When lupus made it difficult for kathy to teach she found a new career with the flexibility she wanted and the fulfillment she needed.
Testimonies living with lupus.
Brain and central nervous system.
I was searching for help for my mom who has lupus.
Staying organized and not afraid to count on others for support.
The lupus foundation of arkansas inc.
Dear jill i am a biomedical scientist and i have a doctorate degree in immunology.
My doctor felt confident enough to say i no longer required the care of a specialist and i didn t need to see him every 3 months.
After prayer in april 2013 against the advice of my doctor i threw out all prescriptions and started oiling and have never felt better.
The lupus foundation of america works to improve the quality of life for all people affected by lupus through programs of research education support and advocacy.
On world lupus day observed on may 10 every year to promote public awareness about the disease these stories of a few lupus patients will make you understand what courage in the face of pain.
Frustration of lupus just another testimonial linda linger d o.
Lupus is a chronic disease that does not have a cure at.
Living with lupus since.
Thank you for supporting the lupus foundation of arkansas inc.
Tammy danna tells her inspiring journey with lupus.
After learning she had lupus webmd community member lenaki alexander rowed her way back to better health and new hope.
Lupus can cause serious kidney damage and kidney failure is one of the leading causes of death among people with lupus.
If your brain is affected by lupus you may experience headaches dizziness behavior changes vision problems and even strokes or seizures.
Because lupus is not only tricky to diagnose but also tricky to understand we asked several people living with lupus to share what it s really like what they wish people knew about this disease.
I found the book lupus recovery diet online a couple of months ago.
Thank you so much for the great book.
After her mom s diagnosis with lupus a year ago kirsten knew she wanted to make her mark in the fight against the disease.
That was my 6 month lupus protocol.