Managing with LupusAfter living with Lupus symptoms for years and being diagnosed 2 years ago. I have learned to get at least 10 hours of sleep per night. I take my hydroxychloroquine...reactions3comments
My Diagnosis Was an Unexpected SurpriseLast year, I decided to make an appointment with the neurologist due to having more than usual nerve pain, especially in my feet and both hands and arms. But the...reactions1comment
22 Years and Still Counting...22 years ago I finally got my diagnosis but for over 25 years I had experienced symptoms. I had been dismissed by so many doctors. I began to think it...reactions3comments
LupiesI was diagnosed with SLE about 6 years ago. I didn't think anything of it because I was never educated by my doctors about what was actually going on in...reactions1comment
This Lupie LifeI was diagnosed with Lupus in 2014. To say it was a game-changer is putting it mildly. I'm glad I found out later in life, or I would really be...reactions3comments
Becoming a Lupus WarriorI was practicing some self-care last summer when I started sweating and felt out of breath and passed out in the spa chair of the nail shop. I woke up...reactionscomments
My Lupus ExperienceMy name is Amanda, I am 36 years old and this is my story. I had my first autoimmune disorder at the age of 18 months old, I started with...reactionscomments
So I'm Not a Hypochondriac...About 6 years ago I went to my GP with a rash across my neck and other ongoing symptoms. He asked me what I did for a job and when...reactionscomments
Showing Lupus Who the Boss IsI was in my early 30's when I was diagnosed. I'm married, I was raising 2 small boys and the doctor told me I had 5 years to live. After...reactionscomments
Lupie LifeI've had Lupus since I was 8 and now I'm 47. I've been in and out of hospitals. I'm so blessed I was able to have one child. I have...reactionscomments
Me, Myself & LupusHi, my name is Sandy. I have been diagnosed with lupus going on almost 4 years now. Let me tell you, at 1st I was angry & disappointed with the...reactions1comment
Becoming a WarriorFor at least three years, I had been experiencing the strangest sensations – like my nerves were on fire and my joints were so inflamed that my hands would sometimes...reactions3comments
I Have Lupus. Lupus Doesn't Have Me.In 1996 my freshman year of college I was given the word Lupus to title all the rashes aches pains hair loss fatigue. I had no place to put this...reactions1comment
Lupus Changed My Life... For Good!Surprisingly, being diagnosed with lupus (and fibromyalgia) in my early 30s changed my life and opened the world. It created a pathway to find more joy in my life and...reactionscomments
Lupus warriorMy name is Kendra and I got lupus when I was 11 years old I am in remission now but still have my ups and downs but I fight it...reactionscomments
Smoldering Myeloma, MGUS and LupusI've had SLE lupus since 1999 and received the news that I have MGUS (monoclonal gammopathy of undetermined significance) on 6/6/2017. When I read your feature story, I was glad...reactions1comment
Poem: "Lupus Is Not a Disease That You See"Lupus is not a disease that you see. It reminds you it’s there like an ‘invisible enemy'. It ravages your body in ways you can never explain. A winding river...reactions12comments
My Long Road to DiagnosisI started having problems when I was 26 years old. I was diagnosed with fibromyalgia finally at 38. Then 6 years later I was diagnosed with Rheumatoid arthritis, during this...reactions3comments
Giving My AllI was found out I had Lupus Nephritis in 2015. Since then I have had my ups and downs. This year has been my worst, or maybe I am just...reactions1comment
Blindsided by Lupus and Autoimmune DiseasesI was diagnosed with SLE Lupus 15 years ago. Since then, I have been diagnosed with Fibromyalgia, Sjogrens, Raynauds and this past November, tests showed my Thyroid is having problems...reactions6comments