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
My Humbling MomentMarch 2020 was the last time I worked as a critical care nurse. Covid came knocking on our doors. Because of my age, 72, my nursing director felt I should...reactions4comments
Always Hopeful2015, the year Discoid Lupus and Subacute Cutaneous Lupus covered my torso and arms in lesions, many of which got infected. The same year, Rheumatoid Arthritis struck. The latter wasn’t...reactions1comment
Taking Charge of My Tangled Web of SymptomsAfter having three babies in three years, I was exhausted. Physically, I’d been through a lot of changes, and emotionally, it was a lot of change for me. I was...reactions6comments
DiagnosisI was diagnosed 28 years ago when I gave birth to my youngest child. After I had her I felt off. I couldn’t lift a brush to brush my hair...reactions3comments
Lupus Nephritis: Now On DialysisI've had Lupus since 2005. It went into my kidneys and now I'm on dialysis. Soon I'll be looking for a Kidney Transplant. I have potential donors, the problem is...reactions5comments
Life with Lupus and RAI just joined Lupus.net today. I actually have both Lupus and RA. I have had RA since 2004 and had to retire from nursing in 2017, as RA started really...reactions1comment
Lupus Symptoms WorseningI essentially have had lupus for 42 years. I was 30, pregnant with my youngest daughter when they first questioned systemic lupus due to 2 daughters born 10 weeks early...reactions1comment
A B-3 vitamin variantI joined this forum because of the benefits of taking a variant in the B-3 vitamin group that my friend had a good experience with. The vitamin is "nicotinamide riboside...reactions4comments