{"id":67925,"date":"2015-07-26T12:00:22","date_gmt":"2015-07-26T16:00:22","guid":{"rendered":"\/news\/?p=67925"},"modified":"2015-07-27T10:03:05","modified_gmt":"2015-07-27T14:03:05","slug":"tiny-super-hero-squad-superhero-capes-help-kids-battling-illness-disabilities","status":"publish","type":"post","link":"https:\/\/archive.liveaction.org\/news\/tiny-super-hero-squad-superhero-capes-help-kids-battling-illness-disabilities\/","title":{"rendered":"TinySuperhero Squad: Superhero capes help kids battling illness and disabilities"},"content":{"rendered":"
<\/div>
\"Anthony

Anthony in his cape.<\/p><\/div>\n

It started as a hobby. Robyn Rosenberger was working a full-time job in corporate America when she made her first super hero cape for her nephew\u2019s birthday. Then she made a couple more, one for her son and one for his dog. When she began selling the capes on Etsy, she had no idea what the future looked like for her newly discovered talent.<\/p>\n

<\/p>\n

But Rosenberger had stumbled upon a blog called Blessed by Brenna, <\/a>about a little girl who was born with a severe skin disorder, and this would change everything. Enamored by Brenna\u2019s strength and determination, Rosenberger decided that Brenna needed a cape of her own.<\/p>\n

This seemingly small moment and act of generosity was the beginning of TinySuperheroes<\/a>. Rosenberger calls it a tiny cape company with a super big mission. That mission is to empower kids as they battle illness and disabilities.<\/p>\n

The plan is simple: every time someone orders a cape, a second cape is donated to a child with special health needs.<\/p>\n

\"_DSC0366_edited-2\"<\/p>\n

The idea took off and after six months of late nights and early mornings, Rosenberger left her job at a software company to focus on TinySuperheroes.<\/p>\n

\u201cI either needed to stop sending capes or figure out a way to make capes my living,\u201d she said. \u201cIt was the biggest leap of faith I\u2019ve ever taken. Fortunately I have a very supportive husband and we just sort of went for it. I believe that if you\u2019re doing the right thing, that things would work out.\u201d<\/p>\n

Things definitely seem to be working out. Since January 2013, Rosenberger has sent out over 6,000 capes. Families visit the company website to either order a cape, nominate a child to receive a cape, or sponsor a child who is on the waiting list for a cape.<\/p>\n

But it\u2019s when the child receives the cape that the real fun begins.<\/p>\n

\u201cI consider it the beginning of the relationship,\u201d said Rosenberger. \u201cOnce they have their cape they are officially in the TinySuperhero Squad. We offer free \u2018missions\u2019 and families keep us up to date on appointments and surgeries on our Facebook page.\u201d<\/p>\n

\"5.26.2013

Super Finn Cunningham.<\/p><\/div>\n

Over the course of the two years that Rosenberger has been creating capes, she\u2019s had the pleasure of learning about different children and the battles they face. Originally, her intention was to bring a smile to a child\u2019s face, but she saw the families were really clinging to the message that comes with the capes: that you\u2019re strong and courageous and brave.<\/p>\n

\u201cThere\u2019s something special about wearing a cape,\u201d said Rosenberger. \u201cYou feel empowered. And that message really translates when I send these capes. For a lot of the families, the capes put an identity to the journey that they\u2019re on and it validates what they\u2019ve overcome. These kids have defied death and the odds and done things that they shouldn\u2019t have been able to do. So when someone from the outside can say, \u2018We see it too\u2019, it just kind of validates that they have done amazing things.\u201d<\/p>\n

So many children have touched Rosenberger\u2019s life including Remedy who went through nine months of chemo and radiation after about a dozen tumors were found on her spine. She lost her ability to walk, but all of her tumors are gone. Nine-month-old Blake is waiting for a kidney transplant, and his cape hangs from his crib in the Neonatal Intensive Care Unit.<\/p>\n

But there is one child whose story changed how Rosenberger viewed her company and her mission.<\/p>\n

\u201cVery early on in this journey, first three months, I never knew what I was walking into,\u201d she said. \u201cI didn\u2019t know what it was like to have a child with a disability. I received an email from a dad that his son had received his cape and had died shortly after and they buried him in his cape. It was a fun hobby that made people feel good, but then I realized there was this need in these families for support. This is the simplest thing ever that I could do. And if I could impact one family in this way, than how can I stop?\u201d<\/p>\n

The company has become family affair as Rosenberger, husband Joe and their boys Rory, age three, and Milo, age one, recently relocated to be closer to family. Rory loves his cape and when Milo goes to physical therapy appointments, he bring capes to give to the other children. Rosenberger says that TinySuperheroes has turned her into a better mother because now her children have the opportunity to not see children with illnesses or disabilities as different.<\/p>\n

\"20150416freshart0050<\/p>\n

Her big vision for the company is to help change the way people think of illness and disability in babies and children.<\/p>\n

\u201cThree years ago if I was walking down the street and saw a girl in a wheelchair I would have found myself not really knowing what to do,\u201d said Rosenberger. \u201cWe don\u2019t want to offend anybody, so we end up not looking at them and not talking to them. And what happens when there\u2019s a superhero cape on the wheelchair is it breaks that barrier and helps start a conversation. We\u2019re walking around trying to be kind and we\u2019re offending people. Superhero capes break walls. We can see kids’ super powers instead of their differences. That\u2019s what pushes me forward. [\u2026] I\u2019m so lucky to have even had the opportunity.\u201d<\/p>\n

All too often, a prenatal diagnosis leads to abortion, since living with a disability is often viewed as too difficult and stressful. Little value is placed on the lives of babies who are seen as different. Instead of using that diagosis to learn about the child’s condition and find the best course of action to provide them with the most normal life possible, parents are often pressured to terminate and try again.<\/p>\n

TinySuperheroes shows that all children are the same and they all want the same things – love, understanding, kindness, life<\/em>, and a little bit of fun.<\/p>\n","protected":false},"excerpt":{"rendered":"

It started as a hobby. Robyn Rosenberger was working a full-time job in corporate America when she made her first super hero cape for her nephew\u2019s birthday. Then she made a couple more, one for her son and one for his dog. When she began selling the capes on Etsy, she had no idea what […]<\/p>\n","protected":false},"author":62,"featured_media":67931,"comment_status":"open","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"om_disable_all_campaigns":false},"categories":[4],"tags":[4389,4351,4350],"yoast_head":"\nTinySuperhero Squad: Superhero capes help kids battling illness and disabilities - Live Action News<\/title>\n<meta name=\"description\" content=\"When Robyn Rosenberger began selling the capes on Etsy, she had no idea what the future looked like for her newly discovered talent.\" \/>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/archive.liveaction.org\/news\/tiny-super-hero-squad-superhero-capes-help-kids-battling-illness-disabilities\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"TinySuperhero Squad: Superhero capes help kids battling illness and disabilities - 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