O.K. so it’s not the most original ice breaker . . . but it’s a start.
I’m a mom of 3 beautiful kids. My daughter, Brenna, has type 1 diabetes. She was dx’d 8/17/06 @ 2 years old. I saw tudiabetes over on Kerri’s SUM blog and thought I’d take a peek.
Thank you, Penny, for inviting me to join the Parents discussion.
Hi! I have three children (ages 2, 6 & 8). My middle child is the one with Diabetes. She is 6 now, but diagnosed in Sept 2004 when she was three years old, two weeks before my youngest child was born. Talk about crazy timing! Between a c-section and a newly diagnosed child, I checked myself out of the hospital after two nights, so that I can keep an eye on her.
So far my daughter is the only with Type 1 in the family. No history on either side (of either type), so this was all a big shocker to us all.
We are using MiniMed 522 as of February of this year and loving it so far!
Noah (my only child) will be 9 in a couple weeks. He was diagnosed in March of 2005 and has been using the Deltec Cozmo since November of 2006. I recently started blogging after reading a ton of d-blogs and getting more information from all of you than I ever did at the doctor’s office. I got inspired and wanted to add our story as well.
I also found out about tudiabetes over at Kerri’s, and when I got here Penny invited me over!!
We were incredibly lucky. Brenna was able to get an Animas pump within about a month of diagnosis. I can’t imagine doing this any other way. Wow. So many diagnosed so young. My husband’s father & every brother and sister (he’s the youngest of 11 kids) have type 2. Brenna’s Type 1 surprised everyone. I’d love to enroll everyone in a study or two (there is a high incidence of diagnosed autism in that side of the family as well).
Hi I’m Amber, mom to Nikki who has D and Quinn who does not. I’m an American married to a Finn, living just outside of Finlands capital of Helsinki. Saw this link on CWD and thought it was a cool site!
I am Angela, mom of David and wife of Dennis, both with type 1. My son was dx in March. I now have been diagnosed with type 2. At least we are all on the same page Neither my husband or son have a pump. We would like to get my husband pumping soon. Waiting on an endo appt. to be set up. This and CWD are great resources for moms like us!
Hi everyone! I am new to the website. My son is 6 1/2 and was diagnosed January 22, 2007. He is curremntly a “pumper” and everything seems to be going well. My wife has quit her job and started a new one as a full time pancreas for Caleb. He attends a private school without a nurse so my wife has become his caregiver at school as well. I just wanted to say “hi” and get aquainted with the website.
So far, everyone we have come in contact with who has diabetes or knows someone with diabetes has been so supportive. I also grew up with a girl who had diabetes, She is actually the one who recommended this site. It means so much to know that yo are not alone when you are new and dealing with your own emotions, your spouses emotions and your childs emotions. I hope to learn a lot here and would like to be able to offer that same support to anyone with a child who has diabetes. Thanks for allowing me to join in.
My daughter Stella was 22 months old when she was diagnosed this Memorial Day Weekend. As you all know so well, my/our world has been rocked. I alternate between being sad, motivated, angry, driven, and oh so very very very grateful that we got to leave the hospital with our daugther (unlike some of the other families in the Peds ICU).
It’s now been a bit more than a month, we’re getting practiced at giving shots, but not at actually controlling the numbers with any decent regularity. I very much look forward to switching to a pump, but Stella’s Dr. says “let’s wait a year.” I’m interested in the experiences of those parents with young children on pumps. At what age? How did you do it? Was your Dr. supportive? Do you have specific advice?
Thank you for this discussion group. I’m getting a lot of comfort from the internet and diabetes blogs.