Dimitri is living with multiple sclerosis (MS), and he experiences dramatic changes in his body temperature every day. These swings can aggravate his other symptoms and leave him feeling suffocated. As he puts it, “a single bead of sweat can bring me to my knees.” You are now seeing hot and cold Photographed by Jamie MacFayden Inspired by Dimitri’s invisible symptoms He worked with photographer Jamie MacFayden to portray his hot and cold sensations as part of the Multiple Sclerosis Society of Australia’s (MSA) Seeing [MS] campaign, which we also posted about on the blog in July (blurred vision) and August (pain). It’s all about raising awareness and showing everyone the invisible symptoms some people are living with because of their MS. Stay tuned for more Seeing [MS] posts. Share this post on Twitter and help spread the word for MS.
“I’m burnt alive every day.” That’s how Stephen Papadopoulos, an Australian living with multiple sclerosis (MS), describes the level of pain he experiences on a daily basis. Pain is the second of nine symptoms portrayed in the Multiple Sclerosis Society of Australia’s (MSA) Seeing [MS] awareness campaign, and Stephen details his experience in the video below: You are now seeing pain Photographed by Garth Oriander Inspired by Stephen Papadopoulos’ invisible symptom We’re highlighting pain this month in an effort to reveal the invisible side of living with MS. You can also read other posts on pain – of particular note, Tam’s story about her private, intense pain. Share this post on twitter and help spread the word for MS.
Hidden – invisible – unnoticed. That’s what symptoms for many living MS are like. So how do you explain them to people who don’t understand? The Multiple Sclerosis Society of Australia (MSA) decided to stop just talking about them and start showing what it’s like to live with MS. Their project is called Seeing [MS] and includes nine photographers depicting nine invisible symptoms in a series of single images. And all of them are inspired by the experiences of people living with the condition – these photographs are what life with MS is like for them. We’ll be highlighting them all on the blog over the coming months to help expose the invisible side of disease. You are now seeing blurred vision Photographed by Toby Burrows Inspired by Emma Giunti’s invisible symptom Emma Giunti talking more about MS and blurred vision. Share this post on twitter and help spread the word for MS.