| Welcome to the Turner Syndrome Society of Canada!
Our non-profit charitable organization shares up-to-date medical information on Turner Syndrome to families, physicians and the public. We also provide local mutual support groups for individuals with TS and their families.
Browse our web site for the latest news or contact us with your questions. We are always looking for new members and volunteers.
34th Annual Conference 2014
"Live, Laugh, Love"
May 22 – 24, 2015
Watch here for conference program and registration information available soon.
We are searching for a new Executive Director to follow Mary Edwards’ retirement in the late fall.
This is a part-time position in the Ottawa area; for more details and application informationclick here.
Membership Campaign on now – new online option
Show your support for YOUR Society: join us as a new member or a renewing
member for the 2014/15 membership year (August 2014-July 2015).
New! Pay online by clicking here
to join or renew your membership online, and pay securely by credit card or authorised bank transfer.
New! – Join or renew online here with our new
online membership form. Secure payment by credit card or direct authorized
You can pay by cheque. Print the membership form here in English or French and mail it to the national office, or the chapter nearest you.
Remember, if you join as a chapter member you also
automatically gain membership in the national organization as well.
Our online newsletter!
- Our newsletter is now available on line in French and English Editions! Check it out here for news about the Society’s activities, personal stories, and highlights from our conferences.
- Winter 2013 (PDF)
- Hiver 2013 (PDF)
Help us raise funds and awareness by purchasing our Awareness Pin.
Order your own by downloading this form and sending it to us.
Turner Syndrome Society of Canada
Top Entries Album
About the photos. (PDF)
Call for participants
Take part in a new study on lymphedema and swelling in girls and women with Turner Syndrome, until September 15, 2014.
Any girl or women with TS over the age of 13, or parents/caregivers of girls under 13 can take part in this study by completing the questionnaire at www.surveymonkey.com/s/turnersyndrome .
Even if swelling or lymphedema has not been a problem for you, it adds to the information that benefits all of us in regard to education and prevention.
__ Featured News & Updates
About the Turner Syndrome Society of Canada
The Turner Syndrome Society of Canada, a non-profit charitable organization, was founded in 1981 by an individual with TS who wanted to share experiences and information. It provides support services for individuals with TS and their families and disseminates up-to-date medical information to families, physicians and the general public.