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    Kids & Family

    Once Upon A Gene

    As a new parent of a child with a rare genetic syndrome, I was lost. There was no guide. There was no rulebook. This was not what I had imagined. As I navigated my way through this new reality, I realized something that should have been simple, but was not. A truth that had always been there, but that I had lost sight of for a time – I am not alone. And neither are you. These are the stories of my family, and of families like ours. These are the stories of how we have persevered, cried, bonded, and grown. These are the stories of children who have been told that they cannot, and that have proved the world wrong.

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    Latest Episodes:
    One of the Youngest Children to be Given Treatment for Spinal Muscular Atrophy I with Kathryn Alexander Jan 27, 2022
    Show notes

    ONCE UPON A GENE - EPISODE 119

    One of the Youngest Children to be Given Treatment for Spinal Muscular Atrophy I with Kathryn Alexander


    Kathryn Alexander is the mother of three kids and her rare disease story starts when she gave birth to twins and a newborn screening on her son came back positive for Spinal Muscular Atrophy (SMA). It's one of the five percent of rare diseases that has a treatment and her son is the youngest to receive it.


    EPISODE HIGHLIGHTS


    Can you tell us about your family?

    I am a mother of three little ones. I have a son named Jack who is 4 years old and twins who were born the first day of the pandemic lockdown in 2020. My twin son, Connor, was diagnosed with SMA Type 1 through newborn screening.


    Did anyone educate you on opting into newborn screening?

    I didn't know that newborn screening existed or that my son was getting screened. No one talked to me about the newborn screening for all these rare diseases or the treatments that exist. Getting the screening is important because if you get a diagnosis and begin treatment right away, your child has the best chance for successful intervention.


    What do you hope to accomplish through sharing your story?

    I want Connor's story to help other people to understand the importance of doing newborn screening and seeking urgent treatment. There aren't currently uniform guidelines across the country for newborn screening and I don't understand the ins and outs of why, but I'm figuring out how to use Connor's story to contribute to change. I have strong feelings around sharing my experience and it helps me cope.


    How did you process the birth of twins, the pandemic, Connor’s diagnosis and beginning treatment all at once?

    Losing someone close to me when I was younger helped me through my experience with Connor because I knew how to cope under extreme duress and I knew how to push and keep going. I keep my focus on the positive in situations and don't sweat the small stuff.



    LINKS & RESOURCES MENTIONED


    Wild: From Lost to Found on the Pacific Crest Trail by Cheryl Strayed

    https://www.amazon.com/Wild-Found-Pacific-Crest-Oprahs-ebook/dp/B005IQZB14

    Tiny Beautiful Things: Advice on Love and Life from Dear Sugar by Cheryl Strayed

    https://www.amazon.com/Tiny-Beautiful-Things-Advice-Sugar/dp/0307949338

    When Bad Things Happen to Good People by Harold Kushner

    https://www.amazon.com/When-Things-Happen-Good-People/dp/1400034728

    When Things Fall Apart: Heart Advice for Difficult Times by Pema Chodron

    https://www.amazon.com/When-Things-Fall-Apart-Difficult/dp/1611803438

    George Mumford Podcasts

    https://georgemumford.com/press/

    ONCE UPON A GENE - Episode 101 - Finding Beauty and Connection When Raising a Medically Complex Kiddo with Melanie Dimmitt - Author of Special

    https://effieparks.com/podcast/episode-101-melanie-dimmitt-m9dga

    ONCE UPON A GENE - EPISODE 059 - Palliative Care & Courageous Parents Network with Founder Blyth Lord

    https://effieparks.com/podcast/episode-059-blyth-lord



    Rare and Relatable on Discord

    https://discord.com/invite/7UFUPAFs8K

    The Disorder Channel

    https://www.thedisordercollection.com/

    EveryLife Foundation

    https://everylifefoundation.org/


    TUNE INTO THE ONCE UPON A GENE PODCAST

    Spotify

    https://open.spotify.com/show/5Htr9lt5vXGG3ac6enxLQ7

    Apple Podcasts

    https://podcasts.apple.com/us/podcast/once-upon-a-gene/id1485249347

    Stitcher

    https://www.stitcher.com/podcast/once-upon-a-gene

    Overcast

    https://overcast.fm/itunes1485249347/once-upon-a-gene


    CONNECT WITH EFFIE PARKS

    Website

    https://effieparks.com/

    Twitter

    https://twitter.com/OnceUponAGene

    Instagram

    https://www.instagram.com/onceuponagene.podcast/?hl=en

    Built Ford Tough Facebook Group

    https://www.facebook.com/groups/1877643259173346/



    Effisode - Oh Goody - Anxiety is Visiting Jan 25, 2022
    Show notes

    Intro music by Scott Holmes


    Ambiguous Medical Plans - How to Figure Out a System Even When it Seems Impossible with Parvathy Raman Krishnan Jan 20, 2022
    Show notes

    ONCE UPON A GENE - EPISODE 118

    Ambiguous Medical Plans - How to Figure Out a System Even When it Seems Impossible with Parvathy Raman Krishnan


    Parvathy Krishnan joins me to discuss being an administrator for your kids and the uncertainty that stems from not having a care plan in place, like when you have an ultra-rare disease kid like she does. She has endured more than most on her rare parenting journey, yet she perseveres every day with courage to advocate and make a difference. To know her is to love her.


    EPISODE HIGHLIGHTS


    Tell me about your rare disease parenting journey.

    About 8 years ago, my son began experiencing bloody stool and he had his first colonoscopy at 6 years old. He had polyps in his colon, so he continued having colonoscopies to see if he improved. Genetic testing didn't reveal any answers. At 8 years old, he had his first major surgery, a proctocolectomy to remove his large intestine and rectum and he got an ostomy bag. Through additional genetic testing, it was revealed that he had a rare condition called Constitutional Mismatch Repair Deficiency (CMMRD). Because it's such a rare disease, there's no treatment or standard of care. My daughter was born around the time my son was having his first colonoscopy done. When she was 6 months old, we were told she had a genetic condition called Bardet-Biedl syndrome (BBS). Through her lifetime, she was identified to have three additional rare diseases and passed away at 4 years old.


    What does it feel like when a doctor says they don't have an answer or don't know what to do?

    It feels honest. When they did genetic testing, we were told our son was the only patient with CMMRD in North Carolina. Then we went to Boston where we were told he was the only patient in the country. We went to Toronto where they run the largest research study on the condition and were told he was the only patient in the world. We realized it would be really difficult to put the puzzle pieces together with no other patients to fill the gaps. The condition is ultra rare and it's been difficult.


    Is there hope in not knowing?

    For us, knowledge is power. We didn't know the affected genes were in our family, but because of our children, five adults in our family now know they're carriers of the defective gene. It's powerful for them to have the information when planning for a family in the future. There’s hope in knowing because we can be proactive in our son’s treatment and screening.


    What resources have you discovered to be helpful to care of your family?

    It's okay to say no when you need to and ask questions before you say yes. My biggest support has been social media and connecting with other advocates that give me hope. We're all rare, but we're not that different. Our struggles and wins remain the same and in the end, we're all connected as patients or parents. Following others, despite their diagnosis or journey, helps me to keep things in perspective. Global Genes and Courageous Parents Network are both great resources and provide comfort as we move through grief.



    LINKS & RESOURCES MENTIONED

    Rare and Relatable on Discord

    https://discord.com/invite/7UFUPAFs8K

    The Disorder Channel

    https://www.thedisordercollection.com/

    Global Genes

    https://globalgenes.org/

    Courageous Parents Network

    https://courageousparentsnetwork.org/

    CPN Family Podcast Series

    https://courageousparentsnetwork.org/podcasts

    EveryLife Foundation

    https://everylifefoundation.org/

    CONNECT WITH EFFIE PARKS

    Website

    https://effieparks.com/

    Twitter

    https://twitter.com/OnceUponAGene

    Instagram

    https://www.instagram.com/onceuponagene.podcast/?hl=en

    Built Ford Tough Facebook Group

    https://www.facebook.com/groups/1877643259173346/


    A Rare Collection - New Beginnings Jan 13, 2022
    Show notes

    ONCE UPON A GENE - EPISODE 117

    A Rare Collection - New Beginnings


    There's power in storytelling- for the listener and the storyteller. A Rare Collection is a monthly series featuring people from the rare disease community, sharing a story with a common theme. In this episode, guests share their stories of new beginnings.


    EPISODE HIGHLIGHTS


    Leah Moore

    In the spring, Leah and her family planted flowers in the garden, but only one flower grew. The single sunflower signified rebirth in the world, but also in the family. After the flower was damaged, someone surprisingly sent a new sunflower in the mail for the family to plant. The generous gift also fostered a realization about supportive friends and the meaning of new beginnings.


    Katie Lloyd

    Katie spent the prior year deep in the trenches of grief with no diagnosis for her son. She was overwhelmed and not coping well. The year was really hard with a raging pandemic that separated her from family and support. It wasn't long after her son finally received a diagnosis, that Katie was making friends with people in the rare disease community all across the world. With the new year, Katie spent time to process her emotions around what she had been through so she could let them go, moving forward, embracing a new beginning of hope for her family.


    Sean Baumstark

    Sean shares stories of starting over, including after a diagnosis of Friedreich Ataxia disease, which robs him of his ability to speak, write and walk. Through his experiences, it's apparent to Sean that things change, and that just as routine as the sun rises, new beginnings will come, but not always as you expect. But every new beginning is an opportunity to assess himself, what's important and how he wants to navigate change. What he makes of new beginnings is where the new happens, where discipline matters and where life gets exciting.


    Angela Rohaidy

    When you become a mom to a child with a genetic difference, you become several different people- the nurse, therapist, pharmacist and advocate. As a mom and caregiver, Angela's self care took a back seat to her daughter Eloise. This year is a new beginning with a focus on her daughter's needs, but also herself.



    TUNE INTO THE ONCE UPON A GENE PODCAST

    Spotify

    https://open.spotify.com/show/5Htr9lt5vXGG3ac6enxLQ7

    Apple Podcasts

    https://podcasts.apple.com/us/podcast/once-upon-a-gene/id1485249347

    Stitcher

    https://www.stitcher.com/podcast/once-upon-a-gene

    Overcast

    https://overcast.fm/itunes1485249347/once-upon-a-gene


    CONNECT WITH EFFIE PARKS

    Website

    https://effieparks.com/

    Twitter

    https://twitter.com/OnceUponAGene

    Instagram

    https://www.instagram.com/onceuponagene.podcast/?hl=en

    Built Ford Tough Facebook Group

    https://www.facebook.com/groups/1877643259173346/



    Effisode - Rare Disease Day Jan 11, 2022
    Show notes

    A Dads Fight to Survive Cancer and the Heavy Burdens of Rare Disease with Luke Rosen Jan 06, 2022
    Show notes

    ONCE UPON A GENE - EPISODE 116

    A Dads Fight to Survive Cancer and the Heavy Burdens of Rare Disease with Luke Rosen


    Luke Rosen is a dadvocate who founded the KIF1A organization to seek a cure for his daughter Susannah who was diagnosed with KIF1A. Luke shares personal details about his recent medical difficulties and opens the raw dialogue around what happens when a caregiver dies.


    EPISODE HIGHLIGHTS


    Can you tell us about your daughter and the KIF1A diagnosis?

    Susannah was diagnosed at two years old with KIF1A and at the time we could only find about 15 people in the world and in literature who had the disease mutation. KIF1A is a neurodegenerative disease with no treatment or cure. We knew we had to find more kids, so my wife Sally and I started the KIF1A organization to pull a community of patients, researchers and clinicians together.


    Can you share about the medical difficulties you're personally facing?

    About 9 months ago, I thought I had kidney stones, which I had before. I took medication, got better and then I couldn't get out of bed one day because I was in so much pain. I went in for a CAT scan and I discovered that I had perforated diverticulitis. I had surgery, experienced some complications and went home after 5 days in the hospital. When I went back for my postoperative follow up appointment, the doctor told me a lot of cancer was removed during the surgery and that I had stage 3 colon cancer. I immediately started to think of Susannah and the research I was doing for her, wondering what would happen when I died.


    As a man and dad, do you identify with keeping struggles to yourself or internalizing feelings?

    I understand the idea of men going it alone, dealing with things independently, but I don't handle things that way. I always go to my father because he makes me a better father through his advice and guidance. My rocks to lean on are my father, my brother and my wife Sally and without them, I couldn't deal with everything myself. I think it's important to check in with yourself and remind those you love to check in with you too.


    What would you share with other parents who can relate to your story?

    For parents of rare disease kids, plan ahead and find a focused community so that if a storm does hit, the team of people around you can keep seeking treatment for your child without you. If you do that, you can relax a little, survive and enjoy the time you have left knowing the work will forge ahead.



    LINKS & RESOURCES MENTIONED

    KIF1A Website

    https://www.kif1a.org/


    TUNE INTO THE ONCE UPON A GENE PODCAST

    Spotify

    https://open.spotify.com/show/5Htr9lt5vXGG3ac6enxLQ7

    Apple Podcasts

    https://podcasts.apple.com/us/podcast/once-upon-a-gene/id1485249347

    Stitcher

    https://www.stitcher.com/podcast/once-upon-a-gene

    Overcast

    https://overcast.fm/itunes1485249347/once-upon-a-gene


    CONNECT WITH EFFIE PARKS

    Website

    https://effieparks.com/

    Twitter

    https://twitter.com/OnceUponAGene

    Instagram

    https://www.instagram.com/onceuponagene.podcast/?hl=en

    Built Ford Tough Facebook Group

    https://www.facebook.com/groups/1877643259173346/



    Create Conversation, Community, and Change with Author of Loving You Big - Leah Moore Dec 30, 2021
    Show notes

    ONCE UPON A GENE - EPISODE 115

    Create Conversation, Community, and Change with Author of Loving You Big - Leah Moore


    Leah Moore won a prestigious award for being teacher of the year in New York, she's the author of the memoir Loving You Big, and she's the parent of three kiddos, one of which was diagnosed with Cri du chat syndrome.


    EPISODE HIGHLIGHTS


    Can you share about yourself and your family?

    I am a high school English and theater teacher in New York and I live in Westchester, which is north of the city with my three kids and my husband. Our ten year old daughter Jordan has a rare diagnosis called Cri du chat which is a deletion of the fifth chromosome. We also have twin boys who are now six, one which has an unnamed disability and the other has Idiopathic thrombocytopenic purpura (ITP), which is a rare autoimmune disease.


    You talk about loving the disability out of Jordan. Was that the inspiration for your book?

    I started writing because my students were doing a personal narrative assignment and they were struggling. To show them how to do it, I wrote what was intended to be a silly example, but what poured out of me was a piece about the irony of language and how I have words and Jordan doesn't. When I read it to them, I realized I was holding on to stories I needed to tell.


    What ideas do you have for people to become inclusion allies?

    It starts with avoiding staring at the playground, asking how to help, asking a person's name and asking someone to play. Saying hi is an easy first step.


    How can we balance chronic stress with joy?

    I personally believe that if we only stay in a negative place, it can color everything. I had to work at how to let it out. For me, it's through writing, through connecting to the people in my circle who I don't feel judgment from, or through watching Netflix on the couch. You have to do the work to figure out where you can let it out safely. I don't quite know the formula, I just know it's imperative.


    How are you and your husband intentional about tending your marriage?

    I think of the days of diagnosis and medical fears as the triage days. One of the fires I needed to put out was not my husband because he was able to take care of himself. And I realized at some point, we were just raising each other's children and our conversations were about milk and epilepsy medication. So I think it's a combination of three things- not taking on too much myself, having a life outside our children, and tapping into each other's humor.


    LINKS & RESOURCES MENTIONED

    Loving You Big Website

    https://lovingyoubig.com/

    Spotlight Series

    https://lovingyoubig.com/spotlight-series/

    Loving You Big book on Amazon

    shorturl.at/brzP8

    Emotional Agility book on Amazon

    shorturl.at/jGL19


    TUNE INTO THE ONCE UPON A GENE PODCAST

    Spotify

    https://open.spotify.com/show/5Htr9lt5vXGG3ac6enxLQ7

    Apple Podcasts

    https://podcasts.apple.com/us/podcast/once-upon-a-gene/id1485249347

    Stitcher

    https://www.stitcher.com/podcast/once-upon-a-gene

    Overcast

    https://overcast.fm/itunes1485249347/once-upon-a-gene


    CONNECT WITH EFFIE PARKS

    Website

    https://effieparks.com/

    Twitter

    https://twitter.com/OnceUponAGene

    Instagram

    https://www.instagram.com/onceuponagene.podcast/?hl=en

    Built Ford Tough Facebook Group

    https://www.facebook.com/groups/1877643259173346/



    Effisode - The Kindness of Strangers Dec 28, 2021
    Show notes

    Intro music by Scott Holmes


    The Bravery of the Brokenhearted - A Big Brothers Perspective on Grief From the Loss of a Sibling with Sanfilippo Syndrome with Noah Siedman Dec 23, 2021
    Show notes

    ONCE UPON A GENE - EPISODE 114

    The Bravery of the Brokenhearted - A Big Brothers Perspective on Grief From the Loss of a Sibling with Sanfilippo Syndrome with Noah Siedman


    Noah Siedman was a big brother to Ben who had Sanfilippo Syndrome, a devastating disease that leads to childhood dementia and premature death. He joins me to talk about his sibling experience and dealing with grief.


    EPISODE HIGHLIGHTS


    As a sibling under potential pressure to not be a burden, do you still carry those feelings even after Ben's passing?

    It's hard as a sibling to see everything your parents are facing that's out of your control. As a sibling, there's a need to be on top of your own care and your own emotions. There were no casual complaints in my family growing up. It was either a disaster or business as usual. Filling in that middle space where you have a bad day and want to talk about it didn't exist. We've had to work on that as a family because that's not how we've functioned.


    What coping mechanisms help you to write and talk about your experience?

    I came to the realization that I was going to be emotionally vulnerable, which is uncomfortable. Knowing I would have to talk about my experience and brother, I had to accept it, put it out front, and get really good at talking about it comfortably. I got more comfortable talking about the progression of my brother's disease and my feelings around him, and I used it as a shield.


    What would you say to the young person who is living the same life you were living and what questions should people ask that person?

    The first thing that I would say, and maybe the best thing to ask that person, is about their roles. When do you feel like a sibling? When do you feel like a caregiver? When do you feel like you're an advocate? When do you feel like you are just you? I got stuck in trying to be a lot of those things at once, where the easiest role to ignore was being just me. But everything you push down morphs into something worse. Frustration turns into resentment, fear turns into trepidation, sadness becomes melancholy.


    What are the misconceptions people have about death?

    The biggest problem with grief is that no amount of experience is applicable. It defies the ability to be prepared for it or to use your past to help you cope. I don't think grief gets easier, I think you get better at it. Those that try to give advice to people that are grieving are hanging on to the idea that that time will heal. It's not that your grief goes away, it's that you get better at it.


    How has your relationship with your sister changed?

    Ben's death brought us closer and we do a good job of communicating despite handling things differently. There's no right or wrong way to navigate life with a sibling who has a genetic disorder, so we don't judge each other and we're honest with each other.


    As a parent, how do you help siblings to have a better experience?

    Abandon the idea that you owe siblings normalcy. My parents put a lot of effort into delivering normal childhood experiences. Instead, put that energy into helping your children articulate what they want. More important than chasing normal is helping siblings decide what's important to them and how to pursue it.


    LINKS & RESOURCES MENTIONED

    ONCE UPON A GENE - Episode 109 - A Rare Collection - What I Know For Sure with Noah Siedman, Grayson Skibington and Nash Hawkins

    https://effieparks.com/podcast/episode-109-what-i-know-for-sure


    CONNECT WITH EFFIE PARKS

    Website

    https://effieparks.com/

    Twitter

    https://twitter.com/OnceUponAGene

    Instagram

    https://www.instagram.com/onceuponagene.podcast/?hl=en

    Built Ford Tough Facebook Group

    https://www.facebook.com/groups/1877643259173346/


    A Rare Collection - Lullabies Dec 16, 2021
    Show notes

    ONCE UPON A GENE - EPISODE 113

    A Rare Collection- Lullabies


    There's power in storytelling- for the listener and the storyteller. A Rare Collection is a monthly series featuring people from the rare disease community, sharing a story with a common theme. In this episode, grandparents share their lullaby stories.


    EPISODE HIGHLIGHTS


    Maria

    In the classic lullaby, Hush Little Baby, when an item is broken, the mama will make it better. But there are things that a mama (or a grandma) can't fix. Emma was diagnosed at 6 months old and her parents’ and grandparents’ hopes and dreams went dark. The grief was all-consuming. There's no way to fix Emma, but her love is pure and perfect and her smile can light up the darkest night. Emma doesn't need to hush and grandma doesn't need to fix, but just be next to Emma along her journey.


    Duane

    When Emma was born, her grandfather, better known as her grandpopotamus, held her on his shoulder and sang the lullaby, Go to Sleep. Emma loves music and her grandfather brings her joy through singing. He strives to find the joy and light in Emma's world so he can broaden it and ensure she enjoys her life to the fullest.


    Mariana

    When her first child was born, Mariana realized she didn't know any lullabies. After her son had an accident, she learned the words to Hush Little Baby and sang it to comfort him in the hospital. As a grandmother, she continues singing Hush Little Baby to her grandchildren when she tucks them into bed. A lullaby isn't about how pretty your voice is, it's about your heart sharing comfort, care and love to a child that you get back a million times over.


    Poppy

    When taking care of his granddaughter Sloan, Poppy sang A Bushel and a Peck as he put her to bed. He sang that song to his own children hundreds of times, but this time was different. Sloan had just been diagnosed with a rare degenerative genetic disorder. The future will bring uncertainty and hardship. As Poppy sang, feelings of panic, worry and hopelessness took over. He loves her so much- a bushel and a peck.


    Alice

    Elijah is beating the odds, proving he has a purpose, blessing and encouraging every person he meets. His grandma has a message for him- to never stop singing his song, never stop dancing and never forget how much he is loved.



    TUNE INTO THE ONCE UPON A GENE PODCAST

    Spotify

    https://open.spotify.com/show/5Htr9lt5vXGG3ac6enxLQ7

    Apple Podcasts

    https://podcasts.apple.com/us/podcast/once-upon-a-gene/id1485249347

    Stitcher

    https://www.stitcher.com/podcast/once-upon-a-gene

    Overcast

    https://overcast.fm/itunes1485249347/once-upon-a-gene


    CONNECT WITH EFFIE PARKS

    Website

    https://effieparks.com/

    Twitter

    https://twitter.com/OnceUponAGene

    Instagram

    https://www.instagram.com/onceuponagene.podcast/?hl=en

    Built Ford Tough Facebook Group

    https://www.facebook.com/groups/1877643259173346/



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