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PANDORA is strong on advocacy and awareness to improve the quality of life of those with NEI diseases. This is being accomplished through multiple approaches:
• Educating the public about
NEIDs
• Educating physicians about
the true nature of NEIDs
• Advocating for state and
national governments to
increase research into NEIDs
• Advocating for government
health policies that will
improve the quality of life of
NEIDs patients. Read More > |
Please sign
this peition
telling the CDC they need
to make changes to their CFS research program.
The CDC has already
made some progress by meeting with patient organizations and working
with other ME/CFS
clinicians and researchers. They have started the
process of refining the CFS diagnostic criteria.
But much more is needed.
They have a long way to go. |
The (NeuroEndocrineImmune) NEI Center will be the first research center of its kind. Patients will benefit from cutting-edge research and clinical care. It will have the computer-aided disease diagnosis and treatment (CADDT) system, which will be specifically designed for multi-system illnesses and complex diseases.
Assistance in accessing social services will also be offered so that patients will feel better, live longer and have an improved quality of life. For more information, visit the NEI Center website. |