This page was printed on:
Welcome to our question and answer page for parents and caregivers of children who need a transplant.
We address the most common information requested by parents or caregivers seeking a transplant for their child and those who want to know more about their child’s treatment. If you have a more general interest in transplantation, we hope you find it helpful as well.
A guide when your child needs a transplant
When you get the news that your child needs an organ transplant, you may react with shock or surprise. Dealing with a child’s sudden or chronic illness can be difficult for any family. You will have many questions, and you may not know where to ﬁnd answers.
The most important thing to know is that you are not alone. In fact, we want to be part of your support group! Call the OPTN's Patient Services line at 888-894-6361. We are parents of young organ transplant recipients. We worked with experts in the transplant ﬁeld to create this guide. It explains the transplant process from a parent’s viewpoint. The guide also brings up issues you and your family may face before, during, and after the surgery. This guide serves as an overview and a place to start. Reach out to your transplant team as you continue on this journey.
We started this project by asking transplant parents a simple question: What is one thing you know now that you wish you had known in the beginning? We received many responses through social media and other sources. We did our best to provide answers and to point to trusted resources that worked for us. We address issues for infants, toddlers, teens, and everything in-between. We tried to focus on topics we found to be important. We also know that each transplant journey is unique. Your doctors and transplant team are the best source of information about your child’s case.
This guide has two sections. The ﬁrst section walks through the transplant process from the time you learn that your child needs (or may need) a transplant. We cover many issues parents and families may face before and during the transplant. These include ﬁnancial concerns, explaining to your child how deceased donation works, and other important issues. The second section offers tips to help you and your child manage life after the transplant. There are many new concepts to learn. We deﬁne terms and share online and print resources you can use.
Here is one term that you may want to know up-front: A pediatric patient is a transplant candidate placed on the U.S. transplant waitlist before their 18th birthday.
If you have more questions or suggestions to improve this guide, we welcome your feedback! And if this guide is helpful to you, please let other parents know about it.
The U.S. Organ Procurement and Transplantation Network (OPTN) Patient Affairs Committee (PAC)
Before and during the transplant
The transplant process
Your child needs a transplant. What now? The path to organ transplantation is a journey. Your family’s transplant journey may begin when your doctor tells you that your child needs an organ transplant, or when you ﬁnd out that your child suffers from end-stage organ disease.
There are seven basic steps in the process before and during the transplant. The process continues after the transplant, which we cover in Section 2.
- Find a transplant hospital
- Get to know your transplant team
- Transplant evaluation
- The waitlist
- Waiting for a match
- The call (organ offer)
- Transplant surgery
Each of these steps is unique to your child’s condition. Your child may have a chronic illness in which a transplant is planned for months or years in advance. Or your child may have an acute illness and need an urgent transplant within days or weeks. In these cases, the ﬁrst steps may be compressed and require quick decisions with the support of the transplant team.
Find a transplant hospital
A transplant hospital is a hospital with health care providers who specialize in all aspects of transplant medicine. All transplant hospitals in the United States are part of the OPTN. Not all hospitals perform transplants and not all transplant hospitals do pediatric transplants.
Your child’s doctor can refer you to a transplant hospital that:
- Specializes in your child’s medical condition,
- Is most conveniently located for your child’s and family’s needs
- Will work with your insurance
Go to the Scientiﬁc Registry of Transplant Recipients (SRTR) website to ﬁnd and compare transplant centers. You can search for U.S. transplant centers by organ and zip code. You can see how many transplants were performed and compare outcomes for adults and children who received transplants at a particular center.
If you have concerns about your transplant center, you have a right to get help or even a second opinion. Feel free to call the OPTN Patient Services line at (888) 894-6361 if you would like to discuss your options with a patient services representative.
Get to know your transplant team
The transplant team will oversee your child’s care. Team members will help you take care of your child’s health issues, identify and create your support system, and work on your ﬁnancial plan. Each transplant hospital is different, and so are the team members.
These are some of the roles that you may ﬁnd:
- Assists and guides you and your family through the transplant process
- At most hospitals, is your family’s point-person
- Helps you meet requirements to add your child to the transplant waitlist
Transplant doctors and nurses
- Manages your child’s care and arrange for tests
- Provide you and your child with specific transplant information
- Performs the operation when an organ is available
- Works behind the scenes to manage the team
- Helps you ﬁnd support and services during your child‘s hospital stay
- Provides letters for work or school, if needed
- Helps a child ﬁnd ways to cope and reduce stress during the transplant process
- Works with a child on taking medications (particularly during teenage years)
- Works with your doctors and discusses your child’s transplant medications with them
- Helps you ﬁgure out how to ensure your child takes all required medications
Registered dietitian nutritionist
- Cares for the patient before, during and after transplant
- Develops nutrition support regimens (tube feeds and IV nutrition), and vitamin and mineral supplements because good nutrition status is vital for a successful transplant
- Helps you create a plan to cover costs before, during and after your child’s transplant
- Advises you on insurance issues, helps you ﬁnd ﬁnancial aid, and explains copay charges
- A social worker also may perform some of these duties at your center
Child life services staff
- Helps children and families cope with chronic illness and time spent in the hospital
- Provides age-appropriate support, including medical play therapy, to explain the transplant process and help children deal with their feelings
- May help arrange schooling options for children in the hospital
- May include chaplains or comfort (palliative) caregivers
Organ procurement organization (OPO) staff
- Identify potential deceased donors and get authorization for donation
- Work with your hospital and the donor hospital during the matching and organ procurement process
In their various roles, transplant team members are there to help you and your family. You can bring any concern to someone on your transplant team. For instance, if you need to take time off from work to care for your child, your social worker or transplant ﬁnancial coordinator may know about a resource that can help.
“At the time of my daughter’s first transplant, it would have been nice to be able to talk to another parent going through it.” — Heather Snow, liver recipient parent
Your transplant team will order medical tests and lab work to evaluate your child for a transplant. These include blood tests, tissue typing, organ-speciﬁc tests and a complete health history. Other tests gauge psychological readiness and social support. Results will help the team decide if your child meets the criteria to be a transplant candidate at their hospital.
The team also will decide how to best manage your child’s medical condition and when your child will be listed for an organ transplant.
The transplant team reviews all of the test results and input from team members to come up with your child’s treatment plan. This includes deciding which patients to add to the national transplant waitlist. The team must inform you, in writing, about their decision to proceed to transplant (or not) and the reason for the decision. The team at your transplant hospital will always be your first and most complete source of information regarding your current medical condition and treatment options. If you have other questions or comments, contact the OPTN Patient Services line at (888) 894-6361 or submit them here.
The transplant team looks at a range of medical, surgical, psychological, developmental, and social factors when listing a patient for organ transplantation. If your child is accepted as a candidate, the transplant hospital will place your child on the national OPTN waitlist. OPOs and your transplant hospital will work together to ﬁnd a match. There is still a possibility that not every transplant candidate will receive an organ because deceased organs are a scarce resource.
If your child needs a liver, kidney, or lung, a living donor transplant is possible at some hospitals. If you, a family member, or a friend wants to be a living donor for your child, you should contact the transplant hospital for information on how to start the evaluation and testing for this process.
“Keep your focus on getting your child healthy. Advocate for your child. Trust your team, but you know your child best. Do your research. Don’t be afraid to ask a million questions and challenge the doctors for answers. Find support from other parents of children with similar issues.” — Amy Antonio-Claussen, liver recipient parent
You may be able to list your child at more than one transplant hospital. This is known as multiple listing. Check OPTN policy for the rules, which vary by organ. You also can ask your transplant team for more information. If you choose to do so, you will need to ensure that you can easily travel between your home and the hospitals. Each hospital will need to conduct a new evaluation. You also will need to check on insurance coverage. Listing a patient at more than one hospital in the same area may not increase chances of transplant.
If your family needs to ﬁnd a new transplant hospital, your new hospital may have to perform a transplant evaluation as well. Waiting time will carry over to the new hospital, but check with your new transplant team to make sure.
The organ transplant system follows OPTN policies, which set organ allocation rules.The national transplant community works together to create and update OPTN policies.
The national donation and transplantation computer system stores medical information about donors and candidates. It uses rules to match organs with patients on the waitlist. Rules differ for each organ. Some of the rules help children who are waiting rise higher on the list because of their disease, complications, or their weight or size.
It may help a child to join the waitlist before they turn 18, depending on which organ they need.
It deﬁnitely affects kidney allocation due to something called pediatric priority. If a child starts dialysis before their 18th birthday but is added to the waitlist after they turn 18, they would not receive priority. Review OPTN kidney policy and check with your transplant team to see if this is an option.
Depending on the organ a child needs and the nature of their illness, there may be other factors that could increase their chances to receive a matched organ. The OPTN deﬁnes those factors as exceptions. They may vary over time, in response to a child’s needs. Your transplant team can advise you. See the OPTN website for a list of OPTN policies that address the needs of some transplant candidates under age 18.
The team’s goal is to make sure that transplant remains the best option for a patient. There may be times when a patient is too sick for transplant.
Sometimes, the transplant team may have concerns that a family cannot manage all of the care required for a successful transplant. The team may discuss this with the family and examine options or services to provide additional care.
If the team decides that a patient is not eligible for transplant, they will explain why and will work with the family to help ﬁgure out the next steps.
Waiting for a match
“When my son was listed, we set up a checklist of everything we needed to do in order to get out of the house and on the way to the hospital.” — Dorie Neuhaus, heart recipient parent
Waiting for a match can be emotionally diﬃcult for your child and your family. See the Parent’s Toolkit later in this section for some suggestions on how to handle emotional concerns.
Some patients wait for a transplant for several months or years. Make sure that your child has a consistent daily schedule during this time. If your child is waiting for transplant at home, talk with your medical team and follow their guidance about activity limits. If a child is waiting for transplant for an extended time in the hospital, talk to the child life specialist. The specialist will provide a schedule and activities appropriate for the child’s age, developmental level, and psychosocial needs.
The transplant team will monitor a child’s condition as they wait for an organ offer. Some children could become more ill and may need to wait in the hospital. If a child is already in the hospital, they may need to move to the intensive care unit (ICU) to wait.
In other cases, transplant may not be the best option for a while. The transplant team may want to wait until the patient’s condition improves. If that happens, the transplant team could change the status on the waitlist from “active” to “inactive.” The patient would not receive organ offers during time on inactive status.
If a patient’s health worsens and transplant is no longer an option, the team could decide to remove them from the list. This is a tough call, but doctors do not want to put a patient through a transplant if it would not be a success.
You have the right to know about all of these decisions. Your transplant team must inform you when they add your child to the waitlist, when they remove them, and the reason they were removed. If you have other questions or comments, contact the OPTN Patient Services line at (888) 894-6361 or submit them here.
Get ready while you wait
Waiting for a transplant can make you feel like you, your child and your entire family are living life on hold. During this time you may feel that there is nothing you can do. Getting ready for transplant can help to provide a sense of control as you wait.
- Keep a records binder or use a smartphone app to manage all your child’s medical information, appointments and medicines.
- Use calendars to keep track of family business (bill-paying, home maintenance, etc.). Checklists also can help.
- Find out the hospital’s visiting rules, ﬁgure out where to park and note details about where to ﬁnd food and where you can store your bags.
- Write down your questions when you think of them so you’ll have them ready the next time you meet with someone on the transplant team. Prepare to discuss your concerns openly. Take notes during meetings and appointments.
- Discuss and decide how you will handle diﬃcult decisions in your child’s care.
- Create a “go” plan and practice it with your family, so you are ready to get to the hospital when it is time for your child’s transplant. Pack those bags! Make plans for care of your other children, your home and pets.
- Set aside money for travel or lodging so it will be easier to get to the hospital.
- If you will be driving to the transplant hospital when your child is called for transplant, plan your route to adjust for driving during the business day and rush hour versus a Sunday morning. Find alternate routes. If you are driving to the airport, make sure you have the same type of plan.
- Plan for you and your child to stay near the hospital, if asked.
- Plan where you will stay after the transplant. Most transplant hospitals ask that families stay in the area for a few weeks after transplant if they live an hour or more from the hospital. Your social worker is the best resource for convenient and affordable lodging.
Keep in touch
- Provide all your home, work and cell phone numbers to the transplant team so they can reach you at any time, night or day.
- Gather contact information for all family and friends and keep it handy. Consider how you would like to provide updates to your circle. If using social media, be cautious about privacy concerns when sharing sensitive information. Review these social media guidelines to learn more.
- Find a primary support person or divide tasks among your group to cover family needs.
- Tell relatives, friends, clergy and others what’s going on in your family’s life. You may want to ask someone in your circle to do that on your behalf.
- Reach out to your transplant coordinator, social worker, psychologist, or your child life specialist to help you with how you are feeling, your concerns, and worries. Talk to them about what you and your family are going through as you wait for transplant.
Many families and transplant recipients ﬁnd help by staying in touch with people in the same situation. Here are some tips to ﬁnd people with whom you can relate.
- Your transplant hospital may have online or in-person support groups; ask them for details.
- Talk to other parents that you may meet while your child is in the hospital. Those relationships can be some of the longest-lasting and most helpful support you’ll ﬁnd. Other transplant parents may be aware of support resources that you don’t know about.
- You may not ﬁnd many people in your area whose experiences are similar to your own, but there are many active communities online.
- Sites like transplantbuddies.org serve as a support system for transplant recipients and their families.
- Talk to organizations that advocate for organ-speciﬁc transplant issues. Some of these groups run their own support forums on social media sites like Facebook.
After you’ve found your way into a support system, don’t be afraid to ask if anyone in that system is aware of a group that might ﬁt your needs more closely.
The call (organ offer)
Your transplant team will contact you when an organ is available that is the best match for your child.
When you arrive at the transplant hospital, get ready for more tests to prepare your child for surgery. At this point, you and your child may feel excited, anxious, afraid, or peaceful. You also may grieve for the family who lost someone, but feel grateful that your child will receive the gift of life. Donor information is conﬁdential and you won’t receive details about the donor, such as sex or age.
You may ﬁnd out that ﬁnal tests show that the organ is not suitable for transplant. You and your child may be disappointed to leave the hospital without a transplant. Your transplant team will use only organs that will give your child the best chance for a good outcome, but this kind of uncertainty can be hard to handle. Your reactions might include anxiety, grief, guilt, depression, anger, and confusion, to name a few. You should lean on your transplant team to help you deal with your emotions. Your transplant coordinator, social worker, child life specialist, psychologist, chaplain, and other team members can help you ﬁnd strength so you can support your child and family.
“The ‘call’ is an overwhelming experience. There is absolutely nothing they can tell you that will prepare you for the emotions that take over when the call comes in.” — Dorie Neuhaus, heart recipient parent
Each transplant is unique, but the surgery generally lasts from four to nine hours. It may take even longer for patients receiving more than one organ. All patients are placed on a breathing machine (ventilator) for the operation, but many patients will need to stay on the breathing machine after surgery too. Your child will likely spend time in the ICU (intermediate care unit).
Each patient recovers differently. Ask your transplant team when your child can expect to eat, walk, and return to normal activities after transplant.
Caring for your family and yourself
A parent is the foundation of any family. Balance the needs of your children with your own needs, and be sure to take care of yourself so you can be there for them. Being in a constant state of crisis, even for a short time, can make you less able to support your family. If you spend your time worrying about the “what-ifs,” it may be tougher to deal with issues happening right now.
Parenting can be a challenge even with healthy children, so having a child who needs a transplant can add extra stress. Here are some points to keep in mind:
- Raising a family is a long-term project. Even though things are not how you wish them to be right now, it will be possible to find a new normal.
- Forgive yourself if you cannot be present for everyone all the time. You have a lot going on. Sometimes, you may just need a short break.
- Take a brief mental vacation when you can, even if for a few minutes at a time.
Manage your reactions
Keep tabs on your emotions. It can be hard to manage your feelings and keep them steady, but it will help you focus on all the other tasks you need to handle. You can show your children a positive example of how to handle tough situations. They can carry your example with them as they grow and develop toward greater independence.
“I wish we had known earlier about getting our family involved in counseling. After the physical, the mental and emotional aspects of transplantation need just as much attention.” — Tim Harrod, heart recipient parent of twins
Each of you will have a different emotional reaction to transplant. Some parents feel guilty that their child needs an organ transplant, even more so if the cause is genetic. Others may be highly anxious, or even suffer from post-traumatic stress. You may need to get counseling during or after your child’s transplant.
There are no right or wrong feelings, but there are people to help. Seeking support is healthy for the whole family. Talk to your transplant team to ﬁnd out about therapy that may be available to you. Your health plan may cover counseling, even if you need it long after the transplant. Faith-based services may be another option for you.
If you are concerned about how hereditary medical issues may affect your other (or future) children, seek out genetic counseling to learn about the risks.
Getting help also should include accepting people’s offers to help. Whether it’s watering the plants at home, bringing you some food, playing cards with you, or something else, it is important to let others in during this time and not try to carry the weight yourself.
You may hear the phrase, “Transplant is not a cure.” Transplant is a treatment that may provide a better quality of life. Most transplant recipients require a lifetime of medications and will need to manage a chronic condition. There may be activity limits, side effects and frequent contact with doctors and nurses. Life is a balance. Help your child learn coping skills so they can handle these realities.
Not every family ﬁnds it easy to laugh together. Connect with your loved ones with a smile, a laugh, or a good memory when you can. It can help to smooth the path to healing and make the hurdles easier to face.
There will be a lot of complex information coming at you. Most of us don’t recall what we hear in a doctor’s oﬃce. It’s especially tough when you ﬁrst learn about your child’s illness and need for a transplant. Keep asking questions until you understand. Your transplant team will explain information that you are unsure about so that you can help your child and family.
Write questions down before doctor’s appointments or rounds. If in the hospital, ask for a pen and paper, use a whiteboard, or keep notes on a phone or tablet. Sometimes it is useful to record doctors (ask ﬁrst) and listen later when you can digest the information more easily.
It may be helpful to have a trusted person come with you to appointments in addition to your spouse or co-parent. They can serve as another set of ears to take in the information and help you process it later.
“One of the hardest things I see families struggle with is the uncertainty. When a child is sick enough to be in the situation of even talking about a heart transplant, families are in crisis mode. We do our best, I hope, to provide a lot of information about what a transplant looks like and what the future will bring, but there is no way a family could realistically either fully understand that or that we could really fully explain it.” — Dr. Jeffrey Gossett, Pediatric Cardiologist
Turn to transplant social workers, child life specialists, psychologists and psychiatrists to help you plan for life after transplant.
- Setbacks happen. Recovery can have its ups and downs. There is no timeline for when to expect grief, guilt, new concerns, new questions or old fears to pop up.
- Speak with your transplant team about when and what activities your child can pursue. See the After the transplant section for more details.
Understanding all the new medications, terms, processes and people involved in a transplant can seem overwhelming. Learning about these things will help your child live life to the fullest. You also will be able to pass along your knowledge.
Explaining the transplant process and deceased donation to your children
Your child will probably have a lot of feelings about the upcoming surgery. Children may feel anxious or angry about so many doctors’ visits, lab tests, and side effects that other children do not have to face. They may show frustration with their health limits and with the need to wait for transplant.
To help explain the process and why many patients have to wait for a transplant, read What Every Kid Needs to Know with your young children. Visit https://unos.dokshop.com/ to access the booklet and to ﬁnd other free resources for transplant patients.
Child life services can point you to other resources or activities for younger children.
You may get questions about where organs come from. One way to describe transplantation to younger children is to explain that a transplant is like changing the batteries in a favorite toy. Most children will have seen a parent do that or even helped their parents “replace a part” that no longer works.
Reinforce the idea that receiving an organ, either from a deceased or a living donor, is a special gift. Older children and teens may express a concern that “someone had to die for me to get an organ” through deceased donation. You can explain the events that led to the donor’s death would have happened, whether or not your child needed an organ.
Siblings may feel hurt or sad that Mom and Dad can’t spend as much time with them. Each person shows feelings in different ways, depending on their age and personality. Sometimes it’s hard for siblings to express negative feelings. They may hurt or ignore each other’s feelings without meaning to do so. One or more family members may need time to process their emotions.
As a parent, you may need extra time as well.
Talk with your children. Ask them questions. Engage in active listening, and be present in the moment. Be open to all questions and let your children know it is OK for them to have lots of different feelings about what’s going on, including feelings they can’t explain.
Focus on what they say and how they say it. If you see changes in the way your children act or behave with each other, you may want to reach out for support from a social worker, psychologist, or counselor.
Financing your child’s transplant
Thinking about paying for a transplant and all of the costs involved can raise many questions and concerns for your family. Your ﬁnancial coordinator or social worker can help you create a ﬁnancial plan.
If living organ donation is in your child’s future, there are programs to help pay for the living organ donor’s expenses. Your transplant team can tell you more about those groups.
What follows are some common options to pay for transplant expenses. Most families use more than one funding source to pay for expenses not covered by health insurance. Some of these sources include savings, other private funds, and fundraising.
Private Health Insurance
If you have health insurance, you may want to start by ﬁnding out what your plan covers. Then you can begin to explore other funding sources. Terms and extent of coverage vary widely and may change from year to year. Read your policy carefully each year and ask your health plan representative what types of costs are covered before, during and after the transplant. Find out if you have to use network providers and when you need to get authorization. If you have questions, call the insurance company directly or contact the human resources department at work. The health plan may assign a case manager to walk through the process with you.
You may have other coverage that will pay for costs or you may have to cover deductibles and other expenses.
Staying on top of medical bills
Your ﬁnancial plan needs to cover costs before, during and after the transplant. Expect a high volume of bills and beneﬁt statements. For your peace of mind, set up a process ahead of time to make sure all of your child’s transplant-related bills are covered. Mistakes happen. If you think something is wrong, address it in a timely manner to help reduce stress.
Medicare is a federal health insurance program available to people:
- Age 65 or older and those under age 65 with certain disabilities, or
- Any age with “end-stage” renal (kidney) disease, or ESRD.
Medicare, like most private health plans, does not pay 100 percent of your costs. You must pay deductibles and other expenses.
To receive full Medicare beneﬁts for a transplant, you must go to a Medicare-approved transplant hospital.
Contact your local Social Security oﬃce or go online to ﬁnd out more.
Medicaid and CHIP
Your child may be eligible for Medicaid or Children’s Health Insurance Program (CHIP). Each state runs its own program, following federal rules.
Check with your social worker or ﬁnancial coordinator. If you are eligible for assistance, provide a copy of your federal tax form or Social Security award letter to the transplant team.
Even if you have medical coverage, you may need help paying for other transplant-related costs and living expenses. Local, regional and national organizations provide patient assistance and sometimes grants.
They can advise you about how to raise funds to help pay for expenses that are not covered or living expenses while you are away from home. Check with your ﬁnancial coordinator, social worker, or insurance caseworker to be sure fundraising does not disqualify you from other assistance programs or if those funds have to be included in your annual income for tax purposes.
The following organizations can help with fundraising for transplants:
- The Children's Organ Transplant Association (COTA); contributions are tax deductible for donors and recipients of COTA funds for their beneﬁt
- National Foundation for Transplants
- Help Hope Live
You may want to look at patient advocacy organizations that cover your child’s illness. They often have funding available to help families who are waiting for transplant.
Some people prefer to fundraise using a crowd-funding site on the Internet. Although these sites are often successful, keep in mind that funds raised through these sites can be subject to fees and taxes, and may also affect eligibility for state programs. Your transplant ﬁnancial coordinator or case manager may be able to help answer your questions about this type of funding.
Taking time off work
Parents who take time off work to care for a child after transplant should talk to a human resources contact at their workplace. Parents should be aware of the Family and Medical Leave Act (FMLA), which will help retain their job while away from work.
Although your family’s transplant journey can be diﬃcult and stressful, your transplant team and many other people can help you through it.
After The Transplant
For kids of all ages
Follow-up care and labs
Your child will have routine check-ups, labs, and procedures to be sure that they are healthy and that the transplanted organ is working well. Most patients are followed very closely in the first few weeks after transplant. Over time, as your child recuperates and the transplanted organ is working well, this monitoring decreases. For many patients, after a couple of years, the transplant team requests that labs be obtained every month or so and that your child have a clinic visit every six to 12 months.
Sometimes, the transplanted organ needs to be checked more closely, and a biopsy is performed. Most patients can have a biopsy done as an outpatient procedure, but some patients spend one night in the hospital.
Imaging studies such as CT scans and MRIs also may be needed more frequently.
After having a transplant, some children may become a little anxious, withdrawn or depressed, especially if they have been in the hospital for a long time. Other children have trouble focusing or interacting with others. If you are concerned about your child’s mood after transplant, please discuss your concerns with your child life specialist, social worker, psychologist, or transplant coordinator. They can help you ﬁnd supportive services in your area.
“I’ve lived more healthy years now due to my transplant than years sick when I was a child. Years that I wouldn’t have if a donor family from Tennessee hadn’t donated their son’s organs. My outcome may not be typical, but it’s possible.” — Kim Uccellini, pediatric kidney recipient
Medical ID tag
You may think about getting your child a medical ID tag. They often come as bracelets or necklaces. Bracelets may be a better option for younger children. The tag should contain the child’s name, diagnosis (including what organ the child received), and contact information for you or your transplant hospital. Smartphones may have a medical ID feature. You will need to update the information if anything changes.
Most patients are prescribed one to three medications to suppress the immune system so that the body will not reject the transplanted organ. After transplant, you and your child will learn much more about these medications. Transplant hospitals usually provide a discharge manual and education to explain why these drugs are prescribed, how they work, and what side effects a patient may have.
Medications may be needed to support the transplanted organ. After a heart transplant, some patients may need drugs to stabilize the heart’s rhythm or to help the kidneys control the amount of acid in the bloodstream.
Other medications prevent or treat infections or help with kidney function. Most patients take an antacid to prevent stomach irritation. Many patients need electrolyte supplements to help keep blood components stable and in normal ranges. These usually include medications to help with levels of potassium, magnesium, sodium bicarbonate, and iron.
If your child takes medications for conditions unrelated to transplant, your transplant team will help coordinate with other providers.
Some things to keep in mind:
- All medications given to your child should be cleared by the transplant team. Provide transplant team contact numbers to your child’s other doctors and health care professionals so they can work together to prevent drug interactions and side effects.
- Tell the transplant team about over-the-counter pain relievers, teething gels and herbal supplements or home remedies you give your child.
- Make sure your child takes the correct dosage in the prescribed time frame.
- Find out how soon you can request reﬁlls. Mark these dates so that you never run out.
- If your child throws up the medication, ask your team when you can give another dose, and how much. Be sure to note times and dosage amounts.
- Your child should avoid grapefruits, pomelos, pomegranate, or juices and soft drinks that contain those fruits. They can interfere with immunosuppression and potentially cause damaging blood pressure levels.
- Some medications increase the risk of skin cancer. Apply sunscreen even on mildly sunny days.
- Ask the pharmacist about medication discount cards.
It is common for medication doses to change over time. Your child may gain or lose weight, need a higher or lower level of immunosuppression, or their electrolytes may be out of balance. Your transplant coordinator will contact you with any medication changes and answer your questions. Never change doses on any prescriptions without talking to your transplant team.
Preventing organ rejection
Rejection is the body’s defense system to get rid of anything seen as “not self” or foreign to your body. Usually this is a cold virus or the community ﬂu but in a child who has had a transplant, the immune system may react against the transplanted organ. Immunosuppressants suppress the normal immune system so that the transplanted organ is not rejected.
What are the common signs of rejection?
Rejection can be sudden (acute) or may occur over time (chronic). You may not be the ﬁrst to notice signs of rejection in your child. Your transplant team will tell you what to look out for. If you are worried or notice a change, talk to your child’s doctor.
How can I help reduce my child’s risk of rejection?
- Give your child the correct dose of prescribed medications on time each day. This is the most important thing you can do to reduce the risk of rejection.
- Exact timing of dosing can be important for some medications, so set up a regular, seven-day-a-week routine.
- Know the signs and symptoms of rejection for your child and contact your transplant hospital if you are concerned your child may have any of these symptoms.
- Contact your transplant coordinator with any changes in your child’s health, particularly in the ﬁrst year after transplant.
- Get your child’s labs drawn as requested by your transplant coordinator.
- Make sure your child attends all required appointments for the clinic, tests, and procedures.
- Check with your transplant coordinator before giving any medications prescribed by another physician, or if you would like to use over-the counter drugs or herbal supplements. Rejection episodes may occur as your child’s immune system adjusts to the new organ. While the risk of rejecting an organ can decrease as time goes on, it never goes away. Your transplant team can provide more details.
Vaccines and staying healthy
Children are exposed to common illnesses at school and elsewhere. These range from the common cold and ﬂu to measles, chicken pox or whooping cough. Immunosuppressants make it diﬃcult to ﬁght disease and make transplant recipients more prone to infections. Ask your transplant team and your child’s doctor about what they suggest for a vaccine schedule. You may want to use the Centers for Disease Control and Prevention (CDC) schedule for transplant recipients as a guide.
“What helped me the most was having a fellow transplant mom tell me about her medicine organization process. It made things so much easier to have a true system when we got home.” — Carie Semenko, heart recipient parent
Some of the required immunizations that are given to children are “live” vaccines. The vaccines work by giving the patient a very small amount of the actual virus so the immune system learns to ﬁght that virus. Most transplant hospitals recommend that transplant recipients do not receive live vaccines after transplant. They also recommend that patients being listed for transplant get any live vaccines before transplant whenever possible.
The pediatrician may use a schedule that moves up the dates of the immunizations to be sure they are given before transplant. Some transplant hospitals advise that family members not receive live vaccines. Talk to your transplant team about what they recommend if other family members need to have live vaccines.
Your child receives added protection if other children, family, friends and others they come in contact with are up-to-date on their vaccines and ﬂu shots. This is called herd immunity.
Ask your child’s school nurse to inform you if any students have a community illness that is controlled by vaccines, such as chicken pox and measles. If your child is not immunized and has been in close contact with that student, there is a risk of getting the illness. Call your transplant coordinator for advice on what to do.
Your child’s immune system is lowered in order to prevent organ rejection, so it is very important to avoid exposure to sources of infection. Good hygiene is part of this, as well as decreasing exposure by avoiding others who are ill and, being careful in public places, where germs may be present on doorknobs or countertops. Carry hand sanitizer in case soap and water are not available.
- If you plan to travel outside the country, check the Centers for Disease Control and Prevention (CDC) website for information about signiﬁcant health problems at your destination.
- If ﬂying, it’s best to pull medications out of your bags and identify them to TSA. They will always get an extra screening, so plan for extra time.
- If traveling for a biopsy, try to limit movement at your child’s surgery site (groin, chest, etc.). Very young children should be in a stroller. A wheelchair may be helpful.
- If you must travel for care, insurance or your care fund may cover the cost of an extra seat for your infant or toddler.
- For long plane trips, keep your child well hydrated. Drinking water during the ﬂight and avoiding caffeine can help reduce jet lag symptoms. This is good advice for you, too.
- Ask your doctor if you can skip magnesium or diuretics that might make your child urinate more frequently.
Travel for vacation
- Ask your hospital for a travel packet. It contains information about your child for emergency responders and hospital staff.
- Ask transplant team members to help you locate the nearest transplant treatment hospitals in your travel area.
- Check with your transplant coordinator before leaving the country.
- Take sunscreen with an SPF of 30 or greater if you travel to an area where your child will be exposed to the sun for long periods of time.
For any travel
- Bring original prescription bottles with labels. You may want to ask your transplant coordinator for a letter listing all medications and medical care that may be needed.
- Bring special formulas and nutrition supplies with you if they may not be available at your destination. Contact airlines in advance to request luggage allowances for these products, if needed.
- Take an extra supply of medicines with you in case you are delayed.
- Keep medicines with you at all times. Never put them in checked luggage.
- Think about time changes and how that might affect when to give medications.
- Talk to the pharmacist about the safest way to transport medications that need to be refrigerated.
Contacting the donor family
When you and your family are ready, you may want to express your gratitude to the donor family by writing a letter. This gesture can be a source of solace to donor families, knowing that their loved one’s death helped others live. Check with your transplant team or your local organ procurement organization (OPO) for guidance.
- Timing for this letter will vary by transplant hospital or OPO.
- Do not include any personal or identifying details. Use ﬁrst names only.
- Share a story about how your child is doing. Tell the donor family about how your child’s health has improved with their generous donation of the gift of life.
- Most hospitals ask you to include a photo of your child.
- Never contact the donor family on your own, through social media or any other way. Always work with your OPO and transplant hospital to contact a donor family, so your letter arrives at an appropriate time as they grieve.
Caring for your child through the ages
Newborns to age 3
Recovery after transplant
Although many children recover well after transplant surgery, some children need support during their recovery. This depends on how sick the child was before surgery, what type of transplant they had, complications they may have had, and how long they were in intensive care and the hospital. Being away from family, friends, school, and their normal routine also can affect how children recover.
Here are some examples of challenges children may have after transplant. Ask your transplant team about therapy or services to address your child’s needs.
- A young child may need to adjust to eating after transplant. It may help to stick to a few basic food tastes and textures to start. Children who have trouble eating or drinking, or with strict food limits, might need a feeding tube. A dietitian can help with a feeding schedule, if needed.
- Some children need help regaining developmental milestones after transplant. For example, a child who was toilet-trained, may not want to use the potty. Talk to your transplant team if you have questions or concerns.
- Infants and children who had a heart or lung transplant will need to be on chest (“sternal”) precautions for six weeks or more. This could cause delays in learning how to roll and other milestones.
- Physical and occupational therapy can help children who experience muscle loss or atrophy after transplant. This can occur when a child is on a breathing tube or heavily sedated for a long time.
- A child’s growth may be a concern after transplant. Discuss issues and options with your doctor and transplant team.
“After transplant, your child is still a child. They will still have tantrums. They will want to play with mud. Just like any kid. That’s why they got the transplant–to be a kid.” — Joseph Hillenburg, heart recipient parent
For children who need additional help after transplant, services may be available on the federal, state, or local level. Many of these programs have speciﬁc guidelines that may differ from one program to another. Ask your transplant social worker or coordinator for details.
Some children with medical conditions may develop more slowly than their peers. Early Intervention (EI) Services (an Individuals with Disabilities Education Act [IDEA] program) provide education and support to help eligible newborns through age 2 reduce the effects of delayed development. Talk to your care team about EI if you feel it would beneﬁt your child.
Your child will be assigned a service coordinator and therapy team to assess them. If the team decides your child qualiﬁes for EI, they will write an individualized family service plan (IFSP). They will include you in the process and will work with you to best meet your family’s needs.
The earlier EI begins, the better chance a child has to succeed and catch up.
There are no-cost public school programs to help your child have a successful and enjoyable school experience. They can help a child catch up on missed schoolwork, manage fatigue, and handle other issues that may impact learning before or after transplant. The following are some of the programs.
Individualized health plan
An individualized health plan (IHP) can help with your child’s medical needs while at school. They may include details about blood pressure checks, taking medicine, use of bathroom and how to handle emergencies. Talk to your child’s school nurse to help you get started.
Section 504 plan
Section 504 of the Rehabilitation Act of 1973 allows you, together with your child’s school, to lay out a written plan that explains how the school will meet the individual needs of your child. A 504 plan makes sure a child who has a disability as deﬁned by law and goes to public school receives accommodations to help them be successful, take part safely, and have the same access to education as other students.
Accommodations could range from home tutoring to extra time to complete homework. The plan helps eliminate misunderstandings. If you are interested in exploring a 504 plan, contact your child’s teacher or school counselor.
Individualized education plan
An individualized education plan (IEP) provides special instruction and services to help children with a disability as deﬁned by the law. It is an agreement between parents and a child’s school to address the child’s unique learning issues and meet their educational goals. If you feel that your child needs more help at school, talk to their teacher about an IEP.
“It’s hard enough being a teenager. Adding a medication to the list of things to worry about makes it that much harder. Take your medicine. That medication will allow you to embrace the many highs that life has in store for you.”— Bill Coon, pediatric heart and adult heart/kidney recipient
Teens: Risky behaviors
Kids face unique challenges as they get older. When your child enters the teen years, things change. Your child may pull away from you and participate in riskier behaviors. This is part of normal teen development, but it is important to stay engaged to help keep your child safe.
Transplant recipients need to stick to a treatment plan to stay healthy. Your transplant team may refer to this as adherence. It includes keeping appointments, completing lab work and medical tests, and managing medications. Younger children depend on parents and caring adults to handle scheduling conﬂicts, health concerns and problems with medications. As your child gets older, adherence can become a challenge. Research shows an increased risk of rejection during teen years, and lack of adherence can be a factor (“Adherence and medical outcomes in pediatric liver transplant recipients who transition to adult services.” Annunziato, et al. Pediatric Transplant, 2007).
Seeking independence is a normal developmental milestone for teens. They naturally start to spend more time with friends and strive to ﬁt in. Not all teens share with their friends that they have had a transplant. This may make it tougher for them to take medications on time and can lead to non-adherence.
Encourage your child to share this information with close friends.
Find ways to help your teen remember to take medications. It could be as simple as setting a watch or clock, or ﬁnding a good smartphone app. You also can help set up a pillbox. All your child has to do is take out the pills needed during the day, without having to think too much about it.
You also can ask your teen what they think will work for them. Some older teens may want to take medications a little later in the morning so they can sleep a little later. They may need to take medicine at school instead of home. There may be side effects that your child does not like. Help your child discuss this with their doctor to see if they can make a change. Teens who own their care are more likely to adhere to it.
“Your child can lead a very fulfilling and relatively normal life. Don’t let a transplant restrict your or your child's dreams.” — Megan McKinley, pediatric heart and adult heart/kidney recipient
If your child begins to slide toward non-adherence, stay on top of the situation. You may need to step in and supervise for a time. A social worker, psychologist, or mental health specialist can help. Talk to the parents of other transplant recipients of the same age. Your child may beneﬁt from meeting transplant peers. They will understand the struggles your teen faces. Some transplant hospitals host teen events or mentoring programs where kids can meet, exchange ideas, and get advice.
Non-adherence can lead to devastating results, including organ failure. It could also affect the possibility of getting another transplant. If you have concerns, talk to your child right away and reach out to your transplant team for support.
Adolescence is already known to be an emotionally charged period in any child’s life, but add in life-threatening illness or disease and the result can be overwhelming. Your child may experience feelings of anger or jealousy as they question, “Why me?” It is important that you keep an open line of communication with your child as they express their feelings of anger, frailty, or injustice.
Your child also may feel isolated or depressed during hospital stays or while they are home recovering from the transplant. Be sure to work with your transplant team if emotional concerns arise to make sure you are able to access counseling or psychiatric support to help your child work through these feelings. Their emotional status is vital to their transplant recovery and follow-up treatment plan.
Your child may feel anxious about their future and what their life might be like after the transplant. Other family members may share the same feelings of anxiety and stress that need to be addressed as well. Working together is the best way to stay strong through turbulent times.
Alcohol and drugs
Peer pressure is powerful and transplant recipients are just like other teens when it comes to trying drugs and alcohol. They may know the risks of these behaviors, but like many people, they believe nothing bad will happen to them. This is normal.
It’s hard to strike a balance between giving a teen some space while making sure that you watch out for their health and safety. Don’t be afraid to discuss this subject openly with your child. Suggest ways to explain to their peers that they can’t drink or do drugs because of the medications they need to take. You also can encourage them to join clubs and activities that do not allow drugs and alcohol. Turn to your transplant team for other suggestions.
Still, many teens will choose these activities anyway. Leave the door open for honest discussions with your teen about what’s going on in their life. It will help them to know they can tell you about drinking or drug use, and that you will work with them to ﬁgure out what happens next.
Some transplant hospitals tell adult (over age 21) transplant recipients that no alcohol is allowed at all. Other hospitals may allow a drink every now and then. Alcohol impairs judgment, which could lead to other risky behaviors or forgetting to take medications.
Transplant hospitals frown on any form of non-prescribed drug use. Your child needs to learn about the risks of infection and interactions with illegal drugs, or marijuana, which may be legal in your state. Most drugs are not pure and may affect the potency of their transplant medications, which adds another layer of risk. Intravenous (IV) drug abuse exposes your child to many communicable diseases that are dangerous for a transplant recipient. If your child ever needs another transplant, active use of illegal drugs could affect future candidacy. Keep talking to your child about these issues through the years.
Sexual activity is a part of life for most adults. Your teen is becoming a young adult and will eventually move in this direction. All parents struggle with this as their child matures. Naturally, you want to reinforce your expectations, but it is even more important to prepare for reality.
Sexual activity includes genital, anal, or oral contact. Many teenagers do not consider it “sex” if it is not intercourse. You and your teen need to know that all sexual encounters can be risky. As your child approaches puberty, your transplant team may start to discuss these issues with your child. Understanding the risks is key to preventing them.
All sexually active teens risk being exposed to sexually transmitted diseases, but an immunosuppressed child is at a greater risk. Because of this, open communication between you, your child, and their transplant hospital is imperative.
Vaccines and condoms will help protect your child against many forms of sexually transmitted diseases. Be prepared to discuss these methods with your child’s transplant team.
Transplant team members may ask to speak with your child without you in the room. Your child may request privacy as well. This allows a child to bring up parts of care that they may not want to discuss in front of you. If the health-care provider starts this process in the young teen years, it becomes a normal part of the clinic visit. It will help your child trust the health care system and teach them that they can speak freely with their doctors.
Your transplant hospital may be able to refer your child to a clinic or program that specializes in sexual health. These clinics can counsel children, educate them about risks and prevention, and offer sexual health screening and birth control. Immunosuppressed recipients who are sexually active may need more frequent follow-up.
Teenage girls should know the risks associated with pregnancy. Some hospitals may advise certain young female recipients that it is not safe to become pregnant. A teen also could be on medication that could harm a fetus. In either case, you should talk to the transplant team about effective and safe birth control, based on your belief system. Barrier methods like condoms or spermicides are generally not considered enough on their own. Your transplant hospital can advise you on the safest method for your child, including birth control pills, IUDs, or something else. Some types of immunosuppressants interfere with the effectiveness of birth control pills.
Some hospitals recommend birth control once a child reaches puberty, even if they are not sexually active. You, your child, and your transplant hospital will decide together what is best. The main goal of these discussions and suggestions is to prevent disease and pregnancy.
Young Adults: Independence and transition
Advanced preparation that takes years
In your child’s early teenage years, your transplant hospital will begin to emphasize independence. Since your children will not always live with you, it’s important that they learn to take care of themselves. Many children are ready to learn about self-care as young as 12 years old, while other children need more time. Whenever the process starts, it should be gradual and involve both the parents and the transplant hospital.
“Empower your child or teen to be independent and learn to take care of themselves. You might not always be around to do things for them or ensure they make smart decisions. I attribute my success to my parents making me be accountable and responsible and not rely on them.” — Kim Uccellini, pediatric kidney recipient
You need to balance letting your child learn on their own and stepping in when needed. Allow plenty of time to prepare yourself for the emotional struggles that go along with change.
Some transplant hospitals have tools that predict how prepared a child is to take care of themselves. These tools help parents and the transplant team know the areas where they are needed most. You can use these tools to mark your child’s progress. As children age, they can learn to manage their own care in the following areas:
They should know the names of medications, doses, and what they are for. They should recognize the pill even when it’s not in the bottle and know when to take it. A perfect time to teach young children about medication names and doses is when you fill their pill box. You can start teaching early if you believe your child is ready, but you should certainly begin by the pre-teen or early teen years. A young teen could begin filling their own pill box while you watch.
Older teens should keep track of medication refill dates on a calendar or on their smartphone. Teach them to call the pharmacy or contact the transplant hospital before prescriptions run out. Make sure they know who to call if they have a medication question or problem.
Children (adolescents in particular) may be unhappy with some of the side effects of their medicine, but these medications keep them alive. If side effects happen, both of you should talk with the doctor about other options.
Your teen should know what type of insurance they have and carry a card. As your child gets older, explain how the health plan works and make sure they know who to call with questions. If they need a specialist, they should know who to call to get a referral.
Communicating with the transplant team
Your child should be comfortable talking with the transplant team. Encourage teens to make their own clinic appointments, and to ask and answer questions during visits. As time goes on, your transplant hospital will talk more with your child and ask them more questions directly. Although it can be diﬃcult for you to remain silent, it’s important for your child to learn this skill and know that you trust them to handle it. Sometimes the transplant team will meet separately with your teen during part of the appointment. This will help them gain conﬁdence.
Encourage them to write down questions ahead of time, so they remember them the day of clinic.
Turning 18, moving out or going away to school
Once your child turns 18, they legally become an adult. From now on, if members of the transplant team want to talk with you about your child’s health, they need their permission. Transplant team members may even ask your child to sign a paper saying that they permit you to speak to the medical team on your child’s behalf. Your child will need to sign all consents and medical documents.
If your child has cognitive delays and is unable or unwilling to make their own medical decisions, you need a legal document stating that you can make decisions for them. The document will become part of your child’s medical record. Discuss this with your child before they turn 18. Your social worker can help you with the details.
Just because your child is legally an adult does not always mean they are ready for total independence. Your child will continue to need your guidance and care. Since children mature at different rates, you are in the best position to know how much support your child still needs.
It is especially important that children learn to take care of themselves before leaving home or going away to college. Giving them gradual independence during the early teen years makes the transition less stressful.
If your child’s college is not near their own transplant hospital, the team may suggest a local hospital that could follow them during the school year. It would be helpful for your child to establish a relationship with this center before they get sick. They should also ﬁnd a local pharmacy.
Talk with your child, the transplant team, and Student Services about any special needs they may have as a transplant recipient.
Moving to an adult transplant center
Eventually your child will need to transfer to an adult hospital. The exact age will differ for each young adult. Some transplant hospitals have formal transition programs, others are informal. The pediatric program will transfer medical records and write a medical summary for the new program. In most cases, coordinators from each program will also talk to one another.
If your pediatric center uses a developmental readiness tool, they will likely use this as a guide to prepare you and to know when the timing is right.
Both children and parents may be anxious during this time. Transitioning to adult care means that the transplant team believes your child is ready to tackle medical issues as an adult. The proper preparation will build independence and help your child succeed during the transition.
“Just like any child they will always need your support. But treat them as though they are no different than any other kid.” — Bill Coon, pediatric heart and adult heart/kidney recipient
Adult programs tend to be larger and have more patients and more providers. This can overwhelm a young adult who may be used to a smaller team. Be sure to work with your child before the transition to get answers to their questions. Would they rather have fewer providers at ﬁrst? Do they want you to go with them to appointments?
You need to know that that adult programs will expect your child to make their appointments and remember to get lab work done. They will be less likely to remind or coddle your child. They will likely give medical information directly to your young adult and expect them to follow up. This is why it’s critical for a young adult be as independent as possible before the transition takes place. They need to know how to navigate the medical system, and they should be willing and able to speak up for themselves.
No matter the age, your child will still need family support. Your child may ask you to attend certain appointments.
Transitions can be stressful for you and your child. Studies show that young adults are more likely to experience organ rejection during this time, especially if they are not well prepared for the change (“Non-compliance and transfer from pediatric to adult transplant unit.” Watson et al. Pediatric Nephrology, 2000). You can lower the risk by getting involved and developing a plan with your child. And know that transition doesn’t stop once your child transfers to an adult program. The transplant team can work with your child to make this transition as smooth as possible.
Put the health and well-being of yourself, your child, and your family ﬁrst. Managing end-stage organ disease can be a long, stressful and challenging situation for any family to endure physically, emotionally, and ﬁnancially. No one is to blame. Throughout adversity, a uniﬁed family provides the best opportunity for a successful transplant outcome and the optimal growth and development of your child.
An organ transplant provides your child with the opportunity to have a second chance at life with a healthy organ, if they follow guidelines for care. Many people will work with you and your child to achieve this goal.
“People always remark to us about how strong transplant parents are. That is not how we see it. We are just ordinary people under extraordinary pressure.” —Joseph Hillenburg, heart recipient parent
Acronyms and terms
Atrophy - The reduction in size of cell, organ or tissue after reaching its normal mature growth.
Biopsy - The removal of cells or tissues from a living body for medical examination.
CT scan - A procedure using a computer linked to an X-ray machine to make a series of 3-D images of areas inside the body.
Immunosuppressants - Drugs or medications that reduce the body’s ability to reject a transplanted organ.
MRI scan - Uses a large magnet, radio waves, and a computer to create detailed images of internal organs and structures.