WISH GRANTED FOR FAMILY OF LITTLE BOY WHOSE MOMMY IS BATTLING CANCER. MEET THE McMICHAELS - TJ, Megan & little Dom.
Here’s the wish we received:
I am writing to you in regards to a little boy named Dom McMichael. He is the son of my friend Megan McMichael. Megan and I grew up together and have been friends since 2nd grade. Unfortunately, she was diagnosed with a rare incurable cancer. As you can imagine this news hit hard for not only Megan, but for her four year old son Dom. Dom is such a brave, amazing, and smart little boy who has such an incredible bond with his mom. I was hoping that there is something special you can do so that this family could experience an unforgettable memory.
We are sending this beautiful family to Wildwood NJ for a week long vacation with boardwalk tickets and Morey's Piers & Beachfront Water Parks tickets.
Dear Bianca’s kids,
I am reaching out on behalf of my son, his name is Hiro & he just turn 4 this month. Last month he was diagnosed of diffuse Astrocytoma stage 2. We are devastated but we have faith that he’s gonna get through this, he’s a fighter and we are fighting with him. My son loves to go to ChuckECheese he’s the happiest kid every time he see he’s favorite mouse but with my husband is the only one supporting our family right now it’s a little tough every time he asked me to go to ChuckECheese and the only thing that I can tell him is we’re gonna see him very soon. it just breaks my heart but he seems to understand and just responds to me “ok we’ll see him soon”. He’s currently undergoing radiation treatment 5 days a week for 6 weeks. I would love to give him a little surprise to go see ChuckECheese I know he will love it so much And he’s into Ryan’s surprise eggs he loves them toys.
Thank you for the time and God bless.
Riva, we are happy to grant this wish god your sweet boy. A check for $100.00 is on it way so you can take Hiro to Chuckecheese & one HUGE “Ryan’s surprise egg” will be at your door tomorrow.
WISH GRANTED FOR 2-YEAR-OLD HERO WHO SAVED HIS SISTER'S LIFE WITH A BONE MARROW TRANSPLANT. MEET THE ADORABLE KAYSON.
Dear Bianca's kids,
Kayson is my 2 year old HERO ! In Jan 2019 he was able to donate his Bone Marrow to cure his sister . He was her 100% match ! The procedure was rough on Kayson and he ended up needed a blood transfusion afterwards.
Since his 6 year old sister is living 2 hours away on medical isolation since her transplant, he's been struggling with not being able to see her ! He will ask for often but we have to remind him Kyn is away so she can get better.
Kayson will be 3 next month and even though he's young I know what would be the best wish that would brighten his spirits. Kayson's wish is for an Ipad so he can facetime his big sister anytime since she already has hers ! Him being able to connect with his sister daily would be the ultimate wish for him !
Thanks for considering Kayson's wish !
When a superhero saves a life, one must not hinder them when they want to talk or see to the soul they saved. We certainly arent going to let that happen. So, one shiny new ipad is on its way to your house so Kayson can facetime with his sister anytime he wants. Its the least we can do for this little angel.
#someangelshavenocouth #miraclemob #biancaskids
Here is the wish we received:
Dear Bianca’s Kids,
My daughter has autism and Bipolar Disorder. I’m a single mom with Lupus and a rare bleeding disorder so finances are a struggle. Sarah was in a residential treatment facility from July 2018-January 2019. She’s home now but still not doing well mental health wise. This is further complicated by the fact I’ve been hospitalized for complications of my physical health conditions 3 times since she’s been home. Once I was in ICU! This has increased her OCD and social anxiety.
She loves photography and it would be a good coping skill. My wish is for her a mini instant camera.
Your wish is granted! One camera and a bunch of film coming right up! Tell Sarah to share some of her photos with us.
Thanks to Dr. Dan Bills & Innovative Orthodontics we made a HUGE wish come true for a special young lady. Meet Madison.
Today, thanks to Dr. Dan Bills & Innovative Orthodontics we made a HUGE wish come true for a special young lady. Meet Madison.
Madison has Mitochondrial Disease and Eosinophilic Esophagitis, also known as EOS, along with a few other medical issues. This sweet girl fights everyday while singing and acting in her school plays. She’s quite the singer.
When we met Madison she told us that she was saving for braces. If any of you have paid for braces you know how expensive they are. It would’ve taken her forever to save the money she needed. So we called on one of our angels, an angel we call on frequently and who never lets us down - Dr. Dan Bills of Innovative Orthodontics. Without hesitation Dr. Bills offered to give Madison braces for free. He has done this for so many of our kids (pre and post braces care too) without a word or desire for acknowledgement. He cares so deeply for children in our community. We are blessed beyond measure to have him on our list of angel/vendors.
We are so grateful to Dr. Bills and his amazing staff for making Madison’s long time wish for braces come true today.
Thank you Dr. Dan! We ️ you.
#miraclemob #someangelshavenocouth #biancaskids
This beautiful young lady is Heaven. She has cerebral palsy and is an activist for the CP community. It is teens like this that inspire other kids with CP to follow their dreams.
Today we granted Heaven’s wish by paying her registration fees & buying her a gown to participate in a beauty pageant in TN this afternoon). Check out our next post to find out how our sweet Heaven made out at the pageant.
Cancer, bone marrow transplant, blah, blah, blah. Nothing is going to hold down today's wish recipient. Meet Laila, the 1-year-old adorable baby/cancer warrior.
We recently received a wish for this adorable child. Laila has been through so much in her short life, but as you can see, she simply asks that you "hold her milk" while she battles cancer and recovers from a bone marrow transplant. She's definitely got this.
Laila's wish was for an awesome play kitchen or washer/dryer set . Laila enjoys cooking, pots and pans , and pretend playing . She also enjoys helping with laundry & getting clothes in the dryer . A kitchen set or a laundry set will get her through this time away from home while recovering from her bone marrow transplant.
Needless to say we got her the most amazing kitchen AND washer dryer set, plus accessories to keep her busy.
Get well soon Laila. #girlpower #someangelshavenocouth #miraclemob #biancaskids
6 yr old sweetheart struggling with with Sickle Cell Anemia, bone marrow transplant and chemotherapy get her wish granted by Bianca’s Kids
Here is the wish we received:
Kynadi is 6 years old and was diagnosed with sickle cell anemia at birth , since day one her life has been filled with pain crisis , hospital stays , doctor visits and an overall limitation on life . Jan 23 th 2019 she was admitted to Texas children’s hospital and started a week of chemo before receiving a bone marrow transplant with bone marrow donated by her two year old brother . Kyn was released after 40 days but can’t go home to her town 90 miles away . She’s currently in an apt close to the hospital and will be there for 3 months . Kyn would love to fill her temporary room and has been asking for an LOL surprise doll house . She is obsessed with LOL dolls and would love the play house ! Thank you for considering her for a wish !
Tiffany (Kyn’s mommy)
This 6 yr old is going through more than most adults. This baby needed some joy immediately. We granted her wish and will be shipping her playhouse this week!
#someangelshavenocouth #miraclemob #biancaskids
SURPRISE WISH GRANTED for tiny patient of Occupational Thrrapist at Weisman Children’s in Sewell, NJ
Recently we received a wish from Kirsten Carr an occupational therapist at Weissman Children’s Rehabilitation Center in New Jersey. Kirsten’s wish was for one of her patients by the name of Naeem Williams. Naeem is 3 years old and was recently diagnosed with autism. He is currently being treated by Kirsten on a weekly basis. However, like many families, Naeem’s family is just trying to make ends meet and they do not have a car. This sometimes results in Naeem missing his therapy appointments. Kirsten’s wish was for an Uber gift card for Naeem’s mom so she could get him to/from his future appointments with ease.
We took it a little further. Today, we surprised Naeem by showing up at his weekly therapy appointment with Kirsten and gifted him a huge basket full of goodies including special sensory toys, a $150 Uber gift card for mom to get him to/from his therapy appointments, a $150 Shoprite gift card for mom to do grocery shopping and an AMC gift card so the family could go to the movies.
Naeem and his family were so appreciative. Every little blessing counts. ️
#miraclemob #someangelshavenocouth #biancaskid
WISH GRANTED FOR TEEN PAGEANT QUEEN & CEREBRAL PALSY ADVOCATE WHO INSPIRES KIDS TO FOLLOW THEIR DREAMS
Heaven Ramsey is a beautiful, smart, giving and talented young lady. She is also a fierce advocate for the cerebral palsy community. Pageants are her passion and her platform. She has won numerous pageants and as such, is a daily reminder to all kids with CP that their disability should never prevent them from following their dreams.
Given the above, we wanted to grant a wish for this beautiful CP warrior and Support her pageant aspirations. So, we are paying for her to attend the
Glamour Miss Pageant in Knoxville, Tennessee on April 4, 2019. No pageant princess would be ready for her walk on the stage without a gorgeous new gown. So we allowed Heaven to choose whatever dress she wanted to wear for the pageant and we purchased thad dress for her. The gorgeous red dress she selected is photographed below.
Good luck Heaven! Heaven Ramsey