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My Awesome Endo Office Appointment

I had my endo appointment last Friday and I haven’t had much of a chance to post about it, so here we go.

I knew going into the appointment that I wouldn’t be meeting with my actual endo that day because she was out of the office, but I would be meeting with a nurse that I’ve known from a past career and ventures that I have done.  A quick background and explanation of that.  I used to travel to a lot of local diabetes event when I worked for a horrible company.  One of the events that I regularly attended was a CEU class that was taught by a diabetes educator and an MSRNP.  This MSRNP is now part of my official diabetes team.

Going into this appointment, I already knew how much respect I had for this medical professional.  Then our first conversation about my specific health issues began, and the respect grew even more.

First, we did not have my Dexcom graphs because their office computer was not working properly with the Dexcom software.  And I use a Mac so was not able to get the results ready before the meeting.  I explained what I was seeing in the results and explained that I noticed a large spike in my blood sugar right after I ate.  I told her that I felt it was because I was not taking my insulin enough time before I was eating.  She agreed.  We worked out a schedule and set a goal in trying to take my insulin 10-15 minutes before I actually eat.  She recommended that I set an alarm on my phone about 15-20 minutes before the times that I normally eat.  I said that this might work because I eat breakfast at 8 a.m. every day, lunch at 12-12:30 and dinner at 7.  I’ve set the alarms and so far they have worked 🙂

The next item we looked at was when she asked me why I was over-riding all of the bolus suggestions from the bolus wizard from the Medtronic pump.  My earlier suspicions were confirmed.  Since I am taking a lot of insulin and I have a 3:1 carb ratio, I’ve been taking more than 25 units at almost every meal.  If I have to take 32 units because of a meal and a correction, my pump maxes out at 25, so it looks like I am over-riding it, but I’m not, I’m just taking the max amount allowed.  Then once that 25 is finished, I have to take the remaining insulin….which never happens because I always forget.  So, there lies a problem.  She said that she never thought about that before and that’s something that Medtronic should fix.  I agree…Medtronic, you should fix that.

Next topic of discussion… where my Dexcom all the time.  Next topic.

Dual wave bolus.  I hardly ever use this, but I have been trying to learn, test and try it more often.  We discussed the 80-20 rule and went over a study from the ADA Scientific Sessions in San Diego about a possible 70-30 rule.  I loved the fact that during my appointment we spoke about studies and I actually remembered hearing something about that during the time the Sessions were going on.

The final part of the appointment was changing my basal rates to get my nighttime / morning sugars to a reasonable level.  My basal rates are ridiculously high, I really need to bring them down.  This is where the conversation moved to talking about my weight and dieting. She mentioned that if I can just cut out some of the meat that I eat, that I could potentially cut down on the amount of body fat that I have.  I am trying this at lunch, but it is damn hard for me.

Once the appointment was over, I started talking to her about the diabetes community and blogging and tweeting and the advocacy and all that fun stuff.  Then she hit me with one of the ideas that she has had, and I told her that I will do what I can to help her.  Her idea is that when she is going to speak to kids with diabetes, or the camps, or whatever group of kids she is working with, they are always in a classroom setting learning about diabetes.  She wants to get the kids active.  Her idea is to create a basketball team, a baseball team, a cheerleading team, some sort of team that can go and compete against others.  Not just any others, but children with diabetes from a different area.  It’s basically like a travel league team, but for diabetics.  I think it’s an awesome idea…. awesome I say.

Get back to me after the New Year and we’ll see how well all of this has been going for me.

Dexcom One Month Later

It’s been about a month since I received my Dexcom and I absolutely love it.  I have only worn it about 12-13 days in the month that I have had it because once a sensor comes out, I tend to get lazy and not put a new one in for a few days.  I need to stop this habit.  I need to try a new location because the two times I tried it on my stomach, it has fallen out within 5-7 days because of intense workouts that I have been doing.  The stickiness is just no competition for the sweat.

I am going to try the sensor on the outside part of my thigh and see how that works. Hopefully that will be my go-to location.  I also have some IV 3000 that I can use for when it begins to peel off my body.

There has definitely been some huge positives that have come out of the Dexcom experience.  The most important thing, I have noticed that after every single meal I eat, no matter what it is, my blood sugar goes above 200 and then comes back down within that 2-3 hours afterwards that I would normally be testing again.  I never knew these spikes were occurring, only when they would stay high once I tested again.

There are not many negatives that I have about the Dexcom.  But there is one major main.  The software is not Mac compatible!!!!  I only use Macs, I don’t use PC’s, I refuse to.  I do have a virtual machine on my Mac that runs Windows, but I use it once every 4-6 months, so when I go to turn it on, it takes several hours just to update all of the Windows service packs and updates and all the other BS that goes with owning a Windows machine.

Dexcom, if you are listening, please create a Mac compatible software.  I think you will make the members of the DOC very happy if you did.

Other than that, Dex, you are my friend and you have taught me a lot in such a short period of time.

Thank You for Your Donation to Diabetes Research Institute

I mentioned back in late October and early in November that I would be donating the commissions in November from my Amazon affiliate link to the Diabetes Research Institute.  First, I want to say thank you for those that remembered to click the little Amazon button down below (right now it’s a Steve Jobs banner) to give me the commission.  The Amazon commission is not a lot, around 3-5% of purchase price.  But I am proud to say that I will be donating $50 in honor of the DOC to the Diabetes Research Institute.

I know $50 does not sound like a lot of money in the big scheme of things, but it’s definitely a lot more than what I thought it would be.  So, in order to reach my larger goal of $1,000 by December 2012, I will be continuing this donation offer.  This is how it works:

  1. You want to buy something from Amazon
  2. From my blog, on the lower right hand corner there will be an Amazon banner (it will change depending on which book I am reading at that time)
  3. Once you click on it, it will take you to Amazon.com
  4. You purchase just like you normally would, no codes needed
  5. The DRI donation fund will receive a 3-5% donation of your purchase price
Pretty simple huh?  So if you’re buying online for  Christmas this year, why not have a percentage of it be donated to the Diabetes Research Institute?
*This post is not sponsored by anybody but my own decisions.  The Diabetes Research Institute is where I choose to donate this money to because of my own personal experiences and opinions.  Any other questions…. e-mail me.

Dear Jay Cutler – Letter to Jay

Some of you have seen lately that I have been tweeting about Jay Cutler and my dream and goal of interviewing him.  So here is an open letter to Mr. Jay Cutler himself.

Dear Jay Cutler,

Thank you for taking the time to read this letter.  It is not very often that somebody considers somebody else close to their own age a role model.  I can honestly say that I am one of those people.  I am truly inspired everyday by your actions of being an NFL quarterback with type 1 diabetes.  Why is this so inspirational to me?  Here’s a little background.

I played QB my entire life.  Had scholarship opportunities to Rutgers before a serious knee injury and ended up playing D-3 ball for a year.  During that year, towards the end of the season, I had began to feel extremely tired and drained of all energy.  I was also drinking a lot of water and gatorade and just didn’t have an appetite.  I started to see a big drop in the output I was getting on the field and in the gym.  Long story short, I was diagnosed with type 1 diabetes a few months later.

So, I understand playing QB with diabetes, but can’t understand doing it at such a high level of the NFL.  For the fact that I am a type 1 QB, and you are an NFL type 1 quarterback has intrigued me to have a goal of interviewing you since you were diagnosed.

I am a Jay Cutler fan, except when you play the Eagles because let’s face it, I’m from Philly and you know nothing comes between Philly and the Eagles.  I believe that the media judges and puts you out to be something you are not.

As “groupie” as this letter sounds, it is an honest letter coming from a guy who is inspired by your hard work ethic and what you do for the diabetes community.

So, I end this letter with, Jay Cutler, will you grant me an interview opportunity?

Thank you.

Chris Stocker

FDA Releases Draft Guidance for Artificial Pancreas

Yesterday was a big step in the process of an artificial pancreas.  You may have your opinions of an artificial pancreas, and that it’s not a cure.  You’re right, it is not a cure, but if it makes your life as a diabetic better, than I am all for it.  This thing is long, so if you don’t like to read long documents, than just wait a few days for the experts to go through it.  The JDRF will be releasing some expert notes and reviews of this draft in the next few weeks.

JDRF CEO and President Jeffrey Brewer is quoted as saying:

“Our initial review of the draft AP guidance indicates that the FDA has been responsive and listened to the recommendations of leading clinicians and researchers in the type 1 diabetes field.  It also appears that the draft guidance lays out a rapid timetable to move from inpatient trials to outpatient trials to prove the AP’s safety and efficacy, and if that turns out to be the case it is good news.”

You can find this guidance document for the artificial pancreas over at the FDA.

The School of Hard Knox – Guest Post from The Poor Diabetic

Today’s post is a guest post from my good friend The Poor Diabetic
.  If you haven’t read The Poor Diabetic before, than you are missing out.  Ronnie’s posts are fun, educating, and just down right awesome.  I met Ronnie for the first time out in San Diego for the Roche Social Media Summit.  After speaking with him, I have been wanting a guest post from him since.  So here we go, on the subject of diabetes education.

I have been a diabetic for about 14 years and the real life experiences that come with that has to account for something when it comes to diabetes education doesn’t it?

Yet a newly diagnosed diabetic is more apt to listen to a first year medical student or a nurse practitioner than they would me right?

The reason is obvious, they purport themselves to be medical professionals and  I do not, In fact I like many other diabetic blogs you read go the further to proclaim this in bold print. The reasoning behind this is obvious as well, someone’s health is of primal importance and giving health advice should be left to said professionals. Woe unto you if you give  medical advice with adverse critical results, it is not just a moral issue but a criminal one as well.


But there is something to be said about life experiences when you are living with a chronic disease like diabetes.

It would be an understatement to portray the lack of diabetes education as a mere lacking.

Truth be told most if not many newly diagnosed patients have little if no knowledge of diabetes beyond the passing fancy and I would venture to say that this knowledge one has is fifty percent fact and fifty percent lies, myths, misconceptions, rumors, or any of the many unknowing words you might use to characterize it.

The learning curve after a diagnosis is steep at best and the learn on the job mentality if you may while it might be wrong is the accepted norm.

If I was to share a typical diagnosis it would be as though I was reading from a prepared script.

“ You have diabetes, you need to check your blood sugar using this machine, watch your carb intake, exercise and good luck to you” make an appointment with a nutritionist for your diet adjustments and a nurse will show you how to use your life saving gadgets other than that you are on your own and If you have any questions then I will be happy to answer them on your next visit six months from now. goodbye and good luck” This was my diagnosis story and am sure it was yours as well with a few minor variations.

I was left with very little in alternatives and back then the web was at its infancy, there was no diabetes websites or education resource or the DOC to say the least.

I learned diabetes management the hard way and even with all the online resources available today diabetes education still has a long way to go just to be proficient.

It would be naïve for me to say that a solution to this problem would be one broad stroke of the brush, the problem is a bit complicated than that. But I have one tangible and easily attainable solution.

The Medical profession is overworked  this we know to be a fact, it is for this reason and many others that most newly diagnosed are left to fed for themselves as it may.

These new diabetics are inevitably going to get online to find information on diabetes so why not steer them to the DOC and real diabetes information online.

The benefits for this process will go along way in laying the ground work for a  real diabetes education