Julie Walters

In this episode of Don't IEP Alone, host Lisa Lightner interviews Julie Walters from The Connected Parent. Julie shares her journey as a neurodivergent parent raising two children with IEPs and how her experiences led her to create The Connected Parent, a national online platform that connects families with disability-related services and resources. Julie offers insight into the challenges of finding specialized services and the importance of creating a supportive community for individuals with disabilities and their families. She also discusses the innovative features of The Connected Parent and how it aims to support businesses that serve the disability community. Tune in to learn more about Julie's inspiring venture and the impact it's making in the lives of families navigating the IEP process and disability-related services. Connect with Julie here: www.theconnectedparent.net www.instagram.com/theconnectedparentsite www.facebook.com/theconnectedparentsite Don't IEP Alone with Lisa Lightner, Special Education Advocate Thank you for listening to this episode of Don't IEP Alone. See you next time! Support the show Other ways I can help you with IEPs: 📚 Order my book

We take some time out to catch up and celebrate that the day has finally come to launch our Brave Bird Pants! Woop woop! We also speak about Will Smith and his very public slap. We considered how we’d have handled the same situation and admitted, rightly or wrongly, we’ve both succumbed to our anger in the past. We also revel in the fact that we got a video message from Dame Julie Walters this week. She’s the patron to the domestic abuse charity we’re supporting ‘My Sisters’ House’ and her public and personal story is bursting of bravery. So to know that she wears Brave Bird Knickers, and took the time to make us a video, just cements her legendary Brave Bird status to us. Thank you Julie! We’d love to have you on this podcast one day. TO PURCHASE BRAVE BIRD KNICKERS: https://www.bravebird.club TO CONNECT WITH SARAH AND LUCY: https://www.instagram.com/bravebirdclub/ https://www.facebook.com/bravebirdclub/ https://www.twitter.com/bravebirdclub/ https://www.linkedin.com/in/sarahoakleyprofessional/ INTRO & OUTRO MUSIC: By Koven and from NoCopyrightSounds: https://youtu.be/0dgMHYThYXw Download/Stream music here: https://ncs.io/LookingForMore DISCLAIMER: The views, thoughts and opinions expressed in this podcast belong solely to the host and guest speakers. Please conduct your own due diligence.

This is it, after a long month winding through the country side, we have climbed the mountain and reached the absolute pinnacle of our life on the rails, where we found Coastal Railways with Julie Walters. We've seen a lot trains and a lot of countryside but we have never seen anything as joyful as Julie Walters riding the train. We're smoking some fish, touring some trailers, eating some lobsters, and learning a lot about victorian train ettiquette. Links: Episode 171 | Norwegian Slow TV (Our Month on the Rails, Part 1) Episode 172 | The Biggest Little Railway in the World (Our Month On The Rails) Episode 174 | SAS: Red Notice (Our Month on the Rails)

In Talking Precision Medicine podcast we sit down with experts on the application of AI and big data analytics in the drug discovery space. Our guests are innovators, business decision makers and thought leaders at the intersection of data and therapeutics. We discuss the promise, practice, challenges, and myths of AI in precision medicine. This show is brought to you by Genialis, and Rafael, our CEO, is your host. Genialis is focused on data integration and predictive modeling of disease biology to help accelerate the discovery and de-risk the development of novel therapeutics. Today we speak with Julie Walters. Julie is the founder of Raremark, an information hub about rare disease for patients and their families. She has a degree in molecular genetics and a background in popular journalism… and is an entrepreneur by nature. In fact, she was a Female Entrepreneur of the Year at the UK’s 2017 Enterprise Awards. Julie believes in harnessing the power of families affected by a rare disease, and our discussion covers many of the ways Raremark aims to do just that.