Acromegaly through the eyes of a Physician, a Nurse, and a Patient
Le 28 Février 2022
– RARE DISEASE DAY WEBINAR –
Acromegaly through the eyes of a Physician, a Nurse, and a Patient
Detection , Diagnosis, Treatment, and Follow-up Care
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)