Contact Kelli 

 Please do not hesitate to reach out with any questions, comments or concerns. 

info@morethanlupus.com
16200 SW Pacific Highway Suite H #121
Portland, OR 97224

All health information on this site is solely for informational purposes.

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About

Kelli Roseta of  More Than Lupus  

Kelli Roseta is a lupus advocate, award-winning blogger, & community liaison.  She is also a 28 year lupus survivor.  Her passion for connecting and validating those in the lupus community began after years of struggling physically and emotionally with the disease.  After attending a lupus support group, she realized what a need there was for those in the lupus community to know  "they are not alone."  Through her ground-breaking Facebook Support Chats, innovative blogs and inspirational speaking engagements, she has given thousands of individuals not only hope, but a voice, in a world where many still don't understand lupus, nor take it seriously.   

More than Lupus was created as a place where those who were just diagnosed, or those that have been living with lupus for decades - can connect, grow and inspire others through the peaks and valleys of their lupus journey.

She welcomes you to morethanlupus.com and hopes that maybe, for the first time, you feel heard, seen, and loved, because, you are so much more than the sum of what is wrong with you.  You are MORE THAN LUPUS

"The hilltop hour would not be half so wonderful if there were no dark valleys to traverse."                         - Helen Keller 

 
Live Facebook Chats & In-Person Support Group

These semi-weekly Live Facebook Support Chats are developed to be a sanctuary.  A place where lupus individuals and their loved ones, can come together in a positive and safe environment to help better understand the illness and validate each others experiences.

Speaking Engagements

Kelli has had the pleasure of conducting numerous camera interviews, has performed local news spots, been on talk shows and PSA's.  She is available for symposiums, Master of Ceremony engagements and seminars.   

No funding, no research. No research, no cure.  Kelli takes her work in community awareness & fundraising very seriously.  Whether it's working with the Lupus Research Program through the DOD, lobbying for lupus funding in Washington D.C. or helping locally through fundraising events.

Live Facebook Chats & In-Person Support Group
Speaking Engagements
Community Awareness & Fundraising 

No funding, no research. No research, no cure.  Kelli takes her work in community awareness & fundraising very seriously.  Whether it's working with the Lupus Research Program through the DOD, lobbying for lupus funding in Washington D.C. or helping locally through fundraising events.

 

Testimonials

 
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