To Tanzania with Love | The Laurita Spina Bifida Project wants to donate wheelchairs

“How sad it is that we give up on people who are just like us.” — Fred Rogers (“Mr. Rogers”)

I don’t really remember what it’s like not being able to walk. As parental anecdotes recall, I was about two years old when I took my first steps. My parents were overjoyed, of course, but probably more than most parents, because I have spina bifida. According to my doctors at the time, I wasn’t supposed to be able to walk.

I may not remember what it was like crawling around the house or not being able to stand up, but, at age 30 now, I am beginning to grasp what it means to have limited mobility. My knees and back hurt constantly, and my wheelchair is getting much more mileage than it used to.

As I recently learned through a good friend I’ve never met, there are people in Tanzania, and in many other countries, who do not know the privilege of owning a wheelchair— what a blessing it is to have the equipment to facilitate mobility.

Little did I know until these past few weeks, that there are people on the other side of the world who would give anything to have the freedom I am often complaining about— the freedom to move.

That’s why my non-profit organization, The Laurita Spina Bifida Project, has offered to help the Association for Spina Bifida And Hydrocephalus Tanzania (ASBAHT) by raising funds so they can purchase wheelchairs, walkers, crutches, and a prosthetic leg for a young girl with spina bifida.

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Image courtesy Sifa Sylvia, ASBAHT 

A shifting perspective

It really gives me pause to reflect on how grateful I am for my “inconveniences.”

Over there, where my friend lives, people aren’t griping because someone took the accessible parking space. Or because their wheelchair won’t fit in their friend’s car when she offers to give me a ride.

They don’t complain about these problems because they don’t exist. Because access to the mobility devices they need doesn’t exist.

Many moms of children with spina bifida and hydrocephalus must push their children in strollers instead of carrying them. If they don’t have access to the brain surgery to have a shunt placed, the children’s heads grow until the parents can no longer carry them. Even these strollers are very hard to come by. As for me, I am only vaguely reminded I have a shunt in my head when the weather changes and I feel a slight headache.

This holiday season, I am fully committed to making the freedom of mobility a reality and not just a dream for at least several people in the Tanzanian spina bifida community…people who are much like me.

Maybe this will make a huge, life-altering difference for them. Maybe it won’t. All I know is, everyone needs someone in their life who refuses to give up on them.

I have you guys. Now, it’s my turn to be that person for somebody else.

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Image courtesy Sifa Sylvia, ASBAHT 

How you can help

What we need, first and foremost, is monetary donations. Whether it’s $5 or $500, every dollar makes a big impact when you add it all up. Trust me on this! How incredible is it that for the price of a latte macchiato you bring us one step closer to giving a deserving human being the gift of mobility?

 

Here’s a rough estimate of what each item costs, in U.S. dollars:

• Wheelchairs – $140.00 each

  • Walkers – $70.00 each

• A prosthetic leg for a youth with spina bifida – $460.00

Other ways to help out

If you own a company or know of a company or organization that might be interested in partnering with us to help raise the funds, please reach out to me at laurita.tellado@gmail.com. I truly believe “it takes a village,” and you are all my shining example of that!

Consider this campaign for your company’s end-of-year charitable contributions. Every donation is tax-deductible.

Also, since there are just so many wonderful social good campaigns during this time of the year, we need your help with getting the word out. Please, post to Facebook, Tweet, share, blog, Pin, Instagram post, etc.! There is truly no action that is too small to make a difference.

Please share / post using the hashtags #TheLSBProject , #SpinaBifida, and #Give5ToThrive (because we want to encourage that no amount is too small!).

Keep up with this campaign by following and connecting with us on social media:

The Laurita Spina Bifida Project on Facebook

@TheLSBProject on Twitter 

@TheLSBProject on Instagram

Remember what it’s all about

Finally, keep in your mind and heart that we are doing this to pay it forward. We have been so Blessed throughout this entire process, and I’m grateful for each and every person who has been part of The Laurita Spina Bifida Project’s journey thus far.

In the words of my friend Sifa of Tanzania, the angel behind-the-scenes who has put me in contact with the ASBAHT: “It will be an honor for ASBAHT to partner with you or any other organization or individuals out there with the heart to help the forgotten children, youth, and adults living with SBH in Tanzania.”

Thank you, Sifa. We’ll do our best.

Love,

Laurita ♥

The Laurita Spina Bifida Project to launch at Hispanicize 2016

Why, yes. It has indeed been a while.

Mea culpa. I may not have been fully “present” on Holdin’ Out for a Hero, but please rest assured…incredible things have been happening behind the scenes– miracles, actually!

Today, after 19 years of wishing, learning, waiting, and hoping, after years of prayers, all answered, not all in the way I anticipated, after much hard work and informal advocacy, it’s happening.

My non-profit organization, The Laurita Spina Bifida Project, is launching today during Hispanicize 2016– in Miami, no less.

Don’t pinch me, please. I don’t want to wake up!

It’s been a long time coming. I mean, really. I remember growing up thinking that starting any kind of organization– for-profit or non-profit– required wealth, and lots of it.

I remember wondering why I wasn’t rich and able to fulfill my dream.

I remember writing my first letter to Oprah Winfrey, and pouring my heart into it, asking her to shoot an episode about spina bifida. And I remember very clearly the polite “no, thank you” letter I received from The Oprah Winfrey Show– at age eleven.

Sometimes I wonder why I just didn’t give up and pursue a different path. I believe anyone with spina bifida can be just about anything within some reason. I could have done anything.

Instead, I chose the road less traveled. The one that hadn’t been trodden before– the one I had to pave myself.

But I haven’t walked it alone. Oh, no. There have been angels. Dozens, hundreds, perhaps thousands of them. And they carried me on their wings whenever I was too exhausted, too angry, too bitter from the failed efforts to keep flying.

It is now that I realize it. My “failures” weren’t failures at all– they were practice; my boot camp. With teachers, mentors, trainers, fellow advocates, cheerleaders, I worked through these failures and got up again.

My initial vision was to host a launch event at a restaurant in Orlando, close to where I live. Instead, I am in the heart of Downtown Miami, surrounded by fellow bloggers, journalists, entertainers, photographers, marketers, and seasoned non-profit industry veterans. Many of these are people I call very close friends.

In retrospect, I cannot imagine launching my precious childhood dream anywhere else, surrounded by so many of the people who are actually helping to make it happen!

Today, as I prepare to meet friends, family, and colleagues for Happy Hour at Toro Toro Miami and our extended community on Twitter at 5:00 p.m., I’m sure we’ll have a lot of last-minute details to think of.

As for me, I’ll also be reflecting on everyone, everything, every incredible moment that has brought me– us– here.

Today, I finally know it was all for good.

Please join us today on Twitter using the hashtags #TheLSBProject and #SpinaBifida (#EspinaBífida para español, también). Be sure to RSVP here to be eligible to win some awesome prizes!

And if you’d like to contribute to our crowdfunding campaign, that’s here.

To see the fabulous press release that my friends and colleagues at Hispanicize Wire published about our launch, please click here.

 

Till tonight! And…thank you. 

Love,

Laurita

Social Good at Hispanicize 2014: Be the Change

Hispanicize 2014 took place in Miami from April 1st through 4th, and this year, the organizers stepped it up by demonstrating that philanthropy is alive and well within the Latino community and beyond.

On March 31st, I attended Social Media for Social Good Training for Non-Profits Serving Latino & Multicultural Communities, a half-day, pre-conference event, sponsored by Florida Blue and open to professionals involved with nonprofit organizations.

 

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The presenters were Alex de Carvalho, founder of Social Media Club of South Florida, as well as Regional Development Director at Constant Contact; Katherine Doble, publisher of Los Tweens and Teens and president of Siren Marketing; and Maricela Cueva, vice president of VPE PR.

The topics covered ranged from strategies for E-mail marketing to the most effective platforms and methods for engaging potential cause supporters using social media.

I personally found the training interesting and engaging, and it was packed with lots of resources for nonprofits and individuals alike.

 

 Yoani_Latinovator

For this cause blogger, one of the most awesome moments of the conference was witnessing Cuban bloguera Yoani Sánchez receive a Latinovator award for her courage and relentlessness in informing the global public on what is going on in Cuba.

The writer and activist has been arrested several times, even beaten, for speaking up.

I was honored and privileged to have the opportunity to meet her last year, when she came to Orlando to speak at my alma mater, Valencia College. After she was interviewed at the Latinovator Luncheon, I got to attend the press conference and ask her a question! What an amazing opportunity. I was thrilled. :)

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I couldn’t believe that Yoani Sánchez remembered me from the Valencia event! I imagine she meets hundreds of new people every week. 

Attending the Positive Impact Awards was yet another amazing opportunity to see social good up, close, and personal. It was also a wonderful time to pay tribute to many awesome Latinos who are making a huge difference in our communities– and in the world.

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I’m very proud to know Hispanicize Founder & CEO Manny Ruiz, and call him mi hermano. Congrats, Manny, on being given the key to the city of Miami!

By far, one of the most emotional moments during the Positive Impact Awards was seeing Hispanicize’s own Founder & CEO, Manny Ruiz, be surprised onstage by being presented with the key to the city of Miami by none other than the Mayor of the City of Miami, Tomás P. Regalado.

I actually had tears in my eyes, watching Manny choke up as he thanked everyone for their support. 😉

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Manny Ruiz gets emotional upon being awarded the key to the City of Miami. Love it!

Even early on in the evening, on the red carpet, I was able to say hello to a few familiar faces…including this one:

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Oh, you know, just hanging out with my friend Edward James Olmos! 

I was so thrilled that actor Edward James Olmos remembered me from last year, when I attended the premiere of “Filly Brown” during Hispanicize! Eeek!

But that wasn’t my only “geek-out” moment of the night. For reals. Yolanda Pagán, whose late husband Louis Pagán inspired the Positive Impact Awards, and I sort of improvised and tag-teamed that evening during the red carpet. It was a really sweet moment as I watched her glide gracefully from interview to interview and from photo op to photo op! Yoli and I have become very close friends ever since we met during Hispanicize last year, and I felt Blessed and honored to witness this shining moment for her.

Well, Yoli came over to me during the red carpet madness, and straight-up told me:

Maria Hinojosa wants to meet you.”

Jaw. Drops. On. Floor. 

“What!?” I gasped. 

“Maria Hinojosa,” Yoli repeated. “She wants to meet you.”

“Why?” I muttered breathlessly. 

“Are you seriously asking that question?” Yoli countered. 

Well…yes I am!  But, no matter. When veteran, award-winning journalist Maria Hinojosa asks to meet you, you ask when and where! 

So, I dashed over to where Maria Hinojosa was being photographed and fawned over. Then, she notices me.

Then, she addresses me.

She said she really wanted to meet me, and that I was an amazing blogger or something like that, but, truth be told, as is the cruel irony in most situations that you should have been taping– I remember very little of what was actually said because of how shocked I was. Understandably. 

But I do recall the million-dollar-moment, as I was basking in my 30 seconds of glory, Yoli watching me the entire time with a huge grin on her face. 

Manny walked over to us (to formally introduce me to Maria, I imagine) and puts his hand on my shoulder and says to Maria (I mean, are we on first-name-basis now!?):

“Laurita is one of the best bloggers in the country.” By this point, I’m fighting back the tears. 

And then Maria totally says, pointedly, to Manny: 

“I know! That’s why I wanted to meet her!” 

By then, whether I was still breathing was questionable. I think I had a pulse, though, because my heart was racing.

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Maria and me. New besties? Here’s hoping! 😉 

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George Torres, founder of the Positive Impact Awards, Yolanda “Yoli” Pagán, wife of Louis Pagán, and Manny Ruiz pay tribute to Louis’ legacy. (Doesn’t she look stunning?)

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Some of the Positive Impact Awards honorees share their moment of triumph onstage. 

I fear I’ve already made this post too long, but I have to share about the panel I spoke on, on Friday! My dear friend and hermano, George Torres, a.k.a., “Urban Jíbaro,” asked me to speak on a panel titled “Hispanic Social Media for Social Good: Corporate Best Practices.”

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(From left to right): Stephen Chávez, founder of Latino Foodie, moderated the #SocialGood panel, which featured George “Urban Jíbaro” Torres, founder of Sofrito Media Group, and Sofrifo for Your Soul, Steven Sánchez, Global Corporate Communications Manager for 3M, Sonia Díaz of Balsera Communications, and me. 

I have been fortunate to be a part of several dynamic panel discussions these past few years, and this one was no exception! Despite being the last day of the conference, and people showing up– *ahem*– at “Latino time” (there were parties every night!), I feel we had an amazing chemistry among our group, and we were able to engage with our audience members.

The best part was being able to tell my story, and hearing everyone else’s personal journeys through social good! I’ll be honest– I came away from this panel learning a lot! 

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With Yolanda “Yoli” Pagán, who is now one of BFFs! I can’t tell you how grateful I am for your support, encouragement, and many pep talks before and during Hispanicize! 😉


Girlfriends

With my longtime amiga, Alsy Acevedo of Catholic Relief Services, Anadel Alberti of Lanugo, and Yoli. Thanks so much, ladies, for supporting me and attending my panel! 😉

Later that day, after I recovered my nerves from speaking, I ran into Matt Wallaert, a behavioral scientist who works with Bing. He wanted to talk to me and introduce me to a group of young students with ASPIRA of Florida that he brought to Hispanicize, so that I could encourage them. Needless to say, I was at a total loss as to what to say to these kids! I have no idea how to foster and nurture young minds; I don’t know what you’re supposed to say to encourage them!

Well, when I saw Matt and a young friend of his, Chantal, they told me that they had attended my panel and that it was great! Matt had walked in with his group of students to watch/hear us! I was so incredibly moved by their show of support, and I realized that, when it comes to the next generation, all you have to really do is be there for them.

The week of Hispanicize was both too long and too fast. There were so many things I would have liked to do but didn’t have the time or energy to do. There’s just so much! That’s why I’m dedicating several posts, here, on Espresso con Leche, and on my hypeorlando blog, to covering everything I can.

By far, the most inspiring and uplifting moments of Hispanicize this year were the ones related to social good. Of course, it feels great to give, and it also feels wonderful to connect with others who are passionate about philanthropy within the social media space.

The best part of using social media for social good is that “the buck doesn’t stop here.” The donation or Tweet that you make, the photo you instagram, the blog post you publish about a cause can have so many impressions and can be shared so many times. Social media knows no boundaries or limits. Social media exists so that we can push our stories out beyond the natural, physical scope of older media channels.

And this week, I got to connect and reconnect with so many others who feel passionate about doing just that!

A hearty shout-out to the following sponsors:

  • Florida Blue, who sponsored the Social Media for Social Good Training for Non-profits Serving Latino and Multicultural Communities training
  • 3M, who sponsored the Positive Impact Awards, this year’s signature event, in addition to sponsoring and participating on our panel, Hispanic Social Media for Social Good: Corporate Best Practices.
  • Toyota Latino for being my sponsor during Hispanicize, and for inviting me to sit at their table during the Positive Impact Awards! I have so much more content to share about you guys, but for now I’ll say that you have truly demonstrated your commitment to social good in every initiative and program you design for consumers. Thanks for taking me under your wings! 😉

 

 

“You must be the change you wish to see in the world.” 

–Mahatma Gandhi

–Laurita ♥

The 2014 SoftRock Holiday Giving Gala #SRGiving

This past Saturday, I was invited by a new friend to attend the SoftRock Holiday Giving Gala at Tier Nightclub in Downtown Orlando! Samantha Weaver is senior writer for SoftRock, a media company that designs software and multimedia for businesses.

The premise of their Giving Gala was to invite guests– in exchange for a pledge to give time in volunteer hours for any charitable organization.

I love that concept. 

Indeed, for me, there is nothing better than encouraging employees to support a worthy cause, or even several!

So, when Samantha invited me to this event, I simply couldn’t resist. 😉

Mami was my plus-one at the gala, and we got the star treatment that night! We were picked up promptly by a car service and taken to Tier Nightclub, a trendy spot in Downtown Orlando.

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I was really impressed to see so many plush, comfy sofas in a club setting! I wasn’t expecting that.

 

SamanthaWeaver_and_meWith Samantha Weaver, Senior Writer for SoftRock

I enjoyed drinks and tasty appetizers with Mami, and did a lot of people-watching!


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Mami and me. :)
 

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Caught live-Tweeting and instagramming! 
 
 
It was great to run into several friends– some of them from way back! 
 
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With Lynn Hoppes, who now works with SoftRock, and who I met as Sports Editor when I was interning at Orlando Sentinel in college. 
 
 
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With my friend, Jen Vargas, of Central Florida Top 5
 
 
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With the ladies! Samantha, Jen, me, and Jeanette Scott of J’s Everyday Fashion
 
 
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With Alec Difrawi, Founder & CEO of SoftRock. 
 
 

I’m so glad I was invited out to the party, and even more excited to start the year off by taking a pledge to volunteer in my community!

Thanks, Samantha– and thanks SoftRock!

Laurita :)

 

5 Simple Ways to Help Someone Living with Spina Bifida / #GivingTuesday

 

Giving Tuesday

 

 

Today is Giving Tuesday, a movement for social good that is taking social media outlets by storm. 

Thousands and thousands of people are sharing ways in which we can all give back to great causes. 

I don’t wish to add to the cacophony of causes by asking you to donate to this or that. Instead, I want to give all of you — even those with limited funds some tips on how you can support a friend or loved one who has spina bifida, or who lives with someone who has spina bifida (caregivers need support, too!) 

So, read on for some musts and must-nots.

 

1. Don’t exclude us from social gatherings. 

I remember how painful it was growing up, and the teen years were just as awkward as my early years. It hurt me deeply when I found out some of my girlfriends were hanging out and choosing not to invite me. The reason? They thought I might bring my mom along. Although it wasn’t true at all, it still hurt. My so-called friends didn’t think I was independent enough to attend a social function on my own, without my parents at my side.

If you have a friend with spina bifida, ask them what hobbies or activities they enjoy. Invite him or her to your next outing. If you have any doubts as to what their capabilities or limitations are, ask, but never assume. 

 

 

2. Ask us for help or advice when you need it. 

Believe me. This can actually be one of the greatest gifts you will give someone with spina bifida. Many of us with spina bifida are so tired of being “helped” all the time, and many times people won’t approach us to ask a simple favor out of fear that we won’t be able to help, or we’re too “burdened” by our lives. That, if you ask me, is an even greater burden.

So, go ahead and ask! The worst possible thing we could say to you is “no.” 😉

You might even find that we have a lot to offer and give to others. 

 

 

3. Don’t tell us about every medical study you’ve read about pertaining to spina bifida! 

No, seriously. We don’t want to hear it. Especially if it involves the prevention of spina bifida, medical research is based on a lot of different variables, and while your intentions may be noble, mentioning something like this can sound like you’re trying to “fix us.” Most people with spina bifida go through countless surgeries and hospitalizations, and often have different therapies to learn to maximize their potential, physically. Many times, if there is a procedure we can benefit from, chances are it’s already making the rounds in online support forums for families with spina bifida!

 

 

4. Don’t tell us God will heal us, or that there’s a reason we have spina bifida. 

I’m a deeply religious and spiritual person, and I have my firm beliefs. I personally do believe things happen for a reason, but if you’re saying this to me after I tell you about spina bifida, you’ll come off like a total jerk. Does that mean God chose for me to deal with spina bifida? Maybe. Then again, there are a lot of great things in my life that have come from having spina bifida, and also, a lot of great things that don’t have absolutely anything to do with that.

Still, never put us on pedestals because of having spina bifida. That’s just…creepy. 

 

 

5. We’re not sheltered. You can talk to us about…anything. 

I don’t know where this crazy misconception was born that people with spina bifida aren’t exposed to certain things– like sex, alcohol, rock n’ roll, the rise and fall of Communism, and Miley’s infamous twerkfest. 

We’re human. We read the tabloids from time to time, usually in the bathroom, just like you do. 

And we also like to party. Hey, you can’t expect us to sit around and watch C-SPAN all day, right? (Fun as it sounds.) 

What’s more, many of us have graduated high school, or even college or grad school. We like to talk. And I love Google and Wikipedia! So, even if I don’t understand what you’re talking about, give me about 30 seconds with my phone to impress you. 😉

Oh, and we also have brag-worthy lives filled with riches and diamonds and yachts and filthy-rich-jetsetting, so make sure not to hog the entire conversation. 😉

 

 

Hopefully that sheds a little light on some basic things you can do to keep someone with spina bifida in your life. (Yes, we grow tired of being overlooked, just like you would!) The most important thing to remember is that our lives don’t revolve around having spina bifida. There are so many facets of our lives, and many of them are similar to yours. 

Also, like you, we hate twerking.

Happy Giving Tuesday!  

–Laurita ♥

Parent & Down Syndrome Activist Eliana Tardio Shines Brightly

Sure, many people are skeptical about “love at first sight,” but have you ever thought of the validity of “friendship at first sight“? I’m not sure if it exists, but if it does, my relationship with Eliana Tardío of ElianaTardio.com is a classic example. Like many people I have met in the last few years, she and I didn’t meet conventionally; rather, we met online and our friendship blossomed.

Eliana and I are both blogueras, Latina bloggers with a cause, a mission, a purpose. While  neither of us can fully understand what life is like for the other, we come pretty darn close. While I have spina bifida, Eliana has two children (not one, but two), and both were born with Down Syndrome.

 

Above photo courtesy of ElianaTardio.com

 

If there’s anyone who I imagine doing more to remove the stigma from life with a disability, it’s Eliana. Whether it’s relating a funny story about her children’s wittiness, or posting a beautiful photo on Facebook for all to see of a tender moment between the two siblings, Eliana is constantly showing the world that her life while raising two kids with Down Syndrome, while at times challenging, is wonderful. 

Her compelling words of love, hope, true beauty, wisdom, and universal compassion challenge her readers to view “disability” in a different way– a positive way.

While I am becoming more and more honest with my own readers, I’m a lifelong cynic when it comes to “letting people in.” But with Eliana, I can’t help but always have my guard down, because to me, she reminds me of my own Mami– beautiful, compassionate, and funny, and fiercely devoted to the well-being of her children.

An incredibly gifted and bilingual writer, Eliana is a contributor for various online publications and Web sites, including BabbleMamiverse, Voxxi, About.com and Blogs de Mamás. She has also worked for the Early Steps program, and for Healthy Start Southwest Florida as an Educational Outreach Liaison.

Lisa and I admiring Eliana's passion and conviction as she speaks during the Blogging for a Cause panel at Hispanicize 2012.

 

As is hopefully the case with most unsung heroes, her community has indeed taken notice of her work. Eliana has been interviewed for several news publications, TV news outlets, and blogs, such as Mamás Latinas, Al Rojo Vivo con María Celeste, Univision’s Viva la Familia, and for Telemundo’s Madres Triunfadoras, to name just a few accolades. And this past May, I was honored to stand alongside her and our mutual friend, Lisa Quiñones-Fontánez of AutismWonderland.com, as together, we spoke up during the White House briefing that was the highlight of LATISM’s Top Blogueras Retreat. It was truly one of the most inspiring moments of my life! This was one of just a few times we’ve met in person, but when I do see her in person, it’s like picking up right where I left off…like meeting with a sister!

 

Eliana speaking passionately about special education at the White House, while Lisa and I (again!) look on in amazement!

 

For these and many other reasons, I have chosen to nominate Eliana for the Yahoo! Women Who Shine campaign. I can’t imagine a better nominee for this campaign, and I was so honored and humbled when she accepted my nomination.

The Yahoo! Women Who Shine campaign aims to “celebrate the women out there who are blazing new trails, touching lives or are just being amazing every single day.” That sounds exactly like Eliana to me, so please be sure to vote for her, and she might have the chance to win $10,000 to help kids like her beloved Emir and Ayelén continue to shine on. Please vote for Eliana here! 

To find out more about Yahoo! Women Who Shine, please visit this link.

Please “like” the Yahoo! Shine Facebook page here to stay up-to-date with great content.

 

 

Also, don’t forget to Tweet using the #womenwhoshine hashtag and visit the site to nominate other fabulous women who rock!

 

Disclosure:  I was compensated for this blog post while participating in the SocialMoms blogging program. The opinions and ideas expressed here are my own. To read more posts on this topic, click here.

Blogging, Speaking, Walking & Rolling: An Update for Good

This year, I feel I’ve especially committed myself to doing whatever God has in store for me. If it’s not meant to be, it’s because He has better plans for me than I could have made for myself. 

As it turns out, the purposes of those plans often overlap with each other– creating just a little confusion in my life! But I need not be too stressed about it– it’s all for good. :) 

So here’s the lowdown on what I’ll be up to in the coming weeks and months: 

  • In just 10 days, I’ll be speaking at CFLBlogCon, formerly known as the Central Florida Blogger Conference, on the topic of “Blogging for a Cause.” (I know, right up my alley, isn’t it?) I’m very excited to be invited to speak at a conference that was founded last year. The very talented organizing team is doing a fabulous job of bringing together bloggers, entrepreneurs, and social media diehards from all walks of life to present a diverse, educational, and entertaining program throughout the day. Check out the Official CFLBlogCon guide for more details!
  • The CFLBlogCon team is also debuting its Blogging for Good program this year, and it aims to raise awareness and funds for some great organizations, among them the Spina Bifida Association of Central Florida, and the Valencia Foundation. While almost everyone already knows why I support the first organization, you might be wondering about the second one. Well, I’m a graduate of Valencia College, and while I completed my Bachelor’s degree at the University of Central Florida, Valencia will always hold a special place in my heart as my first college alma mater. The foundation is committed to improving education for all students, and they have often given me a platform to promote my cause. Of course, I would encourage you all to support the SBACFL through this program, as well. Please visit this link to find out how you can make a difference for good.
  • My goal is to continue the work I began last year as a Team Captain for the Central Florida Walk-N-Roll for Spina Bifida. So, I need your help. Can we exceed our goals from last year and raise the bar? Team Holdin’ Out for a Hero is at it again, and we need more members, and more fundraising. We need all team members to be actively seeking out donations. That being said, any way you can promote it would be awesome. 

  • While I can’t share all the details with you yet, I know I’ll be speaking on a panel at the LATISM ’12 conference in Houston in October!! Yay. I can’t tell you all how excited I am, but because I’ll be in Houston– dun dun dun— I’ll unfortunately be missing out on attending the Walk-N-Roll in person! :( So that’s why I’ll need extra support from you all to make my dream of raising even more funds a reality. We can do this. I do know I’ll be speaking on a health-related panel, so I will definitely be plugging The Cause. :)

So that’s life on the cause front for now. Stay tuned for even more updates. Thanks again to all of you who posted comments, supportive Tweets and wall posts on Facebook in celebration of our 3-year anniversary. Rest assured I read and appreciated them all so much!!

 

Love,

Laurita ♥