at’s journey as a mother has been filled with challenges that most people can’t imagine. Her child was born like any other baby, but he was losing motor neurons every day without her knowing. What should have been a time of joy quickly became a reality of hospital visits, medical care, and uncertainty.
Despite her love and devotion, Cat had to take on the role of a nurse while missing out on precious moments of simply enjoying motherhood. Everyday life became a balance of medical appointments, monitoring her child’s health, and coping with the emotional weight of a rare condition that few understand.
Cat shares her story to shed light on the realities families living with SMA face, to show that these struggles are valid, and to create a space where parents of children with rare and severe conditions feel seen and supported.
Her journey is a reminder that you are not alone. Many families face these challenges in silence, finding strength in sharing their truth and connecting with others who understand.
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Keeley’s journey with her son Isaac has been filled with challenges that most people can’t imagine. Isaac lives with Autism Spectrum Disorder (ASD), Pica Disorder, and Sensory Processing Disorder (SPD). Everyday life for them isn’t simple. It’s navigating constant sensory overload, unexpected behaviors, and the struggle to meet basic needs safely.
Despite her love and dedication, Keeley often faces judgment, misunderstanding, and a lack of support from those who don’t see the invisible struggles her family endures. Simple tasks like mealtimes, dressing, or outings can become overwhelming battles, leaving her physically and emotionally drained.
Keeley shares her story to shed light on the realities families like hers face, to show that these challenges are valid, and to create a space where parents of children with neurodiverse conditions feel seen and supported.
Click to hear Keeley’s story.
Her journey is a reminder that you are not alone. Many families face these struggles in silence, finding strength in sharing their truth and connecting with others who understand.
Share your own story here:
https://docs.google.com/forms/d/e/1FAIpQLSduT5ncgPExhxdXYRxd-GraSB--TMSKhgijL5FwlW4F87xzaA/viewform
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TikTok: @thesilentstruggles
YouTube: @thesilentstrugglespodcast

Kali’s pregnancy became a fight she couldn't win, and she was forced to terminate.She suffered from Hyperemesis Gravidarum, a severe form of morning sickness that goes far beyond nausea. It causes relentless vomiting, dehydration, malnutrition, and extreme physical and emotional exhaustion. For some, it’s life-threatening, leaving the body unable to sustain itself or the pregnancy.Despite her suffering, Kali struggled to find the support she desperately needed. Medical professionals, instead of helping, pushed her toward a decision she hadn’t wanted to make. The pressure, judgment, and lack of empathy made the condition even more dehumanising.Ultimately, Kali made the heart-wrenching choice to terminate her pregnancy. Her story reveals the raw, often invisible toll of Hyperemesis Gravidarum and the gaps in care for those who endure it.Click to hear Kali’s story.Her journey represents many who face conditions that are dismissed, misunderstood, or ignored. You are not alone. Others are walking the same path, finding strength in speaking their truth.Share your own story here:https://docs.google.com/forms/d/e/1FAIpQLSduT5ncgPExhxdXYRxd-GraSB--TMSKhgijL5FwlW4F87xzaA/viewformListen OnApple Podcasts, YouTube & SpotifyConnectInstagram: @thesilentstrugglespodcastTikTok: @thesilentstrugglesYouTube: @thesilentstrugglespodcast