Families dealing with Sickle Cell Disease face the challenges of
the illness
and the trauma of discrimination and ignorance by schools, camps and other programs.
To provide resources and supports for families, the Center for Children’s Advocacy partnered with Citizens for Quality Sickle Cell Care for a “Back to School” training
for parents and children last evening
in conjunction with Connecticut Children’s Medical Center.
Justice Department attorney Vanessa Avery provided valuable information about the American’s with Disabilities Act.
A training on the educational rights of children with Sickle Cell Disease and
a corresponding Informational guide
were developed for the event. The guide is attached as well as the Center’s new guide on helping parents advocate for their children in the
school setting.
If you would like additional information or if your agency would be interested in a training on the American’s with Disabilities Act please contact [log in to unmask].
Bonnie
Bonnie B. Roswig
Senior Staff Attorney
Medical/Legal Partnership Project
Center for Children’s Advocacy
(860) 545-8581