In recent news, Graeme Souness has been reported to have launched a fundraising campaign to find a cure for ‘butterfly skin’. Currently, people online want to know about Graeme Souness Battle with Epidermolysis Bullosa. You should read the article and continue reading for more details. Follow us to know all the ideas. Graeme James Souness, a former professional soccer player, manager and television analyst, hails from Scotland. A midfielder, Souness led the prosperous Liverpool team in the early 1980s and served as Rangers’ player-manager for most of the decade. He also captained Scotland at international level, having spells at Sampdoria, Middlesbrough and Tottenham Hotspur. He continues reading for more details.
Graeme Souness Disease and Health 2023
Before taking the helm at Liverpool, Souness began his managerial career by joining Rangers, where he helped them win four League Cups and three Scottish Championships. Furthermore, he later managed Newcastle United, Galatasaray, Southampton, Torino, Benfica and Blackburn Rovers. Here’s soccer star Graeme Souness’ battle with epidermolysis bullosa. Graeme Souness, a soccer star, intends to swim across the English Channel to help others suffering from a rare skin disease.
The former Scotland, Liverpool and Rangers personality fought back tears as he described Epidermolysis Bullosa as the cruelest disease of all time. After meeting Isle Grist from the Scottish Highlands, he was motivated to attempt the 16-hour challenge. The 14-year-old girl’s ‘butterfly skin’ condition results in skin tearing or blistering at the slightest touch. The former player and coach fought back tears as he called Isla the most unique person he had ever met.
He added that she inspires him to be a better version of himself every day. For the charity Debra, which helps Isla and the 5,000 people in the UK currently living with a genetic disease, the former TV commentator hopes to raise £1.1m. Although mild versions can improve with age, there is still no cure. Here is Graeme Souness’s health and disease update as of 2023. He Continue reading to learn the same.
No, there is no speculation that Graeme will suffer from any disease from 2023. However, he did announce his plans to swim in the canal to raise money for DEBRA. DEBRA is a charity that supports people with epidermolysis bullosa, also known as butterfly skin. After meeting Isla Grist, a 14-year-old girl with recessive dystrophic epidermolysis bullosa, Souness supported the organization. She will now join a team of six, including Isla’s father Andy, to swim the 21-mile distance between Dover and Calais, which can take up to 16 hours.
Furthermore, Souness commented that this will undoubtedly be the most challenging task he has ever undertaken. But he was determined to finish the swim. The serious inherited disorder with blistering of the skin known as EB is also called “butterfly skin”. In severe situations, it can affect any area of the body, including the eyes and internal organs, and can cause the skin to blister and tear easily on the hands and feet. The NHS classifies it as an autoimmune disease because it causes the immune system to attack healthy human tissue.