That's all I've got for now.
Thank you as always for all of the comments, prayers and support . . . it really takes a village!
Hi there. Not sure if I've randomly popped on here before, but I wanted you to know that we've got a little guy with t1d too and have had much of the same frustrations that you've gone through. I wanted to tell you though that it's going to be okay. I say that only because I think that we've got one advantage - my husband. He was dx with t1d at 11 yrs old. He's "normal" (wink, wink), went to a great private school, has a degree a great job and for the most part nobody would know he had t1d. he doesn't hide it, but it's not something that people notice about him first. KWIM?
Anyhow, I really wanted to thank you (warning this will sound odd) for posting pics of your son with his omnipod and dexcom. Isaac is pumping and we've tried out the CGM. I was shocked at the lack of realestate for sites and thankful when I saw that our little guys bum had a matching one in TX! I know sounds weird, but I cried the first time Isaac had a pump site on him. I cried again when he had the CGM and site. Seeing another child allowed me to know that someday Isaac will also see other kids with t1d and not feel alone.
thanks for letting me share and thanks for sharing with me.
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.
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