"My daughter is now 4 and a half and we have been pumping for about a year and half. It was a nightmare for a while with site changes even with cream to numb the area. I think the main issue is having a sense of control. 4 year olds need to have a…"
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Erin Halvorson
- Female
- Rogers, AR
- United States
- Blog Posts
- Discussions (21)
- Events
- Groups (1)
- Photos
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Erin Halvorson's Discussions
Omnipod Coverage with Insurance
Started this discussion. Last reply by Erin Halvorson Jan 6, 2010. 3 Replies 0 Likes
Flying with an Omnipod system
Started this discussion. Last reply by Janet Aug 19, 2009. 4 Replies 0 Likes
Getting insurance coverage for the OMIPOD
Started this discussion. Last reply by Betty Apr 30, 2009. 2 Replies 0 Likes
Erin Halvorson's Page
Latest Activity
Erin Halvorson replied to matilda's discussion 'site change and crying HELP' in the group parents of kids with Type 1
Erin Halvorson replied to Tracy K's discussion 'changing pump sites in children' in the group parents of kids with Type 1"Ella will be 4 in jan. dx at 2. We change every two days. From experience we always have bad numbers if we wait until the third day. That being said the T-SET infusion set with the Minimed has been THE ONLY one that I can trust for 3 days for about…"
Erin Halvorson replied to Natalie's discussion 'Starting Preschool Questions' in the group parents of kids with Type 1"Hi Natalie,
My 3 and half year old is in preschool right now as I type this. Her teacher's willingness is amazing and yes she is overwhelmed. She knows when to ask questions and when to call me. That is a biggie. She has also been teaching…"
Erin Halvorson replied to jellyman30's discussion 'Day one: out of the hospital, into the parents' hand.' in the group parents of kids with Type 1"oooo nooo.. So sorry. Our daughter is now 3.5 years old and dx at 2. It is REALLY hard. Dose for what he eats and let him "graze" as a two year old should. That being said you can prob only dose at 0.5 unit levels which is too much for…"
Erin Halvorson replied to Mark's discussion 'Type 1 + overheating ????' in the group parents of kids with Type 1"My daughter has the same issues!! She gets hot humid and cranky!! I always thought it was her, but now you've got me curious. We used to live in Arkansas and now we are Wisconsin. She is much happier this summer than last summer. hmmmm."
Erin Halvorson replied to GoCeltics's discussion 'Hi !' in the group parents of kids with Type 1"Welcome!! This is my fav and most helpful site by far. My daugther was dx at 2, she is 3.5 now. We are on minimed too!!
I did a local 5K yesterday to support JDRF. May the fight for a cure continue!"
Profile Information
- How do you hope to benefit from TuDiabetes?
- Getting tips and advice on dealing with my toddler with Type1
- Date diagnosed
- January 5, 2009
- Most recent HbA1C %, date of result (optional)
- 8.5
- Type of treatment/devices you use
- Pump, Diet and Exercise
- What pump model do you use, if any?
- Omnipod
Comment Wall (8 comments)
- At 7:39pm on October 5, 2009,
Erin Ball said… - hi my name is erin ball i was diagnosed about a month ago with type 1 who do you know that has diabetes?
- At 12:15pm on April 30, 2009,
Star Lewis said… - I got really lucky and lived in florida at the time and my children had the florida state insurance that covered it. I really do hope that there is a way for you to get a pump soon...I will see what I can find or do to help you out. It is nice to meet another mother of a young diabetic child...If you have any questions at all please feel free to ask me anytime...
- At 6:30pm on March 24, 2009,
Jessica05 said… - Hi, Erin, Just wanted to say hello and welcome to TuDiabetes...I have a 3 year old who's had diabetes for 2 years now who wears a pump. I hope your daughter stabilizes soon...it does take time especially in the beginning. I remember the first year was tough getting used to everything. It's still tough, but I'm thankful for this group of people who have gone before and can give tips and advice. Blessings to you! Jessica
- At 7:45am on February 10, 2009,
Leah D. Rogers said… - Erin, You are NOT alone even if it feels like it sometimes. You have so many people on this site that relate to what you are going through and are with you. I could not imagine not having this site and these people. You have every right to feel the way that you do. Is there a JDRF/support group in your area to go to for some local support? I myself have only been to one meeting but it was only 1 day after my daughter being released from the hospital so I pretty much was in a daze at the time. However, it made my eyes wide open to the fact that we were by far not the only ones going through this. It was a big relief to just see families and kids who have been doing this for a long time and seeing that life goes on and it's just an extra thing that fits into your everyday routine. It's like having a new infant (in my case two at once) when it seems like there is no way that you do everything that needs to be done but somehow you DO and over time it is just everyday life. I will be thinking about you and hoping for a little sunlight in your day. Take care, Leah
- At 7:04pm on January 29, 2009,
Rachel said… - My heart goes out to you! I have a daughter named Ella, too. :) I also have type I. The journey is difficult, but diabetes doesn't have to win!
- At 6:11pm on January 21, 2009,
Penny R. said…
- Welcome to tudiabetes and the parents of kids with Type 1 group. My son, Riley, was diagnosed 3+ years ago at the age of 3. I know too well the pain and shock you are going through now. The parents of kids with type 1 group is a great place to get advice. Or feel free to email me at anytime: pennylane5001@embarqmail.com.
- At 3:27pm on January 21, 2009,
Jen Mangum said… - So good to get a msg from you. I understand and know why you ask those kinds of questions. If you ever need anything please let me know. It keeps me healthy to help others stay healthy, so please anything I can do. Thanks Jen
beachbodyjen@yahoo.com
- At 8:43pm on January 18, 2009,
Diabetic_Iz_Me said… - Hello and Welcome to TuDiabetes! Glad you joined us. I noticed you have a child who was just DX'd. There are a lot of parents in the community who have childern with diabetes. Please feel free to ask questiosn. You will find plenty of support, friendship and knowledge. When you have the chance please visit the "About Us" Section, it will help you navigate around the community. Make yourself at home.
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