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What is an accredited CF Center, and why does it matter? It means that the center has been reviewed by the Cystic Fibrosis Foundation and has nationally-accepted standards. But what it really means is that your child has access to most advanced CF care available today.
Our center provides dedicated professionals who specialize in the treatment of Cystic Fibrosis and in the care of human beings. Your team may include but is not limited to your physician, nurse, respiratory therapist, dietician, and social worker–all in the same location. It's added convenience for patients and, because it allows increased communication between the staff members, detailed attention too.
Whether you're a new patient, an existing pediatric patient, or are seen in our adult program, you'll find one thing in common, exception care. The following information can help assure that your visits are as easy and smooth as possible.
Going the distance
Carol Shepherd is in her 50s, and she was a patient of Dr. James C. Cunningham from 1987 until transferring to the adult program. Once told she would not be able to have children, she is the proud mom of twins–who are now in their 20s. Dr. Cunningham considers her a true role model for others, attributing her great attitude and her participation in research for helping her to stay healthy.
These days, you'll find CF patients enjoying life: playing, getting married, working, having families, going off to college, celebrating the ups and downs of everyday lives; all thanks to the many advancements in care and treatment for children and adults living with CF. Many of them are patients at Cook Children's Medical Center. In fact we currently follow over 300 patients, approximately 200 in our pediatric program and around 100 in our adult program.
Over the past few decades, the outlook for cystic fibrosis (CF) patients has improved dramatically. Today, the median age range is late 30s to early 40s.
The Cook Children's CF Clinic sees patients from birth all the way through adulthood, typically transitioning our kids from our pediatric CF center to our adult CF center somewhere in their late teens.
Cook Children's pediatric center begins caring for a child from the moment they are diagnosed with CF until they are ready to transition to our adult center. Thanks to many advanced in technology, and newborn testing, we are able to diagnose and treat people with CF even before symptoms begin. Our family centered team approach allows us to observe patients, and provide state-of-the-art treatment when needed. We also assure that patients and families have access to education, training and support at each clinic visit to manage the disease and help maintain a healthy lifestyle.
Depending the type and severity of your child's CF, clinic visits will usually be scheduled every 2-3 months. Outpatient care may include some, all, or a combination of the following:
When you have CF, medical issues may arise that require an inpatient stay. Our nationally recognized pulmonology team is at hand and ready to provide excellent care.
During your child's stay, your medical team may also include Child Life specialists, physical and occupational therapists, social workers, respiratory therapists, nutritionists and/or dietitians
Better treatments mean people with CF are living longer than ever before. That means more children are growing up and moving from a pediatric program to an adult program. From the time your child enters Cook Children's CF Clinic, we begin preparing them–and you–for that transition. We teach them about their disease and help them learn to take control at age and maturity appropriate stages of their growth. By the time they are teens we begin encourage them to manage their appointments as well. CF is a lifelong condition, at least until we find a cure. Until then, it important that they learn how to balance their CF and medical needs while developing healthy independence, relationships, jobs and life.
There are also many challenges faced by adults, including work, family, finances and, of course, health. Every aspect of your life is affected in some way by CF, and we provide ongoing care, including treatment, support and education for the various illnesses and risks that adults may deal with, such as:
At Cook Children's CF Clinic, the pulmonologists head the care team, which includes the following members:
At your first visit and once a year after that, you'll meet with all of the care team mentioned above to develop a plan to optimize your child's health. This visit will be longer than a routine or sick visit since you will be meeting with the entire care team. It may include the following tests:
For those over age 4-5 (as developmentally appropriate) there is lung function testing (spirometry)and lung volumes; children not able to have the spirometry test done will still meet with Respiratory to review CPT (chest physical therapy) and nebulizer cleaning methods.
We recommend visits to our CF Clinic at least every 3 months and at the onset of illness. The following are ways to maximize your child's health between visits:
At your first visit and once a year after that, you'll meet with all of the care team to develop a plan to optimize your child's health, or if you are a teen or adult, your own health. This visit will be longer than a routine or sick visit since you will be meeting with the entire care team.
Your initial visit will include a complete medical history as well as any or all of the following:
Your doctor may have you meet the research coordinator, if needed, to review studies you may enroll in to benefit those with CF.
Upon completion of your visit you will check-out and make your appointment for your next visit.
Routine follow-up appointments in the Cystic Fibrosis (CF) clinic may be scheduled every 3 months between annual visits. If your child is sick, has a cold that lingers, or develops a cough or other difficulties, we may advise treatment and/or schedule an "as needed" visit at the CF Center.
Other visits may be scheduled more frequently if your child is having other concerns such as weight gain, or has just recently been diagnosed with CF. In fact, if you are new to CF our center recommends more frequent visits at first, until you feel you have received the right amount of education, have met appropriate team members and feel comfortable with your child's care.
Every patient's visit will be based upon their individual needs, but the following are some things you may expect to happen when at a CF clinic appointment. Please be sure to bring a list of questions for you to ask at your clinic visit.
Please check-in on the first floor of the Dodson clinic building in Registration then with the receptionist at the Pulmonary Clinic. We recommend you arrive 30 minutes prior to your appointment. This ensures you have plenty of time to provide us with any updates in information, such as change of address, change of phone, or change of insurance.
Medical assistants will take following measurements:
Pulmonary functions will do the following:
Your doctor will:
Your dietitian (if needed) will do the following:
Social worker (if needed) can offer
Child Life is available for
Research (if needed) is available to
CF Coordinator will help
While we recommend follow-up visits every three months to keep your child's health on track, there are also ways to maximize your child's health between visits:
A typical yearly visit will average around 2-3 hours. At this visit, you will see your physician, your nurse, get weighed and measured, do pulmonary function tests, have a chest x-ray, do a sputum culture, have blood work done, get a T.B. skin test done, and consult with Nutrition, Social Work, and Child Life.
Once your CF Care Team has decided a hospitalization is needed, your nurse will let you know when to check in at the Admissions desk. This is helpful in case you need to pack or plan for alternative care of siblings. Check in at the Admissions desk usually takes about 15-30 minutes. They wait for the room to be ready before registering your child. Paperwork is completed and a copy of your insurance card is needed. A representative then walks you and your child to the room. Shortly after you arrive in your room, your floor nurse will stop by to introduce her or himself to you. Information will be taken from you and the plan of care your physician has made will be gone over with you.
Since most hospitalizations are for treatment of lung infections that don't respond to outpatient treatment. IV access will be made in the treatment room or child's room if a peripheral line is needed. PICC lines are put in by the PICC team. Ports can be accessed by your nurse in the room.
Infection control is a high priority at Cook Children's. The nurse will go over procedures you and your child should do to prevent acquiring an infection while hospitalized. Staff should always use gowns and gloves when entering the room. Staff encourages you to remind them if they should forget. Additional isolation procedures will be explained to you.
A nursing aide will stop by your room periodically to weigh, take your child's blood pressure and pulse ox. They are a good person to ask for extra blankets, sheets, or toiletries needed for your child.
The Child Life Department helps children and families cope with the medical center experience. Child Life staff provides support and information geared to the child's level of understanding and provides a variety of opportunities for play and expression. Child Life staff members are usually in the playrooms, or you may ask your nurse where to find them.
Respiratory Therapy will stop by your room and go over your treatment schedule with you. They will provide a disinfected therapy vest compressor for your child to use exclusively in the room. They will measure your child for a correct vest size. A disposable vest will then be given to your child for the duration of their stay. Patients may also bring in their own equipment if they prefer.
Physical Therapy will stop by if prescribed by your physician. They can do stretching exercises or bring balls to throw around your room if you cannot leave the room. Or, you will go downstairs to the PT gym where there is a treadmill, exercise bike and other therapy equipment.
Nutrition associates will also stop by to see your menu preferences and for you to order snacks. Please ask them for if your child has a preference for a certain food as they can usually attain it for your child. They will instruct you on how to order meals and snacks.
Your child will be a white board in their room where everyone will write their names for your reference. It is also a good idea to write down your IV infusion times, Respiratory treatments and Physical Therapy time. You can also ask Child Life for assistance with a daily schedule. Always check with your nurse before you leave the floor as they will also know if you have a scheduled treatment coming up.
Being in the hospital doesn't mean you can be as comfortable as possible. In order to make your stay a bit easier, we recommend you bring the following items:
To make an appointment at the Cook Children's Cystic Fibrosis Center, please call 682-885-6299 Monday through Friday between 8:30 a.m.-5 p.m.
After hours and on weekends/holidays:
Why make an extra stop on the way home when you can fill your child's prescriptions right here? Located right on our medical center campus, our full-service pharmacy offers a convenient option to meet your pharmacy needs. We offer:
When you rely on our retail pharmacy, you'll get more than medications, you'll get experts that above and beyond the expected. And that's our prescription for assuring you have a pharmacy you can trust. You can learn more about our Retail Pharmacy services here.
If you have been told your child might have CF, we know you have lots of questions. We can help. To schedule an appointment, refer a patient or speak to our staff, please call our offices at 682-885-6299. After hours and on weekends/holidays, call 682-885-4000 and ask the operator to page the pulmonologist on call.
Contact us at 682-885-6299