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Last year was the first time I had ever done any sort of "walk." I've never been involved with any fund raising before. Heck, I was not even into taking care of myself which is why I call my personal blog "the B.A.D. blog" with the BAD meaning "born again diabetic."
The team name I came up year last year was "Team Beat the Bete!" and take a look at the sweet logo and t-shirts we made!
Well I have decided once again to call the troops to join me in a walk this November to raise money for diabetes research and any other "diabeticy goodness" that the American Diabetes Association deems fit. (READ MORE)

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On Saturday November 3rd I will be participating in the American Diabetes Association's "Step Out to Fight Diabetes" walk. I posted about this a few weeks ago but now I am looking for some help.
I had an idea the other day to have one sentence statements on each of the t-shirts we wear as we walk. Right now, I have about 8 people that are planning on walking for "Team Beat the Bete." I would love to get some ideas from you about what we should have on our t-shirts. (READ MORE)

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Yesterday, the big manila envelope arrived in my mailbox. In it? The application for summer camp at Clara Barton. Already.

Olivia loves camp, so we'll definitely be sending her again but I was dismayed to see that the price has gone up. It's now $2,225 to go for two weeks. Last year it was around $1900. That's a big jump.

I understand why they charge so much - the staff is huge there. The buildings are in excellent condition (way better than any camp I ever attended, that's for sure!) and the grounds are very attractive. Because they have such a large medical staff, I feel really secure sending Olivia there year after year.

Plus, the camp is really great about granting camperships. They also send out information telling you how you can put together your own fund raisers and how to solicit organizations like The Lions Club or Kiawanis to help subsidize some of the cost.
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Hey there! Some notable messages from the email bag this past week.
Carey
I would like to support you and your family in this campaign to find a cure for children's diabetes, most specifically for your Charlie. Your daily routine with Charlie is overwhelming to read and enough to bring a tear to ones eye as I'm sure you have shed many. I realize now how much I take for granted every day and realize, although troubling, the temper tantrums from Ricky because we won't give him anymore apple juice is nothing to get upset about. I won't be able to attend your walk but I can support your efforts. Good Luck with your walk and we'll be thinking of you.
Dave
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The evening was perfect. My friends and I looked like we just stepped out of a magazine. I finally got a dress to work (thanks to an ingenious idea that I'll cover in a future post!). We even valeted the car. Everything was fabulous.

 

After chatting and perusing the silent auction items, we headed into the Ballroom of the Americas for dinner and the main events. I was excited to be there, excited to be part of such a personal and amazing fundraising event. I didn't realize how excited I would be as the night progressed. I didn't realize how carried away I would be by the actual facts.

 

Dinner was magnificent. The food was scrumptious. The presentation was perfect. Dessert was the best part. Chocolate napoleon with chocolate covered strawberries. Two of my favorite things. I even judged the carbs and activity perfectly (I ended the evening at 130).

 

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I just finished reading this post over on Momocrats. To say that my blood is boiling would be an understatement.

It's no surprise to people with diabetes (or those who carry insurance for said people) that insurance companies make you jump thru hoops for test strips and doctor's visits. My daughter's endocrinologist is no longer covered by either of the health plans we will have at my husband's new job. I'm not sure what we're going to do about that. I certainly can't afford to pay out of pocket for that. Do we switch and only go to Joslin once a year? Olivia loves her endocrinologist. She does not want to switch, but she's not the one footing the bill - my husband and I are and we can't afford the out-of-pocket cost.
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Additional considerations. Lately, they're making me crazy. Diabetes serves up a plate load of them. Every. Day.
The insulin pump at my hip - and how to keep it dry. The insulin that goes in the pump - and how to keep it cold. My hip-hopping bloodsugar - and how to make it sit somewhat still. The food I eat - and how to keep it from sending my bloodsugar levels soaring. And all the medicine and supplies - and how to pay for them all.
That last is a big deal. A really big deal. (READ MORE)

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Imagine it's the end of the world.

 

There's a flu pandemic. Or The Plague. Or the sun is burning a hole in the atmosphere and we all have to be herded into caves. There's mass panic and people need medical treatment.

 

Imagine having to decide who is worth saving and who isn't. That was the task of an "influential group of physicians" who drew up a "grim" list of patients who simply wouldn't be treated, according to this story.

 

The idea is to try to make sure that scarce resources--including ventilators, medicine and doctors and nurses--are used in a uniform, objective way, task force members said.

 

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