Simon Del Favero
From MEpedia, a crowd-sourced encyclopedia of ME and CFS science and history
Simon Del Favero is an Australian citizen who developed myalgic encephalomyelitis (ME) after a severe bout of glandular fever in 2011. He was also diagnosed with postural orthostatic tachycardia syndrome (POTS) in 2014. Before becoming ill, Simon had studied architecture at the University of Sydney and was working part-time as an architectural model maker. He was 21, healthy, and physically very fit prior to developing ME.[1][2]
Simon travels to the US to see Dr. Hector Bonilla for management of his ME. In 2017, he met Prof. Ron Davis, director of Stanford's End ME/CFS Project.[1]
Media coverage[edit | edit source]
- Nov 22, 2018, 'I was in denial and ashamed by my CFS'[1]
Online presence[edit | edit source]
See also[edit | edit source]
Learn more[edit | edit source]
References[edit | edit source]
- ↑ 1.0 1.1 1.2 Del Favero, Simon (November 22, 2018). "'I was in denial and ashamed by my CFS'". News. Retrieved November 26, 2018. Cite has empty unknown parameter:
|dead-url=(help) - ↑ Del Favero, Simon (March 27, 2017). "Six years ago I was diagnosed with a debilitating disease called Myalgic Encephalomyelitis". Instagram. Retrieved December 31, 2018. Cite has empty unknown parameter:
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