him and gluten for us...that's not fair to him. I don't want him to be more different than he already is. I will pray.
Posted by Unknown at 7:49 AM 1 comments
Labels: celiac disease, Ethan, football, Lane Michael, twins
Monday, March 28, 2011
A Taste is Too Much
This weekend I was standing in my kitchen, when I realized I didn't feel well, I had a headache, my stomach was sort of cramping, I was light headed and shaky, and a panicked feeling came over me. It was a nervous, sweaty panic. I had 4 nieces and a nephew hanging with us for the day and I was terrified. It finally dawned on me. My sugar was low. I tested and sure enough I was heading low...which is strange since I've never felt anything like this and had eaten that day (I don't usually eat breakfast but had oatmeal and coffee with a little sugar). It wasn't until I had eaten something and started to feel better that I realized that so much of Lane Michael's life is feeling like that. Headaches, shaky, nervous, panic. It was a slap in the face of reality. His reality. I have a new appreciation for what he goes through, I now realize, the pokes, the shots, the blood work...that's the easy stuff compared to that feeling.
Posted by Unknown at 5:18 AM 0 comments
Labels: Lane Michael, type 1 diabetes
Wednesday, February 9, 2011
Mama said there'd be days like this
Posted by Unknown at 11:06 AM 0 comments
Labels: Lane Michael
Monday, July 12, 2010
A Buffet of Auto Immune.
Last year Lane Michael was tested for Celiac, we left the biopsy with our doctor (who we loved and trusted) saying "I am 98% positive that he has Celiac, don't start the diet but be aware that we will call and confirm this in the next few days" A week or so later I was walking through WalMart over my lunch hour, when the hospital called back. Lane Michael has an infection that mirrors celiac disease, he does not have it at this time, be checked again in a year and take this medication for 2 weeks to clear up the infection. The blood work last year showed he had 11 markers for Celiac and anything over 5 was abnormal. So this year I was more prepared, I went with a list of the symptoms he has, a list of concerns and questions. He has constipation, and stomach cramps and he seems thinner. When we sat down with the doctor she said that his bowel doesn't seem to be emptying completely, he went from being in the 58th % to the 45th % and he should not have dropped that drastically in one year. She said the stomach cramps are concerning. and then she told me that he now has 26 markers in his blood work for celiac. This year I'm ok with this diagnosis. Last year I couldn't have handled it. This year I can. I am not facing a new baby in the house, and Todd's job change, this year I am at peace with this diagnosis. I have accepted it, and I'm ready for it. I'm sad for him, for my family, for the changes we'll face, the challenges ahead, Lane Micheal hates pizza, that's a plus but pancakes are his favorite. How will we eat at Bob Evans? How will he share birthday cake with his friends? We will figure it out. More than anything I just want to start living life with him...a normal life. I want so many things for this little person. The thing is I don't worry about him, I don't worry about whether he will be successful, I know he will be. I know that God has great plans for him and this is his path, the path he has to take in life to get there, to be the person he has planned him to be. This weekend a little boy came to the party and was introduced to all the boys at the party, they were all playing video games, they all waved over their shoulders, Lane stopped what he was doing, went to the little boy and said "Hi Alex, I'm Lane nice to meet you" because as much as he has going on, he's still able to care about other people. What a special boy! So I asked the doctor "is there something linking all of this together? something that could explain all of this?" She told me "yes, he is a buffet of auto immune diseases, his body is his own worst enemy and it's just attacking itself, he has an over active immune system" hm. man that sucks. And the kicker? Ethan needs checked. Celiac can cause small stature and hyperactivity, ADD and learning disabilities. Nice, so maybe we can explain some of his ADD stuff!
Posted by Unknown at 5:57 AM 1 comments
Labels: Lane Michael, type 1 diabetes
Monday, October 19, 2009
Six Things About Lane Michael
1. Lane Michael likes school, he's excited to go every morning and last year when I asked the principal how he was doing socially, I was told not to worry...he's a bit of a social butterfly...everyone knows him and really enjoys him!
2. He loves TV...loves it...obsessively! It's hard to make him turn it off, he loves it, he can't help it. He would rather watch TV than do anything! He would never turn it off if that was an option...he even fights me when I tell him to turn it off...it's strange the love he has for TV
3. Lane loves to play board games...he'll take his turn and my turn both, he doesn't care if I'm actually playing as long as I'm sitting with him...and every once in awhile ask who's winning...he's pretty honest about it too! LOL
4. He's a morning person...up before any one else and very happy about it...he tiptoes past our door and heads straight for the basement...to watch cartoons of course!
5. Lane is clumsy....like really REALLY clumsy! He falls UP the stairs at least once a day...at least! It's hysterical!
6. He's really sensitive...he doesn't want to be laughed at and it really hurts his feelings if he is but has no problem laughing at others. He's also easy to cry...Todd and I aren't so dealing with his sensitive side is hard for us...but I've noticed that if we don't brush him off but validate his feelings, he comes around much quicker!
That's my boy...6 things about his super sized personality!
Posted by Unknown at 9:50 AM 1 comments
Labels: boys, Lane Michael


