“I have Super Brexton, Super Adalynn, and Angel Wyatt. Thank you so much Robyn. This isn’t just about a cape, this is our second family. Sending hugs. Thank you all so so much!!! We love you guys!”
“Cooper got an awesome surprise in the mail today!!!! Thank you for the Super Cape! I can’t get it off him … He LOVES it!!”
“Everyone here is familiar with Naylah and they love how she always carries her cape with her. If that cape could talk she would have some story to tell, it has followed her through many procedures. Thank you again and I mean it to be part of such an amazing squad. I am so thankful to have found all of you.”
“I can’t thank you enough for Carly’s TinySuperhero cape. Her five-year-old brother saw it and said, “someone special sent this to sissy because it has the power to catch all the prayers people are sending to her!” You made a very difficult time in our lives a little bit easier. We can never thank you enough♡”
“We received the capes in the mail. They are amazing!! The packaging was so neat, I love how you included so much info. I was able to talk to my four-year-old daughter about the kids on the cards and it was a really nice moment. These capes will be very well-loved and treasured. I posted one picture on your Facebook page but here are a couple more. I can’t wait to get some others done!”
“Thank you TinySuperheroes!! Here is our sweet boy, Hudson, using his powers against his dialysis machine! He is on dialysis every single night for 9 hours. His feeding pump also runs overnight continuously for 9 hours to keep him from getting dehydrated. His cape hangs on his feeding pole at night to help give him the superpowers he needs to fight through dialysis. Thank you for this amazing organization that helps kids look and feel so awesome in their cape!”
“Thank you so much! I know I haven’t even seen the capes in person yet, but I need to tell you how powerful these capes are. I am so incredibly touched by the idea that there are amazing people like you (and your team) out there who are doing something so special for our kiddos.
This is my first child, and my first surgery of any kind (he’s having brain surgery) and I have to tell you that as small as it may seem to some people, having a cape for him means the world to my husband and me.
Sorry if this is all over the place. I just wanted to say how much I appreciate what you all are doing. I can’t wait to spread the word!
I appreciate you checking in on him. His cape has gone with us to each and every neurosurgery and neurology appointment and we always get comments on it. Thank you for providing such a comfort to my son during this crazy, scary time! We truly appreciate you and your team.”
“It was such a warming experience receiving your box in the mail. I completely forgot about applying for them to be on the recipient list for your beautiful capes. I saw a photo from a fellow mom of a beautiful boy on wheels I met at a local WCMX (wheelchair Motorcross) event that had your cape on and that’s how I found out about you! Then I read your story and what your about and it just totally made my day that you provide such a selfless act of kindness by bringing together donors and recipients like this!! It is just absolutely what we need more of in this world.”
“The boys actually checked the mail yesterday and opened the box. It was fine, they were super excited and Maddie didn’t think a thing about not getting one. Thank you for everything. Your company is amazing. The smile it put on Cooper’s face was priceless and then to have Olliver receive one as well (as he is usually overlooked since we have the other two with rare diseases). He was excited.”
“I just wanted to pass along what an awesome thing you are doing with Tiny Superheroes. I bought a cape for a friend’s child and here’s what she wrote to a group of us when she sent out this picture:
‘If you ever know a little one who is sick – go to TinySuperheroes! Aunt Courtney got him a cape and I have now gone on to get all of his heart buddies one as well. A great place to support!'”
“Julian has a rare complex called Sakoda Complex. His cape allows him to go tackle each day like the Super Boy he is. We got his cape on the day we went to Riley Children’s Hospital to (decanulate) take his Trach out. We believe it gave him the Super Strength to leave it out for 8 hrs!! He wears his cape all day and shares it with his stuffed Mickey too!! 🙂 Thank you for the cape he loves it and we appreciate the love, time, and energy you must put into these capes! You’re heroes in our books!”
“This cape symbolizes SO much for us. When I think of who my hero is, it’s this little boy right here. He’s only 3.5 and he has been through more than most adults I know.
He’s been poked, cast, braced, sedated, and tested more times than I can count. He’s transitioned onto and off of medications to control his seizures. He’s dealt with horrible side effects and “yucky” tasting medicines. He’s fallen down … a lot. He’s dealt with frustration from his right hand not working as well as his left. He’s had to repeat himself over and over so people can understand him. He’s worked so hard in therapy (Speech, OT and PT) for almost 3 years now. He’s gone to appointment after appointment and seen specialist after specialist. On top of all of that, he’s dealt with his seizures. The confusion, exhaustion, and everything else that happens after.
And even after all of that (and probably more that I’m forgetting), he is always smiling. He’s is one of the sweetest boys. He loves his sister and his Daddy. He adores his puppy and snuggles with him whenever he gets the chance. He never gives up. He is HILARIOUS and is always making people laugh.
There’s nothing better than the moment when a hero gets his cape “
“Alexa received her tiny superheroes cape in the mail the other day and it’s absolutely perfect! Thank you so much!!!! Alexa was diagnosed with stage 4 neuroblastoma in 2013 at the age of 15 months. She has been fighting for 4 long years with two relapses. She is currently in treatment and shows us every single day what an incredible superhero she is!”
“You have given my TinySuperhero so much confidence! He can’t wait to wear his cape to Children’s Specialized Hospital for his next therapy session! His little brother is ecstatic to have his own cape too! Thank you for putting a huge smile on my boys’ faces!!!”
“Thanks so much Robyn! She sure loves her cape to this day! It is proudly displayed in her room when she is not wearing it! Still so many ups and downs for her, but she often remarks, when she sees her cape, “There are lots of kids with lots of hard times. It’s cool we can all be together with our capes!” TinySuperheroes is so amazing!!!!!!!”
“This girl has had a really rough 10 days. When I picked her up at daycare today she was tired, in pain, and ready to go home and go to bed. She needed this today. Ever since we got the mail she has been a different kid. She is smiling. She has light back in her eyes. I will never be able to thank you for all that you do for these TinySuperheros. I am forever grateful!”
“Just wanted to send a gigantic thank you to you all for everything you do. My superhero lit up tonight when he opened his cape. This is Marky. He is 4 and has common variable immunodeficiency. It’s been a battle and we have struggled lately so this was perfect timing for some extra smiles. Thank you again.”
“I have to share how much confidence Super Nathanial has when he has his cape on! It’s shocked us at how his fears just fade. They come back, but even these breaks are wonderful for him!!! I cannot tell you how much it means to see my boy smile! Tears in my eyes as he flies around the house showing off his new found super powers. Thank you, thank you, thank you!!!!!!”
“We picked up the package at our town post office today. The postal worker was so excited to deliver this surprise addressed to Super William! I opened it right there in line, put his cape on…and wasn’t the only one there teary-eyed. SUPER WILLIAM VANDERWERKEN”
“Wow, I wish I could upload the video of me ugly crying while Dominic and I opened his cape. All the reasons why he is a TinySuperhero went flooding through my mind. The gratitude I feel for the sheer joy you brought him and the sentiment behind the is cape is indescribable and immeasurable. Thank you. This means so much. I hope to find out who donated for his cape. Whoever you are, thank you!”
“Our twins are getting so close to coming home from NICU. One will be home before the other, but we can’t wait. Naturally, I’ve been a little down lately…missing them and wishing they were here. When we got our capes a couple of days ago, it was a much needed pick me up. I have them hanging on their bassinets for when they can come home and wear them. This group has helped me so much. I don’t talk much, but seeing stories and what others are going through helps so much with staying positive and not getting discouraged. Thank you all so much for letting my little boys be part of your group and for sharing your lives with us. 🖤”
“Super Teddy’s cape came and it may just be the sweetest thing we’ve ever seen! Thank you so much for helping show the world how super our little man is!”
“Super Jonathan has to regularly give blood to be tested to make sure his flesh-eating bacteria isn’t trying to come back. He cries EVERY time. He cries when we turn down the hallway because he knows where we’re headed. He cries in the waiting room while I beg him not to scare the other kids. He cries when they take him back and I have to hold him down because he freaks out when they do it. It’s an exhausting experience. Today I put his TSH cape on and told him he wouldn’t be scared this time because he was a superhero. He didn’t cry once. Not even one tear. Thank you, Robyn and everyone at TinySuperheroes and our sponsors!!!”
“He got his cape and loves to race around the house in it! He was so excited to get his own mail. We read the trading cards included and he stated “You guys keep being super and get better!” Which of course was sweet but also opened up dialogue on how each of us is unique and different in our own ways. We are definitely looking into subscription boxes so he can earn badges and continue the conversations on the wonderful differences of all.”
“My daughter had an accident last June in which her lip needed to be reattached to her face. Without TinySuperheroes, I don’t know if we would have gotten through, and without her cape, my daughter would not be where she is today! She still struggles daily with PTSD among other things, but she is our little bit of sunshine! She has healed beautifully and while she still has surgeries in her future, she has come such a long way. Every little step has given us more and more hope that she will eventually be confident in how she looks and that she is gorgeous and beautiful no matter what! Thank you TinySuperheroes, not only for our daughter’s cape (which goes everywhere and is her bedtime blankie), but for the unbelievable support and amazing monthly missions that help her love who she is!”
“First, I would like to give you and your whole company a huge THANK YOU! This was a surprise for Dawson until he opened it up after getting the mail… He was happy to see he received a package, but when he opened his package and saw it was a superhero cape, he was so excited and had the biggest smile on his face. So, for that, our whole family would like to say Thank you.
Dawson asked me to send an email to tell everyone at the TinySuperhero company that he says THANK YOU, that he absolutely loves his cape and he can’t wait to earn some mission patches soon for his “awesome cape”!
Dawson recently had to go to Pittsburgh Children’s Hospital to have more testing done and he wore his cape with confidence and a big smile… He also showed off his cape to everyone too! I think it’s safe to say he really does love it so much and that’s all be you, TinySuperheros made it possible for him to know he’s a superhero himself
Our family greatly appreciates your company, THANK YOU ALL SO MUCH”
“Thank you so much for the cape for Gabe! Our entire week was made when we saw the package in our mailbox on Friday. Words cannot express our gratitude. The thoughtfulness behind the whole package brought us to tears. A special thanks to Elspeth and Eva for the handwritten notes. We have already placed them Gabe’s baby book.
Since the day Gabriel was born (and we found out about his Cleft Palate), he has impressed us with his strength. His cape will serve as a reminder of his Super Strength and will be with us when we travel for his surgery in early December. We have included pictures of Gabe with his cape. We think he looks even more handsome as a Super Hero!
We still bring Gabe’s cape with us to every hospital appointment. Gabe also loves to wear his cape for imaginative play as he slays dragons or flies around our house. The TinySuperhero community has been a wonderful connection to have. We thank you so so much! We try to tell everyone we can about your organization.”
“Charlie and Cooper were SO EXCITED to receive their superhero capes just like Crew’s. I don’t think Cooper has taken it off yet honestly. Thank you so much for always thinking of our Super Crew and his big Super brothers. You are the very best!! It made all of our hearts just as full too! I cannot tell you how excited they were to see their names on a package (and with “super” in front of it as well). We love them so much and will get started on our thank you notes as soon as possible.”
“Thank you so much for Renae’s cape. She loves it. She received this sticker in with it and is convinced it’s her lol. We received this cape on Sunday. Renae was supposed to have her second surgery that Friday but she ended up getting strep the day before and had to reschedule. So it’s amazing how everything worked because now she will have it with her. This will be her second surgery for Cranio. Her first one was only 9 months old so she doesn’t remember it. I’ve let her see her scrapbook I made for her and she can see and feel her scar/bumpy head. But now that she is 4 she is so scared when we take her to the hospital for her test and such. This will make her feel so special. Once again thank you so much for everything you do.”
“It’s amazing 😉 how special they make each kid feel! Koltin got his in the mail this morning and is in love! He even wore it to school to show it to his pre-K friends!”
“We got home late last night, and Jason found a package out front. Once we got the kids settled, we opened it up. Inside we found the most amazing package from Tiny Superheroes. The tears started right away because I felt so honored that you thought of my kiddos. Then I saw the cape for Christian, and my heart just melted. You have no idea how incredibly special this is for my kids. They haven’t seen the capes yet. I can’t wait to show them tonight. I will be sure to take pictures to share!
Thank you so much for your thoughtfulness. This is something we will treasure and remember forever. My kids are definitely my superheroes, and now they have the capes to prove it.”
“Such an amazing organization that goes above and beyond to empower all of our Tiny Superheroes to realize that each and every one of them has truly amazing and unique superpowers that can help them achieve their dreams.”
“Amazing company thank you for Super Saria’s cape.
Not all TinySuperheroes have physical superpowers. My little one may not look super, but she is and always will be super to our family. ”
“We can’t thank you enough, she has been fighting a virus for three weeks now and hasn’t been her happy, go-lucky self that much this week, so to see that smile made our day!! Can’t tell you all, thank you enough!”
“Thank you much for the tiny superhero cape! After being in the hospital last week and having to do a 24 blood pressure today it came at the perfect timing! Keanna was leaping around the house with it on! The best picture is her being a super hero by her dialysis machine her life line! I cannot thank you enough for the confidence the cape has brought her this afternoon!”
“Amazing program for *free* (to start the super process-when added to wishlist) and really gives kiddos the drive to stand up for themselves and others and to be confident in their own skin. My son has difficulty willingly going out to play with the large group of boys in the neighborhood until he wore his cape and became “super”! He no longer fears being different as those are his powers showing though!”
“Ready to take on genetics! Another huge thanks to TinySuperheroes for his cape. This is our first appointment since we got it and he’s a different boy. He flew all the way into the office and hasn’t cried once!”
“I recommend Tiny Superheros because it’s a place you can go and find other families dealing with similar situations, and no one judges you because of it. You can meet n make new friends. I also love the fact that you make it happen for the children with the great capes!”
“Yes! I highly recommend them! These are great people on a mission to help our tiny humans feel like big superheroes 🦸♂️❤️ my 5 month old just recently got his cape today! 🥰 he looks so adorable! All smiles. Thank you too everyone who made this possible for my little man.”
“I can’t explain how happy she was when she received it!!! She had no idea and she was even more excited that it was her favorite color. She loved all the encouraging words in the cape and especially loved that people helped her help others receive a cape. We are putting the items in her scrapbook. Thank you so much for everything!! You are angels🥰”
“My son Kamden just received his amazing cape this afternoon and I am just beyond blessed to have him thought of for this. It brought me to tears! He has been wearing it for hours! Thank you for putting a big smile on my sons face and letting him know he is a superhero!!”
“In Mason’s life, there will not always be special settings and people will not always understand his differences. I just want you to know that what you are doing just fills my heart with so much joy! Wondering about how Mason’s peers will view his differences throughout his life has been and will continue to be one of my biggest concerns- knowing that there are people out there like you helps me sleep at night. The message you are spreading about celebrating differences can apply in so many settings and to more than just the kiddos! LOL! I think my place of employment could even benefit greatly from being reminded of this!
Anyway, I just want to thank you again and let you know that we will be telling all of our family and friends about what you do. We look forward to helping with the fundraising and are so excited about Mason’s inclusion to the Squad!!”
“My daughter received her superhero cape two years ago. I was reminded while watching her video at how for that moment she wore it I felt empowered and not at a loss anymore. I knew how brave she was but the image of her in a superhero cape sealed it. Elsie has now a diagnosis for her epilepsy and she has found much better treatment. We’ve come a long way! We love what you do, thank you so much!”
“My little superhero got his cape today! Mail was delivered right before we left to go see family and he hasn’t taken it off since we left the house! Even sported in the convenient store! He loves the pink! Thank you SO MUCH!!!”
“Super Raylen was at the hospital this week, and this is the most action I’ve seen from him in a while since he wasn’t feeling well. It truly picked his spirit up. I can’t thank you enough. He’s 20 months old and non-verbal. We’ve had a very rough two months and the day it came in the mail happened to be the day we came home from the Ronald McDonald house. I could’ve cried.”
“Super Sammy has been wearing his cape EVERYWHERE! The compliments he’s gotten have made him feel so good, and it’s even opened up a conversation about Prune Belly Syndrome. Thank you so much, TinySuperheroes!”
“I’m an Occupational Therapist and recently, one of my clients, a feisty 2-year-old with Down Syndrome received a beautiful cape from you. I just absolutely LOVE everything you stand for, everything you do and everything you create. Can I come sew with you????!!!! I wish you only the best–thank you for what you do!”
“Super Grace had a cecostomy button placed in October. One of the ways we prepared her for surgery was to show her that Super Naylah has a button on her tummy. She told everyone that she was going to the hospital to get a button like Super Naylah! So nice that these TinySuperheroes can help each other!”
“Kai’s cape was a HUGE hit!! Thank you so much for your hard work and dedication- it literally made her day, brought a smile to her face, and encouraged her to come out of her room! A trifecta of perfection.”
“I have to share how much confidence Super Nathanial has when he has his cape on! It’s shocked us at how his fears just fade. They come back, but even these breaks are wonderful for him!!! I cannot tell you how much it means to see my boy smile! Tears in my eyes, as he flies around the house showing off his new, found superpowers. Thank you, thank you, thank you!!!!!!”
“Super Sammy has been wearing his cape EVERYWHERE! The compliments he’s gotten have made him feel so good, and it’s even opened up a conversation about Prune Belly Syndrome. Thank you so much, TinySuperheroes!”
“Delilah just opened her cape. She was so excited! She just said she feels so awesome right now. Thank you for all you do!”
“My daughter has been depressed lately and the cape lifted her up, she’s back to school and not every day is great, yesterday was hard for her but when she came in she put on her cape and it made her feel safe and joyful. Financially right now we are in a tough place but when we are able to I want to sponsor another cape for a child in the hope that it will lift them up the way it has done for my daughter. From the bottom of my heart and from my family as a whole, I thank you and please keep doing what you are doing. It really means so much.”
“Maxeen received her Tiny Superhero cape Wednesday, just in time to wear it to yet another procedure she was scheduled for on Thursday. She was crying because she was scared, she didn’t want “pokies” (needles). I reminded her she had her Cape to wear and her Mommie read all the words to her and reminded her she was a superhero! She will be wearing her Tiny Superhero Cape next month as they travel to San Francisco to a specialist she is being sent to there. Thank you so much for everything you do!! PS……Mommie wore a Cape too!”
“I just became aware of your organization today when I sponsored my Grandson, Gavin’s cape. I am so impressed with everything that I have read and have to admit, this old guy shed a tear or two when reading the stories on your website. While I have always thought Gavin was a superhero, I know he will feel special when he has the chance to wear his very own cape. Please know that I will do whatever I can to support you in your mission, it is that special and that important. Thank you so much for what you have done and what you will continue to do.”
“My son Avery’s cape couldn’t have come on a better day! He started serial casting on his feet on Monday and was able to come home to find his cape waiting in the mailbox. It definitely helped him feel empowered even through the pain he was experiencing. He’s a former 25 week, 1 lb 3-ounce baby who is now a cerebral palsy warrior. He starts kindergarten next week and can’t wait to tell all his friends about his superpowers!”
“My son Grayson received his cape today along with a few patches and he is beyond happy!! Here’s my sweet boy, he turns 3 next week! He is happy all the time, fearless, knows how to light up a room, and whatever the obstacles he faces he never lets his disability stop him. #opticnervehypoplasia. “
“Thank You SO much! I love this program, I’m doing the best I can and I have so much on my plate that I sometimes forget to make time for the little special moments that become cherished childhood memories. We appreciate you and all that you do, not just for my son but all of the kids whose lives are just a little bit harder.”
“Robyn donated 34 TinySuperheroes capes for the Lydia Cox Memorial Bike Camp this year. Her generosity made year 9, the best year. To see our new independent bike riders with TinySuperhero capes blowing in the wind was priceless. The capes boosted every child confidence in their ability and helped to give them the courage they needed to get back up if they fell. Thank you TinySuperheroes!”
“This is a great organization! My son has been able to battle a lot of obstacles being brave with his cape on! His sidekick brother also got one as well! We got both of them super fast! Thank you for all you do!!”
“Robyn and her team make magical moments happen every day. The love and support that does into creating each Cape transforms these kiddos from the heros they already are to SUPERHEROS!! Never underestimate the power of a cape.”
“My grandson Mason received his Superhero cape today. He was oh so excited when he saw what it was. He put it on and started Running around, saying he was Superman and he can fly 😁. We actually raised enough money from Mason’s Campaign, that there was enough money to make capes for 14 more deserving Superhero’s. I am so thankful for all my friends and family and all who have been on Mason’s Journey for the past few years. Our family is Blessed.”
“My grandson Mason received his Superhero cape today. He was oh so excited when he saw what it was. He put it on and started Running around, saying he was Superman and he can fly 😁. We raised enough money from Mason’s Campaign that there was enough money to make capes for 14 more deserving Superhero’s. I am so thankful for all my friends and family and all who have been on Mason’s Journey. Our family is Blessed.”
“Words will not express how wonderful it is to be a part of this phenomenal group. This is a beautiful thing you are doing here, and it sincerely touches lives. For those who didn’t quite understand our littles before, this helps knock off some of that “unknown” and makes them just a part of something amazing! ❤️”
“TinySuperheroes is so empowering! A place where superheroes of all abilities can come together and unite and support one another. What is most fantastic is the online community built here that brings families with similar diagnoses and has one another for the support!”
“This is an awesome program. It not only gives children that are a bit different a different look at their physical situation. They are superheroes with superpowers when they wear their cape. On the other side of this, it helps fight the stigma that says that it is scary because we are different. With a cape, scary turns into superpowers. When people see our superhero cape-wearing child, they see a child that needs super strength to take a step or even eat regular food, things they take for granted. It changes the outlook of the way children are viewed when they look different or use a gait trainer, AFOs, wheelchair, etc.”
“Super Slade got her first mission finished!!! Thank you TinySuperheroes for giving my Super Hero even more bravery and confidence!!!”
“I did not get a picture of Super Hudson with his new patch yet because I need a new iron, but I wanted to thank you for sending the spina bifida patch. Hudson was so excited to get mail and most excited to read Super Evie’s card because Hudson also has deformities of his feet and had to have surgery when he was 4 for a tethered spinal cord. We didn’t know anyone else besides his older sister who has a tethered cord! It was so awesome for him to see that there are other kids just like him! Thanks again!”
“The love & support from other families is amazing & we have made so many friends & love the missions more than anything. It gives us something more to look forward to each month!”
“I love TSHs. In real life, we don’t belong anywhere. Even online, my daughter is considered severe in most special needs groups. But here, even though she is more severe than many, I still feel like we have a place.
The missions have opened up a whole new world for us. We are doing activities together. No matter what the mission, I can find a way to include her. Crafting? She can fingerpaint, which is a great sensory activity. And there are always choices to make, so she can practice her yes/no switches or sign language yes/no. We’ve worked on missions with her big sister. They are 16 years apart, so doing missions together is a wonderful connecting experience. And we take so many photos of the memories we are creating. And then we get a tangible memento to hold onto forever when we receive her patch.
Every month, we can’t wait for the new mission, and when that patch comes in, we affix it to her cape ASAP. That cape really means something to us because of all of the reasons I mentioned. It goes everywhere with us.”
“The whole staff at Texas Children’s loves and compliments Super Brayleigh’s cape as well as every other doctor she sees. She is known for wearing her cape at all of her appointments.
We will also be taking some more from our Hope mission with us as well. On our follow up 2 months back we saw that the receptionist had at each desk when we left around the hospital. I mentioned we left those our last visit and they asked us if we could bring some more because the kids read and want to take it but they keep them at the receptionist for a word of encouragement. So that’s what we have planned the next few days before our trip. I really wanted to do the Rocks but haven’t had a chance to make it down to the craft store. Thank you for all that you do for our TinySuperheroes.”
“MacKenna became her cousin Super Enzo’s sidekick on 3/4/19. She loves the missions and her cape! It’s a wonderful program for children to get to know one another and know that everyone is not the same!”
“My older kids love being sidekicks and helping our Super April do her missions. Everyone has been welcoming and we just love all our TSH”
“This. Is. Beautiful. When we started talking about growth mindset this month, I wondered if Trenton would get it. It’s a little bit more of an abstract concept then past missions. I thought it was an awesome one for him. And could think of several things he could use a growth mindset for in our daily lives.
But wanted him to try and think of something. We talked about the mission, and a few hours later, he was lying in the living room and said mom I really need to have a growth mindset about the rope swing and giant slide. I was lost for a minute. He said from camp this summer. I didn’t even try them. Cause I was scared. But I’ve gotten a lot of superpowers since then 😁. It was so out of left field to me because it was something from months ago I didn’t even know he had thought about since then.
But perfect timing. Back at camp for a retreat this weekend. We got here last night, and he had a meltdown about going to make his bed. He wanted to go do his stuff NOW lol! So with no fear or reservation whatsoever, my 5 yr old contoured things he was afraid of and thought he couldn’t do…….Because of this group and what it does for him and his confidence and what he’s learned. Thanks, TinySuperheroes, Robyn Rosenberger, and crew. ❤️
Also, I’ve really applied the growth mindset to myself this month about being a mom and feeling completely incapable sometimes. So you are not just helping TinySuperheroes. You’re supporting a whole army of super moms. 😘🥰”
“Thank you for including Knox in these challenges! They ask every day if there is anything in the mail! They are so excited when they come in the mail and want to do it immediately! Knox chose to give one to his brother because he always listens to him and to our friend Seve who just found out he has Leukemia and is fighting to be cancer free! He chose him because he said he is brave! Thank you for your kindness always!!!”
“This is a great organization that helps empower our children who have extra struggles in their lives. They have fun missions for our children every month, which gives them something positive to look forward to amidst the stress of appointments and therapies.”
“We couldn’t have been luckier to become apart of a squad that is THIS incredible. Everything you stand for and everything you do is remarkable. We received our package and when I opened it with Hudson I bawled! It means so much to us and so much to him that you thought of us and sent him this. We loved reading every card, and we loved the drawing as well. We LOVE EVERYTHING. We would love to continue to do what we can to help others as well; if there is anything we can do on top of the missions please let us know! Thanks so much again I wish I could tell ya 100 times over!”
“Our daughters diagnosis is new and not 100 percent complete…. doing these missions has kept my mind off or if while keeping my mind on it at the same time. Tiny superheroes have helped me through this all and have given me something to look forward to every single month and be able to spread awareness about my daughter and her epilepsy. It has also helped us see who of our friends and family we can lean on for support and how willing they are to learn what we have ro teach them! We really appreciate everything you do for special kids including our little Rory!”
“This program breathed hope back onto our family and brought a sense of togetherness and community where there was once fear and isolation. We’re so grateful for that! We LOVE doing the monthly esteem building missions & the patch program, its fun for our whole family! I highly recommend joining the group & nominating kiddos. It’s an awesome program with amazing people running it!.”
“They give kids inspiration to succeed with different missions to accomplish goals and to be the best superhero they can be.”
“It is with great sadness that I tell you our sweet Beckett Hope passed away on November 9th. We had her celebration service on November 15th, and of course, her cape was with her. Beckett loved completing her missions every month. Thank you so much for allowing us to be involved in this special group. Our Beckett Hope was truly a tiny superhero.❤”
“I have it. I have been avoiding texting because every time I start I start to cry. You will never even know how much this means to me. There is no way to adequately say it. There just isn’t. So all I can manage is to say thank you so very much. We are going to have this at the funeral so that people learn about this organization and the incredible people in the world that have supported Sam. Thank you.”
“My son Iza (age 8) includes his cape in everything. He is a big brother to Baby Tre, a TinySuperhero in Heaven. Although he received his cape 2 years ago he still loves it sooo much.”
“We did a drive-by visitation today and had some of Hollis’ favorite toys out there. His beads of courage nd his super hero cape. It was just beautiful!”
“I had nominated Justice Bryant, and after just nominating him, he became very ill again. You rushed him his cape and also made a cape for his twin sister. I am so grateful for all that you did to get them their capes. I’m writing that Justice has passed away. Thank you so very much for his hero cape because this little five-year-old was a true hero. Thank you.”
“I am speechless. I had no idea I was even receiving a cape for her. Keeley Shianne, her 5 short weeks here were not enough to me, but I feel so blessed to have been able to have had those 5 weeks at all. Due to severe preeclampsia, she was born 15 weeks early, at 1 lb even & 11 3/4 inches long. Her growth was restricted, and she was the size of a 22 weeker because my body was depriving her of fluid and what she needed. Her c section was peaceful. I was awake through hers, unlike with her brother, where I had a placenta rupture and had an emergency c section and was put under. So I cherish her peaceful birth. We listened to music as they carefully removed her tiny body from my shaking body. I remember shaking a lot, feeling as if I was freezing from the inside out. She was born alive and breathing on her own, unlike her brother. Her cries sounded almost like a tiny kitten crying out. She was the most beautiful, strong, and fragile thing I had ever laid my eyes on. She was tiny, but she was mighty! She fought off a couple of infections. Went on the vent, off it, then back on it. Then a blood clot. Then mrsa in her lungs. Then it was just much for her little body to take. She fought. Lord, I never seen anything fight like that tiny girl fought. I am beyond proud to be able to say I’m her mommy. I know she watches over her little brother. His birth was a couple of weeks later in gestation than hers, but started a little rougher than hers, & I know she is why he’s here today. For he has a tiny angel on his side. Who before she was an angel, just so happened to be a superhero. Thank you so much for her cape, I can’t wait to put it on her bear and have a picture taken of it at Disney World with her TinySuperhero rainbow baby little brother. I can not express how grateful I am.
“We finally received our sweet boy’s Angel Cape, and we couldn’t be more grateful! Unfortunately, we learned of TSH after his passing, so we never got to see him in his cape, but it is perfect!”
“I just wanted to say THANK YOU for the amazing gift for my sweet angels “angelversary.” It was totally unexpected, and absolutely made my day. It’s always hard around that time, and that package changed my mood completely. We recently moved, and it still found it’s way to me! I am so grateful for all that you do for these kiddos and families. THANK YOU, THANK YOU, THANK YOU, from the bottom of my heart!!!!”