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Amy Stockwell Mercer

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Amy Stockwell Mercer

Monthly Archives: November 2011

Strength in Numbers (Diabetes Forecast Profiles)

30 Wednesday Nov 2011

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advocacy, blood sugar management, Chronic Illness, diabetes, living well with illness, type 1 diabetes, women's health

I met Sysy Morales at the Diabetes Sisters conference last May and was impressed to discover that not only was she the mom of twins, but she was also the co-founder of The Girls Guide to Diabetes blog. Sysy and her younger sister, Ana were diagnosed within months of each other, just like my younger sister and me. The two women share stories on the blog about living with diabetes as a woman-one from the perspective of a mother and the other from the perspective of a college student.

Diabetes Forecast has featured Sysy, Ana and The Girl’s Guide in their December issue about teamwork. There are also profiles of Jessica Apple and A Sweet Life and Mari Ruddy of Team WILD.

Read more here:

Teamwork: Banding Together to Tackle Diabetes

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Insulin: It’s a Good Thing. Really!

30 Wednesday Nov 2011

Posted by alsmercer in diabetes

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Amy Campbell, blood sugar management, Chronic Illness, diabetes, type 1 diabetes, type 2

More great advice from Amy Campbell, CDE and Diabetes and Nutrition Educator at Joslin Diabetes Center on her Diabetes Self-Management blog.

She’s speaking more to type 2′s then type 1′s in this piece but I think it’s a good reminder for us all that insulin is not the enemy and should be used well.

Insulin: It’s a Good Thing. Really! (Show All) :: Diabetes Self-Management.

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Artificial Pancreas, is there really such thing?

28 Monday Nov 2011

Posted by alsmercer in diabetes

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artificial pancreas, blood sugar management, Chronic Illness, cost of diabetes, diabetes, JDRF, living well with illness, type 1 diabetes

According to CNN’s story:

Artificial pancreas could be ‘holy grail’ for Type 1 diabetics

I have such mixed feelings about this because when I read the story I can’t help getting excited, but I also feel like it may be too far off for me to benefit in my lifetime. I like that the research is focused on making our lives easier in the here and now as opposed to waiting for a real “cure” but I wonder what this artificial pancreas would look like…how much equipment would we be wearing? I want to see more photos.

This statistic caught my eye:

According to the Juvenile Diabetes Research Foundation, about 80 people a day are diagnosed with type 1 diabetes. Approximately 3 million Americans are living with the disease. Most of them only have healthy blood sugars 30% of the day. The foundation says it has spent $1.5 billion on diabetes research, $40 million of that on research on artificial pancreas systems.

Healthy blood sugars 30% of the day…..that means 70% of the day most people with type 1 have ‘unhealthy’ blood sugars. wow.

Here’s more:
“Our goal is to drive the development of artificial pancreas systems,” Kowalski said. “This could not only improve tremendously glucose control, and help reduce the risk of these terrible diabetes complications, it could also help people with diabetes live easier. The bottom line is diabetes is a 24 hour a day, 7 day a week, 365 day a year job and if we can make some of that easier that would be a huge step forward.”

Well said.

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Low Blood Sugar And a Child’s Fear

28 Monday Nov 2011

Posted by alsmercer in diabetes

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blood sugar management, Chronic Illness, diabetes, living well with illness, motherhood, parenting, type 1 diabetes, women's health

In 2008 I wrote a post called, “Scary Diabetes Stories.” Here’s what I said:

There was a story in the local paper yesterday about a 5 year old calling 911 because his mother was in a “diabetic coma” and last week, there was a story in the news about a diabetic man getting into a car accident and last night there was an ad on TV preaching about the deadly complications of diabetes. My six year old son can’t read the newspaper, but he did hear the stories on TV. The 5 year old in the paper called 911 from a cell phone and didn’t know his address which slowed EMS’s response time. The boy is quoted on the 911 call as saying, “My Momma is dead.” The reporter stated, “Doctors later told Richardson Burden (the mom) that she would have died if she had not received medical care.”

These stories are like an infection, they snuck up on me without any warning and after I read them, hear them on TV, I feel knocked out and want to crawl back into bed. These are defeating stories, these are Julia Roberts in Steel Magnolia stories, these are stories that scare me, scare my children.

This morning as I sat on the couch reading the Sunday paper, I listened to my boys talk as they built legos in their bedroom. Will, my 6 year old, was explaining to his brother that I would die before them because I was their mom, I was older. He didn’t say anything about diabetes and maybe he has not connected the ideas of death to the ideas about my disease, but he will eventually. And that is the part about this disease that I hate the most, the stories in the news of people who get into car crashes or lose consciousness because of low blood sugar. Maybe they didn’t check their blood sugar before they went to bed or got behind the driver’s seat, maybe that was their mistake, but I’ve done the same thing myself. None of us can be perfect all the time.

So maybe for every negative story that is published in the news and on TV, there should be a positive story to even the balance. Stories about people with this disease who climb mountains, run marathons, write books, raise children and work as educators and doctors in this field. I think my day would start off on a much brighter note with a story of inspiration instead of defeat.

My six year old is now ten and I’m still not sure how he thinks about diabetes and death. I know he and his seven year old brother (the toddler is too young to join in these conversations quite yet), think they are going to live to 100 years old. Yesterday they told me I probably had another 40 or 50 years to go. I told them I wasn’t so sure I wanted to make it to 90 years old and we all had a good chuckle. What I didn’t say is that my diabetes might shave a few years off my finish line. I’m not sure they are ready or even interested in talking too deeply about death. Or maybe they are and I’m not. I’m not a fortune teller and so I’ll let my boys think they will live to 100 and leave the conversation at that.

But their talk of death got me wondering about childhood fears. What scares my boys? When I was their age I was scared of thunder and lightening, fires and the dark. When I was scared at night I would get out of my bed and run downstairs to my parent’s bedroom. They always took me in and between them I felt safe. My boys are pretty solid sleepers and my husband and I don’t often have to share our bed. When there is a storm outside, it’s usually our 13 year old dog that we have to comfort instead of the boys. When I ask, my seven year old tells me he’s not afraid of anything. (Then his older brother reminded him of how he refused to go on the roller coaster last summer and he had to admit that okay, he was scared of the roller coaster.) Other then the roller coaster, I think he’s pretty brave.

I would like to think that feeling scared is an unfamiliar sensation for my children. And not because their lives are sheltered, but because we do a good job of keeping them secure and answering their questions and talking with them about the scarier parts of life. I know that they are scared when I get angry and I do my best to give myself a time out when frustrations start to mount, and to explain my frustrations when I am calm. Seeing fear in my ten year old’s face when I am yelling was humbling. I don’t want to want to make my children afraid.

Not wanting to scare my children makes me work that much harder to keep my blood sugars from dropping. Lows are scary. I used to have the kind of lows where my husband had to revive me. I’ve crashed a car, I’ve been taken by ambulance to the ER, I’ve stumbled and fallen, and I’ve crawled across the floor. But nothing since I became a mother. It’s almost like I flipped a switch between the before and the after. The other day I said to my husband, “Isn’t it amazing that I haven’t had a bad low since the boys were born?” I’ve been a mother for ten years. I used to have a lot of bad lows all the time and not there are none. What changed?

What changed is that I became a mom. The media will do its best to make diabetes sound terrifying to my children, but I will not help. I will do everything I can to keep my diabetes from scaring my children. If it means testing 15 times a day, I’ll do it. As a mom with diabetes, that’s one way I can help my children feel safe.

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