{"id":244734,"date":"2025-09-08T11:07:32","date_gmt":"2025-09-08T11:07:32","guid":{"rendered":"https:\/\/community.skin.club\/?p=244734"},"modified":"2025-09-08T12:10:47","modified_gmt":"2025-09-08T12:10:47","slug":"cs-player-with-rare-disease-shared-his-heartbreaking-story-on-reddit","status":"publish","type":"post","link":"https:\/\/community.skin.club\/en\/news\/cs-player-with-rare-disease-shared-his-heartbreaking-story-on-reddit","title":{"rendered":"CS Player With Rare Disease Shared His Heartbreaking Story on Reddit"},"content":{"rendered":"<p><span style=\"font-weight: 400\">A Reddit user under the nickname Professional_Face337 shared his story about how a rare disease has taken away his ability to play CS at the same level as before. The player suffers from Epidermolysis Bullosa (Dystrophic EB) \u2014 a severe genetic condition that causes damage to the skin and hands. Now he can barely hold a mouse or press keys, so in search of help, he reached out to Team Vitality and told his story to the community.<\/span><\/p>\n<h2><strong>From Childhood Passion to High Achievements<\/strong><\/h2>\n<p><span style=\"font-weight: 400\">Professional_Face337 began his post by recalling his passion for Counter-Strike, before explaining how illness eventually took its toll:<\/span><\/p>\n<p><span style=\"font-weight: 400\">I\u2019ve been a CS player and fan since my early childhood. I grew up playing CS 1.6 and later CS:GO, and I\u2019ve followed the pro scene for years. At my peak, I was a 2200 Elo Faceit player, grinding daily and dreaming of maybe going pro one day. But life threw a huge challenge at me.<\/span><\/p>\n<p><span style=\"font-weight: 400\">I was born with a rare genetic skin condition called Epidermolysis Bullosa (Dystrophic EB). Over the years, this condition has caused severe damage to my hands. Now, I\u2019m at the point where I can barely hold a mouse or press keys properly. My current elo is <\/span><span style=\"font-weight: 400\">down to ~1400-1500, not because I lost my game sense, but because I\u2019ve physically lost the ability to play like I used to.<\/span><\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"alignnone wp-image-244753 size-full\" src=\"https:\/\/community.skin.club\/wp-content\/uploads\/2025\/09\/image_2025-09-08_135712939.jpg\" alt=\"\" width=\"1440\" height=\"1920\" srcset=\"https:\/\/community.skin.club\/wp-content\/uploads\/2025\/09\/image_2025-09-08_135712939.jpg 1440w, https:\/\/community.skin.club\/wp-content\/uploads\/2025\/09\/image_2025-09-08_135712939-225x300.jpg 225w, https:\/\/community.skin.club\/wp-content\/uploads\/2025\/09\/image_2025-09-08_135712939-768x1024.jpg 768w, https:\/\/community.skin.club\/wp-content\/uploads\/2025\/09\/image_2025-09-08_135712939-1152x1536.jpg 1152w\" sizes=\"(max-width: 1440px) 100vw, 1440px\" \/><\/p>\n<h2><strong>A Last Chance for Surgery<\/strong><\/h2>\n<p><span style=\"font-weight: 400\">After describing the daily struggles caused by his condition, Professional_Face337 also revealed that there may be a medical solution \u2014 though one far out of reach without help:<\/span><\/p>\n<p><span style=\"font-weight: 400\">There\u2019s a surgery that can restore some function to my hands, and there\u2019s a specialist in Paris who can perform it. Unfortunately, it\u2019s very expensive, and I have no way to afford it. My government doesn\u2019t fund treatments abroad, and no doctors in my country can perform this specific operation.<\/span><\/p>\n<p><span style=\"font-weight: 400\">I\u2019ve sent a message to Team Vitality sharing my story and asking for help. I\u2019m not sure what will happen \u2014 maybe nothing \u2014 but I still wanted to share this here because CS is a huge part of my life.<\/span><\/p>\n<p><span style=\"font-weight: 400\">Epidermolysis Bullosa, the birth defect he was born with, is a painful and unusual genetic disorder. Even minor rubbing can cause his skin to tear and blister. Through the years, the disease has seriously impaired his hands, making routine activities a chore \u2014 and playing the game he loves, at a championship level, all but impossible.<\/span><\/p>\n<h2><strong>Community Reaction<\/strong><\/h2>\n<p><span style=\"font-weight: 400\">His tale resonated on Reddit, whose thousands of users commented in his support. Many expressed admiration and appreciation both for his tenacity and persistence, and his optimism either that professional esport organizations, or existing players, would come through and assist.<\/span><\/p>\n<p><span style=\"font-weight: 400\">The community didn\u2019t stop at sweet compliments \u2014 it offered practical solutions too. People suggested making a page on platforms like BuyMeACoffee, reaching out to streamers, or promoting the story on Twitter and YouTube in a bid to receive more exposure. Despite all the hurdles he faces in his native land, there was something sure: the CS community is more than willing to come out and show support and prove that no one has to handle it by themselves.<\/span><\/p>\n<h2><strong>Conclusion<\/strong><\/h2>\n<p><span style=\"font-weight: 400\">The journey of Professional_Face337 is a reminder of how fragile even the strongest dreams can be when life brings unexpected challenges. Yet, it also highlights the strength of the esports community when it comes together to support one of its own. For him, Counter-Strike is not just a pastime \u2014 it\u2019s a symbol of hope, resilience, and the will to keep fighting.<\/span><\/p>\n","protected":false},"excerpt":{"rendered":"<p>A Reddit user under the nickname Professional_Face337 shared his story about how a rare disease has taken away his ability to play CS at the same level as before. The player suffers from Epidermolysis Bullosa (Dystrophic EB) \u2014 a severe genetic condition that causes damage to the skin and hands. Now he can barely hold [&hellip;]<\/p>\n","protected":false},"author":46,"featured_media":244813,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"footnotes":""},"categories":[15],"tags":[],"class_list":["post-244734","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-news"],"acf":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.4 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>CS2 &amp; CS:GO Articles, News, Events | Skin.Club Community - CS Player With Rare Disease Shared His Heartbreaking Story on Reddit News<\/title>\n<meta name=\"description\" content=\"CS player with rare disease shared his story on Reddit, seeking help for surgery and finding huge support from the Counter-Strike community.\" \/>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/community.skin.club\/en\/news\/cs-player-with-rare-disease-shared-his-heartbreaking-story-on-reddit\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"CS2 &amp; 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