I’m Paulina - a Lupus Nephritis Warrior. I’m here to help shed some insight on Lupus; an autoimmune disease that is invisible to everyone besides the person who has it. I hope to educate, inform, and support any Lupus Warrior’s or supporters of individuals fighting this disease. 💜 Lastly, I want to remind you all that you aren’t going through this alone - from one Warrior to another - we will get through this! FIGHT ON!
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I’m Paulina - a Lupus Nephritis Warrior. I’m here to help shed some insight on Lupus; an autoimmune disease that is invisible to everyone besides the person who has it. I hope to educate, inform, and support any Lupus Warrior’s or supporters of individuals fighting this disease. 💜 Lastly, I want to remind you all that you aren’t going through this alone - from one Warrior to another - we will get through this! FIGHT ON!
Today I go into what it is like for me to deal with fatigue in my day to day. I also jump in what it was like dealing with lupus and dating. NOT EASY but we do what we can with the hand we were dealt. Reach out on social media @akidney4paulina
Living With Lupus UNCENSORED
I’m Paulina - a Lupus Nephritis Warrior. I’m here to help shed some insight on Lupus; an autoimmune disease that is invisible to everyone besides the person who has it. I hope to educate, inform, and support any Lupus Warrior’s or supporters of individuals fighting this disease. 💜 Lastly, I want to remind you all that you aren’t going through this alone - from one Warrior to another - we will get through this! FIGHT ON!
