Happening TOMORROW! Register now for the Northern California Anti-trafficking Regional Round Table where the CA Alliance will be presenting, along with Casa de Amparo and Mary's Path on services and supports for CSEC. Learn about options and advocacy for our most vulnerable youth in California. Register here: https://lnkd.in/gBHMVgjA
California Alliance of Child & Family Services’ Post
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Our FY 2023 Impact Report is out! Learn more about the impact of our advocacy in the lives of the children and families that we serve. https://lnkd.in/gjHt985H
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Check your inbox! This month's edition of Voices & Views just dropped. If you didn't get our email, but want to stay up-to-date on the latest news in recovery advocacy, it's easy to join our mailing list. Join our newsletter at faces.ly/newsletter!
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At CCRAN, we understand a diagnosis can be overwhelming. That's why we offer a "SEA" of services: Support: Connect with a community that understands. Education: Get the knowledge you need to fight back. Advocacy: Ensure your voice is heard. Together, we can navigate this journey.
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If you are an advocate or educator and would like to learn more about self-care and advocacy, I highly recommend watching the recording of this!
Parents and caregivers, it's your turn to be supported! Join our workshop to discover strategies for recognizing and addressing your own needs, while also enhancing your advocacy skills for your children. Register here: bit.ly/DABC_BalancingActs
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📢From babies to adults, Hyperinsulinism presents unique challenges. By listening to those we support, we tailor our resources, family conferences, advocacy, and training for every stage. Learn more: www.hyperinsulinism.co.uk #CongenitalHyperinsulinism #Hyperinsulinism"
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PhD Candidate, Licensed Mental Health Counselor, Research Assistant & Instructor at University of South Florida
💜 May is #LupusAwarenessMonth. 4 out of 5 people diagnosed are women. It takes an average of 4-5 years and over 4 specialist doctors before they reach a diagnosis. Autoimmunity is a daily battle, effecting every aspect of life for those who are diagnosed and the people who love them. Please consider spreading awareness of this chronic disease and the urgent need for more #research. 💜 #autoimmune #delayeddiagnosis #lupusawareness #lupus
It’s #LupusAwarenessMonth! LRA President & CEO, Albert T. Roy kicks us off with a message of hope – inspiring all to get involved in #lupus research, advocacy, education and fundraising. Learn how you can make a difference today! https://bit.ly/LAM-ALROY #ManyOneCan
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Looking forward to leading a panel discussion this Wednesday on the topic of housing policy and advocacy. A great line up including Christopher Burt, Elizabeth Hansburg, Ian Adam, Marlo Naber Mole, & Wendy Bucknum to discuss what California & our cities are and aren’t getting right, and what we can do about it. https://lnkd.in/gicvDqC4
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Parents and caregivers, it's your turn to be supported! Join our workshop to discover strategies for recognizing and addressing your own needs, while also enhancing your advocacy skills for your children. Register here: bit.ly/DABC_BalancingActs
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Through research, advocacy and raised awareness, the AHA has saved a lot of lives over the past 100 years. Together we’ll do even more in our Second Century. Explore the wealth of knowledge in the Centennial Presidential Advisory: http://spr.ly/6043jya1x #AHABoldHearts
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Parents and caregivers, it's your turn to be supported! Join our workshop to discover strategies for recognizing and addressing your own needs, while also enhancing your advocacy skills for your children. Register here: bit.ly/DABC_BalancingActs
To view or add a comment, sign in
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