contact us

Use the form on the right to contact us.

You can edit the text in this area, and change where the contact form on the right submits to, by entering edit mode using the modes on the bottom right.​

         

123 Street Avenue, City Town, 99999

(123) 555-6789

email@address.com

 

You can set your address, phone number, email and site description in the settings tab.
Link to read me page with more information.

ardenHEADERnew.png

Arden's Day Blog

Arden's Day is a type I diabetes care giver blog written by author Scott Benner. Scott has been a stay-at-home dad since 2000, he is the author of the award winning parenting memoir, 'Life Is Short, Laundry Is Eternal'. Arden's Day is an honest and transparent look at life with diabetes - since 2007.

type I diabetes, parent of type I child, diabetes Blog, OmniPod, DexCom, insulin pump, CGM, continuous glucose monitor, Arden, Arden's Day, Scott Benner, JDRF, diabetes, juvenile diabetes, daddy blog, blog, stay at home parent, DOC, twitter, Facebook, @ardensday, 504 plan, Life Is Short, Laundry Is Eternal, Dexcom SHARE, 生命是短暂的,洗衣是永恒的, Shēngmìng shì duǎnzàn de, xǐyī shì yǒnghéng de

Filtering by Category: OmniPod Blog

I wish I may... have Mac compatible software

Scott Benner

Hello Makers of various insulin pumps, CGMs, and meters.  How are you?  I wanted to drop you a note and say that we really appreciate all that you do!  Your inventions are quite literally saving us (well those of us with good insurance) so I feel just a little weird complaining but nevertheless here I go.  

 

Not one of us wants to keep logs by hand but some of us have to because.  we have Apple computers and your software only runs on a Windows machine.  I know that Apple only holds about a 13% market share in home computing but please keep these things in mind: 13% is second only to Windows, that number is growing steadily, Apple computers are (generally) owned by the more tech savvy section of society and your devices are geared toward those people.  Lastly, it really wouldn’t take that much effort to port your software over to the Mac OS.

 

Anyway, give that some consideration please and let me know what you decide.

 

Signed,

Patiently Waiting

 

**

The following are archived comments from this post. You can post new comments below.

Sophia's Mom
I Emailed Abbott today about this very thing.  I am considering purchasing a no frills laptop just for this purpose but I really can't afford to do that.  Excel is still my friend for now.
Monday, April 19, 2010 - 04:28 PM
Scott
Sophia's Mom,

Like a net book maybe... That's a very good idea! Though I would so dislike using Windows again... :)
Monday, April 19, 2010 - 05:35 PM

 

Well meaning but wrong

Scott Benner

Our children interact with people while they are at school and we as parents can’t control what they hear.  Most days I think of those interactions as moments that enrich my kid’s lives.  They get to hear points of view and thoughts from other people, other cultures and those interactions help to make them into who they are and will be. 

 

This week however, I’m not so thrilled.

 

Arden had photos taken at school yesterday and someone (an adult) told her not to worry if her OmniPod was visible because, in Arden’s words, “it can be photoshopped out so the picture will be pretty.”.  We are not pleased to hear that any overtones were made that indicate that Arden’s pod is in any way, something to be ashamed of.  Whether purposeful or inadvertent comments like that can and will lead to Arden having an unhealthy view of her insulin pump and of herself.

 

We teach Arden that her pod is a normal part of her life, we don’t care if people see it, stare at it or ask about it.  It is what it is and we will not hide, not for our comfort or for anyone else's.  


Arden is “pretty” and would be even if that pod was sticking to her forehead.  We addressed the comment with Arden and with the appropriate folks at the school and I’m confident that my message was heard.  We hold no ill will to the adult and I personally see this incident as just another teachable moment in our life with type I.  It is also a reminder of why good and clear communication between you and your child’s school is so important, this could have been a very uncomfortable moment but it wasn’t.  

 

**

The following are archived comments from this post. You can post new comments below.

Scott
I just spoke with the photography company and they assured me that they won't retouch Arden's picture.
Friday, March 19, 2010 - 04:50 PM
Aunt Megs & Uncle Mike
I would like to correct your blog...Arden is not "pretty", but BEAUTIFUL in and out and we are so proud of her!

Love you Ards!
Monday, March 29, 2010 - 08:52 PM
Amy
did you ever recieve these pictures. I would like to see them.
Sunday, July 18, 2010 - 08:52 PM

 

 

 

 

I’m here for... my insulin pump

Scott Benner

The White House is sponsoring a campaign called, The Final March for Reform.  The campaign is highlighted by people printing out a sign the reads, “I’m here for” and then they fill in the rest...  Arden submitted two photos with Cole, the one that you see here with her proudly displaying her OmniPod... the other is on Daddy’s blog. {link}

 

Arden’s Day steers clear of most everything political.  However, on the issue of health reform we are vocal.  If reform is passed, Arden and every child like her will never again be at risk to lose their healthcare because of a preexisting condition.  No longer will we be scared to switch jobs or fear the day that she is too old to be on our insurance.  Health reform won’t just secure Arden’s ability to stay healthy, it also will relieve a major source of our stress and worry.  Add your voice...

 

http://my.barackobama.com/page/content/finalmarch-visualization

 

Saw a movie, lost a PDM

Scott Benner

This blog entry starts with a movie, moves on to digging through garbage and finishes with me feeling like quite a failure... but it has a happy ending and we don’t get too many of those in Diabetesland so they are extra special when they happen.

 

Valentine’s Day was going to end with us seeing ‘The Lightening Thief’ but instead it ended with me rummaging through the garbage at our local theater.  I don’t know how but I lost Arden’s bag that holds her OmniPod PDM, lancet and test strips, I just didn’t pick it up when we left the theater.  I realized it almost as soon as we got home, I called immediately but it was already gone. I drove back to the theater and dug through maybe 30 trash cans but I just couldn’t find it.  

 

Arden and I went back again to check the theater after the last show ended but still no sign.  She was so sweet, she walked up and down every isle in the theater and stood next to me peering into the garbage, finally after her nose couldn’t take it anymore she said, “it’s okay Dad, it’s not here, we can just buy another one”.  What Arden didn’t know is that a new PDM costs $500.  

 

I am, as most of you are aware, a stay-at-home dad.  I haven’t earned $500 combined in the last decade which makes loosing something that valuable much more painful.  First, loosing Arden’s PDM, the thing that literally keeps her alive, made my heart hurt.  It was like it was my job to remind her to breath and I just forgot to.  Second, the cost is a bit oppressive and as I said, that failure is compounded by the guilt I feel of not having an income.  So sufficed to say I wasn’t having a great night.  Though one bright spot (for my midsection) is that I don’t think I’ll be getting a popcorn the next time we see a movie. While I’m commentating on theater food, note to theater owners: no one drinks their entire soda - smaller cups wouldn’t hurt.  I woke up this morning every bit as dejected as I went to bed.

 

But I feel better now, want to know why?

 

I made the call this morning to Insulet, the company that manufactures Arden’s OmniPod insulin pump to order a new PDM.  I spoke with a wonderful woman named ‘Audrey’ (Hi Audrey, I hope I spelled your name correctly) and I told her just what I told you.  I said as plainly and honestly as I could, “I lost my daughter’s PDM and it’s going to be difficult to raise $500 to replace it”.  We spoke for a few minutes and I shared with Audrey how horrible I felt for losing the PDM and not being able to generate the funds to replace it.  She put me on hold and when she came back she said the nicest thing that maybe anyone has ever said to me, “Arden’s new PDM will arrive on Wednesday”.

 

Audrey worked it out with her manager as a one time courtesy to replace Arden’s PDM at no cost.  Not many good things happen in my day, most days are full of type I diabetes stress and pressure. The stress is so palatable sometimes that it permeates to the people around us.  Some days the poor nurses at Arden’s school sound exhausted after caring for her, our family and friends can’t comfortably have Arden over to play and even as I write this my mind is busy worrying if Arden’s BG is stable as she sleeps in today.  Thankfully, today has a bright spot to chase away those shadows.

 

I want to tell all of you and anyone that will listen that the OmniPod made our lives indescribably better on February 11, 2009 and it continues to, nearly one year to the day later.  Not many companies have a heart but I can say without reservation that, in a life that most days feels full of shadows Insulet and the OmniPod are one of our bright lights.

 

Insulet is online at - http://www.myomnipod.com/ and if you are a type I diabetic or love someone who is, I can’t recommend enough that you check them out.

 

Thank you to Audrey and Insulet!  You saved us today and I won’t forget what you did or how it made me feel.

 

**

The following are archived comments from this post. You can post new comments below.

That really is great news. I am so on the fence as to a medtronic or an omnipod. My CDE was just saying they dont recommend many kids use the omnipod because they are so active and they see them get pulled out.

Your experience seems quite different. And the support for Omnipod sounds really good. You really sound like an awesome dad, doing all you can for your sweet little girl.

I probably wont remember to come back and see if you have any thing to add about your omnipod and your posts, so if you get a chance email at clcooper@gmail.com.

thanks!

 

 

Diabetic U.S. athlete has a point to prove

Scott Benner

BY MIKE BEAMISH, VANCOUVER SUN FEBRUARY 11, 2010

The closet of Olympic cross-country skiing is littered with incriminating paraphernalia: vials, syringes and equipment used by cheats to gain a chemical edge.

 

But nobody in the sport of skinny skis is more open about the use of the needle than U.S. Olympian Kris Freeman, a New Hampshire native who requires them simply to survive.

Indeed, Freeman openly injected himself in plain view to prove two points: that an athlete with Type 1 diabetes can excel at the highest level of sport. Secondly, Freeman's very public injections were a repudiation of those athletes who shoot up illegally and clandestinely.

 

Follow Kris on Twitter @ http://twitter.com/TeamFreebirdXC

 

"Up until two years ago, I was taking 12 shots a day -and I was doing it in the open," Freeman said Wednesday. "In the cafeteria, when all of the teams are sitting together, I'd take out my syringe with insulin and stick myself in the stomach with it. The guys who have cheated in the past did it behind closed doors. They were secretive about it. I'm in the open about it. The IOC knows I use insulin, WADA [World Anti-Doping Agency] knows that I use insulin, FIS [the governing body for skiing] knows that I used insulin. Hopefully, I'll win a medal and everybody in the world will know I use insulin."

Diagnosed 10 years ago with Type 1 diabetes, a life-threatening condition that affects the breakdown of food into energy, Freeman was told to forget about an Olympic career. Yet here he is, a decade later -a 10-time U.S. champion and three-time Olympian talking openly about ending an American drought in cross-country skiing that spans 34 years.

 

Vermont's Bill Koch was the first and last American to win an Olympic medal in cross-country when he took a surprise silver in the men's 30 km at the 1976 Winter Games -a Halley's comet-like performance in a sport thoroughly dominated by Scandinavians and Russians. Since the Winter Games began in 1924, Norwegians, Finns, Swedes and Russians have won 189 of 216 total medals in cross-country skiing. Of those remaining 27 medals, three have been won by Canada, all since 2002.

 

"I've battled two stereotypes since I was a kid," says Freeman, 29. "The first was that Americans could never succeed in cross-country skiing. People would say, 'You may have won junior nationals, but you'll get your butt kicked in Norway.' Then I got diagnosed with diabetes, and I was told I'd never race again. I like to prove people wrong, and I like a challenge. This is the best team I've ever been a part of. "

 

Freeman points to Kikkan Randall, a 27-year-old Alaskan with a swath of magenta-tinted hair who is unique both in appearance and accomplishment. She is the first American woman to win a medal at the world championships.

Then there's Vermont's Andy Newell, one of the world's fastest sprinters, and Freeman himself, who has two fourth-place finishes at the worlds.

 

"It's not a guarantee that we're going to break through for a medal, but it's so possible," Freeman says. "It's not like we're going to need a freak day to do this. We can do it on a plain, even playing field. It just has to be on the right day."

To get his metabolism right, Freeman relies on the OmniPod, a disposable pump that regulates the flow of insulin to keep him from crippling episodes of unbalanced blood sugar.

 

"For a 15K, I need three times the insulin to go into my body that I do for a 30K," he says. "For a 15K, I'm almost anaerobic [using oxygen more quickly than the body can replenish working muscles] for the whole time. My blood sugar rises. When I'm aerobic [efficiently transporting oxygen], my blood sugar falls. It's a really delicate balance, depending on the exertion."

 

He must also be vigilant about getting too amped before a race. "My blood sugar can rise just by sitting there," he says. "So, certainly, the Olympics are going to affect me more. I try to listen to calming music. But it's hard to find calming music I like, because I'm very into heavy metal -Guns N' Roses." Of course, a band with an appetite for booze and hard drugs is in no way an extension of what Freeman represents -an indomitable Olympian breaking down barriers for diabetics. Because skiing truly is in his blood.

 

mbeamish@vancouversun.com

© Copyright (c) The Vancouver Sun

Photograph by: Richard Heathcote, Getty Images, Vancouver Sun

Borrowed from -http://www.vancouversun.com/health/Diabetic+athlete+point+prove/2549954/story.html