Support Groups for People With Chloride Diarrhea

Congenital chloride diarrhea is a genetic disease.

Chloride diarrhea, known formally as congenital chloride diarrhea (CLD) is a rare genetic disease that is present at birth. People with rare diseases can find help and support through a number of organizations.

Symptoms and Prognosis

The key features of congenital chloride diarrhea is watery diarrhea with a high concentration of chloride. The diarrhea is chronic and present from birth. It is important that the disease is diagnosed quickly in order to replace the chloride, water and other minerals that are lost in the feces. Infants born with the disease are often premature and older children and adults with the disease can have kidney problems if they do not receive proper treatment.

Resources

People who suffer from congenital chloride diarrhea can turn to the National Organization for Rare Disorders (NORD) for help. NORD is a collection of organizations which offer support to people who have rare diseases. People with congenital chloride diarrhea can access the extensive database of patient support groups. The Genetic Alliance offers assistance to people with genetic conditions.

Support

The International Foundation for Functional Gastrointestinal Disorders (IFFGD) aims to help people affected by persistent digestive disorders that affect their daily lives.

References

• National Institutes of Health: Offices of Rare Diseases Research: Patient Advocacy Groups
• U.S. National Library of Medicine: Congenital chloride diarrhea in a child.
• International Foundation for Functional Gastrointestinal Disorders