Ensuring rights of parents with children stricken with neuroendocrineimmune disorders (CFS-ME, FM, MCS, chronic Lyme disease), are protected through physician education & community advocacy programs.

This is a special cause that P.A.N.D.O.R.A. supports. Your donation to this cause will help Ryan's family to pay for his medical bills and his legal bills. Recently Ryan was diagnosed with the XMRV virus. You can read Ryan's story at www.bringingryanhome.com. The plight of the Baldwin family begun in 2003, when Ryan fell ill and subsequently was diagnosed with CFS-ME and related illnesses. In January 2009 Ryan was taken from his loving home as his parents were charged with Factitious Disorder by Proxy (FDP). Ryan's story has been repeated in many communities across the U.S. and in other countries too. The lack of understanding by school authorities, local social agencies and medical providers remain a great problem for families with children stricken with neuroendocrineimmune disorders (NEIDs). Go to www.bringingryanhome.com to 1) read Ryan's story and to participate in our efforts to educate, and to prevent this from happening to another family in communities across the U.S. If you can make a donation, and forward the information on this page to your friends on Facebook.

1. Create awareness for chronic fatigue syndrome-ME and related neuroendocrineimmune disorders (NEIDs)

2. Ensure parental rights of families and their children with neuroendocrineimmune disorders

3. Seek fairness for families of sick and disabled children in all areas of local Government

4. Donations to benefit Ryan's medical & legal fund.

5. Ensure efforts to educate physicians in North Carolina as well & in the 50 states remain a priority for local, state & federal health agencies.