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One Breakthrough Way | Las Vegas, NV 89135 | www.Cure4thekids.org New Patient Handbook

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Page 1: New Patient Handbook - Home - Cure 4 The Kids Foundation › wp-content › uploads › 2020 › ...added physicians and nurses who meet our standards for quality and compassionate

One Breakthrough Way | Las Vegas, NV 89135 | www.Cure4thekids.org

New Patient

Handbook

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A Message from the Chief Medical Officer:A MESSAGE FROM OUR PRESIDENT/CEO:

Dear Friends,

It is with great excitement that I greet you from our new state-of-the-art facility located at One Break-through Way on the Summerlin campus of Roseman University of Health Sciences. Together with Roseman University, we have breathed new life into the wonderful building originally created by the Nevada Cancer Institute (NVCI) team. The NVCI team created a truly impressive and unique facility aimed at offering comfort and hope to many; we are honored to pick up where they left off and make this the new home for Cure 4 The Kids Foundation (C4K). As Nevada’s only nonprofit childhood can-cer treatment center, we are thrilled to offer our high quality medical care and research opportunities in such a patient centered location.

Cure 4 The Kids Foundation is in its twelfth year of operation with many remarkable achievements behind us. We still have many more ambitious goals ahead of us designed to bring more programs and services to the children of Nevada. Over twelve years, thousands of patients have been touched by the expertise of dedicated, knowledgeable, caring physicians and healthcare professionals who call C4K and Nevada home. We have been excited to welcome many new team members from across the country. We are thrilled about the recent expansion of our Behavioral Health program, to include behavioral health counseling and social work.

We could not have accomplished these great things without the dedication and support of our amaz-ing staff, our wonderful patients and their families, and our ever-growing community of supporters. We celebrate our progress; yet we know we are just getting started.

With much gratitude,

Annette Logan-ParkerCo-founder, President & CEO

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Table of Contents:

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“Some of the kindest nurses I’ve ever met. They continueto treat us like family from start to finish. We simplycouldn’t have asked for better care.”

Lindsey, Mother of Sidney, 4

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Welcome!No matter which specialty you may be visiting we want you to know that patient care is our utmost focus and concern. We strive to meet, and in many areas, exceed the highest standards in patient care. That is why The Joint Commission awarded us its Gold Seal of Approval® Accreditation in 2014. To keep this important accreditation current, facilities like ours must agree to undergo regular, unan-nounced site visits to ensure high patient standards are continuously being met, if not being sur-passed. As a patient, this is your assurance that you are receiving the best care possible. As medical providers, it is our duty to meet the standards of excellence in patient care.

In addition, we understand that there are many difficult situations and obstacles that may be placed in the lives of our families. We have a plan in place to help patients access the treatment they need. It is an essential portion of our mission to never turn a patient away from treatment due to the inability to pay. Our Charity Care Program assists those families without the ability to obtain medical insur-ance, or who are unable to pay for treatment. We also provide service to those with limited incomes by accepting payment on a sliding scale fee.

If you ever have concerns about your care, or the care of a child at one of our clinics, we encourage you to discuss it with your attending physician. If concerns persist, please notify Katherine M. Sal-kanovic, Patient Experience Manager at [email protected] or call (702) 862-1153.

With warmest regards from the Chief Medical Officer,

Alan Ikeda, M.D.Chief Medical Officer

A Message from the Chief Medical Officer:A MESSAGE FROM OUR CHIEF MEDICAL OFFICER:

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You, the patient, are the most important person in our office. We are committed to providing you with the best possible medical care in a friendly environment. Excellence is our goal. We provide a full range of services and have highly trained and knowledgeable staff. Please do not hesitate to ask us any questions about your medical care; we are here to help you.

In 2006, we created this organization with the goal of building the finest children’s outpatient med-ical center in Southern Nevada. Over the years we have grown our practice very carefully. We have added physicians and nurses who meet our standards for quality and compassionate care.

We are very proud of the full line of services that we offer, including our state-of-the-art procedure rooms and pharmacy as well as our child friendly infusion suite with the best view in the city. We hope that you quickly feel at home in our practice.

While we strive to provide our patients with excellent clinical results, we also work hard to make ev-ery patient have a positive patient experience in our clinic by feeling supported and respected every step of the way. We choose our team members with care, looking for people that embody our culture and values. Our goal is to make sure each patient is treated with kindness, respect, and professional-ism.

We believe deeply in what we do and we are eager to get to know you!

Sincerely,

Katherine M. Salkanovic, CPXP, MBA-HMPatient Experience Manager

Organizational Core Values

AccountabilityAlways maintain an environment where full professional and personal

accountability is not only an expectation but is rewarded.

IntegrityAlways doing the right thing at the right time for the right

patient and the right reason.

Continuous ImprovementAlways looking to make sure we are achieving the best possible outcomes for this patient while searching for improved means for the next patient.

Service ExcellenceAlways striving to provide the highest quality of care and insuring a

healthy and professionally rewarding career environment.

A MESSAGE FROM THE MANAGER OF PATIENT EXPERIENCE:

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Cure 4 The Kids Foundation is Nevada’s only childhood cancer treat ment center and facility for pediatric catastrophic diseases. Founded in 2007, we set out to create a legacy project for our community, not just another business. Our model blends the required structure and rigor of the best clinical practices found in centers of excellence; practices normally reserved for large corporate and/or academic healthcare environments, with the responsibility and generosity of philanthropy.

The primary approach behind our business model is to create a new kind of healthcare facility; one that blended the best of what corporate healthcare, education and research has to offer with the generosity, thoughtfulness, and spirit of charity. This hybrid model allows us to function like a traditional professional healthcare entity in terms of clinical outcomes, yet also allows us to be deeply human in our interactions with patients and their families. We have moved the focus from simply treating patients (children) to a new place of caring for this patient (child). We focus on the difference between what is and what should be; that is what makes us uniquely Cure 4 The Kids Foundation.

Organizational Core Values

AccountabilityAlways maintain an environment where full professional and personal

accountability is not only an expectation but is rewarded.

IntegrityAlways doing the right thing at the right time for the right

patient and the right reason.

Continuous ImprovementAlways looking to make sure we are achieving the best possible outcomes for this patient while searching for improved means for the next patient.

Service ExcellenceAlways striving to provide the highest quality of care and insuring a

healthy and professionally rewarding career environment.

PRECAUTIONS

ABOUT US:

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ACCOUNTABILITY CREEDWe are accountable, reliable, and trustworthy and act with integrity.

We stand ready to be counted upon to do the right thing for the health and highest interest of our patients, our team and for the organization.

We own and are responsible for our actions and outcomes.

We take responsibility for our own work and efforts and do not assign cause or blame toward others for the results we are generating.

We hold ourselves accountable to the agreements we make. It is never ok to simply miss mutually agreed upon deadlines but it is always ok to renegotiate time-lines whenever necessary to accomplish our objectives.

We hold ourselves accountable for the Patient Experience. We are answerable as individuals and team mem-bers for all interactions our patients have with our organization, we are in charge of patient perceptions, across the continuum of care we provide.

We are transparent and open in our communication both individually and as a team.We are open and respectful in our communication. We do not speak poorly of others and bring our challeng-es and grievances openly to our team and manager.

We are responsible for doing our part for patient outcomes through continuous quality improvement and service excellence.

We are focused on personal, professional and clinical excellence and improving our skills and awareness as a contributing team member. We are open to feedback and training to improve ourselves and the organiza-tion.

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JOINT COMMISSION GOLD SEAL OF APPROVAL

In 2012, Cure 4 The Kids Foundation received the coveted Joint Commission Gold Seal of Approval® Ac-creditation.The Joint Commission’s Gold Seal of Approval® Accreditation is considered by many in the medical com-munity to be the most stringent examination of health care standards, practices and policies. To main-tain the accreditation, our clinics have agreed to on-going and unannounced site visits to verify that we continue to meet high medical standards. As a patient in one of our clinics, this is your assurance you are receiving the best care possible. Only a small number of outpatient centers across the country have at-tempted to attain this accreditation, and fewer still have received it. We are proud to have been awarded this special recognition knowing the peace of mind it provides our patients. The Joint Commission’s state of the art standards require that patient care is provided in a safe manner and also measures the organi-zation’s performance in specific areas. The standards are based on consultation with healthcare experts, providers and researchers. Obtaining this accreditation indicates an organization is committed to the highest level of patient safety and care by meeting the rigorous performance standards.

INC 5000In 2018, Cure 4 The Kids Foundation was recognized by Inc. Magazine as one of the fastest growing com-panies in the nation and was ranked #2608 in the magazine’s prestigious “Inc. 5,000.”

50 Best Nonprofits to work for in AmericaIn April, Cure 4 The Kids Foundation received the 2019 Best Nonprofits To Work For designation from the Best Companies Group. Ranked at #23 among the Top 50 nonprofits nationwide, the award is based on a number of factors including Cure 4 The Kids Foundation’s ability to create and maintain workplace excellence, as well as employee surveys —covering eight categories— that showed 90 percent positive survey responses.

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Clinical ServicesAttending PhysicianMid-Level Provider

Nursing teamPharmacy team

Medical Assistant TeamLaboratory Team

Behavioral Health Neuropsychology

Play TherapyFamily Counselor

Social WorkerChild Life Specialist

Supportive Care TeamPatient Experience

Integrative CarePatient AdvocacyPatient Account Representatives

Patient Services Coordinators

YOUR HEALTHCARE

TEAM:

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The vision of the Cure 4 the Kids Foundation is simple. We want to be the community leader in ad-vancing the treatment and prevention of catastrophic diseases in children. We place a particular emphasis on helping those affected by childhood cancer, childhood rheumatic diseases, rare and ultra-rare diseases, genetic conditions and blood disorders.We have taken great care to create an environment that is family-friendly and kid-sized. We never forget the patient is a child or adolescent, and that treatments differ drastically from the way an adult would be cared for. We’ve selected board-certified physicians with highly specialized and unique skill sets from some of the most recognized academic establishments in the country. In addition, we’ve set up strategic affiliations with centers of excellence around the country to provide what’s needed by Nevada’s children.

It is scientifically proven that children who take part in clinical trials have a much higher rate of sur-vival. That’s one reason research is so important to us and why we encourage and participate in those trials. However, they are expensive. They also require additional diagnostic work, monitoring and ed-ucation. Sadly the most vulnerable type of cancer patient, the uninsured, has limited access to these life-saving clinical trials. We believe every child is entitled to the best treatment options that modern science has to offer. This is why we also place a great emphasis on raising money to support access to these trials for all children.

This is a general overview of the services available at the Cure 4 the Kids Foundation. For specific questions or to request a diagnosis, please call (702) 732-1493.

• Pediatric and Young Adult Oncology• Pediatric and Adult Bleeding and Clotting Disorders• Pediatric Rheumatology• Pediatric Neuropsychology• Pediatric Palliative Care• Pediatric Sickle Cell Disease and Hemoglobinopathies• Pediatric Clinical Psychology• Lysosomal Storage Disease and other Metabolic/Genetic Conditions• Rare and Ultra Rare Genetic Disease

We also host:• Board Certified Pediatric Specialists and Sub-Specialists• Procedure Rooms licensed by the Health Department as an Ambulatory Facility• Pharmacy Services-USP 797 Compliant Pharmacy

Specialized Nursing Certifications:• Chemotherapy and Biotherapy certified through Association of Pediatric Hematology and Oncology (APHON)• Certified Pediatric Hematology Oncology (CPON)

YOUR HEALTHCARE

TEAM:

SERVICES:

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• Keep a journal: this reference tool will help you keep track of your child’s treatment, including any reactions or side effects. Also use it to write down any questions between appointments that you want to ask your nurse or doctor.

• Make a special calendar: Your schedule can fill up quickly with appointments, so it may be helpful to create a special calendar to keep track.

• Make a list: Often, friends and family will ask you what they can do to help. Make a list of common duties they can help with such as providing meals, picking up your other children from activities, cleaning the house, doing the yard, etc. Allowing others to fulfill these requests will not only help you, but it will also let the other person feel like they are doing something constructive for you.

IMPORTANT NUMBERS:

Main clinic and after hours: 702.732.1493 Main clinic Fax: 702.732.1080

DO’S AND DON’TS

Do let us know if there is a change in your medical coverageDo let us know if your child has flu-like symptoms Do make yourself comfortable and ask us as many questions as you need.

Don’t smoke on our campus.Please, Don’t leave your child unattended in the facility.

HELPFUL TIPS:

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THINGS TO KNOW AND WHAT TO EXPECT DURING YOUR VISIT:

Knowing what to expect can help you and your child prepare for your visit to Cure 4 the Kids Foun-dation. Here’s a brief overview of what your daily visits may be like.Most families faced with childhood illness would agree that the first few visits are overwhelming. It may be helpful to bring someone with you to take notes during your visit so that you can focus on the discussion with your child’s doctor. A journal is helpful too. Whether you are coming for a check-up or an infusion, please note that space is limited. Sitting space is limited to two accompanying adults per patient. Small children get bored easily in the con-fined space, please try to make arrangements for siblings.

CHECK IN:

Please arrive for your appointment on time. This is extremely important, especially on infusion, labo-ratory and procedure appointments, as delays might cause you to stay late, or be transferred to the hospital. We understand that even the most organized parent can run late sometimes. If that’s the case, call us before your appointment time. We can try to reschedule your appointment for a time that’s better for you! Please note that there may be a $25 fee charge for no-call or no-show appoint-ments.

• Sign in at the front desk and be prepared to have your photo ID and your insurance cards available at every visit. • Wait to be called into your room. • We respect you time and want you to wait the least amount of time. With that in mind, there are days that we have a large number of triage calls (sick visits) that we must accommodate, that might make us run behind schedule. • In the room, the Medical Assistant will begin the triage process.• First, the patient will receive a unique wristband. In this wristband you can find the patient’s name, date of birth, medical records number, and allergies.• Our clinical team will ask you to verify that all the information listed on the wristband is correct. Before any laboratory test, medication, vital signs check, etc., the patient or parent will be asked to verify this information. This is for your protection.• Family Wristbands: To ensure that anyone entering our clinic is an approved visitor, parents, siblings, and other guests of the patient will be asked to wear a “clinic wristband”. For security purposes the color of the wristband changes every day. *Anyone not wearing a wristband (that’s not and employee or volunteer – see badge) will be escorted back to the front desk.• During the triage we start with taking vital signs, temperature, height and weight, blood pressure, and heart rate. You will be asked about medical history, medications, allergies, or sensitivities, and other important questions. • It is important that you bring your child’s medication bottles to the clinic for every visit. This will help us ensure that these medications are being given correctly and dosage accurately.

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During your visit… continued.

We make it FUN!Don’t be surprised to find Spider-Man roaming around the clinic! We keep our patients and families distracted by arranging:• Superheroes visit (Critical Care Comics)• Celebrity Visits (Famous singers, boxers, actors, etc.)• Sports teams (Las Vegas Golden Knights, The Aviators, Las Vegas Lights, etc.)• Seasonal Visits (Easter Bunny, Santa, etc.)

We can help! • We have a limited amount of iPads pre-programmed with kid-friendly games• We have coloring books and crayons (be mindful of tables and walls )• We have a collection of books your child can read• Our Child Life Specialist may have some recreational and diversional activities available foryour child during your visit

Note from our Child Life Specialist:What to pack to the clinic?• EMLA cream –• if your child has a port-a-cath, please apply EMLA cream (a quarter sized glob using Press-and-Seal) when you leave your home…we can always wipe if off if the port does not need to be accessed. If you forget, please let us know when you check in so that we can apply EMLA in the waiting room• Extra bottle and formula • Extra underpants and clothing bottoms – even kids who have long been toilet trained may inadvertently have an accident due to medications or stress

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MEDICATION MANAGEMENT

Our staff will ask you every time you come to the clinic about the medication your child (or you, if youare the patient) is taking. To be prepared to talk about medication management, you need to come prepared with the following information:

• Any medication allergies or sensitivities.• A list of all medication; including prescriptions, over the counter, herbs, vitamins, and natural remedies.• Knowledge of which healthcare professional prescriber which medication.

It is important that you bring the medications bottles with you to every appointment. This way the clini-cal team can review them with you and make sure that nothing is overlooked.

As the patient/parent it is your responsibility to know how to read a medication label and understand the instructions. Do not be afraid to ask questions about any of the medications prescribe to you or your child.

What to do if you do not understand what your healthcare professional is saying?Tell them you do not understand. If you require assistance of an interpreter, we can arrange this for you. It is very important that you understand the instructions given to you.

What is Informed consent?Informed Consent is a document that you will be asked to sign in the event that a treatment needs to be prescribed or a procedure is required. Reviewing the document is an important step in ensuring you know what is happening and why.

Prescription Refill Request • Before you call, please make sure there are no “refills” available on the medication label. If so, please call your local pharmacy.• If there are no refills available, please call our main number and select: Prescription Refill (option 5, then press 2). On your message, please leave: Name of the patient, date of birth, name of the medication and dose. A team member will call you to update you on the request with 48 hrs.

Please note:• Some medications require prior authorization. We will let you know if this is the case. Keep in mind this might delay the process, please plan ahead. • Do not wait until you are out of medications to call us. While we take priority on your request, pharmacies do not stock all medications, and ordering medications could take days.

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If your child experiences a life threatening emergency, please dial 911 immediately!

Triage CallsDuring business hours: If your child isn’t feeling well, please call our office. Our operator will initiate an urgent message with your nurse and physician. The nurse will call you to verify symptoms and give you instructions on how to pro-ceed as advised from your child’s doctor (medication, clinic visit, hospital admission, etc.)

During after-hours:If your child isn’t feeling well, please call our office number. Our answering service will take a message and forward it to our doctor on call.

WE HAVE A DOCTOR ON CALL 24/7. We round at the following hospitals:

Summerlin Hospital and Sunrise Hospital

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Referral RequestsDepending on the diagnosis, our pro-viders might refer your child to other specialists, additional testing, or scans (CT, MRI, PET, etc.).We will obtain the necessary authoriza-tion from your insurance company and set up the referral for you.

Please note:• This can sometimes take several days to complete.• If your insurance denies the referral, we will start an appeal process.

Patient PortalYou have the option to sign up for “Fol-lowMyHealth”, our Patient Portal. After your first appointment you will receive an email invitation.

FollowMyHealth patient portal is an online tool that provides anywhere/anytime access to your personal health record, and enables you to take a more proactive role in managing your care.

With FollowMyHealth you can:• Send secure messages• Send medication refill requests• See upcoming appointments• And much more.

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SafetyIsolation Process:• Your child may be placed on isolation if:• we suspect or know that your child has an infection that can be spread to others in the clinic, or• Your child carries certain types of germs, even if they are not making him/her ill. • If your child gets placed on isolation, your nurse will give you education materials about the type of isolation.• Until your child gets cleared from isolation, you will stop at our “Isolation Station” located by the security desk and pull the items required by the type of isolation (masks, gloves, gowns, bouffant caps, etc.)• You and your child will access the clinic by:• Check in with the receptionist located in the lobby (1st Floor).• Stop at the “Isolation Station”- Collect, and put on required items.• Take the private elevator to the 3rd floor waiting area (more isolation reading material available there).• Use the iPad to check in, and ring the bell. • A member of the Patient Services team will come escort you to your room. • If the patient uses the restroom, please flip the sign from “clean” to “dirty” to notify our crew. • Going home, you and your child will take the private elevators down to the lobby.• A member of the Patient Services team will call you to schedule your next appointment.

Patient Safety GoalsAt Cure 4 The Kids Foundation Clinic, your safety is a top priority for all of us. During each and every visit, you can expect ‘The 4 Important Questions’.

1. What’s your full name? 2. What’s your date of birth?3. Do you have any allergies? 4. Do you know why you’re here?

Why? To ensure accuracy of patient identification!

Infection ControlKeeping hands clean through improved hand hygiene is one of the most important steps we can take to avoid getting sick and spreading germs to others. Many diseases and conditions are spread by not wash-ing hands with soap and clean, running water. • Hand hygiene means cleaning your hands by either using handwashing (soap and water), antisep tic hand wash, antiseptic hand rub (alcohol-based hand sanitizer), or surgical hand antisepsis.• Practicing good hand hygiene is the number one technique in preventing the transmission of infectious diseases from one person to another.• Our patient population is immunocompromised, which means that they have a low immune sys tem that helps them in fighting infections. Their low immune systems are often caused by the treatment they receive in our clinic.• Infectious agents can cause our patients to have a prolonged hospital stay and can be potentially fatal since their immune system cannot fight against infections.

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Facility PolicyPatient safety is of the utmost importance to us, so you may be here we are conducting a fire drill. If this happens, we hope that you don’t mind participating. Your participation will ensure we evacuate safely in case of a true emergency.

Child’s Bill of RightsAt Cure 4 The Kids Foundation, you and your family have the right to:Respect and Personal Dignity - You are important!• We want to get to know you• We will tell you who we are, and we will call you by your name• We will take time to listen to you• We will not talk about you in your room or outside your door unless you know what is happening• We will honor your privacy

Care that Supports You and Your Family - You and your family are important.• We will work together to make you as safe and comfortable as possible.• All families are different. We want to learn about what’s important to you and your family.• There will be a place for a member of your family to spend the night in the hospital with you or near you.

Emotional Support - When you are here, you might feel scared, mad, lonely or sad. You can let people know how you feel. It is OK to cry or complain.• You can have your family with you as much as possible. When this is not possible, the other people caring for you will explain why.• We can help you meet children and families who have had experiences like yours.• You can talk or play with people who know how to help when you have questions or problems.

Make Choices and Decisions - Your ideas and feelings about how you want to be cared for are important. • You can tell us how we can help you feel more comfortable. • You can tell us how you want to take part in your care.• You can make choices whenever possible.

Information You Can Understand - We will explain things to you.• We will speak in ways you can understand.• You can ask about what is happening to you and why.• Someone who speaks your language will help explain things to you.• Someone from your family can be with you when people are explaining things to you.

Quality Health Care - You will be taken care of by doctors, nurses and other people who know about children and teenagers.• You have the right to know all of the people who take care of you in the hospital. You and your family can meet with your health care team to plan what is best for you• We will work with you and your family to make your visit as positive and as comfortable as possible• You have the right to be without restraints whenever possible. • You have the right to cry and make noise of object to anything that hurts you. • You have the right to have your procedures scheduled in a way that does not keep you hungry or thirsty any longer than necessary.• You have the right to be greeted with a smile and receive loving care.

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• You have the right to reasonable continuity of care• You have the right to be advised of the grievance process, should you wish to communicate a con cern regarding the quality of the care you receive. Notification of the grievance process includes: whom to contact to file a grievance, and that you will be provided with a written notice of the grievance determination that contains the name of the facility contact person, the steps taken on your behalf to investigate the grievance, the results of the grievance and the grievance completion date.• You have the right to be advised if the facility/personal physician proposes to engage in or perform human experimentation affecting your care or treatment. The patient has the right to refuse to participate in such research projects. Refusal to participate or discontinuation of participation will not compromise the patient’s right to access care, treatment or services.• You have the right to full support and respect of all patient rights should you choose to participate in research, investigation and/or clinical trials. This includes the patient’s right to a full informed consent process as it relates to the research, investigation and/or clinical trial. All information provided to subjects will be contained in the medical record or research file, along with the consent form(s).• You have the right to be informed by your physician, or a delegate of theirs, of the continuing healthcare requirements following your discharge.• You have the right to examine and receive an explanation of your bill regardless of source of payment.• You have the right to know which facility rules and policies apply to your conduct while a patient.• You have the right to have all patients’ rights apply to the person who may have legal responsibility to make decisions regarding medical care on behalf of the patient.

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PATIENT RESPONSIBILITIESThe care a patient receives depends partially on the patient himself. Therefore, in addition to these rights, a pa-tient has certain responsibilities as well. These responsibilities are presented to the patient in the spirit of mutual trust and respect:

• The patient has the responsibility to provide accurate and complete information concerning his/ her present complaints, past illnesses, hospitalizations, medications and other matters relating to his/her health.• The patient is responsible for reporting perceived risks in his or her care and unexpected changes in his/her condition to the responsible practitioner.• The patient and family are responsible for asking questions about the patient’s condition, treatments, procedures, Clinical Laboratory and other diagnostic test results.• The patient and family are responsible for asking questions when they do not understand what they have been told about the patient’s care or what they are expected to do.• The patient and family are responsible for immediately reporting any concerns or errors they may observe.• The patient is responsible for following the treatment plan established by his/her physician, including the instructions of nurses and other health professionals as they carry out the physician’s orders.• The patient is responsible for keeping appointments and for notifying the facility or physician when he/she is unable to do so.• The patient is responsible for his/her actions should he/she refuse treatment or not follow his/her physician’s orders.• The patient is responsible for assuring that the financial obligations of his/her facility care are ful filled as promptly as possible.• The patient is responsible for following facility policies and procedures.• The patient is responsible for being considerate of the rights of other patients and facility personnel.• The patient is responsible for being respectful of his/her personal property and that of other persons in the facility.

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Your feedback is appreciated...Our main goal is to make your clinic visit a positive experience. We strive to provide you and your family with service excellence. Let us know if your experience was as pleasant as we hoped, or if there is room to make it better. We appreciate you taking the time to give us feedback, please know, that we will use it to evaluate changes and improvements in our clinic.

We invite you to use our “Happy-or-Not” survey platform located around the clinic, and our interactive “happy” touch screen located by the check-out desk. These surveys help us calculate our daily “Happy Score”. You will be able to review our daily Happy Score in our website – coming soon!

For other matters, we encourage you to raise questions or concerns about any aspect of your care or service by communicating with our Manager of Patient Experience. You may address your concern(s) by emailing Katherine M. Salkanovic at [email protected].

Understanding our Billing ProcessDeductibles and co-pays are expected to be paid at the time of services. Payment arrangements may be made by speaking to a member of the reimbursement staff.

As our patient, we care about you and want to help you understand our billing process. The best action you can take as a patient to ensure that your billing is accurate and complete is to make sure that we have correct information about you. This information should include:1. Your Name/Address/Phone Number2. The Name/Address/Phone Number of your guarantor (the person responsible for your bill)3. The name of your insurance company/group number, plan number or other identifying numbers4. Claims filing address and your insurance company’s phone number

IF YOU ARE NOT COVERED BY INSURANCEIf you are not covered by insurance, our Patient Account Representative will provide an estimate of the cost of your care. This estimate will include anticipated hospital, clinic, and physician charges, based on the recommended treatment plan. Please be aware that our estimate may vary from actual treatment cost due to a variety of factors. You are responsible for the full cost of your care.All self-pay patients/parents are asked to sign an agreement to pay for services received. You also may be asked to provide a deposit in advance covering the estimated cost of your treatment. If your estimate has been paid in full in advance, you may be eligible for a discount from the actual charges. For more information, please contacta Patient Account Representative.If your treatment plan changes during the course of your care, you may be asked to agree to a new esti-mate. You also may be asked to increase your deposit.

PAYMENT OPTIONSIf you are a self-pay patient or if you have a financial obligation to Cure 4 The Kids Foundation after your in-surance has fulfilled its financial responsibility, you will be expected to pay the balance due. You will receive a Patient Statement showing all open balances.

If you cannot pay your patient balance in full, it may be possible to arrange a Payment Plan. Our Patient Ac-counts Representative can provide information about the monthly Payment Plans that are available.

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CHARITY CARE PROGRAM:Cure 4 the Kids Foundation believes all patients deserve the chance for recovery and to receive the latest and most current treatment protocols for a variety of specialized diseases such as cancer.That was the idea of our founders when they decided to create Cure 4 The Kids Foundation back in 2007. They saw firsthand that the outcome of many patients facing a life-threatening health crisis was often deter-mined solely by the amount of their medical insurance coverage, or lack thereof.

The Charity Care Program ensures patients who are unable to pay for treatment, or without medical insur-ance, will receive the medical attention they need. Cure 4 the Kids Foundation will never turn a patient away from treatment for financial reasons.

If you have specific questions about the Charity Care Program, and whether you might qualify, we highly recommend that you contact our Billing Department at [email protected] or (702) 862-1134. We strongly suggest you contact our billing department by email or phone to get additional information relat-ed to your specific circumstance.

Frequently Asked Questions About Billing

What should I do if my insurance changes?Please immediately inform our Patient Account Representatives at 702-862-1134. Incorrect information may cause us to miss your insurance company’s filing deadline. You may be financially responsible for services provided.

Why do I still have a balance if my insurance company pays 100% of Reasonable and Customary charges?Some insurance carriers base payment on the average charge for all medical services in a given area. This approach does not take into consideration the specialized nature of the care we provide and may not cover the full cost of the care you or your child receives. You may be responsible for any balance. You are encour-aged to discuss your coverage with your insurer prior to treatment.

How will my payment be applied?Payment in full is applied to hospital/clinic charges and to physician charges as indicated on your statement. If you pay a lesser amount, payments will be applied to the oldest open invoice. To ensure timely and accu-rate payment posting, please include your remittance coupon, which is attached to your statement.

Additional Questions?If you have questions about any phase of the billing process or about your patient statement, please call us at: 702-862-1134

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ADVANCE DIRECTIVES:What is an advance directive?An advance directive pursuant to NRS 449.905 is a document stating one’s wishesregarding end of life decisions, which includes but is not limited to a: living will, healthcare proxy or similar document(s), including organ donor information.

Why do I need an advance directive?An advance directive is the best approach in letting your wishes be known and honored by your family, friends, and health care providers during an emergency or illness.

The Patient Self-Determination Act (Which includes Advance Directives) requires us to inform you of your rights as a patient and of our policies:

1. You have the right to make decisions concerning your medical care.2. You have the right to accept or refuse medical or surgical treatment, including the right to formu late advance directives (declarations and/or durable powers of attorney for health care decisions).3. You have the right to be given information concerning Advance Directives within 24 hours of ad mission to a hospital.4. Upon registration, you will be asked if you have an advance directive.5. It will be documented in your medical record whether you have an advance directive.6. If you have an advance directive you should furnish a copy to Cure 4 The Kids Foundation, so it can be placed in and made a part of your medical record/chart, so our providers are made aware of your medical treatment desires.7. If you have an advance directive it will be honored by the facility.8. For further information regarding advance directives, or to obtain advance directives forms, please contact us at [email protected]. For further information in the community you may contact The Nevada Center for Ethics & Health Policy, (775) 327-2309, http://www.unr.edu/ncehp/ads.html

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Complaints or grievances concerning advance directives noncompliance may be addressed to:State of Nevada Department of HealthState Health DivisionBureau of Health Care Quality and Compliance Licensure and Certification Program727 Fairview DriveCarson City, NV 89701(775) 684-1030

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Alan Ikeda, MDChief Medical Officer, Board Certified Pediatric Hematology-Oncology

Dr. Ikeda joined the Cure 4 the Kids Foundation in 2011. He is a Board Certified in both Pediatrics and Pediatric Hematology On-cology. The Children’s Specialty Center worked to recruit Dr. Ike-da in part because of his skills in managing the complexities and needs of bone marrow transplant patients. His research interests include stem cell transplants as well as cell and gene therapies.

Dr. Ikeda received his medical degree from the John A. Burns School of Medicine where he also completed his residency in Pediatrics. He completed his fellowship in Pediatric Hematology Oncology at the David Geffen School of Medicine at UCLA. He served as the Assistant Director of Pediatric Blood and Marrow Transplant Program at Mat-tel Children’s Hospital at UCLA. He is also a member of the Children’s Oncology Group, an international collaboration of children’s cancer research protocols. Dr. Ikeda has received several grants and awards for his research efforts in Sickle Cell Disease and Gene therapy.

Dr. Ikeda was born and raised in Hawaii and has been known to entertain patients by playing the guitar.

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Jennifer Buitrago, APRNInterim CNO

Jennifer is a Nationally Certified Nurse Practitioner. She is a Cali-fornia native and attended the University of Southern California where she obtained her Bachelor’s Degree in Nursing. She com-pleted a Master’s Degree and received her Advanced Practice Degree in Nursing at the University of California, Los Angeles. Jennifer has been a Pediatric Hematology/Oncology/BMT Nurse for 20 years. She has worked at Rady’s Children’s Hospital, Loma Linda University Children’s Hospital, Comprehensive Cancer Centers of Nevada, Cure 4 the Kids Foundation, Hemophilia Treat-ment Center of Nevada, and most recently Children’s Hospital Los Angeles. Jennifer is one of the original members of the Cure 4 the Kids Foundation clinic staff and was a founding Board Member for Cure 4 the Kids Foundation.instructor for the Association of Pediatric Hematology Oncology Nurses (APHON) Chemotherapy/Biotherapy Provider course for over 10years. She holds two prestigious certifications: Certified Pediatric Oncology Nurse (CPON) and Bone Marrow Transplant Certified Nurse (BMTCN).

Jennifer is also a wife and mother and enjoys spending time with her two beautiful daughters and family.

Waseem Alhushki, MD Long-Term Follow-Up Clinic Lead Physician, Board Certified Pediatric Hematol-ogy-Oncology

Dr. Alhushki joined Cure 4 the Kids Foundation in 2013.He developed a passion for Pediatric Hematology Oncology while working at King Hussein Cancer Center. He is Board Certified in Pediatrics and in Pediatric Hematology Oncology.

In 2006, Dr. Alhushki volunteered in three local missions as part of the medical team of “Operation Smile”, an organization that aims at reaching children all over the world with cleft lip/palate deformities. He also participated in design-ing and conducting workshops on healthy lifestyles, conflict resolution and team work in collaboration with the United Nations Children’s Fund (UNICEF) and the United Nations Population Fund (UNFPA).

In 2007 he joined the Children’s Hospital of Michigan Pediatrics residency pro-gram at Wayne State University and graduated in 2010. He was also honored with the General Pediatric Clinic Outstanding Continuity Clinic Resident Award, Academic year 2009-2010.In 2010 he joined the Children’s Hospital of Los Angeles’ Pediatric Hematolo-gy Oncology program. His fellowship research project focused on the role of weight loss in improving outcome for obese children with acute lymphoblastic leukemia.

In addition to English, Dr. Alhushki speaks Arabic fluently, enjoys reading, play-ing guitar and skateboarding.

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Danielle Bello, Ph.D.Director of Neuropsychology and Long-Term Follow-Up Clinic

Dr. Bello joined the Cure 4 the Kids Foundation in 2015. She is a li-censed clinical psychologist and neuropsychologist. Dr. Bello is originally from New York and completed her bachelor’s degree at Binghamton University with a focus on business management.She obtained a master’s degree in psychology at New York Univer-sity and completed her doctoral degree in clinical psychology at the University of Nevada, Las Vegas. Dr. Bello attended the neu-ropsychology internship at the University of Oklahoma Health Sciences Center. She also completed two years of postdoctoral residency in neuropsychology. Dr. Bello found her interest in psy-chology and helping children while volunteering for nonprofit organizations in New York. She returned to school switching ca-reers from business to psychology. She has interests in examining the cognitive and psychological impacts of various brain injuries.

Dr. Bello has served as a practicum training supervisor for doctoral students and has taught both graduate and under-graduate courses in psychology. She is a member of various

Angela Berg, DNP, APRN, CPNPDirector of Specialty Services, Pediatric Palliative Care Director

Angela Berg DNP, APRN, CPNP achieved her Doctorate in Nurs-ing Practice (DNP) from the University of Utah following a sea-soned career as an RN in a variety of pediatric settings. Her back-ground has given Angela the passion for providing top quality care to children, supporting cost-effective care options, and de-veloping care models to provide for functional care for children.

Angela began the first clinic based outpatient pediatric palliative care program for Nevada right here at Cure 4 the Kids Foundation in early 2016. Angela serves as the Director of Specialty Services Clinic, Pediatric Palliative Program Director, and nurse practitioner for the palliative and rheumatology patients. She is also a founding board member of the Board of Directors for Cure 4 The Kids Foundation.

Angela heads a monthly program we do here at Cure 4 The Kids Foundation called ‘First Friday Happy Healthy Hour’. We look atx x x x x x x x x x x x x x x

professional organizations including the National Academy of Neuropsychology and the American Psy-chological Association. Dr. Bello enjoys spending her free time with her husband and two children.

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Children’s Hospital, Washington University School of Medicine and her fellowship in Pediatric Immunology/Rheumatology at Washington University School of Medicine. While in Navada, Dr Brown has spent a lot of time and photographing Red Rock National Park.

Nicola Longo, MD PhD.Board Certified Pediatric Geneticist

Dr. Longo has been a member of our Visiting Physician Pro-gram since 2009. Currently, he is the Chief of the Division of Medical Genetics at the University of Utah. His past professional experience includes Director of Clinical Biochemical Genetics Fellowships Program, as well as Professor (Tenured) in Medi-cal Genetics/Pediatrics and Professor (Adjunct) in Pathology at the University of Utah. He also served on numerous scien-tific review committees for the National Institutes of Health.

Dr. Longo sees patients in Las Vegas on a regular basis. He also oversees the state of Nevada’s Newborn Screen-ing Program, which tests all newborns for genetic disor-ders so that early treatment can be offered, if needed. Dr. Longo is increasing the amount of time he spends in Neva-da to expand treatment for those patients with Lysosomal Storage Disorders (LSD). Bringing Dr. Longo’s unique and spe-cialized expertise to Nevada allows patients to access a lev-el of care not currently available at any practice in Nevada.

Diane Brown, MD, Ph.D.Board Certified Pediatric Rheumatologist

Dr. Diane Brown is a visiting physicians at the Cure 4 the Kids Foundation. She is a Board Cer-tified Pediatric Rheumatologist, one of approxi-mately 150 such physicians practicing in the Unit-ed States. She travels to our clinic once a month specifically to see patients with rheumatological diseases such as: juvenile rheumatoid arthritis, lu-pus, scleroderma, and juvenile dermatomyositis.

Dr. Brown is an associate clinical professor of Pe-diatrics, Division of Rheumatology and Rehabili-tation, Children’s Hospital of Los Angeles and Uni-versity of Southern California School of Medicine.

She received her M.D. and PhD. degrees from the University of California at San Francisco. She completed her residency in Pediatrics at the St. Louis

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Physical Therapists

Physical Therapists

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Mary Bio

Claudia Bio

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SPECIALTY PROGRAMSThere are many medical conditions that require specialized treatments that are typically only available in major metropolitan areas — most often within large teaching hospitals. The Specialty Services Clinic at the Cure 4 the Kids Foundation has worked for many years to expand these services into Nevada. Through agreements with respected facilities and providers, the Specialty Services Clinic provides ac-cess to highly specialized care that would not otherwise be available in the state.

Child Life SpecialistMost clinics don’t employ their own Certified Child Life Specialist. With our focus on pediatric specialized and medically complex treatments, we understand the many benefits these professionals provide to our patients and their families.

Our in-house Child Life Specialist, Sue Waltermeyer, has more than 30 years of experience in this field, and is trained to help your child and fam-ily understand and cope with having an illness. Sue’s expertise improves care and treatment, increases patient satisfaction, and provides a better experience for the entire family. She can assist you and your child with:

• Developmentally appropriate explanations of their diagnosis and treatment• Identifying and practicing coping techniques to manage anything difficult related to their treatment• Medical play opportunities to increase understanding and coping• Non-pharmacological pain management, including the use of Virtual Reality goggles• Developmental assessments for children 3 and younger• Parenting education and support• Sibling education and support• Recreational and diversional activities

Palliative Care Programxxxxxxxxxxxxxxxxxxx

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StoryBook Homes Long-Term Follow-up ProgramThe most important thing you can do as a childhood cancer survivor is to stay healthy. That’s why we created the Storybook Homes Long-Term Follow-Up Clinic for Childhood Cancer Survivors.

The Storybook Homes Long-Term Follow-Up Clinic for Childhood Cancer Sur-vivors will educate each patient on specific risks from their treatments such as chemotherapy, radiation and surgery. Knowing these possible risks will al-low patients to better monitor their health, address any complications early, and live a healthy and informed life.

Patients are eligible for Long-Term Follow-Up services two years after their final cancer treatment. To make an appointment at the Long-Term Follow-Up Clinic, or for additional information, call (702) 732-1493.

Bleeding & Clotting Disordersxxxxxxxxxxxxxxxxxxx

Pediatric Rheumatology

There are limited Board-Certified Pediatric Rheumatologists permanently based in Nevada. Yet, treating patients for conditions such as childhood lupus, scleroderma, and juvenile idiopathic arthritis are quite different than treating adults with similar conditions. We believe it is important that children get the most appropriate care for their young bodies. That is why we have an agreement with Children’s Hospital Los Angeles, Division of Rheumatology, to bring two Board-Certified Pediatric Rheumatologists to Nevada every month.

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BEHAVIORAL HEALTH PROGRAMPlay Therapyxxxxxxxxxxxxxxxxxxx

Neuropsychologyxxxxxxxxxxxxxxxxxxx

Social Workerxxxxxxxxxxxxxxxxxxx

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EDUCATION CENTER & LIBRARY

Neuropsychologyxxxxxxxxxxxxxxxxxxx

Education Centerxxxxxxxxxxxxxxxxxxx

Social Workerxxxxxxxxxxxxxxxxxxx

ONSITE SERVICES

Pharmacyxxxxxxxxxxxxxxxxxxx

Labxxxxxxxxxxxxxxxxxxx

Infusion Centerxxxxxxxxxxxxxxxxxxx

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Play TherapyEducation CenterLibrary/Tutoring Services

Our Community Partners work closely with us to provide a wide range of services to our (eligible) patients. Some of these services include:

• Education• Transportation Assistance• Financial Assistance• Events• Wish Granting• Hospital Admission Assistance

COMMUNITY PARTNERS:

Contact information

CandlelightersBLURB---xbxbxbxbxbxbxbxXbxbxbxbxbxbxbxbxbxbxbxbxbxbbxnxnxnxnxnxnnxnxnxnxnx702-xxx-xxxx

Make-a-WishBLURB---xbxbxbxbxbxbxbxXbxbxbxbxbxbxbxbxbxbxbxbxbxbbxnxnxnxnxnxnnxnxnxnxnx 702-xxx-xxxx

American Cancer SocietyBLURB---xbxbxbxbxbxbxbxXbxbxbxbxbxbxbxbxbxbxbxbxbxbbxnxnxnxnxnxnnxnxnxnxnx 702-777-7777

Ronald McDonals HouseBLURB---xbxbxbxbxbxbxbxXbxbxbxbxbxbxbxbxbxbxbxbxbxbbxnxnxnxnxnxnnxnxnxnxnx 702-xxx-xxxx

Nevada Childhood Cancer FoundationBLURB---xbxbxbxbxbxbxbxXbxbxbxbxbxbxbxbxbxbxbxbxbxbbxnxnxnxnxnxnnxnxnxnxnx 702-xxx-xxxx

Summerlin HospitalBLURB---xbxbxbxbxbxbxbxXbxbxbxbxbxbxbxbxbxbxbxbxbxbbxnxnxnxnxnxnnxnxnxnxnx 702-xxx-xxxx

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MEDICATION LIST:

Medication Dose Frequency Notes

Ronald McDonals HouseBLURB---xbxbxbxbxbxbxbxXbxbxbxbxbxbxbxbxbxbxbxbxbxbbxnxnxnxnxnxnnxnxnxnxnx 702-xxx-xxxx

Nevada Childhood Cancer FoundationBLURB---xbxbxbxbxbxbxbxXbxbxbxbxbxbxbxbxbxbxbxbxbxbbxnxnxnxnxnxnnxnxnxnxnx 702-xxx-xxxx

Summerlin HospitalBLURB---xbxbxbxbxbxbxbxXbxbxbxbxbxbxbxbxbxbxbxbxbxbbxnxnxnxnxnxnnxnxnxnxnx 702-xxx-xxxx

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NOTES

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