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Recognition of Empty Nose Syndrome

for more information see: http://www.emptynosesyndrome.org/index.html

Statement of Mission

The ENS Association is a nonprofit, 501(c)(3) public charity that was founded in 2005. Our primary mission is to increase medical and scientific awareness of the devastating impact of this disability on the lives of ENS sufferers, promoting the pressing need for a cure.

The Association's mission is to :
  1. Educate patients and their families about Empty Nose Syndrome.
  2. Increase public and professional awareness of ENS.
  3. Encourage research into new treatments and a cure.
  4. Build a member list of ENS sufferers via our registration form.
  5. Raise money for ENS research
Das Petitionsschreiben lesen ▾
We the undersigned wish to convey:
Empty Nose Syndrome is a real disease process that should be recognized and dealt with in an open manner.  These iatrogenic subjects should not be swept under the rug for fear of lawsuits.  Real research and care is needed to correct this situation.
Thank you for openly accepting this disease and working to stop it.
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