One of the world’s top cancer centers has a special place for young people. It’s the MD Anderson Children’s Cancer Hospital. Here, children, teens and young adults get cancer care tailored to their age, size and development. Through clinical expertise, cutting-edge therapies and support programs for patients and families, we offer hope for the future.
Why come to the Children's Cancer Hospital?
MD Anderson is one of the world’s best cancer hospitals. U.S. News & World Report has ranked us as one of the top two cancer centers since the survey began more than 25 years ago, and thousands of patients from around the world come here for care each year. The Children’s Cancer Hospital plays an important role at MD Anderson. What makes us stand out?
- Our primary focus is cancer. We see more types of cancer than any other children’s hospital in Texas, and our oncologists treat more rare cancers in a single day than most physicians see in a lifetime.
- Our pediatric oncologists specialize in specific types of cancer. This gives them an extensive amount knowledge to call on when building treatment plans.
- We’re home to many of the world’s leading cancer researchers. Our patients benefit through clinical trials and new treatment methods.
- We have technologies and therapies most hospitals can’t offer. Patients have access to state-of-the-art treatments like proton therapy, BrainSUITE, robotic surgery, PET/CT fusion imaging, and unique surgeries for rare cancers. We also offer novel therapies for patients fighting difficult or aggressive tumors.
Cancer takes a huge toll on the lives of patients and their families. From educational programs to support groups, MD Anderson is dedicated to helping patients and their families through this difficult time.
Patient- and family-centered care
To ensure every child receives the best care, we welcome parents and caregivers as vital members of the patient’s care team. From their very first encounter, we want family members to be actively involved their experience at the Children’s Cancer Hospital, making decisions and partnering with the care team whenever possible. We’ve also established four patient and family advisory councils. Through these groups, we get ideas and suggestions about how to improve our patient and caregiver experiences.
Some of the diseases we treat:
- Brain Tumors
- Endocrine Tumors including:
- Ewing's Sarcoma
- Germ Cell Tumors
- Hematology Disorders
- Liver Cancer
- Soft Tissue Sarcoma
- Wilms' Tumor
[I] know the joy of belonging to a growing second family - my cancer family, the patients, caregivers and care team I met during my cancer treatment. They are the people who walked this journey with me and who I now walk with as an experienced traveler to guide, help and support.
MD Anderson Resources
When my daughter Aaliyah was diagnosed with Ewing’s sarcoma in November 2016 at age 9, I was shattered, vacillating hourly between two nearly unspeakable fears: the fear that she would not survive, and the fear that during the last weeks or months of her life, she would suffer relentlessly.
Suddenly, thrust into a life I barely recognized, I struggled to navigate what moms who had gone before me kept assuring me would eventually become “a new normal.” I resisted that idea. The last thing I wanted was for life in a cancer hospital to be our new normal.
But time marched on, as it tends to do, and our family did develop a new normal. Eventually, it didn’t feel so difficult to breathe, to eat, to smile, to laugh. Here’s what I recommend to other parents ushering a child through cancer treatment.
Take care of yourself
In the beginning, this feels next to impossible. For the first several weeks, I could barely sleep, eat or remember to take a shower. Friends brought my favorite foods to the hospital, but most of it went to waste due to my nonexistent appetite. I tolerated orange juice, so I drank it constantly, figuring that at least I was getting calories and vitamin C. I lost nearly fifteen pounds before my appetite returned.
While I couldn’t physically nurture myself at first, I did tap into ways to nurture myself emotionally and spiritually. I spent time journaling, praying and sharing my heart online. I also had friends on standby to take my emotionally fragile phone calls at any hour of the night, whenever I found myself sleepless or panicked or overwhelmed.
Some days, though, nothing helped. On those days, I found a place to let myself cry. Sometimes, it was in my closet, my face scrunched into a pillow to muffle the sound. Other times, it was in my car in the hospital parking garage, windows sealed tight as I sobbed with an anguish known only to other parents who have faced a life-threatening illness with their child. Yes, those tears hurt. But they also healed.
So, hydrate. Eat when you can. Nurture your emotional and spiritual health. Your wellbeing will promote your child’s wellbeing.
Find your people and hang on tight
You will identify your people almost immediately. They are the ones who keep texting and calling and showing up — even when you don’t answer your phone, and you don’t text back, and all you do is cry when they do show up.
Let these people know what you need. Friends and family stocked our fridge with groceries, braved Houston traffic to bring our other kids for hospital visits, arranged for weekly house cleanings, provided meals for months on end, organized prayer chains, and gathered donations, cards and gifts. The people who position themselves in your life during this time and stay there really want to help, so give them opportunities!
Use the internet wisely
One night, I couldn’t sleep, so I decided to search for an online support group for parents of kids with Ewing’s sarcoma. In the process, I read one too many stories that fed all of my deepest fears.
There is a time and a place for Google, but it can also cause a lot of anxiety, so use it judiciously. If you’re tempted to do a little online research, consider sending your questions to a trusted friend who can sort through the information and pass along only the information you actually need.
Be kind to yourself
Guilt will haunt you, if you let it. I struggled with all sorts of guilt: guilt that I didn’t notice the enormous tumor in my daughter’s stomach, and guilt that I wanted to escape the hospital room and go on a run even though she was stuck there, attached to an IV pole, with a bedpan in her lap. Guilt that I wasn’t home for our other kids, and guilt that when I was home, I didn’t have the energy to interact with them the way I wanted to. I felt guilty that I literally couldn’t bring myself to vacuum a single room, that I hadn’t cooked a meal for my family in weeks, that I wrote thank you notes and never mailed them, and then I stopped writing them altogether.
Over time, however, I realized that no one is born equipped to deal with a cancer diagnosis. One day, life is normal; the next, you are fighting for your child’s life. So try to let go of any misplaced guilt and be kind to yourself. You will pour every reserve into the fight, and that’s exactly what you’re supposed to do. But, remember this: a cancer diagnosis doesn’t mean you have to stop living or smiling or laughing. Your child needs you to do those three things now more than ever.
When our daughter was diagnosed, her tumor was massive, and her future looked grim. But Aaliyah rang the bell symbolizing the end of her treatment on Sept. 9, 2017, and by the grace and power of God, and through the expertise of her care team at MD Anderson, her cancer was eradicated.
Each new morning brings new hope. Cling to that, and find another reason to smile before the day is out.
Request an appointment at MD Anderson online or by calling 1-877-632-6789.
The Children's Cancer Hospital business hours are 8 a.m. to 5 p.m., Monday through Friday.
713-792-5410 (Current patients)
877-632-6789 (New patients)