At the MACC Fund Center, we treat sarcomas in our musculoskeletal oncology program, a part of the solid tumor oncology program.
Our team includes pediatric cancer experts focused on sarcoma treatment. We provide complete care at each step, starting with the initial diagnosis and even through relapse. We regularly care for more uncommon sarcoma diagnoses.
We work closely with pediatric experts like:
- Orthopedic oncology surgeons
- Radiation oncologists
- Pediatric Interventional Radiologists
During Diagnosis
To us, each patient is a person. We create care plans tailored to your child — from initial surgery, other treatments and follow-up and recovery. The entire team has weekly meetings to ensure we are all up to date on your child's needs. We can also help you learn about and enroll in sarcoma clinical trials.
When needed, we evaluate the cancer cells with genetic and molecular testing. This includes a visit to the COMPASS clinic. You’ll learn about the molecular changes in your child's tumor.
The COMPASS team will review suggestions for adding a targeted treatment to your child’s care plan. Often, we can arrange for your child's main oncology team to deliver the treatment.
Based on the types of care they need, some kids access our Fertility Navigation Program. This is a way to discuss their options for having kids in the future.
In the Hospital
Prompt care and sometimes aggressive treatments are key to the best outcomes for sarcomas. If your child needs to be in the hospital, our care teams create a welcoming, familiar, healing environment. You'll meet daily with our medical teams to get a status update. They'll check that you and your family are comfortable.
Our expert nurses check in with you and your child throughout the day to ensure you have everything you need. To make your time with us as comfortable as possible, we have a:
- Family lounge
- Fully stocked kitchen
- Laundry facilities
- Young child playroom
- Teen center
After Treatment
Our team is here for your family after your child finishes their cancer care. Continuous follow-up care is essential for kids with sarcomas. They may have side effects that come on later, or other cancers that grow.
You can contact your care team or the musculoskeletal oncology program. We can answer questions about long-term care, future screenings and maintenance. You'll also have continued access to counseling, support groups and other resources.
Kids recovering from a sarcoma may need rehabilitation services. This may include physical, occupational and speech therapy.
Young adults who are currently receiving or have received cancer treatment can get support through our young adult oncology group. The group meets monthly to help young adults (18-39) with cancer or recovering from it to share experiences and plan activities.
After treatment, you'll enter the bridge to next steps program. This program helps you and your child transition into post-therapy care. The program consists of two visits. You will meet with a survivorship provider and a psychologist. They'll provide education, a summary of care and support.
Sometime after two years after your child completes treatment, they can enter the Next Steps Clinic. This long-term follow-up program cares for cancer survivors. Our care team monitors for recurrence, manages late effects and promotes overall well-being.