LupusGroupies

Does anyone get a lot of bladder infections? I just had a 6-7 week bladder infection that led to a kidney infection...I still don't feel better after the antibiotics, does anyone else have this issue? #Lupus #Fibromyalgia #infections #ChronicPain #ChronicFatigue #RareDisease #ChronicIllness #LupusGroupies #MightyTogether

Hi Lupies!! 35 newbies have joined within the last month 😍WELCOME!! Please feel free to introduce yourself and tell us your Lupus Journey. We welcome everyone with love and acceptance. This is a safe place to vent or seek advice or just to use as an outlet where people understand and can relate to your sufferings and pain. I'm Brionna or Bri your Community Leader. I was diagnosed in March 2018 and have been struggling with anxiety and depression as well. I'm happy I found the Mighty and I hope I provide some support for my fellow Lupies 💜💜💜💜💜💜💜#Lupus #Depression #LupusGroupies #Anxiety #ChronicIllness #ChronicPain #RareDisease #welcome #MightyTogether

Thank you for everyone who has joined this group. We are all trying to figure out this disease one day at a time! I hope one day there is a cure for all of us. Also let's welcome our 26 new members, please feel free to introduce yourselves and your diagnosis story, we would love to hear from you! #Lupus #LupusAwarenessMonth #LupusGroupies #ChronicIllness #InvisibleIllness #welcome

Hi Lupus Mighties! Sorry I've been a little MIA. Dealing with some at home relationship issues and decided to open up a dialogue about it to see if others can relate. Feel free to vent here or to give/seek advice because that is what the Mighty is for!
I feel like my significant other has unattainable standards for me and I am overwhelmed and exhausted. I have #Lupus and #Fibromyaliga and #Anxiety and sometimes #Depression . I work full-time but he expects me to do all the cleaning, dishes, laundry, grocery shopping, and meal prepping/cooking, and take care of all the pets needs. It's just too much and I can't do it all on my own. Is anyone else experiencing this? I am trying to do it all but I feel like my happiness and personal needs and rest are put on the side burner. Any tips for explaining to your partner you can't do it? How to ask for help? How to set boundaries? Or anyone else experiencing this and want to vent/share? We are all here for each other! Sorry I've taken some time away because I have just been too busy trying to live up to others expectations and I apologize for being absent. Know I'm here for you all 💜 and I appreciate any and all feedback!

How is everyone doing? My anxiety is high and I'm feeling so overwhelmed...anyone else struggling right now?
#Lupus #LupusGroupies #Anxiety #Depression

I wish I could be more vulnerable and open with them, but I always tell everyone I am okay, or they assume I'm okay. I don't know how to talk about mental health with them. Is anyone else like this? Or just me? I can't seem to express myself or make people understand. #MentalHealth #Lupus #Depression #Fibromyaliga #ChronicPain #PTSD #ChronicIllness #LupusGroupies #RareDiseases

Sorry Mighties, I have been absent again for awhile. I am SO overwhelmed. I'm an essential employee so I've been working 50+ hour weeks and trying to plan our wedding--which basically everything was cancelled and we need a new plan, so I'm discouraged and depressed and have so much anxiety. I'm also moving in after we get married so I have to start packing as well, all while dealing with this terrible Lupus or Fibro flare-up and I am in so much pain and just want to cry and quit my job so I can nap. I'm so overwhelmed and I just haven't had the energy to post anything. Sorry for being a bad community leader and especially to my Lupus Groupies who I haven't communicated with in 2 weeks! 😭 I just needed to vent to someone who could understand so thank you!
#Lupus #Fibromyaliga #ChronicPain #Anxiety #Depression #DistractMe #ChronicIllness #LupusGroupies #InvisibleIllness #MentalHealth #RareDisease