Adam Lasher is back on American Idol
Scott Benner
And he made it through to hollywood week with his Dexcom receiver (again) clipped to his guitar strap.
I'm working on finding a time to get Adam back on the Juicebox Podcast...
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.
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: Juicebox Podcast
I'm working on finding a time to get Adam back on the Juicebox Podcast...
Victor Garber stopped by the Juicebox Podcast to talk about his life with type 1 diabetes, his new show on The CW (a spinoff of The Flash called 'Legends of Tomorrow') and a diabetes charity that he supports called 'Beyond Type 1'.
You can listen now with the inline player above, on iTunes, Stitcher or your favorite podcast app - search for Juicebox Podcast. Please don't forget to subscribe!
Its not often that someone is this willing to speak so open and honestly about their life with diabetes. I'm genuinely grateful for Victor's willingness to be transparent about his journey with type 1. It doesn't matter if you are a person living with the disease or someone just hoping to hear about his work on Legends... Victor Garber's kindness and desire for people to learn from his life overflow in this episode - I think you'll love hearing what he had to say, I certainly loved speaking with him!
Learn more about the OmniPod tubeless insulin pump. When you try a free demo pump you are supporting the Juicebox Podcast. Thank you!
Take a moment to learn more about BeyondType1.org, check out their website.
Subscribe to the podcast in iTunes today!
Listen to the Juicebox Podcast online
Watch the trailer featuring Victor as one half of Firestorm!
Episode 42 of my podcast is an hour long conversation with an RN and CDE who recently completed a six week bionic pancreas study at Massachusetts General Hospital.
I'm going to drag you blog readers into the podcast world one way or another, might as well come peacefully... :)
You can listen right hear in the blog post with this player or through iTunes. An hour may seem like a lot of time but you can listen while you do the laundry, do the dishes, grocery shop or while your are in the car.
More photos from Kelly's bionic pancreas trial are available here.
Next weeks episode is an hour with actor Victor Garber. Victor has been living with type 1 diabetes since he was 13 years old and he is about the most delightful person I've ever met. Subscribe today.
Scott talks into the microphone with Basal snoring in the background.
New season of the Juicebox Podcast begins January 5, 2016.
Victor Garber will be on the podcast January 15, 2016 to talk about his life with type 1 diabetes and his long acting career.
Thank you for a great first year... Subscribe today in iTunes - COMING SOON to the Google Play Store!
Not sure how to listen? Scott's four minute podcast tutorial is right here.
#A1cYaLater
After I interviewed Anisha Dharshi from the American Diabetes Association for episode 40 of my podcast, I asked if she'd be interested in preparing a guest post for Arden's Day that detailed how parents and people with diabetes can utilize the ADA's free assistance program (it was a topic we talked about on the show). I sincerely hope that you never need the ADA, but if you do... they can be a great resource!
If something does not feel right, it may not be legal.
Reach out if your child is not getting the right diabetes care at school, or you are not being allowed to test your blood glucose levels at work. The American Diabetes Association can help. The Association has representatives waiting to speak, chat online, or email with you to help avoid problems and find solutions when problems do occur.
Call our Center for Information at 1-800-DIABETES, there a dedicated representative will serve as your personal guide for information on all our programs and events by answering your non-medical questions in English, Spanish or other requested languages.
If you prefer to Email us at askada@diabetes.org, you will receive an reply with information and the next steps to take within 24 to 48 hours.
The Center for Information will give you a form to complete and return to the ADA. If you don’t have time or cannot complete the form, please ask your ADA representative for help.
A Legal Advocate will contact you within 7-10 business days after receiving the form. The advocate can explain the law and help educate your school or business about its responsibilities, help you negotiate a solution and give problem-solving tips, give sample letters and background resources and review your materials. If you need to litigate, the advocate will refer you to a network of local attorneys.
1-800-DIABETES: Monday - Friday, 8:30 a.m. - 8:00 p.m. EDT
Live chat: Monday – Friday, 8:30 a.m. to 5:00 p.m. EDT
askada@diabetes.org is available 24/7/365
The American Diabetes Association has been a resource of reliable information and support to people living with diabetes and their caregivers for 75 years. The Association’s Safe at School® campaign is particularly dedicated to making sure that all children with diabetes are medically safe at school, are treated fairly, and have the same educational opportunities as their peers through tools, resources, and the guidance our legal advocates provide to families. For additional information please visit the Association’s legal assistance webpage.
You can listen to my conversation with Anisha below, on iTunes, at JuiceboxPodcast.com and everywhere that podcast are available.