@violetemors_backup: Having Scleroderma😌🤦🏻‍♀️ sometimes u r so sick that u feel u can’t take it anymore,u feel like giving up😌but having scleroderma giving up isn’t really an option🤷🏻‍♀️ it’s not like u can’t stop being sick💁‍♀️ it doesn’t work that way. So u just have to keep f*gh*ing..it’s what u r always doing, all day long,every single day. When u have Scleroderma every day is a struggle and f*gh* to survive life😌🤦🏻‍♀️ The burden on ur family members who’s standing by u because u can’t do much for urself u need support 😌. And to talk of how expensive health care is for Scleroderma ummm😌🤦🏻‍♀️. Scleroderma is tough but in all Thanks to God for always taking care of me 🙏🏻🤍🥹 always coming through for me even in my downtime when I have no one to tell how I really feel😒 I’m Violetemor Nicholas Onitsha A Scleroderma warrior I’ve been struggling with this autoimmune illness called “Scleroderma” since 2014😌 And for me Giving up is never an option. It’s Scleroderma awareness month June🤍 Scleroderma is an autoimmune disorder that affects the whole body,causing tighten and hardened of the skin and also affects the internal organs. There is no cure to Scleroderma yet. We r hoping for a cure🙏🏻 #scleroderma #autoimmunedisease #sclerodermaawareness #sclerodermawarrior

Violet Emor Onitsha

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Tuesday 17 June 2025 13:35:05 GMT