
Sign up to save your podcasts
Or


Why do so many moms struggle with breast pumping? In this episode, researcher and mom Ashley Mooneyham shares her breastfeeding journey, explains the science behind milk supply and pumping, and discusses how new innovations — including her company Momease — aim to make breastfeeding and pumping easier for nursing and working moms.
Key Takeaways
You can follow and/or get in touch with Archelle by
Subscribing to the ArcHealth newsletter
Following Archelle on
#Breastfeeding #WomensHealth #BreastPump #NewMomLife #Postpartum
What happens when it takes 20 years to get the right diagnosis — and along the way, doctors (and even your family) don’t always believe you?
In this episode, we explore Eva Minkoff’s delayed diagnosis, the reality of invisible illness, and the emotional toll of not being seen in the healthcare system.
Eva shares her journey to being diagnosed with Ehlers-Danlos syndrome, a connective tissue disorder that causes chronic joint pain, dislocations, and fatigue. Her symptoms began when she was a young ballet dancer. But for nearly two decades, she lived in diagnostic limbo — receiving partial answers, normal test results, and, at times, skepticism from both clinicians and family members.
The lessons from this episode go beyond one rare condition:
Answers matter — even when they’re not good news.
If you feel dismissed, it’s okay to keep looking.
Being believed can be as powerful as being diagnosed.
Live by your own owner’s manual — and teach your children to do the same.
A physician-daughter shares what it was like to be in the room when her father chose Medical Aid in Dying. This episode offers a clear, first-person look at how MAID works and what families experience in those final moments.
In this deeply personal and illuminating episode, physician and gastroenterologist Dr. Mandy Powell shares her family’s experience with Medical Aid in Dying (MAID)—also known as Medical Assistance in Dying—through the lens of being both a daughter and a doctor who was in the room when it happened.
Mandy recounts the story of her father, Dr. Ron Gruber, a prominent plastic surgeon in the San Francisco Bay Area, whose second battle with metastatic bladder cancer led him to carefully choose how—and when—his life would end. After a rapid decline marked by repeated hospitalizations and worsening quality of life, Ron elected to pursue MAID under California’s End of Life Option Act.
Over the course of four extraordinary days, Mandy and her family experienced what she describes as a “living funeral”—a time filled with phone calls to lifelong friends, shared memories, and honest goodbyes. On the final morning, Mandy was present as her father self-administered the prescribed medication, offering a rare, first-person account of what Medical Aid in Dying actually looks like in real life.
This conversation offers a humane, clear-eyed look at an end-of-life option that is legal in California, 11 other states, and the District of Columbia, and one that more families and clinicians are beginning to talk about openly.
Resources about Medical Aid in Dying, including educational materials from Death With Dignity, are linked in the show notes.
Links/Resources
Connect with Archelle
What happens when a parent refuses to accept “there’s nothing we can do” for a child with a rare disease?
Amber’s daughter, Willow, was diagnosed at age two with Multiple Sulfatase Deficiency (MSD), an ultra-rare, progressive genetic condition with no known treatment. Instead of stopping there, Amber spent the next seven years learning the science, raising funds, and advocating relentlessly to support research that could one day change the outcome for other children.
Documentary filmmaker Patrick O’Connor followed Amber and her family throughout that journey, capturing what happens when parents are forced to become advocates, fundraisers, and drivers of medical research.
Together, they discuss the emotional moment Amber learned her efforts helped move MSD research to the point where the National Institutes of Health selected it for a pilot gene-therapy program—a milestone filled with both hope and heartbreak.
Key Takeaways
The key takeaways from this episode extend well beyond Multiple Sulfatase Deficiency and may be especially helpful for parents caring for a child with a serious rare or chronic illness:
• Being told “there’s nothing we can do” doesn’t have to be the end of the conversation. Asking questions and seeking options is not denial—it’s loving your child.
• You don’t need to be a clinician or a scientist to advocate for your child.
Asking the right questions opened doors she didn’t know existed.
• Many experts want to help—sometimes you just have to reach out.
Access to scientists and research often starts with a direct email and the willingness to follow up if the first message goes unanswered.
• Not every intervention that is possible is the right one. Recognize when a treatment may be serving the parent, not the child.
• Death is not the enemy. Suffering is. Choosing comfort, dignity, or less intervention can be just as loving and courageous as pursuing treatment.
This is an extraordinary story, but the reality it reflects is one that far too many families live every day. I hope parents listening walk away knowing that their voice matters, their questions matter, and their advocacy matters.
Links & Resources
🎬 The Zebra and the Bear documentary
https://www.thezebraandthebear.com/
🧬 United MSD Foundation (founded by Amber Olsen)
https://www.unitedmsd.org/
Heart disease is the leading cause of death in women—yet women’s symptoms are still too often dismissed, minimized, or misunderstood.
In this episode, Archelle talks to Nina Goodheart, a medical device executive who leads work in heart valve disease. Despite her own expertise, Nina’s own mother had her symptoms brushed off by a physician—simply because they didn’t look “typical.” That experience became a turning point.
In their conversation, Archelle and Nina unpack why heart disease looks different in women, how decades of research and device design have prioritized men, and why knowing your symptoms isn’t enough—you also need to know which heart tests to ask about. They also discuss how to push back when you’re told “you’re fine,” and why bringing someone with you to appointments can change outcomes.
The conversation explores the Letter to My Mother initiative—a powerful reminder that conversations within families can save lives—and why advocating for yourself or a loved one may be the most important health skill of all.
If you’ve ever felt dismissed in a doctor’s office, or wondered whether you should ask more questions, this episode is for you.
Key Takeaways
Links
Learn more about heart valve disease: https://www.medtronic.com/en-us/l/patients/conditions/heart-valve-disease.html
Medtronic Survey on Women & Heart Disease: https://news.medtronic.com/2025-05-07-New-survey-1-in-3-women-have-not-talked-to-their-doctor-about-heart-health,-the-1-killer-of-women
Connect with Archelle:
ArcHealth Newsletter: https://www.archellemd.com/newsletter
Instagram: https://instagram.com/speakupforyourhealth
Facebook: https://www.facebook.com/speakupforyourhealth
Egg freezing has traditionally been an option reserved for women with significant financial means. At the same time, the high cost and transactional nature of traditional egg donation create major barriers for many individuals and couples who want to become parents.
Lauren Makler, founder and CEO of Cofertility, set out to change both sides of that equation.
In this episode, Lauren shares her own fertility journey and how it led her to found Cofertility – a company that makes egg freezing more accessible and egg donation more ethical and human. She talks about the process of egg freezing, the emotional aspects of egg donation, and the importance of women and men being proactive, not reactive about their reproductive health. Whether you’re a woman considering egg freezing as a way to protect your future options—or you’re exploring egg donation as a path to parenthood—this conversation will help you understand your choices.
Key Takeaways
Links
Learn more about Cofertility: https://www.cofertility.com/
Connect with Archelle:
ArcHealth Newsletter: https://www.archellemd.com/newsletter
Instagram: https://instagram.com/speakupforyourhealth
Would you rather pay $1000 for your prescription - or $5? In this conversation, Miriam Paramore, CEO of RxUtility, talks about her personal experiences with healthcare costs and the challenges of medication affordability. She explains how to figure out whether using insurance, combining insurance with a manufacturer copay coupon, or simply paying cash will give you the lowest price for your prescription.
Key Takeaways:
With healthcare costs skyrocketing for everyone as we go
Links:
Miriam Paramore on LinkedIn:
RxUtility: https://rxutility.com/
GoodRx: GoodRx
WellRx: WellRx
Connect with Archelle:
ArcHealth Newsletter: https://www.archellemd.com/newsletter
Instagram: https://instagram.com/speakupforyourhealth
Facebook: https://www.facebook.com/speakupforyourhealth
#SaveOnMeds #CheaperPrescriptions #DrugSavingsTips #MedicationCosts #PrescriptionSavings #HealthTips #SpeakUpForYourHealth #HealthcareFounders #Innovation
After serving as a counter-intelligence agent in Bosnia, veteran Bryan Fuller returned home with invisible wounds—PTSD that upended his life. Then, he discovered rowing. In this episode, Bryan shares how the rhythm of rowing—and rowing across the Atlantic—helped him heal, find purpose, and give back to fellow veterans.
Key Takeaways
London Calling Row: This is where you can donate to Bryan's 2026 trans-Atlantic crossing and/or support veterans: https://londoncallingrow.com/captain-bryan/
Connect with Archelle:
ArcHealth Newsletter: https://www.archellemd.com/newsletter
Instagram: https://instagram.com/speakupforyourhealth
Facebook: https://www.facebook.com/speakupforyourhealth
#PTSD #VeteranStories #HealingJourney #Resilience #SpeakUpForYourHealth
Sexual harassment and abuse can happen in any sport — even youth athletics. In this episode, Carrie Kehring shares her experience after her teenage daughter was sexually abused by her coach. She opens up about the broader issue of grooming and power dynamics in sports and offers practical insight on how to recognize red flags, set healthy boundaries, and navigate the emotional and legal aftermath of abuse. Determined to create change, Carrie founded #WeRideTogether, a nonprofit providing free resources and tools to help parents and athletes build safer sporting environments.
Key Takeaways:
1. If your child/teenager is in sports..any sport...focus on prevention.
2. Learn to recognize grooming. It often starts small with blurring of boundaries: some favoritism, gifts, a little extra attention. It can feel flattering… until it’s not.
3. If you discover abuse or inappropriate behavior, make sure your child is safe — both physically and emotionally - then find an advocate. This can be an attorney, a counselor, or another parent who can help you navigate think through next steps.
4. Be prepared for a long journey. Healing takes time. Law enforcement is essential — but it’s also emotionally difficult. So, be ready for tough questions, and know that your child will need ongoing support.
5. Learn more. Visit WeRideTogether.today — to find resources, videos, and stories that can help you recognize risk and protect the athletes you love.
Links:
Connect with Archelle:
ArcHealth Newsletter: https://www.archellemd.com/newsletter
Instagram: https://instagram.com/speakupforyourhealth
Facebook: https://www.facebook.com/speakupforyourhealth
I’ve always had a strong bias against chiropractic care. But when I met Dr. Scott Salita, a chiropractor who was willing to have a real, evidence-based, and open-minded conversation, I decided to challenge my own assumptions. We sat down for an honest discussion about where chiropractic care truly helps, where it crosses the line, and how patients can make smart, safe choices.
Key Takeaways:
Do your homework. Ask friends for recommendations, review websites for exaggerated claims, and check your state’s chiropractic board for any disciplinary actions.
Be your own advocate. Know your diagnosis, your treatment plan, and expected results. If you’re not improving, seek a second opinion.
Watch out for red flags. Be skeptical of prepaid “treatment packages” or open-ended care plans. Chiropractors deserve to make a living—but not at the expense of your health or wallet.
Links:
Connect with Dr. Salita:
Connect with Archelle
ArcHealth Newsletter: https://www.archellemd.com/newsletter
Instagram: https://instagram.com/speakupforyourhealth
Facebook: https://www.facebook.com/speakupforyourhealth
#ChiropracticCare #alternativemedicine #backpain #neckpain #patientadvocacy #speakupforyourhealth #patientempowerment
From the publisher's feed