Podcasts about neonatal intensive care unit nicu

In this episode of All Things Conceivable, host Nazca Fontes shines a spotlight on the incredible work of NICU nurses—those dedicated professionals who provide life-saving care to the most vulnerable newborns. The Neonatal Intensive Care Unit (NICU) is a place of both immense challenge and profound hope, where nurses and doctors work tirelessly to give critically ill infants the best chance at survival.  This Nurse Appreciation Week, Nazca welcomes two extraordinary nurses, Tori Meskin and Tia Miller. Tori and Tia are co-founders of NICUity, a platform designed to empower NICU nurses by offering essential resources, fostering education, and building a strong, supportive community. Together, they are driving change and uplifting the nursing profession in remarkable ways. Join us as we dive into their journey, their mission, and the impact they are making every day. Love the episode? Learn more about NICUity and join the community that's revolutionizing neonatal care. To keep up with the good work that these women are doing, follow @ThatNurseTia  and @NurseTori on Instagram and @ThatNurseTia and @NurseTori on TikTok. To support the nurses in your life, learn more about ConceiveAbilities #EmpowerNursesChallenge. Interested in surrogacy? Learn more about becoming a surrogate with ConceiveAbilities!

Miracle Child is Wonderfully Made While sitting in the Neonatal Intensive Care Unit (NICU), observing her newborn son and other premature babies fighting bravely for their lives, Melissa Gallagher was struck by the powerful truth the “these little ones were wonderfully made,” her words an echo of Psalm 139. Melissa, who earned a degree in industrial and innovative design from Cedarville University, opens up about her own miracle child — Hudson — on the Cedarville Stories Podcast. Although there were challenging moments, Melissa and her family became cheerleaders for families dealing with the challenges of premature birth. She learned how to embrace every small victory. In watching the tiniest babies achieve milestones in their struggle to survive, Melissa discovered how to inspire and uplift others who faced similar challenges to those she and Hudson encountered. Just seeing Hudson get swaddled for the first time sparked a brilliant idea.  Drawing from her education in design and entrepreneurship, her talent in watercolor art, and firsthand experience as a mother of a premature baby, she brought forth a new business, Wonderfully Made. This company is dedicated to creating swaddles and clothing with tailored watercolor art for the most delicate and precious infants. Through this venture, her goal is to bring hope and encouragement through her personal story, shed light on the NICU journey, and spread optimism for life beyond the NICU.  Walk with Melissa through her experience and catch her infectious desire to encourage others as she tells her Cedarville Story. https://share.transistor.fm/s/6a06ad6bhttps://youtu.be/hUrnUUaLa0o

Emma Justice is a pediatric Speech Language Pathologist, Certified Lactation Counselor and guest speaker serving patients in the greater Boston area. She has worked in both inpatient and outpatient settings including the Neonatal Intensive Care Unit (NICU), pediatric rehab and most recently the public school system.  Emma is the owner of Justice For Infant Feeding Therapy and Lactation where she provides in home and Telehealth services. She also provides parent resources available for purchase and parent coaching . As a NICU graduate herself , Emma knows first hand what families experience leaving the NICU and wanted to assist in access to support and closing  that gap.  Emma has experience evaluating and treating infants born full term in need of support with breast and bottle feeding, as well as infants with complex medical histories.  Looking for more information?  Find us on social media, our website or email us directly!  IG: justice4infantfeeding  Justiceforinfants.com Emmaluj@justiceforinfants.com ____________________________ You can listen to this episode wherever you stream podcasts and at www.3cdigitalmedianetwork.com/telepractice-today-podcast    

While in the hospital, we always aim to keep mum and baby together, and your baby will routinely 'room in' with you. However, if your baby requires more extensive medical support after birth, they may need to be transferred to a Special Care Nursery/Baby Unit, or a Neonatal Intensive Care Unit (NICU). This can understandably be a very distressing situation for a new mum and family, and it is usually quite unexpected. This is where having a plan to support your breastfeeding journey becomes crucial.⁠In this episode I discuss:Common reasons why a mum and baby may be separated at birth and unable to breastfeed.Why nipple stimulation and frequent milk removal are key for building and maintaining supply. The importance of skin to skin with your baby.Hand expressing vs using an electric breast pump. How often to express to protect milk supply. When you book your Postnatal Midwifery Package with us you receive messaging support from your midwife between appointments, and whilst in hospital after your baby is born - this comes in super handy for navigating situations like this as you'll have your midwife cheering you on and supporting you every step of the way. If you're interested in learning more about our postnatal support head here! I would love to hear your thoughts, questions, and ideas for future episodes so please get in touch on instagram - my insta is @heldmidwifery or through my website www.heldmidwifery.com.au. Remember to subscribe so you don't miss any episodes, and if you're enjoying the podcast I would be ever so grateful if you could rate and review  on your favourite podcast player. Disclaimer: Remember as always the info provided in this podcast does not constitute medical, midwifery, psychological, childbirth, pre-natal or post-natal education or other professional medical advice, and is provided for general information and guidance purposes only. Hannah Willsmore will not be liable for any expenses, losses, damages (including indirect or consequential damages) or costs which might be incurred as a result of your reliance on this information, advice, content or materials. This release includes but is not limited to any claim for personal injury, damages and death of any individual which has received information from Hannah Willsmore. Further, Hannah Willsmore does not make any representations or give any warranties about their accuracy, reliability, completeness or suitability for any particular purpose. If you have any health concerns or questions you should speak with your midwife or doctor

Listen to the Empowering NICU Parents' Podcast as we dive into the emotional challenges of having a baby in the Neonatal Intensive Care Unit (NICU). This episode explores the profound feelings of guilt, anxiety, and trauma that NICU parents face, and emphasizes the importance of seeking support.You will learn practical self-care strategies, hear expert insights, and find comfort in knowing you're not alone. Whether you're still in the NICU or have transitioned home, this episode provides valuable resources and encouragement to help you navigate this difficult journey and prioritize your mental health. Subscribe now for support, guidance, and hope.Our NICU Roadmap: A Comprehensive NICU Journal: https://empoweringnicuparents.com/nicujournal/ NICU Mama Hats: https://empoweringnicuparents.com/hats/ NICU Milestone Cards: https://empoweringnicuparents.com/nicuproducts/ Newborn Holiday Cards: https://empoweringnicuparents.com/shop/ Primally Pure: https://empoweringnicuparents.com/primallypure Empowering NICU Parents Show Notes: https://empoweringnicuparents.com/shownotes/ Episode 60 Show Notes: https://empoweringnicuparents.com/episode60 Empowering NICU Parents Instagram: https://www.instagram.com/empoweringnicuparents/ Empowering NICU Parents FB Group: https://www.facebook.com/groups/empoweringnicuparents Pinterest Page: https://pin.it/36MJjmH

Martha Sharkey, founder and CEO of Today Is a Good Day, shares her experience in nonprofit leadership and the mission of her organization to provide support for families who have experienced the Neonatal Intensive Care Unit (NICU). She discusses the inspiration behind the organization's name and the importance of celebrating the good moments in the NICU journey. Martha also talks about the leadership communication lessons she has learned, including empowering her team members to take the lead and solve problems, and the challenge of asking for financial support. She reflects on missed opportunities and the importance of hiring additional staff to support the organization's growth. Martha shares her experiences with taking risks and making big decisions in her organization. She discusses the importance of acknowledging others who are going through difficult times and shares a personal challenge for listeners to reach out to someone in their network who may be struggling. Martha also talks about the skill of thinking on the spot and distilling information into soundbites for media interviews. Finally, Martha discusses the importance of acknowledging others and the power of a simple message of support.   In this episode you will learn: How Martha empowered team members to take the lead and solve problems. Why asking for financial support is essential for the sustainability of nonprofit organizations. How hiring additional staff can support the growth and expansion of an organization. Acknowledging others who are going through difficult times is important and can make a significant impact. Short, concise communication can be powerful and effective in various contexts. A simple message of support and acknowledgement can mean a lot to someone who is struggling. Mentioned in the Episode: “Turnover is Vanity, Profit is Sanity: 9 ½ Steps for Improving Your Profits and Cashflow” – Book by Dan Bradbury “Breeding Gazelles: Fast Growth Strategies for Your Business” – Book by Dan Bradbury About Martha: Martha Sharkey is the Founder & CEO of Today is a Good Day, a non-profit providing personal and financial support for families who experience the Neonatal Intensive Care Unit (NICU). Martha and her husband, Paul, founded Today is a Good Day in honor of their daughter, Claire, and in memory of their daughter, Mary. They welcomed their identical twin girls at just 23 weeks and 5 days on November 14, 2010. Mary was with them only two weeks before passing away. Claire beat incredible odds and came home after 103 days in the NICU at Jefferson Abington Hospital. Following their extended stay in the Neonatal Intensive Care Unit (NICU), the Sharkeys recognized a gap in care for parents and families navigating the NICU journey. They founded Today is a Good Day to fill that gap to support families. Martha has led the effort to advance the mission of Today is a Good Day expanding its reach to 29 hospitals and organizational partners in seven states over the past ten years. Programming for hospital partners includes care packages for families, Navigate the NICU Sessions with current families navigating the NICU journey, Vital Needs Support grant programs for families in need, a podcast, Advocacy resources, and an online community of support. In addition to programs within the hospitals, Today is a Good Day sends care packages upon request across the country and internationally. Prior to focusing fully on advancing the mission of Today is a Good Day, Martha served in several non-profit leadership roles, including Executive Director of the Chestnut Hill Business District and Assistant Director of Corporate Sponsorship for The Franklin Institute. She has received several awards for her non-profit work, including Parent of the Year by Main Line Parent Magazine and the Distinguished Community Service Award from the Glenside Inter-Service Clubs. You can connect with Martha in the following ways: Web: https://www.todayisagoodday.org/ Instagram: @nicutoday Facebook: https://www.facebook.com/nicutoday LinkedIn: https://www.linkedin.com/company/nicutoday/?viewAsMember=true You can connect with Dr. Laura Sicola in the following ways: LinkedIn: https://www.linkedin.com/in/drlaurasicola LinkedIn Business Page: https://www.linkedin.com/company/laurasicola-inc YouTube: https://www.youtube.com/@LauraSicolainc Facebook: Dr. Laura Sicola Twitter: @LauraSicola Instagram: @drlaurasicola Website: https://laurasicola.com Laura's Online Course: virtualinfluence.today See omnystudio.com/listener for privacy information.See omnystudio.com/listener for privacy information.

In this episode, Dr. Frankie Harrison shares her personal experience and professional insights into the often overlooked and challenging journey of parents whose babies require care in the Neonatal Intensive Care Unit (NICU). Dr. Harrison recounts her own journey of unexpectedly facing prematurity and NICU care, highlighting the initial confusion and lack of understanding she experienced. She reflects on the common struggles parents face, including guilt, grief, and traumatic memories, shedding light on the long-term impact of the NICU experience on parental mental health.Dr. Harrison emphasizes the need for greater awareness, education, and support for NICU parents, lamenting the current lack of preparation and resources available. She discusses the importance of addressing mental health needs and providing ongoing support beyond the immediate NICU discharge period. Dr. Harrison advocates for systemic changes in maternity care to better prepare and support parents facing NICU journeys, emphasizing the importance of early intervention and comprehensive support services.This is a must-listen episode for any soon-to-be or current parent of multiples who wants to be informed and learn how to deal with the challenges of a NICU stay. You can connect with Frankie here:Instagram: https://www.instagram.com/miraclemoonuk/Podcast:  https://open.spotify.com/show/4OdVSVmIGW5638zg3p9HqjWebsite: https://www.miraclemoon.co.uk/Thanks for listening! If you are a soon-to-be or current parent of multiples, be sure to head over to my website http://www.fiercekindmama.com to get my FREE resources designed specifically for you! Be sure to follow me on Instagram and Facebook too. Credits:Music from #Uppbeat (free for Creators!):https://uppbeat.io/t/aylex/with-youLicense code: YLMJTQCPKRANEOVB

Join us in this episode as we explore the world of pediatric feeding disorders in the Neonatal Intensive Care Unit (NICU) with Dr. Pamela Dodrill, a Pediatric Feeding Specialist. Together with her co-authors, Pamela developed a consensus definition and conceptual framework for pediatric feeding disorders and she was part of the FOIS-P team, the Functional … EP 29: Pediatric Feeding Disorders in the NICU with Pamela Dodrill Read More »

Hello, everyone! On the next episode of NOON, I'm thrilled to introduce you to Michelle, a retired RN who dedicated the majority of her career to the specialized fields of pediatrics and the Neonatal Intensive Care Unit (NICU). Now, in her well-deserved retirement, Michelle has taken on a new role as the host of the podcast "The Conversing Nurse." This unique podcast is a tribute to the nursing profession, featuring insightful interviews with various nurses and their supporting staff members. Join us for a delightful conversation as Michelle shares her wealth of experiences from the world of pediatrics and the NICU, and how her journey has led her to amplify the voices and stories of fellow nurses through "The Conversing Nurse" podcast. This episode promises to be an engaging exploration of the diverse narratives within the nursing community. Don't miss it! Don't forget to like, follow, and turn on notifications so that you don't miss this or any other episode of Nine One One Nonsense! Bonfire Merch Store (NOON20): https://www.bonfire.com/store/nine-one-one-nonsense/?utm_source=copy_link&utm_medium=store_page_share&utm_campaign=nine-one-one-nonsense&utm_content=default This episode is brought to you by: D.D Finder If you're looking for an amazing book to read, I have a great suggestion: 'Ready Left. Ready Right.' It's a medical thriller written by one of my good friends and favorite new authors, DD Finder. DD Finder believes in supporting first responders and their mental health so with every purchase of 'Ready Left. Ready Right.,' a portion of the proceeds goes to the nonprofits:  Debriefing The Front Lines Inc.: https://debriefingthefrontlinesinc.org 62 Romeo: https://62romeo.com @62_romeo_nonprofit and  The Overwatch Collective: Theoverwatchcollective.com DD finders website: ddfinder.com @ddfinder The book is available on Amazon:  https://www.amazon.com/Ready-Left-Right-D-D-Finder-ebook/dp/B0CJ8WF9Y7?nodl=1&dplnkId=c04cd6b9-6eae-40b7-b9e1-9a6f5db08f39 Don't forget to listen to our podcast interview with DD Finder: https://open.spotify.com/episode/4x1HNnntANZlWlRsZstl4W?si=uZR8QEABSD6Nz-BYrq5Nbw FB Page: https://m.facebook.com/groups/nineoneonenonsense/?ref=share Content Warning: This episode contains discussions about death, including graphic and potentially triggering details. Listener discretion is advised. The episode also covers sensitive topics and may not be suitable for all audiences. If you or someone you know is struggling with suicidal thoughts or mental health issues, please seek help immediately. You can contact the Suicide & Crisis Lifeline by dialing 988 from anywhere in the U.S.  --- Support this podcast: https://podcasters.spotify.com/pod/show/samspursuit/support

Today we chat to Amanda Banks who is the co-producer (with Eleanor Currie) of the new film, Born At Home. Amanda chats to us about why she wanted to create a film about homebirth, the benefits of acupuncture in pregnancy and her two homebirth experiences.  After having a straightforward birth at home with her first baby, her son was unresponsive and needed to be transferred to hospital. Her son was born with Oesophageal Atresia which meant he needed surgery and a 6 week stay in Neonatal Intensive Care Unit (NICU). After having two miscarriages, Amanda fell pregnant with her daughter and had a quick birth and a healing postpartum where she was able to be tucked into her own bed by her private midwives.  Links for Amanda:Website - https://www.amandabanksacupuncture.com/ Instagram - https://www.instagram.com/amandaacupuncture/Links to Born At Home film:Born at Home Website Trailer Instagram Where to buy ticketsOther:Why Not Home Film Dr Sarah BuckleyJess - Mothermoon Hypnobirthing 2LifeDoula- Moran Maet Pearson - It Takes a Village MidwiferySupport the show@homebirthstoriesaustralia Please be advised that this podcast may contain explicit language. Listener discretion is advised.The information, statistics, and research presented in this podcast are for informational purposes only and are not intended to constitute or replace medical or midwifery advice. All information discussed can be found online and is provided in the links in the show notes. It is always recommended to conduct your own research and make informed decisions. We advise you to discuss any topics or concerns with your healthcare provider. While we strive to incorporate the most up-to-date research in our episodes, we do not warrant or guarantee the accuracy of the information discussed on the show.

We have three guests we are featuring on this episode: Tyler Reidy, Teresa Ianni and Laura Hastings. Tyler shares his journey as a NICU music therapist and the ways his work impacts babies and families each day. Teresa tells us more about an amazing quality improvement project in the neonatal intensive unit of a hospital and what her vision is for the future of music therapy. Finally, Laura tells us more about her drive to create the nation-wide network of music therapists working in the NICU. Here is a little more about Tyler, Theresa and Laura: Tyler: A Certified Music Therapist (MTA) and Registered Psychotherapist (RP) living in Guelph, and working in Kitchener-Waterloo. He earned his Master of Music Therapy degree at Wilfrid Laurier University. He is one of the full-time medical music therapists at Grand River Hospital in Kitchener Ontario in the Children's program providing services to the Neonatal Intensive Care Unit (NICU), Inpatient Pediatrics Unit, and the Pediatric Oncology Group of Ontario (POGO) Satellite Clinic. Tyler also works as a Child and Family Therapist at Bloom: Child & Family Therapy in Kitchener . Tyler has further training in the First Sounds: Rhythm Breath and Lullaby NICU music therapy training and in Neurologic Music Therapy (NMT). Theresa: A Registered Psychotherapist (RP) and a Certified Music Therapist (MTA). She has a Master's degree in Music Therapy (MMT) and specialized training in Neurological Music Therapy (NMT) and NICU music therapy (Rhythm Breath Lullaby). Theresa has been working as a music therapist for over 13 years where she has had the opportunity to work with children and adults with developmental delays, neurological impairments and mental health disorders. Theresa currently works full-time at Sunnybrook Health Sciences Centre (Toronto) in Geriatric Care; Alzheimer's' Dementia and End of Life, and has recently completed a Quality Improvement project in the Sunnybrook NICU “Implementing a Music Therapy Program”. Theresa is also the owner and director of a music therapy private practice which supports children and young adults on the Autism Spectrum. Laura: Laura graduated from Capilano University in 2013 after completing her internship at BC Children's Hospital. After practicing for 4 years in Vancouver and the Lower Mainland, she went on to complete a Master's in music therapy at Concordia University in Montreal. There, she joined forces with Capilano graduate Alison Usher-Jones in her private practice working with individuals with autism. After 4 years in Montreal, she returned to the West Coast to work in a Neonatal Intensive Care Unit and in long-term care. Laura is excited to be in the new Board position of President Elect and to support BC music therapists.

We finally did it!  The story of the miracle micro-premie we call son.  Sage is a walking miracle and has impacted so many lives through his trials and tribulations of survival.  10% chance of survival, 10 major surgeries, countless other procedures, and over 7 month residency at Kaiser's Neonatal Intensive Care Unit (NICU).  We bonded with so many nurses, doctors, and other medical staff in the Downey NICU that we still revere every day of our lives.

Almost 1 in 5 babies spend time in the Special Care Nursery (SCN) or Neonatal Intensive Care Unit (NICU) in Australia. For the mothers of these babies, postpartum is very different to what they planned or hoped for and there's often a distinct grief that accompanies the stress of having an unwell or premature baby. We can encourage new mothers to organise meal trains and lie down at every opportunity but we also need to make space for those who are sitting for hours on end in hard hospital chairs, heart aching for their baby and juggling hospital and family life. See omnystudio.com/listener for privacy information.

In this episode, I speak with Rhiannon (an absolute supermum) who shares the inspiring story of her challenging pregnancy and an extremely difficult 76-day stay in the Newborn Services and Neonatal Intensive Care Unit (NICU). Both she and her loving partner show unwavering determination, boundless hope, and unbreakable strength throughout this experience. Throughout this episode we hear firsthand from Rhiannon about the initial moments of uncertainty, the rollercoaster of emotions, and the unexpected twists they encountered along the way. We gain insight into the medical professionals who became not just caregivers, but pillars of support and comfort during this tough period. Rhi shares milestones and breakthroughs that marked their progress, both for the gorgeous tiny fighter in the NICU and as parents themselves. This episode is a reminder that even in the darkest of times, the light of resilience can shine through. Ollie is an incredibly lucky baby to have Rhi as his Mum and Adam as his Dad.

Dean Weaver, EPC Stated Clerk, welcomes Jennifer Prechter, EPC Teaching Elder who serves as a palliative care chaplain at Arnold Palmer Hospital for Children and in the Neonatal Intensive Care Unit (NICU) at Winnie Palmer Hospital for Women and Babies in Orlando, Fla. The two discuss her journey to hospital chaplaincy, and how her ministry provides opportunity for addressing deep questions of life with unchurched people across a wide spectrum of life experience. Prechter also discusses how “longing and lament” can help people process tragedies such as a child with a terminal illness, or the May 24, 2022, shooting at Robb Elementary School in Uvalde, Texas.

In this episode, we are joined by Shan (she/her), a first-time parent to an 18-month-old daughter named Winter, alongside her husband Brad. Before becoming a parent, Shan was working as a beauty therapist and since, she's recently started her career as a sleep consultant. During Shan's pregnancy, her waters broke prematurely at 30 weeks gestation, resulting in a condition known as preterm premature rupture of membranes (PPROM). She later discovered she had Chorioamnionitis, an infection in her placenta caused by the early rupture of the amniotic sac without receiving timely treatment. This led to her body rejecting the placenta and her baby. As her contractions were too advanced, Shan could not have the epidural she had planned for. She was quickly moved to the birth suite, where she gave birth to Winter after just around 8 minutes of pushing. Following the birth, Shan went into septic shock, a condition she only learned about afterward. After birth, Winter was taken to the Neonatal Intensive Care Unit (NICU) due to her delicate condition, covered in tubes and wires. For Shan, not being able to interact with Winter was particularly challenging. She was advised not to stroke her to avoid causing harm. Over the following weeks, Shan and Brad visited Winter in the NICU and Special Care. Adjusting to parenthood was challenging for Shan, who struggled to connect with her baby due to the rapid and unexpected series of events. After bringing Winter home, Shan faced further difficulties with sleep and feeding, leading her to switch to formula after four weeks of feeding Winter her expressed colostrum and milk through a tube. At four months old, Winter experienced breathing difficulties and was diagnosed with a cow's milk protein allergy. Despite the challenges of the first year, Winter's health has improved, and she is now walking and reaching milestones appropriate for her adjusted age. Shan expresses gratitude for the support of nearby family members, which allowed her and Brad some valuable alone time. She also acknowledges that their unique journey into parenthood has brought her and Brad closer together, improving their relationship in profoundly positive ways. Follow our instagram ⁠⁠⁠⁠⁠⁠⁠⁠⁠@definitelybabypodcast⁠⁠⁠⁠⁠⁠⁠⁠ ⁠for photos of weekly guests and episode updates and releases. The Definitely Baby theme music was written by Hagan Mathews and produced at ⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠@sleeplessfootscray⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠. The photo is the podcast logo was taken by @maki.levine. This episode was recorded on the lands of the Wurundjeri Wilam and Boon Wurrung/Bunurong peoples of the Kulin Nation. This always was and always will be the land of the First Nations peoples. Every month, I Pay The Rent and so can you - click ⁠⁠⁠⁠⁠⁠⁠⁠⁠here ⁠⁠⁠⁠⁠⁠⁠⁠⁠to learn more.

Having a baby in the Neonatal Intensive Care Unit (NICU) comes with a wide range of emotions and experiences that can be challenging for new parents to navigate. And many feel like they're facing this challenge alone.   The founders of NICU Nook, Dr. Stephanie Simon and Amanda Neilan, are working to change that!   This episode is filled with encouragement and support with expert advice and practical strategies to help you and your baby thrive. You'll learn strategies for navigating the NICU and cultivating a secure attachment bond that will endure beyond the hospital walls.     I want to hear from you! Send me a topic you want me to cover or a question you want answered on the show!   ✨ DM me on Instagram at @securelyattachedpodcast or @drsarahbren ✨ Send an email to sarah@drsarahbren.com ✨ And check out drsarahbren.com for more parenting resources 

Welcome to the second part of Georgia's story. Georgia (she/her) and her husband, Matt, are parents to triplets Finn, Marlo, and Jude.  In this episode, Georgia shares her experience with her triplets' early days and the rest of their journey in the Neonatal Intensive Care Unit (NICU) and Special Care Nursery (SCU). For five days, the triplets remained in the NICU, which coincided with the isolation length for Georgia's positive Covid-19 status. Subsequently, they were moved to the SCU, where they stayed for a total of 32 days, with 27 days specifically spent in the SCU. Georgia expresses the indescribable feeling of leaving her babies in the hospital while going home. On day 3, her emotions overwhelmed her, and coupled with the hormonal changes, she found herself in tears as she departed the hospital. The unnatural sensation of separation from her babies left her yearning to have them home with her. To ease the transition, Georgia and her partner, Matt, stayed at Georgia's parents's house for two weeks, where they received valuable support. During this time, her parents took care of household chores, cooking, and provided assistance, which proved essential during this period. Contrary to the idyllic portrayal of the "Fourth Trimester" and the "baby bubble" on social media, Georgia's early postpartum experience involved frequent visits to the hospital, instead of rest and relaxation. Reading about these idealised experiences contrasted greatly with her own reality. However, after the 32-day hospital stay, Georgia and Matt finally brought their babies home and began to experience the cherished and serene "baby bubble" they had longed for. Despite being born prematurely at 31 weeks and 4 days, the triplets thrived and remained remarkably healthy, exceeding Georgia's expectations. The process of introducing breastfeeding was calm and gradual due to the premature birth and the babies' underdeveloped suck and swallow reflex. Georgia allowed each baby to spend time on her chest, encouraging their curiosity around breastfeeding by sniffing, licking, and suckling at her breast. Upon returning home, Georgia adopted tandem feeding and began supplementing with bottles, combining half breast milk and half formula. Two of the babies, Finn and Marlo, have naturally weaned themselves from breastfeeding, while Jude is still feeding at night now. Matt played a crucial role in supporting Georgia, taking four months off work to assist with feeding. As he returned to work, Georgia adjusted her feeding routine, utilising bottles during the day and exclusively breastfeeding overnight. Throughout their journey, Georgia and Matt maintained a positive attitude and are grateful for their overall experience. Georgia takes pride in being a mother to her delightful triplets, thoroughly enjoying their interactions with one another. Follow our instagram ⁠⁠⁠⁠⁠⁠@definitelybabypodcast⁠⁠⁠⁠⁠ ⁠for photos of weekly guests and episode updates and releases. The Definitely Baby theme music was written by Hagan Mathews and produced at ⁠⁠⁠⁠⁠⁠⁠⁠@sleeplessfootscray⁠⁠⁠⁠⁠⁠⁠⁠. This episode was recorded on the lands of Wurundjeri Wilam and Boon Wurrung/Bunurong peoples of the Kulin Nation. This always was and always will be the land of the First Nations peoples. Every month, I Pay The Rent and so can you - click ⁠⁠⁠⁠⁠⁠⁠here ⁠⁠⁠⁠⁠⁠⁠to learn more.

In part two this story, Kyla and I talk about life in the Neonatal Intensive Care Unit (NICU) (her experience) and Pediatric Intensive Care Unit PICU (my experience). Kyla says that that time felt like "forever and the same day, over and over"  and I can't think of a better way to say it. Her baby boy, Conner, is now 6 months old and greets each new day with the a gummy smile and shining eyes. Life isn't all rainbows and butterflies, but Kyla and her family know what true gratitude feels like, deep down in their bones.   LIFTS online resource guide: https://hmhb-lifts.org  Specific services relevant to this episode (found on LIFTS.org)Statewide Support Groups Search " early intervention services" on LIFTS online resource guide: https://hmhb-lifts.org Search "counselors" on LIFTS online resource guide: https://hmhb-lifts.org Hand to Hold - NICU Babies, Parent Support (website) Hand to Hold (podcast)For statewide resources please visit the Linking Infants and Families to Supports athttps://hmhb-lifts.org/

In this podcast, we talk with our special guest Michele Derheim about her personal experience of work-life balance and overcoming the feeling of guilt as a healthcare leader. Michele is a Clinical Nurse Director for the Pediatric Intensive Care Unit (PICU), Pediatric Rapid Response Team, and Pediatric Dialysis Unit at the University of Michigan's Mott Children's Hospital. She started working in a Neonatal Intensive Care Unit (NICU) directly out of nursing school and transitioned to the adult ICU. As a bedside nurse, Michele acted in charge nurse and staff educator roles, as well as teaching clinical groups of nursing students in their critical care rotations. In this episode, Michele shares some important lessons about resilience, boundaries, and life priorities from her first formal leadership role. She also shares how she applies the ‘Professional Life and Personal Life Polarity Map®' as a tool to create and sustain dynamic balance in her life. We also talk about how healthcare leaders struggle with feeling guilty for not being able to do more for their staff or being home more for their families and give some personal advice on overcoming the feeling of guilt. For full show notes and links, visit: https://www.missinglogic.com/new-podcast If you found value in this episode, please subscribe and leave us a review on Apple Podcasts! SOCIAL MEDIA LINKS: https://www.linkedin.com/company/missinglogic-llc https://www.facebook.com/missinglogicLLC https://twitter.com/MissingLogicLLC https://www.instagram.com/missinglogic_llc/

"I cannot put to words how that felt being a nurse and not being able to help; there's a level of helplessness when you're taking care of a baby who is dying, but it is even worse when you can't impact their experience in a positive and healthy way. All of those experiences together sparked Walk with You." We are proud to be joined by the founder and president of Walk with You, Kylie Collins. This episode tells the story of Kylie's work within a Neonatal Intensive Care Unit (NICU) and how this experience shaped Walk with You's creation. Walk with You is an organization dedicated to walking with families as they experience the loss of a child from pre-birth through 18+ years of age.

Sharan Widsten, founder of BiblioTake talks to Sara and Marshall about raising money for funding initiatives in the Neonatal Intensive Care Unit (NICU) at Grand River Hospital, and health care appreciation. Find us HERE  

Being a new parent is far from easy: there are so many things to worry about, so many challenges, and things can sometimes spiral out of control. Breastfeeding, postpartum for new moms, preventing infant falls, and so much more are all worries that come with being a new parent. The market is flooded with products that claim to solve these issues and concerns but in reality, you can never be certain that you've chosen the right solution. In response to some of these worries there is a product for new parents, both mom and dad, and it's simply brilliant. The guests on today's episode, Hayley Mullins and Sarah-Almaza Cox, are the co-founders of Joeyband. Joeyband is a baby sling made of yoga pant material clinically proven and designed for prolonged skin-to-skin care in all new born care settings- something every baby needs and deserves. Joeyband™ is the only product in the market that can be used directly on the Operating Room (O.R.) table during repair, Neonatal Intensive Care Unit (NICU) and Labor & Delivery (L&D) unit. This product has been around for a long time, and the impact it has had on babies is simply incredible. Stay tuned to find out more about Joeyband and the ways it can help mothers, fathers and babies connect even more. You can subscribe or listen to previous episodes of the Busine$$ of the V podcast by clicking here. TOPICS COVERED: Meet Hayley Mullins, the inventor of Joeyband and Sarah-Almaza Cox, the co-founder of the company that makes Joeyband. Joeyband is a product designed for skin-to-skin infant fall prevention and breastfeeding support, as we learn from Hayley. Infant falls are far more common than we realize, and the goal of Joeyband is to prevent these falls while keeping the baby safely attached to the parent. As soon as the girls launched their website, people became interested and they realized they were onto something big in the healthcare space. Since Joeyband is a non-sterile product, Dr. Dweck wonders whether it can be used immediately on the operating table, or only after the delivery. As Sarah explains, it is especially important to place the baby on mom after a C-section, and this is where Joeyband can make things better. Another question by Dr. Dweck focuses on the difficulties that can arise when babies sleep in the same bed as their parents, and Hayley states that they do not recommend co-sleeping with Joeyband unless you are being observed. Rachel steers the discussion in a new direction: where do they stand in terms of product development, manufacturing, and distribution? Joeyband is used in many hospitals across North America, and they have collected lots of interesting data on topics such as increased breastfeeding, reduced falls, improved patient satisfaction, and so on. Sarah adds that they are based in Canada and that everything is made within North America, which they are very proud of. As Rachel wants to know who pays for the product and where does money changes hands, Sarah explains that hospitals are currently covering the costs, but their goal is to have insurance cover it entirely. Can men use Joeyband? Hayley explains that during the first day of baby's life dads should have 30 minutes of uninterrupted skin-to-skin contact. Sarah also emphasizes that, apart from dads, Joeyband can also be used by physically disabled parents. Joeyband is made of yoga pant material because many new moms wear yoga pants all the time, and the material is soft, stretchy and breathable. While she was practicing obstetrics, Dr. Dweck used to see many anxious postpartum mothers, and one of their most common fears was dropping the baby. The Joeyband team is fully supported and surrounded by medical professionals who help them adjust the product and adhere to clinical guidelines. When it comes to educating parents, each product comes with instructions and tips for using Joeyband. For those interested in the product, there is a website that they can visit and gather all the necessary information. As for the funding, the Joeyband team decided not to take external funding in order to maintain greater control over their business. HOT FLASH: Newborns are dropped in hospitals during delivery much more commonly than reported. It seems that reports from the UK show there is a drop rate of 50 babies per day during delivery.   QUOTES: “Where the product really came from was one of those horrific parenting moments that nobody thinks they're going to have.” (Hayley) “We don't recommend co-sleeping with it unless there's somebody there to observe you.” (Hayley) “It's a brilliant idea, and obviously your initial response was from the kind of people that you'd want to see it from, and it sounds like there's clinical support.” (Rachel) “One of the things that I love is that it's manufactured directly in Canada. The quality of the product is high, we're bringing jobs, and locally our environmental footprint is low.” (Sarah) “The question that's burning me right now is whether mean wear this because, you know, skin-to-skin is skin-to-skin whether that's slightly hairier skin or not so much.” (Dr. Dweck) “Thirty minutes of uninterrupted skin-to-skin with dad that first day of baby's life actually rewires his brain to bond with the baby.” (Hayley) “Because of the simplicity in the design that Hayley invented, it's perfect for parents who may have a physical disability as well.” (Sarah) “I remember trying to make sure that my baby would live in between pediatrician appointments for my first kid. That was my goal, to keep them alive week after week because you really don't know what you're doing.” (Rachel) “We made a conscious decision not to take external funding just because we would be able to be in control of our business a little bit more.” (Sarah) “Babies held skin-to-skin cry twelve times less than babies that are not skin-to-skin” (Hayley) FURTHER RESOURCES: Joeyband www.joeyband.com Hayley @Linkedin Sarah @Linkedin  LINKS FOR BUSINE$$ OF THE V: Website: www.businessofthev.com Twitter : @businessofthev Instagram : @businessofthev Subscribe to our Youtube channel : Business of the V - YouTube Dr. Alyssa Dweck: https://drdweck.com Rachel Braun Scherl: Home - Rachel Braun Scherl

New mom Sindhu Monica of Coimbatore, Tamil Nadu, has donated the equivalent of more than 40 litres of breast milk to help newborns through Neonatal Intensive Care Unit (NICU) of the Coimbatore Government Hospital. This is an interview with her. - கோவையை சேர்ந்த 29 வயது சிந்து மோனிகா 7 மாதங்களில் 1400 குழந்தைகளுக்கு உணவளிக்க 42 லிட்டர் தாய்ப்பாலை நன்கொடையாக அளித்துள்ளார். அவரது உயிர்காக்கும் முன்முயற்சிக்காக, அவர் Asian book of records மற்றும் Indian book of records ஆல் அங்கீகரிக்கப்பட்டுள்ளார். அவருடனான சந்திப்பு இது.

No matter how beautiful, long, short or difficult your birth experience is, nothing compares to  the agony of your brand new baby being whisked out of your arms and admitted to the Neonatal Intensive Care Unit (NICU) or Special Care Nursery (SPC). Mothers in this position often experience less autonomy and authority over the decision-making and informed consent process than they did in their own birth experiences.  Today, we share the individual stories of three women whose babies ended up in the NICU or SPC with one common thread: Informed consent was insufficient or lacking altogether, interventions were performed without permission, and timely diagnoses for their babies were neglected. Meet Cameron, whose home birth plans were derailed when she went into labor spontaneously at 34 weeks; Nicole,  a mother of five and birth doula whose baby was grossly misdiagnosed until a year of age; and Erin, a mother of three who successfully insisted on breast-feeding in the NICU and followed her instincts to fight for her baby to get an early release from an unnecessarily prolonged stay in the NICU. Each mother shares her story and her battle to feed, hold, comfort and mother her baby within the confines of NICU and SCN procedures and policies. And even though these three moms never met, they each came to the same individual conclusion when it comes to the advice they have for all parents: Know your rights, your breastfeeding expectations and your values, and use your instinct to defend all three relentlessly through your NICU experience.**********Connect with us on Patreon for our exclusive content.Email Contact@DownToBirthShow.comInstagram @downtobirthshowCall us at 802-GET-DOWN Work with Cynthia: 203-952-7299 HypnoBirthingCT.com Work with Trisha: 734-649-6294 Please remember we don't provide medical advice. Speak to your licensed medical provider for all your healthcare matters.

Jared Milrad chats with award-winning animator and director Lauren Aboulafia about her autobiographical short film, SUPER SCAR, which tells the story of a new mom's unexpected struggle to stay sane amidst the madness of the Neonatal Intensive Care Unit (NICU).  Lauren opens up about her traumatic childbirth experience and her approach to creating SUPER SCAR, why it's important for women to share their childbirth stories, and how we can create more transparent, authentic, and inclusive spaces for underrepresented storytellers. We depend on your generous support of Rewriting Hollywood to empower new creative voices and share urgently important stories with the world. Make a tax-deductible donation today: movikarma.org/donate

Guest: Denise Minyard, MS, CCC-SLP, Speech Language Pathologist There are approximately 15,000,000 premature births globally every year. With this statistic, an infant's stay at the Neonatal Intensive Care Unit (NICU) is not uncommon.  Having experience working in NICUs, Denise Minyard, a speech language pathologist at DotCom Therapy, reveals the unseen world of preemies. From therapies, developmental delays, transitions from hospital to home, and the aftercare support parents must have for themselves and their babies - this conversation is sure to open your eyes on how a NICU stay affects development later in life. So stay tuned, and get ready to walk with us as we take this journey into understanding the struggles and the long term effects of NICU stays on families, and most importantly, how to be their support system. Episode Highlights: Denise shares some experiences working in the NICU How NICU stay affects parents and child Struggles and therapies premature babies face in the NICU Differences between premature and full term births Aftercare precautions after getting out of NICU Importance of a support group and where to find them Connect with Denise: LinkedIn | @ denise-minyard Resources Mentioned During This Episode: DotCom Therapy Connect with Wolf+Friends Website | wolfandfriends.com Download the App | Apple Download the App | Google Instagram | @wolfandfriends.community

Emily and Morgan created KC Infant Feeding with one purpose in mind. Balance. Their paths first crossed in the Neonatal Intensive Care Unit (NICU) supporting babies who struggled with feeding. With their skill sets and knowledge they provided parents and caregivers with information and techniques to help dissipate feeding difficulties. However, it wasn't until they both experienced feeding struggles with their own newborns that they realized how essential the inclusion of family mental health considerations are in the development of feeding plans. This balanced approach ensures long term success and thriving infants. They now approach families they support with compassion, knowledge, and empowerment that comes from years of experience working with infants and personal moments of struggle, hope, and success. In this week's episode, we discuss the lasting effects of parenting in isolation during the 2020 quarantine, evidence-based practices for feeding interventions, how support people can care for your loved ones through their feeding journeys, and why, with feeding as with many things in life, we fear what we don't know. We also encourage y'all to stay OFF Dr. Google! In a new segment I like to call, "Meg gets free professional advice from her podcast guests," we discuss helping children eat who are showing picky behaviors, as well as discussing weaning a baby who will fight you if you come between her and breastfeeding, remembering it's okay to set boundaries, because this is your body you're sharing with your little one. Find Emily and Morgan! Website: https://kcinfantfeeding.com/ Instagram: https://www.instagram.com/kcinfantfeeding/ Contact: https://kcinfantfeeding.com/contact/ Thanks so much for joining me for this episode of, Let's Discuss… with Meg Duke. I'd love for you to write a review of my podcast on your app, and don't forget to subscribe so you get a notification when new content is posted. Take a moment to leave a 5-star rating, too! You can also support this podcast by purchasing a monthly subscription at the amount of your choosing at https://anchor.fm/letsdiscusswithmeg/support. Follow me at @TherapyByMeg on Instagram and find Meg Duke LCSW-S on Facebook. You can also look for Let's Discuss… content by searching the hashtag, #LetsDiscussWithMeg. Let's Discuss… with Meg Duke is executive produced by David Presley and produced by Meg Duke. Our theme song was written and performed by Antwone McDuffie.

LaResa Janousek, NNP, neonatal nurse practitioner at St. Luke's Neonatal Intensive Care Unit (NICU) in Boise delivers a didactic presentation on Neonatal Opioid Withdrawal Syndrome (NOWS).

The birth of a baby is a wonderful, yet very complex process. There are many physical and emotional changes that occur for both the mother and the baby. Alena Smith tells her story to the ladies this week of how she and her husband were blessed with two miracles that unfortunately arrived prematurely and experienced staying in the Neonatal Intensive Care Unit (NICU) 6 years apart.

Videos: 1. Stefan Oelrich, head of Bayer's Admits COVID-19 Vaccine is Gene Therapy (0:40) 2. Munk Debate on Ukraine – John Mearsheimer Closing Statement (3:06) 3. Jonathan Pie: ‘Boris Johnson Is a Liar' | NYT Opinion (7:42) 4.  “Uniquely Stupid:” Dissecting the Past Decade of American Life | Amanpour and Company (18:09) 5. New Rule: The United States of Dumb-merica | Real Time with Bill Maher (HBO) (10:00) 6. You're Not Going To Believe What I'm About To Tell You – The Oatmeal (7:53) Researchers investigate cancer-fighing properties of mango Texas A&M University In addition to being one of the most important tropical fruits consumed worldwide, recent studies by researchers at the Institute for Obesity Research and Program Evaluation at Texas A&M University in College Station have shown that mangoes also may help prevent breast cancer. Talcott and others recently completed one in vitro study and one using mice to see if the polyphenols found in mango did, in fact, exhibit inflammation- and cancer-fighting properties. “There was already some research done showing that polyphenolic compounds, such as those found in the mango, have cancer-fighting properties,” Talcott said. “Those compounds appear to have antioxidant properties that may contribute to decrease oxidative stress, which can lead to the onset of chronic diseases such as cancer. In addition to that, polyphenolics have been shown to be anti-inflammatory.” Talcott said interest in mango has been increasing in recent years and experimental data has already shown bioactive compounds present in mangoes exert anti-inflammatory, anti-carcinogenic, antiviral and antibacterial properties.  “Based on this premise, we extracted mango polyphenols and tested their effects in vitro, or separate from their normal biological context, on commercially obtained non-cancer and cancer breast cells,” she said. These results of the study indicate that the cell-killing effects of mango polyphenols are specific to cancer cells, where inflammation was reduced in both cancer and non-cancer cells, seemingly through the involvement of miRNA-21 – short microRNA molecules associated with cancer,” Talcott said. A second study by this research group using hairless mice showed mango polyphenols also suppressed cell proliferation in the breast cancer BT474 cell line and tumor growth in mice with human breast carcinoma cells transplanted into them. (Next) Ginseng can treat and prevent influenza and RSV, researcher finds Georgia State University Ginseng can help treat and prevent influenza and respiratory syncytial virus (RSV), a respiratory virus that infects the lungs and breathing passages, according to research findings by a scientist in Georgia State University's new Institute for Biomedical Sciences. In a recent issue of Nutrients and an upcoming publication of the International Journal of Molecular Medicine, Sang-Moo Kang reports the beneficial effects of ginseng, a well-known herbal medicine, on human health. He partnered with a university and research institutes in South Korea that wanted international collaborative projects to study if ginseng can be used to improve health and protect against disease because of the potential benefit in fighting these viruses. There are no vaccines available for RSV, which affects millions and is the leading cause of inflammatory bronchiolitis pneumonia and viral death in infants and in some elderly adults. In his study published in Nutrients, Kang investigated whether red ginseng extract has preventive effects on influenza A virus infection. He found that red ginseng extract improves the survival of human lung epithelial cells infected with influenza virus. Also, treatment with red ginseng extract reduced the expression of genes that cause inflammation. (Next) New study illustrates that potato protein ingestion strongly increases muscle protein synthesis rates at rest and during recovery from exercise Maastricht University, The Netherlands Exercise enthusiasts have long presumed animal protein to be superior to plant-derived options for muscle protein synthesis due to its essential amino acid profile. While many plant proteins are deficient in one or more essential amino acids necessary for optimal muscle growth and repair, a new randomized controlled study published in Medicine & Science in Sports & Exercise shows that plant-derived proteins can still induce strong anabolic responses. Researchers at Maastricht University, The Netherlands, found that consuming 30 grams of potato-derived protein concentrate following resistance exercise strongly increased muscle protein synthesis rates to levels that did not differ from the response following the ingestion of an equivalent amount of milk protein concentrate. In general, plant-derived proteins are considered to have lesser anabolic properties, due to their lower digestibility and incomplete amino acid profile. The results show that ingestion of 30 g potato-derived protein will support muscle growth and repair at rest and during recovery from exercise.” (Next) Antipsychotic medication during pregnancy does affect babies Monash University (Australia)  A seven-year study of women who take antipsychotic medication while pregnant, proves it can affect babies. The observational study, published in the journal PLOS ONE, reveals that whilst most women gave birth to healthy babies, the use of mood stabilisers or higher doses of antipsychotics during pregnancy increased the need for special care after birth with 43 per cent of babies placed in a Special Care Nursery (SCN) or a Neonatal Intensive Care Unit (NICU), almost three times the national rate in Australia. As well as an increased likelihood of the need for intensive care, the world-first study shows antipsychotic drugs affects babies in other ways; 18 per cent were born prematurely, 37 per cent showed signs of respiratory distress and 15 per cent developed withdrawal symptoms.

Dean Weaver, EPC Stated Clerk, welcomes Jennifer Prechter, EPC Teaching Elder who serves as a palliative care chaplain at Arnold Palmer Hospital for Children and in the Neonatal Intensive Care Unit (NICU) at Winnie Palmer Hospital for Women and Babies in Orlando, Florida. The two discuss Prechter's journey to hospital chaplaincy, and how her ministry provides opportunity for addressing deep questions of life with unchurched people across a wide spectrum of life experience. Prechter also discusses how “longing and lament” can help people process tragedies such as a child with a terminal illness, or the May 24 shooting at Robb Elementary School in Uvalde, Texas.

God is with us during our dark seasons, but does He prepare us for them too? Mom of 3 and founder of Praying Through ministries, Jessika Sanders shares how her obedience to God's calling prepared her for one of the greatest battles in her life when her newborn son had to immediately be admitted to the Neonatal Intensive Care Unit (NICU) after birth. She also talks about the intense spiritual warfare she faced when she felt the pull of the devil to end her life and how God saved her from that moment. Through these difficult seasons, God led her to start a ministry that is blessing families all around the world who are walking through NICU and PICU seasons as well as child loss. Jessika's story will show you:- God doesn't just step in during our dark seasons… He goes ahead and prepares us for them too- He can turn bad things for good beyond what we can ever imagine- Our purpose can be found through obedience and surrender -----Connect with Jessika and find ways to support Praying Through ministries on their website, Facebook, and Instagram. Episode mentioned: - The Self-destructive Lies We Tell Ourselves- Easter Tribute (Who is God Starts at 7:30)Enjoying the show? Rate us on Apple, Spotify or Momsgrabcoffee.com.Follow our Facebook page: https://facebook.com/MomsGrabCoffeeSupport the Moms Grab Coffee Podcast

Babies born prematurely or with illness can receive specialized care in an Neonatal Intensive Care Unit (NICU) or Neonatal Intermediate Care Nursery (IMC). Hear as we dive in to what it means when a newborn baby has to stay in the NICU. 

For this week's episode on The Balanced Parent Podcast, we are going to talk about a topic that is a little bit different from what we have tackled before and is quite personal in my own parenting journey. Many of you know that while I was pregnant with my second daughter I got into a car accident that started me down a path that eventually lead me away from academia and into my work with you all. But something I rarely talk about is my first daughter's traumatic birth that resulted in a Neonatal Intensive Care stay. During both of these incredibly difficult moments, I had to dig deep to figure out how to support myself and how to be fully present with my family. I struggled with my self-worth, knowing what was right, and feeling like I was constantly failing. During both of these incredibly difficult moments, I had to dig deep to figure out how to support myself and how to be fully present with my family. ​ It wasn't easy and at the time I felt incredibly alone. ​ ​I am speaking more about this experience TODAY in this online retreat, I'd love to have you join me!​ I know now that my emotions and experience in response to these stressful situations were incredibly common and understandable and that I'm definitely not alone. And while you maybe haven't had these exact experiences or had a medically complex child, I know that there have likely been times, especially over these past two years, where things have felt very heavy and hard. And that's what I want to support you with in this week's episode with my guest Tanisha Burke-Wormley. She is a NICU mom of a medically complex child who supports moms all over the world as they move through the space of having to stay in Neonatal Intensive Care Unit (NICU) with their child. Her son, Jaleel, is a NICU and Kidney Warrior who she helps conquer Chronic Kidney Stage 5 everyday as a Stay-at-home Medical Mom. She also has a healthy daughter, Jameela, that she gave birth to at home in October 2020 during the Covid pandemic. To get more support, follow Tanisha on social media and join her Facebook community. She is a grad student and donates much of her time to these causes, so supporting her by giving her a follow or spreading the word to moms you know who need support is hugely appreciated! ​ Instagram: @medicalmomsofnicu​ Facebook Page: www.facebook.com/MedicalMomsofNICU​ Facebook Group: Medical Moms of NICU Group​Find more show notes here: www.laurafroyen.com/podcast

Dr. John Pardalos is the Chief of the Neonatal Intensive Care Unit (NICU).

A Note from Hope Katz Gibbs, creator, Inkandescent PR + Publishing Co. — I am thrilled to host an Inkandescent interview on Sunday, Jan. 16 with authors Stephen Gilliland, a professor at Claremont Graduate University, and his brother Jim Gilliland. They have a big goal, a giant job, and a determination to keep the premise of their new book simple. "We promise to each other to do at least one exercise activity every day. It doesn't matter if you are sick, traveling, or tired. And to keep each other honest, we share one pic doing our activity every day," the authors and brothers share on their book website: pushingupbook.com. The dynamic duo embarked upon a journey of crazy workout challenges that increased in intensity as the year progressed; 10,000 push-ups each in March became 30,000 push-ups by December. Authors Stephen Gilliland and Jim GillilandAt the time, they were each searching for something more – more from their relationship as brothers and more from their middle-aged bodies. And as each month passed, they discovered the unexpected gift of what it means to live more fully as connected brothers, fathers, husbands, and successful leaders. I am excited to share their story with you and invite us to join them in the journey. "We hope you  uncover scars you didn't know you had, grow muscles and inner strength, and find authentic support in connecting more deeply with someone else," Stephen says, about the tome which will take you on an inner journey of life through lessons on: Taking the "I will" commitment and achieving audacious goals. Asking for help and finding a genuine connection. Recognizing limits and preparing to fail. Embracing "should be fine" as a mantra against doubt. Practicing empathy and reaching out in times of loss. Here's to Pushing Up! Click here to learn more about the book. Scroll down to check out the introduction. From Pushing Up! Introduction by Stephen Gilliland and Jim Gilliland It was out of the blue, but it was not. We had just spent the holidays together; my daughter and her husband recently moved to Vancouver, where Jim and our parents live, and we all had a big family Christmas. Jim gave me a book for Christmas – Living with a SEAL: 31 Days Training with the Toughest Man on the Planet. In this book, Jesse Itzler describes a month of physical punishment that resulted from having a Navy SEAL live with him and train him daily. The journey defies typical workout wisdom by eschewing "recovery days" and pushing each day harder than the last. Itzler was in decent shape at the start of the month. By the end, he was running with a 50-pound vest and completed 1,000 push-ups in a day. Some of the workouts he described seemed insane. But he pushed through the insanity for physical and mental gain. I saw Jim reading this book shortly after he bought it. He finished it in a couple of days. He gave it to me and asked me to read it right away. JG: Have you finished the book? SG: Just a chapter. I am reading it to Cindi. JG: Okay, once you are done, I have a New Year's resolution workout proposal for you. That filled me with fear. What would he be proposing? Would I be able to handle it? I was in good shape for 51 but not great. My wife expressed her concerns. "You're not going to do any of those crazy Navy SEAL things with Jim, are you?" But I was also excited. Workouts had become boring. Runs had become shorter. And I was five pounds heavier than I had been in my late 40s. When I think about it, the workouts and physical challenges were not as big a concern for me as the commitment. Could I commit to a greater focus on working out? I don't want the exercise to run my life. I have always been the opposite of a weekend warrior when it comes to workouts: I am pretty good during the week but usually take weekends off. It's a break from work and working out, a break from schedules. I don't take commitments lightly, and this was going to be a big one. But it wasn't just about the workouts and commitment. Part of my excitement was the growing connection with my brother. Jim is seven years younger than me, and as kids, it was almost like we grew up separately. Our older brother, Brian, is fewer than two years older than me, and he and I were inseparable growing up. We tried to include Jim, but he was so much younger. When I was 18, I moved 500 miles from central British Columbia to Edmonton, Alberta, to go to university. Jim was ten going on 11 at the time. Or maybe it was ten going on 16. He had always seemed older and wiser than his age. Many people I have talked to have found that, as adults, they grew more distant from the siblings they were close to growing up, but Jim and I have been the opposite. Two separate childhoods: For Jim, it was almost like being an only child. But in adulthood, we developed a strong bond even when contacts were infrequent. When I went through a divorce from my first wife in graduate school, Jim was the family member who flew out to spend time with me, making sure I was okay. He was 17 at the time and a freshman in college. But we could also go for four or six months without ever contacting each other. We lived separate lives with a strong bond between us. So, another thought that crossed my mind when Jim presented me with the idea of a challenge was excitement over the prospect of more regular contact with one of the smartest and kindest people I know. Jim's Turn Growing up, it almost seemed that I had four parents. My brother Brian was nine years older and moved out of the house when he was 16. My brother Stephen was seven years older and left home when he graduated high school. My Dad was working in Vancouver, so it was just my Mom, and having Stephen gone left the house very empty. His trips home during the holidays were an intense time where I could tell him everything that had been bottled up since his last visit. Also intense was my dread near the end of his visit with the knowledge that he would be leaving back to school soon. Since that time, the intermittent intensity would describe our relationship. Flying to East Lansing to help him through his divorce. The occasional visit to Tucson to see our niece and nephew grow up. A meaningful connection, always there in the background but intermittent. A relationship I didn't fully appreciate until that phone call in the hospital. My wife Jenny was only 30 weeks pregnant and was recovering from the surgery of an emergency C-section. Our twins, a 2.5-pound daughter, and a 3.5-pound son were both very sick in the Neonatal Intensive Care Unit (NICU). I remember that feeling of complete shock and helplessness. My only thought was, "I need my brother, and I need him now." "Stephen, Jenny's been in an accident. I need you; I need you so bad." "Jim, where are you?" "John Muir Hospital, Stephen, please get here. I can't do this. I can't." "Just hang on; I'm on my way. I will get the next flight. I will be there. Just hang in there." I counted the hours until he arrived and did everything I could just to hold it together. In the years that passed since that day, we sustained a strong bond—a deeper connection from his supporting me at a time in my life when I needed it most. But again, as time passed, our contact became more occasional. As I approached the New Year and the inevitable emptiness of his latest departure after the holidays, my thoughts turned to resolutions. I wanted to find a way to increase the interaction from a distance. I wanted to create something important together. This relationship was too important not to make a priority. We hope that by sharing our journey, we can entertain, provoke, and perhaps even inspire. This is not a book about getting in shape. Truth be told, after all the workouts, I still carry that extra five pounds. Instead, this is a book about a powerful journey for two brothers and the lessons for life that were uncovered on that journey. About the Authors Stephen Gilliland (pictured left): Dr. Stephen Gilliland is a University Professor at Claremont Graduate University where he teaches organizational psychology and is responsible for developing executive education and leadership development programs. Stephen is originally from British Columbia and studied psychology at the University of Alberta and Michigan State University. For 24 years, Stephen was a professor of management at the University of Arizona, where he served in a variety of leadership roles. His research examines the fairness of leadership practices. Through this merging of psychological, social, and managerial issues, he has authored over 50 journal articles and book chapters. He has published eight books in the series Research in Social Issues in Management. He is a Fellow in the Society for Industrial and Organizational Psychology and received the Early Career Award from the same organization. Stephen has taught numerous courses on leadership, organizational behavior, healthcare, social entrepreneurship, human resource management, and leadership ethics. He has consulted with small and large organizations and conducted leadership training for companies around the world. He has served on the boards of several organizations. Stephen is married to Professor Cindi Gilliland and lives in Southern California. They share a wide variety of hobbies, including surfing, gardening, winemaking, and playing music. They spend time traveling to see their two adult children who always find interesting places to live. Author Jim Gilliland (pictured above, right) — Jim is President and CEO of Leith Wheeler Investment Counsel, one of Canada's largest fully employee-owned investment management firms.  He brought extensive investment experience in Canadian and U.S. investment markets through his time at HSBC Asset Management/M.K. Wong & Associates in Vancouver and Barclays Global Investors (BGI) in San Francisco. Among his achievements were building out and managing a team of professionals covering interest rate strategies, corporate credit, securitized credit, and emerging markets; launching and managing a successfully fixed income hedge fund; developing platforms to manage risk; and developing customized client solutions and liability-driven solutions. Jim is a graduate of the University of British Columbia (B.Comm with honors). After his work at HSBC, Jim earned his Master's degree in Financial Engineering at the University of California, Berkeley.  Jim lives on a horse farm with his family in the Fraser Valley of British Columbia and volunteers his time at a variety of educational and professional not for profits.

Many hospitals have a dedicated social worker on staff to support NICU families. How do you access the social worker? What questions should you ask as a new parent in the NICU? We are speaking on today's episode with Shannon Davis and Leah Heyel from Nemours/Alfred I. duPont Hospital for Children. Shannon received her Bachelors in Social Work from West Chester University and Masters in Clinical Social Work from Widener University. She also has her License in Clinical Social Work. Shannon has just been accepted through Postpartum Support International to take her Perinatal Mental Health Certification. She began her career working for the Chester County Children, Youth, and Services agency. During that time, she also worked part time at Crozer Chester Medical Center as an on call social worker for Traumas and weekends in Maternity and the NICU. She later joined the team in the Psych Med Surgery Unit. Shannon currently works in the NICU at Nemours. She is excited to continue her education in Perinatal Mood and Anxiety disorders to further provide support for families in the NICU and Advanced Delivery Program (ADP). Leah Heyel is a Licensed Clinical Social Worker for Nemours A.I. duPont Hospital for Children. Since 2018, she has provided support for patients and families in the Neonatal Intensive Care Unit (NICU) and the Advanced Delivery Program (ADP). Leah joined Nemours initially supporting the tracheostomy/ventilator and general pediatric patient populations after receiving her Master of Social Work degree from Delaware State University in 2015. Dedicated to helping NICU & ADP families, Leah has recently focused on expanding her understanding around perinatal mood and anxiety disorders with plans to complete her Perinatal Mental Health Certification later this year. Prior to Nemours, Leah worked six years in the Addiction field as an outpatient Level 1 substance abuse counselor for adults and adolescents. On this episode you will hear: - Shannon and Leah discuss their work and share insights into how social workers can help you. - You'll hear about why the role of a social worker can be confusing for families not knowing how they can help and who can access that help. - We'll discuss what families, like yours, should know about the role of a social worker. - What you should ask a social worker in your hospital. - The most common question families ask social workers, like Shannon and Leah. - You'll hear about how social workers can help families, like yours, fill out paperwork for social security benefits, secondary insurance, etc. - You will find out how often you can speak with a social worker at your hospital. - We discuss some of the resources you, as parents, can have access to through your social worker during your NICU stays. - Many times parents feel at fault for why their baby ended up in the NICU especially if they arrive prematurely, you will hear how social workers help families through those feelings. - You will get Shannon and Leah's biggest pieces of advice for families when meeting with a social worker. Please subscribe to the TODAY is a Good Day Podcast, wherever you enjoy your podcasts, or on our YouTube channel. This episode was produced and directed by Tony Lopes, of SoftStix Productions LLC (www.softstixproductions.com), in collaboration with co-producer and director of photography Michael Leary, of One Fifteen Films LLC (www.onefifteenfilms.com), and editor David DeLizza. Copyright 2020 to 2022, SoftStix Productions LLC.

"Highly sensitive people need a little bit more time to adjust to changes and new experiences because we are processing so much information at any given time." - Anna King In this episode of Moonwise, we speak with clinical social worker and perinatal mental health specialist Anna King about parenting as a highly sensitive person. We talk about the characteristics of this evolutionary trait and some of the gifts and challenges that it presents. Anna shares tips for dealing with overstimulation and how to support HSPs so that they can thrive in parenthood. She also shares her unique insights about why HSPs are at a higher risk for postpartum depression and anxiety and some of systemic and cultural barriers for understanding this trait within communities of color. We also talk about: HSPs and altered states of consciousness Inequity in maternal mental health The myth of the “strong black woman” Expanding our concept about what it means to be a parent Anna King, LCSW, PMH-C, (she/her) is a licensed clinical social worker and certified perinatal mental health specialist who uses an integrative, trauma-informed approach in her work grounded in reproductive and transformative justice. Anna serves as Clinical Training Specialist at Maternal Mental Health NOW, where she curates training events and curriculum and facilitates live and pre-recorded training to educate providers on perinatal mood and anxiety disorders (PMADs). Prior to joining the MMH-NOW team, she served as a full-time social worker in the emergency department and eventually found her home when she transitioned to serving a birth center and the Neonatal Intensive Care Unit (NICU). Throughout her experiences, Anna has realized the significant barriers to care for birthing people, especially for Black, Indigenous and people of color (BIPOC), and queer, trans, and gender diverse individuals and families. Her work centers on the embodied liberation of marginalized groups in reproductive spaces. She is also currently a part-time psychotherapist with ARC Counseling and Wellness and a third-year Ph.D. student in the Integral and Transpersonal Psychology program at the California Institute of Integral Studies (CIIS). Her research interests include spiritual activism, the highly sensitive person (HSP) trait, birth and postpartum tradition, and the transition to parenthood as a rite of passage. Links: Maternal Mental Health NOW ARC Counseling and Wellness The Highly Sensitive Parent Rooted pregnancy journal —> Leave us a written review on Apple Podcasts, and get a shout out on the show! --- Send in a voice message: https://anchor.fm/moonwise/message

1 in 10 infants in the United States will spend time in the Neonatal Intensive Care Unit (NICU) each year. NICU admissions and NICU staff save countless lives a year but the experiences can be traumatic, emotional, exhausting, and yes, even inspiring and hopeful. Join us as we welcome NICU veteran mom Patrice Guzman as she shares her honest and brave story and that of her miracle daughter Vivianne. Patrice shares what she has learned, tips for other NICU parents, and what she wishes NICU professionals and pediatric therapists understood from a parents' unique perspective. Most importantly, Patrice shares the tools she has found helpful for self care so that she can ensure well being and health for herself and her daughter. We hope this conversation will be supportive, healing, and hopeful for anyone anticipating or experiencing a NICU stay or for those who have spent time or work with NICU babies. 

SERIES 4 | EPISODE 1: Neonatal Palliative Care - Treatment ApproachGUEST: Nikki Berza RN, MN-NP Program Student (NP-Peds in a few months!) This episode explores myths and misconceptions surrounding palliative care in the NICU, defining palliative and end-of-life care terms, and highlighting the importance language plays in difficult discussions surrounding the death of a neonate. Nikki discusses her personal experiences with end-of-life care in the NICU setting; focusing on empathy, compassion, and the importance of integrating palliative care into neonatology. Nikki Berza is a Registered Nurse in the Neonatal Intensive Care Unit (NICU) at McMaster Children's Hospital and a Pediatric Nurse Practitioner (NP) student at the University of Toronto. She had the privilege of completing her first NP placement with the Quality of Life and Advanced Care Team (QoLA Care) at McMaster Children's Hospital and has found a passion for palliative and end-of-life care, especially in her work and role in the NICU. She has accepted an NP position at the NICU following her masters education and is looking forward to integrating the philosophies learned through QoLA Care in advocating for infants and families at the end-of-life.   

The ladies of the Scrub Caps and Sippy Cups podcast are joined by fellow CRNA mom, Alex Pudwill as she shares her son’s journey with congenital Cytomegalovirus (CMV). Her son Sam was suspected to have been exposed to CMV in the third trimester of pregnancy. Alex explains the signs and symptoms of CMV at birth and how she and Sam’s medical providers came to realize he had congenital CMV. Alex shares her struggles with mom guilt and how their family focuses on Sam’s milestones to keep them going. Alex is here to spread awareness about congenital CMV and help prevent this from occurring.  There are two groups of people that are most at risk for contracting CMV, immunocompromised individuals and unborn babies. Alex and Sam’s medical providers did not have any reason to suspect Sam had CMV in utero. He was growing fine and there was not a cause for concern during prenatal exams. She was shocked when she first saw him and he was covered in petechiae and had a blueberry muffin rash. Sam was sent to the Neonatal Intensive Care Unit (NICU) where he was cared for in the coming days.  Alex shares the struggles ahead for Sam and what it is like to have a child with CMV. From making the decision to have Sam receive cochlear implants to a brain bleed that will cause long-term issues and how she and her family overcame these obstacles.  Laci asks if there is any treatment for moms in the event that they are found to be positive for CMV while pregnant. Alex explains that there are antivirals available, but the treatments are experimental at this time. Ellen discusses the concerns from a perspective of being pregnant and not knowing what she could come in contact with and if that would have an effect on her baby. For many parents, this is currently a COVID concern. What effects does this have on the baby?  Alex gives tips on how moms can help decrease their chances of getting CMV while pregnant and shares some statistics with our listeners.   “91% of women are unaware of congenital CMV. 1:200 children are born with CMV each year and 1:10 of those are born with a disability.” Alex wants to get the message out about congenital CMV and what we can do as moms and healthcare professionals to prevent this virus from spreading. Please share this episode with a friend who could benefit from this information!  Alex Pudwill is a CRNA mom from Sioux Falls, SD. Her son, Sam, was born with congenital CMV. Ever since then, she has been trying to educate as many moms and soon-to-be moms as possible to prevent this very preventable disease. You can follow Alex Pudwill @aapudwill on Instagram and on Facebook at https://www.facebook.com/alex.hughes.1238 Let's connect! Follow the girls on Instagram - @mslacilea @ellenlauletta @stl_injector Email: scrubcapsandsippycups@gmail.com Or you can leave us an audio message that could air on a future podcast episode! https://www.speakpipe.com/Scrubcapsandsippycups Facebook: Scrub Caps and Sippy Cups Instagram: @heysmartmommas Twitter: @heysmartmommas

Welcome back! On this week's episode of #MDTribe we have Dr. Kathryn Winn, Board Certified Neonatologist at Winnie Palmer Hospital in Orlando, Florida. Dr. Winn is an attending at the largest Neonatal Intensive Care Unit (NICU) in the nation and shares her experience on how she became a neonatologist, as well as the challenges and rewards that come with this career. She graduated from the University of Florida with her Bachelor's and continued her medical education at Florida State University College of Medicine. She graduated with the Class of 2013, where she also met her husband Dr. Patrick Gill, Board Certified Internal Medicine Physician. Dr. Winn couples matched with her husband for residency and shares her amazing road trip experience for interview season! Dr. Winn tells us about her day to day activities as a neonatologist and the complexities that have been added with the COVID-19 pandemic. She explains the difference between the NICU and Pediatric Intensive Care Unit (PICU) and what ultimately called her to serve the babies in the NICU! Despite caring for the sickest and tiniest of babies, she absolutely loves her career and has learned how to navigate between breaking difficult news and celebrating miracles! She hopes that by sharing her journey she can inspire others to pursue their dream careers in medicine! Are you inspired or what? Listen to this week's episode for some much needed inspiration! Leave a review to support #MDTRIBE! & Subscribe for new episodes every week! Full Episode on Youtube: https://youtu.be/V-Tq_PCXeHA --- Support this podcast: https://anchor.fm/nataliacorreamdtribe/support

  An extended cut of our episode with Logan Hussein. Logan Hussein had a complicated arrival on November 26, 2008 at the Queensway Carleton Hospital. He was born with a collapsed lung and was immediately taken to CHEO’s Neonatal Intensive Care Unit (NICU) in a specialized incubator. Logan remained in the NICU for nine days. From the day Sue and Wael Hussein took Logan home from the NICU, they knew their lives would never be the same. Filled with gratitude on their son’s recovery, they wanted to find a way to give back to CHEO, help save the lives of other children and give families hope. Logan’s ultimate goal is to raise $200,000 for a Neonatal Transport Incubator. Logan is the youngest recipient of the CHEO Foundation’s ORDER of the GOOD BEAR. He also participates each year in the CHEO Telethon and his family participates in CN Cycle for CHEO. At the 2019 AFP Ottawa Philanthropy Awards, Logan was awarded the Youth Philanthropy Award.  

Logan Hussein had a complicated arrival on November 26, 2008 at the Queensway Carleton Hospital. He was born with a collapsed lung and was immediately taken to CHEO’s Neonatal Intensive Care Unit (NICU) in a specialized incubator. Logan remained in the NICU for nine days. From the day Sue and Wael Hussein took Logan home from the NICU, they knew their lives would never be the same. Filled with gratitude on their son’s recovery, they wanted to find a way to give back to CHEO, help save the lives of other children and give families hope. Logan’s ultimate goal is to raise $200,000 for a Neonatal Transport Incubator. Logan is the youngest recipient of the CHEO Foundation’s ORDER of the GOOD BEAR. He also participates each year in the CHEO Telethon and his family participates in CN Cycle for CHEO. At the 2019 AFP Ottawa Philanthropy Awards, Logan was awarded the Youth Philanthropy Award.

Nakiea has two very unique stories. Her Daughter was born at 23 weeks gestation, while her Son was a planned c-section at 38 weeks. They have two very different experiences. No Parent wants to experience the NICU twice. NICU Parents just want to bring their Babies home. However, their life is shared with the Neonatal Intensive Care Unit (NICU). Moms, Dads, Siblings & Families from around the World can identify with her story. Take a listen to the Founder of NICU Stories very own NICU Story. 

Welcome back to another episode of the ACN Podcast. In today's episode I speak with an incredible clinician and academic, Dr Rosemarie Boland. Rose has extensive experience in the Neonatal Intensive Care Unit (NICU) at the Royal Children's Hospital; has been an educator for the Paediatric Infant Perinatal Emergency Retrieval (PIPER) service for over 20 years; is an experienced academic; midwife and business owner. There are so many golden pieces of advice in this episode from the career of an incredible clinician.

WOW. That is what we have to say about this week’s episode. Elana Meyers Taylor embodies Mum’s the Word and did not hesitate to get into the tough conversations about balancing motherhood and being a US team athlete. In a sport like bobsled where a lot of the training and competing focusses on explosive power, we heard about how Elana, under the coaching of her husband Nicholas Taylor (also a USA bobsled athlete) adapted her training to monitoring her heart rate and keeping her power lifts capped below maximum. Morning sickness sometimes reared its ugly head during training runs so they adapted the program to fit with what Elana was capable of that day. This powerhouse of an athlete was instrumental with the recent rule changes for female USA Olympic athletes maternity stipend payments and insurance coverage through pregnancy and one year post pregnancy. This is a momentous step in the right direction in the fight for equality between male and female elite athletes.  Ever the competitor, Elana and Nic never went into birth expecting complications and planned for a totally natural birth to match their natural lifestyle of organic food, gluten and dairy free diet, limited medications...a self confessed “crunchy”. After 48 hrs of labor and hours in the 2nd stage (the pushing stage) the couple and medical team made a game time decision to proceed with an emergency C-section.  Having experienced her baby spending time in the Neonatal Intensive Care Unit (NICU), Elana expressed how these was some of the hardest moments of her life and the impact it’s had on her. Elana also explained the impact that the Covid-19 pandemic has had on her competition schedule which Sarah could relate to in sailing.  If you are loving the show so far please go and subscribe where you get your podcast and leave us an apple podcast review. Follow along the Mum’s the Word team and breaking news about upcoming guests on our social medic channels Instagram and Facebook @wispsportsmumtheword, and onTwitter @spmums. Hosts: Sarah Newberry Moore & Pam Relph Jones Podcast length: 45 mins Subscribe to WiSP Sports or WiSP Sports Mum's the Word on your podcast app. For more information, links and resources plus conversations from the world of women’s sport including articles, blogs, videos and podcasts visit wispsports.com. WiSP Sports is the World’s First and Only Podcast Network for Women’s Sport with more than 60 hosts, 1300+ episodes across 50 shows and over 7 million plays and downloads. WiSP Sports is on all major podcast players. Follow WiSP Sports on social media @WiSPsports. Contact us at info@wispsports.com.

WOW. That is what we have to say about this week’s episode. Elana Meyers Taylor embodies Mum’s the Word and did not hesitate to get into the tough conversations about balancing motherhood and being a US team athlete. In a sport like bobsled where a lot of the training and competing focusses on explosive power, we heard about how Elana, under the coaching of her husband Nicholas Taylor (also a USA bobsled athlete) adapted her training to monitoring her heart rate and keeping her power lifts capped below maximum. Morning sickness sometimes reared its ugly head during training runs so they adapted the program to fit with what Elana was capable of that day.This powerhouse of an athlete was instrumental with the recent rule changes for female USA Olympic athletes maternity stipend payments and insurance coverage through pregnancy and one year post pregnancy. This is a momentous step in the right direction in the fight for equality between male and female elite athletes.Ever the competitor, Elana and Nic never went into birth expecting complications and planned for a totally natural birth to match their natural lifestyle of organic food, gluten and dairy free diet, limited medications...a self confessed “crunchy”. After 48 hrs of labor and hours in the 2nd stage (the pushing stage) the couple and medical team made a game time decision to proceed with an emergency C-section.Having experienced her baby spending time in the Neonatal Intensive Care Unit (NICU), Elana expressed how these was some of the hardest moments of her life and the impact it’s had on her. Elana also explained the impact that the Covid-19 pandemic has had on her competition schedule which Sarah could relate to in sailing.If you are loving the show so far please go and subscribe where you get your podcast and leave us an apple podcast review. Follow along the Mum’s the Word team and breaking news about upcoming guests on our social medic channels Instagram and Facebook @wispsportsmumtheword, and onTwitter @spmums.Hosts: Sarah Newberry Moore & Pam Relph JonesPodcast length: 45 minsFor more information, links and resources plus conversations from the world of women’s sport including articles, blogs, videos and podcasts visit wispsports.com. WiSP Sports is the World’s First and Only Podcast Network for Women’s Sport with more than 60 hosts, 1300+ episodes across 50 shows and over 7 million plays and downloads. WiSP Sports is on all major podcast players. Follow WiSP Sports on social media @WiSPsports. Contact us at info@wispsports.com.

Today I have the privilege of airing the interview that I did with André and Kayleon Elliott about their experience with the Neonatal Intensive Care Unit (NICU). September is NICU awareness month and the Elliott’s story is a great one to share during this time. André and Kayleon live just outside of Charlotte, North Caroline with their little girl, Ariah. They both have a background in Ministry and Kayleon is the founder of By Grace Not Perfection. In today’s show, André and Kayleon share their story about having their baby prematurely and spending her first 45 days of her life in the NICU. The goal of our conversation is to bring awareness and advocate for NICU parents. Lets jump into the interview: In this episode we discuss: Kayleon shares about Ariah’s birth storyThe Elliott’s experience in the NICU How they got into NICU advocacyKayleon has created:NICU Keepsake JournalNICU Moms PlannerHow to get in touch with André and Kayleon: Two Hosts are Better website: https://www.twohostsarebetter.com/Two Hosts are Better podcast: https://www.twohostsarebetter.com/podcastInstagram: https://www.instagram.com/twohostsarebetter/https://www.instagram.com/bgnpllc/Facebook: https://www.facebook.com/bgnpllcThank you so much for listening to the show today. This conversation was particularly impactful for me because my middle sister, Lauren, was born prematurely and with a complication that required surgery and a month long stay in the NICU. I was only 4 years old when she was born, but I remember it being a very scary and stressful time for my family. I’m so glad that the Elliotts are doing the work that they are for NICU advocacy. If you are interested in doing more or finding out more, I would encourage you to check out their resources listed above, as well as March of Dimes.org. Thank you for listening to the show today!Support the show (https://www.patreon.com/findingyourvillagepod?fan_landing=true)

Instagram @persichetti.triplets Lauren and Vincent share their story on the triplets being at the the Neonatal Intensive Care Unit (NICU). --- This episode is sponsored by · Anchor: The easiest way to make a podcast. https://anchor.fm/app

In today's News: Preemie babies saved in Louisiana Thousands of people from Lake Charles, La, were forced to evacuate as Hurricane Laura approached from the Gulf of Mexico last week. The powerful Category 4 hurricane threatened 150 mph winds and catastrophic storm surges, causing nearly one-million people to flee from Texas and Louisiana, with the Lake Charles area ultimately the hardest hit. Yet a small group of brave people remained behind to care for babies who weren’t able to leave. Nineteen babies remained in the Neonatal Intensive Care Unit (NICU) at Lake Charles Memorial Hospital, and a team of 14 nurses, two neonatal nurse practitioners, three respiratory therapists, and one doctor stayed behind to make sure they stayed safe. Some of the babies weighed as little as one pound, others relied on ventilators, feeding tubes, and respirators, and some were born premature as early as 23 weeks. The team slept in shifts when they could to make sure someone was always caring for the babies. The babies had been moved from the women’s hospital to the main hospital in advance of the storm, as the main building had a generator and was built to withstand hurricane-force winds. California churches fight to stay open As California officials continue threatening residents for exercising their First Amendment right to religious assembly, one Christian pastor is standing up to offer to pay any legal penalties for those who worship in defiance of state mandates. Democrat Gov. Gavin Newsom has banned indoor religious services, along with various types of secular gatherings, in 29 counties representing 80 percent of the state’s population, in the name of containing the spread of covid-19. Numerous churches have defied the order, including Grace Community Church of Sun Valley, Cornerstone Church of Fresno, Destiny Christian Church of Rocklin and Harvest Rock Church of Pasadena. Last week, Pastor Ché Ahn Of Harvest Rock Church announced that he would pay for any tickets given to those who choose to attend in person despite the order, Pasadena Now reported. Local officials have threatened Ahn with fines, jail time, or worse for his civil disobedience. Another pro-abortion group accused of racism The National Organization for Women (NOW) appears to be the latest pro-abortion group accused of racism at the highest levels of leadership. Abortion giant Planned Parenthood has dealt with numerous accusations of racism in recent weeks, as has NARAL Pro-Choice America. NOW, founded in 1966 by feminist icon Betty Friedan, fractured after two pro-abortion men, Lawrence Lader qnd Bernard Nathanson, convinced Friedan to add abortion rights to the organization’s platform. Lader maintained that in order for abortion to be legalized, the eugenic agenda must be hidden from the public, and “women… and some blacks” must be kept “out front” once recruited to the cause. Recently, The Daily Beast reporter Emily Shugerman conducted interviews with nearly a dozen members and employees of now who claim that women of color were being “heckled, silenced, or openly disparaged at now meetings and offices.” As a result, 26 of 35 now state chapters signed a letter demanding the resignation of NOW’s president, Toni Van Pelt.

The Neonatal Intensive Care Unit (NICU) is not a place any parent anticipates meeting and caring for their newborn. But when they do, they find it a place where science, technology, tiny humans and strong emotion meet head-on. And as COVID-19 spread across the globe, it added another layer of planning and anxiety for pregnant people anticipating how different their pregnancy could turn out should they or their newborn test positive for the virus. In this episode, we hear from Nicole Lincoln MSN, RN, FNP-BC, CCNS about her work on NICI, a radical reimagining of the infant incubator. What started as an idea to create a low-cost, portable, and single-use incubator for our smallest and most fragile citizens, morphed into new concepts about how the incubator could be used in new ways, new places, and solve new problems.  For additional resources, visit our website at www.seeyounowpodcast.com  Contact us at hello@seeyounowpodcast.com 

Gracielle cries in this episode when speaking to amazing parents Jessica and Mathew when Mom Jessica water breaks at 14 weeks. They talk about their experiences with Preterm Premature Rupture of the Membranes (PPROM) and the Neonatal Intensive Care Unit (NICU). Jessica and Mathew give some words of wisdom who also maybe going through a similar journey. --- Send in a voice message: https://podcasters.spotify.com/pod/show/miraclebaby/message Support this podcast: https://podcasters.spotify.com/pod/show/miraclebaby/support

This is a story about loss - In memory of SaulThroughout her life, Kimberly was told and thought that as long as you strive to do your best good things would happen to you. So she did that, followed the rules, followed the order of things - got an education, fell in love, got married, and then pregnant. In her mind, there was no reason for her to think that this next phase of her life wouldn't go "right." With no early indication, in 2014, Kimberly and Aaron Novod's son, Saul, was born prematurely at twenty-eight weeks and six days. He was whisked to the Neonatal Intensive Care Unit (NICU). Initially, they thought he was going to do well and would be bringing their baby home. Yet, baby Saul passed after twenty days in the NICU due to a brain bleed. In that experience, Kimberly realized that there was no "justice"; her previous mindset had shielded her from the mass inequities of the world. There were limitations to medicine, to doctors, to life, and she fell as she describes into the "rabbit hole of grief."As a way to process through their grief and work on healing, Kimberly and her husband Aaron created Saul's Light. During their time of need, their community surrounded them in love and support, which was an integral part of their healing process. Thus, making it their mission to provide the same outpouring to all NICU and bereaved families. A vital part of the support provided to families is through mobilizing people, organizations, and resources directly from their community. Families are offered social-emotional support through peer and whole group support groups and events. Partnering hospitals have cooling cots that allow families who may lose children to create and have memories with their babies. They also have established patient assistant funds allocated towards parents' need for transportation, food, and other expenses that might arise. Along with educating families, there is education provided to hospital staff about being culturally responsive and preparing them to have end-of-life discussions.In the sharing of her birth story, Kimberly makes it clear and points that we cannot ignore the disparities that black and brown babies are overrepresented in the NICU and the graveyard. When parents are present for their babies and present in their care, they have better outcomes. Saul's Light allows for families to have that, responsive to the whole experience of NICU and also addressing infant mortality. It is a communal embrace, reminding families that their community cares about them, and they're not alone!Resources:Nicole Diggins CNM, MSN, MPH | midwife and founder/CEO of Sista Midwife Productions

In Episode 5, Amar Patel speaks to Dr. Tara Bastek, a neonatologist, bioethicist and simulation educator with a Master’s degree in Public Health from Harvard University.Currently serving as Chair of the Medical Ethics Committee and Associate Medical Director of the Neonatal Intensive Care Unit (NICU) for WakeMed Health, Dr. Bastek offers her views on isolating with family, where to find factual information and the COVID-19 impact on society and healthcare. “I myself ended up as a person of interest. I was in a strict quarantine for 72 hours until my test results came back... wondering if I had exposed my family to this.” Dr. Tara Bastek Associate Medical Director of the Neonatal Intensive Care Unit (NICU) for WakeMed Hospital in Raleigh, North Carolina

Hey, mi gente! In this week's episode, we speak with our good friends Annie and Kyle from the innovative NICU Fam Podcast for those looking for support and community that have children or know something that has been in the Neonatal Intensive Care Unit (NICU). Tune in to learn more about their journey and what their podcast is all about. Shoutouts: Podcast: @nicufampodcast @LongBeachCoffeeClub - Come join us on the LBCoffee Club's live video this Wednesday at 12pm talking about coffee, the podcast, and the world. --- This episode is sponsored by · Anchor: The easiest way to make a podcast. https://anchor.fm/app Support this podcast: https://anchor.fm/latinx-nation4/support

A snapshot into the life and times of a Dad with a Premature baby or sick baby in the Neonatal Intensive Care Unit (NICU). We will discuss what Dad's go through mentally and emotionally with their little preemy/premmie delight!

On this episode, our guest Shantel Burchell-Baptiste shares her story about having her daughter Shaniya Baptiste at 26 weeks weighing 2lbs. She spent three months in the Neonatal Intensive Care Unit (NICU). Shaniya had three blood transfusions at six weeks old and was also diagnosed with chronic lung disease.After growing through the loss of her first child and then giving birth to a premature baby one year later, Shantel decided to start her own business "We Thank God Apparel."Her social media information is as follows: 1) Instagram @wethankgodapparel  2)Facebook: @wethankgodapparel 3)Email: wethankgoda@yahoo.comFeel free to send your questions or contact us at itsallaboutevolving@gmail.comYou can find on us on social media platforms too our Instagram handle is @Its_all_about_evolvingFacebook Page & Private Group: @itsallaboutevolvingTwitter Account: @allabtevolving

At 86, Carol Bauer is still on call around the clock in the Neonatal Intensive Care Unit (NICU) at Norwalk Hospital in Connecticut. This fiery and charismatic volunteer and interfaith chaplain spends long days and many late nights supporting families in crisis, advising staff, comforting and cuddling sick babies, and helping parents cope with unimaginable loss. Supporting Norwalk Hospital is a family affair. Carol’s husband, George Bauer, a respected executive who spent more than 30 years with IBM, has served as a member of the Norwalk Hospital Board of Trustees, the Norwalk Hospital Foundation board, and WCHN Board of Directors. --- This episode is sponsored by · Anchor: The easiest way to make a podcast. https://anchor.fm/app

At 86, Carol Bauer is still on call around the clock in the Neonatal Intensive Care Unit (NICU) at Norwalk Hospital in Connecticut.  This fiery and charismatic volunteer and interfaith chaplain spends long days and many late nights supporting families in crisis, advising staff, comforting and cuddling sick babies, and helping parents cope with unimaginable loss.Supporting Norwalk Hospital is a family affair. Carol’s husband, George Bauer, a respected executive who spent more than 30 years with IBM, has served as a member of the Norwalk Hospital Board of Trustees, the Norwalk Hospital Foundation board, and WCHN Board of Directors.--- This episode is sponsored by · Anchor: The easiest way to make a podcast. https://anchor.fm/app

Martha Sharkey is the Founder and CEO of TODAY is a Good Day. Their mission is to provide personal, spiritual, and financial support to families of premature babies during their time in the Neonatal Intensive Care Unit (NICU).For Martha and her husband, Paul, this is a very personal mission. In July 2010, they learned that their journey to starting a family had begun. Shortly thereafter, they learned they were expecting twins! Unfortunately, their journey took a dark turn when Martha delivered Mary Gladys and Claire Josephine on November 14th, 2010, a full 16 weeks premature. Unfortunately, Mary Gladys passed away on November 28th, at just 14 days old. However, Claire Josephine has survived and will be celebrating her 9th birthday this year! (On a side-note, our founder, Ryan Martin had the privilege of meeting Claire Josephine at another podcast interview and she is a wonderful little girl) On their journey, Martha and Paul learned that while the neonatologists and other medical staff are amazing and knowledgeable, they need to take a clinical and therefore, somewhat removed approach. They realized that NICU parents need an extra layer of emotional support and this led to TODAY is a Good Day. Connect with TODAY is a Good Day: • http://www.todayisagoodday.org/ •• https://www.facebook.com/TodayisaGoodDayPA • • https://www.instagram.com/today_is_a_good_day_pa/ •Connect with Luxe Podcast Production by visiting luxepodcasts.com or following us on Instagram @luxepodcasts.

On this episode of The Self Made Strategies Podcast, we sat down with Martha and Paul Sharkey, of the nonprofit organization, TODAY is a Good Day (www.todayisagoodday.org/). About our guests: Martha and Paul Sharkey are the founders of the nonprofit TODAY is a Good Day. The mission of TODAY is a Good Day is to provide personal and financial support to families of premature babies during their time in the Neonatal Intensive Care Unit (NICU). TODAY is a Good Day offers monthly grants for families at Abington Memorial Hospital and Crozer Chester Medical Center, including support of utility bills, car seats, transportation expenses, pack-n-plays, lodging, and other needs. TODAY is a Good Day also offers care packages that are distributed through several area hospitals, including Abington Memorial Hospital, Crozer Chester Medical Center, Einstein Montgomery, and Einstein Philadelphia. TODAY is a Good Day also partners throughout the year with The Superhero Project to donate items for care packages provided to families at Holy Redeemer Hospital. In addition, care packages are sent across the country upon request.On this episode of the Self Made Strategies Podcast, you will learn about:• TODAY is a Good Day's mission and how TODAY is a Good Day helps families with a baby in the Neonatal Intensive Care Unit ("NICU").• How does TODAY is a Good Day helps families who just need someone to talk to.• How family or friends, of those families with babies in the NICU, can help a family member or friend during a NICU stay or after a loss.• The volunteer opportunities that exist for those who want to support TODAY is a Good Day.• How entrepreneurs or business owners can get involved with or help TODAY is a Good Day.• The programs TODAY is a Good Day offers for those looking for Corporate Social Responsibility programming.• How nonprofit involvement, in organizations like TODAY is a Good Day, can help an entrepreneur or business owner to improve their personal brand and network.After you’ve listened to the episode, go to SelfMadeStrategies.com for more information about our show, exclusive content and to contact the Self Made Strategies show hosts.You can also connect with us on: • https://www.facebook.com/selfmadestrategies/ •• https://twitter.com/SelfMadeStratGs •• https://www.instagram.com/selfmadestrategies/ •• https://www.linkedin.com/company/self-made-strategies/ •

Giving birth to a baby pre-term can lead to all kinds of challenges for parents. Leaving the hospital without your baby being one. The stress and anxiety of seeing them in the Neonatal Intensive Care Unit (NICU) is another. Not being able to touch them. Now research has shown that the parents of premmie babies are more likely to suffer from postnatal depression than their counterparts with full term babies. Melinda Cruz is the founder of The Miracle Babies Foundation (miraclebabies.org.au), and a mother who had three babies in NICU. She explains what it was like having babies in NICU, and what parents in this situation really need.

A woman who once fought for her life as the smallest baby born in Texas now works at the same hospital that saved her life. Born at 24 weeks old, Tammy Lewis spent three and a half months at Scott and White Hospital's Neonatal Intensive Care Unit (NICU). Lewis was considered a micro preemie / ˈmaɪkroʊ ˈpriːmi /, a baby born weighing less than 800 grams. Because of this, the doctors were unsure whether she would live and beat the odds. Now, after 34 years, Lewis works at the same NICU that took care of her when she was a premature baby. Even while she was still studying, Lewis had always known that she wanted to work with children. She was choosing between a profession in teaching and the medical field. However, Lewis claimed that she fell in love with the medical field when she began researching on it. Now, Lewis works as a respiratory therapist for premature babies. Part of her job is attaching premature babies to ventilators and breathing tubes, just like the ones that helped her survive years ago. Incidentally, Lewis is now working alongside some of the staff who took care of her as a baby. Lewis said that it is an honor to be able to pay it forward and take care of children who are in the same situation that she was in. According to Lewis, nothing feels more rewarding for her than seeing premature babies grow big and healthy enough to go home. She added that being a survivor lets her become a beacon of hope for parents with premature babies in the hospital.

We chop it up with author and self-care advocate, Alena Smith. Trust Your Strength is about keeping the faith when the odds are stacked against you. Have you ever been faced with a battle so tough that you didn’t know how you were going to get through it? Has your strength been tested and you needed a reminder of how amazing God is? This book will take you on our journey, including the highs and lows of becoming parents, losing a child, and then being blessed with two miracles. Both of our son’s journey began in the Neonatal Intensive Care Unit (NICU) 6 years apart for a combined total of 368 days before going home. Through our testimony, you will gain strength to remind you that no battle is too big or too hard for you. You will also read scriptures throughout the book to remind you to hold onto God’s faith while you journal your own thoughts of staying strong through your battle.

Kristen Nagle is a Registered Nurse (RN) working in the Neonatal Intensive Care Unit (NICU). She "fell down the rabbit hole of holistic health" after having her first son, enrolled at the Canadian School of Natural Nutrition and became a Registered Holistic Nutritionist. She cofounded Sweaty Successful Moms to "help the busy mom who wants to do it all gain confidence, energy and time." Show notes Eco-nutrition and why you're not getting everything your body needs from the food you eat How to pick quality supplements (see details below) The 80/20 rule for practicing good nutritional habits Tips and resources for busy mom's trying to do it all Vaccines, Autoimmunity, and the Changing Nature of Childhood Illness by Dr. Thomas Cowan The End of Food by Paul Roberts

In the first hour, hosts Brad Gray and Jeanine Bitzan began by visiting with Courtney Ehlers about a place called the Neonatal Intensive Care Unit (NICU) and how physical touch plays an important role in helping young babies who end up in this unit. Our hosts then visited with Roxane Salonen about our response in times of turmoil when it comes to deciding if we will stick with Jesus and the Church or abandon them both. Finally, Brad and Jeanine joined Alicia Hunt-Welch of Birthright in Rochester, MN to talk about how this organization helps offer love, support, and resources when a woman is facing an unplanned pregnancy and needs help.

Mia Grant is a mother of three grown children and grandmother of five. She works as a registered nurse in the Neonatal Intensive Care Unit (NICU) and in the Maternal and Newborn Care Unit of a major hospital in New York. Twelve years ago, her twin grandchildren, Ava and Mikey, were born five weeks premature. She helped care for Ava and felt the need to be there to share my love. That nights she woke her husband up to share with him that she was shifting careers to be a NICU nurse. Two weeks later, she was enrolled in school. She finished her bachelor's Degree in Science of Nursing after four years. Listen up as she shares a bit into her life and a new career after becoming a grandma.

Order your pre-launch copy of the book DOUBLE HAPPINESS MULTIPLIED - What you need to know about having Twins, Triplets, & Quads HERE:  https://www.doublehappinessmultiplied.com/twins-triplets-quads-book/ On this episode, we discuss taking care of your children while you have babies in the Neonatal Intensive Care Unit (NICU). Psychologist Dr Monique Robinson has some tips to help normalise the situation as much as possible. Joanne Beedie shares her heartbreaking story of grieving for her baby boy who died inutero while watching her surviving twin fight for his life in the NICU. And, Senior Social Worker Clare Dimer explains the pressures facing families in this situation. Psychologist Dr Monique Robinson tells us that when you’re going through your NICU journey you will need support, however, asking for help doesn’t come easily to some people and it’s okay to feel overwhelmed and not completely in control. The Reality of NICU Even if you knew leading up to the birth your babies were going to come early, there can often be a sense of this isn’t what I was expecting. This is not what I signed up for, this is not what I imagined having twins would be. “As much as it sounds like it’s just a revision of plans, for many women that total change in expectations, and the change in the plans for the future, and where they thought they were going to be at what time is really difficult.” ~Psychologist Dr Monique Robinson~ Tweet This Dr Robinson says it’s normal to feel overwhelmed and to accept that this is your reality for a while. And,...

Order your pre-launch copy of the book DOUBLE HAPPINESS MULTIPLIED - What you need to know about having Twins, Triplets, & Quads HERE:  https://www.doublehappinessmultiplied.com/twins-triplets-quads-book/ On this episode of the Double Happiness Multiplied podcast, we talk with Consultant Neonatologist Doctor Patricia Woods from King Edward Memorial Hospital in Western Australia about what to expect when you have babies in the Neonatal Intensive Care Unit (NICU). Mum of quadruplets Jannelle Snaddon walks us through her NICU journey. Psychologist Doctor Monique Robinson offers practical advice about taking care of your emotional wellbeing when you have babies in NICU. I’ll share my NICU story with you and I’ll read a moving letter from a micro-premmie mum written to other parents of premature babies. What does pre-term mean? A Preterm or Premmie baby is defined as being born alive before 37 weeks of pregnancy are completed. There are sub-categories of preterm birth, however, based on gestational age: Extremely preterm, or micro premmies, are born at less than 28-weeks’ gestation, Very preterm are those babies born between 28 and 32-weeks’ gestation, And, moderate to late preterm, which are babies born after 32 weeks and before 37-weeks’ gestation. Why does preterm birth happen? There are many reasons preterm births occur, the most common causes include multiple pregnancies, infections, and chronic conditions such as diabetes and high blood pressure. However, oftentimes no cause is identified but may be due to...

Guest: Michelle Emanuel is the developer of the TummyTime!™ Method and has over 20 years experience as a Neonatal / Pediatric Occupational Therapist.  In this episode, we will cover: why Tummy Time is so important for your baby and how it helps with head flattening, breastfeeding and brain development when you should start Tummy Time, how long and how often you should do it what to do when your baby doesn't seem to like Tummy Time how to do the 8 Stages of the Tummy Time Method to get the maximum benefit  Resources mentioned in the conversation: Michelle Emanuel's website: www.TummyTimeMethod.com link to find a Tummy Time trained professional YouTube video of the newborn Breast Crawl  About Michelle Emanuel: Michelle Emanuel has over 20 years experience as a Neonatal / Pediatric Occupational Therapist.  She has worked in Neonatal Intensive Care Unit (NICU), pediatric critical care, outpatient and private practice. Michelle was a Level II staff OT at Cincinnati Children’s Hospital Medical Center for over 17 years, working directly with patients as well as participated in research and education. Her private practice, Whole Body LLC, TummyTime!™ Method Headquarters and the Infant Neurodevelopmental Training Center for Professionals is located in Cincinnati, OH. Michelle has a wide variety of knowledge and skills that includes Embryology, Newborn/Infant Development, Pre & Perinatal Psychology, Autonomic Nervous System Regulation and Resiliency, Infant Sensory Processing, Polyvagal Theory, Baby Massage and various forms of Manual Therapy.  She developed and began teaching TummyTime!™ Method classes over 10 years ago.    Michelle is licensed and registered as an Occupational Therapist, a National Board Certified Reflexologist and 200 hour Registered Yoga Teacher.  She is also certified in CranioSacral Therapy, Divine Sleep™ Yoga Nidra, Reflexology, Infant Massage, Baby's First Massage, Butterfly Touch Massage, Neonatal Oral Motor Assessment Scale (NOMAS) and the Infant Behavioral Assessment (IBA). Michelle has trained in evaluation and scoring of the Test of Infant Motor Performance (TIMP).   She is reliable in the General Movements Assessment at the Advanced Level.

Paying It Forward Paying it forward matters.  Top-selling Realtor, Debbie Henninger knows how.  In addition to her real estate career, advising women on protecting their real estate assets during divorce, and sitting on several community boards, Debbie has a passion – improving lives of pre-mature babies and their parents.  She raises funds to improve and expand MedStar Franklin Square Medical Center’s Neonatal Intensive Care Unit (NICU). Debbie is putting on a new fundraiser this year.  In conjunction with Damian Bohager and his company, “The Gathering” they’ll be putting on The Gateway Gathering and Music Festival at the Crossroads in Middle River, Maryland on Saturday, May 7th, starting at noon.  It will combine great Music and great Food Trucks all to benefit the Franklin Square NICU.  Come out and listen to live music, have some great food, and improve the lives of newborns and their families. The NICU provides a full spectrum of Neonatal services to approximately 2,700 delivering mothers per year. Approximately 40% of the OB patients who deliver at MedStar Franklin Square Medical Center require neonatal care at the time of the delivery. The Neonatal medical team is made up of Neonatologists and Neonatal Nurse Practitioners. They collaborate with Registered Nurses, Respiratory Therapists, Occupational/Physical Therapists, Pharmacists, and Social Workers who are specially trained in Neonatal Care. The NICU provides 24-hour care 7 days a week. Join Mark and Carolyn, and Debbie as we talk about the joys of paying it forward. Let's Coach

Babies born premature or with troubling medical conditions are cared for around-the-clock by Saint Peter’s University Hospital’s staff of neonatologists, pediatric specialists, neonatal nurses, neonatal nurse practitioners, neonatal respiratory therapists and pharmacists. The Neonatal Intensive Care Unit (NICU) at The Children’s Hospital at Saint Peter’s University Hospital is one of the most experienced and one of the largest specialized facilities of its kind on the East Coast, with 54 intensive and special care bassinets. Preemies require a special brand of care. And the parents of those premature infants are often faced with numerous unknowns.