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役に立つ非営利団体

The Non-Profits below are ones we personally work close with.

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France

An association under the 1901 law recognized as being of general interest, it was founded with the aim of supporting, informing, raising awareness and participating in the improvement of care pathways and the management of patients suffering from Nutcracker, Cockett/May-Turner, Wilkie and Dunbar vascular compression syndromes. 

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Spain

AESCOV is a non profit organization made up of members who suffer from vascular compression syndromes. These compressions include Nutcracker Syndrome, May-Thurner Syndrome, Superior Mesenteric Artery Syndrome, Median Arcuate Ligament Syndrome, Inferior Vena Cava Syndrome, Pelvic Congestion Syndrome, Thoracic Outlet Syndrome, Budd-Chiari Syndrome, among others. Our aim is to help everyone who is in this maze of vascular compression syndromes and simultaneously claim a medical and social treatment comparable to the one that patients from common diseases receive.

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We are a group of patients with Ehlers-Danlos Syndrome (EDS) and Abdomino-Pelvic Vascular Compression Syndromes, which include Dunbar Syndrome (MALS), Nutcracker Syndrome (NCS), Wilkie Syndrome (SMAS), May-Thurner Syndrome (MTS), and Pelvic Congestion (PCS/PVI). We know what our fellow patients are going through. Our mission is therefore to accompany them on the difficult journey through these diseases. To learn more, read our site and become a member of our patient group.

Slovokia

United States of America

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Superior Mesenteric Artery Syndrome Research Awareness and Support is a registered 501c3 nonprofit organization. They are solely unpaid volunteers. They are also the first and only SMAS nonprofit organization to provide financial assistance to SMAS Patients. They are dedicated to promoting healthcare opportunities for underinsured individuals and promoting research for improved healthcare for all members of the SMAS community. They also strive to educate both the medical community and the public about SMAS with the hope of increasing the chances of early diagnosis. They also work under the name of SMAS Patient Assistance.

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最初に知ってください!

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デダム、MA 02027

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著作権 ©2020 National 正中弓靭帯症候群財団、Inc. 無断複写・転載を禁じます。 National MALS Foundation は、登録された 501(c)(3) 非営利団体です。 National MALS Foundation は、MALS 患者および臨床医コミュニティの利益のために、この Web サイトの情報を提供していることに注意してください。 National MALS Foundation は、医療提供者または医療施設ではないため、MALS を診断したり、特定の医療処置を承認または推奨したりすることはできません。患者は、MALS の診断と治療に関する情報を求める前に、資格のある医療専門家の個人的かつ個別の医学的アドバイスに頼らなければなりません。

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