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Thread just for us old Type-1 diabetic insulin pump wearing Spyder Ryders

I'm unaware of whether or not i have hpypoglycemic unawareness. I've started seeing a kind of sparkly pattern(very poor description) in my vision while it's dropping, but still often miss it. My doctor recently told me not to try to keep too tight a control because while highs damage blood vessels and nerves, repeated lows damage the heart. A real loose/loose.

As far as wearing the pump 24/7, I've gone from it bothering me all night to where I semiconciously move it around while I sleep and don't think about it. I love/hate it alarming all nigh, but that does allow me to respond to highs and lows.

I agree with you Bob - we live at constantly 5 years from the cure. Kind of like when me kids used to tell me they were "about" to clean their rooms.

I went on a pump in 2000, and my control went from awful to awfully good in a short time. It is a lifechanging product. Not perfect, still with risks of short term and long term complications, but infinitely better than trying to maintain tight control with shots.

An aside - when I was 9 I read one of the Joslin clinic books on diabetes my mom had bought, and it stated that doctors could keep most young diabetics alive until they were in their thirties. I was elated, I thought "Man, I'll be sooo old when I die".
 
I went on a pump in 2000, and my control went from awful to awfully good in a short time. It is a lifechanging product. Not perfect, still with risks of short term and long term complications, but infinitely better than trying to maintain tight control with shots.

:shocked: We must have gone to different High Schools together... :D
I got my 508 pump in 2000.
Prior to the pump; my BEST A1c was 10.5 :opps:
Right out of the blocks: I dropped it to 6.2
 
just a note that the iphone can be set to never auto lock or screen save if that's what you want

You're correct, and that is a more effective solution than the awkward one I'd devised. Thanks.


Between the two of us; we've had 102 years of this... :shocked:

Bob - your story and mine, which we've discussed in pieces before, seem to be incredibly parallel. Someday we definitely need to meet.
 
I am very sensitive to blood glucose levels and treat any Hypo early whether on or off my bike ...

I use an Animas "Ping" insulin pump. My special "OneTouch" glucose meter communicates wireless to my Ping Pump. So any adjustment is as simple as testing and sending the results wirelessly to my Ping Pump (which at times is tucked three or four layers down).

When it gets really warm (desert heat) I put my pump into a specially designed "Frio" hung from my belt. The Frio is a evaporative cooling pouch built for the purpose ...

http://ecx.images-amazon.com/images/I/61NxTevuvBL._SY450_.jpg
 
The idea of keeping the pump cool (or extra insulin) while ryding is appealing. We don't have the desert heat here in Alabama, just humid heat. I may purchase one of these for long trips.

I had one-touch meters that broadcast my BS to the pump, and now I use a Bayer Contour Next that also broadcasts. It's a small thing, but it is convenient not to have to put that reading into the pump manually to let it calculate boluses.
 
Nothing new here, but here's some guidelines on overheated insulin

[FONT=Helvetica Neue, Helvetica, Arial, sans-serif](Not from me, I copied this off of another website)

Insulin is made up of proteins that do not respond well to overheating or freezing. Insulin should never be frozen, left in a car overnight or stored in direct sunlight. A car can get very hot in the summer months and the heat will cause the insulin proteins to break down and deteriorate. So even though it may look fine, it will no longer work the way it should. It is best to keep insulin at temperatures less than 86 degrees and greater than 36 degrees. Room temperature is best for vials or pens that are in use. Unopened insulin pens and vials should be stored in the refrigerator and are good until the expiration date on the bottle. The longer the insulin is left in a very hot or cold environment the more the proteins will break down. The best option at this point is to throw it away and start with a new bottle or new insulin pen.
[/FONT]

Read more at http://www.diabeticconnect.com/diab...away-or-attempt-to-use-it#lqDsG5Wy6gKdKdCe.99

I will definitely purchase a frio.
 
Even though the Bayer BG tester uses a much smaller blood sample; I still miss the One-Touch monitors... :thumbup:
When i got my first pump(MM-722) it came with a one touch ultra-link then four years later i got a new pump(MM-723)it came with a Bayer link meter but when i got on medicare they would not cover there strips so i went back to my one touch,in all these years i think i only changed the batteries twice and that was only because i thought i should every so often not 'cause it said i should(i've had to call for a new case twice as i wore them out and need a new one now.)
 
Spyders on the Bayou

Just took a 1500 mile trip from Birmingham, AL to New Orleans to attend Spyders on the Bayou. Wonderful fun event, lots of great rydes all around the N.O. area, great fried catfish and red beans and rice.

I used the setup I described on the first post in this thread where I could monitor my blood sugar everywhere I went and did pretty well. I bought a waterproof case for my phone (it rained EVERY day).

At least twice I saw my BS start to rise quickly. I tried to use some of the techniques in the book "Sugar Surfing" with moderately good results. I was able to counter the rise when I saw it start without overcompensating. (I know the pump well enough that I could bolus by touch only, and used the feedback on the phone to let me know I'd done it properly)

More importantly I caught the drops. I kept some hard candy in my glove box and used to to keep the drops from going too low.

My main concern from what I'm trying to over-responding to too much insulin. I still have some fine-tuning to do, but the techniques I'm using with the monitoring set up are working to keep me out of trouble.
 
Glad to hear that you've got it all working for you! :clap:
Next Month; I'll be "playing the game", during SpyderFest!
I travel with Gummie-Bears for the lows, and I've got my 530 set up to bolus .5 units per push of the "Up" button. (I can also run it without peeking!)
 
I saw this on www.nbcnews.com. Glad that transplants are becoming increasingly feasible and that standards are being set, disappointed they are not so much for glucose control as for clearing up hpypoglycemic unawareness.
 
Since I'm completely unaware of hypoglycemic episodes; it makes good sense for me! :D
I'll ask my primary care physician to look into this... in about six months or so... :thumbup:
 
Update...

Next Spring: Medtronic will be releasing their newest pump... The 670.
It will rely on much more accurate blood glucose sensors, and be the first pump to automatically dispense basal insulin as needed.
You'll still need to handle the blousing chores for meals, but this is the first step toward the "closed-loop" system. :yes::yes::yes:
It will also alter basal deliveries based upon predictive alerts... Current pumps only will warn of a predicted hypoglycemic episode, and shut down if your blood glucose levels drop to an pre-set level.
This will allow the pump to be more pro-active, and catch highs and lows earlier than ever! :clap:
I'm due for a new pump in January: I may just wait until this one is ready! :2thumbs:
 
I am a 52 year type 1 Diabetic under decent control, taking 2 injections daily for most of my life. I am now 68 years young. I still use a glucometer, none of the modern gadgets, and am happy with the results.
 
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