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The members of our society have offered a wealth of support for over 20 years. We understand that every person’s needs are unique as Turner Syndrome affects each girl and woman in a different way.
Education is our foremost goal whether you are a member of our society or a guest, you can access the latest Turner Syndrome Clinical Guidelines, attend our National Conference, get support from parents and adult women that “have been where you are”, and access local chapter and support group information, plus many other resources.
Membership to our society allows us to continue to offer valuable services to all those touched by TS and also gives individuals, families, and professionals the opportunity to access more resources. Click here to join. Read more about the benefits of membership here.
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Plan on meeting us in beautiful Portland, Oregon in July of 2009. Dates will be determined soon and the theme will be announced early so that everyone can anticipate another great experience. The 22nd Annual Conference (2009) will add an optional tour for a Thursday outing. We'll also give much info. in the next TSS Connect.
About Our New Website
Please be patient as we are
in the final stages of updating and transitioning our new site for a
more user friendly format. The design element will take place last and
it will surely be a sight we'll all be proud of. You may experience
problems with logins, donations, and membership. Please contact the
national office at 800-365-9944 for assistance. Thank you for your
support and patience.
The 2008-2009 TSSUS Educational and Awareness Programs
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