#tealitup

[sofyscleropbcwarrior]

Being an autoimmune disease warrior is not for the faint of heart. Despite the major flare I'm having, I have to pick up and keep on going. And it sucks. It sucks big time.

This has been become a normal part of life for me. Some of the people in my life have asked what it's Ike. It's tough to describe, but lately it feels like a low grade fever with body aches, but times 1M.

I'm always in pain but today I may take some ibuprofen for relief. I've been like this for a week and I'm exhausted by it. I try to keep unnecessary meds, fried foods and alcohol out of my diet as much as I possibly can. It does not help the Primary Biliary Cirrhosis for me to consume these things. So please recognize that what you consume is a prescription within itself!

My skin has felt like its on fire lately, I have been itching like crazy and I know its because my liver enzymes are elevated... with all the stress I've been under - end of school, running my business, job interviews, finalizing divorce, not eating or sleeping right - everything has just caught up to me.

So I'm working extra hard to maintain a positive attitude, because it go a long way in helping me with my mindflow! I heard someone say emotions are energy in motion and we need to work on making it positive and contagious 💜

[leeshamurphy-blog]

Did you know that September is PCOS Awareness Month? PCOS, poly cystic ovary syndrome, is something that so many women have, but many people have no idea that it even exists. I didn't know about it until one my closest friends was diagnosed, then a year later, I was diagnosed (since then I've met so many wonderful women impacted by it, too.) Throughout the month, I am going to be sharing some information about PCOS to help raise awareness and provide education. #tealitup #pcoswarrior #pcosawareness #strongerthanpcos

[thetragicdoll]

Literally trapped in my own skin. Scleroderma can go to hell. #scleroderma #irockteal #tragicdoll #thetragicdoll #tealitup #awareness