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Posted Nov 27, 2017, by terrymonkaba
It’s hard to believe that it has been 31 years since we attended our first convention in Cincinnati.  It was July of 1986. Ben was just six months old – and I was sleep deprived – but I still have so many vivid memories of that weekend... More about The WSA Convention... Life Changing Then and Now
Posted Oct 23, 2017, by lauriej1
The WSA is proud to partner with Team IMPACT (TI) to spread the word on how young individuals with Williams syndrome can participate in the inspiring program. Team IMPACT is a two-year commitment and relationship between college sports teams and individuals with special needs that “connects children with serious and chronic illnesses to local college athletic teams, forming life-long bonds and life-changing outcomes.” More about The Power of Teams: WSA Partners with Team IMPACT
Posted Aug 11, 2017, by lauriej1
Do you have a vision for your child with Williams syndrome?  Is it written down so you can refer to it, update it, and remember exactly why you are working so hard every day to overcome the obstacles in your child’s path?  Lisa and Ned Portune read all the things that their child... “probably wouldn’t do," and then set out to help Erin be the very best she could be.More about Unwavering Expectations
Posted Jun 20, 2017, by lauriej1
Thank you for a successful Williams syndrome awareness month! Click to read the thank you blog and view the special video that highlights the amazing types of awareness that happened all over the country. More about Thank you for a Wonderful Awareness Month!