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!
In this episode I go over my UCLA SM Hospital stay and why I believe UCLA SM hospital isn’t fit for long term stays. I stayed at UCLA SM for about a month and throughout my stay I went through various stressful events that could’ve been avoided with proper resources, and proper staff training. Follow me on insta @akidney4paulina — ask me your questions, give me your comments — next episode coming next Sunday
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!
