A
September
to
Remember....
As many of you know, my grandmother passed away in June from ALS, better known as Lou Gehrig's disease. I can't even say how much I miss her. Everyday I come across some instance where I needed to call her for an answer or just to chat. Before she died, I was working on getting a wheelchair accessible van so she could get out of the house. I had talked to numerous people about financing options and fundraisers to help this process. When her health just went downhill so fast, there was no need for the van. So after she passed away, I asked my dearest friend, Katie to help my family do something in her honor. She of course said yes, and I know how much work she is having to do, so it was a big deal for her to say yes...THANKS KATIE!
We all decided to do host a black tie affair at Savanah's Riverfront Cafe, her family owned restaurant. That place was my grandmother's heart and soul. She loved the restaurant. She loved cooking. My grandparents have owned several businesses but this one is special. I truly believe it kept her going, even when she didn't know she had the disease.
The event is taking place on September the 14, 2009 from 7 to 11 p.m. It is semi-formal. We are having dinner and dancing. There will also be a live auction and silent auction. We are looking forward to this event. All the proceeds are going to ALS national organization in honor of my grandmother, Nelda Strecker, in hopes that eventually we can start our own ALS chapter in central Arkansas. The tickets are $100 per person or $150 per couple. Seating is limited and the tickets must be purchased by August 31st. You can purchase tickets by calling Savanah's (479)-229-3425. Or if you would like to make a donation please send an email to septembertoremember2009@gmail.com with details and contact information.
We are hoping to make this an annual event and will be giving the money to ALS in hopes that someday there will be a cure or treatment for the people who are suffering with this disease. I can't tell you how hard it is to see someone who is so vibrant about life be tortured by this disabling disease. So many families are affected by ALS and the treatment options are extremly limited. Please help us fight against this disease. If not by monetary donation, just by volunteering your time and most of all praying that one day there will be a cure!
For volunteering information please visit http://www.alsa.org/ and click on in your community.
Birth Photography
8 years ago

No comments:
Post a Comment