Started this discussion. Last reply by Sarah May 14. 6 Replies 0 Likes
My 10 year old daughter has been using the Dexcom G4 since September. For the past several months we've been placing the sensor in the back of her arm. Last week when I inserted a new one she…Continue
Tags: dexcom
Started this discussion. Last reply by TuDiabetes Administration Nov 18, 2011. 136 Replies 3 Likes
My eight-year-old daughter was diagnosed in March, 2011 with Type 1. When she was diagnosed she was put on four insulin shots per day. After returning from vacation in June I decided the family…Continue
Sarah replied to Shana's discussion 'Dexcom hurting after insertion'
Shana replied to Shana's discussion 'Dexcom hurting after insertion'
AliciaM replied to Shana's discussion 'Dexcom hurting after insertion'
Kate replied to Shana's discussion 'Dexcom hurting after insertion'
Shana posted a discussion
Shana replied to c.schambers's discussion 'How does your child carry their Pump?' in the group parents of kids with Type 1
Sophia'smommyLori liked Shana's blog post Ten months post Type 1 diagnosis and still off insulin
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Shana commented on mompoptoo's blog post 'glicemic index help'
Shana posted a blog postPosted on February 2, 2012 at 3:01pm 0 Comments 1 Like
It is highly unusual that Kendal is still not on insulin, 10 months after diagnosis. A lot of people ask me about this so I thought I would write about it this week.
http://bebalanced52.com/2012/02/01/type-1-ten-months-and-still-no-insulin/
Posted on January 5, 2012 at 8:27am 1 Comment 1 Like
And continue to learn! I feel like I've just "dipped my toe" into the world of diabetes management and trying to keep it all in balance will be a huge challenge. bebalanced52.com
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Kate said… Hi Shana - I just wanted to drop you a note to say that I was dxd at age 15 (back in the mid-90's). My mom thought I had a UTI and took me to the drs. That's where they diagnosed T1. I was put on Regular and NPH insulins. I was taking about 2 units of NPH and 1 unit of Regular twice a day. Looking back, I'm pretty sure that I could have gone without insulin if my diet were lower carb or low gi. I believe that the endo put me on that regimen to get me used to shots and the whole process so that when my honeymoon eventually ended I would just increase my rates and be "good to go".
You made a comment about "grieving" all over again when your daughter starts insulin again. I think that is an apt comparison. I know that I grieved over what was lost. I hope that you are able to find hope and peace in the midst of these ever changing times. I see many similarities to your daughter's story and my own. I wish you both the best and hope that you continue to share your journey with this community.

Doris D said… You do what u must. I just read through the whole Forum discussion. I was diagnosed with Type 1 at 10 & my daughter was diagnosed with Type 1 at 11. Like Judith I hope u won't let a few outdo the good of more.U have a beatiful daughter keep on doing as u need to and all of us will be back here encourging u alone.

Judith said… Hey Shana----I've read through the whole discusson. While I am a T2 in my 60s, diet and exercise only so far, I have learned sooo much from my T1 friends and I always check in---my grandson's best friend is T1, for instance, so I want to "know stuff"! I joined when there were only 800 members and believe this site has saved my life and sanity often. I hope you will stick with us. It really sounds like you are doing a great and enlightened job in caring for your beautiful daughter. Brava!!!...Judith in Portland
BadMoonT2 said… Forgot to mention, my daughter used to live in Loveland and now resides in Greeley. Beautiful area of the country, I read about geology a lot, so when I visit I'm in hog heaven.
BadMoonT2 said… Shana, Although I did not participate in your recent discussion I have read through all of it. I think you are doing exactly the right thing, and you seem to realize that at some point diet will stop working on its own. By doing frequent testing you are insuring that when your daughter needs a change in treatment you can do so quickly. I have noticed that when flame wars start here the instigator usually has an ax to grind and does not take the time to read and understand the posts. You handled the attacks with grace and never lost you cool, kudos to you.
I hope you will not let this bad experience discourage you from further participation in TuD. If you disregard the flame war, I think you got some excellent advice. Actually this forum is generally characterized by tolerance and respect for the views of others. In my experience posters who go off the rails and attack others soon either leave on their own or are banned. I myself am a T2 who is a confirmed low carber(T2 nutjob?) but I try to be a nutjob who respects the views and experiences of others. Best of luck to you and your daughter
Scott E said… Shana, just wanted to write you a note and wish you luck in finding the advice you are seeking. That question you posted got way out of control (through no fault of your own), and I must say I've never seen a response anything like it. I sure hope you don't give up on TuDiabetes as a result. You may have seen my comment on page 9, but as I read through this discussion, I can't help but be impressed at how much you know and understand about diabetes and health-management in general! For someone who's dealt with this for only 8 months, you sure are smart! I'm sorry I can't relate and offer you the specific advice you're seeking, but I do hope you find someone who can, and I wish you and your daughter all the best - in health and in life.

Donna H said… Hi Shana, saw what happened on the discussion you posted. Had to stop by here to share that the tone some of the people took there is not the norm for this place. Not sure what stirred up those few -- a full moon perhaps. :) Also, wanted to laud you for how you are managing your daughter's disease. This is tough stuff! And i think you are absolutely spot on by doing what you can to extend the honeymoon period. The diabetes/celiac combo makes it all the tougher to manage. The things you are doing now to really understand the nutrition and manage the disease so triumphantly is going to be a benefit to your daughter for the rest of her life. She's clearly got an amazing mom!

Donna H said… Welcome to TuDiabetes! Check out some of the groups -- it's a great way to get to know the community.
Marie B said… here's a discussion on MODY
http://www.tudiabetes.org/forum/topics/i-might-have-mody-diabetes
let me know if you'd like any more links.

Doris D said… WELCOME TO ONE OF THE GREATEST FAMILIES YOU WILL EVER MEET MY FRIEND!!!! WE'RE GLAD YOU JOINED US!!!!!!!!!! Please introduce yourself on our forum. Questions??? Just ask one of us or post it on our forum and you will get many answers there.
Here's a link to help our new member's get to know us better: http://www.tudiabetes.org/notes
Manny Hernandez(Co-Founder, Editor, has LADA)
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Bradford (has type 1) |
Lorraine (mother of type 1) |
Marie B (has type 1) |
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