Just so you all know--- Jimmy John's is unwilling to provide information on ingredients. I am now avoiding them completely (for myself as well, because I think it's bad business practice).
talk soon!!
n
Wednesday, August 24, 2011
Wednesday, March 3, 2010
Grant's Wish Fundraiser: March 20
It's cool, we don't have so many followers on our blog :)
However, for anyone out there... this is important. On the outskirts of Chicago, we will be hosting our first attempt at a fundraiser. Grant's Wish is to showcase our wonderful children and the wishes for their future. Grant, and the rest of our children, have a genetic disorder called Galactosemia. We are having this fundraiser to (1) help families afford to go to the bi-annual conference (this year in Minneapolis) and (2) help fund research to hopefully find a cure or manage a way to live a better life even with this disorder.
Every parent has hopes and dreams for their children. Most of us found out this disorder existed when our child was diagnosed. Some people caught it quickly and had less complications, some were not that lucky. We hope that our children can avoid or at least manage the complications that come with Galactosemia.
Please join us on March 20 for our fundraiser (please see details on pgcmidwest.com) or check out the website to see how you can donate. There are also many incredible donations that are already online for our silent auction.
However, for anyone out there... this is important. On the outskirts of Chicago, we will be hosting our first attempt at a fundraiser. Grant's Wish is to showcase our wonderful children and the wishes for their future. Grant, and the rest of our children, have a genetic disorder called Galactosemia. We are having this fundraiser to (1) help families afford to go to the bi-annual conference (this year in Minneapolis) and (2) help fund research to hopefully find a cure or manage a way to live a better life even with this disorder.
Every parent has hopes and dreams for their children. Most of us found out this disorder existed when our child was diagnosed. Some people caught it quickly and had less complications, some were not that lucky. We hope that our children can avoid or at least manage the complications that come with Galactosemia.
Please join us on March 20 for our fundraiser (please see details on pgcmidwest.com) or check out the website to see how you can donate. There are also many incredible donations that are already online for our silent auction.
Tuesday, March 10, 2009
Shop and Share
I posted on our faceBook site as well. i will be sending an email in the next 2 or 3 days with all the info for our Shop and Share fundraiser going on the week before easter. I will also be picking up 300 pre-printed slips next week and so if anyone wants me to send some their way, please give me your address and I will do that. Hoping to raise at least $1000!
Thursday, January 29, 2009
More Logo Designs
Ok... I really went too far with the "rough" thing.... I also made one without the blue wrap-around as suggested. They are both more "cleaned up". Alright. Now what do you think?
Sunday, January 25, 2009
Logo?
Hey everyone,
I was messing around with some ideas for a logo. I am not a graphic artist so if anyone can come up with something that looks more professional please do. I will not be offended or discouraged. Here are two color schemes I came up with. I was thinking of a hand as drawn by a child. A helping hand. Inside the hand is a rising sun, the symbol of hope and new beginnings. Let me know what everyone thinks. Any suggestions would be helpful.
Monday, December 15, 2008
Facebook Group
Ok... I caved in and started on Facebook. I created a group for us there. Just look up Parents of Galactosemic Children Midwest. :)
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