Today we have the unique opportunity to hear  the perspective of someone who has lived her entire life with Williams Syndrome.  She shines a light on some of the challenges that she has faced and currently faces.  Becky Carlson shares her heart to advocate for people with special needs and to educate others on how to treat and be there for people with disabilities.  She shares one of her big dreams with us!

Williams syndrome | Genetic and Rare Diseases Information Center (GARD) – an NCATS Program (nih.gov)