I suddenly became paralyzed from the neck down and nobody knew why. I spent 8 months in the hospital. I was a medical mystery. After exhaustive research from a tertiary hospital, I learned I have a genetic rare blood disorder called Porphyria. My type is called Variegate Porphyria, a form of Acute Hepatic Porphyria. Symptoms during an attack for me begin with excruciating abdominal pain, neurological issues and nausea.

I had one setback after another. I was admitted to ICU multiple times, with near-death experiences. I was told there was no hope. My family was told to prepare to say goodbye to me. I couldn't be more grateful for them and their unyielding love and support! They were finally able to bring me home.

I was paralyzed for nearly a year and had to relearn everything all over again. I still have some residual issues, but I remain determined.

Life is hard for all of us sometimes. As my journey unfolds, I'm sharing my story, discussing how I continued to persevere, and to show that there is always hope.

Support the show

https://HopeBlvd.org - Podcast episodes and more.

https://GeriCarlson.com - Geri's story, About her, the services she provides, and more. To inquire about Geri's counseling or coaching services, go to the Contact page and leave her a message. There is also info on the Counseling page.

https://Porphyria.org - My type is Variegate Porphyria (VP), a subtype of Acute Hepatic Porphyria (AHP). I am an ambassador (advocate) for The United Porphyria Association. I also serve on the UPA's President's Council board.