[Diabetes-talk] Accessible CGM

Mon Jul 11 14:39:59 UTC 2016

Hi Veronica,

Another thought: Besides the armband, you can also get a waistband. I got
mine at Sports Authority, which won't help you because they are either out
of business or going out of business, but any sports store should have one.
I wear my tops on the outside of my pants or skirts, so it's fairly easy to
get at the phone under the top most of the time. Either the armband or the
waistband can work. I had to learn to carry my phone when I got an Apple
Watch, which isn't nearly so important, but now I keep it with me much of
the time--except at home! That's still difficult, because I walk away from
it if it's not yet attached!

Sandi

-----Original Message-----
From: Diabetes-Talk [mailto:diabetes-talk-bounces at nfbnet.org] On Behalf Of
Bernadette Jacobs via Diabetes-Talk
Sent: Monday, July 11, 2016 7:45 AM
To: Diabetes Talk for the Blind
Cc: Bernadette Jacobs
Subject: Re: [Diabetes-talk] Accessible CGM

Veronica, got a suggestion for you. And it should work for almost everyone
else. For those of us who have to worry about clothing without pockets for
our phones question there is an armband that can be purchased from Best Buy,
or even Walmart. You put The phone in a little slot in the band. You were
the band on your arm. Winners and sports people use these. You can't do
everything with your phone. And sometimes it can be a headache. But, if you
don't have a pocket, it's better than nothing. I use mine a fair amount.
Again, if you're doing a lot with your phone you might want to take it out
of the band. I do.

Bern

Sent from my iPhone

> On Jul 11, 2016, at 7:57 AM, Tom Ley via Diabetes-Talk
<diabetes-talk at nfbnet.org> wrote:
> 
> Hi,
> 
> Two items. 
> First, I completely agree with Veronica regarding the fantastic help a CGM
would be when pregnant and managing diabetes. That being said, it is a great
help for most type ones. I just returned from a national conference named
Friends for Life" which is hosted by the Children With Diabetes (CWD)
organization - it is for parents of children with type one. Almost every
single one of the children at the conference, over 500 by my estimate, had a
CGM on. And, the new Dexcom G5 Mobile systems make it a snap to share the
data with another person, like a parent. All the parents had their phones
out watching how their children's blood sugars were doing, even when their
children were off at Disney or another part of the hotel. Pretty cool. 
> 
> Second, hang in there Veronica, you will eventually master getting the
sensors on without the tape sticking together. I don't have a second thought
any more when I have to put on a new sensor, but it took a few months to get
there. 
> 
> I wear my sensor anywhere from ten to 14 days, based on how long I can
keep the tape stuck on. 
> 
> Tom
> 
> 
> I've been using the Dexcom sensors for a couple of years, and now 
> almost never have any issues with applying the sensors without
> 
> -----Original Message-----
> From: Diabetes-Talk [mailto:diabetes-talk-bounces at nfbnet.org] On 
> Behalf Of Veronica Elsea via Diabetes-Talk
> Sent: Sunday, July 10, 2016 2:11 PM
> To: 'Diabetes Talk for the Blind' <diabetes-talk at nfbnet.org>
> Cc: Veronica Elsea <veronica at laurelcreekmusic.com>
> Subject: Re: [Diabetes-talk] Accessible CGM
> 
> Hi Bridgit and all.
> First, boy, I would think that these days a CGM would be a must have 
> during pregnancy. Anytime you're really trying for tight control 
> without trouble, there's nothing like really finding out what happens
when.
> As for testing, in general, I test about the same number of times I 
> usually do, five or six times a day. You have to do two tests after 
> your new sensor warms up and anytime you get a concerning number, 
> right now the advice is to test and make your insulin or food 
> decisions still based on your meter. But for me, being able to look at 
> the number and notice, oops, it's starting up, I can catch it before 
> it gets away from me. And who knows what I'll end up doing once I 
> settle in with this thing as well. The sensor is supposed to last 7 
> days although I've heard some people say they use them much longer 
> than that. I just don't see how they keep them on. <grin> But I've 
> already made changes based on what I've learned. By asking my hubby to 
> look at the graph in the morning, I did figure out where my basals 
> were getting off during the night. I figured out that I was going high 
> about an hour and a half after meals, then coming down, sometimes not 
> in the nicest way before my next meal. My endo had me take my meal 
> bolus about 10 minutes before my meal, instead of right with it and 
> wow! Down came those post meal numbers and I actually got to cut back 
> on the amount of insulin. So there's no question that I can see the 
> benefits to this. For me, I just had to start getting used to carrying 
> my iPhone everywhere and I've not completely solved that one. My phone 
> doesn't stay in many of my pants pockets if I'm crawling around on the 
> floor and I'm forever leaving it somewhere, then having to call it to 
> see where it is. <grin> The first week wearing the sensor with the 
> transmitter, honestly I felt like I had two-ton Lizzie hanging off of 
> my belly. <grin> I'm assuming that over time I'll get over being 
> nervous for three days before I change the sensor, worrying about the 
> tape. At least they're good about replacing bad sensors. Right now I 
> just think they should automatically send out extras. I'm a little 
> curious about how people travel with this. The sensors come in a giant 
> package and all I could think when I first got mine was man, there 
> goes any room in my suitcases. <grin> So while in my book there are 
> things to refine, buttons to label and changes I'd like to see, I really
want to make this work because I can sure see how one would get used to
having easy access to that information pretty much round the clock. Hope
this helps.
> Veronica
> 
> 
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