Wednesday, October 20, 2010

Today...

I spent the majority of today watching Lily...and thanking God for every second that I have with her. Every precious second that she blinks, or laughs, or cries, or takes a tiny breath. Sometimes this is all too much. It doesn't seem like too much to the average eye. And it shouldn't. It is not their responsibility. It's not their flesh, their blood, their sole reason for being alive. I don't want sympathy for my daughter or for myself. Anyone can die. At any time. And every parent does their absolute best to protect their children. Life is not always as we plan for it. I learned that with our diagnosis. But we take on what is given to us and we give it the very best fight we've got inside of us. And we teach our children to fight and love and be thankful and live every day to the fullest. We teach them that they cannot live in fear of the unknown. If you do...life will pass you by very quickly. It's out of our hands...our fate. I am not a religious person and never have been, but I do know that we cannot control all that happens. Life happens and there are too many factors. My heart feels like a weight today that I have been dragging around...sometimes stopping and trying my hardest to get it off the ground. And sometimes just stopping to rest to take a breath and realize how heavy I feel. I have not stopped thinking about the family that lost their daughter for one second. I have been dealing with my life...living my life...checking my daughter...doing every day things...and not one second has this family left my mind. And they never will leave my mind. We are all a family. And thank God for that.

My thoughts and prayers and love and heartache go out to you all.

3 comments:

  1. Ditto. This one reason why I blog. To educate and advocate. The "invisibility" of this disease detracts from the seriousness AND the NEED for a cure.

    I am with you, I will not live in fear. I will continue to do all that is humanly possible to keep my son safe and to advocate for all persons and families with diabetes.

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  2. I found mealmommy.com and was going to sign up, but I have a question first? If I select the 10$ a month option, is it every month I will be drafted or do I pay month to month? I hope I am not inconviencing you... I think you are so great to have started mealmommy, I am a mother to 2 beautiful little ones, and I was diagnosed 1 year ago(oct 8th 2009), with T1 Diabetes, and Grave's(a form of hyperthyroidism). I thk I need something like your site to help me get on the right track with carb counting-T1 friendly meals for my family. I enjoy cooking but mostly have no clue where to start with doing a better job of preparing meals for proper management! THank you so much!
    Naomi

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  3. Hi Naomi! So sorry it's taken me a while to get back to you!

    You can email me directly at kimberly@mealmommy.com

    The site is $10 a month and is drafted through Paypal. It is so much fun for me to do and since food is the only thing I can somewhat control with diabetes, it is what I have focused on. Hope this helps!!

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