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Lupus Awareness Month 2017
Lupus Awareness Month Fact of the Day 2017
LSI Brochures by Dr. Robert Katz
What Causes Lupus
Diagnostic Tools for Lupus
Warning Signs and Prevention of Flares
Working with Your Doctor
Lupus and Quality of Life
Pregnancy & Contraception for Women with Lupus
Research & Treatments
More Lupus Research Information
October 2017 Support Group Meetings
Illinois Lupus Walk 2017
Tara Joseph - 2017 NS Lupus Walk Ambassador!
Kanefus Walker - 2017 SS Lupus Walk Ambassador!
Corrin Stines - 2017 WS Lupus Walk Ambassador!
Maddie Handley - 2017 Chicago Walk Ambassador
2017 Bank of America Chicago Marathon Lupus Charity Runners Team
2017 Aware for All Chicago
2017 Lupus Educational Event
Advancing Lupus Care Through Research & Advocacy
2018 Bank of America Shamrock Shuffle 8K
2018 Bank of America Chicago Marathon Lupus Charity Runners Team
Programs & Services
Individual Peer Support
Living Well With Lupus Story Sharing Project
The Lupus Voice Grows
Father's With lupus: A Son's Story
Still Alive: Kay Mimms, Lupus Warrior
There is Hope
Living with Lupus for 30 Years
A Mother's Journey
Mari Gonzalez: Chicago Lupus Walk Ambassador
Kerri Horan: Western Suburbs Walk Ambassador
A Brighter View
Coping with Lupus
Marathon Story - Courtney
Finding Comfort in the Uncomfortable
How I Met Lupus
2014 Bank of America Chicago Marathon Lupus Charity Runners Team
I Am Still Alive
I Don't Have Lupus, Lupus Has Me
Attack of the "Itis"
Learning to Accept
Living with Lupus Since 1980
Marathon Story - Aaron
Marathon Story - Dana
My Lupus Journey
A Runner's Story
A Special Day: A Lupus Story
The Symbol That Represents Me
This is Our Story
One Runners Story
What Do You Mean I Have Lupus?
Yoga and Lupus: In Good Company
So...What Was That About Yoga?
Beyond the Mat
How LSI's Advice Got Me The Treatment I Needed
Lupus Community Navigator Program
Rush University Medical Center Doctors answer Lupus Questions
News You Can Use
Lupus & Chemo & Cancer
Hair Loss and Lupus
When should I tell my employer I have lupus?
Diagnosis Disputes: What to do when one doctor says you have lupus and another says you don't
Illinois Rehabilitation Services
Lupus and the Lungs
Anti-Malarial Drugs and Lupus
Statewide Support Opportunities
UV Rays and Lupus
Plaquenil/Hydroxychloroquine Prescription Costs
Beware a Cure for Lupus
Dentistry: More Than Just Teeth
How to Find a Doctor
Managing Infections for Lupus Patients - Highlights from Dr. Curran's Presentation
Resources for Men with Lupus
The Internet & Lupus
Lupus Update with Dr. Katz
About Dr. Robert Katz
National Lupus Initiative
Board of Directors
Lupus In The News
Medical Advisory Board
Lupus PFDD Meeting
Lupus Charity Runners
Volunteers with Special Skills
English to Spanish Translation
#GivingTuesday Volunteer Survey
Achieving the Mission
Donate/Donate Monthly Online
Host Your Own Fundraiser
Griffins Red Wagon Project
Donate Your Car
Lupus Charity Runners/Lupus Charity Riders
Welcome to the Lupus Society of Illinois' Living Well with Lupus Story Sharing Project submission form. This submission form is designed to help you tell your lupus story - you do not have to complete the survey in its entirety and if you would prefer to submit your story in a different format, it is equally welcome. You are welcome to post your story anonymously or if you like you can invite feedback by agreeing to including your contact information.
Once you have submitted your story (either via the survey or another format), the LSI will review it and contact you with a final draft prior to posting the story on its website. You are welcome to withdraw your story any time you like by contacting the LSI at firstname.lastname@example.org or calling 312-542-0002.
If you have any questions, please do not hesitate to contact Mary at email@example.com or 312-542-0002.
Thank you for your participation!
Living Well With Lupus Story Sharing Survey
When were you first diagnosed with lupus?
How long did it take for a correct diagnosis?
Were you misdiagnosed first?
How has your life changed since your diagnosis?
How has your diagnosis affected your family and friends?
Has a lack of public awareness about lupus affected your quality of life?
I don't know
If so, how has a lack of awareness affected your quality of life?
Is your employer supportive of your diagnosis?
Share your story:
How did you find the Lupus Society of Illinois?
How has the Lupus Society of Illinois helped you?
What would you want the world to know about lupus? Why?
Please include my contact information
Include my name
Include my email
Include my telephone number
No thank you
Select all that apply.
What is the title of your story?
Lupus Society of Illinois
411 S. Wells Street, Suite 710; Chicago, IL 60607 | 312-542-0002 or 800-258-7872 | firstname.lastname@example.org |
Serving Illinois Since 1973