Today is the last day of D-Blog Week.
The topic is to share a few of our favorite things from the week.
I find that kind of hard to narrow down.
It was a very busy week for me with all the ballet recitals and the trip to Lab City that I didn't get to read as many posts as I would have liked. I will definitely be reading up the next few nights.
I think my favorite thing is to see more people read my blog.
I have a very small readership, but I don't really promote my blog either. To be honest, I'd say there are very few people in my circle that actually know that I blog.
I feel its my way to connect with other D-parents. and I need that.
From the bottom of my heart, I thank all of you that have read my thoughts this week, and those who have taken the time to reach out to me and comment as well. You will never know the impact that you have had.
THANK YOU!
Sunday, 18 May 2014
Saturday, 17 May 2014
D-Blog Week: Day 6
Today's topic is as follows:
Back for another year, let’s show everyone what life with diabetes looks like! With a nod to the Diabetes 365 project, let’s grab our cameras again and share some more d-related pictures. Post as many or as few as you’d like. Feel free to blog your thoughts on or explanations of your pictures, or leave out the written words and let the pictures speak for themselves.
Feb 25, 2012. Just 2.5 short weeks after Amy was diagnosed.
She was vomiting profusely, I knew it was a stomach bug. Her sister and cousin were both sick as well. She couldn't keep anything down. She was on NPH twice daily and Rapid twice daily. I was dealing ok. She had some ketones. But I wasn't sure if I should give her bedtime insulin or not. (2 weeks in remember).
I decided to bring her through our emergency department. At this point, we had only ever seen a family physician, CDE and dietician, I didn't have any contact numbers for our children's hospital that we now visit every 3 months for diabetes clinic.
We saw a doctor, and he tried to tell me that she had a UTI, that was what was causing the ketones. I tried to explain that she had diabetes, and I wasn't sure what to do. He told me not to give her insulin yet. He hooked her up to some fluids (Normal saline), and let us go when it was run in, and then to give the insulin 4 hours late.
When we got to our car, she started vomiting again. I called in to the building and they told me to bring her back in. The doctor told me there was nothing wrong, that she had a UTI and handed me a 27 page document about diabetes. I told him what he could do with his document, and took her home and managed the best that I could by reviewing the papers I was given at diagnosis and looking up as much as I could on the internet (I'm not saying that everyone should do this!)
Luckily we haven't had this happen again, but I keep this picture to remind me that I ALWAYS need to advocate for my child, especially when she is unable to do it herself.
Back for another year, let’s show everyone what life with diabetes looks like! With a nod to the Diabetes 365 project, let’s grab our cameras again and share some more d-related pictures. Post as many or as few as you’d like. Feel free to blog your thoughts on or explanations of your pictures, or leave out the written words and let the pictures speak for themselves.
Feb 25, 2012. Just 2.5 short weeks after Amy was diagnosed.
She was vomiting profusely, I knew it was a stomach bug. Her sister and cousin were both sick as well. She couldn't keep anything down. She was on NPH twice daily and Rapid twice daily. I was dealing ok. She had some ketones. But I wasn't sure if I should give her bedtime insulin or not. (2 weeks in remember).
I decided to bring her through our emergency department. At this point, we had only ever seen a family physician, CDE and dietician, I didn't have any contact numbers for our children's hospital that we now visit every 3 months for diabetes clinic.
We saw a doctor, and he tried to tell me that she had a UTI, that was what was causing the ketones. I tried to explain that she had diabetes, and I wasn't sure what to do. He told me not to give her insulin yet. He hooked her up to some fluids (Normal saline), and let us go when it was run in, and then to give the insulin 4 hours late.
When we got to our car, she started vomiting again. I called in to the building and they told me to bring her back in. The doctor told me there was nothing wrong, that she had a UTI and handed me a 27 page document about diabetes. I told him what he could do with his document, and took her home and managed the best that I could by reviewing the papers I was given at diagnosis and looking up as much as I could on the internet (I'm not saying that everyone should do this!)
Luckily we haven't had this happen again, but I keep this picture to remind me that I ALWAYS need to advocate for my child, especially when she is unable to do it herself.
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