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  • 8/14/2019 DiaTribe - Research and Product News for People With Diabetes - Issue #5

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    conference pearls

    American Diabetes Association 67thScientific Sessions (Chicago, June 22-26, 2007)

    In late June, diaTribe sent our team to Chicago to attend the 67th Annual Scientific

    Sessions of the American Diabetes Association. Referred to simply as ADA, this meeting

    is the biggest in diabetes; this year over 11,000 researchers, doctors, educators, nurses,

    dieticians, and other professionals gathered to present new scientific data, hear fromclinical thought leaders, and generally expand the

    knowledge base in diabetes. We came back from

    the grueling five-day meeting exhausted but newly

    optimistic about ongoing work in diabetes care as well

    as the many exciting new drugs and products that we

    expect to become available within the next few years.

    See below for our ADA pearls!

    Pumps, patches, and ports new insulin

    delivery technologies for type 2s are just

    around the corner. One interesting trend this year

    was the large number of small companies working on

    new insulin-delivery technologies that may provide

    affordable alternatives to injections within the next few

    years. The h-Patch is a disposable insulin patch pump

    for type 2s being developed by Valeritas; this device

    would be simpler to use than traditional insulin pumps.

    Each h-Patch lasts a day, after which it is discarded.

    The patches infuse a fixed basal rate of insulin but also

    have the ability to deliver additional units as needed

    for meals. We think this technology has the potential to

    make it easier for type 2s to go on basal-bolus insulin

    therapy although it would not be appropriate for type 1patients because each pump uses a standard basal rate that patients are unable to change.

    Alternatively, insulin ports are another way of getting around injections; these are similar to

    the infusion sets used for insulin pumps, removing the need to give many daily injections;

    patients would only need to pierce their skin every few days when it came time to change

    the port. We believe this would also be very useful for patients interested in using Symlin

    (see our Learning Curve on Symlin in diaTribe #3) to reduce their post-meal blood glucose

    levels but who dont want to take more shots per day.

    V O L U M E 1 I S S U E 5

    Conference Pearls .......... 1

    ADA and CWD two big

    meetings of 2007

    From the Editor .............. 2

    What a summer.!

    FingerSticks ................... 2

    Inhale, exhale

    Test Drive ........................ 7

    Jim Hirschs candid take on

    the Omnipod and the SEVEN

    Diabetes Dialogue ......... 9

    Jeff Hitchcock and the

    inspired, inspiring Children

    with Diabetes organization

    Logbook.......................... 15

    A challenge to the Acting

    Surgeon General

    Learning Curve ............... 17

    Olive oil, wine and the

    French Paradox

    Profile .............................. 19

    Chronic disease: working

    extra hard to work

    Trial Watch ...................... 21

    Sign me up!

    What Were Reading ...... 22

    So you dont have to!

    NewNowNext ................ 23

    Whats in

    in this issue

    research and product news for people with diabetes

    To subscribe todiaTribe, visit

    www.diaTribe.us.1continued on page 3

    T1/2

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    from the editor

    From conferences to Avandia to burritos...What a trip!

    Happy day! We are all in terrific moods here at diaTribe as

    the summer ends weve attended some great conferences,

    read some wonderful research papers, and had some terrific

    conversations with leading doctors, nurses, and scientists. Were all in

    the diaTribe offices just winding down on a Friday afternoon, drinking a beer and thinking

    about how lucky we feel. Thanks to all of you for checking in let me tell you about this,

    our fifth issue of diaTribe!

    Weve been thinking big thoughts about diabetes since we returned in late June from

    the American Diabetes Meeting (ADA) in Chicago there was so much to see! Eight of us

    traipsed around the city for four days taking in news on type 1 diabetes, type 2 diabetes,

    exercise, lifestyle, psychology .. you name it, if it concerns diabetes, we looked, listened,

    took notes, and discussed it! We also went to the Children With Diabetes Meeting in

    Orlando and felt more hopeful about diabetes than we had all year see why inside.

    For our Test Drive, our gadget-avoiding Jim Hirsch tells us about his experiences withdisposable pumps and continuous sensors. It isnt always pretty, but it is encouraging. Find

    out how he fared on page 7.

    Thats it from San Francisco weve finished our beers and most of the team is off

    to find some of San Franciscos finest food in the form of burritos in our Mission district!

    Im running to find baby Lola, Coco, and John and to thank them again for an amazing

    summer. Cant wait to see you next time if you have anything on your mind, or ideas for

    diaTribe, as always dont hesitate to write me at [email protected].

    Yours,

    Kelly

    fingersticks

    D I AT R I B E R E S E A R C H A N D P R O D U C T N E W S F O R P E O P L E W I T H D I A B E T E S

    2

    diaTribe staffEditor in Chief

    Kelly L. Close

    Managing Editor

    James S. Hirsch

    Contributers

    Kaku Armah

    Daniel Belkin

    Michael Chen

    Jenny Jin

    Amy TenderichDaniel Trecroci

    Mark Yachoan

    Design

    Gina Wilson

    diaTribeadvisory board

    Jennifer Block, RN, CDE

    Dr. Zachary Bloomgarden, MD

    Dr. Bruce Bode, MD

    Dr. Nancy Bohannon, MD

    Dr. Bruce Buckingham, MD

    Dr. Wendell Cheatham, MD

    Dr. Steven Edelman

    Dr. Barry Ginsberg, MD, PhD

    Debbie Hinnen, ARNP,

    BC-ADM, CDE

    Dr. Irl Hirsch, MD

    Jeff Hitchcock

    Dr. Lois Jovanovic, MDDr. Francine Kaufman, MD

    Dr. Aaron Kowalski, PhD

    Mirasol Panlilio

    Dr. William H. Polonsky, PhD

    Michael Robinton

    Jane Jeffrie Seley, NP, CDE

    Virginia Valentine, CNS,

    BC-ADM, CDE

    Dr. Howard Wolpert, MD

    Gloria Yee, RN, CDE

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    What to do about Avandia? An expert panel weighs in. More than four thousand

    doctors packed into an enormous auditorium to hear from Cleveland Clinic cardiologist Dr.

    Steven Nissen, the author of the original paper that started the Avandia controversy. As

    readers probably saw in the popular press, this paper suggested that Avandia, an insulin

    sensitizer commonly used for type 2 diabetes, increases the risk

    of heart attack by 43%. Other expert panelists at this symposium

    included Dr. Philip Home, a well-known UK researcher; Dr. John

    Buse, the highly regarded president of the American Diabetes

    Association; Dr. David Nathan of Harvard Medical School; Dr.

    Barry Goldstein of Thomas Jefferson University; and moderator

    Dr. Richard Kahn of the American Diabetes Association. The panel

    was not able to answer the question of whether Avandia is actually

    harmful we simply do not have rigorous clinical trial evidence

    to decide one way or the other but Dr. Kahn did pose a very

    interesting three-part question to his colleagues: What would you

    do with 1) a patient who is not on Avandia, 2) a patient who is ingood glycemic control on Avandia, and 3) a patient who is not in

    good control on Avandia? Dr. Buse led the panelists in recommending that 1) someone

    who isnt taking Avandia yet should be started on one of the many alternative medications

    available, 2) someone who is doing well on the drug should remain on it until we know

    more about it, and 3) someone who isnt doing well on Avandia should be evaluated for

    therapeutic intensification and possibly discontinuation of the drug.

    An FDA panel met July 30 to deliberate on the controversy and on August 14, a black

    box warning was issued for Avandia as well as Actos, a drug from the same class (called

    thiazoladinediones). The warning emphasizes that the drugs may cause or exacerbate heart

    failure, especially in certain patient populations. Both drugs will, however, remain on the

    market this warning doesnt address heart attack risk, the risk originally raised by Dr.Nissen. We believe all patients should make sure their healthcare team is watching out for

    safety first if you have not done so recently, we encourage you to check in with your

    healthcare team to make sure you are on optimal therapy. If your A1c is over 7 and your

    therapy has not changed in more than six months, your doctor or educator may wish to

    optimize your routine they will be the best judge, but as always, it is very important for

    you to follow your own progress and to manage your diabetes to the best of your abilities.

    A new paradigm for continuous glucose monitoring (CGM): Improving

    A1c without increasing hypoglycemia. One of the most important trials presented

    this year was the STAR 1 study, the first randomized controlled trial to compare continuous

    glucose sensor-augmented pump therapy against traditional insulin-pump therapy without

    CGM. Dr. Irl Hirsch from the University of Washington gave a brisk presentation to a

    packed auditorium of more than a thousand professionals. The trial enrolled 138 adults and

    adolescents with type 1 diabetes; all were already using insulin pumps. These participants

    were randomized into two groups. One began wearing the Medtronic Paradigm 522/722

    pump, which can be used with a real-time CGM sensor. Continuous glucose data were

    displayed in real time on their pump screens. The other group went on the Paradigm 715

    smart pump, a standard insulin pump without CGM. After six months, A1c dropped from

    8.5% to 7.8% in both groups, but only the CGM group was able to do so without an increase

    in hypoglycemia. University of Virginia mathematician Dr. Boris Kovatchev nicely summed

    up this finding when he said that we should think of CGMs primary benefit as the ability to

    D I AT R I B E R E S E A R C H A N D P R O D U C T N E W S F O R P E O P L E W I T H D I A B E T E S

    3continued on page 4

    The panel was not able

    to answer the question

    of whether Avandia is

    actually harmful we

    simply dont have

    rigorous clinical trial

    evidence to decide one

    way or the other.

    PHOT

    O:MARKYARCHOAN

    Doctors Refuel on Diabetes Research at ADAcontinued from page 1

    Tough inter-booth competition

    as drug and device companies

    battle for the attention of

    healthcare providers.

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    reduce hypoglycemia; this in turn allows patients to intensify therapy and reduce A1c and

    long-term complications. We note, however, that to everyones surprise, in STAR 1 there

    were actually more episodes of severe hypoglycemia in the CGM group than in the control

    group (11 vs. 3). In case your doctor might note this or might seem otherwise unenthusiastic

    about the study results it is key to know that Dr. Hirsch attributed this result to unique

    problems that occurred at one of the study sites rather than to the use of CGM itself. STAR

    1 was the first of three major trials that Medtronic is sponsoring to show the benefits of

    continuous glucose monitoring. The trial was at least in part intended as a practice study

    to help the research investigators prepare for the current STAR 3 trial. STAR 3 is the largest

    of Medtronics CGM trials the yearlong trial was expanded recently to 550 patients - and

    will likely also be the most important one in helping convince insurance companies to pay

    for CGM. Unlike STAR 1, it will compare sensor-augmented therapy against multiple daily

    injections (MDI) of insulin guided by fingerstick glucose values it is comparing against

    MDI rather than standard pump therapy because MDI is still the way most type 1 patients

    take insulin.

    For Byetta enthusiasts who wish they could take fewer injections, next-

    generation incretin therapies are on the way. The next big drugs in the GLP-1

    class to which Byetta (exenatide, made by Amylin/Lilly) belongs will be liraglutide (Novo

    Nordisk) and Byetta LAR (Amylin/Lilly), which stands for Byetta long-acting release. Bothare expected to be on the market around 2009 see this issues What Were Reading for

    more details on how they work. Liraglutide will be a once-daily injection with a fine needle,

    while Byetta LAR will be a once-weekly injection with a slightly wider needle. Just before

    ADA began this year, Novo Nordisk released some intriguing data from a large six-month

    trial for liraglutide. In this trial, liraglutide produced a 0.2% greater A1c drop than Lantus

    insulin in patients not achieving their A1c goal on metformin and/or sulfonylureas. Oral

    medications like metformin and sulfonylureas are rarely enough to keep type 2 patients

    at A1c goal for more than a few years, after which insulin therapy becomes necessary.

    However, in the future it may become common practice for patients who have stopped

    responding to oral medications to try a GLP-1 drug like Byetta or liraglutide before going on

    insulin.Unlike insulin, which causes weight gain, GLP-1 drugs are associated with weight loss,

    though the actual amount of weight change varies greatly among individuals. Dr. John

    Buse, ADA president, presented new data showing that patients in the original phase 3

    Byetta trials who continued taking Byetta for three more years continued to lose weight

    and maintain the same A1c drop that they had after six months of Byetta treatment. These

    are very promising results, especially since the current twice-daily formulation of Byetta

    is actually degraded too quickly to provide 24-hour effects. Byetta LAR should overcome

    this problem, which is why clinicians are excited to see the results of the currently ongoing

    large phase 3 study of Byetta LAR. If the results from a much smaller trial with Byetta LAR

    hold up, the once-weekly formulation could produce greater A1c improvements (perhaps a

    drop of 1.7% in A1c, as seen in the smaller trial) and weight reductions than the twice-daily

    formulation. Amylin/Lilly stated they expect to release the results of ongoing phase 3 study

    of Byetta LAR well update you when they do

    Why Janumet may be better than Januvia. Researchers from Merck, which

    makes both of these drugs, presented some interesting data that suggest metformin

    and Januvia (sitagliptin) may have synergistic mechanisms of action. Januvia belongs

    to the DPP-4 inhibitor class of drugs, which work by inhibiting the action of the DPP-4

    enzyme, which breaks down GLP-1. The net result is that it works by increasing the level of

    active GLP-1 in the bloodstream by about two-fold (Byetta effectively raises GLP-1 levels

    considerably more, which is why it produces different effects than Januvia). Metformin

    D I AT R I B E R E S E A R C H A N D P R O D U C T N E W S F O R P E O P L E W I T H D I A B E T E S

    4continued on page 5

    The combination pill, Janumet

    STAR 3 is the largest of

    Medtronics CGM trials

    and will likely also

    be the most important

    one in helping convinceinsurance companies to

    pay for CGM.

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    D I AT R I B E R E S E A R C H A N D P R O D U C T N E W S F O R P E O P L E W I T H D I A B E T E S

    5continued on page 6

    is one of the oldest diabetes drugs on the market, but its mechanism of action remains

    somewhat of a mystery. This year, researchers revealed that metformin also raises levels

    of GLP-1 in the bloodstream by about two-fold, but while Januvia works to prevent the

    breakdown of active GLP-1, metformin seems to increase the total production of GLP-1.

    Thus, when taken together (i.e., Janumet), the two drugs produce an additive effect on

    GLP-1, increasing levels by about four-fold. This may account for why Janumet produces

    a more robust A1c drop than either metformin or Januvia alone. The ADA recommends

    metformin as first-line therapy for type 2 diabetes, followed by either a sulfonylurea(generic), a thiazolidinedione (Actos or Avandia), or basal insulin (Lantus or Levemir). At

    the time of the recommendation, Januvia was not yet approved by the FDA, but these new

    data suggest that Januvia might not be a bad idea for combining with metformin in patients

    who dont reach A1c goals on metformin alone.

    No one is safe from hyperglycemia, especially during pregnancy. The results

    of the HAPO study were alarming for people both with and without diabetes. HAPO was

    the first study to ever look on a wide scale at pregnancy in women without diabetes. The

    investigators discovered that there were no cut-offs for increased risk when it came to

    glucose values. In other words, women with fasting plasma glucose values from 75 mg/dL

    to 100 mg/dL showed a linear relationship between glucose level and adverse pregnancy

    outcomes (note that 100 mg/dL is the cut-off for prediabetes and 126 mg/dL is the cut-off for diabetes). These included outcomes for the probability of the baby being large for

    gestational age (LFGA), rates of primary C-section, neonatal hypoglycemia in the newborn

    baby, and unusually high levels of insulin production. These findings are a reminder that

    we should all be striving for glucose levels as near to normal as possible, even before we

    reach diagnostic cut-offs for prediabetes and diabetes; to a certain extent, these cut-offs are

    only arbitrary values especially during a pregnancy.

    See even more Pearls online at www.diatribe.us/issues/5/conference-pearls.php.

    Children with Diabetes Friends for Life

    Conference and Expo (Orlando, July 11-15, 2007)Friends for Life, the national Children with Diabetes (CWD) conference, took place inOrlando, Florida, from July 11 to July 15. The conference exercised both mind and body

    while experts discussed the latest treatments in diabetes, professional athletes ran sports

    camps. The exciting exhibit hall featured the latest continuous glucose monitors, insulin

    pumps, and tasty sugar-free products. In the midst of it all, we had our diaTribe stand.

    See our Dialogue with founder Jeff Hitchcock for more on how the conference began!

    There is often a gap between the advice from health care providers

    and what patients actually understand. This dearth of health literacy was the

    focus of US Surgeon General Ken Moritsugus keynote speech. We thought long

    about his message: to close the gap, both parties need to work toward bettercommunication. It is challenging because much of the time, healthcare providers

    are pressed for time if your doctor is not, you are among the lucky! We do

    strongly encourage working with a diabetes educator no matter how good your

    diabetes management is. They can help you figure out how to improve your

    management and can probably even give some communication advice not

    only with your doctor but also with your friends and family. Moritsugu also encouraged

    patients to make a point to stay informed about the goings on in the world of diabetes. We

    at diatribe urge you to check out diabetes resource dLife at www.dLife.com where you can

    ILLUSTRATION:DANIELBELKIN

    T1/2

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    D I AT R I B E R E S E A R C H A N D P R O D U C T N E W S F O R P E O P L E W I T H D I A B E T E S

    6

    find nutrition information, recipes, and even MSNBC Hardballs Chris Matthews talking

    about his experience with diabetes. We would absolutely agree with Moritsugu that you

    should work to close the communication gap by using your knowledge and experience to

    help others. For more on what Moritsugu shared, see this months Logbook.

    Ready, set, pump! Dr. Henry Anhalt, a noted pediatric endocrinologist and

    CDE spoke extensively about Why we pump. He said his type 1 patients would

    insist that they were accurately delivering fractional insulin doses with a regular syringe

    but would fail miserably in a reproducibility test. As many readers know, and as Dr. Anhalt

    stressed, insulin pump therapy allows you to deliver exactly how much you need, and leads

    to better glycemic control. Better control of course means lower risk of both micro and

    macrovascular complications. Dr. Anhalt discussed pumping for children in particular;

    since school nurses are not allowed to give insulin shots, some parents find it difficult

    putting their children on an optimal MDI schedule, and pumping is one solution that many

    parents find helpful.

    The artificial pancreas, a device-based cure, is on everybodys mind.

    Dr. Aaron Kowalski, who is leading the effort toward the artificial pancreas by the JDRF,

    talked about the current state of the art. The ultimate iteration of the artificial pancreas

    will be a closed loop, fully automated insulin delivery system based on continuous

    glucose monitoring. In this context, a closed loop refers to the device systems capacity towork effectively to maintain healthy glucose levels without any input from the wearer it

    would be like having an electronic pancreas. Earlier versions will be a hybrid closed loop,

    requiring at least some input from the wearer; a closed loop is extremely difficult to achieve

    for many reasons. For example, in non-diabetic patients, simply thinking about or smelling

    food starts the pancreas producing insulin. The device system, at least with current

    monitoring technology, cannot replicate this. It must be reactive to changing glucose levels,

    rather than proactive like the non-diabetic human body, resulting in imperfect timing of

    insulin delivery and a perpetual game of catch-up. On the other hand, a hybrid closed loop

    allows wearers the option of manual bolusing before meals to eliminate the catch-up factor

    Other barriers to a true closed loop from our perspective include the availability of a top-

    notch sensor the current ones are getting much better but still have issues with accuracy(especially at low levels), the availability of very good algorithms (in development), and

    timing there is still a lag between the time that insulin goes into the system and the time

    it begins working and with a perfect artificial pancreas there wouldnt be a lag, just as there

    isnt in non-diabetics. But heres to progress we do feel like there is much more of it in the

    last year or two and were excited about the research on this front, since most patients have

    been hearing this is about five years away for decades!

    People with type 1 diabetes do not need more insulins; they need smarter

    insulin. The current insulin therapies can require over 30 minutes to reach their peak

    activity. That means ideally when you see a movie, you take your insulin, watch the first 30

    minutes of the movie, and then start eating your popcorn. Dr. Irl Hirsch, insulin expert at

    University of Washington commented on Biodels Viaject, a new subcutaneously injected

    formulation of insulin, noting that this insulin may be absorbed much more quickly it is

    in phase 3 tests and is expected to be available by 2009. Well be looking out for this.

    And on a related (or not) note whats the weirdest injection site you can

    think of?According to Dr. Irl Hirsch, there is research being done to find alternative

    routes for insulin administration. These include ocular, rectal, intra-vaginal and per lingual

    (through the tongue) routes. Current insulins are not fast enough, but they act faster or

    slower depending upon the injection site due to differing rates of absorption per site. There

    is even some research to suggest the scrotum is one of the more optimal places to inject! Do

    not try this at home.

    The current insulin

    therapies can require

    over 30 minutes

    to reach their peak

    activity. So when you

    see a movie, you take

    your insulin, watch the

    first 30 minutes of the

    movie, and then start

    eating your popcorn.

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    D I AT R I B E R E S E A R C H A N D P R O D U C T N E W S F O R P E O P L E W I T H D I A B E T E S

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    test drive

    A Technology Laggards Foray into Insulin Pumpsand Continuous Sensors

    By James S. Hirsch

    Its fair to say that Im a technology laggard and that even on my best days I have alove-hate relationship with gadgets. Im not even on speaking terms with my cell phone.

    But two years ago, I began using an insulin pump, primarily because I had a bad low and

    figured I needed to so something different. I went on the Animas. Then earlier this year,

    Roche wanted feedback on its new Accu-Chek pump, so I tried that for four months.

    When that trial was over, I took another detour and bought the OmniPod, which

    unexpectedly led me DexComs continuous glucose monitor. I had resisted CGM for

    the same reason Ive resisted having a Blackberry: I avoid most new technologies. But

    OmniPods manufacturer, Insulet, for various reasons wanted me to use its insulin pump

    in conjunction with CGM, so it paid for three months of supplies. I got another break when

    DexCom kindly upgraded me to its seven-day sensor, even before it was available to the

    public.So for one who barely knows how to use the television remote, I was now wearing

    the latest, most sophisticated diabetes technology in the world. Have I found glycemic

    paradise? I wouldnt go that far. But after three weeks, I can say that the OmniPod at

    least for me is an incremental but clear improvement over traditional pumps, while

    CGM has the potential to transform care. I also believe the real power in these devices is

    less physiological than psychological, tools that can shape and manipulate behavior in

    unexpected ways. I compare my CGM to a benevolent mother-in-law whose intrusions can

    be overbearing but who ultimately has your best interest at heart.

    Heres my rule of thumb about diabetes technology: small is better than large; fast is

    better than slow; streamlined is better than fragmented. By that measure, the OmniPod has

    obvious advantages over traditional insulin pumps, which require filling a cartridge with

    insulin, knocking out air bubbles, dropping the cartridge in the pump, activating the piston

    rod, attaching and filling the tube, priming, checking for more air bubbles, inserting the

    cannula, and connecting the tube to the infusion set. While using conventional pumps, I

    tried three or four infusion sets until I found one with relatively little discomfort (some

    were outright painful), but my biggest problem centered on occlusion errors, which occur

    when the insulin doesnt reach the body, typically when bolusing. This happens, I was told,

    with certain body types (lean and muscular, which overstates my own physique, but at

    my age, Ill take any compliment I can get). Each occlusion error required me to detach the

    tube and reprime the pump, a maddening experience that led me to consider returning to

    shots.

    The OmniPod is different. As my colleague Kelly Close described in our last diaTribe

    issue (www.diatribe.us/issues/4/test-drive.php), the pod is the first tubeless pump.Attached to the body, it delivers insulin via signals from a wireless hand-held Personal

    Diabetes Manager (PDM), and the pods are replaced every three days. The infusion process

    is automated, quick, and easy. No priming. No air bubbles. No piston rods. The automated

    insertion is less painful than a fingerprick, and Ive had no occlusions.

    The device still has flaws and is not for everyone. If you forget your PDM before going

    to a restaurant, you cant bolus, which means you cant eat. That would be a big drawback

    for my 6-year-old diabetic son, whom I fear would lose his PDM with the same zeal that he

    loses his baseball caps and mittens. Another problem: You cant take the pod off your body,

    and after three days on one site, it begins to feel heavy. Keeping the pod on while playing

    continued on page 8

    T1

    So for one who barely

    knows how to use the

    television remote, I was

    now wearing the latest,

    most sophisticated

    diabetes technology

    in the world.

    DexCom STS 7 Continuous

    Glucose Monitor Sensor and

    Receiver

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    D I AT R I B E R E S E A R C H A N D P R O D U C T N E W S F O R P E O P L E W I T H D I A B E T E S

    8

    certain sports is another challenge; Ive already ripped one pod off the side of my arm just

    when taking off a t-shirt. The pod automatically deactivates after 72 hours, regardless of

    how much insulin is left. Those shortcomings aside, the simplicity of the product makes it a

    superior pump, at least for me.

    A friend of mine with diabetes once said to me: I just dont know how I feel. Well, real-

    time CGM finally tells us how we feel, at least in terms of blood sugar. The DexCom comes

    with an applicator, which injects or inserts the sensor probe beneath the skin. Attached

    on top of the skin is the transmitter, which signals a glucose reading every five minutes to

    a receiver, and the receiver displays your most recent reading plus trend lines over the past

    one, three, and nine hours.

    My first few days on the DexCom STS the companys first generation product were

    disappointing, because I had so many data gaps and noise. The first night, the alarms

    woke me up just to tell me the receiver wasnt receiving any information. Couldnt that

    news wait until morning?

    Ive had better success with the SEVEN, the companys next generation sensor that can

    stay in your body for seven days. The most obvious difference is just that longer duration,

    fewer insertions of new sensors. But the insertion itself is less painful, as a smaller needle

    is used. Ive also learned to be more forgiving. It appears to take the sensor about 24

    hours to get used to its new surroundings, so that first day will have some data gaps andinaccurate readings; but then it becomes more consistent. The receiver also requires daily

    maintenance: it must be charged once a day like a cell phone, and it must be calibrated

    every 12 hours by doing a fingerstick with a OneTouch meter and then

    uploading the meter onto the receiver with a cable.

    The DexCom is not approved to replace fingersticks, and its true that at

    times there have been 40 or 50 point differences between my DexCom receiver

    and my meter reading. So I dont entirely trust the DexCom, but the longer Im

    with it, the more faith I have. Its already caught three or four mild nighttime

    lows that is, it began vibrating while I was still sleeping. (I believe Ive had

    these lows because with the OmniPod, Im no longer losing insulin from air

    bubbles in the tube.) It helps to have a tolerant partner with you in bed. Onenight, when my DexCom alarm buzzed and sent a frisson of electricity across

    the mattress, my wife lifted her head and said, Youre vibrating.

    Of such pillow talk are great marriages made.

    The glucose readings provide fresh insights into familiar actions. Ive always known

    how easy it is to overtreat a low, but I really understood it when I drank a modest glass of

    orange juice and saw the glucose trend line spike from 60 to 183. The sharp decline while

    exercising is equally fascinating.

    There is something futuristic about the entire enterprise. I see the trend line falling

    rapidly. I dont feel anything yet, but I know I have to act. I eat a snack and patiently watch

    the receiver. Finally, I see the trend line straighten out, and I want to announce, Glucose

    stabilized . . . Beam me up, Scotty!

    On another occasion, my blood sugar started to fall when I was stuck in a traffic jam

    about the worse time possible, of course, to become hypoglycemic. So I started eating

    some Skittles and watching the receiver eating and watching watching and eating

    until it finally felt as though I were treating the receiver and not my blood sugar. And who

    can blame me? If I went low, my DexCom would buzz, alarm, reprimand, scold, hold me

    accountable, and all but lecture me on my failure to take proper precaution. Not the most

    pleasant riding mate, but it beats passing out at the wheel.

    I will remain skeptical about new technology, and I know that these gadgets in particular

    continued on page 9

    Heres my rule of

    thumb about diabetes

    technology: small is

    better than large; fast is

    better than slow;streamlined is better

    than fragmented. By

    that measure, the

    OmniPod has obvious

    advantages over

    traditional insulin

    pumps.

    One night, when my

    DexCom alarm buzzed

    and sent a frisson of

    electricity across themattress, my wife lifted

    her head and said,

    Youre vibrating. Of

    such pillow talk are

    great marriages made.

    The OmniPod

    PHOTO:DANIELBELKIN

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    D I AT R I B E R E S E A R C H A N D P R O D U C T N E W S F O R P E O P L E W I T H D I A B E T E S

    dont always work, theyre cumbersome, and theyre expensive; but their ability to change

    behavior is their underlying power. For either CGM or insulin pumps to work, patients

    must be highly motivated uploading, calculating, calibrating, counting, trouble shooting,

    and observing. Always observing. That will exclude some, and perhaps many, diabetics who

    dont have the time, interest, or resources to invest in their health.

    But if you believe that diabetes is an endless dance to the same old song, we now have

    some new partners who can engage, enrapture, and even awe us, long into the night.

    dialogue

    Jeff HitchcockJeff Hitchcock is the founder of Children with Diabetes, an organization

    whose Web site (www.childrenwithdiabetes.com) has become an indispensible source of

    information and support for countless families around America and beyond. In the 1990s,

    Hitchcock was an Internet pioneer, using this new technology to help patients, but he was

    less a visionary than a desperate parent: his daughter had diabetes, and he knew that

    other parents had the same questions, fears, and hopes that he had. Hitchcocks company

    now sponsors multiple conferences a year the Friends for Life Conference in Orlandojust took place and he plans to expand that part of his business abroad, with the first

    international conference taking place in Toronto shortly. In this interview with diaTribes

    Jim Hirsch and Kelly Close, he talks about the origins of Children with Diabetes, the

    evolution of care, and the history of the organizations conferences.

    Jim: When was your daughter Marissa diagnosed with diabetes? What was the hardest

    part for her?

    Jeff Hitchcock: Marissa was diagnosed when she was just 24 months old, in September

    1989. It was a long time ago, and the tools used to manage diabetes then were certainly

    crude by todays standards. I guess the biggest challenge we would have faced was trying

    to reconcile a toddlers normal eating behaviors with the action of insulin. A smart child

    quickly determines that food is a powerful manipulative tool, and if you sit down for dinner

    and give X and Y and they say Im not eating, mom and dad get rather anxious.

    Jim: Sounds like our house. And does this bring us to how Children With Diabetes came

    into being?

    Jeff Hitchcock: For many years after she was diagnosed, I worked in the high-tech

    software industry. There was one forum in particular on the old CompuServe forums about

    diabetes. The postings on there dealt primarily with adults who had diabetes; the number

    of people who had online access was very small back then - this is way before the Internet.

    There was nothing there to help parents, and absolutely nothing for kids. In the fall of 1994

    I was in a company that got access to the Internet. It was clear that this medium was theperfect place to build a support environment for kids who had diabetes. At the time, there

    were a couple of sites online. The biggest was called the diabetes knowledge-base run out of

    the University of Wisconsin Madison. And again, the content was adults with diabetes, both

    type 1 and type 2. Nothing for parents.

    As luck would have it, I found myself laid off in the summer of 1995. I called my

    Internet service provider and said Im launching this site today; I need a full-time modem

    connection. CWD launched the day I got laid off, with a page about Marissa and some

    wacky graphics. And I had no real thoughts on what it would become.

    continued on page 10

    T1

    Jeff Hitchcock; founder of

    Children with Diabetes

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    Kelly: At that point, how many people had you communicated with who had children with

    diabetes?

    Jeff Hitchcock: None that I recall, to be quite honest. There was nothing there

    for families who had kids with diabetes. CWD was sort of my attempt to pass on our

    philosophy, which was really to live your life and fit diabetes into it, not the other way

    around.

    Kelly: How had you developed that philosophy over time, and who influenced you?

    Jeff Hitchcock: Well, when Marissa was diagnosed, her endocrinologist at the Childrens

    Hospital in D.C. left us with for lack of a better term a very positive diagnosis

    experience. We left feeling that we could make a big difference in her life. Those were pretty

    much the words he gave to us. And that we shouldnt really worry. I think he had seen

    changes in diabetes care beginning with home-glucose monitoring recent studies have

    shown that kids diagnosed post home-glucose monitoring have a very different long-term

    outcome than kids diagnosed in the 60s, before there was home-glucose monitoring.

    So we never had sort of a meltdown, the worlds over, all that kind of stuff. We may

    have been very naive, but we just didnt have that.

    Jim: Going back to the organization, how did it evolve as you got your feet wet?

    Jeff Hitchcock: I made some overtures to companies and was told, The Internet thats

    pornography. We dont want to be there. There was no financial support.

    I did receive a contract from the JDF, as the JDRF was called at the time, to build and

    host their initial website, which was called jdfcure.com. That lasted about 18 months before

    they took it in-house.

    Back then, the Internet was very new. One of the things that helped us is someone at

    Yahoo discovered the site and featured us in a whats new page. Once that happened, our

    traffic began to just grow and grow and grow and grow. And the growth has not stopped.

    Kelly:What was it like having people writing directly to you?

    Jeff Hitchcock: CWD has always been free and anonymous. That has been one of the

    things Ive always wanted. In maybe late summer like October-ish I probably got the

    first email to Dear Dr. Hitchcock, please tell me about my insulin. About that same time,

    an endocrinologist in Kansas City ran a site called Diabetes Monitor, which still exists, and

    his Internet service provider was having problems keeping his site up. So I asked him if he

    would answer these questions in exchange for me hosting and keeping his site up, and he

    agreed. And that served as the foundation for what is now the Ask the Diabetes Team part

    of the site.

    Jim:Were you still thinking at that point that this could be a business?

    Jeff Hitchcock: No. At that time, having been told that no companies wanted to beonline, from a sponsorship perspective, I had no delusions that this was going to be

    anything other than a hobby. It remained that until Im not even sure. If you go basically

    to late 1999, CWD was not bringing in any financial support to speak of. And it was to the

    point where Id almost wanted to just turn it off, because it was so time-consuming.

    It was in the fall of 1999, when people were investing a lot in the Internet, and Internet

    health in particular, that myself and two other people created Diabetes 123, our company,

    and took over running the website from what was the CWD Foundation, which is now a

    separate entity. We then promptly watched the NASDAQ crash.

    So that was another very scary year. Another go a long time and not get paid kind of thing.

    10

    D I AT R I B E R E S E A R C H A N D P R O D U C T N E W S F O R P E O P L E W I T H D I A B E T E S

    continued on page 11

    I made some overtures

    to companies and was

    told, The Internet

    thats pornography.

    We dont want to be

    there. There was no

    financial support.

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    D I AT R I B E R E S E A R C H A N D P R O D U C T N E W S F O R P E O P L E W I T H D I A B E T E S

    11continued on page 12

    Jim: Did you quit your job?

    Jeff Hitchcock: I walked away from what was a very nice job thinking that this was an

    easy business. Youve got to kind of go back to the 1999 mentality and what we all thought

    was possible. Some of the things we had thought about doing just did not make sense in

    retrospect. Online diabetes education is a very expensive endeavor from an infrastructure

    perspective, and online sales of diabetes-related products has become something that the

    Wal-Marts and the Walgreens manage, not the small boutique companies.But the other thing that happened in 2000 was Laura Billetdeaux, a mom on our parents

    list, sent a note out to that list and said, Who wants to come share a vacation in Orlando?

    Which became the first official CWD event in June of 2000. Her vacation email invitation

    went to the CWD list and 110 families 550 people showed up in Orlando. That was 1995

    and the rest is history.

    Kelly:Was that the first time that the companies had kind of reached out?

    Jeff Hitchcock:We had some financial support from LifeScan. I think that came in about

    1997 to fund a section of the site about camps. But that was pretty much it. There were a

    couple of little companies, but not enough to pay a mortgage and all that kind of stuff.

    When it became clear that it wasnt just five families going to show up at Disney, thatthis was a serious thing, she began calling various diabetes companies. TheraSense stepped

    up and was the first company to provide financial support for a CWD event. This was prior

    to them actually having a product on the market.

    They took a leap of faith in us that this was going to be something that was both

    worthwhile and would obviously be beneficial from a corporate perspective. You want

    them to feel that. But it was really a big leap of faith in us, that this sort of ragtag group of

    Internet people were going to do something.

    After spending a day at Sea World and a day at the Magic Kingdom, we asked the

    families what they wanted, and the feedback was that people wanted real conference kinds

    of stuff. These were parents who had gone to trade shows and conferences and such as part

    of their regular work, and they knew what these things could be. From that came the formatfor Friends for Life as we know it now educational sessions, focus groups, a lot of social

    activities.

    Jim: So, when did CWD in effect become your full-time job?

    Jeff Hitchcock: I think sometime in 2002. We finally had enough both online support

    and sponsorship at the conferences that I could put aside the separate job. Of course, a

    deciding factor was health insurance. We were able to get a policy. Its basically a group

    policy with two families, my familys and Lauras. Without that, it would have been very

    difficult to do this.

    Jim: Switching gears for a moment - what do you think the biggest problems are, either

    from a parents or a patients perspective, in diabetes?

    Jeff Hitchcock: I dont know that theres a one biggest issue. I think a familys struggle

    with suboptimal care; going to clinicians who dont keep up or arent aware of the latest

    management tools and strategies, and who impose purely artificial barriers to adoption of

    new tools, such as pumps.

    Nothing is more frustrating than hearing a parent say, My doctor wont prescribe a

    pump until my teenagers blood sugars are perfect. They may not be able to achieve those

    goals without that pump those are the kinds of frustrations I see.

    Nothing is more

    frustrating than hearinga parent say, My doctor

    wont prescribe a pump

    until my teenagers

    blood sugars are

    perfect. They may not

    be able to achieve those

    goals without that pump

    those are the kinds of

    frustrations I see.

    Laura Billetdeaux; Her

    vacation email invitation

    went to the CWD list and 110families 550 people showed

    up in Orlando. That was 1995,

    and the rest is history.

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    D I AT R I B E R E S E A R C H A N D P R O D U C T N E W S F O R P E O P L E W I T H D I A B E T E S

    Jim: What do you think are the biggest misconceptions or misperceptions among parents

    and patients?

    Jeff Hitchcock: Ill give you an example that just came up in the last couple of days on

    our forums. A dad posted that his son was newly diagnosed, and he was very anxious about

    the long-term effects of type 1. He was just very worried that his son, who is now 16, is

    going to suffer what his aunt did 20 years ago.

    I think theres this enormous misperception about type 1 versus type 2 in the generalpopulation, and a lack of appreciation for the dramatic advances that medicine has made

    in caring for type 1 diabetes in the last 10 or 20 years. I think that people new to this and

    who arent left with a good diagnosis experience, leave feeling really anxious and depressed

    when I dont think they need to be.

    Jim: The first time we met, you said to me that you think complications are a thing of the

    past. What did you mean by that?

    Jeff Hitchcock:Well, there was a study published in Diabetes Care this year. Basically

    they looked at the incidence of nephropathy in kids who were followed for over 20 years.

    When they looked at kids who were diagnosed very young say zero to four and

    they followed them for 20 or 25 years, zero not one had developed nephropathy.Historically, kidney disease has been a very bad thing if you have type 1 diabetes. And this

    study showed very strongly that the world has changed. In kids who are diagnosed older

    say the five to nine and 10 to 14 ranges the incidence was just one percent for the five to

    nine year olds and just over two percent for the older kids. That is in stark contrast to kids

    diagnosed many, many years ago who had very high incidence.

    Thats the kind of positive news that families need to hear. Now that comes with the

    qualification that you take care of yourself. That you dont just dismiss it. But again, that is

    really a very positive message.

    Jim: How have the products improved?

    Jeff Hitchcock:When we compare glucose monitors from 1989 to today, we go fromthe best meter on the market that took 120 seconds and a drop of blood that would have

    made a bricklayer cry, to meters today that are in the three- to five-second range, with sub-

    microliter volumes. And integrated data management, or connections to computers to help

    identify patterns and improve management strategies.

    We look at insulins regular and NPH was the norm, and now both short acting and long

    acting analogs have given us incredible dosing options and much better predictability. They

    reduce low blood sugar, which has always been the limiting factor on optimizing control.

    And insulin pumps, which in 1989 were available but really were not something you

    would have put on a two-year-old, are now so small and so lightweight that you can put

    them on toddlers. And those tools are what has made that nephropathy study a reality.

    These tools make living with diabetes easier. And theyve given patients the opportunity

    to basically have complications be something that they dont need to worry about like they

    used to.

    Kelly: Can you talk about what product out there is doing really well with customers, and

    what makes it such a good product. Is it price? Is it great education? Is it that they like the

    color?

    Jeff Hitchcock: I think the biggest deciding factor on products is customer service. If

    you look at insulin pumps, for example, thats a big cash outlay no matter how you cover

    it; a lot of supplies every month. And, effectively, youve entered into a relationship with

    12continued on page 13

    When we compareglucose monitors from

    1989 to today, we go

    from the best meter on

    the market that took

    120 seconds and a drop

    of blood that would

    have made a bricklayer

    cry, to meters today

    that are in the three-

    to five-second range,

    with sub-microliter

    volumes.

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    D I AT R I B E R E S E A R C H A N D P R O D U C T N E W S F O R P E O P L E W I T H D I A B E T E S

    13continued on page 14

    a company, because most people buy their supplies from their insulin pump company.

    People talk about what happens when things break. Insulin pumps are mechanical devices,

    and like any mechanical device, some number are going to break or have a failure. And its

    more how the insulin pump company responds to those episodes of crisis because a pump

    failure is always a crisis that determines how patients and future customers will view

    that company. People dont complain so much about the fact that their pump broke. They

    complain about the fact that their pump broke and they didnt get a replacement for three

    days because their rep was out of townand the company didnt think they were important

    enough to make a delivery that night. Thats where a little investment goes a long way.

    Jim:What would you say for meters? Because meters typically dont break down, whats

    the deciding factor there for patients?

    Jeff Hitchcock: For our audience parents who have kids with diabetes having a

    second meter that you dont have to go buy, so that you can leave one at school and have

    one at home, is a big thing. So a meter company that will accept a phone call to their

    customer service where Mom says, Tommy is in school. Can you send me another meter

    this is what he uses so that we dont have to keep schlepping it back and forth? Then

    they send it out, and it arrives the next daythats what they should be doing.

    Jim:We see more TV advertising for diabetic products than ever before. How would you

    assess that trend?

    Jeff Hitchcock: There is no question thats changed. And you just have to look at the

    television to see all of the commercials for meters. The message adds things that matter

    to the patient, not to the clinician: its painless, or it doesnt require coding; or the things

    that make a difference to the family. So its very obvious that there is more direct consumer

    marketing in the glucose meter space.

    Jim:What impact do you think thats actually had on the companies themselves?

    Jeff Hitchcock: I have no idea. But I think its a good thing if it raises the awareness that

    there are multiple tools. Its not just whatever you left the doctors office with three years

    ago. You should be aware that there is innovation. And if it does nothing other than get

    someone to go and ask either the pharmacist, or their doctor, or somebody online, whats

    out there now, they may find a tool thats better for them. But it does sort of put some

    pressure on companies to continue to innovate and come out with new models and stuff.

    Kelly:Your conference this year in Orlando was absolutely fantastic. So much incredible

    learning and meeting so many increidbly interesting people. Year after year, more and

    more families come to your Friends for Life Conference. What is most drawing them to

    Orlando?

    Jeff Hitchcock: One very important thing is that families who come and have a great

    experience want to come again, because they see that its made an enormous differencein their childrens lives and in their own. At the end of each conference, the teens are just

    sobbing as they part. Its mystifying. But theyre literally just bawling their eyes out because

    theyre not going to see the friends theyve met until the next conference.

    And thanks to cell phones and email, theyre able to communicate throughout the year.

    But these kids from different parts of the country and, in some places, different parts of the

    world have become friends in a very powerful way. They share something with these other

    kids with diabetes that they just dont share with their peers at home. And the families, the

    moms and the dads, have the same kind of experience.

    a pump failure is

    always a crisis that

    determines how patients

    and future customers

    will view that company.

    People dont complain

    so much about the fact

    that their pump broke.

    They complain about

    the fact that their pump

    broke and they didnt get

    a replacement for three

    days because their rep

    was out of town...and

    the company didnt think

    they were important

    enough to make a

    delivery that night.

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    D I AT R I B E R E S E A R C H A N D P R O D U C T N E W S F O R P E O P L E W I T H D I A B E T E S

    So we have this growing body of families who come. When they go back to their

    communities and meet in their support groups, they talk about what it was like. And word

    spreads, basically. We are able to bring these world-class researchers and clinicians to come

    and meet with the families and talk to them about daily care strategies and whats coming

    in a very relaxed atmosphere. And thats just an incredible opportunity for everyone, me

    included.

    Jim: On a related note, whats been most satisfying about what you have built over these years?

    Jeff Hitchcock: When I sit here and look online at the traffic statistics, theyve gone

    up consistently. But those are just numbers, and its difficult to have an emotional

    experience with that pool of data. But when Im standing onstage in front of 1,500 people

    and watching a slideshow of our kids over the years, growing up healthy and happy, and

    interacting at conferences and the like, that is very rewarding. It cant not be. So while the

    website, obviously, has a chance to reach many more people than our conferences can, the

    conferences have become the heart and soul of what we do.

    Jim:What frustrates you or concerns you the most about diabetes today? Youve spoken

    about how much things have improved, but there must be things that still get you

    frustrated.

    Jeff Hitchcock: I think a very significant, unaddressed problem is access to these tools.

    And that gets to how we fund health care in the US. And, at some point and I dont

    know how soon as a nation, I think we have to realize that access to what we know to be

    good health care practices, whether its in diabetes or cardiac health or anything, makes a

    difference for us as a nation, both economically and otherwise.

    Its foolish in my mind that companies like General Motors have to worry as much about

    health insurance as they do about the quality and features of their automobiles. Those

    companies should be building cars or computers or whatever they do. And, as a nation, I think

    we need to step up and realize that healthcare matters as a nation, and were just not there yet.

    Jim: Do you envision ways of expanding what youve already got, or are you kind of gettingready to wrap things up and retire?

    Jeff Hitchcock: I cant retire until we have scheduled the Children Who Used to Have

    Diabetes Conference. Were not there yet, though I do look forward to that.

    14

    I cant retire until we

    have scheduled the

    Children Who Used

    to Have Diabetes

    Conference. Were not

    there yet, though I do

    look forward to that.

    Jeffs daughter Marissa (2nd

    from right) with children at the

    CWD conference. Marissa is an

    inspiration indeed she was an

    active staff member at the 2007

    conference and is in the midst of

    study to be a CDE.

    PHOTO:WWW.CHILDRENWITHDIABETES.COM

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    D I AT R I B E R E S E A R C H A N D P R O D U C T N E W S F O R P E O P L E W I T H D I A B E T E S

    logbook

    A Challenge to the Acting Surgeon General

    By James S. Hirsch

    He sees no patients. He doesnt submit insurance claims. And he

    doesnt run any clinic or hospital. But the U.S. Surgeon General isthe most important doctor in America.

    Sometimes called Americas top doc, the surgeon general is appointed

    by the president, and his or her job is to promote the health of the nation

    through education and to advise the president on health care policy. Some

    surgeon generals have been controversial while others quite influential: Dr. C. Everett

    Koop, who held the post from 1982 to 1989, used the bully pulpit to help change the

    countrys policies on tobacco and AIDs.

    With diabetes now making a legitimate claim as the countrys number one public

    health threat by the governments own estimate, one in three Americans born in this

    century will develop the disease we would hope that the surgeon general would make

    diabetes a national priority. But thats not the case. The surgeon generals web site (www.

    surgeongeneral.gov/index) identifies five public health priorities: disease prevention,

    eliminating health disparities, public health preparedness, improving health literacy, and

    organ donation.

    All of these intersect diabetes but do not focus full attention on the disease itself and do

    not send any clarion call to action.

    A Diabetic Patient in High Places

    Which might be a little odd, because since August of last year, the acting surgeon general

    has been Rear Admiral Kenneth P. Moritsugu, who was diagnosed with diabetes seven

    years ago at age 55. Prior to his current appointment, he had been deputy surgeon general

    since 1998 (in 2002, he briefly served as acting surgeon general).

    In many ways, Dr. Moritsugu is an inspiration, showing that diabetes has not impairedhis ability to work at the highest levels of government. He has also had to overcome

    stunning personal tragedies that make his professional accomplishments stand out even

    more.

    He was recently the keynote speaker at the Friends for Life Conference in Orlando for

    the Children with Diabetes organization. Standing in his white gold-braided navy uniform,

    his chest bedecked with ribbons, he slipped his Animas insulin pump out of his pocket to

    show the children that he was one of them.

    I am also a patient, he said, stressing that everyone including himself needs to

    better understand health literacy.

    But does Dr. Moritsugus employer the federal government understand the scope

    of the diabetes epidemic? Consider the governments spending for medical researchfor diabetes: between 1980 and 2006, the NIH budget for the disease increased by 240

    percent, to $1.1 billion, but its total expenditures grew by 261 percent. So the percentage

    given to diabetes slightly declined even as the number of diabetics had doubled. (Even

    more sobering: the NIH in 2004 spent $68 for each diabetic, compared to $16,936 for each

    patient with the West Nile virus.)

    Blame It on Congress

    In an interview with me, Dr. Moritsugu blamed the funding shortfall on Congress. We can

    only administer those programs for which we have authority, he said, and we can only

    15continued on page 16

    I am also a patient, he

    (Dr. Moritsugu) said,

    stressing that everyone

    including himself needs

    to better understand

    health literacy.

    Acting Surgeon General Ken

    Moritsugu; Americas top doc

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    distribute those funds which have been legislatively appropriated to us . . . As a patient, I

    see that the federal government is doing a good job with the funding that it has.

    If anything, Dr. Moritsugu said, diabetic patients should look less to the federal

    government for help and more to themselves. From my experience of 36, 37 years as a

    career officer in public health services, I have seen programs come and go, and the biggest

    mistake is if everything is leveraged on federal funding, as opposed to a partnership on the

    federal level, the state level, the community level, private organizations, and foundations.

    From that perspective, it is less us who have the power to affect the federal component of

    funding for research than you, meaning the constituency who actually has better access to

    the ears of those who make the appropriations.

    My first reaction to those words was: ugh, what a cop out. Yes, I can write a letter to

    my congressman, but I dont have the megaphone that a president has, or a senator, or an

    acting surgeon general. Why are none of them doing what President Franklin Roosevelt did

    for polio make its defeat a real priority?

    Dr. Moritsugu said the emphasis by the surgeon generals office on disease prevention

    is very much tied to diabetes. (The Web site identifies diabetes, along with heart disease

    and many forms of cancer, as examples of preventable chronic diseases that kill 70

    percent of Americans each year.) The first priority is prevention, he said. I think

    overweight and obesity will put this smack dab in the middle of the radar screen. Hedescribes the complications of weight gain and obesity heart disease, kidney failure, etc.

    as the domino effect.

    Connecting the Dots

    Prevention is a laudable strategy to curb the type 2 epidemic, but is diabetes per se just

    another domino? Of course not, its the entire game board, and Dr. Moritsugu said that

    he understands the vast challenge before us: changing lifestyles, improving health care

    delivery, and increasing biomedical research. He calls the challenge connecting the dots.

    Many of us want to do good things for the health of America, but what we do is not

    really integrated into an overall strategy, he said. We need to look at overweight and

    obesity and diabetes as not simply a health issue but a dietary issue thats the Departmentof Agriculture. Its a Housing and Urban Development issue. Its a Transportation issue.

    Its an Education issue. Its a Commerce issue. You say, Eat well, but in some of our

    communities there is no supermarket within a reasonable distance, so we have to bring

    commerce into the neighborhood and we have to help people help themselves do the right

    thing. . . This is a long way of saying, Connect the dots.

    But Dr. Moritsugus integrated strategy begs the larger question Who will connect the

    dots? Who will unite these disparate entities, across all levels of government and all walks

    of life, to fight a common foe?

    Looking for a Leader

    Perhaps the best qualified person in America is Dr. Moritsugu himself. While he lacks the

    charisma of a Colin Powell, the resources of a Bill Gates, or the power of the president, he

    has a remarkable personal story of triumph and heartbreak that commands attention.

    Born in Honolulu of Japanese descent, he has both a medical degree and a masters degree

    in public health. He entered the Public Health Service in 1968 and has held numerous

    positions, including medical director of federal prisons, and has won a slew of honors,

    including the Surgeon Generals Medallion. (I dont know what that is, but it sounds

    impressive.)

    Resume aside, what distinguishes Dr. Moritsugu is family tragedy: he lost his wife in

    an auto accident in 1992, and then his daughter was killed four years later, at age 22, in a

    D I AT R I B E R E S E A R C H A N D P R O D U C T N E W S F O R P E O P L E W I T H D I A B E T E S

    16continued on page 17

    We need an integrated

    strategy that looks at

    overweight, obesity, and

    diabetes as not simply a

    health issue but a dietary

    issue we should

    involve the Departments

    of Agriculture, Housing

    and Urban Development

    Transportation, Education

    and even Commerce.

    You say, Eat well,but in some of our

    communities there is

    no supermarket within a

    reasonable distance

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    separate car accident. Dr. Moritsugu has used these tragedies to promote organ donation.

    Both his wife and his daughter were donors, and he found comfort in knowing their organs

    saved others. (A retired policeman received his wifes heart.) Organ donation stands as one

    of the health priorities of the surgeon generals office.

    Dr. Moritsugu, who has remarried and has two daughters, will return to his position as

    deputy surgeon general once the current nominee is approved. Asked about the leadership

    vacuum in diabetes, Dr. Moritsugu told me: Waiting is passive, instead of what I know is

    part of the fabric of America, which is that people come together and raise their voices and

    say, Hey, pay attention to that issue, and here is the science, and here is the evidence, and

    here is the emotion.

    But what role should you play?

    He paused before answering, then looked me in the eye. I have engaged in the

    challenge, he said. I have engaged in the challenge with the Office of the Secretary (for

    Health and Human Services). I have engaged in the challenge with our former surgeon

    general, and there is another nominee, and I have engaged him.

    But how many people in America know about Kenneth Moritsugu about his life story,

    about his experiences, and about his commitment to diabetes?

    Basically, Im holding myself out to the department and saying, Use me. I am the one

    who has the disease. It is very personal as well professional.With a glint in his eye, he thanked me for pressing the issue.

    I hear your challenge, he said, and I am willing to rise to it.

    learning curve

    The Mediterranean Diet

    By Daniel Trecroci

    The Mediterranean Diet Makes Sense of the French Paradox

    It was first publicized in 1945, but it took more than 50 years to get its name the

    Mediterranean Diet. By the 1990s, researchers noticed that people living in Mediterraneancountries consumed high amounts of fat, but unlike their fat-consuming counterparts in the

    U.S., they were at less risk of heart disease.

    This is sometimes referred to as the French paradox, but it really isnt a paradox at all:

    Americans consume higher amounts of saturated fats, while in the Mediterranean world,

    monounsaturated fats are more likely to be consumed.

    But fats alone are not responsible. What really puts the gusto in the Mediterranean diet

    what has drawn so much attention is the wine.

    Its the Type of Fat That Counts

    But dont overdo the happy hours. Moderation, of course, is paramount, and there is more

    research data on monosaturated fats than on Merlot.In the Mediterranean diet, the main fat is olive oil, with a very high content in

    monounsaturated fatty acids and more than 200 microcomponentsmany of which exert

    beneficial properties to health, Dr. Antonia Trichopoulou, a researcher at the Department

    of Hygiene and Epidemiology at the University of Athens Medical School in Athens, Greece,

    told diaTribe.

    Dr, Trichopoulou, as well as researchers from Harvard School of Public Health,

    published a study in the New England Journal of Medicine (July 26, 2003) that found that

    a greater adherence to the Mediterranean Diet is associated with a significant reduction

    in total death. Dr. Trichopoulou told diaTribe that, combined with physical activity and

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    PHOTO:MARKYARCHOAN

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    weight control, the Mediterranean diet is ideal for a person with type 2 diabetes. One of his

    more recent studies in the Journal of Internal Medicine (June 2006) found that increased

    consumption of eggs and saturated fats was associated with significant increase of death in

    people with diabetes while monounsaturated fats were found to be preferable for diabetic

    persons.

    The Mediterranean Diet Explained

    According to the American Heart Association (AHA), the common Mediterranean Diet

    has these characteristics:

    A high consumption of fruits, vegetables, bread and other cereals, potatoes, beans,

    nuts and seeds

    Olive oilan important monounsaturated fat sourceused for cooking and dressings

    Dairy products, fish and poultry that are consumed in low to moderate amounts

    A minimal consumption of red meat

    Eggs are consumed zero to four times a week

    Low to moderate consumption of full-fat cheese and yogurt

    Moderate consumption of wine, usually with meals

    Reliance on local, seasonal, fresh produce

    An active lifestyleMore than half the fat calories in a Mediterranean diet come from monounsaturated

    fats (mainly from olive oil), says the AHA. Monounsaturated fat doesnt raise blood

    cholesterol levels the way saturated fat does.

    Data Everywhere Support the Mediterranean Diet

    According to data from the Lyon Diet Heart Studya randomized, controlled trial

    designed to test the efficacy of a Mediterranean-type diet in people who have had a heart

    attackpatients following the Mediterranean-style diet had a 50 to 70 percent lower risk of

    recurrent heart disease.

    A study in the Archives of Internal Medicine (June 11, 2007) found that individuals at

    high cardiovascular risk who adopted one of two traditional Mediterranean diet (TMD)patterns TMD + virgin olive oil or TMD + nutsshowed significant reductions in cellular

    lipid levels and LDL oxidation.

    In another study, in the American Journal of Clinical Nutrition (August 2006),

    data suggested that of the several components of the Mediterranean diet, alcohol, nuts

    and whole grains showed the strongest association with adiponectin concentrations in

    women with diabetes. Adiponectin is a protein hormone secreted from fat tissue into

    the bloodstream that changes a number of metabolic processesamong them, glucose

    regulation. Researchers discovered that, Close adherence to a Mediterranean-type diet is

    associated with higher adiponectin concentrations.

    Talk with Your Healthcare Provider

    As with any diet, be sure to talk with your healthcare provider if you are thinking about

    starting this one.

    18

    Americans consume

    higher amounts of

    saturated fats, while

    in the Mediterranean

    world, monounsaturated

    fats are more likely to

    be consumed What

    really puts the gusto in

    the Mediterranean diet

    what has drawn so

    much attention is

    the wine.

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    D I AT R I B E R E S E A R C H A N D P R O D U C T N E W S F O R P E O P L E W I T H D I A B E T E S

    profile

    A Coachs Creed: Balancing Work and Life for theChronically Ill

    By Amy Tenderich

    In 1980, Rosalind Joffe was on the verge of landing her dream job with a multimediaproduction company when she unexpectedly developed multiple sclerosis (MS). Her

    immediate ambition was derailed, but not her life. She bore two healthy daughters and

    became a communications professor at Boston University.

    Then in 1993, she was diagnosed with ulcerative colitis, which left her weak and

    sometimes unable to walk. Suddenly, any job requiring her presence on a regular basis was

    too much. She quit her teaching position but did not want her career to end.

    I still wanted to work, but I had to find a whole new career that would be flexible

    no matter what my health was like, says Joffe, 48, who lives in the Boston suburb of

    Newton. Lots of people thought I was crazy. Theres no precedent for people who are sick

    continuing to work.

    Working from home, she started a consulting/executive coaching business, but thatevolved into something even more specialized: a business that helps others with a chronic

    illness develop their own balance between work and life.

    Four years ago, Joffe launched CIcoach.com, offering individual and group consulting.

    She focuses on living with a chronic illness and the specific workplace issues it presents.

    To date, she has helped over 60 people diagnosed with an array of illnesses cancer,

    MS, lupus, Crohns disease, and of course, diabetes explore their own altered capabilities

    and work/life priorities.

    In reality, anyone with chronic illness is dealing with essentially the same stuff, Joffe

    says. Fatigue, frustration, guilt over spending time away from the family. But as long as we

    dont talk about it to our bosses or others, nothing will be done about the problems people

    encounter with chronic illness until its too late, and the person goes out on disability.

    While a chronic disease used to be considered an aberration, those days are long gone.

    More than 125 million Americans and 40% of Americans in the workforce now live with

    at least one chronic health condition, according to the think tank Partnership for Solutions

    at Johns Hopkins University. More than 60 million Americans have potentially life-

    threatening conditions such as heart disease, hypertension, cancer, arthritis, and diabetes,

    and nearly 10 million American people continue to work despite a disability.

    Helping Clients Connect the Dots

    Joffe offers an approach thats a little like What Color is Your Parachute? for the

    chronically ill: through a series of phone calls and visualization exercises, she helps

    clients identify what is possible and agreeable to them in the workplace.

    Each time we talked, Rosalind was able to connect the dots on a lot of things I wassaying about what was important for me, says Mark E. in Minneapolis, a client with MS

    who works for a large healthcare software company. [Like other clients interviewed for this

    story, Mark asked that his last name not be disclosed in part because he wants to control

    who knows about his illness.] The big aha was that being on the fast track to a high-level

    management position wasnt really a good fit for me right now. What I needed was more

    flexibility and less stress.

    Some common missteps occur when people try to ignore their illness altogether, or

    simply attempt to charge through it and perform as if their health didnt matter. In

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    Life balance expert

    Rosalind Joffe

    Lots of people thought

    I was crazy. Theres no

    precedent for people

    who are sick continuing

    to work.

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    response, Joffe has developed guidelines on how to discuss your illness in the workplace

    and any special needs you may have.

    After working with Joffe for about six months, Mark E. was able to scale back from a

    national sales position requiring a 14-hour workday, including a two-hour commute, plus

    his responsibility for a dozen employees, to a position in business development where he

    works from home. With Joffes help, he was able to do this without losing face at work or

    compromising his own pride.

    She helped me present myself as a still-valuable employee, who still wants to work

    hard, still wants a challenge, and is still loyal to the company. I just need to do things

    differently right now, he says.

    Clients say the magic that sets Joffe apart from other career coaches is her natural empathy

    and her personal experience working with a chronic illness in the corporate world. Other

    coaches dont get the aspects of being ill, and how it affects your life and family, Mark E. says.

    Jackie V., a 23-year-old school teacher in Connecticut diagnosed with MS fresh out of

    college, was plagued by a sense of inadequacy. I was so exhausted all the time, but I didnt

    want to ask for accommodations at work. The coaching helped me see that asking for help

    is not a sign of weakness. Im not giving in. Its healthier to remain in work and go about

    your life rather than stay at home hiding.

    Her talks with Joffe focused about 60% on work issues and 40% on personal matterssuch as pivotal relationships and stress at home. Taking Joffes advice to approach her

    boss with an upbeat attitude and specific compromises in mind, Jackie was pleasantly

    surprised by her colleagues reaction. She now works four hours a day instead of eight,

    and says she feels much healthier both emotionally and physically.

    Joffe has had similar results with her diabetic patients. In one instance, a woman was

    diagnosed following her third pregnancy. She was briefly in diabetic coma, and her husband

    had begged her to stop working. She was confused and emotional.

    She was basically ignoring her diabetes, and her husband thought stopping work was

    the solution, Joffe says. Through our sessions, she came to the realization that she loved

    her job. She decided to cut back temporarily, to give herself time to acclimate to living with

    the disease, but she did not want to stop working permanently. This client recently wentback to work full-time, now confident that she can balance her career with caring for her

    health and her family.

    Spreading the Word

    For many clients, a core issue is disclosure. Who should they tell, and how? According to

    Joffe, very few people struggling at work due to chronic illness engage the Human Resources

    (HR) Department. HR simply isnt trusted, since people assume its members will always have

    the companys interests in mind, and they may not keep the information confidential.

    The thinking is, if they know about your condition and they think youre a problem,

    theyll be angling to get rid of you, Joffe says.

    Client Steve D., in his 30s and also living with MS, was grappling with the disclosure

    issue for two reasons. First, having a secret is very isolating, he says. Secondly, although

    his position at a biotech research company in Seattle requires mostly brain work, the

    job description also called for a fair amount of work in a laboratory, which meant hours of

    standing on his weak legs. His father pointed him to CICoach for help.

    First we talked about the legal issues what are my rights? And then Rosalind helped

    me put a positive spin on things, identifying what I can do for the company to still be of

    value, rather than talking about what I cant do. Basically, its doing a little bit of sales for

    yourself, Steve says.

    Joffe suggested limiting disclosure on a need-to-know basis, identifying the critical

    20

    In reality, anyone with

    a chronic illness is

    dealing with essentially

    the same stuff

    fatigue, frustration, guilt

    over spending time away

    from the family Some

    common missteps

    occur when people try

    to ignore their illness

    altogether, or simply

    attempt to charge

    through it and perform

    as if their health didnt

    matter.

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    people, and then discussing it with them in the right light. The strategy worked, as

    Steves boss was very responsive to his request for an altered schedule. Joffe emphasizes

    to her clients the importance of finding a boss who is sympathetic and flexible though, of

    course, many workers dont have that luxury.

    While Joffe instructs her clients to carefully disclose information about their health,

    its also important that enough people know about any illness in case of an emergency.

    Anyone with an invisible and chronic illness faces these issues, she says. But as long as

    its continually swept under the rug, were kind of living in silos.

    Ultimately, Joffe says, patients have to be their own best advocate. If we can band

    together, we can have a voice, which would be really helpful in educating employers,

    managers, and colleagues so the workplace can be a more supportive place, she says.

    Theres power in numbers and a lot of comfort around the sense that youre not alone.

    Learn more about chronic illness in the workplace at:

    www.cicoach.com

    www.keepworkinggirlfriend.com (Rosalind Joffes co-authored blog)

    www.partnershipforsolutions.org

    http://www.advocacyforpatients.org/

    Amy Tenderich is author of the popular web log www.diabetesmine.com, and

    coauthor of the valuable book, Know Your Numbers, Outlive Your Diabetes.

    trial watch

    Anti-CD3 mAb Treatment of Recent Onset Type 1 Diabetes

    This study will test whether a single 14-course treatment with an anti-CD3

    monoclonal antibody will prevent the loss of insulin secretion capacity in type 1s who have

    been diagnosed for a duration of 4-12 months. Previous studies have shown that treatment

    with CD3 antibodies can preserve residual beta-cell function in type 1s. This is a JDRF/Yale

    sponsored phase 2 trial started in September 2006 and researchers are looking to enroll

    60 participants at the two study sites; Yale University, New Haven (CT) and University

    of California, San Francisco. Check out the website at: http://clinicaltrial.gov/ct/show/

    NCT00378508?order=3.

    Diabetes Technology Study of Real-Time Glucose Alerts in the Team

    Management of Diabetes

    Have you ever had a particularly good week of blood glucose results that you could not wait

    to share with your doctor or educator? If so, this Diabetech-sponsored study has your name

    all over it. It will use a special glucose meter to send wireless alerts to a team of healthcare

    providers of your choice. This will give them a chance to review your glycemic levels before

    your next appointment. We believe the possible advantages to this are two-fold. Your

    provider will be better informed when you next see him/her and they would spend less time

    when youre in the office looking at logbooks/glucose meters and more time looking at you!Who knows what applications could come parents could even receive a blood sugar text

    message from their child at school during a hypoglycemic event if the technology takes

    off. We believe ultimately its more about self management than physician management

    (the truth is they probably dont all have time to look through mountains of numbers

    its probably better for you to look at the key ones!) But all these trials will be great for

    researchers to learn more on the technology so were all in favor. The research team is

    looking for 1000 participants and they expect to complete the study in December 2007.

    Check it out on the web at: http://clinicaltrials.gov/ct/show/NCT00322478;jsessionid=66

    016FA616632B9A9142F556554019F8?order=4.

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    what were reading

    GLP is the 1 For Me: Recent Literature Shows Promising New

    Formulations of GLP-1 on the Horizon

    Byetta has been the first of a relatively new class of diabetes drugs called incretin

    mimetics or GLP-1 analogs. GLP-1 is a gastrointestinal hormone, or incretin, which

    is released in the body during meals to enhance the insulin response to the new glucoseload. We discovered several years ago that GLP-1 does not merely help the insulin release

    but actually caused about 70% of it. Without enough GLP-1 in the body, ins