APPS informs, supports, and empowers Alberta pituitary patients,

caregivers, and health-care professionals to help patients live fulfilling lives.


Light Up for Rare February 28

1 Feb 2022 8:00 PM | Anonymous member (Administrator)

#LightUpForRare

This Rare Disease Day, participate in the Global Chain of Lights and share your colours.

Light or decorate your home with the Rare Disease Day colours at 7 p.m. MST on February 28, 2022. Take a picture and share on social media with the tag #LightUpForRare

For more information, see the attached toolkit.

Webinar Feb 24: Rare Disease Day

The Canadian Organization for Rare Disorders (CORD) is hosting a webinar on Canada’s Rare Drug Strategy on Thursday, February 24 from 10–11 a.m. MST. For more information and to register, click here.

Webinar Feb 28: Acromegaly Through the Eyes of a Physician, a Nurse, and a Patient

The World Alliance of Pituitary Organizations (WAPO), the Federation of International Nurses in Endocrinology (FINE), and the International Society of Endocrinology (ISE) are jointly hosting this webinar on Monday, February 28 from 8–9:30 a.m. MST. For more information and to register, click here.



Copyright 2019 Alberta Pituitary Patient Society 


Powered by Wild Apricot Membership Software