Who are we? 

The Chronic Illness Advocacy & Awareness Group (CIAAG) envisions a world where those with disabilities and chronic illnesses are guaranteed palliative care and access to prescription life sustaining medications without stigma, fear or push-back, particularly from the medical community. We shape social narratives to promote inclusion of disabled rights and individualized patient-centered care. We lobby against political agendas and misinformation campaigns that interfere with patient's access to vital medications and palliative care.  We support patient populations with the following:

Would  you  be  willing  to   give  up  a cup  of



  coffee  to  make  a  change?


We are a small lobbying non-profit,run by two very sick disabled women. Any "change" for change  you can spare, would make a world of difference. 

Check out  our  blog, 


Words of Pain.  

Want   to    print   out   flyers   to   send   


​to   your


legislators? 

Check out our tool's tab, where we offer informational flyers to help you better advocate for your patient rights! 

Our  Social   Media 

Meet  Our  Team

Lauren     L.  DeLuca, CPCU, API, AINS 

Jayne     Flanders 

Founder  &  President

Vice   president  

CURRENT ISSUES


CIAAG TOOLS & FLYERS


REACH OUT  TO YOUR  LEGISLATORS
​

DONATE 

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