I have had Lupus for eight years and along with it came RA, chronic fatigue, bursitus, depression, and what seems like a million other serious conditions. I take 26 pills a day and am currently fighting for my disability. The pain is dibilitating everyday and dealing with the fatigue is so hard. No one understands....my kids know to some extent that I'm sick but they mostly just think I'm lazy. My husband supports me but you tell there are days he wishes I would just get off the couch and do something. I miss doing the things Ii used to do like gardening and working, sometime the depression is more than I can stand.
I would love to talk to others who understand.