Special Teams Chat – April 30 with guest author, advocate @AutismMomExpert
It’s hard to find a reason not to participate in the March of Dimes’ March for Babies. The event is all about working to help give babies a more welcome entry into the world – what could be a more noble cause than that???
As a walker, it’s good for your health. As a sponsor, it’s tax deductible. And if those are not reasons enough – how about a shot at seeing @aspiringmama’s infamous Mexi-fro on display?
Earlier today I was happily tweeting away about Metallica when things took a sharp right turn into a parallel dimension. The result? My muse and one other, that of Wendy (a.k.a Sparrowbug), are locked into a cage match. Two muses enter … one leaves …
The challenge? Post around 500 words of our current works in progress (WIP) written within the last week.
Wendy’s entry – a YA that might end up being horror – can be found here.
(…. and as a last minute challenge, Pauline a.k.a. @aspiringmama is going to enter the fray ….)
My WIP is a narrative nonfiction survival guide for parents, caregivers and supporters of ill or special needs kids currently titled Born into Battle: Surviving and Thriving Amidst a Child’s Complex Medical Situation.
SpecialTeams chat – March 26, 2010 featuring @kadiera
|Twitter chat transcript with guest @BarbDittrich talking about her #specialteams and Snappin Ministries|
The Special Teams community is congregated over at our new Ning community!!!
It’s a judgement-free space for parents, caregivers, advocates and supporters of ill or special needs children to gather, share and learn from each other’s journeys. Find us here:
Please come visit, join and post any material you think is relevant!
I’ve kept the Special Teams page here on my personal blog for reference – and because I will still be blogging occasionally about related issues.
One of the most wonderful things about social media tools like Twitter and Facebook is the ability to locate and connect with people who care about the same issues as you do – and try to do something about them.
The Twitterverse is loaded with great individuals and groups hoping to raise awareness and campaign on everything from human trafficking to health care, from sports teams draft choices to saving favorite television shows.
(Yes, #heroes fans, I’m getting there!!!)
Here’s just a sampling of my evergreen favorites:
- Women’s issues/rights: @safeworld4women, @thewip, @GlobalFundWomen and @Womens_eNews are just a few of the tweeters out there raising awareness on women’s issues
- Rare Disease: @GlobalGenes and @rarediseaseday are among those raising awareness about #raredisease and what families face in battling rare, debilitating conditions
- Autism Spectrum: @autismtoday and @AutismMomExpert are among hundreds campaigning for #autism awareness and acceptance
- HumanTrafficking: @27millionslaves and @TrafficInPeople are among those campaigning to end #humantrafficking
- Human Rights: @witnessorg , @EnoughProject, @AmnestyUK and @jonhutsun
Most mothers will do anything to protect their child’s best interests and help them succeed. It’s part of being a mom – a reflection of that overwhelming, all-encompassing love that we feel for our tiny mini-mes.
So I guess it’s hardly a surprise that battalions of mothers (and fathers!) out there have joined together to support the campaign effort to raise awareness about Rare Disease Day, February 28. The slogan for this year’s campaign is “Hope – It’s in your genes.”
These parents are simultaneously just moms and dads like any of us, and amazing individuals willing to step forward and try to make a difference. They, and the campaign, deserve our support.
For years I’ve told the stories of men, women and children struggling to survive amidst conflict, poverty, human right abuses and a wide array of life’s challenges. Every single one of them had a story to tell that contributes to the diverse tapestry of the global family.
And now it’s my turn.
At a time when globalization and the Internet have connected people across the world in more ways than ever possible before, it’s profoundly disconcerting to feel completely alone. And yet, as my family battled to not only survive – but thrive – though my son’s special needs reality that is exactly how I felt.
Most friends, family and colleagues simply could not understand, no matter how much they loved us. When it came time to put in a feeding tube or make the difficult decisions concerning our son’s health, we were inexorably alone. And scared. And angry. And overwhelmed by the amazing love we felt for our son.