The Endocrine Society of the Republic of China (Taiwan)

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【轉知國際會議】2/28(一)ISE Rare Disease Day webinar-Acromegaly through the eyes of a Physician, a Nurse, and a Patient

 

- RARE DISEASE DAY WEBINAR -

Acromegaly through the eyes of a Physician, a Nurse, and a Patient
Detection , Diagnosis, Treatment, and Follow-up Care    


Monday, 28 February 2022
16:00 - 17:30 CET

(台灣時間2/28-23:00~3/1-00:30)

 
Together with the World Alliance of Pituitary Organizations (WAPO) and the Federation of International Nurses in Endocrinology (FINE), we would like to invite you to explore the challenges faced by physicians, nurses, and patients in terms of detection, diagnosis, treatment, and follow-up care in acromegaly.

Join Susan Webb (Spain)Chris Yedinak (USA), and Sheila Khawaja (Italy) on 28 February to commemorate Rare Disease Day and learn more about this condition from the speaker panel sharing their experiences as a physician, a nurse, and an acromegaly patient, respectively.

 

We encourage you to invite anyone in your network working in the field of acromegaly, suffering from acromegaly themselves, or supporting a family member
with this condition.

SAVE YOUR VIRTUAL SEAT HERE, FREE OF CHARGE
When: Monday, 28 February, 16:00 - 17:30 CET 


After the live webinar, you will be able to access the webinar recording on the
ISE Global Education Hub. 

To learn more about WAPO and FINE, please follow these links:

•    World Alliance of Pituitary Organizations (WAPO) 
•    Federation of International Nurses in Endocrinology (FINE)
 
Register for this Webinar >>

Learn more about Rare Disease Day 2022

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.

Thousands of events in more than 100 countries will be held to recognize Rare Disease Day on the 28 February in 2022. Learn more about how to support the campaign and participate on the link below!
Rare Disease Day 2022 >>