Call Noble
Phone:
888.843.2040
E-scribe Noble
E-scribe:
"Noble" in Syracuse, NY

Cystic Fibrosis

Specialty Solutions for Cystic Fibrosis

Cystic Fibrosis

The ability to breathe is considered a luxury for many who were NEW Cystic Fibrosis Enrollment Form 9.2018.jpgCystic Fibrosis Enrollment Form born with the inability to take it for granted. For the 30,000 U.S. Americans currently struggling with a cystic fibrosis diagnosis, limitations on daily life are a given without the proper treatment regimen. Here at Noble Health Services, our team enables you to push the limits of a diagnosis and strive to live better with cystic fibrosis.

Cystic fibrosis is a genetic disease of the mucus glands that primarily affects the respiratory and digestive tracts of the body. Normally, the body’s glands produce both sweat and thin, slippery mucus to prevent the respiratory and digestive system tissues from drying out. Those that are diagnosed with CF produce thick and sticky mucus and often lose large amounts of salt when perspiring which can result in mineral imbalance within the blood. The thicker version of mucus that is produced causes significant accumulation within the lungs and intestines which poses the threat of clogging and irreparable damage to the systems.

While the symptom severity of living with CF varies depending on the stage of the disease’s development, common difficulties that patients encounter include persistent coughing, frequent lung infections, shortness of breath, salty skin, difficulty with bowel movements, male infertility, weight loss and inflamed nasal passages. A variety of treatments are used to tame symptoms and elongate life expectancy while correspondingly improving quality of life.

Incidence – The progressive condition of CF causes a thick wall of mucus to build up within the walls of the respiratory and digestive systems, hindering normal function.

  • Approximately 1,000 new cases of cystic fibrosis are diagnosed each year in the U.S.
  • More than 75 percent of people with CF are diagnosed by age 2.
  • Cystic fibrosis is most common in Caucasian people of Northern European ancestry.

Cause – Cystic fibrosis is a progressive condition caused by a hereditarily passed gene mutation.

  • Both parents must have at least one carried copy of the defective CF gene.
  • There are more than 1,800 known mutations of the CF gene.
  • Certain types of the mutation are associated with different symptoms of CF.

For two parents that each carry one copy of the defective CF gene:

With advances in medical research constantly progressing, the diagnosis of cystic fibrosis has become less daunting in regards to life expectancy. On average today, those with CF are able to live well into their twenties and even thirties without a diminished quality of life. Therapy regimen is primarily the reason for the outrageous change in prognosis and continues to be innovated at every opportunity. Here at Noble Health Services, cutting-edge treatments and education are available to you through our dedicated and enthusiastic team of professionals.

Learn more about our Management Program.