ooh, boy, it’s on the way!

I just got a call from MiniMed that my pump will arrive Thursday –
that’s WAY sooner than I expected, and I’d figured on starting in
mid-August. But they said I could do a saline start Thursday
afternoon…then add insulin the week of the 19th (when my husband and
son get back from vacation).

Talk about excited and nervous!

Laurie, not quite believing it yet

www.authorspotlights.com/campbell

26 Responses to “ooh, boy, it’s on the way!”

  1. carolann_70 Says:

    GRRRREEEAAAATTT!
    Jan

    ] ooh, boy, it’s on the way!

  2. elmo_15 Says:

    Don’t be nervous Laurie there’s nothing to it.
    fp

  3. rodney_800 Says:

    Sorry I haven’t posted to this group and let you know I got my 508 last
    Thurs. I love it, this is my fourth pump.
    What I really like is the remote control and the vibrating.
    Had a little trouble at first then got my son to help me program it, he can
    do things like that. I could of programed it, but could not see the screen.
    So he helped me program it for vibrating and it is great. Haven’t gotten
    into the square wave thing yet (can only teach an old dog so many new
    tricks at a time).
    Does anyone else use the vibrator, how long do you batteries generally last
    using it?
    I found out Fri they are going to remove my cataracts on both eyes. Hoping
    my vision will be where it was last fall and if so I can see the screen
    with light and my glasses.
    Gail

  4. elmo_15 Says:

    getting rid of those cataracts will help immensely, Gail. Good luck
    fp

  5. kristan_180 Says:

    What did you upgrade from?

    I am on my third pump, the 507, and wondering if the added features are worth
    upgrading now, or waiting for the next model?

    David

  6. carolann_70 Says:

    I *heard* a 511 in is the making.
    Jan

  7. poole_110 Says:

    In *other* news… I’m one step closer to getting my
    pump! Saw the doc that I needed to see yesterday to
    get a refferal to the pump clinic, but the next set of
    classes isn’t until July/August so I’m looking at two
    months at best. Oh well, I’ve been diabetic over 8
    years, I think I’ll last another 8 weeks! :) It’s
    unclear WHEN exactly I’ll get hooked up… I should
    know more in the next couple weeks though…

    -Sara

  8. rodney_800 Says:

    Thanks fp, I am counting on it.
    Gail

  9. rodney_800 Says:

    David,
    I upgraded from a 506 and really needed to, I had been on it for over six
    years.
    Gail

  10. rodney_800 Says:

    Me too, Frank, and like I said this was not my first. The four months of
    insurance red tape was ridiculous. I had been on a pump for 18 yrs. They
    (the insurance co.) wanted six months of bgs test….why?
    Gail

  11. carolann_70 Says:

    Gail,
    Did you end up supplying the ins. co. with what they wanted, or was 18 years
    on a pump sufficient?
    Jan

  12. rodney_800 Says:

    I didn’t have six months since I throw my test away after see the dr each
    time. MM called and had my dr write a letter on necessity of pump. Can you
    believe that.
    Gail

  13. dorothea_140 Says:

    Sorry I haven’t posted to this group and let you know I got my 508 last
    Thurs. I love it, this is my fourth pump.
    What I really like is the remote control and the vibrating.
    Had a little trouble at first then got my son to help me program it, he can
    do things like that. I could of programed it, but could not see the screen.
    So he helped me program it for vibrating and it is great. Haven’t gotten
    into the square wave thing yet (can only teach an old dog so many new
    tricks at a time).
    Does anyone else use the vibrator, how long do you batteries generally last
    using it?
    I found out Fri they are going to remove my cataracts on both eyes. Hoping
    my vision will be where it was last fall and if so I can see the screen
    with light and my glasses.
    Gail

  14. carolann_70 Says:

    How old is your pump?
    Jan

  15. carmelo6 Says:

    << How do all of you afford to get pump after pump? Sorry if this is too
    forward. Does your insurance cover it each time? I would love to have the
    newest model! >>

    HEY IM GLAD YOU ASKED THAT I WAS WONDERING THE SAME THING!!! CHRISSY

  16. dorothea_140 Says:

    I’ve not even had it for a year. Does the insurance cover it?

    re:
    How old is your pump?
    Jan

  17. kristan_180 Says:

    I agree that upgrading is the best deal, but it can be expensive.

    My first two pumps were covered by insurance, but now I am supping at the
    Medicare trough, so no more coverage. Also, no coverage for infusion sets,
    insulin, and any other medication. But, test strips are, but it takes a
    specific letter from the MD to get enough to make it worth while. In may
    case, the MD authorized 250/month, and these are fully covered by Medicare
    and the Medicare supplemental insurance.

    So, if I decide up upgrade in the future, I will get a sizable trade in
    discount from Minimed, but the cost still will be $3000 or more.

    David

  18. rodney_800 Says:

    David,
    Medicare does cover the pump now, go to the Mini Med site and it tells
    about medicare.
    gd

  19. kristan_180 Says:

    Thanks! That’s news to me….

  20. carolann_70 Says:

    Is this the one for T-2’s and is disposable??

  21. kristan_180 Says:

    I checked the Minimed site, and found that there are severe restrictions on
    Medicare coverage for the pump.
    First, you must be type I, and you have to have ’severe swings’ in Bg, what
    ever that means. How is this defined? I would define any type I as
    probably having severe swings, regardless of medication., but also one could
    have reasonable control using multiple injections as well as the pump. So
    what is the big deal with ’severe swings"? Politicians mucking around
    with things they know nothing about, I fear.

    Also, there is no coverage for infusion sets or insulin, which is a major
    cost. One could use up to 100 infusions sets/year, which depending on the
    set, can be a considerable sum. In my case, I use bent needles, which are
    the least expensive, and easiest to use, from my perspective.

    So more work is needed!

  22. kristan_180 Says:

    I have read the detailed statement of Senator Susan Collins on the
    Introduction of the Medicare Insulin Pump Coverage Act of 1999, and find
    this a bit disingenuous.

    She clearly is setting the legislation to be in support of a constituent,
    not for the benefit of type I diabetics, or diabetics in general. The
    individual involved claims that control is impossible without the pump; I
    find this hard to believe. If one counts carbs, uses multiple injections
    of R and then adjusts basal rates properly with two injections of NPH or
    Lente, I don’t see much difference in the pump and the standard treatment.
    I am sure the pump does better, but to claim that control is impossible
    without it strikes me as self serving.

    Did this act actually pass? It is not clear from the site that it did;
    only the introduction by Sen. Collins is offered. I may have missed

    something elsewhere, though.

    David

  23. rodney_800 Says:

    I don’t know how much medicare will pay on a MM, but I do know their site
    tells about it and if my insurance had not paid for all mine, they were
    going to bill medicare. I have insurance through my husband, but am
    disabled, so I also have medicare.
    Gail

  24. gerry_1400 Says:

    Multiple injections doesn’t cover Dawn Syndrome unless you want to get up in
    the middle of the night every night. Also, I had post-exercise lows because
    of my Lente "amping up" with my vigorous exercise sessions. The pump has
    eliminated both, which were "lowering the quality of life" or some ridiculous
    "buzz phrase" being used by the factions fighting for Medicare coverage.
    There are several criteria, not just wide swings and I believe any one of
    those criteria being met and certified by doctors’ recommendation would
    satisfy Medicare. Kaiser, my HMO, is very up on the legislation and follows
    whatever Medicare is doing, so when I moved from California to Ohio and lost
    my durable medical equipment coverage, Kaiser was willing to keep me on and
    pays for all my supplies because they paid for the original pump and feel
    that they should always provide at least what Medicare provides to their
    members. Kaiser gets a lot of bad press, but they have been ABSOLUTELY
    FANTASTIC for me–it just takes some dedication and cooperation on my part
    and they will do everything they can to help me keep myself in control and

    healthy.

    Janet

  25. kristan_180 Says:

    I agree with everything you say, but that does not change my basic
    complaint.

    The legislation is based on the idea that you cannot survive without the
    pump for those with ‘extreme fluctuations’ of Bg’s. It is certainly more
    difficult to handle diabetes with multiple injections (sure you have to get
    up in the middle if the night), but why should legislation be created for
    just a minor percentage of the diabetes population, and perhaps a small
    group that don’t have the diligence to do what is necessary with what is
    available to them?

    What is needed is a broad approach to the problem, not to rifle shoot for a
    few complaining constituents, made to a singe politician.

    David

  26. carmen15 Says:

    David:
    Medicare just approved the pumps, so I would suggest you check the medical
    criteria which is very strict with them. Since you are already on the pump,
    it may take some wheeling and dealing, but you may be able to succeed…Give
    it a try. Joan:)

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