My Story Living with Lupus

Lupus Butterfly

Educating and Empowering Those Living with Lupus

Hypertrophic Lupus Erythematosus
Lupus Butterfly Rash
Photosenitivity
Bullous Lupus Erythematosus
Chilblain Lupus Erythematosus
Discoid-Lupus-4 Hair Loss.

ABOUT OUR HEALTH FORUM

The Full Story

We promote the inclusion of everyone who would like to get involved in the discussion. The topics at My Story Living With Lupus often pave the way to surprising and compelling dialogues between our forum users.

 

Our Health Forum is dedicated to enhancing the forum experience by offering plenty of opportunities for users to engage with each other in an interesting and safe online environment. Feel free to join the conversation by seeking advice, sharing your knowledge, or just shooting the breeze today.

***MEDICAL DISCLAIMER. The information on this site is not intended or implied to be a substitute for professional medical advice, diagnosis or treatment. All content, including text, graphics, images and information, contained on or available through this website is for general information purposes only. And is based on my experience seeking medical help and treatment for Lupus***

FORUM RULES

Keep it Clean

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NO OFFENSIVE CONTENT

Posting content that incites hatred, promotes discrimination, or is prejudiced (anti-religion, homophobic, racist, sexist, etc.) is not permitted. These posts will be removed immediately and users may be subject to disciplinary actions.

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NO ILLEGAL CONTENT

It is forbidden to post or share illegal content on our forum. This includes pirated material or someone else’s original work without proper citation. Repercussions for violations will follow from a thorough investigation.

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QUALITY POSTS ONLY

Please read through all posts in each discussion before posting something on a message board. We strictly adhere to high quality standards at our forum, and we ask that users make sure each post is relevant and original.

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WELCOME TO MY STORY LIVING WITH LUPUS

Share Your Thoughts

Welcome to your Health Forum. Join our community today and start reading the latest information about lupus. If you have any questions, please get in touch.

 

HELP CENTER

Additional Info

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Questions

DO I NEED TO REGISTER IN ORDER TO COMMENT IN A FORUM?

Yes.  Be thoughtful, write clearly and concisely, and consider adding written as well as visual examples. Make sure that if it was the first time you were visiting the site, you’d understand your answer.

Answers To Questions

CAN I GET POSTS REMOVED FROM THE SITE?

Yes.  If we find your post to be offensive to others it will be automatically deleted. 

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WHO CAN SEE MY PROFILE?

Privacy notice: This website, blog, podcast are all HIPPA compliant.  While you may give your email address to subscribe to the website posts or to post information on the website/blog. I will never share your information with any third parties without your written explicit permission.

NEWS & RESOURCES

What’s Happening

Athletic Woman

THE IMPORTANCE OF KEEPING YOUR BODY MOVING THROUGH EXERCISE.

Business Woman Typing

WHAT’S TRENDING? SEE WHAT IS TRENDING IN THE LATEST RESEARCH FOR LUPUS.

Customer Support Representative 2

RESOURCES THAT ARE AVAILABLE TO YOU.