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Sunday, October, 12, 2008

Type One for More Than 35 Years!

by  Victoria in San Antonio
Tuesday, July 22, 2008
Victoria in San Antonio

Victoria in San Antonio

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Well Hello.  I have had type 1 for many, many years.  I was first diagnosed way back when the only way of telling how your sugar levels were while at home was with a test tube and drips of urine.  Ring a bell, anyone?  But now a days, I am happ...

  1. welcome!
    Laura
    Tuesday, July 22, 2008 at 04:34 PM

    Hi Victoria, 

     

    Welcome to the site! I'm glad you've found us. I know our community members will truly benefit from having someone with your years of experience to learn from!

     

    Can you tell us what the biggest difference in your diabetes management has been since switching to the pump?


    reply
  2. Test tubes LOL!,
    shoofly
    Saturday, September 06, 2008 at 12:53 AM

    Howdy Victoria!Wink

     

    To this day I can't stand that deep green color that means "shot time"!  OH, sharping your own needles, pits, glass syringes...that didn't last long thank goodness. School that's another nightmareSealed, and parents who wouldn't let there children come over, could be contagious ya know.

     

    The Honeymoon period, my first heartbreakCry....took 7 years for my islets to kick it, it was hard on a kid, who still believedInnocent...

     

    Blaming my parents for the 'diet' of sugar they fed me, LaughingROTFL! Even 1 of 3 brothers came home from school wondering why he didn't get candy too.

     

    Bells ringing? Sounds more like the Gong Show Ha Ha ha

     

    Really wouldn't have changed it for anything. We are stronger, healthier and most of us are over-achievers =) Smile

     

    Thank you sooo much, I needed the boost you gave!

    Bless your heart, Giggles and Grins to all,

    Shoofly & Moose Service Dog-retired

     

    PS. Just found the smiley, what fun!


    reply
    re: Test tubes LOL!,
    Victoria in San Antonio
    Monday, September 08, 2008 at 10:43 PM

    Hey Shoofly-

     

    Thanks for the walk down memory lane... You made me laugh and nod!  I remember getting a detention in school one day for asking to go to the bathroom too many times - boy, we have all come a long way in understanding diabetes!  I hope every child who happens to be diagnosed with diabetes is introduced to one of us long timers - the support and understanding alone would make a huge difference! 

     

    Someone in an earlier post asked What is the biggest difference the pump has made?  I would like to say, there are so many great things about the pump, it makes me very aware of my diabetes which is instrumental to heading off tricky situations at the root.  It has also given me a sense of power and stripped away a certain amount of  "helpless" with this disease.  I think not having to carry around syringes and a delicate glass bottle is also a fairly HUGE relief.  Still, finding a secluded place to use my blood glucose meter posses the same dilemas.  You know what I mean, like having to sneak off so those who don't know you very well won't feel uncomfortable... that sort of thing.  However, nothing compares to being able to push a couple of buttons and magically get a dose of insulin right at the table of a restaurant!! I love my pump. I have earned my pump and now I only wait for the arrival of the Glucometer Watch or better yet, how about a Glucometer Cell Phone!! Your comment really touched me, so true:

    We are stronger, healthier and most of us are over-achievers =)

     

    Right back at cha!!

    Keep up the smilies - they really show your spirit!

     

    Victoria Wink


    reply
    re: re: Test tubes LOL!,
    Bev
    Saturday, September 13, 2008 at 09:13 PM

    Hi: I'm 54 and have had type 1 diabetes for 43 years. I've been on a pump for about 20 years, was one of the subjects in the first human trials of human insulin, published the first paper about glucose monitoring in pregnancy in 1980 (I'm also a CDE) and asked my pediatric endocrinologist in 1970 if I could use the Dextrostix at home to check my BG that we had used at the camp where I was a counselor for kids with diabetes. She STERNLY told me that no one would ever be willing to stick their own fingers to check their glucose and absolutey forbid me to do soLaughing . Fern's blog touched me heart. Fern, you can be OK. You'll find the strength to change one thing at a time. Keep all your dreams, but make your first dream taking control of your life, most improtantly, your diabetes. Don't see your only identity as a diabetic---you are clearly many, many things; student, artist, adventurer (notice how none of those labels end in "ic")---you also happen to have diabetes. Owning that part of your human condition will help you see ways that you can accomplish whatever you want to do in your life. Take your antidepressants--no shame there!  Good luck to you and God bless.


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