2023 Mid-Atlantic & National Virtual Walk (DC, MD, VA, WV, Nationwide)

Remembering Dee Petros 2013-2023

Thanks for visiting our "Remembering Dee petros, 2013-2023 Team Page! 

I hope that you will join the team and help to increase awareness and raise funds to support the work of the Sjögren's Foundation!

You can read more about Dee on Ekaterene "Kathy" Lawrence's personal page. Kathy's sister, Dee sadly lost her battle with Sjogren's 10 years ago in 2013.  

For thos wanting to know more about Sjögren's (pronounced Show-grins), please continue reading.

Did you know that upwards of 4 million Americans are living with Sjögren's? It is Systemic, Serious & Prevalent. While hallmark symptoms include dry eye, dry mouth, fatigue and joint pain, Sjögren’s is a systemic autoimmune disease, which means it can also attack any organ or body.  

You can help make a difference by joining our team and help us to get the word out! We need your help to support research, education and to increase Sjögren’s awareness! 

Join the team and help to make Sjögren's known. It is simple to set-up your personal webpage and become part of the team!  It is also an easy way to receive donations which is also fast and totally secure. It is also the most efficient way to support your fundraising efforts. Then reach out to your friends and family by sending them a link to your page so they can learn more about Sjögren's and support your efforts. 

Thank you in advance for your support! Go Team!

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