WAPO believes that the strength of a global network of national pituitary patient organizations will lead to improved diagnosis, treatment and care for pituitary and adrenal patients worldwide.

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WAPO is a non-profit, umbrella organization that brings together national pituitary patient organizaitons around the world.
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WAPO SUMMIT

Andrei opens Summit 2016

Wapo Summit 2017

Given the 2016 WAPO Summit was such a success it was agreed that we would organize it annually. The new Board agreed that the WAPO Summit 2017 should take place in Amsterdam on 12-14 of May 2017.
Find out more!

ALL WAPO MEMBERS

WAPO members map April 2017

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Webinar: ‘Adult GHD: an interactive debate about diagnosis, dosage and treatment’

Dec 13, 2019, 12:00 PM in Universal Time UTC Registration link: https://zoom.us/webinar/register/WN_QNK9MJOoTrGFk5uMfqq4rQ                                                                                       

Rare Disease Day

Rare Disease Day takes place on the last day of February each year. The main objective of Rare Disease Day is to raise awareness amongst the general public and decision-makers about rare diseases and their impact on patients’ lives. The campaign targets primarily the general public and also seeks to raise awareness amongst policy makers, public authorities, industry representatives, researchers, health professionals

WAPO Summit 2020

Event for WAPO Member organizations to meet & discuss, share best practices, learn from HCPs incl. Q&A, and receive training on March 20 and 21. Annual General Meeting, Action points 2020-2021 incl. discussions and poster contest on March 22, 2020.

ENDO 2020

ENDO is the place where leading experts, researchers, and the most respected clinicians in the field will converge to share the latest findings in hormone science that lead to the next breakthroughs in clinical care.

Cushing’s Day

Global campaign to raise awareness for undiagnosed and diagnosed people with the rare disease Cushing’s Syndrome (incl. Cushing’s Disease).

The European Conference on Rare Diseases & Orphan Products (ECRD)

The European Conference on Rare Diseases & Orphan Products (ECRD) is recognised globally as the largest, patient-led rare disease event in which collaborative dialogue, learning and conversation takes place, forming the groundwork to shape future rare disease policies. It is a biennial event, providing the state-of-the-art of the rare disease environment, monitoring and benchmarking initiatives.

22nd European Congress of Endocrinology (ECE 2020)

The European Congress of Endocrinology is the European Society of Endocrinology’s premier event, attracting over 3,500 international delegates each year across the spectrum of endocrinology. The event is a showcase of the best of science and clinical practice across the fields of endocrinology and metabolism, and aims to deliver to all audiences interested in the

19th International Congress of Endocrinology (ICE)

ICE 2020 will be a worldwide event, gathering more than 5,000 delegates and leaders from different endocrinology fields, becoming an excellent opportunity for best-practice exchanges between colleagues. Bringing together the leading experts, researchers and the most respected clinicians, ICE 2020 will represent a convergence of practice and science that will highlight and reflect the latest