Preparing for your infusions
Plan your time accordingly
Each infusion of POTELIGEO takes at least 1 hour. This does not include the time it takes for travel, preparation of the infusion, and monitoring after your infusion. If you’d like to better understand how long these steps may take, contact your infusion center for more information.
Commit to your infusion schedule
You may need to adjust your everyday routine to stick to the infusion schedule. These tips can help you stay on track.
Review medications
Tell your doctor about any prescription or over-the-counter medications you take, as they may interfere with your infusion. Ask a healthcare professional if there are any medications you should take prior to your infusion that may help decrease your risk of side effects like rash or drug eruption (skin reaction).
Getting comfortable on infusion day
Try activities to keep you busy. Remember, a trained healthcare professional will be available to assist you and answer any questions you may have during your treatments.
Watch a TV show
Call a family member or friend to catch up
Read a book
Listen to music
Pick up a new hobby
Wear warm, comfortable clothing |
Pick your clothes out the night before. Wearing loose-fitting, warm clothes like a sweatshirt or sweatpants will make it easier for you to stay warm and comfortable while your healthcare professional gives you an infusion and checks your vital signs. Being warm and comfortable will also make the infusion more enjoyable for you. |
Consider bringing a friend or family member |
Depending on your infusion center, you may be able to bring in a family member or a friend for company or support. It is recommended that your loved one drive you to and from your first few infusions. |
Find your support system |
Beyond the person accompanying you to your first few infusions, it’s important to find a group of people you can lean on—a support system. Your support system may include people who are there for you in your daily life, like your family, friends, and the cutaneous T-cell lymphoma (CTCL) community. If you aren’t sure who you would include in your support system or you’d like more information about engaging with the MF and SS community, reach out to your doctor for help. |