Daniela Delgado is just like any other 8 year old girl. She goes to school, loves reading and participating in running club, and spending time with her family.
But Daniel is also extraordinary. She and her family make beautiful birthday cakes for kids who are dealing with hardships. She hand delivers them to the birthday boy or girl and sings them “Happy Birthday.” All while fighting her own battle.
Daniela took some time out of baking and running and reading to answer a few questions for OperationalizeBeauty.
(Warning: you may experience renewed feelings of hope for our future after reading this interview.)
Who she is: Daniela Delgado from Daniela’s Little Wish
What she does: Bake birthday cakes at no cost for kids with life threatening illnesses or disabilities and kids suffering a sad situation in their lives.
Where she does it: Stamford, Connecticut, but I travel all around Connecticut to deliver my cakes and now I am starting a project to deliver cake toppers to other states (sadly not the cakes, I cannot send them).
Meet Daniela
I am 8 years old and I am from Stamford, CT. I do not have siblings. I live with my parents, both are immigrants from Colombia (my mom) and Mexico (my dad) and I am so proud to call myself Colombian-Mexican-American. Like a normal girl I play with my dolls, I love reading books (it is my passion, too) and do exercise (I am in a running club to be healthy). I have a beautiful 3 pound of “hair” yorkie and I love to camp. I love nature and animals.
My mom always said that I am very mature for my age and I agree! I help my parents not to worry about me. I am never mean to anybody and I am very respectful to others and especially adults (I love to talk with them). My parents are raising me well, teaching me good values and morals.
I love to help others. I am so happy with myself!!
P.S I am a little disorganized but I am working on that!!
What is Von Willebrand and how does it affect you?
I have a health condition called Severe von Willebrand Disease Type 1. It is a condition that can cause extended or excessive bleeding. The condition is most often inherited (my mom has it too) and it is a deficiency in our impairment of a protein called von Willebrand factor, an important component in your blood-clotting process. In general, it takes longer for people with von Willebrand disease to form clots and stop bleeding when they’re cut.
I live a normal life. I just have to be very careful not to hit my head, my stomach, or my inner arms. I have to avoid contact sports and stay away from heights of more than 8 feet. I always carry with me special medication that could save my life in case of minor and big accidents. My school and my classmates have to know about my condition and avoid rough play with me. I feel special because I have a nurse in school that takes care of me and the secretary of my school, Patti, always takes care of my minor boo-boos and calls my mom about the incident. I am having nose bleeding episodes without a reason and my mom taught me how calm I have to be, lay down, pinch my nose in a special place, take my medicine and rest for a while. I always wear a medical bracelet with my condition and it is good because in case of accidents doctors and paramedics know what to do. My body is changing, so I can expect any effect related with my condition. I do not feel shy or different to anybody, I just have to be careful with myself.
Tell me a little about Daniela’s Little Wish. When did you start DLW? What inspired you to start? What exactly do you do?
Well, I started this community group when I was just 4 years old. My mom and dad were making a cake and I raised my magic wand (spatula) and wished that I could make cakes for kids suffering in this world with sickness, disabilities, domestic violence and any situation that makes them feel sad or different.




