Jacqueline Rush Foundation

Determined to inform the public & medical community about Lynch Syndrome & help people realize the power of knowing what’s in their genes

[Jacqueline Rush Foundation @JRushFoundation]

https://t.co/6k98XeJe6q

[Jacqueline Rush Foundation @JRushFoundation]

Encouraging news for the Lynch syndrome community. 💜

The FDA has granted Fast Track Designation to NOUS-209, an investigational immunotherapy being studied for cancer interception and prevention in individuals with Lynch syndrome.

#LynchSyndromeAwareness #NatureMedicine

[Jacqueline Rush Foundation @JRushFoundation]

March 22 is Lynch Syndrome Awareness Day. 🧬

Lynch Syndrome is the most common hereditary cancer syndrome—yet ~95% don’t know they have it. When it’s known, cancer can often be prevented or caught early.

Knowledge is powerful. Please share 💜
#LynchSyndromeAwarenessDay

[Jacqueline Rush Foundation @JRushFoundation]

When research reaches Nature Medicine, it signals something important.

The Phase 1b/2 NOUS-209 trial in Lynch syndrome carriers highlights growing momentum in cancer interception & prevention.

Progress happens step by step and this is a hopeful one. 💜

[Jacqueline Rush Foundation @JRushFoundation]

We’ll be exhibiting at the Penn Medicine Lynch Symposium and the Dana-Farber LYNKED IN Conference.

If you’re attending, please stop by and say hello, we’d love to connect.

[Jacqueline Rush Foundation @JRushFoundation]

Have Lynch syndrome or work with Lynch patients?

GWU is conducting a research study on lifelong cancer screening + prevention.

🧬 Zoom interview
🎁 $35 gift card
🔗 https://t.co/bVDf6utjbd

[Jacqueline Rush Foundation @JRushFoundation]

The holidays can hold joy and grief at the same time. For many, that contrast makes loss feel louder; not because love is gone, but because it’s still here.

We’re holding space for all who are missing someone this season. 🤍

[Jacqueline Rush Foundation @JRushFoundation]

As National Hereditary Cancer Week comes to a close, we’re reflecting on the amazing research that has happened in Lynch Syndrome since the Jacqueline Rush Foundation started. Since 2015 when the Foundation was founded, our motto has always been to “Live in Your Genes.”

[Jacqueline Rush Foundation @JRushFoundation]

Happy Mother’s Day 💐 “A mother is not defined by the number of children you can see, but by the love she holds in her heart.” ~ Francesca Cox
Thinking of all for whom this day is joyful, painful, or both. You are seen. 💜 ~ Joan Rush, Jacqueline’s mom

[Jacqueline Rush Foundation @JRushFoundation]

We attended AACR in Chicago and were present when the results of this study were presented. These results of the study are very exciting for the Lynch Syndrome community. To learn more about the study visit the link in our bio. #cancerinterception #LynchSyndrome

[Jacqueline Rush Foundation @JRushFoundation]

Happy National DNA Day! 🧬 On this day, we celebrate the groundbreaking discoveries in genetics that have paved the way for personalized medicine and understanding of inherited diseases. #NationalDNADay #Genetics #liveinyourgenes #lynchsyndrome #lynchsyndromeawareness

[Jacqueline Rush Foundation @JRushFoundation]

From my garden to yours. Enjoy all that nature brings. Happy Earth Day! ~ Joan Rush

[Jacqueline Rush Foundation @JRushFoundation]

Lynch Syndrome is surprisingly common but mostly unknown! Only 2 out of every 100 people with it are diagnosed. We MUST change this statistic! 💜

Around 1.2 million people in the US are living with Lynch Syndrome, but many don’t know they have it until after cancer strikes.

[Jacqueline Rush Foundation @JRushFoundation]

On #LynchSyndromeAwarenessDay, we honor Jacqueline’s memory. At 23, she lost her life because we didn’t know Lynch Syndrome ran in our family. Her kindness and mission to impact others live on. 💚

Share the knowledge about Lynch Syndrome to help save lives.

[Jacqueline Rush Foundation @JRushFoundation]

🧬 Today, March 22, is #LynchSyndromeAwarenessDay! Did you know that Lynch Syndrome is the most common hereditary cancer syndrome and raises the risk of colorectal & endometrial cancers? Sadly, most people (95%) are unaware until after cancer diagnosis.

#LynchSyndrome

[Jacqueline Rush Foundation @JRushFoundation]

@AparajitaSingh0 @ExactSciences @CologuardGolf @Stewartcink1 An amazing experience!

[Jacqueline Rush Foundation @JRushFoundation]

This weekend in Tucson, AZ, the Jacqueline Rush Foundation joins the PGA Champions Cologuard Classic Golf Tournament, bringing together 78 pro golfers, 350+ advocates, colorectal cancer survivors, caregivers, and those honoring loved ones lost to the disease.

[Jacqueline Rush Foundation @JRushFoundation]

Today is #DressInBlueDay 💙! We wear blue to raise awareness for colorectal cancer and efforts to end this disease. Honoring those impacted.

Post a photo wearing blue and tag us to show your support. 💙

#ColorectalCancerAwarenessMonth #LynchSyndrome #JacquelineRushFoundation

[Jacqueline Rush Foundation @JRushFoundation]

So grateful that at the #CologuardClassic by @ExactSciences golf tournament, PGA TOUR Champions @ChampionsTour Professional @stewartcinc will be playing in memory of Jacqueline Rush wearing a ribbon with her name all 3 days (March 7-9). Tune-in to @GolfChannel & help us cheer!

[Jacqueline Rush Foundation @JRushFoundation]

March is National Colorectal Cancer Awareness Month!

This Virtual Town Hall by the University of California San Francisco is open to all, not just those with a high risk family history or Lynch Syndrome. Register to learn to prevent and lower your risk now.