It's 11:10 PM CST ---- not much time to bust this post out. I normally write my posts the night before and post them the next morning. Things got hairy yesterday and I haven't had any time to sit down and do anything much less write a blog post.
Short and Sweet just like Sophie:
Most of you know Sophie has been sick again for a few weeks I blogged about it here. We've been in to the hospital a couple of times to do blood work and stool studies. Sophie is on a 1st name basis with all the lab techs at CMC-Legacy and even tells them that she prefers room #3 because it has the best stickers (Tangled). We are there a lot.
As Sophie's GI and I had been mulling over meds and treatment plans we were both really struggling with our next step. Her GI loves her, is so kind and seems to genuinely care about Sophie and her well-being. He called Friday and told me her lab results were back and Sophie has C-Diff.
11:46 PM --- why did this take so long? I'm going to bed now.
On the side of your blog it says, "just a mom." Nothing could be further from the truth. You are more than "just" a mom. You are a warrior...hear you roar! I know that your children were meant to be with you...that your love will see them through every trial. Thank you for blogging, and educating. You make a difference in this big world, and you especially make all the difference in the world of your children. Love you warrior mom!
((Hugs)) I'm sending love all the way from the beautiful Pac Northwest to your lovely girl...may a quick recovery and fun times come here way quickly!
BTW my mother-in-law was just diagnosed with ulcerative colitis or possibly lymphocytic colitis. She's been in a lot of pain, too - for her and your daughter's health I hope they soon find better treatments for these belly troubles. :)
Your little Sophie is always so strong. All your kids are. You, too. Good luck as you fight this. Even though she won't be at school, I know you'll be able to have some very special moments at home that you'll always remember. And...the part about logging numbers, horrid. I've totally dropped this part of our diabetes life. For now.
I've been following along as you write Sophie's story and it's been difficult to read nevermind live it. I am always hoping to read some good news that you've found a treatment that helps or works or something. Anything. What an awful thing to go through. Your kids are strong because you are strong. Keep doing your best.
Oh, Laura. My heart goes out to you and Sophie. I am so sorry she is having to go through this. I can only imagine how hard it all must be.
What I do KNOW is that there are few mothers out there like you. You are a true blessing to your girls and Nate. God gave them you as a mommy for a reason!!! He knew you were strong, and he knew that you would fight for them! You can hold your head high knowing that you are their hero.
Laura, everytime I see a picture of your little Sophie, I can't help but tear up and smile at the pure joy and beauty that shines from her face. That kind of beauty doesn't come just from her gorgeous features. It has a lot more to do with the strength of her spirit and the security that comes from knowing she is loved and cherished beyond reason. I can't even begin to imagine how tough everything she goes through is on the both of you, but once you've both won these battles, she is going to be one amazing, gorgeous and incredible girl! Know that you're all in my prayers and if there's anything I can do for any of you, it'd be an honor to be called on to help your family!
Laura, I just shake my head and wonder why these sweet little people have to endure so much. I have to believe that it is bigger than we are...the reasons. You are so so strong Laura and Sophie is so lucky to have you as her "so much more than a mom"! Praying for your sweet girl.
Laura, I am catching up on blogs now. I am so sorry to hear that Sophie had another setback and especially that she has to miss school. It really breaks my heart to hear this. I will be praying for her and you....you are an amazing Momma! Hugs to you and your girl.
Just a Mom
I AM a wife.
I AM the mom of 3 wonderful children.
I AM my son's pancreas.
The information provided on this blog is from our personal experiences with Type 1 diabetes. Because something works for us does not mean it will work for you.
Please consult your doctor if you have any questions or concerns about your health care options.
- ► 2016 (15)
- ► 2012 (25)
- #30 Ramblings of a Crazy D Mamma #NHBPM
- #29 Nick Jonas talks about Type 1 #NHBPM
- #28 The Blue Heel Society #NHBPM
- #27 Making it look easy #NHBPM
- #26 Dr. Google and Diabetes #NHBPM
- #25 Words to live by . . . #NHBPM
- #24 - Free Pass - Happy Thanksgiving! #NHBPM
- #23 A Re-Post - Welcome to Holland #NHBPM
- #22 - Hope on 2 Wheels #NHBPM
- #21 - Bedtime and Diabetes #NHBPM
- #20 - OmniParty #OmniPod #NHBPM
- #19 - A Normal Boy with Diabetes #NHBPM
- #18 - Pod Parts #NHBPM
- #17 - Diabetes Dude takes on Times Square #NHBPM
- #16 - Confessions of a D-Mom
- #15 - Happy Faces Through It All #NHBPM
- #14 - World Diabetes Day Post #NHPBM
- #13 Big Blue Test #NHBPM
- #12 - C-Difficile Colitis #NHBPM
- # 11 - People with diabetes ROCK - Dr. Nat Strand ...
- #10 - WDD is coming soon! Help me! #NHBPM
- #9 - Remission Intermission #NHBPM
- #8 - Weighing it all out . . . #NHBPM
- #7 - Blaming Diabetes #NHBPM
- #6 - The Continuous Glucose Madness #NHBPM
- #5 - Invisible Diabetes #NHBPM
- #4 - After I publish #NHBPM
- #3 - 1 in 20 #NHBPM
- #2 - Catching Diabetes #NHBPM
- #1 - Saving the Pancreas one post at a time #NHBPM...
- ▼ November (30)
- ► 2010 (136)