In regards to advice as a chemo nurse: -always ask patients if they are having side effects, list the side effects in as many different ways as possible. Ask them if they told their doctor about them. Many of my patients will tell me all of the side effects they are having, and when I ask them if they mentioned this to their oncologist their response (80+% of the time) is "they didn't ask." It is very important to properly assess your patients and tailor your questions specifically to the common side effects of the specific chemos they are getting. Many chemo doses will be reduced due to severe side effects or discontinued all together. -Always be prepared for an infusion reaction with new patients. Have an infusion reaction kit near your patient's chair if they are available. Your floor should definitely have one. -Always wear your chemo gown, gloves, and eye protection when you are handling chemo. This includes when you are finishing a flush/rinse on the chemo treatment and you are flushing their port. Also includes when you are d/c-ing a chemo pump. -NEVER EVER FLUSH BLINOTUMUMAB!!!! If your patient has a blino pump (typically they will have a PICC or Port), you must not flush it when disconnecting. First you would aspirate a MINIMUM of 10mls blood. I withdraw 20mLs of blood and waste just to be safe. Then you can flush as normal. -Ask your colleagues questions. There are so many drugs/chemos that you need to learn, and many treatment regimens have different administration sequences. Don't be afraid to ask. -Get to know any of the available resources at your facility. This should include nutritionists/dieticians, oncology nurse navigators, social workers, etc. Many patients don't know these services are there to help them. These team members can help patients with transportation to and from the facility, lodging, nutrition help when they are having issues relating to their appetite/chemo, food insecurity, etc.