Aug 05, 2015


Blog Carnival for Spina Bifida: Raise Funds & Awareness for the Cause

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Promoting Awareness of Spina Bifida
October is Spina Bifida Awareness Month and to help increase awareness about Spina Bifida, we’re joining Laurita Tellado of HoldinOutforaHero.orgin a Blog Carnival Fundraiser to raise funds for Laurita’s Walk-n-Roll event on October 29th. Through Laurita’s

To Donate $5 or more, click HERE.  Gracias!

Add your own personal intro…


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October is an eerie month, filled with monsters, mummies, and the macabre. But while the occasional witch or skeleton might freak you out, one must concede that there are indeed more frightening things– like finding out your child will be born with spina bifida.

And yet, each day in the U.S., an average of eight families welcome a child with spina bifida into the world. Annually, an estimated 1,500 infants are born with spina bifida each year in the U.S.

I was born with spina bifida nearly two and a half decades ago. The diagnosis came as a total shock to my family, along with an entire set of secondary complications. I was also born with hydrocephalus, or “water on the brain.” During the first ten years of my life, it seemed I was in the hospital every other week with a bladder infection or shunt malfunction. I’d be lying if I said this wasn’t really scary at times.

But then, at age ten, I discovered a fantastic way to defeat my worst fears– knowledge. I vowed I would educate myself and read up on the condition that, up until that point, seemed to be taking over my life. Much like a child who imagines a ghost is in his closet, grabs a flashlight and realizes it’s only an old coat, I had come to the realization that, when you take the time to learn about something, no matter how terrifying it may seem at first, everything is less scary in the light of knowledge.

According to the Spina Bifida Association of America, “spina bifida remains the most commonly occurring birth defect in this country.” Just how common is it overall? PubMed Health, the Web site of the U.S. National Library of Medicine, reported in March of this year: “Myelomeningocele [the most severe form of spina bifida] may affect as many as 1 out of every 800 infants.”

As a 21-year member of the Spina Bifida Association of Central Florida, I’m doing my part to shed light on this condition by raising money for the Walk-N-Roll for Spina Bifida. When my parents and I moved from Puerto Rico to Orlando, Florida in search of better educational and healthcare opportunities for me in 1990, we found a support system away from our family and homeland in joining the SBACFL. My personal search for a public spokesperson for the spina bifida cause, as well as my work as a current member of the SBACFL board of directors, have helped me find my true purpose– galvanizing as many people as possible to support the spina bifida community.

So, in the spirit of shedding light on a little-known condition, and in honor of October, which is Spina Bifida Awareness Month, here are some statistics about spina bifida that might spook you a bit:

  • Spina bifida is more common than muscular dystrophy, multiple sclerosis, and cystic fibrosis combined.
  • Latinos have the highest incidence of spina bifida out of all the ethnic groups.
  • Ireland is the country with the highest incidence of spina bifida in the world.
  • About 50 percent of babies with spina bifida areselectively aborted after being diagnosed with spina bifida.
  • Doctors recommend that every woman of childbearing age consume 400 micrograms of folic acid daily to help prevent neural tube defects like spina bifida up to 70 percent of the time. In spite of this, there are currently an estimated 166,000people in the U.S. living with spina bifida– up from just 76,000 just last year.
  • About 90 percent of people with spina bifida are also born with hydrocephalus. Many need a shunt inserted near the brain to drain the excess cerebrospinal fluid– and many requiremultiple shunt replacements during their lives.
  • Other very common secondary conditions include bladder and bowel incontinence, as well as frequent urinary tract infections.
  • After the onset of puberty, young people with spina bifida are more prone to clinical depression than most people. Researchers think this may be due in part to social isolation.


Being able to share this information with all of you today is without a doubt the most empowering and inspiring aspect of my life. I’d love nothing more than to give you that very sense of empowerment. Please publish this post on your own Web site(s), and feel free to add your own personal intro that will make it relevant to your blog followers. As many people as I’ve managed to rally in support of this cause, you have an advantage that I don’t–your audience. So, please share this information with everyone you come into contact with.

Below is a video that explains just why the Spina Bifida Association of Central Florida means so much to me, and why I’m participating in the Walk-N-Roll.

I will be raising money online for Team Holdin’ Out for a Hero until October 29th, when we have our Walk-N-Roll event. Donations can be as small as $5 or as large as $50,000. (Yes, I do like the $50,000 better!) Every cent counts! Every cent of every dollar will go towards supporting families affected by spina bifida in 22 counties in and around the Central Florida region and supporting educational and awareness efforts.

Yes, to the new parent, or even to the already-grown individual, spina bifida can seem like a scary thing to deal with. But there’s a power in numbers and a strength in awareness– a strength that gives us the courage to open the closet, shine the light in the ghost’s face, and reduce it to nothing but an old coat.

Thank you for helping me conquer my biggest fear– ignorance of spina bifida.

~ Laurita Tellado,


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Angélica Pérez-Litwin

Angélica Pérez-Litwin

Dr. Perez-Litwin is the Founder & CEO of ELLA Leadership Institute, a multi-platform professional development organization designed to advance the careers and leadership of women. She's the creative force behind the LATINAS THINK BIG™ national tour, sponsored and live-streamed by Google.

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  1. Angelica, you have proven to be a true and genuine friend. And to think I’ve only had the pleasure of meeting you once! I am sending you a BIG cyber-hug until we can meet again.

    No sabes cuanto aprecio tu apoyo. It means EVERYTHING. <3

  2. I love it! I wish i could go! May I re-post?

  3. You can count on my blog!


  4. Jes, of course you can repost!!! Love ya, chica! :)

    Vicky– I visited your site. The badge looks great! FYI it does not link to a post or anything. The badge is supposed to link to this post on New Latina. Just wanted to let you know. I hope you’ll be posting the post on your blog today! ;) Gracias!

  5. Scheduled to publish the post on 10/29 at Excellent cause & proud to be a part of it!

  6. Hello Laurita,

    I followed you from @ATGTranslations and now following you from my new @LatinaComm. This is set up to go up tomorrow in Hope this helps!

  7. This is such an amazing cause and opportunity to promote awareness. Thank you…I posted here: :)

  8. Lisa Renata says:

    Here is mine!

  9. I am happy to participate in this worthy cause!



  10. I am very honored to be part of this blog carnival. I have place the post as of this afternoon & will also share on The Latin Cooking Diva Facebook page.

    I want to say that I have the badge & will place it on my new website going live by next week. For some reason, is not “set-up” tp permit badges on the ezine =(

    Until then I have placed the badge twice in the post.

    Thank You again for allowing me to participate!


  11. This is a great example of Latinas Unidas. Thank you Laurita for inspiring all of us. And thank you Angelica for your leadership and generosity. Love you all!
    Here’s the LATISM post in English:
    y aqui esta en nuestro idioma:

  12. so cool to see so many blogueras coming together and sharing these blog posts.

  13. Done~

    So thank you for the opportunity to participate!

  14. Hi Laurita! Here’s my entry for the Blog Carnival. Un Abrazo!!

  15. I love this! And think you are doing amazing things :)

    I’ve been so crazed this month, haven’t had a chance to write anything yet. But I will participate! XOXOX

  16. I wasn’t able to post but I donated a little something. So awesome what you are doing! You should be proud of yourself!!


  1. […] Bifida Blog Carnival encourages bloggers and online media to publish a “call to action” using existing content created by Ms. Tellado on Wednesday, October 25, 2011. Concurrently, participants are encouraged to […]

  2. […] through the Spina Bifida Association of Central Florida.  To participate in this blog carnival, learn more here.  Thank you so much in advance for your […]

  3. […] through the Spina Bifida Association of Central Florida.  To participate in this blog carnival, learn more here.  Thank you so much in advance for your […]

  4. […] While I didn’t get my brief moment of local fame today, this day is also very meaningful to me for another reason related to this cause. In honor of the Walk-N-Roll, my bloguera friends Angelica Pérez, Chantilly Patiño and Midy Aponte have teamed up to organize an online event that is the first of its kind: The Walk-N-Roll for Spina Bifida Blog Carnival Fundraiser. […]

  5. […] The Walk-N-Roll Spina Bifida Blog Carnival is being led by another amazing Latina, Angélica Pérez-Litwin, PhD, publisher and CEO of New Latina. […]

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