Showing posts with label T1D. Show all posts
Showing posts with label T1D. Show all posts

May 8, 2013

Joslin: Challenges and Opportunities in Type 1 Diabetes Research


The Joslin Diabetes Center hosted their first Type 1 Diabetes (T1D) Symposium on May 6 at the Harvard School of Medicine. Titled “Challenges and Opportunities in Type 1 Diabetes Research” there was an impressive group of speakers on a range of Type 1 research. 



The presentations were fascinating. Seeing the eager interchange between speakers was particularly encouraging. I left with a renewed confidence in the quality of work being accomplished and hope for success in taming T1D. Maybe my most significant take away was to recognize the passion that the researches have is akin to what we as parents of Type 1 kids feel. Those passions can come together when those of us living with T1D help support this work directly and through our elected government’s programs.

There were presentations on the autoimmune attack. Obviously understanding the autoimmune process is critical in being creative about how to stop that attack.    I found it amusing that the process was referred to as an “insult” to the beta cells. Makes me want to tell the beta cells to man up and take a little flack. Apparently it isn’t that easy. 

We were shown detailed images of how the macrophages attack beta cells.  One point that stuck with me was that the autoimmune attack may come in waves over a long period. This suggest that a treatment that mitigates the autoimmune process would need to also be in the body for a long period, be effective when there was a periodic attack on the pancreas and the rest of the time not harmful to other immune processes between those rounds of beta cell insults. 

Other presenters spoke on growing new beta cells. It seems that people must do so. Almost all of Joslin’s 50 year medalist, those folks with 50+ years of type 1, who donated their pancreas posthumously for research had functioning beta cells. So beta cells either last a lifetime or, more likely, they can regenerate. As one presentation discussed beta cells pretty much suck at reproducing. Ok that isn’t *exactly* how it was said but you get the idea. There is a small host of inhibitors of cell reproduction hanging out in beta cells. The good news is researcher knows they are there and maybe how to inhibit the inhibition. The closing presentation was on betatrophin which may help beta cells suck less at reproducing. 

Ed Damiano gave a presentation on progress towards a dual hormone artificial pancreas. He made a convincing case for the need for both insulin and glucagon as part of the system. He brought both the passion of a researcher and a dad to the table. It is not that he wants his son wearing a bionic pancreas, it is not the final solution. A cure is. Ed was humble, his research may give kids, like his, a better life while the search continues for a cure. 

That humility was clear throughout the symposium. This was not a day of headlines we so often see blazing about cures but humble presentations that were as much about what researchers didn’t know, as what had been discovered. Accompanying that was a clear desire, often expressed from the podium in reply to questions, to work with other and bring separate efforts together to perhaps jointly find what had not yet been found separately. 

It was a privilege to be there and being somewhat overwhelmed by the individuals giving presentations and asking questions. I can think of little that would have improved the day.    Well, other than a cure. 

My thanks to the Joslin Diabetes Center for extending me an invitation to attend as a member of the diabetes online community. Thanks also to Joslin’s co-sponsor, the Leona M. and Harry B. Helmsley Charitable Trust.


March 1, 2013

An AP by Any Other Name: Animas HHM

Artificial Pancreas is in the news again. This time the press release is from Animas. Yesterday the news was of an article in the New England Journal of Medicine.

Everyone's favorite bard said, "A Rose by any other name would smell as sweet." Sorry Bill,  I am beginning to think you were wrong.  I think the first steps of AP smell sweeter with different names.



My experience talking with other parents is that the term Artificial Pancreas is all wrapped up expectations of it doing what they really, really want. That is magically managing diabetes so well they don't need to worry about it. Being reasonably smart people, who are regularly frustrated by their child's diabetes varying in inexplicable ways, the discrepancies of life, liberty to eat and CGMs, they conclude that the present technology can't deliver that magic.

No kidding. It can't.

There is a whole bit on this in Forbes by David Kliff, Stretching The Truth About An Artificial Pancreas to which others and I replied.

Here is what matters to me as a dad of T1D kids - the NEJM article says the first steps of AP can lessen the number of hypos and keep kids in range longer. This is where the Animas release kicks in, remember the Animas press release? This is a story about the Animas press release.

In the Animas release they don't call it AP. Go ahead go read it. Search it for the word Artificial. It ain't there.

The story is about, "a first-generation closed loop insulin delivery system." I will give you that AFGCLIDS is no rose. They got that.  They call it HHM for Hypoglycemia-Hyperglycemia Minimizer. I would call it Hypblurglycimic Minimizing System. Then I would go for a whole Gilbert and Sullivan operetta - HMS Pancreas.  But I digress.

Like LGS (Low Glucose Suspend) the idea isn't to manage precisely to target. The goal is to help minimize bad sh*t from happening. Preventing bad sh*t, is a good thing.

Progress happens incrementally. Regulators are gonna be more comfortable regulating incrementally and payers will probably be more likely to pay if academia (see NEJM above) can show incrementally better outcomes and hopefully incremental savings in the reduction of expensive hospital visits.

Staying in range more means better long term outcomes. That may not be actually magic but it is a nice parlor trick.


Oh and my apologizes to centuries of British culture.






February 15, 2013

...and about Fido.


I just wrote about mice and my pal Mike remedied me that there are stories about dogs and gene therapy in the news. 

So that it is a different model than than mice

I have joked that you can spit on a NOD mouse and cure it. Still I welcome studies in animals to help find cures. If / when science get there, there may well be a variety of things that are cure-like. I expect better treatments will come first but I digress.

So a quick read of reports on the dog study finds interesting things, promoting insulin production and insulin regulation. Both of which lost in T1D with distraction of beta cells. Both are way cool and I hope lead to more discoveries and progress.

I would caution, as the reports do, that there is the issues that the dogs don't have an autoimmune process attacking the beta cells. In this case the beta cells were killed chemically.  So it maybe the gene thing is part of the process. Stopping the auto immune process seems the big part too. 

It maybe that the ability to reproduce beta cells is there in full onset but the autoimmune process overwhelms it. Consider for example Joslin has 50 year T1D Medalists who still have some beta cell function. That sure suggests that beta cell can rejuvenate even in long term full onset T1D. (Looking for the citation and I think it was mentioned on 'Rents Blog Talk Radio with John Brooks III.)  So the a key then is also stopping the auto immune process that kills them. 



http://www.popsci.com/science/article/2013-02/gene-therapy-cures-diabetic-dogs
http://www.newscientist.com/article/dn23163-gene-therapy-cures-diabetic-dogs.html?cmpid=RSS|NSNS|2012-GLOBAL|online-news

February 8, 2013

Ryan Reed Racing with Roush Fenway and ADA

T1D NASCAR racer Ryan Reed was on Speed TV's Race Hub last night announcing he will be running a Mustang with Roush Fenway. The #16 sports American Diabetes Association colors.


(including more cool pictures) 



October 23, 2012

Wanted: Patients Voice in Diabetes and Emotional well Being


A few days ago I wrote about research were patients were not seen as a stakeholder in research. There were some good comments and I encourage you to go read them. If researcher are part of the problem so at times maybe are patients. I think at times we don't participate as much as we should (arguably because we don't see the results as being to our benefit or even accessible.) We need to step up when we can. Here is place we can. 


Glu has a survey for adult T1D about emotions of diabetes and T1D support. Any #DSMA regular knows this is an issue near and dear to the hearts of the DOC. Here is a chance to help patient views be part of the conversation. 

Here is how to share your voice:
  1. Join Glu www.myglu.org (if you haven’t already.)
  2. Scroll down to the bottom on the home page, in the glu u section click October’s Survey.
  3. Look over the terms and agree as appropriate, this is being run by real researchers so yes there is a real consent process. (I think that approachable research is a good thing). Enter you password so they know it's officially OK with you. 
  4. There are a number of questions each has its own page. A few of pages is a little cumbersome yes but it is a good start and an important topic. 
  5. Participate, spread the word and help make it better.
Full disclosure. I was part of a group that offered views on how to start this process and communicate it to the DOC. I would love to see it succeed not because I had a tiny part in getting the ball rolling but because I think patients voices need to be a bigger part of the research process. Here is a chance to do that. Lets all help make the effort a success so they keep doing it.

Why not parents? As I said this is being done by real researchers with review boards and all that that involves. Doing research with kids, even parents sharing information about their kids is anther level of dotting I(s) and crossing T(s). It should be.  Kids deserve to  be protected with a little extra diligence. In the mean time parents of T1D kids share this with friends in the adult T1D community OK? 

Thanks.  

October 12, 2012

Little Help? Spouses and Significant Others of Adult T1Ds


From the Behavioral Diabetes Institute: 


Just For PartnersDevelopment of an Online Program to Address Emotional Distress in the Spouses and Partners of Adults with Type 1 Diabetes

Help Needed!
WHO WE ARE: A joint project of the Behavioral Diabetes Institute (which is run by William H. Polonsky, PHD, CDE) and the Bringing Science Home initiative (directed by Nicole Johnson).
GOAL: We know that sometimes it can be tough and frustrating when you have a partner with type 1 diabetes.  So we are developing the first Web-based program that is designed to help you, the spouse or partner of an adult with type 1 diabetes, to cope more successfully.  In early 2013, this program will be available to partners all over the world at no cost.    
WHAT WE NEED: In this first phase, we are looking for partners/spouses of adults with type 1 diabetes to complete an online questionnaire.  We will use the initial results of this questionnaire to help us understand how partners are struggling and what might be needed to help them.  We will then use these findings to build the tools for the final online program.  
Please note that we will not be asking you for any personal information that will identify you in any way.   The questionnaire is completely anonymous.
WHO IS ELIGIBLE: Anyone who has an adult spouse or partner with type 1 diabetes.  Must be fluent in English.
WHAT WE WANT YOU TO DO: If you are willing to participate, please access our private and secure study website at: http://justforpartners.behavioraldiabetes.org.  The questionnaire will take approximately 15 – 20 minutes to complete. 
WILL THERE BE COMPENSATION: Well, no.  Sorry about that.  But you will have the pleasure of knowing you have helped us move this important project forward and that you will be contributing to a project to help other spouses and partners deal more effectively with type 1 diabetes!

September 30, 2012

Of Kayla and Chenmistry

Tom Kayla friend and fellow dad of T1D kids has a great post up called, “Parents, Diabetes, IS Not Yours, Give it Back.” In that article he talks about diabetes and families. This is my response, compliment, echo and building from his piece. You should probably read his first so feel free to click over there, this will still be here when you are finished.
http://diabetesdad.org/2012/09/29/parents-diabetes-is-not-yours-give-it-back/ 

Also you should be warned now I like Mr. Wizard, Bill Nye the Science Guy, Magic School BusThrough the Wormhole and many other similar TV shows. (Feel free to suggest  more to the list in comments, riffing on TV shows is fun.) If a tiny amount of science isn't your thing, bail out now.



I have often said Diabetes is a catalyst.  In chemistry that is something that makes reactions happen that would not have happened or makes reaction happen faster. Folks often talk about family chemistry. So it is my bet then is that catalysts are true of families as with petri dishes.

Diabetes, in many ways, makes kids grow up faster and take on responsibilities that parents may not be ready to give up. I think all parents struggle with giving kids appropriate and increasing amounts of independence.

Diabetes is a catalyst for that. More responsibility, sooner is hard. Diabetes often speeds the process of independence. Kids start independently dealing with their day to day diabetes care long before we give them keys to a car and other freedoms in their lives.


In ways that is perverse or at least reveres of what we would want. Think about it. What would you rather see your kid do first; dose and take a lifesaving but potentially fatal drug multiple times a day or drive and be responsible with a curfew? I am willing to take odds on drive and curfew.

So many of us T1d parents have had to do that the other way around. It is hard to believe we are sane. Honestly, I am willing to take odds few of us are sane or at least many are overly cautious.

It is hard to give that independence and maybe see BG rise. Hopefully that is a short term thing that leads to long terms successful self management. We would rather strive for a false perfection reflected in hour to hour numbers than the uncertainty of independence.

Many parents of T1D kids, who share my age and cultural habits, are likely to face diabetes ourselves, T2D. The day to day management of T2D is different than T1D and it is oh so easy to see T2 as less significant for those differences. Diabetes is a rat bastard as well as a catalyst. In my own case that rat bastard, and my parental inclinations are to do for my kids first, meaning I am tempted put aside my own care to worry about the kids’. Again to betting on a false short term misconception and giving T2D odds in the long term.

I am trying to not to let my understanding of T1D be the an inhibitor of T2D care.  That is the opposite of a catalyst. Something that slows down a reaction, my reaction to my own diabetes. I am not doing very well at it.

There is a different diabetes. One that is mine. One I should care as much about it as I do my kids'.  

May 10, 2012

Grail-like Glucagon

From the News Wire:

LATITUDE Pharmaceuticals, Inc. Develops a Stable Liquid Glucagon Formulation
SAN DIEGO--()--LATITUDE Pharmaceuticals, Inc. (LPI) announced today that its scientists have developed the first ever, ready-to-inject, stable liquid glucagon formulation (Nano-G). A glucagon formulation with these properties had been a highly sought after Holy Grail of drug developers for decades. 
Currently, glucagon is indicated for emergency treatment of insulin-induced hypoglycemia and as a diagnostic aid for radiological examinations. Researchers have long been interested in evaluating glucagon for hypoglycemia prevention, the bi-hormonal insulin/glucagon pump and the treatment of obesity but have been thwarted by the absence of a stable injectable glucagon formulation. 
Glucagon is a notoriously insoluble and unstable molecule and is therefore provided as a dried powder. Before use, the glucagon is dissolved in an acid solution by following a cumbersome, eight-step procedure that becomes an outsized task during life-threatening hypoglycemia.
Glucagon, while useful stuff, kind of fall short of my Holy Grail Test. Sure cures fall into Grail status. I think prevention would come real close too. I have also written about side orders to go with the grail like some basic integration of management tools. We each seek our own Grail and I am happy that stable liquid glucagon was someone's.

I am a big fan of progress. Automation in the prevention of hypos would be progress. There are smart smart folks working to AP projects. That is great. For me this is better and Better is Better. Dual hormone pumps with very good logic tools to support them is better. Staying in range more of the time is better. Glucose responsive insulins that make hypos history would be that much more.

The Grail? Cures. Not a cure, Cures. 'cause I know enough about type 1 diabetes to know that one size doesn't fit all. I also know enough to know progress is one step at a time.

Mostly I know this about Grails, nobody ever find them (except for Sean Connery & Harrison Ford.) When you find what you thought may be a Grail you discover a new passion.



So lift your glass and toast pursuing passion.  

April 7, 2012

#TwoBits - One Post by @momof2T1s

#TwoBits is a way of pointing to great stuff on the DOC. Pointing out two sites helps show there is a wide span of these great ideas. I do this as much to make myself seek out other work as anything else. I feel an obligation to point stuff out. A very good friend very passionately spoke recognizing and sharing others work not competing with it at some ungodly hour in the lobby at MedtronicDAF. She was so so right. #TwoBits also helps me do that.

So here it is one link with #TwoBits. I write because… by Christina. I so love what she writes about wearing hats and when they are they are worn. It helps that Christina is a mom to two T1s. That is bit #1.



#2 is how she recognizes Kerri. It is both Funny and appropriate. That ties back to the whole idea of recognizing others. A good friend of the DOC at Medtronic spoke about borrowing from other and in a reply to my post emailed the source of that document making the point that when boldly borrowing from other to cite the source. So thank Lane Desborough for teaching me Proudly Found Elsewhere and that it came from Proctor and Gamble.

More importantly thanks Christina for expressing why I write too.  

March 26, 2012

Proud of the Kid

Connor spoke at the American Diabetes Association's Greater Philadelphia Area Chairmans's Reception the other day.

Did a nice job.



Proud of the kid, even if he is not much of a kid any more.


March 22, 2012

Beta Cell Stress Could Trigger Type 1 Diabetes @JDRF


Before T1d Stresses patients, stress on the beta cells may trigger T1D. Which matters because understanding how it works help find cures. So knowing what you don't know helps.

Study provides important clue in type 1 diabetes; could help scientists identify and validate potential drug targets to alleviate ER stress and preserve beta cell mass in T1D
In type 1 diabetes (T1D), pancreatic beta cells die from a misguided autoimmune attack, but how and why that happens is still unclear. Now, JDRF-funded scientists from the Indiana University School of Medicine have found that a specific type of cellular stress takes place in pancreatic beta cells before the onset of T1D, and that this stress response in the beta cell may in fact help ignite the autoimmune attack. These findings shed an entirely new light into the mystery behind how changes in the beta cell may play a role in the earliest stages of T1D, and adds a new perspective to our understanding how T1D progresses, and how to prevent and treat the disease. 
More about the study, published in the March 22 issue of the journal Diabetes, the researchers, led by Sarah Tersey, Ph.D., assistant research professor of pediatrics, and Raghavendra Mirmira, M.D., Ph.D., professor of pediatrics and medicine at the Indiana University School of Medicine is online here: 
http://www.eurekalert.org/pub_releases/2012-03/jdrf-rfb032212.php 

March 14, 2012

Body of Proof - Type 1 Diabetes Stops Nothing


In last night’s episode of the coroner crime drama Body of Proof, the character of the  daughter of the lead was diagnosed with type 1 diabetes. It was done very well.

Life is going on and nobody seems to see anything coming. Grandma is at home with the teen while mom is at a business function. The teen is rushed to the hospital but nobody is sure why. Test show it is DKA associated with T1D.

Later we see mom and daughter in a hospital room. The girl has a bunch of IV tubes hanging. She is scared. Mom is scared. The girl doesn’t understand how she can have diabetes if she isn’t over weight diabetes.

Mom tells her that is type two and it is acquired but her diabetes is different.

The girl knows diabetes is incurable. She is afraid she will loose her legs or go blind.

Mom says, “You forget everything you have ever heard about diabetes. Okay? Those are misconceptions. It is a completely manageable condition...  and I am going to be with you every step of the way. Okay.”

So many things right here:

  • Diabetes sneaks up on you - you don’t see it coming. 
  • It is scary, for everyone in the family. 
  • There are different types of diabetes. 
  • Type 2 and type 1 are not the same thing.
  • There is no cure.
  • Forget the misconceptions. 
  • I am going to be there with you every step of the way. 


There was more.

After the broadcast ABC ran a little PSA with the actresses Dana Delany and Mary Mouser on the set. They mention JDRF and speak of the kids and adults diagnosed by type 1 everyday, “like me” says the teen actress.

Wait! kid and adults... like me!

Yes. Mary Mouser, teen actress has T1D.

On the her twitter feed @MaryMMouser she wrote her goal “was to prove that Diabetes stops nothing! :)”

As the father of an aspiring young actor who also happens to be T1D the message that diabetes stops nothing is particularly poignant.

Thanks ABC.
Thank Body of Proof.
Mostly, thanks Mary.

Diabetes stops nothing!


(You can watch the episode here: http://abc.go.com/watch/body-of-proof/SH5580165/VD55179081/identity. The scene with the mom and daughter is at the end time at 40:30. Sadly the Public service announcement at the end of the broadcast is not included.)

Update: Scott posted a link the PSA in the comments, thanks Scott, here it is:

March 2, 2012

Hey DOC! Welcome Maryam #TwoBits


Hello my Diabetes Online Community friends. Meet Maryam or Myrm as my son calls her, all though I have no idea how that nick name is spelled. (Regular YDMV reades will know I have no idea how anything is actually spelled and not be surprised.)
She bring the DOC the much needed sound of young america which is actually the name of a PRI show but you get the point.   
Here is the bio for her blog: 
Maryam Elarbi is an 18-year-old freshman in college who was diagnosed with Type 1 diabetes at the age of 10. Eight months after her diagnosis, Maryam’s family began attending the “Children With Diabetes” conferences, which changed their entire view on Type 1 and how to cope with it. Over the past eight years, Maryam has been actively involved in advocating for people with Type 1 through these conferences, as well as fund-raising for diabetes research through JDRF’s annual “Walk to Cure Diabetes.” In her spare time, Maryam enjoys reading (especially works by Jane Austen and Kurt Vonnegut), writing, spending time in the beautiful city of Philadelphia, and defeating her brothers in the new “Dance Central 2″ game.
She and the brothers she thrashes at Dance Central 2, helped my son feel welcome at CDW years ago. What a great gift. You can see her almost live in theBetesNOW's fashion report form the FFL Red Carpet. So DOC welcome Maryam! Here’s two of her recent posts:
Adventures in Hypoglycemia
The Importance of Consistency




YDMV on the Goal of diabetes management and teens

.

February 29, 2012

We Hold TheseTruths to be Self-Evident, Except Trials are Required.

Medtronic has a press release out today that says with Low Glucose Suspend (LGS) folks spend less time in hypos. That seems kind of intuitive to me but hey the studies need to be done. It it wasn't a small difference IHMO. 19% less time in hypos.



You can read the press release here or click this graphic to see what is said in markets that aren't the USA and where people with diabetes can get a LGS pump.



YDMV has burned a fair number of electrons on and around LGS. Here is hoping this helps the FDA focus on the value this step brings living safe lives with insulin infusion.

What do yo think?
Would you like LGS?
Would you use it?

.

Anyone have a Dummies Guide to @ANTPlus

Or maybe a not so dumb but new to it patients guide to how ANT+ may impact the diabetes space?



The headline reads:

ANT+ Expands Established ULP Wireless Ecosystem to Further Support Mobile Platforms and Augment Unique Use Cases in Sport, Fitness and Health

and down in the text it has this bullet: 
  • Dexcom Continuous Glucose Monitoring (CGM): showing real-time glucose information at a glance. ANT+ technology will be incorporated into future products to enable connectivity with personal electronic devices.
Anyone up on this? 'Cause I aint and I would like to be. Here's why in case you forgot:

Best Diabetes Parenting Advice - Updated

As theBetes:NOW has reposted a short video of my diabetes parenting hero.



At my first CWD Friends for Life I heard this dad simply say, "My wife and I are our daughter’s primary care team.”

Brilliant. This piece of wisdom had been updated when theBetes:NOW caught up a few years later. The new message,"She'll become her own Primary Care Giver.



What do yo think, who is the primary care giver in your diabetes life?

Previously on YDMV: Of Independence and Angry Mobs

February 28, 2012

#TwoBits on Green and Orange at CWD Conshy

Children with Diabetes held a tech conference in Philly, will Conshy (Conshohocken) PA over the weekend. A very good friend asked why I go to these. Simple because when it is all said and done I need to recharge the batteries to have the energy to do the right stuff as opposed to the easy stuff. Diabetes Burn out takes different forms with parents, doing to little or even worse doing to much and making diabetes the focus of life.

So for me the focusing on diabetes for a day helps me focus on not over focusing on diabetes the rest of the time.


Here two other great views of the event form around the DOC. Kerri talks about some of the frustrations and diabetes burn out stuff and definitively defines CGM'er and Art Panc.

I finally got to briefly meet another DOC dad, Scott Benner, (Like the DOC needs another Scott, someone needs to do a study of the name Scott and the correlation to T1D.) He is someone I have admired from a far (and someone I swiped a this image from, Thanks Scott). We're both orange but I would say we bleed green.

Love to know who else is orange or green.

February 27, 2012

@GlookoInc Upgrade: Carbs

Glooko has an upgrade out. Makes it easier to look up carbs and "with one click add the value to your note."

Their email goes on to say,"Say goodbye to your bulky carb counter book and hello to a comprehensive digital food database. No more adding up carbs in your head, or recording them on paper. Use Glooko Logbook to search nutritional information, adjust for serving sizes, and automatically enter in your logbook.  Tracking the food you eat anytime, anywhere on your iPhone and putting it context of your blood glucose readings, helps you stay on top of monitoring diabetes.   

Upgrade to the newest version of the Glooko Logbook app on iTunes." 

Click here for a previous YDMV Glooko post

Check them out on the web http://www.glooko.com/
or Twitter: http://twitter.com/GlookoInc

February 23, 2012

Dexcom Acquires Sweet Spot. Is Dewy on the way?


Dexcom released their earnings call online today. (Listen here for your self to see how off I am in my reporting.)


These calls are like a crystal ball. Fun but future looking. I looked for a picture of a Dexcom and a crystal ball ad found Kerri's Dexcom isn a glass with a super cute cutest Birdie picture. Close enough.

Right off the bat I found it interesting. Terry Gregg announced the acquisition of SweetSpot http://www.sweetspotdiabetes.com/.

Even the most casual reader of YDMV knows I have a particular interest in diabetes data. SweetSpot was identified on the call as adding sophisticated diabetes data management to the Dexcom portfolio. Terry Gregg identified two shortcoming in the Dexcom offerings; CGM pump integration and universal data integration. Ultimately they hope to see seamless data flow from the CGM to a mobile device and into the cloud.

Dexcom also mentioned the recent Tandem and Roche agreements. Interestingly the used the term “open architecture” repeatedly on the call in the CGM pump context.

Generation 4 sensors were said to be expected to be submitted to the the FDA end of Q1 early Q2 2012 and it sounds like CGM/Pump about a quarter days after Gen 4. YDMV.

Gen 5 was briefly mentioned and in the context of connecting out to open architecture devices including mobile and the cloud. Also accuracy was said to be at therapeutic levels.

The business model for sweet spot was covered in a question. At times it sounded a little big brother like with the VA, clinics and possibly insurers being customers of the data service. Naturally I would love to hear more about patients and later in the call they noted that the current product is approved for clinics.  Patients can see see what the clinic sees gets, so i guess (key word guess) patients aren't approved recipients of SweetSpot. A desire for a more patient centric data model was shared by one of the Dexcom C suite dudes. Anything is ways off in the future. There was also mention of criticism from the physician community of Dexcom for not having a means of connecting Dexcom information to the clinic. The future is digital and the acquisition of SweetSpot look like good positioning of the future.

At about 36 minutes into the call there was an interesting exchange on the Gen 5 product and the FDA. Specifically comments about the FDA concern that the health data being primary in on the mobile device. There were some interesting real world comments about os upgrades and aps running on devices. It was brief but good to know someone is having the conversations with the FDA and helping move the ball forward. I am sure the conversations are happening elsewhere but still it comforting to hear about the exchanges. Also interesting comments at about 56 min about their relationship with FDA. I'm "happy" with the FDA, industry has to make an effort.

On a personal note my kids don’t like carrying another thing so getting the CGM into the pump and ultimately the cloud is a step that may help them choose to wear sensor more.

Full disclosure, I own Dexcom shares.

http://www.ydmv.net/2012/01/of-fantasy-diabetes-devices-sheldon.html