Our trip to the endocrinologist went well today. Alyssa's A1C was 7.9 (recommended between 6-8 for her age) and there was no change to her regimen. We did discuss the pump and we both agreed that Alyssa will let us know when she's ready. They sent us home with a sample OmniPod (without the connection) so she could try wearing it and see how it felt. The omnipod is tubeless, but they also gave us information about the Paradigm Real-Time Revel and the OneTouch Ping.
Right now Alyssa is dead set against the pump. Her biggest concern was wearing it during gymnastics, cheer, or when she swims; but, we have found out that some pumps can be removed during these activities and some are also waterproof. She doesn't know anyone that has a pump, so I'm hoping once she meets someone that has one, she'll be more open to it. We are going to a pump class next month so that we can have some hands on time with different pumps and also for her to meet others that are considering getting the pump.
Alyssa rarely complains, but on occasion, she asks 'why does she have diabetes?'. On a recent FB post, I shared my answer "Its His plan and maybe its because one day you'll help other T1 kids". And then we discuss how her beta cells in her islets of Langerhans do not produce enough insulin to turn her food into fuel....she thinks the islets of Langerhans is a funny name. So she laughs and that's usually enough. However today, sadly, while we were waiting for the endo, Alyssa said to me that she thought she was going to die early. Diabetes does not run in our family, but my (step) dad was diagnosed with T2 many years ago and is insulin dependent. Currently he is suffering with complications of the disease. He has been recently diagnosed with diabetic retinopathy and moderate chronic kidney disease (stage 3). She may not fully understand these conditions but she knows they are terrible and this is very scary to an 8 year old little girl. My reply to her statement was that she is going to live a long healthy life and that the reason I make sure she checks her blood sugar, eats healthy, and gets insulin injections is so that will happen. This is a double edge sword, on one had you want to shelter your child from the scariness of this disease and on the other, you want to stress how important it is that she take care of her health.
Thursday, April 5, 2012
Tuesday, April 3, 2012
Spring Break
Normally we travel 'somewhere' during the kid's Spring Break, but after my hub's trip to the Middle East and our short get-a-way to the Keys, we decided to push our family vacay back to the summer.
Home for Spring Break=Princess LuLu's Boredom=Hunger
Lu: "I'm Starving!" Me: "How, you just ate lunch?" So the snacking begins......
Alyssa's Top Ten snacks (all under 15 g of carbs)
(light) low fat vanilla yogurt
sugar free pudding cups
100 calorie snack packs
4 pk peanut butter crackers
low-fat, no sugar added ice cream cups
medium apples
grapes
cucumber slices with ranch
string cheese
Caprisun's Roarin Water
Home for Spring Break=Princess LuLu's Boredom=Hunger
Lu: "I'm Starving!" Me: "How, you just ate lunch?" So the snacking begins......
Alyssa's Top Ten snacks (all under 15 g of carbs)
(light) low fat vanilla yogurt
sugar free pudding cups
100 calorie snack packs
4 pk peanut butter crackers
low-fat, no sugar added ice cream cups
medium apples
grapes
cucumber slices with ranch
string cheese
Caprisun's Roarin Water
Wednesday, March 28, 2012
Type 1 Diabetes Research
My posts have been few and far between lately….mainly because I am a full-time wife, mother, business owner, and student… This semester three of my classes all require extensive paper writing so honestly I haven’t had much time to blog. I have really missed it, so I have decided I will at least try to blog twice a month.
I want to begin with how EXCITED I am about the recent FDA approval for testing the artificial pancreas. This study is already under way in other countries. Although I know it will take some time for testing and for it to be made available to patients suffering with Type 1 Diabetes, at least we are on the road!!
Now, for the naysayers who say JDRF is wasting valuable funds researching this artificial pancreas that could be used towards finding a cure~~ WTH!?! JDRF’s mission is also to fund research that improves the lives of those living with this disease. Without research there never would have been insulin, meters, insulin pumps, medication ect…. All of these discoveries keep our Type 1 loved ones healthy and ALIVE! There is still much research going on about beta cell replacement….which if it works…will help the pancreas make insulin on its own. Research takes time and new developments are happening all the time. I do not claim to be a ‘diabetes expert’, however, I love and am the primary care giver of a child who lives with Type 1 and I make it my business to support, advocate for, and research anything that will make her life a little bit easier.
Ultimately, Diabetes SUCKS!! And when I sit and think about what lies ahead for my daughter~ I cry, I get angry, I even scream sometimes…my job is to protect her and there are times I feel helpless. But then I remember there are so many other diseases out there and many other parents who’s children are suffering with untreatable, incurable diseases and I’m thankful that at least we can somewhat control diabetes and I believe we will see a cure. And we are blessed that more and more options are on the horizon.
JDRF First Outpatient Artificial Pancreas Trial Approval
I want to begin with how EXCITED I am about the recent FDA approval for testing the artificial pancreas. This study is already under way in other countries. Although I know it will take some time for testing and for it to be made available to patients suffering with Type 1 Diabetes, at least we are on the road!!
Now, for the naysayers who say JDRF is wasting valuable funds researching this artificial pancreas that could be used towards finding a cure~~ WTH!?! JDRF’s mission is also to fund research that improves the lives of those living with this disease. Without research there never would have been insulin, meters, insulin pumps, medication ect…. All of these discoveries keep our Type 1 loved ones healthy and ALIVE! There is still much research going on about beta cell replacement….which if it works…will help the pancreas make insulin on its own. Research takes time and new developments are happening all the time. I do not claim to be a ‘diabetes expert’, however, I love and am the primary care giver of a child who lives with Type 1 and I make it my business to support, advocate for, and research anything that will make her life a little bit easier.
Ultimately, Diabetes SUCKS!! And when I sit and think about what lies ahead for my daughter~ I cry, I get angry, I even scream sometimes…my job is to protect her and there are times I feel helpless. But then I remember there are so many other diseases out there and many other parents who’s children are suffering with untreatable, incurable diseases and I’m thankful that at least we can somewhat control diabetes and I believe we will see a cure. And we are blessed that more and more options are on the horizon.
JDRF First Outpatient Artificial Pancreas Trial Approval
Friday, February 10, 2012
Diabetes is Ugly
Diabetes has been showing its ugliness.....The last few weeks have been a roller coaster for Alyssa's diabetes. The week before last, I got a call from school 4 out of 5 days saying that Alyssa's glucose levels were high....300 + every morning at around 8:30a. She eats breakfast at 6:30a and gets 2 injections (regular insulin and then a long lasting insulin). So, her sugar should have been within normal range 2 hours later? Over that weekend, her levels were great! Last Monday, I decided to up her regular insulin .5 units (a very little) and I got a call at 8:30a saying her sugar was low. ughhh...so on Tuesday, I backed down the dose....8:30 ~another call and low!! Wednesday and Thursday, the same thing. Weekend was pretty good, a few highs but in the low 200's and likely because she snacked a little more. This Monday morning, a call at 10:00.... sugar was 59! Lowered insulin from her normal dose and Tuesday no call! Thought we were in the clear! Wednesday was an early release day, so I kept her home from school because it would mean she would have to eat lunch at 10:45a, which throws her whole schedule off. Levels were great! Yesterday, call at 10a, sugar 300! What the heck!! Today (Friday) same thing! I swear, I'm losing it! What is insane is that these extreme lows and highs are effects of a minute amount of insulin! The picture below (on the left) is the actual syringe scale. She gets 1 unit for every 25 grams of carbs, usually 2 1/2 units. So,as you can see, 1/2 u is a tiny amount.
Those of you who know me and Alyssa know that I am borderline obsessed with managing her diabetes. I measure EVERYTHING she eats and have learned to adjust for her activity levels. Thank God we have a great Endocrinologist! I know I've called and emailed her 10+ times. Finding that perfect dose has been a challenge and unfortunately what worked one day, has not been working the next!
I'm at the point I think there is another culprit besides the pancreas. I know stress can elevate glucose levels. The blood sugar of type 1 diabetics can increase when they’re stressed because of the production of stress hormones. In most people, these hormones help improve the body’s stress response because the liver releases more glucose for additional energy. For diabetics, however, this extra glucose can result in a dangerously high blood sugar level. My husband was in the Middle East for 2 weeks, and I know she missed him. I tried to keep as much from her as possible, but she knew that he was in dangerous areas at times. Now that he's home, I'm hoping things get back to normal and that her glucose levels balance.
I'm at the point I think there is another culprit besides the pancreas. I know stress can elevate glucose levels. The blood sugar of type 1 diabetics can increase when they’re stressed because of the production of stress hormones. In most people, these hormones help improve the body’s stress response because the liver releases more glucose for additional energy. For diabetics, however, this extra glucose can result in a dangerously high blood sugar level. My husband was in the Middle East for 2 weeks, and I know she missed him. I tried to keep as much from her as possible, but she knew that he was in dangerous areas at times. Now that he's home, I'm hoping things get back to normal and that her glucose levels balance.
Thursday, January 5, 2012
We made it through the holidays!!
Happy New Year!!
Again, it's been a while since I blogged....
Alyssa was diagnosed just 3 days after Christmas in 2010. Facing the holidays in November and December were pretty scary as this would be our first Thanksgiving and Christmas since her diagnosis. I feared that we wouldn't be able to take part in all the holiday baking traditions we had in previous years. Alyssa loves to help me bake so I began to search for recipes for our family's favorite holiday desserts where I could substitute out sugar. We did make regular peppermint sugar cookies and yes Alyssa did have 1 here and there, but we adjusted her insulin. She said it was totally worth it!! Alyssa also loves chocolate pie, so I found a recipe for chocolate chess pie and substitute the 3 cups of sugar with Splenda. A little sugar-free whipped topping made for a happy girl!
Santa was on board this year, and instead of filling her stocking with loads of candy, he opted for hair accessories, lip gloss, nail polish, bracelets, and coloring books. She was ecstatic! And you know what?? She never once asked about where her candy was, even with her brothers who had chocolate and candy canes in theirs. I do let Alyssa have sweets occasionally...everything in moderation. I try to keep her diet as 'normal' as possible. The time of day, her activity level, and bgl just determine the amount of insulin or if any is given. Her endocrinologist assures me she is doing great, her A1C was 8 at our last visit (within range for someone her age) and she's growing so tall. She has gained up to 59 lbs, which is a little on the low end, but like her Endo said, not many 8 year old's are on this strict of a diet. In Sept. 2010, (pre-diabetes) she weighed 56 and then in October she weighed 52 (during our journey to find out why she was sick). The day she went into the hospital she was down to 46lbs. So, I think gaining 13lbs in the last year is pretty good. Trust me, she eats ALL the time! Her food is just healthier options, controlled carb intake, and very little sugar.
Looking back on December 28, 2010 I'm blown away by how different our lives are. Honestly, at that time, I did not think I could handle this situation-- this illness that would change Alyssa's life forever. But today, through education, research, support, and Alyssa's amazing endocrinology team, I feel optimistic for her future. Those that know her, know she is a FIRE CRACKER and even though she drives me crazy at times :), she continues to amaze me with how she has learned to accept what life has dealt her.
Again, it's been a while since I blogged....
Alyssa was diagnosed just 3 days after Christmas in 2010. Facing the holidays in November and December were pretty scary as this would be our first Thanksgiving and Christmas since her diagnosis. I feared that we wouldn't be able to take part in all the holiday baking traditions we had in previous years. Alyssa loves to help me bake so I began to search for recipes for our family's favorite holiday desserts where I could substitute out sugar. We did make regular peppermint sugar cookies and yes Alyssa did have 1 here and there, but we adjusted her insulin. She said it was totally worth it!! Alyssa also loves chocolate pie, so I found a recipe for chocolate chess pie and substitute the 3 cups of sugar with Splenda. A little sugar-free whipped topping made for a happy girl!
Santa was on board this year, and instead of filling her stocking with loads of candy, he opted for hair accessories, lip gloss, nail polish, bracelets, and coloring books. She was ecstatic! And you know what?? She never once asked about where her candy was, even with her brothers who had chocolate and candy canes in theirs. I do let Alyssa have sweets occasionally...everything in moderation. I try to keep her diet as 'normal' as possible. The time of day, her activity level, and bgl just determine the amount of insulin or if any is given. Her endocrinologist assures me she is doing great, her A1C was 8 at our last visit (within range for someone her age) and she's growing so tall. She has gained up to 59 lbs, which is a little on the low end, but like her Endo said, not many 8 year old's are on this strict of a diet. In Sept. 2010, (pre-diabetes) she weighed 56 and then in October she weighed 52 (during our journey to find out why she was sick). The day she went into the hospital she was down to 46lbs. So, I think gaining 13lbs in the last year is pretty good. Trust me, she eats ALL the time! Her food is just healthier options, controlled carb intake, and very little sugar.
Looking back on December 28, 2010 I'm blown away by how different our lives are. Honestly, at that time, I did not think I could handle this situation-- this illness that would change Alyssa's life forever. But today, through education, research, support, and Alyssa's amazing endocrinology team, I feel optimistic for her future. Those that know her, know she is a FIRE CRACKER and even though she drives me crazy at times :), she continues to amaze me with how she has learned to accept what life has dealt her.
Friday, November 11, 2011
What's been going on....
Well, it has been a while since I've blogged.... I've been a very busy girl. Since my last entry in September, we participated in our first walk for diabetes. Our team, Alyssa's Angels, raised about $2400!! We are so grateful for all the people who donated and for all our family and friends that walked with us!!
A lot of things have changed around her since I went back to work. I can tell you that my husband has really stepped up and helped me around here. Outside of the classes I have at the college, I also am taking 2 online classes. So, much of my time at home is spent studying and doing homework. He's cooked many dinners, kept Alyssa when she was home sick and taken the kids to doctor appointments so I wouldn't have to leave work. He's self-employed, so his schedule is much more flexible. The kids have also had to do a lot more. I created a spread sheet with the monthly schedule and chores. My oldest has saved me several times when I wasn't sure I'd get to after school care to pick up Alyssa in time....so glad he can drive!! Trust me, he's super safe now that he's had a car wreck and had a deer hit him!
We had a little break!! Hubby and I took a trip to Key West and Alyssa spent several days between her 2 grandma's. The grandmas did a great job taking care of her!! It was a nice break for us and I'm sure for Alyssa too. The poor thing never gets to spend the night away from home....
Back to reality......Alyssa has adjusted well to our new busy schedule. Right now my schedule consists of morning classes and working 32 hours a week at a medical office. Everything has been going along smoothly until we had a battle with a cold last week that threw her sugar off the charts! Just when you think you have a handle on this disease, it throws you something else. She made it through only 1 whole day of school last week, came home early Monday of this week with a level near 400, but thankfully she's been well since Monday afternoon!
Alyssa has been taking gymnastics once a week for the last 2 months, but beginning next week we are going to add a private lesson as well. She is really enjoying it and learning so much! Because her glucose levels are so sensitive to activity, we check levels and give a snack to cover what she'll burn during the class. Then re-check after class.
The clinic I work at is an integrative health practice. I have learned so much about the holistic approach and I am currently researching the effects of chromium on diabetes. What I have found so far is that it is an insulin potentiator, so it makes the body's own insulin production go further. I'm still researching....
A lot of things have changed around her since I went back to work. I can tell you that my husband has really stepped up and helped me around here. Outside of the classes I have at the college, I also am taking 2 online classes. So, much of my time at home is spent studying and doing homework. He's cooked many dinners, kept Alyssa when she was home sick and taken the kids to doctor appointments so I wouldn't have to leave work. He's self-employed, so his schedule is much more flexible. The kids have also had to do a lot more. I created a spread sheet with the monthly schedule and chores. My oldest has saved me several times when I wasn't sure I'd get to after school care to pick up Alyssa in time....so glad he can drive!! Trust me, he's super safe now that he's had a car wreck and had a deer hit him!
We had a little break!! Hubby and I took a trip to Key West and Alyssa spent several days between her 2 grandma's. The grandmas did a great job taking care of her!! It was a nice break for us and I'm sure for Alyssa too. The poor thing never gets to spend the night away from home....
Back to reality......Alyssa has adjusted well to our new busy schedule. Right now my schedule consists of morning classes and working 32 hours a week at a medical office. Everything has been going along smoothly until we had a battle with a cold last week that threw her sugar off the charts! Just when you think you have a handle on this disease, it throws you something else. She made it through only 1 whole day of school last week, came home early Monday of this week with a level near 400, but thankfully she's been well since Monday afternoon!
Alyssa has been taking gymnastics once a week for the last 2 months, but beginning next week we are going to add a private lesson as well. She is really enjoying it and learning so much! Because her glucose levels are so sensitive to activity, we check levels and give a snack to cover what she'll burn during the class. Then re-check after class.
The clinic I work at is an integrative health practice. I have learned so much about the holistic approach and I am currently researching the effects of chromium on diabetes. What I have found so far is that it is an insulin potentiator, so it makes the body's own insulin production go further. I'm still researching....
Thursday, September 22, 2011
Strep Throat & Diabetes
So, Alyssa woke up this morning with a fever and sore throat! She has had sniffles for the last few days, but so has everyone in my house. I was hoping it was just allergies, but when my hubby took her to the pediatrician this morning they gave her a strep test and it came back positive. So, now she will be taking amoxicillin for the next 10 days and out of school until Monday. My oldest son also had a sore throat and stayed home from school, so their doctor went ahead and prescribed him an antibiotic as well and suggested he stay out of school until Monday too. At least he can stay with her tomorrow while I am at school.
Catching a cold or the flu is no fun, but it can be even worse if you have type 1 diabetes. Some over-the-counter cold treatments contain sugar, which can make blood sugar levels higher. Also, dehydration, fever, and nausea can cause blood sugars to rise and for ketones to be released. Colds can lead to pneumonia and other serious health problems. People with diabetes are three times more likely to suffer from these conditions than non-diabetics.
This afternoon, she said she felt shaky as if her bgl were low. But when we checked her levels it was 134?? And when I checked her temp, it was 102. It was close to dinner, so I had her try to eat. I’m always concerned when she isn't feeling well that her levels will drop, but it always tends to run a little higher. Crazy!
Anyway, she had some children’s ibuprophen and her first dose of amoxicillin and was able to eat a bowl of chicken noodle soup and some orange slices. Thankfully her fever is down for the moment…..keeping my fingers crossed!
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