Being admitted for a stem cell transplant can feel overwhelming. There's a lot happening---new faces, unfamiliar equipment, and routines to adjust to.
Your care team is here to support you every step of the way.
| Role | What They Do |
|---|---|
| Doctors | Oversees your treatment and medical decisions |
| Nurse | Provides daily care, medications, and education |
| Pharmacist | Manages your medications and dosing |
| Social Worker | Supports emotional, financial, and family needs |
| Psychologist | Helps with coping, stress, and mental health |
| Nutritionist | Guides your eating plan and nutrition goals |
| Child Life Specialist | Supports children through play and emotional care |
| Care Coordinator | Helps organize appointments, resources, and communication |
Each morning, your care team will visit your room for rounds.
This is a great time to:
Ask questions about your treatment plan
Share how you're feeling
Raise concerns or changes you've noticed
Get clarity on next steps
Blankets -- hospital rooms are often cold
Mattress toppers or sleeping bags -- hospital beds can be uncomfortable
Hand lotion (like Cavilon) -- the air is dry, and frequent handwashing can cause irritation
Entertainment -- books, puzzles, playlists, or crafts help pass the time
Chargers and headphones -- stay connected and entertained
Comfort items -- photos, small decorations, or favorite snacks
Ask how you can make your room your own (photos, art, lights, etc)
Set realistic expectations -- hospital stays can be long and unpredictable
Plan for breaks -- caregivers need rest too; ask for about support services or respite options
It's okay to speak up. Whether it's a physical symptom, emotional need, or something that doesn't feel right---your voice matters.
Ways to raise an issue:
Use morning rounds to ask questions and share concerns
Keep a notebook or notes app to track symptoms, questions, or changes
Use "I" statements like "I've noticed..." or "I'm feeling..." to express your experience clearly
Ask for a huddle or quick team check-in if something feels urgent or confusing
Bring a caregiver to help advocate and remember details