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.[1] He was also diagnosed with postural orthostatic tachycardia syndrome (POTS) in 2014. Before becoming ill, Del Favero had studied architecture at the University of Sydney and was working part-time as an architectural model maker.[2]
Del Favero travels to the US to see Dr. Hector Bonilla for the management of his ME. In 2017, he met Prof. Ron Davis, the leader of the Open Medicine Foundation's End ME/CFS Project. His experiences with ME are featured as part of Emerge Australia's Member Stories campaign.[3]
Media coverage[edit | edit source]
- Nov 22, 2018, 'I was in denial and ashamed by my CFS'[2]
Online presence[edit | edit source]
See also[edit | edit source]
References[edit | edit source]
- ↑ Del Favero, Simon (March 27, 2017). "Six years ago I was diagnosed with a debilitating disease called Myalgic Encephalomyelitis". Instagram. Retrieved December 31, 2018.
- ↑ 2.0 2.1 Del Favero, Simon (November 22, 2018). "'I was in denial and ashamed by my CFS'". SBS. Retrieved November 26, 2018.
- ↑ Del Favero, Simon (December 2, 2019). "Simon". Emerge Australia. Retrieved December 20, 2019.
