OPWSA: Newsletter & Annual Report

Newsletter & Annual Report

Contact & Donation Info

Membership Info

Conference 2008

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The Ontario Prader-Willi Association is a registered non-profit charity organization, established in 1982.

CHARITABLE #:
11906 8203 RR0001

Newsletter

"The OPWSA Newsletter is produced on a quarterly basis. Each letter includes a report from President Heather Ann Lowry and a report from Executive Director Nita Goldband. It's also a place for celebrating our community! If you want to keep informed on the latest research on PWS or on what's happening in our Ontario organization- this is the place to find it. In order to receive a copy of the Newsletter, please consider becoming a member for the low annual fee of $25.00 for families and individuals or $30.00 for professional organizations."

Heather Ann Lowry, OPWSA President
Robyn Heaton, Newsletter Editor

Annual Report

Click here to view OPWSA's 2005 Annual Report

	This OPWSA website is intended to provide information only - not to diagnose or advocate particular treatment options. The diagnosis and treatment of Prader-Willi Syndrome should be made through a qualified medical professional. Thus, it is strongly urged that patients do not change treatment without first consulting their doctor.
	Web design courtesy of Jennifer Gignac. Site updated & maintained by OPWSA. 2006