A Milton couple knew their youngest daughter was experiencing some learning and developmental delays growing up, but they didn't know why until about three years ago. That's when Alyssa Okeyo was diagnosed with a rare genetic condition known as Williams syndrome. Check out their story.
There's still time to participate in this survey about the healthcare transition for adults with Williams syndrome. By providing your input, you contribute to early research that can impact the quality of care received in the future! This online survey is intended for caregivers of an adult (18+) with Williams syndrome.
If you previously began taking the survey but still need to complete it, you still have time to finish it! The survey is available until October 19th.