04/07/2025
Hi everyone, I have created this page to spread awareness on Lupus and Autoimmune Diseases. As I will be sharing my own experience and journey with all the information that I have acquired over the past few years. It all begins with the time I was diagnosed with Systemic Lupus Erythematosus (SLE) in February 2021. It started with Dengue fever, rashes, feeling extremely fatigue all the time and vomiting to being diagnosed with something I had no clue about, as a 20-21 year old my life had completely changed, it began with a lot of self doubt to researching while all of this was happening when Covid was going on. I honestly dont know how but for a period I thought this was something I could deal with very easily, as I been very strong emotionally since childhood, never afraid of doctors, injections or hospital. It just gave me a sense of strength that I could tackle anything in life only before I started discovering more symptoms which was devastating. Being a girl who never showed her true emotions it took me on a toll of emotional stress which I couldn't share. Until one day my hair started to fall, being someone who loved her Long curly hair and wouldnt let anyone touch them since childhood to seeing them being cut short. That day something in me had changed, as nothing mattered more now. Today when I think about it, I feel so stupid that as women or young girls, we associate our beauty with hair, looks, complexion, figure and other irrelevant things but usually forget that beauty is actually within us.
Stay turned as I share more about my journey, as there is still so many things and experiences to share with all my fellow Lupus Warriors.
So if anyone of you reading this has recently being diagnosed with Lupus and still struggling to understand it, do DM on this page or comment below for any questions or help required.
