Take a look at these photos.
Our sweet little wish recipient Bryson just received the IPAD we sent him. When you donate to BK, you are helping to improve and enrich the lives of struggling children. The beauty of our organization is that you actually get to SEE where your donating dollars go. Bryson appreciates YOU!
Bryson was born in October 10, 2013 with congenital hydrocephalus. Since that time, this little guy has battled. He’s in the hospital as we speak and we ask for prayers for Bryson. Meantime, we wanted to grant a wish for cutie pie.
Bryson’s IPad recently broke and we are replacing it. For children like Bryson, with frequent doctor visits and hospital stays, an IPad helps to occupy him. They are a priceless tool for special needs kids.
To follow Bryson’s journey click here:
BIRTHDAY WISH GRANTED FOR LITTLE BOY WITH GENETIC DISIRDER SO RARE HE IS ONE OF LESS THAN 60 IN THE WORLD. MEET JUDE
We have been following Jude’s page for a while. This adorable little guy just celebrated a birthday and we needed to gift him an awesome birthday present. His grandma advised that Jude’s mommy had been wishing for a Keentz 7s multi seat stroller. This special stroller would allow Jude to enjoy nature during long strolls. We were honored to grant that wish today.
~A little about Jude~
Jude Sullivan Peters has a very rare genetic disorder called Rhizomelic Chondrodysplasia Punctata (RCDP for short). He is one of less than 60 in the world. His chances for survival at birth were slim to none. His parents, Sully & Hannah Peters, have fought so hard for their baby boy, whom we affectionately call the “Brave Little Warrior.” He sees dozens of specialists, as well as occupational, physical, and speech therapists; he is defying odds every single day. Sully and Hannah travel to Delaware every few months for him to see his main medical team at Alfred I. duPont Hospital. His story is one of hope and faith in adversity. It has brought light and love to thousands of people all over the world! His facebook page is:
When a child dreads unavoidable surgeries, hospital stays and long car rides to/from the hospital, who do you call? BIANCA'S KIDS! Meet Teaghan.
Here's the wish we received via our website:
Dear Bianca's Kids,
Teaghan has a right ear cholesteatoma which we discovered during a tube placement in August of 2016, even though it is not classified as a tumor, it is just as destructive with a high re growth rate, Teaghan just completed her 4th surgery and the cholesteatoma was back, she has had to have her ossicles, ear drum, cochlea, tasting nerves removed, some bone removed, and have several skin grafts with ear canal widening surgery, she has also lost her hearing. The hospital she attends for these surgeries and follow ups is a 3 hour drive for us, she is extremely bored in the car and dreads the ride and hospital stays, she has been requesting a ipad however with 7 other children I just cannot afford one. Her dream would be met by having one and make her surgeries and car rides go by quicker.
Lindsay, I am happy to report that Teaghan's wish for an Ipad came true today. We are confident that it will serve as a great distraction and also a great learning tool. It's been ordered and will be to your door by April 11th. Enjoy!
WISH GRANTED - LITTLE GIRL WITH DOWN SYNDROME GETS ONE YEAR OF GYMNASTICS CLASSES PAID BY BIANCA’S KIDS!
Dear Bianca’s Kids,
I was searching for grants to help my little Amelia with her gymnastics classes that I unfortunately cannot afford and could not find any foundation that would be willing to provide this kind of assistance. When I was reading about Bianca from the website history, I though it is wonderful that Bianca had a passion for bringing joy to children because kids with disabilities need it very much.
We are a family of three: Amelia, my son, and myself. In August 2008, my husband brought us here from Belarus, a little country in Eastern Europe. When Amelia was born in 2011, and we found out that she has Down's Syndrome, it split our family.
I would like Amelia to live a full life and try new things, especially things that she enjoys like music and gymnastics. Aim High Academy has Stars of the Future (Special needs class), but SoonerCare (Amelia's medical insurance) will not cover classes like dancing or gymnastics. Even though I spent countless hours on the phone with them, trying to explain that she will learn by watching and copying other students in class, and it is much more important than one on one physical therapy. I strongly believe gymnastics will help her with balance and coordination, strengthen her muscles and build up her immune system, but also she will acquire social skills that will help her find a way in this life and become somebody.
Please, consider helping my little Amelia!
Katerina, I am so happy to advise that we are granting your wish for Amelia! We are paying for one year of classes, the registration fee and for Amelia’s leotard. We know this is going to be great for her!
WISH GRANTED FOR LITTLE BOY WHOSE MUSCLES TURN TO BONE. THIS HANDSOME FELLA IS A HUGE EAGLES FAN. WE’RE TAKING HIM TO MEET THE SUPER BOWL CHAMPS!!! MEET AJ GONZALES
We received the following wish vis our website from Heidi Salerno:
My wish is for AJ Gonzales to get a chance to meet his favorite football team! The EAGLES! AJ is battling FOP ( aka “stone mans disease-where his muscles turn to bone. An excruciatingly painful disease). AJ is a funny, strong, courageous little guy who despite his battle always manages to have a smile on his face!!! I can’t think of a more deserving child than AJ!!!!
Heidi, thank you for bringing AJ to our attention. We are so happy to grant your wish.
WISH GRANTED FOR BABY GIRL BORN ADDICTED TO DRUGS. WE GIFTED HER EVERYTHING SHE COULD POSSIBLY NEED.
We received a wish from the foster mom of a 5 month old baby girl who was born addicted to drugs. For privacy purposes we’ll call the baby Abby. As foster mom’s children are grown, she didn’t have a lot of the things Abby needs to live comfortably. Today we changed that!
Thanks to our friends at BabiesRus in Mays Landing, NJ we were able to provide our foster mom with EVERYTHING she needed and more for Abby. Thanks to BabiesRUs we were able to probide Abby with the following (all items brand new):
A Davinci crib/toddler bed
Bedding, crib bumper & sheets
Addition throw blankets
2 car seats
Baby food & cereal
A plethora of clothing
toys and books
When you are giving enough to take in a newborn baby like Abby, the least we can do is help make life a little easier by reducing the financial stresses of baby items.
Thank you Babies"R"Us (Mays Landing, NJ)!!!!!
That’s right! We asked 15 yr old cancer warrior Dalton what his #1 wish was. His ultimate wish was for Biancas Kids to send him, his mom and his two sisters (who he adores) on a Disney Cruise. We granted that wish! When Dalton is done his chemo treatments in August, we are flying him and his family to Florida where they will board and enjoy an all inclusive paid vacation on a Disney Cruise Ship! Wooohoooooo!!!!
Dalton knows that with each chemo treatment he completes, he is one closer to going on his cruise. It is the best incentive for him to battle this monster.
Have fun Dalton! Take lots of pics.
HE’S AMAZING, HE’S ADORABLE, AND HE’S THE BIGGEST EAGLES FAN OF ALL TIME. MEET OUR NEXT WISH RECIPIENT GIOVANNI!!!!
WE HAVE A COUPLE OF SURPRISES FOR THIS LITTLE GUY. THE BIGGEST WILL TAKE PLACE THIS SUMMER. BY THE VIDEO BELOW, IM SURE YOU KNOW WHAT WE HAVE UP OUR SLEEVES FOR GIOVANNI.
This is our first surprise for little Giovanni. As a die hard Eagles fan and more importantly, a Carson Wentz fanatic, the Eagles commemorative super bowl football featuring Carson was a must. There will only be 10,000 of these speciality balls made. Each come numbered with a certificate of authenticity. It’s a perfect piece of Eagles history and memorabilia for its #1 fan.