Your transplant team prescribes anti-rejection medications to keep you healthy and to prevent your immune system from attacking your transplanted organ.
After you’ve had a transplant, your body sees your “new” liver, kidney, heart, lung, or intestine as something foreign.
Taking your transplant medications every day—correctly and on time—is one of the most important things you can do to protect your health.
Filling your weekly pillbox is a big step toward taking charge of your own health.
Life is busy! Here are some tips for remembering to take your meds and finding a schedule that works for you.
As you take on more responsibility for your transplant health and daily medications, learning how to handle pharmacy visits and refills is a big step toward independence.
Getting labs is a normal part of life after having a transplant.
Even though you take medications to keep your immune system calm, rejection can still happen.
A Primary Care Provider (PCP) is your main medical provider when you move into adult care.
Taking care of your transplant health —and you! —may seem to be a lot, but you’ve got this!
After your transplant, you take medicines to protect your transplanted organ.
Being active with your family or exercising with peers should be a part of healthy living – and it’s fun!
Learn how to protect yourself against STIs.
Living with an organ transplant – a heart, lung, liver, kidney, or intestine - is a lifelong journey.
Your transplant story is part of who you are—but how, when, and with whom you share it is your choice.
Self-advocacy - learning to communicate independently with your transplant team- is a big part of transitioning to adult care. Many teens and young adults build these skills over time, with support from their caregivers - and lots of practice.
Taking the Lead in your Transplant Care: Self-Advocacy