Wednesday, September 4, 2013

Thankful!

My 5 year old daughter Bella loves horses, she loves to draw, especially fairies and she just learned to ride her bright pink and purple bicycle without training wheels. She has long blonde curly hair that catches everyone's attention and she has enough "sass" to make even a stranger shake their head and hide a smile. My daughter Bella was diagnosed with Type 1 diabetes in February. This means that her body cannot make the insulin that it needs to turn her food into energy for her body. Her father and I must give her insulin injections, shots, multiple times a day. In the 6 months since Bella was diagnosed she has had over 550 injections. Thankfully, she now has an insulin pump that administers her insulin, instead of shots she only has to change her infusion site every three days. It has been a godsend! However, we must still check her blood sugar 8-12 times per day. This means pricking her tiny little finger tips with a needle and squeezing blood out to apply to a test strip. These readings let us know if her blood sugar is high or low, how much insulin to give her, or if she needs juice or food or worse, an emergency injection called Glucagon to raise her blood sugar. Just like the pump made administering her insulin easier on her, and so much more effective as well- There is a device called a Continuous Glucose Monitor. This "CGM" has a fiber-optic sensor that sticks under her skin and stays in place for a week. The sensor takes a reading of her blood sugar every few second sand every 5 minutes it displays the average. Not only does the CGM give us the real time reading but it plots these readings out so that we can see if her sugar is rising or falling quickly, allowing us to catch any dangerous lows and stop dangerously high blood sugars. However, her insurance will not cover it. It's not a required item, even though it is considered the standard of care in the diabetes community. A CGM costs almost $1600 and the monthly supplies average about $300. This is beyond what our family can afford. Thankfully, we have wonderful friends. We have friends who are going above and beyond, creating fundraisers to help raise the money to purchase Bella what she needs, what we need to keep her tiny little body as healthy as we can.

 I dont know how to make it click-able... but here it is!

https://www.giveforward.com/fundraiser/f303/bellacgmfund