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'Lupus Doesn't Define Me': Milwaukee Teacher's Struggle & Resilience With Lupus | WUWM 89.7 FM

Elizabeth Kosmach is an elementary teacher in Milwaukee who was diagnosed with Lupus when she was in college. ....

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Virtual Butterfly Walk aims to raise $25,000 by June 5 to support people battling lupus, fibromyalgia

Virtual Butterfly Walk aims to raise $25,000 by June 5 to support people battling lupus, fibromyalgia
and last updated 2021-05-24 07:25:30-04
NEWPORT NEWS, Va. - On June 5, put on your purple and walk anywhere in support of people battling lupus and fibromyalgia.
The Social Butterflies Foundation s annual Butterfly Walk is going virtual for the second straight year.
Last year was our first virtual due to the pandemic and everyone just had a great time, said Chastity Corbett, Founder and CEO for the Social Butterflies Foundation.
Corbett says she founded her non-profit, named for a symbol representing lupus, after seeing the gaps in support services that national organizations were leaving. ....

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Lupus Awareness - NOW Magazine

NOW Magazine
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May is Lupus Awareness Month and to help drive conversation, Lupus Ontario is inviting everyone to wear purple for Lupus on Friday, May 21st. Wear something purple and post on social media using #PutOnPurpleForLupus @LupusOntario (Instagram) @LupusON (Twitter) and @LupusOntarioOfficial (Facebook) to join the conversation.
Lupus Ontario will be hosting the Virtual Walk for Lupus Ontario in communities across the province. August 21, 2021 has been chosen as the day for you to walk, run, cycle, do a craft, challenge your friends to an activity, etc. to increase lupus awareness and to raise funds for lupus research, and patient support and education programs. ....

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3 Sisters Diagnosed with Lupus are Striving to Spread Awareness

May is Lupus Awareness Month. This is a disease that has heavily affected my life over the past few months, and I wanted to shed some light on the effects of Lupus and the damage it can inflict. A lot of people have no idea what Lupus is, what the symptoms are and how serious it can be. You look at me and probably would never guess I m dealing with an auto-immune disease that is effecting my organs.
I was honored to be able to have a conversation with Aniysha, Sakeema and Kareema Trice the other day; three sisters who were all diagnosed with Lupus in their 20s. Because of their experiences, hardships and trials they decided to start an organization based in Philadelphia called ASK Lupus. According to their website, they are a non-profit organization that is dedicated to lupus advocacy, supporting those that have been diagnosed or are in the process of a diagnosis with lupus within the community. ....

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Lupus Awareness Month Resources

Lupus Awareness Month Resources
With May being Lupus Awareness Month, we wanted to share some facts and resources about a disease that impacts over one and a half million Americans, the majority of whom are women between the ages of 15 and 44. Recently, it has been reported that women of color are two to three times more likely to develop Lupus with Lupus.org saying that 1 in 537 African American women will develop some form of Lupus. Although 10-15% of individuals with Lupus may die due to complications of the disease, most, with the right treatment/management, live a normal life span. ....

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