Wishes In Waiting
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Kade
Nousha: Fighting Lymphoma
My whole life has been a struggle. I have had 7 open heart surgeries. With that comes a lot of being sick and in the hospital. I had a pacemaker which restricted activities. I've spent many years there if you were to add up all the time.
After my heart transplant in 2016 I was doing good and then I went into rejection in 2018. That was terrible because I felt so bad a spent most of the summer hospitalized. I started to recover and feel better for a few years. In 2023, I started to feel bad again. I couldn't eat much because of my stomach, my hair started to fall out, and my skin was really bad and just plain uncomfortable all the time. Biopsies determined that I have PTLD.
I am now doing photopheresis therapy 2 days a week. They take out my blood to treat the bad cancer cells and then put them back in the treated blood. It takes several hours. I am in transition for all my care to come from the adult hospital now, which is also scary. I feel a little better now that they stopped the medication, but it also puts me at risk.
What Nik's wish are you thinking about and why?
I would like to go to Las Vegas. I really love music; it helps me through my worst and best times. I would like to see one of my favorite bands perform or a show. I would also like to go to Gordon Ramsey's restaurant. I think Las Vegas would be a good place to take me away from the cold and treatment
Nousha
Nousha: Fighting Desmoplastic Small Round Cell Tumor
I was a recent college graduate who had the best college experience ever, made the best friends, and always got good grades. My goal was always to become a journalist, preferably in broadcast. About 6 months after graduation, I was able to get a dream job in my competitive dream field as an assignment editor. I was just getting my career started, feeling like I was getting a good grip on my job, loving every moment of it. I had amazing coworkers and bosses. I wanted to make some travel plans to explore the world more on my time off. Then at 23 years old, several months back, I got diagnosed with an extremely rare and aggressive type of cancer called desmoplastic small round cell tumor (DSRCT) that put my life at a big halt. It felt like my life was over when I heard that diagnosis. It is a type of sarcoma. Less than 1 in a million people have had it, and there are only around 200 recorded cases in its history. The complexity of this cancer is resulting in a lot of different treatments to save my life, including multiple surgeries, over 40 chemotherapy rounds, innumerable doctor visits, and costly medications. It's been very hard to keep up with everything on a daily basis now for me and my family.
I was living with chronic pain for about a year leading up to diagnosis and had to go to over 20 doctors before one believed my pain needed to be investigated, performed surgery, and found the cancerous tumor. This resulted in me pretty much saving my own life through my self-advocacy with the help of this trusted doctor and a physical therapist. A bunch of doctors brushed me off before the diagnosis, saying my abnormal health findings were "normal" for someone my age. Previous providers told me the pain was all in my head. I wish to become an advocate in this space, especially for young women, and promote screenings for cancer detection once I hopefully get through all this, making a real difference after this experience. Now, I am fortunate enough to receive specialized, expert care for this rare cancer.
It is unimaginable that I was a recent college graduate, just starting my career, living a normal life one minute, savoring every moment of my young adulthood, and now have to be inpatient in the hospital constantly during treatment, dangerous side effects of treatment, and pain management. There are so many awful side effects that make me feel really ill all the time. I still try my best to stay as brave, strong, and positive as possible despite the circumstances.
What Nik's wish are you thinking about and why?
A trip to Hawaii with my mom (my main caretaker right now), preferably to Disney Aulani or somewhere in Oahu
Ryan
Ryan: Fighting Hodgkin's Lymphoma
Life after being diagnosed has been scary and uncertain. Whenever I get sick, that could be a simple cold. It is terrifying not knowing if the cancer is back or if it is just a cold and I will be better in a few days. Unfortunately, I have not been able to live a normal life nor plan for a normal life. I had to delay starting college because of my first relapse which was crushing because I was looking forward to start on my future. I graduated in May of 2025 and started looking for a full-time job in my area of study in which I had to pause because of my relapse. These are situations that have me uncertain of what my future will look like and the constant thought of could my cancer be back. I try to look on the bright side of things but some days it is very hard to find the light at the end of the tunnel.
What Nik's wish are you thinking about and why?
I am thinking about the Hawaii trip with my family because of my experience from being in the hospital not being able to go home during the holidays and all the pain I went through. During my stay in hospital, I was stuck in a small room for weeks because I could not walk or because I was at risk of catching an infection from others outside those four walls which made me appreciate the ability to go outside and explore the world. This has taught me that I have to take advantage of every opportunity and live life. Hawaii is a dream destination that I financially would not be able to take let alone with my whole family. This would be a great experience for all of us especially since they have also suffered alongside me.
Jamauri
Jamauri: Fighting Neuroblastoma
Before I got diagnosed, I was able to go places and be around family, work, ride four wheelers, play basketball, just chill with my family and friends. After being diagnosed I finally had an explanation for what I was experiencing, which brought a sense of relief and clarity. The diagnosis helped me learn better ways to manage my challenges and seek the right support. Even though there are still obstacles, I feel more confident and hopeful now than I did before.
What Nik's wish are you thinking about and why?
Player two prime nzxt base model the reason I would like this so I can play games and I really wanna start my own clothing brand. And find other stuff I can do with it.
Mmesomachukwu
Mmesomachukwu: Fighting Hodgkin's Lymphoma
Before being diagnosed with cancer, I was in my second year of college for nursing. I had a few hobbies I loved to do when I wasn't studying - reading, playing my saxophone, learning Igbo, writing my book, doing my hair, and the newest one I picked up, sewing (with a sewing machine). Things were chill then, but I always had this breathing problem, like asthma. I went on a road trip with my cousins. It felt like there was a lump on my chest when I lay down, and I could hear this very slight wheezing sound, but it wasn't serious - not then at least - so I ignored it. But when I went back to college, things started to get real because there's a lot of walking up hills, stairs, and regular paths, something that forced me to exert myself. The wheezing sound grew more frequent to the point that if I talked too long or laughed too hard, I'd break out into a cough, which turned into wheezing, and eventually the wheezing became a permanent thing. You could always hear my breathing, and it didn't sound pretty. So, I told my mom, and we decided that when I came back home, I'd go see the doctor (because I live out of state and fly home). Eventually, the doctor's visit came, which eventually led to a pulmonary function test being ordered, and when I failed that, it led to a chest x-ray, which then turned into a visit to the ER after they found the mass in the middle of my chest. This was the night I found out I might have cancer.
It was hospital appointment after hospital appointment after that. That's when I knew I wouldn't be able to go back to school. I had my biopsy, and my results came back only a few days later, and that's when everything became official - I had Hodgkin's lymphoma; I had cancer. I've had to live with that possibility, but in the back of my mind, I knew it was 100% certain; I just needed that biopsy to prove it.
I've been out of school since then, returning there only to gather my belongings. The hospital appointments only continued until the big one came, my first round of chemo, It's not something I dreaded - I looked forward to it in fact. Not because I want cancer (no, nobody wants that c word), but because it was an obstacle placed before me and I love a good challenge. This wasn't going to be an easy one, but I knew it was one I could face if I could just keep the positive attitude I've always had. I like to see the positive in the negatives, because it makes the hard times seem less daunting, like a movie where I'm the main character and I know I'm going to win at the end, but don't know exactly how. My first round of chemo has been the worst so far, but not horrible. I had terrible nausea to the point I couldn't sit up for long (I had to lie down to eat sometimes), was so drained I'd sleep like 75% of the day, dizzy, lightheaded, couldn't stand for long either or drink water. My mouth also tasted weird, and I got mouth sores that eventually led me to get admitted to the hospital because I had a fever - 100.6ºC and climbing. My blood dropped so low that I needed a blood transfusion. Being in the hospital for those 48 hours isn't an experience I'll forget; it's made me realize the power nurses have, and I'll be sure to be the best nurse for all my patients because I now know what it's like to be in that bed, and gosh do I hate that bed, but the nurses made it so much better. The doctor at the hospital told me it gets easier, and she was right.
I recently finished my second round, and I had little to no side effects except mild nausea and the usual lightheadedness/dizziness. I did end up losing all my hair, though; the first round really loosened it all up. But I like the new look - I might even stay bald when my hair starts growing back. My next round is in a few days, and I'm hoping it goes smoothly, too. Life's been interesting living with cancer and seeing how other people react to my disease is also interesting. I've seen a type of love that's so new and refreshing, that makes my heart smile knowing they care. It also makes me wonder what they would do in a hypothetical world (because I don't want it to ever happen in this one) where they got cancer. I hope they can smile through and stay positive even when it's hard, because an attitude alone can make all the difference in the cancer journey.
Every day hasn't been easy. Sometimes I'm in bed all day, other times I'm able to get up and work on another sewing project, read a book, or even simply watch a movie. Sometimes I feel awful, unproductive, like I'm wasting my time (because I'm the type that loves to make the most of my days), but overall, in the grand scheme of things, I've been feeling great. I can't wait to be done with chemo, because I know the person I'll become won't be the same person I was before, but i know she'll be beautiful.
What Nik's wish are you thinking about and why?
I have a lot of hobbies, but my biggest one has always been writing. I want to be an author in the future, along with being a nurse. I've been using my Mac to work, but it's old now and laggy. I would really love a new MacBook Pro M5 Max with the Apple Creator Studio preinstalled. It's got all the RAM, storage, and CPU power for writing, but most importantly, the newest hobby I've been hoping to start with a new Mac - animation. When I was in the hospital and couldn't sleep, I'd play some music in my AirPods, close my eyes, and imagine fun animated lyric videos with pictures telling a story until they sang me to sleep. Except, these lyric videos don't exist - they're all in my head. I've been wanting to bring them to life since then and hopefully share them with the world, because I believe music with visuals completely elevates the listening experience, and as someone who always has music in my ears 24/7, that's an experience I want to give others.
Arturo
Arturo: Fighting DIPG
Life before cancer: Arturo was a straight A student in his senior year of high school. He has 3 younger siblings (12yo, 7yo, and 5month old) and he is the best big brother. He loves anime! Alex and his family were visiting San Diego on a family vacation and when he started to have stroke-like symptoms, they brought him to the hospital where they found a tumor in his brain.
Now: Arturo is unable to walk anymore and has limited speech. He is currently admitted to the hospital as he was having some concerning symptoms (impaired speech, weakness). He is currently on steroids, which the medical team hopes will improve his symptoms and he can regain function.
Wish and Why:
VIP Comic Con experience
He is a big anime fan and wants to experience the anime culture
Erin
Erin: Fighting Medulloblastoma
I was just a typical 18-year-old girl. I had just graduated and was trying to figure out what I really wanted to do with my life. I was looking for internships when my health became an issue. It was a complete surprise that I had a brain tumor.
The last 16 months have been some of the hardest of my life. I had to have emergency brain surgery, endure 6 weeks of radiation, and then a year of chemo. My memory has become problematic, and my mobility continues to be affected. Even though I'm frustrated with losing the life I thought that I would have had, I'm looking forward to my future even though I'm not sure exactly what that looks like yet.
What Nik's wish are you thinking about and why?
I'd love to go to Hawaii and visit the Lanai Cat Sanctuary!
I've always loved cats, some may even say I'm obsessed with cats. I have 4 indoor cats and 2 barn cats - all who I adore.
Mathew
Mathew: Fighting Choriocarcinoma
Before cancer, my life felt pretty normal. I was a freshman in college, staying active all the time. I would run, play pickleball, go hiking, and just be outside a lot. I didn't really have to think about my health, I was a healthy individual and didn't worry about being around people who were sick. I could exercise without getting out of breath or feeling my heart race too much. I also got to see my friends whenever I wanted and worked my way from a part-time employee to a full-time employee. Eating was never something I stressed about either. I could eat whatever I wanted, like deli meats or sushi, and didn't worry about food safety or how things were prepared.
Now with cancer, everything is kind of the opposite. I can't stay active the same way, and even simple things can make me feel tired or out of breath. I have to be really careful about being around people who might be sick because my immune system is weaker. Seeing friends isn't as easy anymore, and I can't work like I used to. I also have to be more cautious with food, making sure everything is safe to eat and properly prepared. Overall, life feels a lot more limited and requires way more planning than before.
What Nik's wish are you thinking about and why? - Undecided
Diante
Diante: Fighting T-Cell Lymphoblastic Lymphoma
Before cancer, Diante had so much ahead of him. He was in barber school and working toward launching his own clothing line. Then his diagnosis turned his world upside down, and treatment brought intense challenges, including complications that led to repeated hospitalizations and debilitating pain. After relapsing during maintenance and preparing for a bone marrow transplant, his disease progressed before he could receive it, and he now faces a terminal diagnosis.
Through it all, Diante never let go of who he is. He stayed committed to his craft, achieved his dream of becoming a barber, and even began building his clothing line. Despite every setback, his kindness, resilience, and gentle smile continue to shine, bringing comfort and light to everyone around him.
What Nik's wish are you thinking about and why?
Travel with family.
Katie
Katie: Fighting B - ALL
I am a single mom who has always been active and involved in activities with my son. I used to work and go to school at the same time because I wanted and still want to give him a better life.
It has been really hard for me because I feel like I've been missing out on so much of my son's life since I'm always in the hospital. Before I was diagnosed, doctors told me I was depressed, but I didn't feel depressed at all. I just felt tired all the time like I slept but never truly rested. I was constantly having nosebleeds, and sometimes they would get worse. I thought maybe I just needed vitamins, but in the U.S., they don't usually prescribe vitamins unless it's necessary.
After I finished my semester, we decided to take a short vacation to visit my family. After a check up there, I never imagined I would have to stay. I ended up staying for a week and a half. It was a nightmare. My arms were covered in bruises, my platelets were very low, and my blood counts were dangerously abnormal. They even told my parents that I might not make it because of the condition I was in.
Sometimes I feel useless because I have a four-year-old who needs me, and I'm always tired. I can't play with him like I used to. I feel like this has impacted his life even more than mine, and that truly breaks my heart. I used to be with him all the time, and now, because I'm in treatment, I can't even see him since they don't allow children in the hospital.
What Nik's wish are you thinking about and why?
My wish is to take a vacation to Hawaii because my son loves the beach, nature, and animals. My dream is to always make him happy, spend quality time with him, and create beautiful memories together. I would love to take him to the aquarium, explore nature, and do fun activities as a family. My mom and friends who have been there say it's an amazing place.
Erika
Erika: Fighting ALL
Before cancer, life was truly fun and beautiful. I had graduated as a licensed practical nurse. With the new job, I was able to help my family with housing bills and expenses. I had also become engaged. I got accepted into nursing school to become a registered nurse. It was completely stressful, but it was a dream of mine to become a registered nurse and to help my family for all they have sacrificed for me over the years. I was also in the best shape of my life. I weighed 155 pounds and was determined to work out and maintain a healthy lifestyle while attending school. I was also involved with my community in church. I would attend church every Sunday and Wednesday and to other side events the church would hold.
I remember being in school and feeling fatigued with body aches and chills. I felt completely off and went to get checked out at the ER after school. After a certain test they concluded that I had leukemia. I remember the day like it was yesterday. My entire world completely crashed. I immediately broke down and cried with my mother. I remember my mother comforting me and told me she would be with me through every step of this journey. I remember telling my fiancé that we should separate and go on our own paths because neither one of us asked for this. Fortunately, he has stayed with me through every step of the way until today.
Life after being diagnosed with cancer was very difficult. For one, I had to postpone my fiancé and I's wedding. I was almost done with 3/4 semesters of nursing school. Due to the circumstances, the nursing program gave me a year to get treatment and be able to continue where I left off. Unfortunately, I needed more treatment than anticipated, and the year has passed. If I want to go back to school, I will have to start the program all over from the beginning. The hardest part was seeing my mother's dreams not come true. At the time, she was working as a nurse assistant at a rehab center and attending the same school as me but studying to be a licensed practical nurse. Having cancer required me to have a caregiver with me 24/7, and my mother was determined to be my caregiver. Her program also did not allow her to come back to finish school and so she also had to drop out. My mother has been the biggest support in my life, and I will always be appreciative of her. Due to the circumstances, my mother had to take care of me and missed out on my sisters' first year of high school and my brothers' first year of college. I was not able to see my siblings as much and so my mother and I would try to take weekly trips to come down to McAllen to see my siblings as much as we can. I needed six rounds of chemotherapy and a stem cell transplant in august 2024. Losing my hair was really difficult, I had long curly hair and to see it fall off and buzzed off completely hurt me. I felt like my hair held a lot of my identity. I also dealt with nausea, vomiting, fatigue, weight loss, mouth sores, stomach pain, back pain, headaches, and frequent infections. Dealing with the physical symptoms was one thing, but dealing with it mentally was another task I had to face. It felt like a death sentence was slapped in my face. It's one thing to know you are going to die, but another to think you'll die soon. I was in remission for about 3 months until I relapsed. That took a toll on me. Relapsing gave a worse feeling than being diagnosed. It felt that all the chemotherapy and transplant my body had been through was for nothing, and my own body rejected me. I also went through a Car-T-cell therapy. It was a painful process, and my body did not respond at all to the new cells. I did another stem cell transplant and that was the hardest therapy. Recovering was the most difficult part. I had lost over 30 pounds, weighing 94 pounds. I had also lost all my hair again. Eating was challenging. I lost all appetite for food and had nausea and vomiting along with stomach pains. It took about 3 months to recover, but I can thankfully say I am able to eat more, walk more, and do more tasks on my own. Today, I am still recovering from my transplant and happy to announce I am in remission. These last 2 years have not been the easiest, in fact it was probably the worst years of my life. But I can also say it was the best years of my life. Sure, it was filled with pain and suffering, but it was filled with so much joy and peace. I made a lot of friends along the way who knew exactly what I was going through. My mom and I were also blessed to have housing for free while I was undergoing treatment. I also have a completely different outlook on life. I am appreciative of all things in life. I will never take for granted the simple task one can do on their own such as breathing, walking, or even talking. I have built a closer relationship to God who gives me complete peace. I am no longer afraid of treatment because of my identity now in Christ. Cancer completely sucks, but without this chapter in my life, I would not be who I am today.
What Nik's wish are you thinking about and why?
I would love to take my family and fiancé on a trip to Hawaii to eat different foods and go on different adventures. I was told in January 2026 that I was in remission again and I want to close this chapter of my life with a nice vacation where I can thank my family for their support and patience.
Heagan
Heagan: Fighting B- ALL
I was in three different basketball programs, hoping for a scholarship from one of the college coaches watching me. One day at practice, we were just warming up, and I began to feel very weak, then I passed out. Without knowing why I passed out, we decided it was just dehydration. A few weeks later, I went back to basketball, and the same thing happened once again. So at this point, I was taken to the doctor. The doctor said, "Let's monitor your heart", so we monitored my heart. During this time, my doctor is telling me I should take a break from playing with my AAU teams, and I am not the brightest person when they say that. Halfway through the summer, my heart monitor came back, and my heart was perfectly fine. The cardiologist shoves us away, then tells me I just need to drink more water. At this time, summer was coming to an end with still no diagnoses, but I did get to make it to one last basketball game. After the entire summer with no summer workouts and barely any practice, I was out of breath. Of course, I barely played because there was still something wrong with me, but we just wanted me to play so I could try and get college coaches looking at me.
On the first day of senior year, I started to feel like I was getting the flu or something like that. We had an assembly, and I am in the yearbook, so it was my job to take the first day of school pictures. Fast forward to Friday Night Lights, I feel like I'm genuinely dying, but I have to be there for the yearbook to teach and take pictures. After FNL and the weekend, I felt better, then we had a volleyball tournament in which I'm still not playing any sports, so I brought my own camera to start taking photos of athletes. While I used my camera, I also made video edits along with an Instagram page for the work I did. Sometime had gone by and we finally got a doctor's appointment to see the rheumatologist, so I got to the doctors office. They run more blood tests, which is good, but we also have to wait a week. As the week goes by, I get sick once again. I'm mostly not at school that week because of volleyball tournaments, so I still go while feeling sick. The weekend came by again, and I never thought my life would change. My mom had gotten a call from the doctor himself saying we needed to pack a bag and take me to the hospital. Then I was diagnosed with B-cell acute lymphoblastic leukemia, having it take over 75% of my body.
Looking back, as I am about to get a transplant, I really do believe that God gave me this path for a reason. It might be a challenge, but I figured out if I can't play sports anymore, I want to take pictures, enjoy art, and picture the moment. Some days cancer really beats me, but I still love to take pictures even if it's on my phone, anywhere I go. I just love it.
What Nik's wish are you thinking about and why?
The Nik's wish I am wanting is a X2D ll 100C Hasselblad + XCD 2.5/25V
Logan
Logan: Fighting ALL
Logan was a healthy child overall; he was born with down syndrome and other disabilities. However, he did not allow that to define who he was and still is to this day. Logan from day one was an inspiration to his family, friends and just to everyone that knew him. Logan has had challenges over his lifetime. Logan was diagnosed with cancer at an early age, and his life took a turn that no one expected. Logan and his family then learned of his biological fathers passing away. It was devastating for Logan and his family. As he was a big part of their family. Logan loved his father immensely, and still to this day. Logan will say my father passed away, its okay. I know that he is here with me watching over me in heaven. He just has a heart so big and loves everyone. His family thought that Logan had beat his cancer and was so happy. Once more, tragedy hit his family. Logans, stepdad, who he calls Dad, also, had been hit with Cancer. So, for Logan and his family it was like reliving it all over again, Logan was a huge support for TJ his stepfather (Dad). TJ did go into Remission and life resumed as it had before all the diagnosis.
Then years later one day in November 2024. Logan's life took another unexpected turn. Logan was diagnosed with Acute Lymphoblastic Leukemia and has remained under continuous medical supervision and has been receiving care from his oncologist since the diagnosis and to date. Logan, despite the Leukemia coming back, almost losing his life several times has remained a positive light. Logan will say it's all right, I am going to be fine. I will beat this and Dewayne Johnson the ROCK has been such a role model and inspiration for Logan and really got him through all of this. Logan, dresses like the ROCK, he literally wants to be just like the ROCK. It would be totally amazing if we could make his lifelong dream of meeting the ROCK in person come to reality. Please help him make this a dream come true.
What Nik's wish are you thinking about and why?*
Dewayne Johnson the ROCK has been such a role model and inspiration for Logan and really got him through all of this. Logan, dresses like the ROCK, he literally wants to be just like the ROCK. It would be totally amazing if we could make his lifelong dream of meeting the ROCK in person come to reality.
Braeden
Braeden: Fighting ALL
As a child, Braeden had nicknames, such as "Bump and Go and Ricochet". He has always been Happy, Energetic, and a leader on his Sports teams and among his friends. Known not only for his faith and dedication but also for his talent, Braeden is one of the top ultimate frisbee players in the nation, holding five national championships. In fact, in the State Ultimate Frisbee Tournament in April 2024, about a month before high school graduation, Braeden played at the peak of his performance, was voted Runner Up for MVP Ultimate Frisbee in the State of Utah, and added to the All-State Team. He was training for his third High School Nationals Invite Ultimate Frisbee tournament in June. He also had recruiters from Team USA ultimate approach his coach about him and when asked his plans for summer, Braeden kindly told them he'd be serving a mission for his church, but that he was grateful and flattered for the offer.
AN UNEXPECTED DIAGNOSIS: Braeden's life took an unexpected turn when he was diagnosed with a rare form of Leukemia at 18 years old. In the weeks leading up to this moment, Braeden had some significant back and rib pain. He went to a couple Instacares and got X Rays, and was told both times that there were no broken ribs or bones, and that he had sustained a sports injury and likely just bruised ribs. He kept going to frisbee practice, noticed he was more tired, and in more and more pain. Braeden was taking mission photos with a group of his best buddies who were also set to serve missions soon. He was in so much pain and was so fatigued that he had a hard time standing to do the photos and by the end of the hour, he was laying down in the car. After a lot of encouragement from his mom he was taken to the ER that night and days of testing and imaging began. The Doctor at the ER was in Hematology/ Oncology and he told us that Braeden had "blast cells aka cancer cells" in his blood. Braeden was diagnosed with ACUTE LYMPHOBLASTIC LEUKEMIA (ALL), If left untreated, ALL can spread quickly to lymph nodes and other parts of the body. They told him it would be a marathon, not a sprint.
The first month was rough, Braeden's strength diminished even further, he was unable to use his fingers to button things or open things, he developed drop-foot, where he would fall while walking, he couldn't climb stairs, he lost his hair, he developed temporary type 1 diabetes, and he developed kidney stones from the chemotherapy side effects. Braeden spent most of his time in bed sleeping or throwing up, but through it all, he still managed to have a smile on his face, and always expressed gratitude and his sports-like toughness mentality. His Dr. (and medical team) have been phenomenal-and even though at 18 years old he didn't qualify for Make-a-Wish benefits-people have been so kind and generous, showing up with treats and cards and puzzles, anything to help brighten our days! Braeden's leukemia journey continues to see it's share of ups and downs from rare side effects to chemotherapy, including pancreatitis, neuro-toxicity, mucositis, blood infections, nightly fevers for a time, lots of ER visits, and very prolonged hospital stays. Each challenge has been met with a fierce determination to conquer and win this battle. Braeden is a true WINNER!
What Nik's wish are you thinking about and why?
Braeden would love to attend a World Cup Soccer game in the US this summer. He has a friend coming back from his church mission and he would love to travel with this friend, who he hasn't seen since diagnosis and watch the World Cup with him. Braeden's Hero is Lionel Messi, so it would be amazing to see an Argentina game to see Messi in person.
Zachary
Zachary: Ewing Sarcoma
Growing up I played travel hockey, soccer, and loved to be outdoors. I decided to leave schooling after my sophomore year of college and join the workforce as a CAD Detailer for a Caterpillar Dealership. I then left that job to get a career as a sales engineer at an agriculture company . I started coaching my high school soccer team, playing hockey weekly, playing pickleball with my coworkers, and became very active in my church. Everything was going great except for this pain in my left hip. I went to the doctor and went through physical therapy, a steroid injection, and an MRI. That's when everything changed in my life.
At 21 years old, I never thought I would hear the words, "you may have cancer" come out of my orthopedic surgeon's mouth the day of discussing my MRI and attempting to get surgery on my Hip. I thought he was joking at first or that he just had to say that to rule out the big clear obvious "NO" on the list of things to go through. He then sent me to Northwestern Hospital to be seen by an orthopedic oncologist and they did another MRI and found many tumors in my femur and pelvis.
I was shocked. I went from one month before of trying to get hip surgery to finding out I have tumors in my femur. This news broke me and I broke down instantly. It then began the process of going to Chicago, Illinois which is 2.5 hours away almost weekly to find out what my diagnosis would be. After PET/CT/MRI and Bone marrow biopsy, we had an answer to what was causing my pain in my hip. I was diagnosed with Ewing Sarcoma.
This put me into a funk for a couple weeks. At the beginning I was 290lbs and by the day of my first treatment I was 218lbs. I lost weight, my mental strength, and my will to be happy because I didn't know what life was about to be like.
I started treatment #1/14 with the chemotherapy being distributed every two weeks and would alternate between 5 different drugs, VDC/IE. The first treatment was 2 days and the other treatment was 5 days in the hospital. I was worried about what my effects would be like Nausea or being extremely tired on top of all the pain I was having. It turns out my body was responding well to the chemotherapy after 1 day of treatment and I had no side effects from the chemo. I was shocked! No pain, no sickness, no fatigue, and I felt normal again. I am now as of today finished with 8 treatments and have 6 left until I will have my scans to see if I can begin a life in remission. I started proton radiation therapy and will complete 31 treatments. My final day of chemo therapy will end on April and I have never been so excited to be able to beat this cancer and be a walking testimony for everyone in my life and everyone around me going through the battle of cancer.
WISH: San Jose Sharks game -- with brothers.
Rafith
Rafith: ALL
I am a student living far from home, without family, sharing my life with friends. Everything changed when severe back pain led to an MRI that revealed a spinal fracture with a tumor, and soon after, a diagnosis of leukemia.
Before treatment even began, I faced the hardest part of my journey. I endured relentless headaches-10/10 pain for nearly 40 days. Despite multiple emergency visits and high-dose painkillers from my primary doctor that worked only for a few hours, the pain kept returning. Those long days and nights tested my patience and faith deeply.
Chemotherapy was toxic and exhausting, but I was never alone. My doctors, nurses, and friends became my family when mine was far away.
WISH: Undecided
Victoria
Victoria: Leukemia
Just a year ago, I was a regular 21-year-old, balancing school for medical billing and coding with hobbies I love like spending time with friends, attending car shows, and enjoying the great outdoors. Life felt vibrant and full of possibilities.
However, after undergoing a bone marrow transplant, my circumstances have dramatically changed. I've had to move back in with my parents, and unfortunately, I've found myself housebound as I focus on recovery. During my treatment, I developed foot drop and severe neuropathy, which now requires me to use a walker to get around.
I'm currently waiting for my counts to come up so I can gradually return to more of my normal activities. It has been a tough adjustment, but I'm trying to stay positive and find joy in the little things.
What Nik's wish are you thinking about and why?
NY Bronco has always been my dream vehicle. When I was 15 years old, my dad found a Bronco in rough shape, and he traded his car to bring it home. We embarked on a father-daughter project to restore it together.
Over the years, we have made substantial progress. The Bronco is now mechanically sound and has received a fresh coat of paint. However, we are facing financial constraints that have made it difficult to finish the interior restoration.
While I'm not looking to be on the show, I would love to inquire if there's a way for the Garage Squad team to assist us in our project. My parents and I watch the show all the time and love the way they let the family help.
I would like to humbly request your consideration in helping us complete this project. It would mean the world to my dad and me to see this dream come to fruition.
Thank you for taking the time to read my request. I am hopeful that Nik's Wish can help us in this journey.
Olivia
Olivia: Breast Cancer
Before being diagnosed, my life was full, active, and deeply rooted in the future I was building. I was working full time as a CNA at the hospital, caring for patients and finding purpose in serving others. The long shifts were tiring, but I felt strong and capable. I was also a full-time student, balancing coursework with work and still making time for the people and commitments that mattered most to me.
Outside of work and school, I helped my fiancé on the farm, caring for the cows and learning more about the responsibilities that would one day be part of our life together. We were planning to show cows this summer, this was something we were both excited about and I was also preparing to help at a two-week student youth group trip through our church, this one was going to be extra special because it was where me and my fiancé met 2 years ago. My days were busy, but they were meaningful. I felt independent, dependable, and confident in my ability to manage it all. Most of all, I was looking forward to the future. I am only 20 after all and after getting engaged this past summer, so many of our conversations revolved around building a life together, our wedding, our home, and the family we hoped to have someday. Having children was always part of that picture.
After my diagnosis of breast cancer and learning that I carry the BRCA1 gene mutation, everything shifted. My life no longer feels predictable. Physically and emotionally, I have had to slow down and reevaluate what I can handle. Working as a CNA, keeping up with school, helping on the farm this all of it now requires more energy and intention. Plans for the summer have drastically changed. One of the hardest changes has been the conversations about our future family. What once felt like an exciting, natural next step has become complicated and uncertain. My fiancé and I have had to talk about the possibility of fertility challenges, preventative surgeries, and even the reality that we may not be able to have children the way we once assumed. Those conversations have been emotional and heavy, filled with fear, grief, and unknowns. But they have also been filled with honesty and love. We have had to lean on each other in ways we never expected this early in our engagement. This diagnosis has tested my independence, but it has also revealed my strength and the strength of our relationship. I am learning that resilience does not mean doing everything on my own. It means adapting, asking for help, and continuing to hope even when the future looks different than planned.
Life after diagnosis is not the life I pictured, but it is still a life filled with purpose, faith, and commitment. I am still a caregiver, a student, a fiancée, and a woman with dreams. The path to those dreams may have changed, especially when it comes to building a family, but I am determined to face that path with courage, honesty, and the support of the man who has promised to walk beside me through all of it.
What Nik's wish are you thinking about and why?
I would love to do a family trip with my family, we haven't done anything in years because my dad has had his own health issues and my brother is leaving for college this year and I just miss being all together as a family. Its weird even asking for something as I still don't feel deserving. I remember times as a kid as a family and it just seemed so carefree and fun, we would bicker like normal siblings but we had such good memories. Time seems to go so quickly now and I just miss those times and worry if I will every get them again. I worry since I have the BRCA1 gene that my little sister will go through the same stuff that I am going through. I just want a time we can remember together. I prefer the mountains to the beach, not a huge sand person, even though I competitively swam in college funny enough. I think visiting Yellowstone or the Utah National parks or Lake Louise would be amazing. My mom and I always talked about going there with my sister because we all the middle name Louise, so do my grandma and my aunts and my aunts kids. I just want time together where my mom doesn't have to worry about everything going on or how to afford things. Doesn't have to be in any real capacity other than that.
Orin
Orin: Fighting Glioblastoma
I faced the kind of news that shifts the ground beneath your feet. What I assumed was just persistent fatigue, and headaches turned out to be something far more serious. I was diagnosed with glioblastoma brain cancer. In that moment, everything changed: my routine, my education, my social life, and my understanding of what it meant to be strong. Facing a life-threatening illness at an age when most teenagers are planning prom or stressing over exams felt unfair. Especially, when I prided myself on always being active in sports such as wrestling and debate. I actively had an enrollment at the YMCA and embedded myself and countless activities. I would help my mother, who is a single parent, with a lot of duties in the home and with my brother and sister. As the eldest of three, I always pride myself on being a structured role model for my siblings. I was active in church and community. During the summer, I kept active in sports such as swimming and running, which kept me in the best shape. So, I'm sure you can understand that the impact of this diagnosis completely shifted my life and turned my world upside down. But through that darkness, I found strength I never knew I had, a deepened sense of purpose, and a clearer vision of the future I want to build.
The months that followed my diagnosis were filled with treatments, hospital visits, and uncertainty. I had to undergo surgery and transition towards a new way of living my life, temporarily, missing out on valuable academic time in classroom interaction as I was placed on home instruction and the comfort of normal teenage life. One of the biggest challenges I faced during this period was maintaining my mental health while enduring physical and emotional suffering. Radiation took a toll not only on my body but on my spirit. 33 treatments, I remember one particularly difficult night when the pain and isolation overwhelmed me. I had lost my hair, most of my energy, and all sense of control. But that night, I made a decision that I wasn't going to let this illness define me. Instead, I would use it as a foundation for growth and determination.
A challenge I overcame during this time was pushing forward into completing school while simultaneously still enduring treatment. My body was still weak, and I had fallen behind in what felt like, academically I would not recover or finish my studies and graduate senior year on time. However, I was determined not to let cancer derail my dreams or my senior year of high school graduation. With the support of my mom and teachers, I created a rigorous homeschool schedule and often worked late into the night preparing material even through the aches and pains of treatment. I persevered and learned that my determination paid off as I completed my final semester with a 95-class average and even excelled in several subjects. That experience taught me not only resilience but also how to challenge myself physically, mentally, manage time efficiently, and maintain a long-term vision even when the short term feels overwhelming.
Beyond personal recovery, I found purpose in giving back. As someone who received so much support from my community and church family, family friends delivering meals to local nonprofits helping cover medical costs, I felt a strong desire to pay that kindness forward. I began community outreach by giving food to the less unfortunate and became a member of the discipleship group at church providing meals and discussions of hope. I also organized a small online group chat with fellow students at my school that streamlined youth development and peer-to-peer discussions that encouraged and enriched student engagement. Participating in these efforts not only helped others, but it gave me a sense of empowerment and purpose during a time when I often felt helpless.
Additionally, Education has always been important to me and helping others gain confidence in their abilities is deeply rewarding. This season in my life has strengthened my commitment to service.
Looking forward, my faith is strong and I will continue working towards my goals as I am committed to continuing my education, pursuing a degree in law specifically, criminal defense. I want to one day contribute to a bigger platform in the world and economic development. I envision working internationally in government legislation. While in college, my mission is to support students and families with community development programs in faith-based programs while learning the values and skills needed to practice law. Help other families who are impacted by life-threatening conditions. The path of law has always been my passion for as long as I can remember. Debating on various legal topics opened my mind to the many unresolved issues that people face surrounding the judicial system. I look forward to breaking down some of the many barriers that exist. It is my hopes and aspiration to become a successful lawyer and advocate for the rights of people. In any capacity.
Being diagnosed with brain cancer was the most difficult information to receive and experience of my life. But it also became the catalyst for personal growth, and a deeper commitment to serving others, and understanding my purpose. I will continue to emerge from the storm more resilient, more compassionate, and more determined than ever to make a meaningful impact on the world. I am ready for the next chapter that this life has, and I will face it, not as a victim of circumstance, but as a survivor determined to thrive.
What Nik's wish are you thinking about and why?
Trip and travel help for life-saving surgery.
Brieanna
Brieanna: Fighting Epiteloid & Rhabdoid Sarcoma
I was just trying to be a normal 19-year-old kid. I worked 2 jobs security and housekeeping. I was trying to work towards getting my own car and my own place. My foot started hurting months before the actual diagnosis. I worked through the pain until I couldn't do it anymore. I called my mom and she said we would go get it checked out again. I had been to multiple hospitals trying to find out what was going on with my foot. Why there was a lump and why it hurt so bad. After months of being told it was a plantar fascia injury, I did not have much hope of truly finding out what was going on. So, my mom brought me out to the emergency department. They also did an x-ray but with the visual deformity they decided to do what my mom and I had been asking all the other places to do for at least 6 months. They did the ultrasound, and we were greeted by the entire cancer team. I was immediately admitted the following morning and they did an MRI. That's when the cancer teams and orthopedic surgeon came in and told me I had cancer in my foot. And that it had taken my entire foot over. We got the phone call confirming what was already suspected. It was cancer. They said it is both epithelioid and rhabdoid sarcoma. I was immediately scheduled for a below the knee amputation set for October 9th. Also noted in the PET scan, the lymph node in my left groin area also showed suspicious. So, during the amputation surgery they also took that lymph node. It came back positive for the same very difficult diagnosis of epithelioid & rhabdoid sarcoma. The same day I was released from the hospital to begin my life as an amputee at 19 years old. Then we got the news the cancer had spread to my lungs, and it was very concerning as it was a new spot and it measured 6cm. A treatment plan was built using tazeometostat a chemotherapy pill & after a lot of research ivermectin/membendazole.
I have had multiple issues with pains in my chest, dangerously low blood sugars, and really bad headaches. I pray every day that when I get the results that the cancer is going to at least be stable with no spread. I pray every day that the cancer is gone!! On the bright side I have not lost my hair, which has been a huge fear. I can deal with losing my foot but my hair I just can't even think about that. My life went from being a free teenager trying to get my life put together. To having a very rare VERY aggressive cancer. Working security, I got to see so many bands play at the concert venues! I have not been able to work either of my jobs at this point my life is on hold. My dreams are to get my prosthetic and try to restart my goals of a car and my own place. One thing that has been paramount in my life and now my cancer journey is my momma. She has been my Rock, my support, and the only person that has been right beside me through it all. Without her, I am not sure where I would be.
What Nik's wish are you thinking about and why?
I would really love to go see Bad Omens at the T-Mobile Center on February 26th. It would be my mom and me. It would be really amazing if we could get VIP/backstage tickets. To have just one VIP experience in my life where I can forget the diagnosis even if it's just for a moment. There are other things like seeing the ocean and the northern lights on my list. Bad Omens is my first!
Kevin
Kevin: Fighting T Cell All
I am 18 years old, just graduated high school and planned on attending SIUE to major in Electrical engineering. While working at T.J. Maxx, I started to experience symptoms. First it started with enlarged lymph nodes in my groin, which then proceeded to grow in my armpits and finally within my chest. I then started to feel very fatigued. My dad insisted we go to the emergency room. That's when I was told of my diagnosis of T-Cell Leukemia. Since then, I've been constantly in treatment and as of right now, I'm currently in my final phase of intensive treatment: delayed intensification.
What Nik's wish are you thinking about and why?
Probably a vacation with my family, we initially were very excited last year to plan out our vacation and get ready to go, but very soon after everything went left and I was diagnosed with cancer and our worlds turned upside down.
Kaite
Katie: Fighting B Cell Acute Lymphoblastic Leukemia & Avascular Nechrosis
I was 5 days into senior year at Shenandoah University in their fine arts conservatory majoring in Theatrical Design and Production (lighting). I had just moved into my first ever apartment with two best friends. Life was good. I awoke one morning with unbearable arm pain. A friend drove me to the ER and found I was deathly anemic and had leukemia! That started a full-on battle for my life, with more than 80% of my blood full of leukemic cells. I never got to live in that apartment and had to step out of college due to illness and out of state treatments. My mom has been with me every step of the way. We are very fortunate that she has been able to work remotely, and my university has been supportive. I completed my two senior capstones, designing all lighting for two live main stage shows from our remote location. It was hard, but we figured it out. My friends have graduated and moved on.
What Nik's wish are you thinking about and why?
I would like a trip to take my mind off all the medical challenges and treatments. My top wish is to go to see TaskMaster, a British comedy which I just learned is touring in various locations in the US (or to see their normal show which is in England). Secondly to go to see comedian Josh Johnson in person or backstage visit to the studios of Sam Reich's "Dropout" an American comedy production company in Los Angeles.
Calvin
Calvin: Fighting B-Cell ALL
Initially diagnosed with Acute Lymphoblastic Leukemia (ALL) at 4 years old and went through 3.5 years of chemo treatment. I survived and lived a normal life for the remaining childhood and teenage years, finished elementary, high school, and college.
I graduated college in 2023 and work for Capital One as a Software Engineer. I had a relapse and was diagnosed with the same Acute Lymphoid Leukemia (ALL), the same cancer I had 20 years ago. I went through various chemotherapy and immunotherapy treatments and now I am currently going through Bone Marrow Transplant (BMT) treatment.
The treatment and recovery for the BMT procedure should last 6-12 months. Thanks for reviewing and considering my application for the Nik's wish program.
What Nik's wish are you thinking about and why?
The Nik's wish I am thinking about are:
1) Family Vacation to Hawaii
My family has spent a lot of their time and hours taking care of me. This will be a good opportunity for them to take some time off, relax, and enjoy family time together.
2) Lakers Game - Floor Seats
I am a long-life Lakers fan. This will give me an opportunity to watch the Laker's game and meet some of the players who I really love to watch play.
Andrew
Andrew: Fighting Diffuse Midline Glioma of the Spine
Meet Andrew: I was Carefree. I had the use of both legs, just graduated Highschool with over a 4.0 GPA and I was ready to start college. I was ready to make my family proud and set an example for my siblings.
Now life is difficult, I deferred school and i am confined to a wheel chair. I feel dependent on my family. I have 2 younger sibling and I worry about being forgotten.
What Nik's Wish are you thinking about and why?
If i am fortunate enough to attend Howard next year, my wish is to enter the school as a business man and philanthropist. My wish is something that will help my family and others. I would like to start a faith inspired T-shirt business and donate 20% of the proceeds to Nik's wish and 10% to Lasalle Prep my high school. I would like my Dad to design the shirts and my Mom to help runt he business with me.
What i am asking for is startup support, mentorship and guidance in creating a name for myself and helping others.
Aviva
Aviva: Fighting Hodgkin's Lymphoma
Meet Aviva: Hi my name is Aviva and I am currently 23 years old. Before I was diagnosed with cancer I had finished my BA and psychology and was working on applying for my masters in social work. I was working two jobs one in a preschool and one at a mental health clinic but of which I loved! Before I was diagnosed I was extremely fatigued and it got to the point that when I wasn't working I was sleeping. One day I woke up with extreme chest pain and ended up in the ER later that night. Over night my life changed when I learned they had found a large tumor that had reached capacity in the cavity between my sternum and heart. The tumor had also attached itself to my lung. After two needle biopsies (one of which my lung collapsed and numbing and anesthesia did not work) a pet scan, and finally a surgical biopsy I was diagnosed with Hodgkin's Lymphoma. I got my port put in and started chemo. I kept working as long as I was able to keep my life as normal as I could. I finally had to stop when the chemo no longer allowed me to and that was deviating for me. Besides for the brain fog and terrible nausea and all the many horrible side effects that comes along with chemo. A really hard part for me was watching my friends move on with their lives. Going on trips, getting married, having babies, and knowing that I was stuck wear I was. Thank GD I made it through! I am back to working and I start my masters program in September. I have been working on regaining my strength and getting back to myself. I am truly grateful for how much I have matured and grown through this experience. I am definitely not the same person I was before.
What Nik's Wish are you thinking about and why?
I am not exactly sure yet but I know I want a cool experience! I love music and musical theatre and I have a passion for singing so maybe something around that.
TyQuareon
TyQuareon: Fighting Nasopharyngeal Cancer
Meet TyQuareon: At the age of 18 I had to show incredible strength and courage while facing the challenges of cancer treatments. Before my diagnosis I enjoyed going to school, hanging out with my friends, and I loved to ride four wheelers and play my PS5! But as soon as I learned about my treatments I knew that my life would be different. That meant traveling back and forth, weekly frequent hospital stays, painful side effects and missing out on the cool normal teenage activities. But, I knew that it had to get done if I wanted to live! Now that I am off my treatments I still continue to fight daily to live, enjoy life and I pray that the cancer does not come back. I took a hard hit at life due to the treatments my mom and I even had to relocate for treatments for almost 2 months living in a hotel. I am now doing my best to continue to live and recover.
What Nik's Wish are you thinking about and why?
My dreams of a special wish that would bring me hope, joy and a sense of normalcy back into my life is to one day be able to go to a live Chiefs Patrick Mahomes and Travis Kelcey football game and experience the excitement of seeing my favorite players in person. Throughout the cancer journey, football has been something that kept my spirits up and gave me something positive to look forward to. Watching the Chiefs on TV helped me get through long hospital stays and difficult treatments, but being there in the stadium feeling the energy of the fans and cheering for my team would mean so much more. I also would be able to create unforgettable moments with my family. I would love to take a picture with them and get a signed autograph!
Kamryn
Kamryn: Fighting Synovial Sarcoma
Meet Kamryn: I received my diagnosis when I was about to begin my fourth semester of my Master's program. I was working full time and in school full time. Before I received my diagnosis I was always busy and on the move doing something. I was going to football games at my sister's school, going out with friends, going to concerts, and traveling. I had been going to doctor appointments for a year before I received the diagnosis of synovial sarcoma. Many of the doctors had told me nothing was wrong or that I just needed vitamin supplements. It wasn't until a doctor finally ordered an MRI scan for me that I was able to finally get answers. Since I received my diagnosis, I have tried to not let it affect my life in terms of what I can and can't do. I am not someone who really likes to slow down or take breaks. However, I had to drop down to part time in school during my treatment which was difficult for me to accept. I continued to work after receiving my diagnosis and only took off what I absolutely needed to for my rounds of chemotherapy and surgery that I just received in November 2025. In some ways I think my life has not changed as much physically as it has mentally. Having to live with the weight of knowing you have cancer and it being such a scary concept to fully grasp and accept has been the most challenging. I try to keep up with everything I still want to do while living with this diagnosis. I am on track to graduate with my Master's in Special Education and applied behavior analysis in summer of 2026. I am surrounded by so much support from family and friends which has been so helpful in dealing with my diagnosis.
What Nik's wish are you thinking about and why?
The Nik's wish that I am thinking about is Hawaii. I have always loved everything about the outdoors, swimming, nature, and I love to travel. I love being in the water so much that I actually got a tattoo of a wave on my ankle when I was 18 years old. I think it would be so fun to be able to experience a vacation away from everything that I have going on. I never truly gave myself a break from everything when I received my diagnosis. I continued on with working and completing my schoolwork and just added cancer and all the terrible things that came with it onto my plate. I think that taking a trip like this could give myself and my family who have been there through everything a chance to really relax and just have fun with each other.
Bianca