Podcasts about for chloe

Episode 103: Raising a Child with STXBP1 With Guest Chloe Weber  In this we discuss rare genetic disorder called STXBP1. Guest Chloe Weber's son Remy has a rare genetic disorder called STXBP1. This condition affects syntax and binding protein. For these individuals, their bodies don't make enough of the protein,the protein  is misfolded, and the proteins can affect the brain. The condition can cause delays, cognitive impairments, ataxia, apraxia, parkinsonian tremors, and epilepsy.   Remy was referred to early intervention at 9 months, as he was not developing as expected, although Chloe first started seeing signs at 4 months. He was then referred to genetics and neurology. He was diagnosed with a genetic disorder at 2.5 years old.   Although her son has a lot of impairments, Remy remains happy and in the moment, even during this therapies. His seizures started when he was 2 years old, around the time he was diagnosed. For treatments, they manage seizures, stress, insomnia, and any symptoms that arise. There is no cure. They have tried intense therapy programs, CBD, oxygen therapy, supplements, movement therapy, ozone therapy, hyperbaric therapy, neurofeedback, and floor time. Remy needs constant supervision, even at night, due to having nocturnal seizures.   Chloe discusses all of the advocacy work she has had to do to help Remy, including advocating for him to be allowed to attend school. Remy was kicked out of school twice, causing them to have to move, and uproot her company and leave behind family and friends. When Remy was 3, there was an inclusion program that he was able to attend through the school system, with a lot of supports. As Remy got older, Chloe started getting phone calls to come pick up Remy because the school didn't want to deal with his behaviors. He is now in a great program in Colorado, although the paraprofessionals are mostly in charge of the children, rather than the special educator. For Chloe, she copes by being easier on herself, using positive self-talk, uses Fight Camp, being in nature, and using meditation.     Remy's Revenge Radical Roots Herbs Email Brain Balance Program Family Hope Center Fight Camp NAPA intensive therapy     Links: Email us if you have any questions or ideas! We are now on instagram! Check out updates on our website. Follow Thriving on Twitter. Check us out on Facebook! We are also on Pinterest!     Please subscribe to our podcast in the iTunes store, or wherever you find your podcasts, Leave us a 5-star review, to help us know what you like and what you don't like, and to make sure other like-minded people find support through this podcast. Show Music: Intro Outro: Intro Outro 2 by Mattias Lahoud under CC-BY 3.0 License (www.freesound.org) Theme Song: 90s rock style by monkeyman535 under CC-BY 3.0 License (www.freesound.org) Self Care Song: Green and Orange No Water by Duncan Alex under CC-BY 3.0 License (www.freesound.org)   Hosted by: Jessica Temple and Lewis Temple   Disclaimer: Our show is not designed to provide listeners with specific or personal legal, medical, or professional services or advice. Parents of children with health issues should always consult their health care provider for medical advice, medication, or treatment. Copyright 2021 Jessica Temple

On this bonus episode of Knockin’ Doorz Down, we’re joined by Elaina Vieira, President of the Carlos Vieira Foundation, to discuss the Race to End the Stigma Scholarship with Breanna Smith, Chloe Mendoza and Isabella Porras.  Breanna shares her struggle with the aftermath of the deadly Camp Fires, and confronting mental health matters in childhood, home life, socially in her high school environment, culturally, and the positive steps she's taking to end the stigma surrounding mental health. For Breanna's essay- https://www.carlosvieirafoundation.org/programs/race-to-end-the-stigma/scholarship-recipients.html#qxt-qx-tabs-4934088 Chloe shares her aim in helping her fellow students discuss mental health in high school, and confronting mental health matters in childhood, home life, culturally, and the positive steps she's taking to end the stigma surrounding mental health.  For Chloe's essay - https://www.carlosvieirafoundation.org/programs/race-to-end-the-stigma/scholarship-recipients.html#qxt-qx-tabs-4934082  Isabella shares her struggle with never having a stable home environment, confronting mental health matters in childhood, socially in her high school environment, culturally, and the positive steps she's taking to end the stigma surrounding mental health For Isabella's complete essay- https://www.carlosvieirafoundation.org/programs/race-to-end-the-stigma/scholarship-recipients.html#qxt-qx-tabs-4934080 This is Breanna Smith, Chloe Mendoza and Isabella Porras in their own words on Knockin’ Doorz Down. For more on the Carlos Vieira Foundation and the Race to End the Stigma campaign visit https://www.carlosvieirafoundation.org/ The Race to End the Stigma Scholarship was created by the Carlos Vieira Foundation to start the conversation about mental health. The $2,000 Race to End the Stigma Scholarship is granted annually to graduating high school seniors who are interested in mental health awareness or who are willing to share their stories about mental health in an effort to end the stigma. https://www.carlosvieirafoundation.org/ https://www.facebook.com/CVFoundation/ https://www.instagram.com/carlosvieirafoundation/   For Carlos Vieira's autobiography Knockin' Doorz Down https://www.kddmediacompany.com/ For 51FIFTY use the discount code KDD20 for 20% off! https://51fiftyltm.com/ https://www.facebook.com/51FIFTYLTM https://www.instagram.com/51fiftyltm/ https://twitter.com/51fiftyltm For more on the Knockin' Doorz Down podcast and to follow us on social media https://www.kddmediacompany.com/podcast https://www.instagram.com/knockindoorzdown/ https://www.facebook.com/knockingdoorsdown/ https://twitter.com/kddmediacompany https://www.youtube.com/channel/UCUSJ5ooBFqso8lfFiiIM-5g/   

Meet Chloe Songer, founder of Thousand Fell - more than just a manufacturer of foot wear, but a leader in the movement to build a circular economy. Motivated by the enormous waste in the fashion industry and a desire to make a difference, Chloe took it upon herself to learn everything she could about the production process. She was introduced to manufacturing working for the Alexander Wang Group in China and later moved to Gap where she got an education in supply chain.   Chloe’s experience in China empowered her vision to build her own brand utilizing sustainable materials. Currently, 2.4 billion pairs of sneakers are sold in the U.S. every year and 300 million pairs go straight to a landfill within their first year. Today, the fashion industry is the poster child for change with entrepreneurs like Chloe leading the way to make better products, eliminate waste, and create a safer environment. For Chloe - she gets to practice the best advice she ever got -- “to be the person who brings people together.” Hear more about Chloe’s journey on the WAM Podcast. Learn more about your ad choices. Visit megaphone.fm/adchoices

Meet Chloe Songer, founder of Thousand Fell - more than just a manufacturer of foot wear, but a leader in the movement to build a circular economy. Motivated by the enormous waste in the fashion industry and a desire to make a difference, Chloe took it upon herself to learn everything she could about the production process. She was introduced to manufacturing working for the Alexander Wang Group in China and later moved to Gap where she got an education in supply chain.   Chloe’s experience in China empowered her vision to build her own brand utilizing sustainable materials. Currently, 2.4 billion pairs of sneakers are sold in the U.S. every year and 300 million pairs go straight to a landfill within their first year. Today, the fashion industry is the poster child for change with entrepreneurs like Chloe leading the way to make better products, eliminate waste, and create a safer environment. For Chloe - she gets to practice the best advice she ever got -- “to be the person who brings people together.” Hear more about Chloe’s journey on the WAM Podcast. Learn more about your ad choices. Visit megaphone.fm/adchoices

While most of the time, FIRST Looks gets the opportunity to speak with members of FIRST Robotics Competition and FIRST Tech Challenge teams, we always look forward to our experiences with FIRST LEGO League team members. These students, while very young, are some of the most energetic and passionate, both about their teams and about FIRST in general. During ROBOTICON Tampa Bay 2018, the team spoke with Chloe from the Tie Dye Gummy Divas, Team 30648. The adorable team name came from combining one word from each team member, making it a true team effort.Showing the team's excitement for the season, the team members all have a similar, but unique look. All of the girls were wearing a team shirt, matching rainbow tutu, and space-themed leggings, which match the theme for the season. Each member, however, had their own design for their leggings, getting to show off a little about themselves. This is a big part of the FIRST LEGO League program, with awards being given to the team with the most "team spirit."For the Gummy Divas, there aren't exactly roles. The students get the opportunity to try different aspects of the build and research project and then focus on the aspects that they enjoy the most. For Chloe, that's been all about programming and building, while her friends have focused on other aspects of the season, like the research project. The project for the year is to think of the problems that would be encountered by people trying to live in space and help address those problems.When thinking about the future of space travel and exploration, Chloe is very excited. She says that "it takes your breath away, figurately and literally." Profound words from a very smart girl. She believes that, in the future, we will find a way to live in space for more than just a few years, with colonies being built. She's also excited about the things that she's learning now in FIRST about robotics could one day help astronauts on other planets.Sponsored by: Support our coverage by shopping Amazon here. Whether you're programming a robot, playing a game or doing homework, the Microsoft Surface is the tablet that can replace your laptop. Get yours at the Microsoft Store.

While most of the time, FIRST Looks gets the opportunity to speak with members of FIRST Robotics Competition and FIRST Tech Challenge teams, we always look forward to our experiences with FIRST LEGO League team members. These students, while very young, are some of the most energetic and passionate, both about their teams and about FIRST in general. During ROBOTICON Tampa Bay 2018, the team spoke with Chloe from the Tie Dye Gummy Divas, Team 30648. The adorable team name came from combining one word from each team member, making it a true team effort.Showing the team's excitement for the season, the team members all have a similar, but unique look. All of the girls were wearing a team shirt, matching rainbow tutu, and space-themed leggings, which match the theme for the season. Each member, however, had their own design for their leggings, getting to show off a little about themselves. This is a big part of the FIRST LEGO League program, with awards being given to the team with the most "team spirit."For the Gummy Divas, there aren't exactly roles. The students get the opportunity to try different aspects of the build and research project and then focus on the aspects that they enjoy the most. For Chloe, that's been all about programming and building, while her friends have focused on other aspects of the season, like the research project. The project for the year is to think of the problems that would be encountered by people trying to live in space and help address those problems.When thinking about the future of space travel and exploration, Chloe is very excited. She says that "it takes your breath away, figurately and literally." Profound words from a very smart girl. She believes that, in the future, we will find a way to live in space for more than just a few years, with colonies being built. She's also excited about the things that she's learning now in FIRST about robotics could one day help astronauts on other planets.Sponsored by: Support our coverage by shopping Amazon here. Whether you're programming a robot, playing a game or doing homework, the Microsoft Surface is the tablet that can replace your laptop. Get yours at the Microsoft Store.

How much you believe… In yourself? Can you put your feet on the ground in the morning are you focusing on your power… Or limitations? Chloe Cohen was diagnosed with relapsing remitting MS in 1998. She had a Trumatic head injury and within hours she was having tremors on her left side. She was only 20 years old and an aspiring cellist. That all changed. The early years after diagnosis were lonely for Chloe as they are for a lot of us. In order to find some people to share with, she cofounded an MS support group. And I’m so thankful she did. I’ve been involved with this group since 2007 and you can see Chloe‘s personality stamp on it because the meetings are always very positive and upbeat. Like she is. I have known Chloe for over 10 years and that time I have seen her belief, trust herself skyrocket. It hasn’t been easy, but she’s created a recipe That allows her power to shine despite any limitations the MS has brought on. Chloe knows she didn’t get MS at such a young age to cry about it. She’s here to teach and share her story. Whether it be in the gym and lifting more weight than she ever thought she could, speaking at MS events or in her writing She is a true example of how hard work, tenacious persistence and soulful desire can lead to amazing things. Chloe has written a book and the ebook comes out in May 2019. Chloe and I have been honored to be involved in the most recent national MS Society‘s awareness campaign. Through black-and-white pictures and heartfelt videos we got to tell our stories and it was profoundly touching for both of us. In this podcast Chloe mentions walking in the photo shoot while I was getting my picture taken and it brought her to tears. I think that’s the power of this campaign in that it touches our soul. For me it’s my daughters. For Chloe it’s the loss of her musical abilities.   Buy Chloe’s book - https://www.amazon.com/Making-Lemonade-out-Lemons-Story-ebook/dp/B07PGR64T7/ref=sr_1_2?keywords=Chloe+Cohen&qid=1552144568&s=books&sr=1-2   Whatever It Takes Campaign -  pics and videos of Chloe and Jim - www.nationalMSsociety.org/Chloe

We talk with Chloe O’Neill, founder of "More Than Lyme." She’s had Lyme Disease for most of her young life. For Chloe, the vague, intermittent, but often debilitating symptoms of the disease have impacted her life view in both negative and remarkably positive ways. Many of the lessons its taught her are surprisingly universal - whether that's becoming more at ease with gray areas or redefining personal strength. Stay tuned for the end of the episode, there's a sneak peak of our new podcast, "Women on the Road," hosted by Laura Hughes. Subscribe on Apple Podcast, Stitcher, Google Play, and wherever you stream stories. Learn more about it in an essay by Laura. Sponsored by Oru Kayak. Music is by Lee Rosevere and Josh Woodward via the freemusicarchive.org. Find out more at She-Explores.com/podcast and www.morethanlyme.org.

Welcome! My guest today is an experienced commercial research consultant who was born and raised in the UK. Dr. Chloe Peacock earned a Ph.D. in Consumer Brand Participation and is an expert in Semiotics. She loves beaches, traveling, the outdoors, and all creatures. She is the founder of the UK Lifestyle Network for Childfree Women and The League of Fabulous Women. Her hope is to gently shift and soften cultural perceptions of women without children and to help these women connect with each other. You can find her on Facebook, Twitter, and at www.tlfw.co.uk. In this episode, you’ll learn the following about Chloe: Chloe has always been very comfortable with her ambivalence about motherhood. Even as a childfree woman, you can still be a caring, nurturing person and have children in your life. We all have different peak life experiences that we view as huge and fulfilling. In her mid-30’s, Chloe considered her “fertility window” but never felt the compulsion to plunge into motherhood. Like many childfree women, Chloe has dealt with pressure from family and friends: “You’d make a GREAT mom! You’re such a caring person!” The issue of legacy is important to Chloe and she has had many conversations with her father about this topic. Ultimately, you have to follow your own path. The League of Fabulous Women started small, as a product of her own experience, and then it grew rapidly. It exists for the purpose of connecting childfree women in friendship. Like many childfree women, Chloe noticed a dramatic shift in her social life because of others’ pregnancies. She read about Melanie Notkin’s work and then began meet-up groups of her own. Women over 40 without children are an increasing demographic for the present and the future. Not being a mother is no less natural or feminine than being a mother and having children. There is much cultural mythology surrounding motherhood as THE ultimate feminine experience. Chloe likes to express her creativity through creating relationships. For Chloe, the major benefits of NOT having children are the sense of freedom, being able to travel, and being the author of her own life. The League of Fabulous Women now has meet-up groups in Brighton, Bristol, Manchester, and London.  Connect and find out more at www.tlfw.co.uk   I do hope you enjoyed this episode. Please subscribe and share with a friend. For more episodes go to www.michellemariemcgrath.com