Vivir con ictiosis laminar: El impactante caso de Bobbi | Dos entre un millón
My name is Bobbi, I'm 49 years old, and I was born with lamellar ichthyosis, an extremely rare genetic condition that causes the layers of my skin to build up so quickly that they don't shed until they are extremely thick. The result is skin that looks like reptile scales and a grueling daily routine to avoid potentially fatal infections. We follow Bobbi in her daily struggle: from soaking and filing her skin to the constant use of petroleum jelly to prevent bleeding cracks. Following her recent divorce, Bobbi faces the biggest challenge of her life: finding a job to afford the medication that keeps her skin under control, in a race against time and infections in the scorching Arizona desert. 00:00 – Bobbi's reality: What it's like to live with lamellar ichthyosis and the impact on her body. 03:15 – Fighting for health: The exhausting daily care ritual to avoid life-threatening infections. 5:40 – An Uncertain Future: The Challenges After Divorce and the Urgency of Paying for Treatment #DKISS #TwoInAMillion #LamellarIchthyosis #MedicalCases #Health #OvercomingAdversity #Documentary Follow us on our social media: Instagram: / dkisstv TikTok: / dkisstv_es Facebook: / dkisstv Twitter: / dkisstv

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