4 more miles running today. Treadmill run as I couldn’t get my act together to get out before dark.
However, 4 more miles towards reducing my cardiovascular risk. You know, since I’m in a high risk category. Gotta fight for yourself.
All of the CGM’s are still in, post 4 mile run. I’ll really test them in the am with my 6-7 mile run. I don’t know if the researchers are ready to deal with this PITA…..
Now, time to clean up and go find something to eat. Never had trouble with that in Boston.
General thoughts during my run…..(uh,oh, this should be good….)
1. How much money will it take to get the AP to commercial market?
2. What are the remaining hurdles to get it to market?
3. How many T1D’s would wear it?
Let me know what you think….
Just met my AP for the weekend! AND got the four (4) sensors installed. You’ll see the following:
Two (2) Navigators
One (1) Dexcom G4 (not on the market yet, don’t be jealous)
One (1) Minimed EnLite
Now to check in at the hotel, get a run in and get some dinner.
While the AP (on a med pole) isn’t yet ready to go for a run with me, I am excited to see how well it all works together.
You guys getting excited yet?
I have been planning for this for some time.
I am participating in a JDRF funded research study for the Artificial Pancreas. Crazy, I know. Who, in their right mind, CHOOSES to participate in a research study? Well I do. And maybe I’m not in my right mind, but I have been living with T1D for almost 30 years and BOTH of my children are producing 2 of 4 antibodies known to kill islet cells and cause T1D. So, maybe I’m not in my right mind, but I choose research.
Technically, this study is the combination of multiple medical devices already on the market: Continuous Glucose Meter (CGM) and Insulin Pumps, (2 are used, 1 for insulin and 1 for glucagon) that are networked together with a computer algorithm that controls the pumps based on the information from the CGM’s.
But what this really is, is something greater. I am participating in this study to feel, for the first time in 30 years, what its like not to worry about what my blood sugar is.
In case you didn’t catch that the first time….From Friday at 12 noon to Sunday at 6pm I will not have to worry about what my blood sugar is. Let that soak in for a minute…………………….
Now that is something.
I will get into the details of what the Artificial Pancreas is, what it means to me, and what it can mean to all of those currently living with Type 1 Diabetes. Follow along and find out what is happening for those already with T1D, for those who are at increased risk, and to cure T1D.
Mikes Miles is the efforts of myself (Mike) and my family to raise awareness and funds for Type 1 Diabetes. I am living with T1D, and have been since my diagnosis on November 26th, 1982. This also means that my family has lived with this autoimmune disease as well. Our experiences are different, but similarly powerful and impactful to our lives.
80 people per day are diagnosed with T1D, and we want to be a resource for those who are newly diagnosed. We want to be a resource for those who we know and connect with on a daily basis for when the time comes when they unfortunately are diagnosed.
We also choose to work and fund raise for the JDRF, who has been the greatest financial supporter of T1D research since 1970. Many of the advancements in care, prevention and knowledge for the eventual cure have come from JDRF funded research.