Spina Bifida of Greater New Orleans

serving all of Louisiana

 

01/15/12

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President Update -

Dear SBGNO members,

As the calendar approaches Thanksgiving, I have started to look back at the past year. I want to thank all of the SBGNO members and friends that have volunteered their time to help make a difference in the lives of individuals with Spina Bifida and their families. 

Our year starts off with our first fund raising event and family outing in April. High School students for all over the Greater New Orleans areas form teams for Slam and Jam. This is a volleyball tournament that raises funds to support Camp Friendship. During the event SBGNO members pass out information about Folic Acid Awareness. We also had our annual Family Picnic with about 50 family members in attendance, this is a laid back chance for families to enjoy the day together and share information with each other.  

It’s May and things are getting very business for SBGNO, 2nd Annual Red Bug Hill Challenge was a huge success. I would like to thank Jordy Rourke’s Family for all the long hours and hard work that went into making this event into a wonderful way to honor their son who had Spina Bifida and passed away. SBGNO has used funds from this event to help young adults with SB attend the national Spina Bifida Conference the last two years. SBGNO members manned the water and rest stations during the races. Great event and I look forward to next year. 

In June, SBGNO members attended the National Spina Bifida Conference in Anaheim, California. This year 17 members made the trip. Conference is a 3 day event with speakers on a wide range of subject matter. It a chance for individual with SB to spend time with others that are going thru the same issues that they are. SBGNO was able to cover the registration fees for all members and $300 toward hotel expenses for each family attending. Due to the success of all the fund raising this year we are going to raise the hotel stipend to $450 for the next Conference. 

July, Camp Friendship, what more do I need to stay. Kids from all over the state, southern Mississippi, and even a few other states attended this year. Ms. Cindy and her staff put on another wonderful camp. No where else can a kid with Spina Bifida enjoy a wonderful week of fun with other kids just like themselves than at Camp Friendship. During camp this year Judy Otto lead our chapter with our 1st Annual Parent Conference. Twenty parents attended the two day conference, which had 2 Doctors and staff from Families Helping Families of Jefferson share valuable information with the attendees. SBGNO made sure that moms and dads had the chance to attend and learn, a Sib Camp for the brothers and sister of campers at Camp Friendship was held at the same time. Both were a first for SBGNO. 

The month of October is Spina Bifida Awareness Month, and SBGNO did more to raise awareness and to promote prevention of Spina Bifida than ever before. We mailed information about Folic Acid Awareness to every Louisiana State Health Unit, all Universities Student Health Units, all 10 Families Helping Families centers and local Greater New Orleans Doctors. SBGNO had a booth at the 2nd Annual Baby Fest, members passed out promo items that had our Folic Acid message and our Folic Acid Brochures. Ms. Julie attended a Conference for medical professional and also passed out information about SB and Folic Acid Awareness. At the end of the month we held the 5th Ghost Bowl a thon and had many first for the event.

Here are some of them:

24 teams this year vs. 18 last year, 8 outside volunteers vs. none last year, 64 bowlers registered on line vs. none last year, 41 bowlers created a fund raising page vs. 5 last year, 23 bowlers received donations on line vs. 5 last year, Avg. amount per fund raising page was $ 337.40 vs. $97 last year. Before expenses we raised over $20,000 this year vs. $17,018.47 last year. A special “Thank You” goes to Gwenn Marelo, who recruited 10 teams to bowl this year. 

I am thankful to all who have volunteer their time this year working with SBGNO to help improve the lives of all who have Spina Bifida and their family members. Your hard work has paid off in many ways during the year.  

I am also thankful to have a Board of Directors that are dedicated to our mission and have answered every request I have made of them during the year.   

Happy Thanksgiving and Merry Christmas. 

Al Hitt

Board President

 

 

 

 

 

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This site was last updated 01/08/12