My Journey To Diagnosis Pt. 2 See The Invisible: Living With An Invisible Or Rare Disease podcast

See the Invisible: Living with an Invisible or Rare Disease « »

3+ y ago 42:53

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In the second part of this episode, we will finish the story of my journey to the diagnosis. Our journeys to find out our actual diagnosis may take years. During that time, we suffer through physical, emotional and mental pain, but because science has not put a name on it, it doesn't seem to exist. But it does, and it is creating challenges for us everyday.

While I always say that I want to focus on being positive, I think that it is important to address the obstacles that we faced to just put a name to the illness that was invading our life. It will show that no matter what, we are fighters, survivors and we deserve to be seen and heard.

6:42 Podcast after Introduction begins

Information on Multi-System Inflammatory Syndrome in children after Covid: Multisystem inflammatory syndrome in children (MIS-C) and COVID-19 - Symptoms and causes - Mayo Clinic

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Email: Seetheinvisible2020@gmail.com

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54 episodes