My life didn't end after my lupus diagnosis... #shorts

I have had lupus for more than half of my life but some of my best memories were made post-diagnosis. Don’t let your illness stop you from living your best life. It’s not always easy but take the time to listen to your body and take care of it. You’ll find plenty of memories worth making. ✨

#lupus #lupuswarrior #chronicillness

[CaSweety]

I was diagnosed just before high school and lupus definitely didn’t slow me down except during flares. In college I was even busier! Good for you for continuing with your life.

[cruzleonelramos]

My wife has lupus and was diagnosed in 2016. She has had a journey from hell and has had treatments, surgeries and medication for years. She at most times feels well but at least twice a year that beast wakes up and makes her life difficult. 💔 As of today in 2024, she feels good and strong enough to participate in marathons. Don’t give up, don’t back up and do not kneel to lupus ever. Always keep pushing forward and surround yourself with warriors and you’ll see what you can accomplish.

[Gaming-zg]

Exactly!! Same here with lupus and sjogren, it’s only making us stronger 😉

[LittleLulubee]

That’s awesome that you still got to play sports! 👍

[hk]

Ohw..feel emotional just found out today I most likely have it :( sadly its affecting my skin alot..heart ache

[flacaf]

So, were you able to keep playing volleyball after your diagnosis? how did you handle that? Very encouraging to see that! ❤

[mihribancan]

Merhabalar ben de Türkiye de lupus hastasıyım ve Steroid azatoprine ve plaquenil kullanıyorum sizin tedavi şekliniz nasıl