“We Will Get Through This” ~J-NOTT
Supporting awareness for Lynch Syndrome in loving memory of Jeremy Nottingham
J-NOTT-GTT was created to honor the legacy of Jeremy Nottingham. A son, brother, and friend; “J-Nott” was diagnosed with colorectal cancer as a result of Lynch Syndrome at age 28, and fought it relentlessly until his passing on November 22, 2021. Jeremy wanted his story to spread awareness of this condition, knowing that lives can be saved through genetic testing for Lynch Syndrome and early detection of life-threatening cancers.
The Latest from J-NOTT-GTT
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New Team, Same Goal: Ish Smith Continues his Support for J-NOTT-GTT
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J-NOTT-GTT Featured on NPR
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Brandon Graham and the Eagles Support J-NOTT-GTT
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Nottinghams Receive Letter from President Joe Biden
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J-NOTT-GTT visits WFU and Northside Lanes
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Pool Table Donation in Memory of Jeremy
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Ish Smith Supporting J-NOTT-GTT
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Washington Capitals Ticket Raffle
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Blog Post on facingourrisk.org
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Jeremy’s Story in the Winston-Salem Journal
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Family testimony from Jeremy’s father, Junius Nottingham, Jr.
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Lynch Syndrome PSA in memory of J-NOTT
BUT GOD: A JNott Podcast
Hosted by Junius Nottingham, Jr. and Pastor Frank Robinson
BUT GOD: A JNott Podcast is a space that will bring together special guests from various areas.
Dedicated to the Memory of Jeremy Nottingham
Scan here to access BUT GOD: A JNott Podcast on your mobile device.
Community Outreach
J-NOTT-GTT participates throughout the community via speaking engagements, tabling events and conferences, and hosting fundraisers in order to spread awareness about Lynch Syndrome. The more people know Jeremy’s story, the greater chance that one more life can be saved through early detection.
Please contact us at jnottgtt@gmail.com if you’d like us to come to your event!
J-NOTT-GTT has partnered with local businesses, national brands, and Wake Forest University in order to extend the reach of Jeremy’s story. With the help of our partners, Jeremy’s legacy has raised over $20,000 in its first year towards fighting Lynch syndrome.
Friends of J-NOTT-GTT
The key to fighting Lynch syndrome is through education. J-NOTT-GTT works closely with CCARE Lynch Syndrome in order to keep the public informed on how to get tested for Lynch syndrome and what you need to know if you’ve been diagnosed with Lynch.
Lynch Syndrome Education
Every dollar donated goes to spreading awareness about Lynch Syndrome and honoring Jeremy’s life. This includes hosting events, attending medical conferences, and also funding the Jeremy Nottingham Pro Humanitate Award, a scholarship fund at Wake Forest University. Please consider giving in Jeremy’s honor.
How can I help?
Contact
Feel free to contact us with any questions.
Email
jnottgtt@gmail.com