Team Pasta party:
Save the date for the NF Endurance Team Pasta party. It will be held at 5:30 pm, Saturday, March 3rd (at Arkansas Children’s Hospital – directions to come). It’s a great way to meet your team, NF Heroes, and be inspired! (pasta party is free to fundraisers, and $10 per person otherwise. Please RSVP to loslica@gmail.com if attending)

Team Finishers Tent:
On a similar ‘food’ note, plan to meet up with your family and friends after the race at our NF Endurance Team Finishers tent to celebrate your accomplishments. Team Volunteers will be preparing freshly grilled burgers and hot dogs along with other refreshments – free for you and your supporters who join us in our team colors…NEON.

Course Support:
We will have Team volunteers at the start line and along the course if you need to shed jackets or other apparel. Volunteers will take all clothing that is collected from their team mates back to the finishers tent where you can pick it up. (be sure to put your name in your clothing that you might shed along the way).

Hotels:
If anyone is in need of a hotel, the NF Endurance office has a block of hotel rooms. Please contact Chrissie Conner’s at the NFE Office cconnors@ctf.org as soon as possible to arrange getting a hotel room in your name.

Friends/personal support:
If you have friends coming to cheer you on, be sure to get them a team support shirt so they too can join the neon nation in LR. Here is a link to order your support shirt (shirts can be picked up in advance at the expo booth or pasta party, or the day of the race at finishers tent). Click the link to reserve the size you need http://tinyurl.com/NFSupportVolshirt

Expo Booth:
Please stop by and see us at the NFE Expo booth! We will have volunteer shirts for those that ordered one and answer any last questions about race day.

If you have any other questions about the marathon, our team, or events, please feel free to email or call me at loslica@gmail.com or 501-920-5588 or Pete at pete@rock-pond.com.

There are several ways you, too, can participate in this event – as NF Endurance Team runners, walkers, and cheer supporters along the course of the marathon. All of these areas are very important to our Marathon Team. We understand that not everyone is a marathon runner. However, having enthusiastic people on the sidelines cheering us on as we go by gives us the motivation to continue running.

Our primary goal is to raise money for NF research. However, we also want to bring awareness to a condition that has impacted our lives. If you would like to help us raise money for research, then you can also join the team as fundraisers. Any area of participation is important to this cause and to our CTF of AR Marathon Team.

Here are a few marathon-related events that we are very excited about. We’re still trying to verify all of the details, and we will post the most recent information as soon as it’s available to us.

Team Pasta Party – Night before the marathon to meet and greet runners, walkers, and cheer supporters. Everyone is invited to attend.
Marathon Celebration – At the end of the marathon at the NF Team tent where we will cook burgers and hot dogs with all the trimmings.
Mini-medical Symposia -  For NF Families – more details to follow!

Tentative Schedule:
Saturday, March 3rd from 3:00 – 5:00 – NF Information Meeting/Medical Symposia: Meet Dr. Shbarou, medical director of NF Clinic, and a social worker from ACH
Saturday, March 3rd from 5:00 – 7:00 – NF Endurance Team Pasta party (also open to NF Families attending Medical Symposia)
Sunday, March 4th 8:00 a.m – 1:00 pm – NF Endurance Team participates in Little Rock Marathon

IMG_3684 IMG_3686 IMG_3687 IMG_3688

IMG_3690 IMG_3691 IMG_3692 IMG_3693

IMG_3694 IMG_3696 IMG_3698 IMG_3699

IMG_3700 IMG_3701 IMG_3702 IMG_3704

IMG_3705 IMG_3707 IMG_3708 IMG_3710

IMG_3712 IMG_3713 IMG_3715 IMG_3716

IMG_3717 IMG_3719 IMG_3720 IMG_3721

IMG_3723 IMG_3724 IMG_3725 IMG_3726

IMG_3727 IMG_3728 IMG_3730 IMG_3731

IMG_3733 IMG_3735 IMG_3736 IMG_3738

IMG_3740 IMG_3741 IMG_3742 IMG_3743

IMG_3744 IMG_3745 IMG_3746 IMG_3748

IMG_3750 IMG_3752 IMG_3753 IMG_3754

IMG_3755 IMG_3757 IMG_3759 IMG_3760

IMG_3761 IMG_3762 IMG_3763 IMG_3764

IMG_3765 IMG_3766 IMG_3767 IMG_3768

IMG_3770 IMG_3772 IMG_3774 IMG_3775

IMG_3776 IMG_3778 IMG_3780 IMG_3782

IMG_3783 IMG_3785 IMG_3787 IMG_3789

IMG_3791 IMG_7556 IMG_7557 IMG_7558

IMG_7559 IMG_7560 IMG_7561 IMG_7562

IMG_7563 IMG_7564 IMG_7565 IMG_7566

IMG_7567 IMG_7568 IMG_7569 IMG_7570

IMG_7571 IMG_7572 IMG_7573 IMG_7574

IMG_7575 IMG_7576 IMG_7577 IMG_7578

IMG_7579 IMG_7580 IMG_7583 IMG_7584

IMG_7585 IMG_7586 IMG_7587 IMG_7588

IMG_7589 IMG_7591 IMG_7592 IMG_7594

IMG_7595 IMG_7596 IMG_7597 IMG_7598

IMG_7599 IMG_7600 IMG_7601 IMG_7602

IMG_7603 IMG_7604 ]]> http://ctfarkansas.com/2011/10/photos-dancing-w-our-stars/feed/ 0 http://ctfarkansas.com/2011/10/in-the-news-soiree-magazine/ http://ctfarkansas.com/2011/10/in-the-news-soiree-magazine/#comments Tue, 11 Oct 2011 01:07:55 +0000 admin http://ctfarkansas.com/?p=199

In the News: Soiree Magazine (PDF)

• 2011 Dancing w/ Our Stars – Invitation (PDF)
• 2011 Dancing w/ Our Stars – Response Card (PDF)

The Children’s Tumor Foundation and the Red Carpet for Research Committee is excited to present to you Red Carpet for Research – Dancing with Our Stars gala. On September 15, 2011 at the Chenal Country Club in Little Rock you will have the opportunity to be wowed by the dancing of six of Arakansas’ finest and enjoy a plated meal, drinks and dancing. We thank you so much for your continued support of the Children’s Tumor Foundation and our mission to end neurofibromatosis through research.

*Please note – online registration will close Monday, September 12th, at midnight. Advance registration required, contact Lesley Oslica at 501-920-5588 for more information

Location: Chenal Country Club
10 Chenal Club Boulevard, Little Rock, AR

Time: 6:30 PM
Thursday, September 15, 2011

Click here to Register Online!!

Fred Brown
I am a DAD, who is excited to be able to dance in the Children’s Tumor Foundation’s – Dancing with Our Stars Event in honor of my daughter who has neurofibromatosis. Our family has attended every gala in support of our NF Hero – hoping to make a difference for her, and all those with NF.

Jacob Jones
You may know Jacob Jones from Jones & Son Fine Jewelry, he is also on the board of directors of the Wolfe Street Foundation and was chair of Oscar Night America 2011. Jacob was asked to dance and accepted to help the Children’s Tumor Foundation to hopefully be an extension of the philanthropy work that he and his father annually give as the “official jeweler” of Arkansas Children’s Hospital’s Miracle Ball.

Rob Lambert
When I’m not dancing, I am a cardiologist in North Little Rock, husband to a beautiful lady, and the proud father of five children. My daughter, Eleanor, has neurofibromatosis; it is for her and finding a cure for her disease that I dance.

 

 

Aiyana Cristal
My name is Aiyana Cristal and I am originally from Tacoma Washington but my career has moved me all over the country and the latest stop is here in Little Rock. I am a Sports Anchor/Reporter at KTHV and I am excited to be a part of Dancing with Our Stars especially since it’s for a great cause. I think it is extremely important to Help the Children’s Tumor Foundation find a cure.

Leah Thorvilson
I am from Minnesota and moved to Little Rock in 1999 on a track and cross country scholarship at UALR. After college I found my passion for running increased with the distance, and I began running marathons professionally. I am currently training to compete in the US Olympic Trials Marathon, which will determine the 3 women who will go on to the 2012 summer Olympics in London. Trying to live out my dream as a runner has required a lot of emotional and financial support from sponsors and the community. Because of this, I try to give back through my abilities any way I can. I am honored to have been asked to participate in Dancing with Our Stars, and know that our efforts will help to find a cure for NF.

Angelica Rogers
I am the wife of John, mother of Lexie, John Matthew and Gabriel. I am passionate about many causes, heart disease, cancer, the arts, at risk youth and now the Children’s Tumor Foundation. I have a special young friend with neurofibromatosis and I am dancing for her!