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My New Normal: A Lifetime of Chronic Migraine with CarmenRose Fiallo

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Contenido proporcionado por Sabreen Haziq. Todo el contenido del podcast, incluidos episodios, gráficos y descripciones de podcast, lo carga y proporciona directamente Sabreen Haziq o su socio de plataforma de podcast. Si cree que alguien está utilizando su trabajo protegido por derechos de autor sin su permiso, puede seguir el proceso descrito aquí https://es.player.fm/legal.

This episode of The Lavender Fix podcast features CarmenRose Fiallo, a 25 years old Queer Latina disability advocate - originally from Portland, OR, now residing in NY.
Exactly a year ago, CarmenRose received a formal diagnosis of her invisible disability: Chronic Migraine, that put her on her own island of loneliness where she grappled with making anyone around her understand what she was going through on a daily basis. Having chronic migraine meant facing medical gaslighting. It meant waiting for over 6 months just to check in with her doctor. Living with chronic migraine meant constantly having to explain herself and how she was feeling, because none of her symptoms were visible.
What led to this new normal? What is it like to live a life with such a diagnosis? How is CarmenRose coming to terms with her reality? What is the path forward?
Tune in to find out!

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Disclaimer: This post contains affiliate links. If you make a purchase, I may receive a commission at no extra cost to you.
Follow us on Instagram: @the.lavender.fix.podcast

  continue reading

56 episodios

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Manage episode 358975517 series 2887923
Contenido proporcionado por Sabreen Haziq. Todo el contenido del podcast, incluidos episodios, gráficos y descripciones de podcast, lo carga y proporciona directamente Sabreen Haziq o su socio de plataforma de podcast. Si cree que alguien está utilizando su trabajo protegido por derechos de autor sin su permiso, puede seguir el proceso descrito aquí https://es.player.fm/legal.

This episode of The Lavender Fix podcast features CarmenRose Fiallo, a 25 years old Queer Latina disability advocate - originally from Portland, OR, now residing in NY.
Exactly a year ago, CarmenRose received a formal diagnosis of her invisible disability: Chronic Migraine, that put her on her own island of loneliness where she grappled with making anyone around her understand what she was going through on a daily basis. Having chronic migraine meant facing medical gaslighting. It meant waiting for over 6 months just to check in with her doctor. Living with chronic migraine meant constantly having to explain herself and how she was feeling, because none of her symptoms were visible.
What led to this new normal? What is it like to live a life with such a diagnosis? How is CarmenRose coming to terms with her reality? What is the path forward?
Tune in to find out!

Buzzsprout - Let's get your podcast launched!
Start for FREE
Disclaimer: This post contains affiliate links. If you make a purchase, I may receive a commission at no extra cost to you.
Follow us on Instagram: @the.lavender.fix.podcast

  continue reading

56 episodios

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