When the ER Cannot Help You and Your Autoimmune Disease

Where do you go when you feel the worst you’ve ever felt in your life? Where do you go when you feel like you need immediate medical attention or something bad is going to happen? The last resort when you just can’t handle it anymore? Most of us would answer, the hospital! Well that is … Continue reading When the ER Cannot Help You and Your Autoimmune Disease

Grieving the Person I Was Before Chronic Illness

  “Click, click” is all I hear while I sit in front of my computer screen biting my lower lip trying my hardest not to cry (telling myself I need to be strong). “Oh no,” I can feel a tear fall down my face; there is the beginning of me grieving the person I used … Continue reading Grieving the Person I Was Before Chronic Illness

My Answer To You, When You Ask “Why I Don’t Have Real Kids?”

  I can hear the whispers and I can see the laugher. The way you look at me when you pass then look into the stroller I am pushing and you see furry animals instead of a human baby. I feel embarrassed and the look on your face makes me feel like I should be … Continue reading My Answer To You, When You Ask “Why I Don’t Have Real Kids?”

How Lupus Changed Who I Thought I Would Be In My 20’s

Currently, I am 26 years old, going to be 27 in just a few months. Unfortunately, since I can remember, I have never felt completely “normal,” but I can say 16 was probably the best I ever felt. Looking back now 10 years ago, I had a vision of what now might look like. I had this image that … Continue reading How Lupus Changed Who I Thought I Would Be In My 20’s

How I Thought My Diagnosis Would Bring Me Closer to ‘Normalcy’

I remember the day as clear as yesterday. I remember the feeling – lost, hopeless, and petrified. A few moments later my hands became stiff and I could no longer use them. I felt the beating of my heart like it was exploding through my chest. I was sitting at my desk at work when … Continue reading How I Thought My Diagnosis Would Bring Me Closer to ‘Normalcy’