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Courtney Waller is the co-Founder of Timothy Syndrome Alliance, and mom to a 5 year old daughter with the condition.
She has been a legislative advocate for the rare disease community for the past five years. Primarily working on legislation by state. She is the founder and principal of Policy Served Rare, a patient centered think tank focusing on policy that focuses on health and mental health care for the rare disease community.
Website: www.SADS.org/TSA
Twitter: @Timothy Syndrome
Facebook: Policy Served Rare @policyservedrare
By PodcastDX4.9
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Courtney Waller is the co-Founder of Timothy Syndrome Alliance, and mom to a 5 year old daughter with the condition.
She has been a legislative advocate for the rare disease community for the past five years. Primarily working on legislation by state. She is the founder and principal of Policy Served Rare, a patient centered think tank focusing on policy that focuses on health and mental health care for the rare disease community.
Website: www.SADS.org/TSA
Twitter: @Timothy Syndrome
Facebook: Policy Served Rare @policyservedrare

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