10 hours ago As a volunteer, you’ll join thousands of people across the country who are helping add tomorrows to the lives of people with cystic fibrosis. Skip to main content Utility. Search; Local Chapter; español; Main navigation Intro to CF Managing CF Research & Clinical Trials Support ... >> Go To The Portal
The CF Foundation Patient Registry collects information on the health status of people with cystic fibrosis who receive care in CF Foundation-accredited care centers and agree to participate in the Registry.
CF Foundation-accredited care centers play an important role in research. They collect information on the health status of their patients with CF who agree to participate, and report that data to the CF Foundation Patient Registry.
The Patient Portal give patients 24x7 access to their medical information from the comfort and privacy of their own home or office. Patient Portal This is your personal electronic medical folder. Here you can communicate and e-mail your doctor.
Volunteers are special people, called to a service of healing at Community First Medical Center – where the gifts, the power and the worth of one person’s care for another is as important as the clinical technology we use in the overall healing process.
Volunteers have been providing support to staff, patients and their families since 1968. There are two categories: Teen: men and women 16-17 years of age Adult: men and women 18+ years of age A minimum of four hours of service weekly for at least three months is requested.
Volunteers work under the supervision of the Volunteer Department or a member of the hospital staff and serve in most areas of the medical center.
Electronic Health Records, or EHRs, are a computer based system of patient medical records that focus on the total health of you, the patient. Everything that had been written by hand is now entered into a computer. This secure EHR system permits direct access to certain areas of our office and to your Personal Health Information (PHI).
Have you ever been away from home and in need of medical care? Instead of undergoing needless tests, your doctor will be able to send and receive information about you to other doctors, hospitals, labs and pharmacies.
Improve the quality of your medical care by providing your doctor with information to diagnose and prevent disease
COTA helps Cystic Fibrosis (CF) patients of all ages. Since its founding in 1986 the Children’s Organ Transplant Association (COTA) has assisted hundreds of CF patients — many of whom have received a life-saving lung, liver or kidney transplant.
Danny Quesada became a COTA patient in early 2019 when a lung transplant became a necessity to continue his life-long battle with CF. Danny’s family, friends and local community rallied around him and showed tremendous support through their lung transplant fundraising efforts.
COTA’s initial CF patient fundraising goal to raise $200,000 was met in early 2020. These funds are already being used to help fund unmet transplant-related expenses. And, with the growing number of CF patients progressing to transplant today, the Danny Quesada Memorial Cystic Fibrosis Fund will be a lifeline for these patients and their families.