The CCCA is one of the Sacramento area's oldest patient support groups for patients, family and friends who are trying to manage Chronic Fatigue and Immune Dysfunction Syndrome (CFIDS), also known as Chronic Fatigue Syndrome (CFS) or Myalgic Encephelomylitis (ME).

This page will present various documents, including sample letters, that we hope you will find useful for encouraging supportive public policies among our government officials and educating those who have heard little about this illness.

Congressional Call for Action, 2008

The following documents were written to help you lobby our legislatures for more effective representation of CFIDS/CFS.

These documents may be downloaded to your computer by right-clicking on them and selecting the Save (or Download) option. 

Click the following for "How to use these documents":
    How to use this Call for Congressional Action

Microsoft Word (2000) documents
    Congressional Call for Action

WordPerfect documents
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