2022 West Coast Virtual Walk for Sjogren's (CA, ID, NV, OR, WA)

InStyle with Sjogren's

Thanks for visiting our Team's Page, InStyle with Sjögren's!

Hello and welcome to our page,

My name is Andrea and I am the captain of InStyle with Sjögren's. I am a wife, mother of 2, and small business owner, and I have Sjögren's. My story in short, I was feeling drained ALL of the time and slacking on my business and home duties. In 2018, I started talking to my doctor about how I was feeling and all of the things that was going on with my body. I had been going to different specialist looking for answers. After multiple lab work, medical tests, different medications, and misdiagnosis, I was diagnosed with Sjögren's Syndrome on June 10, 2022.

This is a fairly new disease, and is often misdiagnosed and can take years to pin point. Research is on going and we could use your help.

Together we can make a difference and impact the future of Sjögren's!

To learn about Sjögren's Syndrome, you can visit: 

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! 

When did you first learn about Sjögren's (pronounced Show-grins)?

Did you know that upwards of 4 million Americans are living with Sjögren's? 

Sjögren's is very common yet still little known, 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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