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Hello from New Mexico

Discussion in 'Introductions' started by browneyesjt, Feb 26, 2009.

  1. browneyesjt

    browneyesjt Approved members

    Feb 24, 2009
    My name is Julia and I live in New Mexico. I have 6 children (ages 16, 14, 11, 8, 5 & 6 months) and two of them have diabetes, type 1. My 14 year old son, Javier, was diagnosed in November 2005 and my son Angel (8) was just diagnosed on January 19, 2009. I am glad to have found this group with members who really are going through the same things we are and share some of our frustrations, triumphs, sadness, etc....

    Angel is officially "honeymooning" so we have cut down on his Novolog these last couple of days. Javier is not honeymooning (I think ) and still struggling with some of his BG's.
    My husband and I have really been struggling with our situation and I now freak out whenever one of my non-D kids tell me their stomach hurts, or I see them drink water. We are trying to decide if we should get our kids tested for antibodies for type 1? I would really appreciate any feedback on this....
    Also anyone else here from New Mexico?

    Julia-Mom to Javier (14), dx 11/05, Angel (8)- dx 1/09 both on Lantus & Novolog, Andres (16, nonD), Joanna (11, nonD), Joel (5, nonD) and Angelica (6 months nonD)
  2. Connie(BC)Type 1

    Connie(BC)Type 1 Approved members

    Nov 11, 2005
  3. Reese'sMom

    Reese'sMom Approved members

    Jan 18, 2009

    You found the right place to come for support! :)
  4. Christopher

    Christopher Approved members

    Nov 20, 2007
    Welcome, I hope this site helps you as much as it has helped me. Good luck...:cwds:
  5. CButler

    CButler Approved members

    Dec 1, 2007
    Welcome, and sorry you have two kids with type 1.:(
    I can understand why you would be concerned about
    getting the others tested.
    We did not test our other three, but they do get a finger-prick
    occasionally just for peace of mind.
  6. 2type1s

    2type1s Approved members

    Nov 23, 2008
    Welcome...I also have 2 kids with type 1. We had our oldest tested for the antibodies. You should look into the TrialNet study. If you don't have a local hospital, I can give you the name and number of the person who is in charge of it here in TN at Vanderbilt. They send a kit to a lab local to you, or even your pediatrician. It's a simple blood draw. It's critical research, and think about it as a possible lead to a cure.
    It is very hard having 2 kids to remember all the details with, and I am so sorry for your family. It does get easier...God bless... PM me if you want the name and number...Sharon
  7. tiffanie1717

    tiffanie1717 Approved members

    May 16, 2008
    Welcome. I have two D kids two with the latest being dx in Feb 09. This is a great place for info and support! glad you found us!
  8. hsmommyofmany

    hsmommyofmany Approved members

    Jan 31, 2009
    welcome, from a fellow mommy of 6!! i only have 1 child with D, diagnosed just 1 month ago, i can not imagine having to remember all of this stuff for 2 of them...i totally understand about the stomache ache and water thing...everytime someone asks for water or wets the bed or throws up, my first thought goes to diabetes now...it is really stressful constanly worrying about someone else getting it. i have called for the trialnet package that some of the others posted about, you can get the link on this site. this is a great site and the people here are very helpful and always available.
  9. Jensmami

    Jensmami Approved members

    May 17, 2007
    Welcome to CWD, you will find information and support here, we all learn so much from each other. I am not from New Mexico, but I love it there. We are at least once a year in Albuquerque.:)
  10. AmberO

    AmberO Approved members

    Oct 31, 2005
    I'm not sure if there are any other NM's here. I'm from Las Cruces but have lived over seas for a few years now. Welcome!

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