Cystinosis is a rare, multisystem genetic disease that accounts for nearly 5% of all childhood cases of kidney failure. Cystinosis occurs in only about 1 in 100,000-200,000 children, so it is not widely known nor understood.
Learn more about cystinosis by selecting a subject from the list below.
You have probably been hearing the word "cystinosis" for several years now. As you may already know, cystinosis is an ultra-rare condition that is usually diagnosed in childhood. But what is cystinosis really?
Cystinosis is a rare genetic condition. A genetic condition means that it is passed down through families.
Cystinosis leads to a buildup of cystine (a natural protein in your body) in a part of your body's cells called lysosomes. As cystine builds up, it forms crystals that cause the cells to die. Eventually, these dying cells can cause damage to organs, including your kidneys and liver.
Over time, cystinosis leads to permanent kidney damage and kidney failure. Each person is different, and some people with cystinosis will develop kidney disease as a child or adolescent while others may not until early adulthood. As kidney disease gets worse and the kidneys lose the ability to function, your will need to start dialysis or have a kidney transplant to live.
Prepare for your next virtual doctor visit
Telehealth lets you see your doctor from home – or wherever you are. Download this guide for tips on how to prepare for your next virtual visit. If you do not have a computer or internet access, the Cystinosis Research Network (CRN) and PCs for People may be able to help. Learn more here.
The educational information on this page can be downloaded or ordered in a paper toolkit format and mailed to your home for free by submitting this form.
Having too much cystine can damage different parts of the body. Talk to your doctor to learn more about ways that cystinosis can affect your body:
Visual or learning issues
Sensitivity to light (photophobia), blindness
Poorly working thyroid (hypothyroidism) leading to slowed growth
Fanconi syndrome (a type of kidney disease)
Muscle weakness and decreased muscle mass (myopathy)
Softening or weakening of bones (rickets)
Cystinosis and your kidneys
Cystinosis leads to permanent kidney damage and kidney failure. Kidney failure means the kidneys are unable to remove waste from your blood. The extra waste builds up in your body and makes you sick. When the kidneys lose the ability to remove waste from the blood, there are two treatment options:
Start dialysis, a treatment that connects your body to a machine that cleans your blood
Have a kidney transplant, a surgery that replaces your sick kidneys with a healthy kidney from someone else's body
With cystinosis, it is highly likely that you will need more than one kidney transplant during your life. You may get a kidney transplant when your kidneys are close to failure, as a prevention measure before you need to start dialysis. It is also possible you may start dialysis while you wait for a kidney transplant. Kidney transplant surgery is considered safe and is usually very successful. However, as with any surgery, there could be some risks involved.
Preparing for kidney transplant
The kidneys are two bean-shaped organs, about the size of a fist. They are vital organs, meaning everyone needs at least one healthy kidney to survive. The kidneys have many functions, but their most important role is removing waste from the body by filtering your blood and eliminating waste through the urine.
Cystinosis can damage the kidneys over time, leading to kidney failure. Once the kidneys have failed, you must start dialysis or have a kidney transplant to live.
Remember, a kidney transplant treats kidney failure. It does not cure cystinosis. After getting a transplant, it is important to keep taking medicine for cystinosis to protect your new kidneys.
A kidney transplant is a surgery in which a healthy kidney is removed from a person's body and given to someone whose kidneys are not working. Transplants can come from deceased donors (who have recently passed away) or living donors. No matter where the new kidney comes from, doctors test it to make sure it is safe and healthy for your body.
When your medical exams begin showing signs of decreasing kidney function, you and your family should start preparing for a kidney transplant.
The first step to getting a kidney transplant is working with your parents/caregivers to find a transplant center and schedule KIDNEY TRANSPLANT Remember, a kidney transplant treats kidney failure. It does not cure cystinosis. After getting a transplant, it is important to keep taking medicine for cystinosis to protect your new kidneys. a transplant evaluation. Every transplant center requires different tests for a transplant evaluation, but all will include:
Tests of physical health (e.g., blood tests)
Psychosocial exam to make sure you are mentally and emotionally ready for transplant
Conversations with your family about finances and health insurance to ensure that you can afford the surgery
If the transplant team decides you are ready for transplant, the next step will be for your transplant team to help you find a kidney match from a living or deceased donor.
Types of kidney transplant
A deceased donor transplant comes from someone you may or may not have known who has just passed away but had a healthy kidney.
Getting a deceased donor transplant requires being on a waitlist for several months or years.
As soon as a deceased donor kidney becomes available for your child, you will get a call to come to the hospital for surgery right away, usually in a matter of a few hours..
To increase your chances of getting a kidney transplant as soon as possible, you can get waitlisted at multiple transplant centers. If you are listed in multiple areas, you must be able to reach the center in a short amount of time if you are called.
Check with each center to ensure that they allow patients who are listed at multiple centers.
Deceased kidney donor transplants last an average of 10 years but can last for a longer or shorter amount of time.
A living donor kidney transplant comes from a living person who offers to donate one of their kidneys.
A kidney donor does not need to be a family member.
The donor will have to go through medical testing to make sure they are healthy and a good match.
If you can find a kidney donor match, you can schedule the date of the transplant surgery
Living donor kidney transplants last an average of 15 years but can last for a longer or shorter amount of time.
Benefits of a transplant
There are many things you may experience that you can look forward to after receiving a new kidney including:
Being able to eat some of the things you may have not been able to eat before
Eventually having to spend less time visiting the doctor
Experiencing a growth spurt if you are still growing
Having more energy to do the things you love
Did you know? Transplants last longer if you take care of your health and take all your medicine; including your cystinosis medicine!
Preparing for kidney transplant: You've got this!
Getting a kidney transplant is exciting, but it can also be a little scary. It is okay to feel nervous! Asking questions is one great way to feel prepared for the transplant surgery. You can use our question tool or write down your questions in a notebook to ask your transplant team. Examples of the type of questions you can ask include:
Can I have medicine if I feel pain?
Can I still play sports after the surgery?
How long does the surgery last?
How soon can I go home?
Will I be fully asleep during the surgery?
Will my diet change after the surgery?
Preparing for surgery
It is okay to be a little nervous about the surgery. There are ways you can prepare for it, for example:
Talk to someone who has gone through a transplant if you feel nervous or anxious. Your transplant team may be able to recommend someone you can talk to.
Consider reaching out to the Cystinosis Research Network (Cystinosis.org) to connect with peers who have gone through something similar.
Talk to your transplant team about how long your surgery will take and how long you will need to be in the hospital for recovery.
Always let your care team know if you have questions or need anything before or after the surgery.
Once you know the available schooling options, talk to your child about what option they like best.
Consider schooling options
After the transplant surgery, you will need time to recover at home and temporarily avoid crowded places with lots of germs, like school.
Talk to your parents about what schooling options are available and decide which option you prefer.
You may be offered the options of home schooling, online learning, home visits by a teacher, or virtual classrooms.
Let your school and teachers know that you will be absent for about six weeks as you recover from the surgery, and that avoiding infection will be a top priority.
Life after kidney transplant
Receiving a new kidney is a major game-changer. Many people say they feel better quickly after surgery, if their new kidney starts working right away. Although you may feel great, you still must take medicine to protect the health of your new kidney and to continue feeling good.
Immunosuppressants, also called anti-rejection medicines, protect your new kidney from getting attacked by your immune system. Your immune system protects your body from outside invaders (such as germs and bacteria), and it may treat your new kidney as an outside invader, too. It is important to take immunosuppressant medicines exactly as prescribed to stop your immune system from attacking the new kidney.
Since it is likely you will need a second and maybe even a third kidney transplant during your lifetime, it is important to extend the life of your transplant by taking care of it. A big part of taking care of your new kidney is taking immunosuppressive medicines exactly as instructed. If you skip even one dose of your medicine, your body can start rejecting your new kidney.
For a period of time after the transplant surgery, you will need to take extra precautions to stay healthy.
Avoid being around pets since they can carry germs.
Avoid being near people who are sick.
Avoid participating in sports until the doctor tells you it is safe.
Keep your surgery spot clean and dry to prevent infection.
Limit physical activities like riding a bike, jumping on a trampoline or playing sports until the surgery area is fully healed.
After you come back home from the transplant surgery, you may feel much better, but you will need to take it easy for a while. During the first three months after surgery your immune system is much weaker than normal, meaning you can get sick very easily. For this reason, your doctor will recommend you mostly stay at home during this time and avoid crowded places like school, restaurants, and public transportation.
The time during the recovery period can feel isolating, so it is important to prepare yourself mentally by finding other ways to stay busy and keep in touch with your friends or classmates. Just remember, you have had a very important surgery that will change the course of your life.
Once your recovery is complete and your doctor says you can return to your regular lifestyle, there are many activities you can look forward to enjoying. Are any of these activities on your list?
Eating more of the things you like
Going to school/college
Hanging out with friends
Getting a job
Taking cystinosis medicine
Take your medications for cystinosis as prescribed at the same time every day. Adherence is extremely important. Even after you have had a kidney transplant, you
will still need to take medicines for cystinosis. If you stop taking your cystinosis medicine, your new kidney transplant could stop working and other symptoms of cystinosis will get worse. Although it can be challenging, you must take your medicines for cystinosis for the rest of your life and take immunosuppressant medicines for as long as your kidney transplant lasts.
Have an honest talk with your parents and health care team if you are having trouble taking all your medicine, whether it is because of the side effects, a busy schedule, or simply not wanting to. Your parents and doctors may have solutions that could make things easier.
Make taking medicine easier
Try some of these techniques to remember to take medicines when you are on the go.
Set alarms or reminders on your phone.
Carry your medicine in a pill case or small sack. You can even use a "disguised" pill case like an empty and clean mint container.
If you do not like taking medicine in front of others at school, tell your teachers and school nurse that you want to take your medicine in complete privacy.
Identify where you can take your medicine if you are going out. Keep extra medicine in your backpack or car in case you ever forget your medicine at home.
Remember, taking care of your health today is the first step to living your best life. Prioritize taking your medicine and managing your health so that you can continue doing all the other things you like and spending time with those you love.
Emotional health after transplant
Getting a transplant is usually an exciting event, but because it is also a major life change, it is normal to feel a mix of emotions afterward. If you feel anxious, depressed, scared, stressed, or unhappy, please know that you are not alone. Many people who receive transplants experience these feelings at first, for many different reasons.
After transplant some people experience:
Changes in mood, which can sometimes be a side effect of the immunosuppressant medicine you are taking
Feelings of stress or anxiety about your new lifestyle
Guilt about getting a kidney from a living or deceased donor
Family members who have emotional changes as they adjust to your new lifestyle
You do not have to deal with these feelings alone. Getting a kidney transplant is a major life change, and it is okay to feel stressed and anxious about events that change your life.
You have been through a lot after living with cystinosis for so many years. Sometimes it is not possible to deal with everything alone. Reach out to your family and friends when you need to talk.
There may be times when you do not want to talk to someone you know or would rather talk to someone new. Tell your parents or social worker that you would like to be connected to a counselor. Also, let your transplant team know about your emotional changes so they can help support you and adjust your medicines if needed.
Your transplant center may host local support groups in your area. You can also join other trusted support groups to talk to people who have been in your shoes.
If you believe you are experiencing depression, anxiety, or having thoughts of self-harm, call:
NATIONAL SUICIDE PREVENTION LIFELINE: 1-800-273-8255
NATIONAL ALLIANCE ON MENTAL ILLNESS: 1-800-950-6264 TEXT NAMI TO 741741
Remember, you are not alone!
Living your best life with cystinosis
Everyone deserves to live their best life, including you! As a young person, you have your whole life ahead of you, so here are some ways to make the most of it:
Advocate for yourself – help others learn more about cystinosis and what they can do to help.
Find a hobby – start doing something you enjoy and find interesting, like photography, painting, cooking, biking, writing, dancing, or playing an instrument.
Help others – give back to your community and those in need by volunteering.
Make new friends – surround yourself with supportive people who make you happy.
Stay active – find a sport or outdoor activity you enjoy, and your doctor approves of.
Practice positivity – a positive attitude is key to success; try meditation, mindfulness, or positive affirmations.
Set goals – whether you want to go to college or start working after high school graduation, set high goals for yourself.
Share your story – inspire and motivate others by sharing your journey.
Support causes you believe in – whether it is protecting animals, equal rights, or the environment, take a stand.
Participate in advocacy – use your voice to support laws relating to cystinosis or kidney disease in general. Anyone affected by kidney disease can join the American Kidney Fund's Advocacy Network, where you can work to make a difference in the lives of others.
Talking to others about cystinosis
It can be frustrating or awkward having to explain cystinosis to people all the time. Remember: cystinosis does not define you as a person, and it is only one part of your life. If you feel comfortable sharing your diagnosis with others, then keep it up! If you need some time before opening up to others about your condition, then that is perfectly okay and very normal.
If you do decide to tell other people about cystinosis, here are some tips to help you have the conversation:
Explain the basics of cystinosis. It will be easier for others to remember key points, rather than a lot of detailed information at once.
Be honest about what you may not be able to do and tell others what you can do instead.
Let others know that you take care of yourself by taking medication and seeing a doctor.
Inform others that you do not want to be treated differently (if that is the case).
If you do not want to talk about cystinosis anymore, steer the conversation in a different direction.
You do not have to answer every question if you do not feel comfortable. Instead, you can direct others toward resources like the American Kidney Fund or Cystinosis Research Network to get more answers.
Let's take these tips and see what they would look like in a real-life situation.
Videos: How parents can help their child with cystinosis
Preparing for your child's transplant
When your child's medical exams begin showing signs of decreasing kidney function, you should start preparing your child for a kidney transplant. Here are some important considerations for parents supporting a child through transplant.
Up Next: Helping your child manage their kidney transplant
Helping your child manage their kidney transplant
Receiving a new kidney is worthy of celebration! However, it is important to recognize that a transplant does not cure cystinosis and a new kidney comes with new responsibilities. After the transplant survey, your child will stay in the hospital for about a week to recover.
Up Next: 5 tips on supporting your child with cystinosis
5 tips on supporting your child with cystinosis
Cystinosis is a rare, multisystem genetic disease that accounts for nearly 5% of all childhood cases of kidney failure. Cystinosis occurs in only about 1 in 100,000-200,000 children, so it is not widely known nor understood. Cystinosis can be tough on children, but there are ways you can support them and help them cope. Here are a few tips for parents supporting a child with cystinosis.
Thank you to our sponsor:
Educational content made possible by Horizon Therapeutics plc.