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Parents of Children with Type 1 | Forum profile
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Forum profile page for Parents of Children with Type 1 on http://www.childrenwithdiabetes.com.
This report page is the aggregated overview from a single forum: Parents of Children with Type 1, located on the Message Board at http://www.childrenwithdiabetes.com.
This forum profile page summarizes the general forum statistics such as: Users Activity, Forum Activity, and Top Authors, which are reported in either a table or graph below for a given reporting time period.
Additional forum profile information for "Parents of Children with Type 1" on the Message Board at http://www.childrenwithdiabetes.com is also shown in the following ways:
1) Latest Active Threads
2) Hot Threads for Last Week
Warning: These statistics are generated using 'best efforts' and can experience delays and reporting errors at times. Please note that such statistics do not constitute a forum's popularity and/or exact posting volumes at any given reporting period.
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Posting activity on Parents of Children with Type 1:
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Week
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Month
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3 Months
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Threads:
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423
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1,516
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4,239
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Post:
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2,957
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10,624
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29,489
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Parents of Children with Type 1 Posting activity graph:
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Top authors during last week:
user's latest post:
what are your basal rates these...
Published (2009-11-25 14:43:00)
12 midnight 1.10; 1am 1.05; 1:30 am 1.0 (this number can be pushed forward until 2:30am as she sometimes needs more until 2:30am); 5am 1.05; 8am 1.10(schooldays, weekends 1.05 all morning); 12 noon 1.05; 3pm 1.25; 4pm 1.35; 5pm 1.6; 6pm 2.1; 7pm 2.2; 10pm 1.9. Right now her TDD is about 50 units a day, more or less. She gets 55 to 60 percent of her TDD basal, rest bolus (at least the last time I checked balance). The hours of 6pm to 1 am,...
user's latest post:
please pray for this family.. (...
Published (2009-11-25 23:07:00)
Quote: Originally Posted by Darryl I was talking about data I have observed, and how that data has led me to believe that testing only once overnight may not be sufficient to insure safe BG's over a 10-hour timeframe. I was not making judgements about you. Thank you for that Darryl Happy Thanksgiving to you and yours
user's latest post:
Question for Parents on CWD
Published (2009-11-26 12:03:00)
Quote: Originally Posted by CTuban What made you join CWD originally? Looking for people going through the same things as my family. How easy are you able to find the information you are looking for on CWD? Pretty easy. I use the Search button on the forums a lot, or browse through the CWD drop-down menu. What feature do you use most often? Forums What do you like most about CWD, and why? The Forums - post a question or comment, get different...
user's latest post:
need advice on which pump to pick
Published (2009-11-25 21:37:00)
Considering how small she looks in your picture, I would think the biggest drawback of the Omnipod would be its size. And I don't know if she'd be ok with the smallest basal amount being 0.05u/hr. The Ping does as low as 0.025u/hr.
user's latest post:
Question for Parents on CWD
Published (2009-11-25 17:46:00)
Responses are numbered as per your list below: 1. n/a 2. access to great scope and depth of information 3. information is well-organized and presented 4. forums 5. the ability to exchange ideas and information with other parents of kids with D 6. several reference texts, and other websites 7. none comes close to CWD 8. I'd suddenly have a lot of time on my hands but I'd feel cut off from a valued source of information, peer support,...
user's latest post:
Question about the 30 point drop...
Published (2009-11-25 14:56:00)
Quote: Originally Posted by StillMamamia Is it only for MDI (using Lantus or whichever background insulin) or for the pump as well? I'm a bit confused. Sorry. Thanks. I think in general it would be the same?
user's latest post:
Help - sensor placement. - Page...
Published (2009-11-25 13:26:00)
Quote: Originally Posted by Ali The arms are almost impossible to do on your own if you are not using the Navigator. deafmack, I did not quite follow your description of how to use the upper rear area. Would you mind explaining again. Ali I've heard the same thing at a CWD conference. They recommend using the same cheek a few times, and then switching to the other cheek. Going in rows, basically, on the same cheek, just moving the site...
user's latest post:
Growth spurt???
Published (2009-11-24 23:41:00)
Don't be to surprised if you see a week of steady #'s followed by lows...we almost ALWAYS see that with growth spurts!
user's latest post:
please pray for this family.. (...
Published (2009-11-25 21:23:00)
Quote: Originally Posted by Dad of Daughters Sarah, I didn't say if you don't agree with the post you should be quiet. But 3 days ago on another thread, you did... Yes, in some ways a different situation. But in some ways the same. The other day, the OP wanted to start a discussion about possible triggers/causes of T1D. Here, for what could be many reasons, the OP wanted to share this sad story. In the same way you pointed out that...
user's latest post:
MIA - message to CWD friends -...
Published (2009-11-24 14:31:00)
That is so sad. I can't say how sorry I am and I know there's nothing anyone can do but pray for you and their family. My heart breaks just reading it.
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Latest active threads on Parents of Children with Type 1::
Started 2 days, 15 hours ago (2009-11-25 12:49:00)
by Skyefire
Quote:
Originally Posted by CTuban
I'm a member of a group working with Jeff Hitchcock and Laura Billetdeaux from CWD. We are looking at ways to help CWD continue to meet the needs of families living with diabetes. To help us, we'd like your thoughts on the following questions - please feel free to respond to any or all of these ...
Started 1 week, 2 days ago (2009-11-18 11:56:00)
by StillMamamia
If there are ketones, I smell them, yes.
Probably not what she meant though
Started 1 month, 3 weeks ago (2009-10-03 16:44:00)
by hawkeyegirl
I've always assumed that Jack's "trigger" was the virus that we all had right before he started showing symptoms. But I think he would have gotten it eventually anyway. It was just a matter of time.
Started 3 days, 10 hours ago (2009-11-24 18:01:00)
by Becky Stevens mom
Oh Sherry Im sorry There are lots of members on here that have kids with Hashimotos that you will be able to get support and advice from. I hope the adjustment is not too difficult
Started 2 days, 17 hours ago (2009-11-25 11:00:00)
by OSUMom
Some of you remember that my son was diagnosed just before leaving for college. His endo spoke to him that summer about alcohol and his diabetes without us in the room. I thought this was smart, and I totally respected this.
Started 4 days, 6 hours ago (2009-11-23 21:24:00)
by Sarah Maddie's Mom
It sounds like you stood your ground AND kept your cool. Not easy to do, I'm sure.
Started 4 days, 11 hours ago (2009-11-23 16:42:00)
by hawkeyegirl
I would get it. If you don't need it, fine, but if your child is bothered by site changes, it's a godsend.
For us, it makes site and sensor changes completely painless. My opinion is that our kids go through enough. Why not numb them up if they prefer it that way?
Started 2 days, 14 hours ago (2009-11-25 13:38:00)
by jcanolson
Started 2 days, 18 hours ago (2009-11-25 09:29:00)
by fredntan2
I think they are around 1.0 to 1.8
I'll look later,
she averages 60 units day
Started 2 days, 5 hours ago (2009-11-25 22:50:00)
by My_Dana
This would really simplify life!
I didn't know about it.
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Hot threads for last week on Parents of Children with Type 1::
? - 69 new posts
Started 1 week, 1 day ago (2009-11-19 18:08:00)
by Kalebsmom
http://www.philly.com/philly/educati..._exercise.h tml
Started 5 days, 4 hours ago (2009-11-23 00:10:00)
by Brynn Senior Member
I have to admit, I am horrible, I have never carried it, and this is what is worse, I don't even think I have a prescription for it. We've had to call the paramedics a few times, once when the glucagon was right there and my family didn't even consider using it...
Started 1 week, 1 day ago (2009-11-19 06:25:00)
by cindyrn6617
Started 4 days, 9 hours ago (2009-11-23 18:53:00)
by Kayeecee
I have no problem with her not giving insulin before lunch and that's likely what I would have done with my own child. However, if there is any fault to be found, it would be that she didn't have the child return after lunch to re-check BS. That may have happened and just didn't make it to the fact pattern. With a 40, I worry that whatever took the BS down that low will repeat ...
Started 1 week, 1 day ago (2009-11-19 11:02:00)
by BrokenPancreas
Quote:
Originally Posted by WendyTT
Can someone explain what is "supposed" to happen if a child's blood sugar goes low during the night and it is undetected? Also, what "can" happen? We get up and check Lindsay every night at 2-3am. Every once in a blue moon we will not wake up with the alarm and realize in the morning ...
Started 3 days, 4 hours ago (2009-11-24 23:31:00)
by sisterbeth43 Senior Member
That is very sad and it has always been one of my biggest fears.
Started 1 week, 2 days ago (2009-11-18 18:46:00)
by melissajm
Oh no!! Time will probably make it easier...hopefully & Tyler won't give up!
Started 1 month, 3 weeks ago (2009-10-03 16:44:00)
by hawkeyegirl
I've always assumed that Jack's "trigger" was the virus that we all had right before he started showing symptoms. But I think he would have gotten it eventually anyway. It was just a matter of time.
Started 4 days, 18 hours ago (2009-11-23 09:30:00)
by sammysmom
December 18th is pleanty of time to find someone, get them trained and have them run up to the school and do the bolus. You really don't know if a parent will bring somethimg in that day and he will want to eat it. I really think your best bet is to get someone trained.
Started 1 week, 2 days ago (2009-11-19 02:39:00)
by kim5798
we had high cholesterol too. Hashimoto's thyroid. Then diagnosed celiac in June. Last blood test, no mention of cholesterol & currently on no meds for thyroid since starting gluten free diet for celiac.
kim
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