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    Kids & Family

    Inside the Children’s Hospital

    Inside the Children’s Hospital shares real stories from parents, caregivers, and pediatric healthcare professionals navigating the emotional realities of caring for a hospitalized child with honesty, compassion, and hope.

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    Latest Episodes:
    Episode 136 | Jaime's Story - A daughter with limb loss and Tetralogy of Fallot Sep 07, 2022
    Show notes

    "It's not a time to say I'm sorry, It's a time to acknowledge that, yes in fact you had something you did not plan for, a traumatic event. But also you did have a baby and to step into that joy and gratitude and not lose sight of those things.-Jamie Cline

    Jamie shares how her daughter Callie has persevered with tetralogy of fallot and later on a limb loss.She learned about her daughter's tetralogy of fallot just hours after having her 7 weeks premature. When Callie turned one, she shares how they came to the decision to do a lower leg amputation. Jamie shares Callie's journey of learning to walk with a prosthetic as well as the emotional journey she embarked on as a mother.

    [3:00] Jamie shares about their family and hobbies

    [4:50] Close monitoring during Jamie's pregnancy due to her pre-existing type 1 diabetes

    [5:37] Callie was born 7 weeks early via c-section

    [6:43] Learning of Callie's heart condition, Tetralogy of fallot

    [8:30] The grief and anger to follow the initial diagnosis

    [10:35] Feeling cheated of hopes and dreams she had

    [11:40] Sharing the emotional challenges of others saying they are sorry rather than celebration

    [13:12] Callie had to be transferred to a different hospital for the surgery

    [15:00] How their community rallied around supported their family

    [17:18] Callie went between the NICU and PICU for close to 3 months

    [20:40] The best Christmas gift- Callie got to come home for Christmas

    [21:40] Noticing Callie's limb difference shortly after birth

    [26:05] At 19 months old, Callie had her amputation surgery

    [27:30] Decision making process

    [30:08] How grief was a big part of Jamie's journey to healing

    [32:00] Jamie shares how she took care of her self during this difficult time

    [36:00] How Callie has changed their lives and the positive things she has gleaned from being her mother

    Connect with Jaime:

    Instagram

    Website

    Whether you are a parent or professional, we want you to join our community. Sign up for our newsletter here.

    Parents, download our free parent starter kit.

    When you download our starter kit, you'll learn how to:

    • Give medicine to your child without it becoming a wrestling match
    • Prepare your child (and yourself) for a shot so they can feel less anxious
    • Create and use a coping plan for any medical appointment or procedure

    The first sign of sniffles, or worse, shouldn't send you into a tailspin. Feel confident in your role as a parent and advocate, no matter what medical situation you're facing.

    Child life specialists, get affordable PDUs on-demand here.

    Shop for your CLOC gear here.

    Catch up with CLOC on Instagram, Facebook and meet Katie for a Q+A every Monday at 10 AM CST.


    Episode 135 | Judith's Story- A twin with albinisim Aug 31, 2022
    Show notes

    Judith shares how one of her twins was born with albinisim and how she stayed positive during the diagnosis and beyond. This episode will absolutely touch your heart, Judith is a natural story teller and captures hows she embraced her daughter's albinism and has seen the beauty through it all.

    [3:15] Judith shares her busy life and routine with the twins

    [6:25] She shares about her high risk her twin pregnancy journey

    [7:27] How the ultrasound tech noticed the bridge of the nose on both of the babies

    [8:20] Overwhelming feeling that finding out about one issue after a next,

    [8:49] Joining a support group felt like accepting the mis-diagnosis she received

    [9:57] The doctor noticed her daughter stopped growing and told her she needed a c-section

    [11:12] Soon after birth, she noticed her skin was light in color and Judith wondered if she had albinisim

    [13:14] Baby girl had to stay a little longer to gain some weight when brother got discharged.

    [15:25] Judith and her family were concerned about others not accepting her

    [19:45] How her faith helped her maintain positivity during trying time

    [21:45] While trying to become pregnant, Judith's faith that she would become pregnant with twins was walked out when she prepared the extra bedroom for children

    [25:55] Confirming the gender of the babies

    [29:00] How she felt like going to a support group for parents of blind children was accepting that her daughter would be blind

    [32:00] Sharing how people in her culture treat albinisim

    [33:40] Judith shares how she explained to her daughter how she was beautiful and that different is beautiful

    [35:05] Sharing how she is confident in school and speaking to others about her differences

    [36:50] How she uses her story to help others and inspire parents going through it

    [40:00] Embracing the journey of albinism and seeing the beauty in it all

    CONNECT with Judith:

    Instagram

    Learn more about albinism at www.albinism.org

    Whether you are a parent or professional, we want you to join our community. Sign up for our newsletter here.

    Parents, download our free parent starter kit.

    When you download our starter kit, you'll learn how to:

    • Give medicine to your child without it becoming a wrestling match
    • Prepare your child (and yourself) for a shot so they can feel less anxious
    • Create and use a coping plan for any medical appointment or procedure

    The first sign of sniffles, or worse, shouldn't send you into a tailspin. Feel confident in your role as a parent and advocate, no matter what medical situation you're facing.

    Child life specialists, get affordable PDUs on-demand here.

    Shop for your CLOC gear here.

    Catch up with CLOC on Instagram, Facebook and meet Katie for a Q+A every Monday at 10 AM CST.


    Episode 134| Rebekah's Story - A teen with food allergies Aug 24, 2022
    Show notes

    "I've connected with food allergy patients and we have all come together. That is the most important thing, to make sure that nobody feels alone."-Rebekah Wallace

    Rebekah shares her life today as a teen with food allergies. This episode brings perspective to our listeners about how we can take our challenges and turn them into advocacy and awareness. Rebekah, shares her first memories of having food allergies and how she and her family learned to cope. She shares how she coped with the news and what she is doing today to bring awareness to food allergies.

    [3:15] Rebekah shares her about her every day life as a teen with food allergies

    [5:30] The struggle as a young child not understanding why she couldn't eat certain foods

    [6:40] She began to understand the importance of the allergies around age 10

    [7:45] Rebekah shares the first time she had to use an EPI pen

    [8:00] She explains how remaining calm during a reaction is key

    [10:30] How Pageantry made her feel confident to speak up about bringing awareness to food allergies

    [11:55] The Allergy bet book she created to share with young children about food allergies

    [15:45] Being able to connect with other peers going through the same thing was so helpful

    [16:00] All children need is just love and support

    [17:45] Rebekah shares her dream of being a oncology nurse

    CONNECT

    Instagram- @Rebekahreacts

    Whether you are a parent or professional, we want you to join our community. Sign up for our newsletter here.

    Parents, download our free parent starter kit.

    When you download our starter kit, you'll learn how to:

    • Give medicine to your child without it becoming a wrestling match
    • Prepare your child (and yourself) for a shot so they can feel less anxious
    • Create and use a coping plan for any medical appointment or procedure

    The first sign of sniffles, or worse, shouldn't send you into a tailspin. Feel confident in your role as a parent and advocate, no matter what medical situation you're facing.

    Child life specialists,get affordable PDUs on-demand here.

    Shop for your CLOC gear here.

    Catch up with CLOC on Instagram, Facebook and meet Katie for a Q+A every Monday at 10 AM CST


    Episode 133 | Expert: A Hard of Hearing Child Becomes an Audiologist Aug 17, 2022
    Show notes

    "I really feel like I'm paying forward with everything that I lived and everything I've experienced as a professional. My program is my heart in a basket for them."- Dr. Michelle Hu, Audiologist

    Dr. Michelle Hu shares how she was diagnosed as hard of hearing as a young child and what lead her to become an audiologist. This episode is packed full of wisdom.

    [3:12] Michelle's teacher encourages her mom to get her hearing checked

    [3:49] Getting hearing aids after a mild hearing loss diagnosis

    [4:44] The hurricane feeling her parents felt after receiving her diagnosis

    [5;26] Struggling with the news of hearing loss

    [6:14] Seeking second opinions after struggling with the diagnosis

    [7:00] How Michelle's parents processed her diagnosis

    [9:15] The inspiration behind creating a community for parents

    [10:18] Through the community she has created, she feels like she is paying it forward

    [13:00] Creating tools to helped newly diagnosed families

    [16:00] Katie+ Michelle discuss how parenting is full circle

    [17:33] How Michelle decided to be an Audiologist

    [20:10] Providing the cliff notes to help each other and win is the goal

    CONNECT:

    Instagram

    Website

    Whether you are a parent or professional, we want you to join our community. Sign up for our newsletter here.

    Parents, download our free parent starter kit.

    When you download our starter kit, you'll learn how to:

    • Give medicine to your child without it becoming a wrestling match
    • Prepare your child (and yourself) for a shot so they can feel less anxious
    • Create and use a coping plan for any medical appointment or procedure

    The first sign of sniffles, or worse, shouldn't send you into a tailspin. Feel confident in your role as a parent and advocate, no matter what medical situation you're facing.

    Child life specialists, get affordable PDUs on-demand here.

    Shop for your CLOC gear here.

    Catch up with CLOC on Instagram, Facebook and meet Katie for a Q+A every Monday at 10 AM CST.


    Episode 132 | Tanisha's Story - A son with Lower Urinary Tract Obstruction Aug 10, 2022
    Show notes

    Tanisha tells a story of strength and perseverance as her son Jaleel was born with a lower urinary tract obstruction. This story highlights the powerful ways Tanisha and her husband, Quentin work together as a team for Jaleel and their family. From her experiences in the NICU and beyond, Tanisha created a community to support NICU Medical Moms.

    [3:52] The journey to motherhood for Tanisha

    [6:13] Learning that Jaleel had a lower urinary tract obstruction at her 20 week anatomy scan

    [9:30] How Tanisha's husband helped her feel included in Jaleel's care

    [14:16] Healing is on-going for Tanisha and her family

    [18:39] She describes how she had the urge to walk one evening and the next morning learned she was in labor

    [20:35] Jaleel was born and was immediately rushed to the NICU for respiratory issues

    [22:57] Tanisha explains the emotional reunion in the NICU

    [24:51] Her husband advocated for Tanisha become involved in Jaleel's care to connect with him

    [26:49] Tanisha shares how she went into learning mode to not be stressed

    [28:42] Child Life specialists put up pictures of Jaleel's progress in the NICU and decorated his room the theme of his nursery

    [31:33] Getting a G-Tube was key to getting Jaleel ready for transplant

    [33:30] Moral support from Mom to Mom was key for Tanisha

    [37:43] Tanisha shares how she was enrolled in her Master's Degree program and how she was supported by faculty

    [42:00] Tanisha shares how she feels she is getting to live her dream in a new way

    [45:24] How Child Life Specialists shaped Jaleel's interest in music

    Connect with Tanisha:

    Medical Moms of NICU Facebook Group

    Whether you are a parent or professional, we want you to join our community. Sign up for our newsletter here.

    Parents, download our free parent starter kit.

    When you download our starter kit, you'll learn how to:

    • Give medicine to your child without it becoming a wrestling match
    • Prepare your child (and yourself) for a shot so they can feel less anxious
    • Create and use a coping plan for any medical appointment or procedure

    The first sign of sniffles, or worse, shouldn't send you into a tailspin. Feel confident in your role as a parent and advocate, no matter what medical situation you're facing.

    Child life specialists, get affordable PDUs on-demand here.

    Shop for your CLOC gear here.

    Catch up with CLOC on Instagram, Facebook and meet Katie for a Q+A every Monday at 10 AM CST.


    Episode 131 | Paola's Story - A son with ADA-SCID Aug 03, 2022
    Show notes

    Paola shares the shocking diagnosis her son received as a newborn of ADA-SCID (Severe Combined Immunodeficiency.) This powerful story a he shares how she navigated hospital life during the beginning of the pandemic and her journey with postpartum depression. She shares words of wisdom on how to deal with the feelings that come when your child gets a life altering diagnosis.

    [5:22] Paola describes the grief she experienced with Jakob's diagnosis

    [7:10] She describes the shock and acceptance of the news that Jakob has ADA-SCID

    [9:12] Postpartum depression struggles during isolation

    [11:10] Sharing the importance of opening up about your struggles

    [13:44] Being a first time Mom and medical mom

    [15:03] Paola describes how she fights the good fight

    [17:44] Her cervical cancer diagnosis after Jakob's diagnosis

    [19:29] Paola's campaign to fight for Jakob's treatment

    [20:21]She describes how her cancer diagnosis was her moment to pause

    [26:50] Coming up with a plan and leaning on community helped Paola cope with the diagnosis

    [30:12] She shares how Child Life specialists have helped reduced the trauma Jakob has had to endure

    [31:28] Jakob has taught Paola to be brave and to have courage

    [32:20] Paola has created an environment that helps Jakob have some normal day to day activities despite being isolation

    [33:45] She shares how her motherhood journey was so different than what she anticipated, she feels fierce and does not take no for an answer

    In My Magical Bubble Book

    Connect with Paola:

    Instagram

    Facebook

    Website

    Whether you are a parent or professional, we want you to join our community. Sign up for our newsletter here.

    Parents, download our free parent starter kit.

    When you download our starter kit, you'll learn how to:

    • Give medicine to your child without it becoming a wrestling match
    • Prepare your child (and yourself) for a shot so they can feel less anxious
    • Create and use a coping plan for any medical appointment or procedure

    The first sign of sniffles, or worse, shouldn't send you into a tailspin. Feel confident in your role as a parent and advocate, no matter what medical situation you're facing.

    Child life specialists,get affordable PDUs on-demand here.

    Shop for your CLOC gear here.

    Catch up with CLOC on Instagram, Facebook and meet Katie for a Q+A every Monday at 10 AM CST.


    Episode 130 | Belinda's Story - A son with autism, low tone and epilepsy [A BELOVED MENTOR] Jul 27, 2022
    Show notes "Never listen when they tell you your child will not, encourage them to do the best they can do"- Belinda Hammond, CCLS

    Belinda shares her son's journey with low tone, epilepsy and autism and how her professional and personal experiences collided, giving her an invaluable perspective as a parent and professional. This episode is in our top 5 most downloaded episodes to date.

    [4:39] Belinda notices her son is not meeting some major developmental milestones

    [5:17] Receiving a low tone diagnosis as an infant

    [10:00] Belinda shares a touching moment in her son's journey to run a 5k

    [12:39] Finding activities your child likes to incorporate into therapy

    [13:34] She gets a phone call from Justins school, Belinda begins to search for answers

    [14:57] Additionally, she learns her son is having absent seizures and after a neurology referral learns he has Epilepsy

    [15:41] After hearing feedback from her son's school, Belinda decides to homeschool Justin

    [19:53] Getting her Masters degree helped her become a stronger advocate for her son and patients

    [22:45] In addition to low tone and seizures, Belinda shares about Justin's mild autism spectrum diagnosis at age 5

    [24:50] Belinda describes how going back to school was self-care for her

    [28:54] Working on self-confidence

    [30:09] Justin's amazing attitude and ability to push forward is inspiring to Belinda

    If you would like to connect with Belinda, you can email her, or connect through her website and Facebook pages.

    Whether you are a parent or professional, we want you to join our community.

    Sign up for our newsletter here.Parents, download our free parent starter kit.

    When you download our starter kit, you'll learn how to:

    • Give medicine to your child without it becoming a wrestling match
    • Prepare your child (and yourself) for a shot so they can feel less anxious
    • Create and use a coping plan for any medical appointment or procedure

    The first sign of sniffles, or worse, shouldn't send you into a tailspin. Feel confident in your role as a parent and advocate, no matter what medical situation you're facing.

    Child life specialists, get affordable PDUs on-demand here.

    Shop for your CLOC gear here.

    Catch up with CLOC on Instagram, Facebook and meet Katie for a Q+A every Monday at 10 AM CST.


    Episode 129 | How to Explain Covid-19 to Kids [2nd MOST DOWNLOADS] Jul 20, 2022
    Show notes

    This episode originally aired in March 2020 at the beginning of the pandemic. This topic is so important and rightfully so, it is our 2nd most downloaded episode of all time. When it comes to COVID-19, how we inform our children is incredibly important. If you're wondering how we can talk to our kids about COVID-19 when we as adults still don't know exactly what's happening, you're not alone. This episode covers suggestions for age-appropriate language to use as well as general considerations to keep in mind as you talk to your children about COVID-19. Children are looking to adults for honest, easy-to-digest information. Give a listen to learn how to break it down into a way that they can understand.

    [3:20] Katie explains that children and adolescents crave a strong compassionate leader who establishes boundaries

    [6:00] It's important to remind children that a lot of the information they hear may not be factual

    [8:53] Katie explains to empower your children by validating what they are already doing

    [9:19] She shares how hand-washing is an easy practical way fuel empowerment when discussing COVID-19

    [10:10] t is ok to admit that there are unknowns about COVID-19 and acknowledging that we don't know the answers and that is ok

    [11:06] Katie shares the importance of setting a good example.You want to model behavior that your children will follow

    [12:00] Offer to have a check in with your child if they are feeling worried

    [12:22] Katie's key to success is to be a strong and compassionate leader and exhibit the behavior you want your child to have. Be a buffer!

    Whether you are a parent or professional, we want you to join our community. Sign up for our newsletter here.

    Parents, download our free parent starter kit.

    When you download our starter kit, you'll learn how to:

    • Give medicine to your child without it becoming a wrestling match
    • Prepare your child (and yourself) for a shot so they can feel less anxious
    • Create and use a coping plan for any medical appointment or procedure

    The first sign of sniffles, or worse, shouldn't send you into a tailspin. Feel confident in your role as a parent and advocate, no matter what medical situation you're facing.

    Child life specialists, get affordable PDUs on-demand here.

    Shop for your CLOC gear here.

    Catch up with CLOC on Instagram, Facebook and meet Katie for a Q+A every Monday at 10 AM CST.


    Episode 128 | Maura's Story - A son with Down syndrome [MOST SHARED] Jul 13, 2022
    Show notes

    On this episode of the podcast, you will hear an amazing story of resilience and hope.This episode originally aired back in August of 2020. This is the most shared of all of our podcast episodes; you will quickly learn why after listening to this inspiring story. Meet Maura Senneff, mom to sweet Ryan. Ryan is a thriving 8-year-old boy who has Down syndrome. The amazing advocate by his side, his momma Maura, describes that "zooming out" and looking at things from a wide lens helped them turn Ryan's health around.She talks about small changes and the "no limits" attitude their family lives by.

    [1:39] Maura shares about her family and introduces us to Ryan and his journey with Down syndrome

    [2:40] Maura explains how resilient Ryan is despite his struggles with chronic illness for his first six years of life

    [3:27] Never giving up was key to their success at navigating Ryan's diagnosis of Down syndrome

    [4:00] Maura shares how Ryan's diagnosis with Down syndrome was not going define him and put limits on what he can and can't do

    [4:56] Maura shares the deep meaning behind advocating for Ryan; it meant the idea of unlocking potential and removing barriers for generations to come

    [5:23] Maura explains how they came to learn of Ryan's unexpected Down syndrome diagnosis at birth

    [7:12] Maura shares that during her prenatal care there were no markers on any of her ultrasounds for Down syndrome

    [8:04] Maura began to have what she thinks are braxton hicks contractions but learns she is in labor

    [9:07] Maura describes Ryan's quick delivery and the time that lapsed before getting to see him

    [9:32] She describes how Ryan wasn't latching and crying like her first baby and something felt wrong

    [10:45] Maura describes the moment she told her husband Jack that she thought Ryan may have Down syndrome

    [10:56] She explains through tears how she feels sad about the emotional roller coaster of emotions she went through the first few days and how there is immense joy despite the diagnosis

    [12:51] Ryan goes to the NICU for additional testing and Maura describes how she was mentally preparing for the diagnosis of Down syndrome

    [13:45] Maura shares how her husband saw their family pediatrician come in with his Saturday work clothes on and was how it was an indicator that something serious was happening

    [14:07] Maura explains the emotional moment they heard the official diagnosis of Down syndrome

    [15:30] Maura explains how with Down syndrome, there is a variety of health complications and Ryan was fairly healthy despite the circumstances, but struggled with acute illness

    [18:26] Maura shares how she and her husband didn't know much about Down syndrome and special needs before meeting their son

    [19:57] Ryan was reading before he learned to talk. Maura did not know if he was going to talk but ensured that he had access to as much therapy as possible

    [22:37] Maura shares how she advocated for Ryan during one of his ICU stays

    [24:02] Ryan had a low white blood count at birth and had several emergent blood draws over the years and Maura shares her desperation for answers

    [26:09] Maura explains how an ABA therapist was a pivotal force for Ryan to potty train

    [28:00] Ryan did swimming lessons at 18 months old, could roll over and do things in the water before he could do them without his walker

    [29:46] Maura shares how other people have reached out to her after finding her on instagram and how his story has given them hope

    [31:00] Maura shares about the language surrounding Down syndrome and how it made her feel

    [33:50] When children have a diagnosis, it is important to not put what they can or can't do in a box

    [35:40] Maura explains how the school called her about Ryan's therapy, stating that he did not need it any longer. She had his therapists train the teachers on his behavior plan

    [37:25] She shares the one thing she wished she would have done in early Ryan's diagnosis is to meditate and how many medical professionals urged her to do so as it is a part of their daily practice. It helped her not get overwhelmed in her thought life

    [41:00] How their family added meditation into their daily routine for calm minds,manage stress and think clearly

    [43:05] Maura explains how going through the emotions and feeling like your head is spinning is normal but you don't need to stay there. Meditation is so crucial to her to get through the days.

    [48:00] Maura explains how ABA therapy was a game changer and how she wishes that she would have started Ryan in this type of therapy at birth

    [50:00] She shares about how when she broke her foot badly and told the doctor she would do anything to help her broken foot.. He sent her to a Chinese medicine doctor for acupuncture and had immediate pain relief. She vented to the doctor about Ryan's situation and she suggested she bring him in for treatment

    [54:00] Maura explains how thinking outside of the box and trying things that are not typical are SO impactful to their experience. Find your tribe that will sit in the trenches with you.

    [55:50] Within 2 weeks of using functional medicine, Ryan was able to have regular bowel movements and his far-sighted vision changed by a third then even more in the weeks to come. Ryan's labs were all in normal range within a few weeks.

    [01:00:00] Maura shares how Ryan's thyroid level changed drastically after acupuncture

    [01:03:42] She shares how Ryan has shown them that ANYTHING is possible and how much he has taught them about achievement

    [01:06:45] How Maura honed in on working on gross motor skills for Ryan as she knew it would help change many things for him. They improved drastically after 5 or 6 treatments

    [01:07:43] Maura had Ryan participate in a study that focuses on brain function in children with Down syndrome and the doctor doing the study could not tell that Ryan had Down Syndrome by looking at the MRI.

    CONNECT WITH MAURA:

    Instagram

    Whether you are a parent or professional, we want you to join our community. Sign up for our newsletter here.

    Parents, download our free parent starter kit.

    When you download our starter kit, you'll learn how to:

    • Give medicine to your child without it becoming a wrestling match
    • Prepare your child (and yourself) for a shot so they can feel less anxious
    • Create and use a coping plan for any medical appointment or procedure

    The first sign of sniffles, or worse, shouldn't send you into a tailspin. Feel confident in your role as a parent and advocate, no matter what medical situation you're facing.

    Child life specialists,get affordable PDUs on-demand here.

    Shop for your CLOC gear here.

    Catch up with CLOC on Instagram, Facebook and meet Katie for a Q+A every Monday at 10 AM CST.


    Episode 127 | Courtney's Story - A daughter born at 25 weeks [MOST DOWNLOADED] Jul 06, 2022
    Show notes

    Episode 127 | Courtney's Story - A daughter born at 25 weeks [MOST DOWNLOADED]

    At just 25 weeks pregnant, Courtney was diagnosed with pre-eclampsia and was hospitalized. Just 5 days later and after a terrifying emergent c-section, she would meet her daughter, McKenzie. In this episode, Courtney talks about her entire experience from her own hospitalization and her daughter's 5-month stay in the NICU and eventually going home. She talks about the balance of being a single, working mom and the struggles that come along with having a child with medical needs. Courtney will leave you feeling inspired and in utter awe of how she loves and supports her daughter.

    [2:47] Courtney is informed she has high blood pressure and is admitted to Labor and Delivery

    [4:24] Courtney is transported to a larger hospital that has a higher-level NICU

    [6:35] Courtney asks tough questions about her condition and her daughter

    [9:12] Courtney is informed she will need to have a c-section

    [11:12] Courtney is informed she will need an emergency c-section as she has developed HELLP syndrome

    [15:44] Courtney describes the overwhelming emotions she felt meeting her daughter for the first time in the NICU

    [19:44] A primary nurse keeps Courtney accountable in the NICU about pumping. Courtney shares how important this was to her and her journey with McKenzie.

    [21:24] Learning how to do McKenzie's care in the NICU helped Courtney feel empowered

    [22:45] Courtney describes the roller coaster ride she experienced while McKenzie was in the NICU

    [24:20] She explains how she stayed in the hospital recovering from HELLP syndrome

    [24:50] That punch in the gut feeling Courtney felt after learning the significance of a white flower posted outside of a neighboring NICU room

    [26:50] Courtney shares how she advocated for McKenzie, even when others did not agree with her

    [29:35] She shares about life after the NICU + rooming in with McKenzie

    [33:15] Courtney shares about McKenzie's feeding journey and oral aversion and the ups and downs with her feeding including developing, GERD and getting an NG tube

    [36:41] She recalls how McKenzie's nurse, now friend, came to the rescue to help drop McKenzie's NG tube

    [38:32] Courtney shares how she came to the decision to get McKenzie a g-tube and how it affected her as a mother

    [40:15] She shares the love and hate relationship with the feeding tube and how she came to the understanding that even though it wasn't preferable it helped her nutrition

    [43:00] Changes she had to make in her life to support McKenzie including staying in during cold and flu season

    [43:50] The beautiful gesture of friends supporting her during their NICU stay, bringing her to lunch each Sunday, and giving her weekly care packages.

    [45:35] Courtney shares her struggle of finding quality childcare for McKenzie and how difficult it was to find someone whom she could trust

    [48:12] Courtney relied on her faith and prayer to cope with what was going on in her life and with McKenzie

    [50:18] Courtney's friend Ebony, encourages her to get help and go to therapy after she describes some dreams and things during her day that remind her of being in the hospital

    [54:00] She shares how difficult it was for other people to understand what she was going through

    [55:09] Courtney describes how she puts her own needs aside to give McKenzie the selfless care and love she needs and deserves

    CONNECT WITH COURTNEY

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