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  Knowledge is key – information about and an understanding of SBS, its impact on daily life, and the methods that can be used to manage it are crucial and can help give a much greater sense of control.
 
  Communication is essential – both the people with SBS and their family and friends must be willing to express needs, frustrations, disappointments, anger and other emotions that will inevitably arise; it is equally important to communicate with doctors and other healthcare providers.
  
  Support networks are extremely helpful – these groups may consist of family, friends and groups of others with similar life situations and problems; the support groups may be physically meet or may meet through chat rooms on the internet.
  
  Other aids to coping are available – these include stress management skills and other psychological counseling with specially trained professionals.

 

 

Introduction

Everyone approaches disease or physical injury differently. This is especially true for people with SBS because the nature and severity of this syndrome vary depending on the length and condition of the remaining bowel, the type of nutritional regimen required (ranging from oral to intravenous nutrition), and other complications and diseases that may impact survival and quality of life. Your attitude, expectations and how you cope with the condition all influence your individual sense of well-being. The more knowledge you have about your particular type of SBS and methods for coping with it on a day-to-day basis, the more likely you are to enjoy an improved quality of life and a greater feeling of control over your situation.

 

 

 

 

This information is provided as a general educational service
and is not intended to recommend any particular treatment plan
or to replace the advice of physicians. It is important that patients
seek and rely on the advice of a healthcare professional
about their individual medical conditions.

  
  
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