My 10-Year Lupus Diagnosis AnniversaryThis is my 10th anniversary of being diagnosed with lupus, and I am so happy I made it this far. Being diagnosed with lupus at age 17 was a lot... By Jokiva Bellard2 min readBookmark for later
CPAP Therapy: An Unpleasant Solution for My Fatigue ProblemsSometimes, taking responsibility for your health kind of sucks. Have you been there – where you just want to do the right thing for your health but the process feels... By Ava Meena4 min readBookmark for later
Not Enough Providers Know About Autoimmune ConditionsI have been in the medical field for over 15 years. I’ve seen it from the inside out. I have seen providers of all kinds, from my "fellow" nurses, to... By Amber Blackburn3 min readBookmark for later
My 10-Year Lupus Diagnosis AnniversaryThis is my 10th anniversary of being diagnosed with lupus, and I am so happy I made it this far. Being diagnosed with lupus at age 17 was a lot... By Jokiva Bellard2 min readBookmark for later
CPAP Therapy: An Unpleasant Solution for My Fatigue ProblemsSometimes, taking responsibility for your health kind of sucks. Have you been there – where you just want to do the right thing for your health but the process feels... By Ava Meena4 min readBookmark for later
Not Enough Providers Know About Autoimmune ConditionsI have been in the medical field for over 15 years. I’ve seen it from the inside out. I have seen providers of all kinds, from my "fellow" nurses, to... By Amber Blackburn3 min readBookmark for later
My 10-Year Lupus Diagnosis AnniversaryThis is my 10th anniversary of being diagnosed with lupus, and I am so happy I made it this far. Being diagnosed with lupus at age 17 was a lot... By Jokiva Bellard2 min readBookmark for later
CPAP Therapy: An Unpleasant Solution for My Fatigue ProblemsSometimes, taking responsibility for your health kind of sucks. Have you been there – where you just want to do the right thing for your health but the process feels... By Ava Meena4 min readBookmark for later
Not Enough Providers Know About Autoimmune ConditionsI have been in the medical field for over 15 years. I’ve seen it from the inside out. I have seen providers of all kinds, from my "fellow" nurses, to... By Amber Blackburn3 min readBookmark for later
Dealing with Covid and LupusAfter almost 3 years, Covid finally got me. Unfortunately, my husband fell ill first. The day after Thanksgiving, I saw that he was wearing a mask. I asked him what... By Geri Rodriguez3 min readBookmark for later Reactions 0 reactions Comments0 comments
Life With An Invisible IllnessWhen I first became sick with lupus, nearly everything about my life changed. I had once juggled my college classes with work and a social life without too much difficulty... By Meghan Bea2 min readBookmark for later Reactions 0 reactions Comments0 comments
My Eyes Are Open Now!I have been a very healthy person until 5 years ago. I began to think my doctor just got tired of hearing the same old whining from me. Just within...Bookmark for later Reactions 0 reactions Comments8 comments
Will You Take our 2023 In America Survey? The Lupus Foundation of America estimates that 1.5 million people in the United States have a form of lupus. Our 2023 In America survey aims to better understand the patient...Bookmark for later Reactions 0 reactions Comments0 replies