Here's a list of my lupus rules ( these are MY RULES, THAT I LIVE BY)
Please don't get dramatic and start spreading childish Facebook rumors saying "Theresa made up some #lupus rules" NO, THESE ARE MY RULES.. OKAY..continue😂😂
1.I Don't post about EVERYTHING that's causing me pain, example..a person can stub their toe and they'll upload a video of them crying.( I'm not talking about ppl who post about pain, I'm talking about
the people who overdo it) I'm sure ppl are going to say "Theresa you're wrong for saying that, when y'all know good and well y'all want to say it too.)
2. There is a big difference when you ask for resources in order to get medication you can't afford,
instead of trying to get money out of other sick people.
3.when I say I'm here for you, that doesn't mean financially, encouraging words go a long way in my book.
4. Having a journal is a good thing, it helps with venting.
5.Family and real
friends that you can talk to also helps with venting.
#Lupus awareness month is almost over, and let's be honest, some crazy crap has taking place, because of that, ppl who work their butt off by going to different states talking to mayors and governors
demanding for more research when it comes to #lupus may become skeptical when they see a post about someone in need.
So, THANK YOU TO THE SCAMMERS, WHO USED #LUPUS AS A WAY TO GET OVER ON PPL WHO GENUINELY CARED ABOUT Y'ALL... NOW Y'ALL SCREWED EVERYTHING
To my fellow #lupies
who went hard and always go hard for #lupus, I thank you from the bottom of my heart.
I also want to thank those beautiful souls who supported us lupies this month, and every month.
My last rule..LAUGHTER IS THE BEST MEDICATION.
DON'T NEED OR WANT A PITY PARTY
THAT'S WHY THEY CALL US #WARRIORS✋✋✋✋✋
THANK Y'ALL SO MUCH.