{"id":12,"date":"2021-03-23T13:34:07","date_gmt":"2021-03-23T20:34:07","guid":{"rendered":"https:\/\/globalnmo.org\/?page_id=12"},"modified":"2025-06-25T10:50:15","modified_gmt":"2025-06-25T17:50:15","slug":"home-page","status":"publish","type":"page","link":"https:\/\/globalnmo.org\/","title":{"rendered":"Home Page"},"content":{"rendered":"\n
\n
\"Multiracial<\/figure>\n\n\n\n

\n\t\tJoining Hands
Around the World
for NMO Patients\n\t<\/h1>\n<\/div>\n\n\n\n

\n\t\tStronger together\n\t<\/h2>\n\n\n\n

In an effort to join hands around the world, the organizations shown here have a strong, heartfelt commitment to building bridges where there were none. These organizations are committed advocates for patients who walk the path of NMO on a daily basis. We are one global voice and the world is our platform. Please join us in supporting our international patient family and help us raise awareness for this rare, debilitating disease known as NMO.<\/p>\n\n\n\n

You can learn more about each organization that advocates for NMO patients by selecting any\/all of the site links below. Thank you for joining us in our work to support our global patient community.<\/p>\n\n\n\n

 <\/p>\n\n\n\n

Please note that this collection of websites has been created solely for the purpose of sharing contact information for NMOSD patient advocacy support organizations around the world.  The content of these sites has not been reviewed by the site administrator, and the site administrator does not intend by listing any such organization to endorse or recommend its use or the accuracy of any information shown on its website.<\/p>\n\n\n\n

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Patient Advocacy<\/h2>\n\n\n\n
\n
\n
\n
\"Guthy-Jackson<\/a><\/figure>\n\n\n\n

The Guthy Jackson Charitable Foundation<\/h4>\n\n\n\n

United States of America
<\/strong>For more information, contact:
Cori Woolf<\/a><\/p>\n\n\n\n

\n
Visit Website<\/a><\/div>\n<\/div>\n<\/div>\n<\/div>\n\n\n\n
\n
\n
\"Siegel<\/a><\/figure>\n\n\n\n

Siegel Rare Neuroimmune Association (SRNA)<\/h4>\n\n\n\n

United States of America<\/strong>
For more information, contact:
Gabrielle deFiebre<\/a><\/p>\n\n\n\n

\n
Visit Website<\/a><\/div>\n<\/div>\n<\/div>\n<\/div>\n\n\n\n
\n
\n
\"Sumaira<\/a><\/figure>\n\n\n\n

The Sumaira Foundation for NMO<\/h4>\n\n\n\n

United States of America<\/strong>
For more information, contact:
Sumaira Ahmed<\/a><\/p>\n\n\n\n

\n
Visit Website<\/a><\/div>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n\n\n\n
\n
\n
\n
\"NMO\u4e4b\u5bb6\"<\/figure>\n\n\n\n

NMO\u75c5\u53cb\u4f1a<\/h4>\n\n\n\n

China<\/strong>
For more info contact:
Jenny Zhang<\/a><\/p>\n\n\n\n

\n
Visit Website<\/a><\/div>\n<\/div>\n<\/div>\n<\/div>\n\n\n\n
\n
\n
\"Logotipo<\/figure>\n\n\n\n

NMO Brasil<\/h4>\n\n\n\n

Brazil<\/strong>
For more info contact:
Daniele Americano<\/a><\/p>\n\n\n\n

\n
Visit Website<\/a><\/div>\n<\/div>\n<\/div>\n<\/div>\n\n\n\n
\n
\n
\"NMO<\/figure>\n\n\n\n

NMO France<\/h4>\n\n\n\n

France<\/strong>
For more info contact:
Souad Mazari<\/a><\/p>\n\n\n\n

\n
Visit Website<\/a><\/div>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n\n\n\n
\n
\n
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Your Patient Advocacy Organization Here<\/h4>\n\n\n\n

Please send the title of your organization, country, logo, url, and contact email address to:\u00a0cwoolf@thegjcf.org<\/a><\/p>\n<\/div>\n<\/div>\n\n\n\n

<\/div>\n\n\n\n
<\/div>\n<\/div>\n<\/div>\n\n\n\n
\n

Access to Therapeutics<\/h2>\n\n\n\n
\n
\n
\n
\"The<\/figure>\n\n\n\n

The Assistance Fund (TAF)<\/h4>\n\n\n\n

United States of America<\/strong><\/p>\n\n\n\n

For more info contact:<\/p>\n\n\n\n

Stephanie Marshall<\/a><\/p>\n\n\n\n

\n
Visit Website<\/a><\/div>\n<\/div>\n<\/div>\n<\/div>\n\n\n\n
\n
\n
\"NORD<\/figure>\n\n\n\n

National Organization for Rare Disorders (NORD)<\/h4>\n\n\n\n

United States of America<\/strong><\/p>\n\n\n\n

For more info visit:<\/p>\n\n\n\n

\n
Visit Website<\/a><\/div>\n<\/div>\n<\/div>\n<\/div>\n\n\n\n
<\/div>\n<\/div>\n<\/div>\n\n\n\n
\n

\n\t\tAbout NMO\n\t<\/h2>\n\n\n\n

Neuromyelitis optica (NMO) is a central nervous system autoimmune disorder that primarily affects the eye nerves (optic neuritis) and the spinal cord (myelitis). NMO is also known as neuromyelitis optica spectrum disorder (NMOSD) or Devic’s disease. NMO is a rare-occurring, demyelinating disease that impacts patients globally.<\/p>\n<\/div>\n","protected":false},"excerpt":{"rendered":"

Joining Hands Around the World for NMO Patients Stronger together In an effort to join hands around the world, the organizations shown here have a strong, heartfelt commitment to building bridges where there were none. These organizations are committed advocates for patients who walk the path of NMO on a daily basis. We are one […]<\/p>\n","protected":false},"author":1,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"footnotes":""},"class_list":["post-12","page","type-page","status-publish","hentry"],"jetpack_sharing_enabled":true,"_links":{"self":[{"href":"https:\/\/globalnmo.org\/index.php?rest_route=\/wp\/v2\/pages\/12","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/globalnmo.org\/index.php?rest_route=\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/globalnmo.org\/index.php?rest_route=\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/globalnmo.org\/index.php?rest_route=\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/globalnmo.org\/index.php?rest_route=%2Fwp%2Fv2%2Fcomments&post=12"}],"version-history":[{"count":0,"href":"https:\/\/globalnmo.org\/index.php?rest_route=\/wp\/v2\/pages\/12\/revisions"}],"wp:attachment":[{"href":"https:\/\/globalnmo.org\/index.php?rest_route=%2Fwp%2Fv2%2Fmedia&parent=12"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}