Did you know that April 14th is Raise Your Voice for Type 1 Awareness Day? You didn't? Well, now you do.

What Ruby (4) has to say about her Type 1 Diabetes:
"I have to care about my Diabetes to make sure I eat no sugary stuff without my Mom there. A lot of my friends know that I shouldn’t have sugary stuff. May-May doesn’t have Diabetes; I’m the only one in the family that has it. When I die, I won’t have Diabetes anymore; they don’t have Diabetes in heaven. When I get to eat something, my Mom pumps my insulin but no one else can touch it and one time Braylen touched it but nothing happened so it was ok. I feel good about my Diabetes but I wasn’t very good about it back when I picked my pump color because I wanted red or pink, not green. I don’t like brown. I like rainbow. I don’t like black. I only like red, pink and purple. And hot pink. But they don’t have those colors. If I knew other kids with Diabetes, I wouldn’t say anything to them about it because I wouldn’t want to hurt their feelings. And if they had a pump, I wouldn’t push any of the buttons, either."

What I, Ruby's Mom, have to say about Type 1 Diabetes:
-it's the pits--the big, stinky, hairy kind but with all things that are big, stinky and hairy, it has made us stronger.
-when I meet a child with Type 1, the first thing I want to do is hug them. The second thing I want to do is hug their mother.
-There is a huge difference between Type 1 and Type 2. Type 2, you can help prevent by eating right and exercising. With Type 1, the Great Wall of China couldn't prevent it. Also Type 1 requires shots. Lots of them, daily. Type 2, you can take a pill. Big difference.
-I've mentioned this before, but let me re-iterate: If you meet someone who's child has Type 1, do not proceed to tell them about how your uncle/cousin/half-brother/etc. who has Type 1 just had his foot amputated/kidney transplant/went blind, etc.
Just don't.-Also, if your cat has Diabetes, don't launch into a pity party and try to compare your situation with my kid's. Because:
a) I hate cats and you will receive not an ounce of sympathy from me.
b) YOUR CAT IS NOT YOUR CHILD. Your cat is your cat. Did you carry your cat in your womb for 9 months? Did your cat make you gain 50 pounds? Did you wake up three times each night to nurse your cat for the first 6 months of its life? Did you sit by your cat's hospital bed and have to try to explain to her why she has Diabetes? Did you have to tell your cat at birthday parties that she can't have any birthday cake but you brought a nice cold string cheese for her to chew on while the rest of the kitties happily dig into their cake and ice cream? Do I really need to keep going?
c) Please refer to letter a.
-The thing about Type 1 that really kills me is this: it never goes away. It's always there. Ruby never gets a break from it. I never get a break from it. I've heard that teenage boys think of sex every 7 seconds. That's me, but with Diabetes.
-We're coming up on Ruby's 2 year diagnosis anniversary and I think, just in the last little while, that I've finally completed the 5 stages of coping...for the 10th time.
-We need to help our children, especially our girls, have a healthy body image, which is hard to do when we, as adults, struggle with it as well. This is particularly important to me, as I have girls and one of them is diabetic. A study in 2005 showed that 25% of all girls with Type 1 Diabetes develop eating disorders. This freaks me out.
-Yes, my other kids have a higher chance of developing Diabetes as well. Sometimes I look at May and wonder if there's a ticking time bomb in there somewhere.
-I just want to thank all of our friends and our families. Thank you for your support, concern and love that you have shown to Ruby. Thank you to my Las Vegas family, who came to see her in the hospital and brought her fun things to play with and didn't make her feel like a freak. Thank you to friends everywhere who sent emails of encouragement and phone calls of reassurance. Thank you to our friends here in PA who think of Ruby's condition when planning a function; you have no idea how much I appreciate the inconvenience, the hassle, but especially the thought. The more children (and adults!) who know about Diabetes, the more accepted it will make Ruby and other children with Type 1 feel so thank you for learning about and teaching your children about Type 1 Diabetes.
To learn more about Type 1 Diabetes, check out these sites:
American Diabetes Association - Type 1JDRF - Juvenile Diabetes Research Foundation InternationalSix Until Me Blog