16
Juin

Emily Travis was 16 when she began to faint regularly.

Diagnosed with Fetal Alcohol Spectrum Disorder as a 12 lb., year-old infant, her health trajectory had been atypical from the start. But when Travis told her doctor she suspected the fainting was linked to her FASD, she was met with a dismissive response.

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16
Mai

An announcement from the Ontario government earlier this month committing $26 million in the province’s budget to support youth and families affected by fetal alcohol spectrum disorder (FASD) is being met with a mixed response.

The strategy lists six initiatives, which include providing one-stop access to information, funding for 56 FASD workers and parent support networks, increasing access to FASD initiatives developed by Indigenous partners, establishing consultation groups, and creating a research fund.

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21
Avr

Do children with disabilities and their families know they have rights? Does Canada respect their rights? In Giving a Voice to Children’s Rights, a blog posting on March 31, 2017, Dr. Keiko Shikako Thomas laid out these intersecting issues arising in childhood disability and human rights in a Canadian context.

A few days later, Shikako-Thomas, co-lead of the Network's KT Core policy engagement project and other members of a Canadian delegation of civil society organizations (CSOs) appeared before the United Nations committee overseeing the Convention on the Rights of Persons with Disabilities. Dr. Shikako-Thomas presented on the status of children with disabilities and responded to detailed questions as part of a compliance review in Geneva April 2-4. Canada became a 2010 signatory to the convention, and both the federal government and relevant NGOs participated in the review process.

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