Podcasts about disabled children

The UK Supreme Court rules that the legal definition of a woman is based on biological sex. BBC correspondent Catriona Renton joins Nuala to discuss the ramifications of the ruling. Parents of disabled children are being forced to spend thousands of pounds of their own money to plug funding gaps in the health and social care system, according to new research by the disability charity Sense. Nearly half of mums polled have had to give up work as they don't get enough support to care for their child, and many families are turning to loans, credit cards and even crowdfunding to plug the gaps. Nuala is joined by Harriet Edwards, Head of Policy at Sense, and mum-of-three Kimberley Hind. The Irish writer Edna O'Brien died last year at the age of 93. The last person to be granted an interview with her was the documentary director Sinéad O'Shea. Her new film Blue Road weaves those final interviews with archive and readings from Edna's own diaries to tell the story of her extraordinary life. How does parental infidelity impact children, even years later when they become adults? Juliet Rosenfeld, a psychoanalyst and author of Affairs, and Tanith Carey, parenting expert and author of What's My Tween Thinking, join Nuala to discuss.Presenter: Nuala McGovern Producer: Dianne McGregor

The expert team at Amelia Home Care (929-333-3955) can offer you the relief you need through their pediatric home care services, available now in the Bronx. Apply today at https://ameliahomecareny.com/pediatric-home-care/ Amelia Home Care City: Brooklyn Address: 3007 Ocean Parkway Website: https://www.ameliahomecareny.com/

This podcast episode from our Twinkl SEND podcast "SEND in the Experts" hosted by Georgina Durrant, focuses on supporting children with Special Educational Needs and Disabilities (SEND). Georgina is joined by Joe Faultley, an autistic and neurodivergent advocate with dyspraxia and anxiety, who works at the Council for Disabled Children and is an active member of the SEND and education community. Joe shares his personal experiences, insights on autism advocacy, and advice for improving education for autistic students, emphasising the importance of supporting children and young people with sensory processing differences, communication needs, and anxiety. He highlights his work in promoting awareness, acceptance, and understanding of neurodiversity through media and delivering training. This episode offers practical tips for educators to better support SEND learners, in particular autistic learners. Find out more about using Twinkl Symbols to support children and young people with communication here: https://www.twinkl.co.uk/l/ypt3j or download the free Twinkl Symbols AAC app: https://www.twinkl.co.uk/l/1asrsnFind out more about supporting autistic children and young people here: https://www.twinkl.co.uk/l/140sia

Services for children with special education needs and disabilities (SEND) in England are ‘unviable'. That's the judgement from a report out today by the Public Accounts Committee, who look at the value for money of government services. Anna Dixon MP, who sits on the committee, joins Nuala McGovern to explain more, alongside Katie Ghose, Vice-Chair of the Disabled Children's Partnership.Four Women's Championship football clubs will take part in a new pilot scheme beginning this month to allow fans to drink alcohol in the stands. This is something that's been banned for supporters of the men's game in the top five tiers. Head of Women's Football at the Football Supporters' Association Deborah Dilworth discusses the plans and what this could mean for women's football matches.Holly Bourne, bestselling author of How Do You Like Me Now? and the Spinster Club series, is back with So Thrilled For You, her most personal novel yet. It's a story about four friends navigating motherhood, career ambition, and societal pressures, all unfolding during a sweltering summer's day at a baby shower. Holly explains what inspired her to write this funny, sharp, and moving exploration of friendship, and her experiences with early motherhood.According to stats from Cycling UK, 75% of cycling trips in the UK are made by men - but women are increasingly turning to the gym and indoor classes for their biking fix. Nuala discusses how we can get more women cycling, inside and outside, with Michelle Arthurs Brennan, digital editor at Cycling Weekly, and Clare Rogers from the London Cycling Campaign women's network. Presented by Nuala McGovern Producer: Louise Corley

Episode 187: Tucker's House. Helping Disabled Children. Something That's Still GREAT in This World. Helping Disabled Children in HUGE Ways with Very Little Budget. Interview with Director Graham Honeycutt, Formerly "Rory Uhtredson" on This Podcast.If you want to see something that is still GREAT in this world, where passionate people who instill hope, encouragement, and practical life-long solutions to disabled children and their families through personal sacrifice, check out the Tucker's House website at: Tucker's House - Making Homes Accessible - Franklin, TNTo watch episodes of their new show "House to Home" on Youtube, here's the link to that: Tucker's House - YouTubeGraham's personal journey to Tucker's House during and after the death of his disabled daughter in Episode 110 of this podcast:  Episode 110: No One Would Gue - It All Ties Together - Apple PodcastsGraham's second interview on this podcast on Episode 147:  Episode 147: Rory Uhtredson R - It All Ties Together - Apple PodcastsSend a text to It All Ties Together

This week we're joined by retired Irish Army Captain, Senator Tom Clonan. Tom is a fully Independent Senator - with no links to any political party. He is seeking re-election in the upcoming Seanad election, hoping to continue holding the government accountable.  Tom has been a tireless campaigner for the Rights of others - as an Army Whistleblower on Gender-Based Violence and as a Parent campaigning for the rights of Disabled Children, Adults, and the Elderly.  Tom is a strong advocate for Irish Military Neutrality. In this episode, we talk about Tom's first term in Leinster House, his advocacy for people with disabilities, and we ask him to put on his military analyst hat to discuss the global security picture.

Parents of disabled children are responsible for navigating a number of complex systems, from educational services and accommodation to medical care. Author Kelley Coleman, whose son has an undiagnosed genetic syndrome, says that parenting a disabled child can be hard–but hard is not bad. That's the central framework of her book, Everything No One Tells You About Parenting a Disabled Child, which came out earlier this year. In today's episode, Coleman speaks with Here & Now's Deepa Fernandes about their joyful and difficult parenting moments, how to access the support needed for kids to thrive, and teaching self-advocacy.To listen to Book of the Day sponsor-free and support NPR's book coverage, sign up for Book of the Day+ at plus.npr.org/bookofthedayLearn more about sponsor message choices: podcastchoices.com/adchoicesNPR Privacy Policy

It's no secret that parenthood is expensive. But when it comes to parenting a medically complex kid, the dial is turned up to 100. Everything with an “accessible” label is marked up 10x. We have to make renovations to our homes and vehicles with little to no financial assistance. And that's often on top of career and work changes that have made our finances tighter to begin with. In this episode, I'm bringing back Alyssa Nutile and Amanda Griffith-Atkins to sort through the thoughts, feelings, and anxieties from this community about the financial aspect of this life. We cover many of the stressors, the guilt and shame associated with feeling like you can't provide for your child, and some of the resources and routes other parents have used to ease some of the financial stress. This episode touches on some deeply personal territory for many of us, but I think it'll leave us all feeling less shame and loneliness. Let's dive in! Links: Visit the ABLEnow website to learn how to open an account for your child! Visit SupportNow to start a registry and share with your community. Join The Rare Life newsletter and never miss an update! Fill out our contact form to join upcoming discussion groups! Follow Alyssa on Instagram @caffeinated_caregivers! Follow Amanda on Instagram @amanda.griffith.atkins! Follow us on Instagram @the_rare_life! Listen to previous episodes with Alyssa: Ep 170 on Hospitalizations Ep 140 on Alyssa's Story Ep 125 on Traveling with Disabled Children & on our recent season opener and finale episodes! Listen to previous episodes with Amanda: Ep 159 on Sharing the Mental Load Ep 156 on Getting a Divorce Ep 153 on Hurtful Things Loved Ones Say Ep 147 on Sex and Disability Parenting Ep 142 on If My Disabled Child Outlives Me Ep 135 on Career and Family Roles Ep 132 on Self-Care Ep 131 on Chronic Stress Ep 130 on Anticipatory Grief Ep 99 on Family Planning Ep 85 on Parental Identity Ep 81 on Health Anxiety & our holiday season eps: Being Hospitalized During Holidays - Isolating at Home During Holidays & Why Holidays Can Suck. Donate to the podcast or Contact me about sponsoring an episode. Follow the Facebook page. Join the Facebook group Parents of Children with Rare Conditions. Access the transcript on the website here. And if you love this podcast, please leave us a rating or review in your favorite podcast app!

In this episode, Amy Brown interviews Megan Amrich, author of the book 'Show Up and Bring Coffee: How to Support Your Friends with Disabled Children.' They discuss practical ways to support parents of children with disabilities, including being knowledgeable but not a know-it-all, being an extra set of hands, and making events and celebrations accessible. Megan emphasizes the importance of asking your friends what they need and being open to learning about their child's diagnosis. She also encourages friends to share their big news with sensitivity and understanding.Be knowledgeable, but not a know-it-all, about your friend's child's disabilityOffer to be an extra set of hands and help with specific tasks, such as feeding tubesMake events and celebrations accessible by asking your friends what they need and providing accommodationsShare your big news with sensitivity and understanding, recognizing that your friend may be processing their grief Introduction and Welcome02:51 The Importance of Practical Support06:15 Trusting Your Friend's Knowledge10:35 Being an Extra Set of Hands17:19 Finding the One Thing That Would Benefit Your Friend20:41 Small Acts of Help Can Make a Big Difference25:18 Making Events and Celebrations Accessible36:14 Sharing Big News with Sensitivity41:33 Conclusion and Where to Find MeganMegan's Website Rad AdvocatesMegan's IGIf you enjoyed the show:Have you purchased our new book, The Other Side of Special? Subscribe to our newsletter on the Take Heart WebsiteGet our free resource on finding Gratitude, Peace, and HopeReview and like us on Apple Podcasts Share us with others from wherever you listen to podcastsFollow us on Instagram @takeheartspecialmomsFind Amy at www.amyjbrown.com/  or on Instagram @amyjbrown_writerFind Carrie at www.carriemholt.com or on Instagram @carriemholtFind Sara at www.saraclime.com or on Instagram @saraclimeSupport the show

Beware the post-menopausal women who doesn't give a damn, says 63-year-old TV presenter Carol Vorderman. Carol, a self-described ‘old bird with an iphone' joins Nuala McGovern to discuss her new book: Now What? On a Mission to Fix Broken Britain. Part memoir, part tool kit the book relates Carols campaign to defeat the last Tory Government, and urges millions to find their voice and hold the new Labour Government, and all future governments, to better account. Following on from the Woman's Hour SEND programme yesterday, we now focus specifically on SEND provision for black and Asian minority ethnic families. Nuala is joined by Stephen Kingdom, Campaign Manager for the Disabled Children's Partnership, who shares exclusive findings from a report they have conducted. Plus, co-founder of the Sikh disability charity SEN Seva Praveen Mahal tells Nuala about her own personal experience. The pioneering photographer Lee Miller worked as a fashion model and an artist before becoming a war correspondent for British Vogue in the 1930s. Her images taken during World War II are some of the most arresting and enduring of the conflict. A new film about her life, which stars Kate Winslet, focuses on the period in her life when she defied convention to become a war photographer, travelling to the front lines. The film's director Ellen Kuras explains how they captured Lee Miller's adventurous spirit.Last night saw the first - and so far, only scheduled - televised presidential debate in the USA ahead of the election in November. Kamala Harris and Donald Trump spoke for 90 minutes, each accusing the other of lying. Women's issues were on the table for debate including a heated exchange on abortion. Nuala discusses with New York Times columnist Amanda Taub.Presented by Nuala McGovern Producer: Louise Corley

A BATTLE with SATAN & THE DARKNESS! NDE | Eric TaylorToday we're talking with Eric Taylor

*NEWS FLASH*This just in…Connie needs some help understanding research for a school project, so she asks her trusty Uncle Chris and her lovely customers if they know anyone who could help her out!‘Wow, it's like the Batcave…Look at all the robots and machines.'

Another episode dedicated to election-related topics suggested by you, the audience.This time round, we look at mental health, Special Educational Needs and Disabilities (SEND), housing and how, for many immunocompromised, disabled people, the COVID pandemic never ended.This week's panel – Fazilet Hadi from Disability Rights UK, and veteran of our previous panel; Sam Carlisle from Disabled Children's Partnership; and Nil Guzelgun from mental health charity Mind – look at what the seven main parties standing in the General Election on 4 July are offering on those issues.Presented by Emma Tracey Production by Daniel Gordon and Natasha Mayo Sound recording and editing by Dave O'Neill Edited by Farhana Haider

Text us your financial questions! Chief Investment Officer Troy Harmon, CFA, CVA, along with Senior Associate Logan Daniel, CFP®, CRPC®, and Tax Manager Jessie Thomas, CPA, from Henssler CPAs & Advisers, offer valuable tax advice for a couple with a disabled child. They share insights on what may qualify as a medical expense deduction.  Read the Article: https://www.henssler.com/essential-tax-tips-for-families-with-disabled-or-special-needs-children 

Welcome to Empowering Homeschool Conversations, where we delve into the heart of crucial topics affecting homeschooling families. In today's insightful episode, we're honored to host James Lange, a distinguished CPA/Attorney and passionate advocate for families with disabled children. Join us as we unravel the complexities of financial strategies tailored specifically for these families. With James's unique perspective as both a professional advisor and a dedicated special needs parent, get ready for a conversation that promises invaluable insights and empowering guidance. Our special guest this week on Empowering Homeschool Conversations was James Lange, CPA/Attorney and special needs parent. James Lange is the President of two interrelated companies that provide financial services to IRA and retirement plan owners: 1) Tax planning and preparation CPA firm 2) Registered investment advisory firm that provides cutting-edge Roth IRA conversion strategies and money management James Lange one of the few CPAs who is also an Attorney, Financial Advisor, and a 3-time best-selling author. He provides advice on the topics of retirement, estate planning, and Roth IRAs has been featured on CNN, CBS, MSNBC and in the Wall Street Journal, Financial Planning Magazine, Kiplinger's, and hundreds of other sources. Viewers like you funded similar episodes, and other free resources from SPED Homeschool. To learn how you can support the work of SPED Homeschool and this broadcast, visit https://spedhomeschool.com/donate/ To connect with James and his resources, use this link: Get your free digital book and to learn more about the 3-day virtual summit, Financial and Life Planning Summit…for Parents of a Child with a Disability from June 18 to June 20. Go to https://DisabledChildPlanning.com/Podcast To find out more about SPED Homeschool, visit our website at https://spedhomeschool.com/ To learn about the other Empowering Homeschool Conversations Co-Hosts and their resources, visit: https://annieyorty.com/ https://www.youtube.com/@LivingWithEve https://elarplearning.com/ https://solimaracademy.com/  Join our mission to empower homeschool families!: https://spedhomeschool.com/donate/ Discover more Christian podcasts at lifeaudio.com and inquire about advertising opportunities at lifeaudio.com/contact-us.

Episode #123: Kimberly is joined by Lindsey and Ryan Goldman where we discuss detailed events that lead up to their son Skylar suffering birth injuries. We get a peek into how they responded and what they are creating today for disabled children to play at their local park. We also discuss what it means to teach your children about how to be inclusive with people with disabilities and to be the most supportive you can be.  They are looking to raise 500k and are only 80k away from being able to build their dream for the entire community!  Donate by going to www.morrisonparkplayground.com follow them on Instagram @morrisonparkplayground

Welcome back to Voices of Your Village! I got to hang out with Kelley Coleman. She is the author of Everything No One Tells You About Parenting a Disabled Child. Kelley is a feature film development executive turned author and a passionate advocate for parents and caregivers and individuals with disabilities. She is the parent of two amazing boys, one of whom has multiple disabilities, and her book, Everything No One Tells You About Parenting a Disabled Child draws upon over a decade of advocacy with candor, humor, and relatability earned in her prior career of writing and developing talking animal movies. She was recently named best mom ever by her two discerning children and received a congratulatory mug. I had a blast hanging out and chatting with Kelley. There are a lot of nuances in the conversation and think that this is really key for all humans. Whether you are parenting a disabled child or not, there's so much learning for us all to do as a community about systems and support and the worth of every human on the planet. All right, folks, let's dive in.  Connect with Kelley: Instagram: @hellokelleycoleman Website: https://www.kelleycoleman.com/ Order the book: Everything No One Tells You About Parenting a Disabled Child: Your Guide to the Essential Systems, Services, and Supports  Connect with us: Instagram: @seed.and.sew  Podcast page: Voices of Your Village Seed and Sew's Regulation Quiz: Take the Quiz Order Tiny Humans, Big Emotions now!  Website: seedandsew.org Music by: Ruby Adams and Bensound This show is brought to you by BetterHelp. Learn more about your ad choices. Visit megaphone.fm/adchoices

The boys lunch on “Naked ‘Nola Benedict” and surprise dessert!RJ is the voice of god, Jimmy photographs St. James Cemetery for Disabled Children, Johnny is fascinated by people's fascination with the Royal Family, and Brogan (basically) calls for a British Revolution. https://2charactersandaclown.comhttps://www.buymeacoffee.com/2CandaC

In this episode, Emma Tracey gets reaction to Chancellor Jeremy Hunt's spending plans from Fazilet Hadi of Disability Rights UK. Plus Stephen Kingdom from the Disabled Children's Partnership on the Budget announcement that £105 million is to be spent on building schools for students with Special Educational Needs and Disabilities. There's also an interview with Henry Fraser. Once an aspiring rugby player, he was paralysed from the neck down in a diving accident and has since become famous for painting using his mouth and a specially-adapted paint brush.The episode was made by Daniel Gordon with Niamh Hughes and Emma Tracey. The editor is Alex Lewis. Recorded by Hannah Montgomery. Sound design by Dave O'Neill. To get in touch with the team email accessall@bbc.co..uk or find us n X, @bbcaccessall. Don't forget to subscribe by finding us on BBC Sounds.

If you have a child with a disability in the public school system, you are familiar with the language of special education, IEPs, and 504 Plans. If it's new to you, stick around for today's conversation because I'm joined by two trusted experts in the thick of the IEP world. We begin with Dr. Lesley Cook, a clinical psychologist and repeat guest on the show, as she explains what parents need to know to be prepared and informed ahead of IEP meetings. My second guest is Kim Kizito, a fierce advocate who meets with families and consults with them as they navigate the public school system to get educational services for their children with various disabilities. Join us to learn more! Show Highlights: From Dr. Lesley:  ●      Dr. Lesley's path to becoming a trusted expert witness in due process cases dealing with neuropsych assessments ●      Understanding IEPs–individual education programs for students who have a diagnosis that interferes with their education ●      The difference between bad goals and good goals in an IEP ●      Dr. Lesley's advice to watch out for the word “comply” in an IEP goal ●      Turning bad goals into better goals that are affirming and realistic ●      Considerations around behavioral disorders, PTSD, and triggering environments ●      3 kinds of interventions and supports that should be included in IEPs ●      A look at the intense pressure that parents feel in the IEP process–and why the law regards them as equal members in the process ●      Examples of common accommodations that parents can ask for ●      The problem with color charts as a behavior management tool ●      Dr. Lesley's tips for parents and guardians who want to be more informed and prepared for IEP meetings   From Kim:  ●      Most parents don't realize what services are available for children ages 0-3 through ECI (Early Childhood Intervention) ●      The importance of a special education advocate in helping families ●      Understanding the difference between a 504 Plan and an IEP ●      The three-pronged process for a child to qualify for an IEP ●      Lightning round questions for Kim about the excuses schools give to parents ●      Kim's strategy to “get through” to the school to get evaluations and services for a child ●      Top tips for parents in protecting their child's educational rights ●      A manifestation determination hearing—when it is appropriate and what it means   Resources and Links:  Connect with Dr. Lesley Cook: TikTok  Mentioned by Dr. Lesley: www.understood.org  Connect with Kim Kizito: Website, Instagram, Facebook, and TikTok  Connect with KC: Website, TikTok, Instagram, and Facebook Get KC's book, How to Keep House While Drowning We love the sponsors that make this show possible! You can always find all the special deals and codes for all our current sponsors on our website: www.strugglecare.com/promo-codes.  

When you first discover you'll be parenting a child with disabilities, the road ahead can seem daunting and lonely. Kris Burbank and Linda Hoopes join me to shed light on this path, offering wisdom from their book "Embracing Another Normal." Together, we unpack the resilience necessary for such a journey, sharing personal stories and strategies that resonate not just with parents, but anyone facing adversity.The podcast unfolds the reality of raising children with unique needs, unwrapping the complexities like the layers of an onion. We discuss the importance of fostering connections and nurturing positivity, even when the isolation feels profound and the challenges insurmountable. Our conversation is filled with genuine experiences and practical advice, aiming to build a lifeline of resilience for families navigating these waters.Finally, we tackle the notion of strategic decision-making and energy management, with Kris and Linda presenting their framework for resilience that can be applied across life's challenging terrains. Listeners will come away with a sense of empowered grace, learning that it's not about avoiding obstacles, but rather, reframing them into opportunities for growth. Join us for a heartfelt exchange that celebrates the strength found in vulnerability and the triumph of the human spirit in the face of life's unexpected turns on a special hiatus episode of Navigating Life as we Know it!Use this link to order your own copy of Embracing Another Normal from Amazon: https://a.co/d/5lZFmbKSupport the showThank you for listening to our podcast and for your continued support! We're taking a break to recharge and plan some exciting new things for the show. We'll be back with a fresh season featuring more in-depth explorations of disability issues, along with new segments and interviews. If you'd like to learn more about NLAWKI please visit our facebook page and if you'd like to support our program more directly, stop by our Ko-Fi and make a contribution! But the most important way you can help our program is by sharing NLAWKI with someone you know!

Our kids touch the lives of everyone around us, but especially our close family and friends. But we don't always get to hear that perspective from the outside. So on this episode of The Rare Life, we'll finally get to hear from those close to us about what it was like to watch us endure trauma, explore parenthood with a medically complex child, and try to figure out the best ways to support us. Kassie Harbath, auntie of Sloan, a little girl with CHARGE syndrome, joins us to sort through all these complex feelings.And, this episode is so well-timed, because we're also starting our Family + Friends Fundraiser!  Get more info on the fundraiser at https://therarelife.org/fundraiser. Also, thanks to the many families and friends who have already donated and sponsored episodes, including the loved ones of Alyssa Nutile, mom of Gemma who has Pyruvate Dehydrogenase Complex Deficiency (PDCD). We couldn't do it without you!   Links: Join us for The Family + Friends Rare Disease Day Fundraiser and see how you can help The Rare Life continue for years to come! Donate to the fundraiser here. Hear the story episodes of the loved ones whose family and friends who shared today: Alyssa Ep 140, Libby Ep 95, Bek Ep 133, Marci Ep 114, Brianna Ep 105, Madhura Ep 117, Suzy Ep 124, Kari: Ep 123, Ep 10, and Ep 11. Listen to Ep 146: The Dad Perspective. Listen to Ep 104: How to Support the Parents of Disabled Children. Read Show Up and Bring Coffee by Megan Amrich. Follow us on Instagram @the_rare_life! Donate to the podcast or Contact me about sponsoring an episode. Fill out our contact form to get a reminder about upcoming discussion meetings and the Skype link to join! Follow the Facebook page. Access the transcript on the website here.

Get ready for an enlightening and heartfelt episode as The Wolf Of Queen Street Podcast welcomes Frian Wadia, a devoted mother to three teens with a range of sensory, learning, and neurodevelopmental disabilities. Based in Tāmaki Makaurau, Frian's personal experiences have fueled her passion to advocate for systemic change, ensuring inclusion and equity for disabled children and their families.

Study highlights inadequacies in Care Dependency Grant for disabled children by Radio Islam

A lesbian couple has attracted fierce criticism by deliberately having a deaf baby. Plus, rapper Ice Spice has released a musical masterpiece with a new song called... "Think You The Shit (Fart)." And, I am launching a rare defense of Ilhan Omar after she was accused of 'treason' for a speech where she allegedly unapologetically declared she is "Somalia first." Ep.272 - - - Binge ALL 10 episodes of Convicting a Murderer here: https://bit.ly/3RbWBPL Grab some “Yes We CANdace” merch here: https://bit.ly/3Amm13Y - - -  Today's Sponsor: Beam - Get 40% off for a limited time! http://www.ShopBeam.com/Candace - - - Socials: Follow on Twitter: https://bit.ly/3RNly1c Follow on Instagram: https://bit.ly/3U5DF4a Follow on Facebook: https://bit.ly/3Ug6Thd Subscribe on YouTube: https://bit.ly/3d9dZ6k

Parenting is both a blessing and a challenge, and this is especially true when your child has a disability.  Steph Hubach has firsthand experience with the demands of caring for a disabled child.  She joins Chris Brooks to encourage those who parent special needs children and to offer wisdom for the rest of us who walk alongside them. EQUIPPERS - Our next EQUIPPER WEBINAR is February 1!  REGISTRATION DETAILS ARE IN YOUR E-MAIL INBOX.  Not an Equipper and want to attend?   Become an Equipper Today

Parents of disabled children say they are being “pushed out” by a Kent zoo after new restrictions were placed on carer passes. Rule changes at Wingham Wildlife Park have left some families concerned they won't be able to afford to take their kids. Also in today's podcast, the government's Rwanda scheme is back in the national spotlight today - there'll be a debate over amendments in the commons ahead of a vote tomorrow. A Kent charity is calling for the scheme to be scrapped completely following the death of five asylum seekers in the Channel over the weekend. The Church is facing a huge backlash over plans to build 23 homes between an A-road and ancient woodland near Tenterden. Those backing the proposals say it  will “make a positive contribution” to the community but critics says it's going to make the A28 a "nightmare". You can find out which Kent councils have the highest level of debt.News figures also show where money is being spent across the county. And a supermarket cafe in Kent has been told to clean up its act after inspectors found evidence of mice in the kitchen.The eatery was also told it needed to tackle poor food hygiene after they were found to be keeping food past its use-by date.

How can the design of a home transform the daily life of a child with disabilities and have a lasting impact throughout their lifetime? How does this transformation affect their family and caregivers?   This episode features Marcel Hernandez Development Director of Tucker's House, a nonprofit in Tennessee that customizes homes for disabled children. They focus on creating accessible spaces that cater to each child's needs, considering their future growth and independence. Marcel emphasizes the importance of a holistic and therapy-informed approach, not only making physical adjustments but also alleviating emotional stress for caregivers, acknowledging their critical yet often unnoticed role. He also discusses the "House to Home" video series, which illustrates the profound impact of these home transformations on families.    Tune in to hear firsthand how compassionate home designs and builds are breaking barriers and bringing joy to families in need.      [00:01 - 04:29] Opening Segment Tucker's House is a Tennessee-based nonprofit that specializes in home modifications for families with children who have disabilities The organization, active since 2009, estimates its impact on approximately 1200 to 1500 individuals, working annually with about 100 to 120 individuals Tucker's House is fully funded through private donations, including grants from foundations, corporate partners, and individual community champions, covering all costs for their core AIM program The AIM program involves a comprehensive process with a program manager, occupational and physical therapists, architects, and construction partners, to create personalized, practical modifications in homes     [04:30 - 08:11] Building for a Lifetime: A Lasting Solution for Families and Caregivers Tucker's House focuses on long-term, sustainable home modifications for children with disabilities, considering their growth and evolving needs to provide lifetime solutions The organization's approach includes not just physical modifications but also aims to provide emotional relief and support for caregivers, recognizing their crucial role Their high client satisfaction and attention to detail in modifications underscore their commitment to delivering quality solutions without the need for major re-installations   [08:12 - 13:40] Inspiring Stories Behind Accessible Homes Tucker's House not only modifies homes but also assists with ordering and installing durable medical equipment (DME), ensuring a perfect fit for each family's unique needs Their therapy-informed approach goes beyond typical remodeling, prioritizing the family's voice and choice throughout the process for personalized solutions The "House to Home" series offers a behind-the-scenes look at the challenges faced by families with disabilities and how accessible modifications alleviate these struggles This series also highlights the crucial role of caregivers and the physical and emotional toll of caregiving, underscoring the importance of ergonomic home design Tucker's House collaborates with financial partners who are also featured in the series and play a significant role in supporting and facilitating their initiatives   [13:41 - 20:48] Navigating the Demand for Accessibility  The organization is primarily referral-based, receiving clients through healthcare providers and gaining increased exposure through media and their House to Home series Their service criteria focus mainly on children but are flexible, considering each family's unique situation, including financial constraints and healthcare needs Marcel also talks about similar organizations that serve people of all ages    [20:49 - 28:46] Closing Segment Marcel is deeply committed to setting a strong psychological foundation for his children, emphasizing the importance of a stable, nurturing home environment His nonprofit work, including founding Be About Change, reflects his dedication to elevating young people's trajectories, paralleling his role in Tucker's House to support children physically and psychologically Marcel finds inspiration in the resilience and positivity of those facing mental and physical challenges, which is evident in the impactful stories shared in the House to Home series     Want to connect with Marcel? Reach out directly through marcel.hernandez@tuckershouse.org or contact 615 953 9572. Visit https://tuckershouse.org/ to learn more about their work and watch Episode 1 of House to Home: Zola's House Transformation on YouTube.   Key Quotes:   “We really focus on providing that lifetime solution. While some are looking for kind of a day-to-day impact, we really focus on going perhaps just an inch wide, but a mile deep in terms of the impact that we make with each household.” - Marcel Hernandez   “We do everything to preserve the family's voice and choice through the entire process so that it is really their plan and we're facilitating the realization of that plan.” - Marcel Hernandez   “I have a belief that the individuals that struggle mentally, physically, or both are, in my estimation, what I would just say closer to God, closer to divinity” - Marcel Hernandez Please check out videos of many of the podcast episodes on my YouTube channel: Accessible Housing Matters.   To learn more, share feedback, or share guest ideas, please visit my website or contact me on Facebook and Twitter.   Like what you've heard? Please review us! That helps let other people know about the podcast.   Accessible Housing Matters is dedicated to raising awareness about important issues around accessibility and housing and getting conversations going.   I'd love to learn more about what's on your mind and get your feedback about the show.   Contact me directly at stephen@accessiblehousingmatters.com to share your thoughts or arrange a call.  

Did the Russian Government Alter Disabled Children's Appearance to Resemble Aliens?? - 10/15/23See Privacy Policy at https://art19.com/privacy and California Privacy Notice at https://art19.com/privacy#do-not-sell-my-info.

Claiming to tell unknown stories about the iconic singer, alongside songs some of his much-loved songs, this world premiere musical hopes to reflect his enduring legacy. His youngest daughter Tina, one of the producers, and the director and choreographer of the show, Kathleen Marshall join Emma Barnett. We discuss the possible decision to cancel another part of the high speed rail link - HS2 - and the impact it could have on women with Dr Mary-Ann Stephenson, co-director of the Women's Budget Group, a Feminist Economic Think Tank and Zoe Billingham, Director of the IPPR North - based in Manchester. Between 1975 and 1980, Peter Sutcliffe murdered 13 women and attempted to murder at least seven more across the North of England.  A new ITV drama series, The Long Shadow, portrays the women who were killed, and their families, as well as the hardworking but flawed and misogynist police investigation.  Joining Emma are Willow Grylls, executive producer of the show and Meg Winterburn, who worked on the investigation as a police sergeant. Exclusive research shared with Woman's Hour claims that £60m is ‘wasted' in England every year on Tribunals for children with Special Educational Needs and Disabilities. Local authorities ‘fight' thousands of parents of disabled children about what support the child gets and where they go to school  – but 'lose' 96% of those cases. This comes on the day that one of the country's leading experts delivers a valedictory lecture after a 40 year career advocating for disabled children. Dame Christine Lenehan, Director of the Council of Disabled Children, part of the National Children's Bureau, Presenter: Emma Barnett Producer: Lisa Jenkinson Studio Manager: Duncan Hannant

In this episode we are talking to Katie from Child Life On Call.  Katie is the CEO and Founder of Child Life On Call, an app, podcast, and website dedicated to closing the resource gap through the intersection of child life services and technology.We discuss: how to support the siblings of disabled children,what a child life specialist is,and how to support your local child life specialists.Here are some links that were mentioned in the show:Supporting Siblings: How Child Life Specialists Can HelpKatie's Favorite Things on AmazonKatie's Podcast Child Life on CallPlease follow Katie on Instagram @childlifeoncallPlease subscribe, leave a review, and follow us on social media to know about upcoming episodes and to participate in this podcast.Instagram - @raisingdisabledpodcastFacebook - Raising Disabled Podcast

A new charitable centre to help disabled children develop has opened its doors in Palmerston North. Little Stars is the brainchild of a family who know only too well what access to therapy at an early age can do. Our reporter Jimmy Ellingham paid a visit.

Caring for a disabled child often goes unthanked and unrecognized in this world. But God sees every sacrifice, and he will reward you.This show is part of the Spreaker Prime Network, if you are interested in advertising on this podcast, contact us at https://www.spreaker.com/show/3279340/advertisement

Caring for a disabled child often goes unthanked and unrecognized in this world. But God sees every sacrifice, and he will reward you.

In this episode, Michael Reddington engages in an incredible conversation with Shaun Haines, a remarkable multilinguist. Shaun shares his unique language learning journey, starting with sign language and expanding to Spanish, Portuguese, Italian, and more. Discover how Shaun's motivation, focus, and passion for grammar made learning languages as an adult easier, while also exploring the profound connections language creates between cultures. Additionally, Shaun shares his diverse career path, from supporting the disabled to serving in the military and becoming an attorney, which has shaped his empathy and understanding for others. Timestamps: (00:00:16) - Introduction to Shaun Haines(00:08:24) - Working with adults with disabilities and its impact(00:23:10) - Being a 31-year-old in boot camp: the challenges and rewards(00:27:31) - Young soldiers with attention problems and disciplinary issues.(00:32:51) - The importance of connection and understanding differences.(00:41:14) - Law student finds success through investigative work.(00:50:03) - Learning languages as an adult.(01:01:34) - Understanding and valuing communication across languages.(01:06:56) - Closing sentiments and thank you to the sponsors.Sponsor LinksHumintell: Body Language - Reading People - HumintellEnter Code INQUASIVE25 for 25% discount on your online training purchase.Emotional Intelligence Magazine: HOME | Emotional Intelligence Magazine + (ei-magazine.com) International Association of Interviewers: Home (certifiedinterviewer.com)Podcast Production Services by EveryWord Media

Today Jan is joined by Saida Mahoney, activist and advocate for the disabled of all types and kinds, Miss Amazing winner, author, artist, and Thrivivor. Saida's history of abuse is daunting, but she still finds a way to keep her vision of the world bright and does all she can to live to the max and help others live to their full potential.Keep up with Saida in all ways possible:WONDERGIRLSAIDA PodcastFollow her on Twitter, instagram and Wordpress @WONDERGIRLSAIDARead her writings on WattpadThis episode is sponsored by Betterhelp Online Therapy. Get in touch with the right therapist today! Use our link to get 10% off your first month: www.betterhelp.com/janSubscribe / Support / Contact:

The longest legislative walkout by Oregon Senate Republicans in state history had meant the death of any number of bills. Now that legislative leaders have reached a framework for a possible deal to bring lawmakers back to the capitol, some may have new life. But the fate of one caregiving proposal was unclear even before the partisan boycott: a bill to allow parent caregivers of severely disabled children to continue to be paid for their work. Advocates say the program, which began in the pandemic, has resulted in dramatically lower health care costs and a reduction in the number of hospitalizations. According to these parents, “Of families that participated in the parent caregiver program, 80% reported reduced hospitalizations, 73% reported reductions in calls to 911 or crisis intervention, and 82% reported extreme concern about the risks to their children's health since the program ended in May.” Parents rallied last week at the capital in an effort to call attention to what they say is truly an emergency, and in lieu of the bill, get support for a budgetary note to continue this funding. We're joined by Calli Ross, who cares for her 8-year-old son who manages severe disabilities.

The longest legislative walkout by Oregon Senate Republicans in state history had meant the death of any number of bills. Now that legislative leaders have reached a framework for a possible deal to bring lawmakers back to the capitol, some may have new life. But the fate of one caregiving proposal was unclear even before the partisan boycott: a bill to allow parent caregivers of severely disabled children to continue to be paid for their work. Advocates say the program, which began in the pandemic, has resulted in dramatically lower health care costs and a reduction in the number of hospitalizations.According to these parents, “Of families that participated in the parent caregiver program, 80% reported reduced hospitalizations, 73% reported reductions in calls to 911 or crisis intervention, and 82% reported extreme concern about the risks to their children's health since the program ended in May.”Parents rallied last week at the capital in an effort to call attention to what they say is truly an emergency, and in lieu of the bill, get support for a budgetary note to continue this funding. We're joined by Calli Ross, who cares for her 8-year-old son who manages severe disabilities.

Dad's Series: “The Additional Needs Blogfather Part 2” with Mark Arnold We continue our Dad series with author, speaker, advocate, ministry director and co founder Mark Arnold, also known as the Additional needs Blogfather.  Mark brings a wealth of knowledge and experience working with churches all over the UK.  He is also a dad of a son with Autism, so he understands the joys and challenges of a raising a child with special needs. Dads, after listening to this episode and Eric and Mark's conversation you will definitely walk away feeling seen and heard. Join in the conversation and connect with other Dads who get it at our upcoming Dad's Meet Up this Thursday and be watching for our annual Dad's Day Out event COMING in THIS SUMMER! Connect with Mark at: Episode Links and Resources: Mark Arnold is the author of The Additional Needs Blogfather blog.  You can follow his blog and reach out to him on his website at https://theadditionalneedsblogfather.com/ Mark Arnold (The Additional Needs Blogfather) is the Additional Needs Ministry Director for Urban Saints' pioneering additional needs ministry, including training, consultancy, conference speaking and resourcing: http://www.urbansaints.org/additionalneeds He is co-founder of the ‘Additional Needs Alliance', a learning and support community of almost three thousand organizations, children's & youth workers, parents and more who are passionate about inclusion and belonging in the UK and beyond: http://www.additionalneedsalliance.org.uk Mark is founder of ‘The Dads Fire Circle', a place for dads and dad figures for children, young people and young adults with additional needs to gather, share and support each other: http://www.thedadsfirecircle.com He is a ‘Churches for All' partner, a member of the ‘Council for Disabled Children' the ‘European Disability Network' and the ‘Living Fully Network', serves on the executive for ‘Children Matter!' and writes a monthly additional needs column for Premier Youth and Children's Work (YCW) magazine as well as being a writer/contributor for Firefly Community, Key Ministry, The Mighty, Different Dream, DAD.info, and BRF Parenting For Faith. Mark is the author of ‘How To Include Autistic Children And Young People In Church' creating a place of belonging and spiritual development for all: https://grovebooks.co.uk/products/y-65-how-to-include-autistic-children-and-young-people-in-church-creating-a-place-of-belonging-and-spiritual-development-for-all Mark is dad to James, a 19-year-old Autistic young man, who journeys with Epilepsy, Learning Difficulties and Anxiety.   Connect with Us: If you enjoy this podcast please share us with others and be sure to follow us so won't miss an episode.  We'd love to hear from you so please leave us a comment or rating and connect with us on social media or on our website. Website: hopeonthehardroad.org Instagram:https://www.instagram.com/hopeonthehardroad/ Facebook:https://www.facebook.com/hopeonthehardroad/ Facebook Group:https://www.facebook.com/groups/2621447987943459/?source_id=105530184205752 Free Youtube Resource Library https://www.youtube.com/playlist?list=PLsSAfvTkSy87X-fEqtVR2qvo7w9UQBuxz

BARRI COHEN is an award-winning writer, director and producer of documentary films. Among her awards and nominations are those for her feature doc, Toxic Trespass: Children's Health and the Environment (WGC winner), and the recently co-produced Phyllis Ellis film, Toxic Beauty – which garnered an International Emmy nomination and several CSA awards. Cohen's latest film, Unloved: Huronia's Forgotten Children, premiered at Hot Docs in 2022, won the 3rd prize Audience Award, a DGC Award, and has been nominated for four CSA awards.Read more about Barri and Unloved: Huronia's Forgotten Children here: https://variety.com/2022/film/global/barri-cohen-hot-docs-unloved-1235261842/ --As always, thanks so much for tuning into Breaking Brave! If you like the show, please subscribe, review, and/or send us your suggestions or questions via the platforms below! For more from Marilyn Barefoot or to get in touch with her directly, please connect via:Marilyn's website: https://marilynbarefoot.com/ LinkedIn: https://www.linkedin.com/in/marilynbarefootbigideas/ Twitter: @MarilynBarefoot Instagram: @marilynbarefoot ABOUT Marilyn Barefoot, the Host of Breaking Brave:Breaking Brave is Hosted by Marilyn Barefoot, one of the foremost business coaches & creative ideators in North America - Marilyn gets hired by several of the world's biggest brands, companies, and organizations (the NHL, McDonald's, Deloitte, Coca-Cola, MTV, Viacom, The CFL, Forbes Magazine; to name just a few) to help them get unstuck and generate big, creative ideas.It helps us so much to have your feedback which goes a really long way in helping us shape the future of Breaking Brave and host the guests you're most interested in hearing from! So if you have the time, please subscribe, review, and connect with Marilyn on social media or through her website! And as always, thanks so much for tuning in!

Dad's Series: “The Additional Needs Blogfather” with Mark Arnold We begin our Dad series with author, speaker, advocate, ministry director and co founder Mark Arnold, also known as the Additional needs Blogfather.  Mark brings a wealth of knowledge and experience working with churches all over the UK.  He is also a dad of a son with Autism, so he understands the joys and challenges of a raising a child with special needs. Dads, after listening to this episode and Eric and Mark's conversation you will definitely walk away feeling seen and heard. Join in the conversation and connect with other Dads who get it at our upcoming Dad's Meet Up this Thursday and be watching for our annual Dad's Day Out event COMING in THIS SUMMER! Connect with Mark at: Episode Links and Resources: Mark Arnold is the author of The Additional Needs Blogfather blog.  You can follow his blog and reach out to him on his website at https://theadditionalneedsblogfather.com/ Mark Arnold (The Additional Needs Blogfather) is the Additional Needs Ministry Director for Urban Saints' pioneering additional needs ministry, including training, consultancy, conference speaking and resourcing: http://www.urbansaints.org/additionalneeds He is co-founder of the ‘Additional Needs Alliance', a learning and support community of almost three thousand organizations, children's & youth workers, parents and more who are passionate about inclusion and belonging in the UK and beyond: http://www.additionalneedsalliance.org.uk Mark is founder of ‘The Dads Fire Circle', a place for dads and dad figures for children, young people and young adults with additional needs to gather, share and support each other: http://www.thedadsfirecircle.com He is a ‘Churches for All' partner, a member of the ‘Council for Disabled Children' the ‘European Disability Network' and the ‘Living Fully Network', serves on the executive for ‘Children Matter!' and writes a monthly additional needs column for Premier Youth and Children's Work (YCW) magazine as well as being a writer/contributor for Firefly Community, Key Ministry, The Mighty, Different Dream, DAD.info, and BRF Parenting For Faith. Mark is the author of ‘How To Include Autistic Children And Young People In Church' creating a place of belonging and spiritual development for all: https://grovebooks.co.uk/products/y-65-how-to-include-autistic-children-and-young-people-in-church-creating-a-place-of-belonging-and-spiritual-development-for-all Mark is dad to James, a 19-year-old Autistic young man, who journeys with Epilepsy, Learning Difficulties and Anxiety.   Connect with Us: If you enjoy this podcast please share us with others and be sure to follow us so won't miss an episode.  We'd love to hear from you so please leave us a comment or rating and connect with us on social media or on our website. Website: hopeonthehardroad.org Instagram:https://www.instagram.com/hopeonthehardroad/ Facebook:https://www.facebook.com/hopeonthehardroad/ Facebook Group:https://www.facebook.com/groups/2621447987943459/?source_id=105530184205752 Free Youtube Resource Library https://www.youtube.com/playlist?list=PLsSAfvTkSy87X-fEqtVR2qvo7w9UQBuxz

Chad discusses a shameful vote in Oklahoma against a ban of corporal punishment towards disabled children.in schools.

No matter how professional you are, EVEN home health care providers can be thrown off guard from time to time!THEY CAUGHT one of the kidnappers in Mexico responsible for the death of 2 Americans!WHY ARE PEOPLE GOING TO MEXICO! I'll tell you why!Most recent crime statistics released indicate ONCE AGAIN, Oklahoma Texas Arkansas and Louisiana is the most dangerous places to live in America!TEETH WHITENING CAN COST YOU YOUR NOSE!!!!!!!!!!!! True story!!!Kim Basinger bought a new nose! We saw it at the strip club baby shower!A 64 year old/29 year old RELATIONSHIP?THE PEOPLE OF OKLAHOMA SAID "NO" to question 820! Wish I knew why!

Scripture says we will be saved “if we believe in our heart and confess with our mouth that Jesus is Lord.” But what about those who cannot speak?

Special Needs Ministry Series: “The Additional Needs Blogfather” with Mark Arnold You guys are going to love today's episode from our Special Needs Ministry Series. Mark Arnold brings a wealth of knowledge and experience working with churches all over the UK.  He has a passion to see churches worldwide embrace the special needs community and develop programs to meet their needs.  Let's get started.   Episode Links and Resources: Mark Arnold is the author of The Additional Needs Blogfather blog.  You can follow his blog and reach out to him on his website at https://theadditionalneedsblogfather.com/ Mark Arnold (The Additional Needs Blogfather) is the Additional Needs Ministry Director for Urban Saints' pioneering additional needs ministry, including training, consultancy, conference speaking and resourcing: http://www.urbansaints.org/additionalneeds He is co-founder of the ‘Additional Needs Alliance', a learning and support community of almost three thousand organizations, children's & youth workers, parents and more who are passionate about inclusion and belonging in the UK and beyond: http://www.additionalneedsalliance.org.uk Mark is founder of ‘The Dads Fire Circle', a place for dads and dad figures for children, young people and young adults with additional needs to gather, share and support each other: http://www.thedadsfirecircle.com He is a ‘Churches for All' partner, a member of the ‘Council for Disabled Children' the ‘European Disability Network' and the ‘Living Fully Network', serves on the executive for ‘Children Matter!' and writes a monthly additional needs column for Premier Youth and Children's Work (YCW) magazine as well as being a writer/contributor for Firefly Community, Key Ministry, The Mighty, Different Dream, DAD.info, and BRF Parenting For Faith. Mark is the author of ‘How To Include Autistic Children And Young People In Church' creating a place of belonging and spiritual development for all: https://grovebooks.co.uk/products/y-65-how-to-include-autistic-children-and-young-people-in-church-creating-a-place-of-belonging-and-spiritual-development-for-all Mark is dad to James, a 19-year-old Autistic young man, who journeys with Epilepsy, Learning Difficulties and Anxiety.   Connect with Us: If you enjoy this podcast please share us with others and be sure to follow us so won't miss an episode.  We'd love to hear from you so please leave us a comment or rating and connect with us on social media or on our website. Website: https://hopeonthehardroad.org Instagram:https://www.instagram.com/hopeonthehardroad/ Facebook:https://www.facebook.com/hopeonthehardroad/ Facebook Group:https://www.facebook.com/groups/2621447987943459/?source_id=105530184205752 Free Youtube Resource Library https://www.youtube.com/playlist?list=PLsSAfvTkSy87X-fEqtVR2qvo7w9UQBuxz

Kay Morgan-Gurr was 14 years old when she decided to advocate for children with disabilities in the U.K. A few years later, Kay was diagnosed with a disability herself.“I could just see the church needed a big education when it came to disability.” Listen to her story in Part 4 of this 5-part podcast series, “More Than Our Abilities.”Visit Kay's blog and The Pondering Platypus resource pages. Follow Kay on Facebook, Instagram, and Twitter.You can connect with us through email at gps@billygraham.org or on Billy Graham Radio on Facebook.

When you have a child with a disability or other medical complexity, the holidays can feel like a minefield, as trauma triggers, anxiety, and grief for what we wish the holidays could have been for our families lurk around every corner. And on top of that, having to manage schedules, special diets, gift expectations, and uncomfortable commentary from friends and family can be emotionally and physically draining. The season often leaves parents of disabled children feeling left out, over-worked –and occasionally– like the celebrations might just be more trouble than they're worth. In today's episode, Amanda Griffith-Atkins and I discuss listener feedback and contributions about how complicated the holiday season feels for parents of disabled children, suggestions for how to make the holiday season feel just a little bit more manageable, and how adjusting our expectations has made a big difference for each of our families. Links: Listen to Amanda's previous episodes: Ep 81: Health Anxiety, Ep 85: On the “Disability Parent” Identity, & Ep: 99: Family Planning. Listen to Ep 20: Anticipatory Grief with Katie Peterson. Check out Ep 104: How to Support Parents of Disabled Children. Thank you to our listeners who sent in recordings: Heather, Maddison, and Lysa! Donate to the podcast via Buy Me a Coffee. Follow Amanda on Instagram. Follow me on Instagram. Follow the Facebook page. Join the Facebook group Parents of Children with Rare Conditions. Access the transcript on the website here. And if you love this podcast, please leave us a rating or review in your favorite podcast app!

Having a child with a disability or rare disease can be a lonely experience, often in ways that parents never anticipated. Their lives have changed dramatically and the relationships they used to rely on might feel suddenly distant. Family and friends may want to reach out, but they don't always know how to offer the support that is most helpful for parents. Their “encouraging” comments sometimes miss the mark and can cause even more heartache for the parents they are trying to help. Or, they might be so at a loss for how to offer support that they just stay away altogether. It's easy to find lists of things not to say and not to do for parents caring for children with rare diseases, but what about the ways that family and friends CAN offer support? In this solo episode, Madeline shares suggestions from listeners about the kind of support they want from those close to them as they care for their children with disabilities. Parents of children with medical complexities need —and want— their people to stay in their lives, and these tips can help strengthen these relationships. Links: Check out Annette Moreau's courses. Follow me on Instagram. Follow the Facebook page. Donate to the podcast via Buy Me a Coffee. A big, big thank you to everyone who contributed thoughts and suggestions to this episode: Kenya Davis @sunflowers_sea Catherine Hoffman @cathsheahoff Grace Bongiovanni @grace.bongiovanni Huang Hsin @becky812 Maddison Ward @maddisonjward Michel-Anne Bridges @mrs.mabridges Jenna @donotfeedwildlife Shannon Read @mrs_read_15 Jill Jones @jilllatimer294 @jenangarita Siobhan and Jamie @jamies_gdd_diary Victoria Shaver @vicgs Kate McGregor @kate_mcgregor_ Kate Rolfes @kate.rolfes Krystal Hatch @mrs_katch @linavilela Sarah Harris @sarah_harris_insta Katie Peterson @katiebpeterson Chloe @chloerose1127 Marci Dunning @freyasluckyarm Libby @libby.shidel Karissa Taylor @the_advocating_mom @jenangarita Hailey @Growing_juniper Rachael Carlucci @rachaelmcarlucci Julianna Morasse @howlinghive Kari Harbath @Kariandsloan Tricia @triciajeanb Ashley Garrison @ash.garrison