Showing posts with label teens. Show all posts
Showing posts with label teens. Show all posts

December 31, 2008

Two Teens with Lupus Win Spots in the Rose Parade with Kaiser Permanente

The Lupus Foundation of America applauds their efforts to raise awareness of lupus in children.

Two southern California teens living with lupus will be among the riders aboard the Kaiser Permanente float in the 120th Annual Tournament of Roses Parade on January 1, 2009. Nathalie Gonzales and Jessica Southern will appear on the float with 12 other riders, ages 12 through 18, who are battling life-threatening diseases, including lupus, cancer, and sickle-cell anemia. Kaiser Permanente Health Plan physicians nominated the teens based on their positive attitudes and persevering spirits.

With the theme, "Propel Your Dreams," the float design centers on Kaiser's ongoing health message, "Thrive." The float is a colorful and imaginative flying vehicle powered by inspiring children who cycle, row, and jog above floral clouds of solid roses.

"We are excited that these girls have been chosen to have this once in a lifetime experience," said Sandra C. Raymond, LFA President and CEO. "We appreciate the efforts of Kaiser Permanente, Nathalie, Jessica, and their parents to raise awareness of lupus in children."

Although not as common in children as it is in adults, lupus in children may develop early and tends to be more severe with multi-organ system involvement. While there have been no drugs approved by the U.S. Food and Drug Administration specifically for lupus in 50 years, research and advances in the science of lupus has improved the future for children and teens affected by lupus. There is hope on the horizon that young teens, like Nathalie and Jessica, won't have to suffer and wait another 50 years for new treatments. Today, there are more lupus treatments in development than ever before.

The Lupus Foundation of America (LFA) is on the front lines of the effort to advance the science and medicine of lupus and to bring down barriers that have impeded progress in lupus research. The LFA has established the Michael Jon Barlin Pediatric Lupus Research Program to enhance key understanding of research issues specific to lupus in children and identify novel, innovative basic/translational/clinical pilot projects. Earlier this year, the LFA launched its new Center for Clinical Trials Education (CCTE) through its website as a resource for people interested in learning about and joining lupus clinical trials.

On January 1st, turn on your TV and look for Nathalie Gonzales and Jessica Southern on Kaiser Permanente’s Rose Parade float!

In the following weeks, Nathalie and Jessica’s experience in the Rose Parade will be featured on the LFA website, http://www.lupus.org/. They will be documenting their experience on the float with video and pictures that will be posted on the LFA website, and here in our blog.

Read more about lupus and children, teens, and young adults.


Photos: Nathalie Gonzales (top right); Jessica Southern (lower left)

January 23, 2008

There's More To Lupus Than You Know: A Public Service Announcement Brought To You By The Lupus Foundation of America

Good morning everyone ... it's another cold day here in the nation's capital. Going to the low 40s today, which is warmer than it has been. I have been freezing the last few days so I'm dressed "in my snuggies" as my aunt would say. Perhaps a few hot chocolates would help take the chill out.

Quick reminder ... this afternoon, Wed., January 23 at 3 p.m. Eastern is the Lupus Foundation of America's Webchat with Dr. Peter Chira. Again, the topic is Teens & Lupus. We hope you can join us then.

Coming Attraction: Our Webchat on February 13: Women's Heart Health with Dr. Amy H. Kao.

And finally, I wanted to share another public service announcement (PSA) with you. This one is called There's More to Lupus Than You Know. It's a 30-second clip. Take a look.



If anyone reading this is interested in posting this PSA, or any of the LFA's PSAs, on your blog, please feel free to do so.

I wish everyone a great -- and warm -- Wednesday.

Until next time, Wick


January 18, 2008

Teens & Lupus: The Wed., Jan. 23 Webchat at the Lupus Foundation of America

Morning all ...

Ever notice that you don't realize how dependent you are on technology, until that technology is temporarily unavailable? Let's just say ... I've experienced that in the last 24 hours.

And now to lupus news.

Wanted to give you a quick reminder about the Lupus Foundation of America's second Webchat for January 2008.

This coming Wednesday afternoon, January 23, at 3 p.m. Eastern Time, Dr. Peter Chira, an instructor of pediatric rheumatology at Stanford University School of Medicine at Lucille Packard Children's Hospital, will host a Webchat on Teens & Lupus. (This was to have originally taken place in December and was rescheduled to Jan. 23.)

Dr. Chira graduated from medical school from Albert Einstein College of Medicine and completed his pediatrics training at Children's National Medical Center in Washington, D.C. and Children's Hospital, Oakland, CA. He did his pediatric rheumatology fellowship at Stanford.

Dr. Chira's research interests focus on improving the transition and educational process for adolescents with rheumatic diseases, including those systemic lupus erythematosus, and evaluating the role of information technology in this transition, with a past project looking at the role of an online chat room support group for teens with rheumatic conditions.

Currently, Dr. Chira is working on a project looking at designing a personal health record for teens with chronic health problems.

You can submit a question in advance.

We hope you can join us for the Webchat on Wednesday, January 23. It should be interesting.

Have a great holiday weekend, everyone!

Until next time, Wick


December 10, 2007

Teens & Lupus: This Week's Webchat at the Lupus Foundation of America

Morning all ... wanted to give you a quick reminder about the Lupus Foundation of America's December Webchat.

This Wednesday afternoon, December 12, at 3 p.m. Eastern Time, Dr. Peter Chira, an instructor of pediatric rheumatology at Stanford University School of Medicine at Lucille Packard Children's Hospital, will host a Webchat on Teens & Lupus.

Dr. Chira graduated from medical school from Albert Einstein College of Medicine and completed his pediatrics training at Children's National Medical Center in Washington, D.C. and Children's Hospital, Oakland, CA. He did his pediatric rheumatology fellowship at Stanford.

Dr. Chira's research interests focus on improving the transition and educational process for adolescents with rheumatic diseases, including those systemic lupus erythematosus, and evaluating the role of information technology in this transition, with a past project looking at the role of an online chat room support group for teens with rheumatic conditions.

Currently, Dr. Chira is working on a project looking at designing a personal health record for teens with chronic health problems.

You can submit a question in advance.

We hope you can join us for this Wednesday’s Webchat. It should be interesting.

Until next time, Wick