Concussion & CTE Foundation

Concussion & CTE Foundation The Concussion & CTE Foundation's mission is to support athletes, veterans & all affected by brain trauma.

04/09/2026

When you have post-concussion syndrome you realize how many tasks require brain power! Even something as simple as having a conversation with friends for an hour can flare up symptoms for days. It can be so hard trying to decide when to use your cognitive energy, and that can oftentimes leave you feeling isolated and lonely. If you’re feeling that way right now, we get it! It’s HARD. And you’re not alone.

and share their experiences with PCS on Episode 11 of Invisible Impact: a Post-Concussion Podcast. 🎙️
📺 Watch on YouTube
🎧 Listen on Spotify or Apple Podcasts

04/07/2026

Research shows NFL players are nearly 4x more likely to die of ALS than the general male population. We sat down with Dr. Dan Daneshvar, Chair of Physical Medicine and Rehabilitation at Mass General Brigham and Harvard Medical School to understand why. He explains that while the exact cause isn’t fully understood, repetitive head impacts, like those suffered playing years & years of tackle football, are known to produce brain changes associated with both CTE and ALS.

The family of Chicago Bears legend Steve "Mongo" McMichael has announced through the Concussion & CTE Foundation that he...
04/07/2026

The family of Chicago Bears legend Steve "Mongo" McMichael has announced through the Concussion & CTE Foundation that he was diagnosed with stage 3 CTE by researchers at the Boston University CTE Center. He was a key member of the Bears’ 1985 Super Bowl championship team and a Pro Football Hall of Famer. Mongo died in April 2025 after a nearly 5-year public battle with ALS.

A 2021 study led by researchers at Harvard Medical School and the Boston University CTE Center study found NFL players are more than four times more likely to develop ALS compared to the general male population. McMichael pledged to donate his brain while he was alive, saying it was important to him to contribute in any way he could.

Mongo will be honored at our Race to End CTE event later this month in Chicago. More information on the event and how to make a donation in his name can be found at https://give.concussionandcte.org/event/3rd-annual-chicago-race-to-end-cte-reception/e776435

04/05/2026

Liz Nicholson Sullivan doesn’t sugarcoat it.

She talks about the fear. The violence. The years she had to leave. And the reality that CTE can show up in ways many families find hard to share.

Her husband Gerry was a Cleveland Browns offensive lineman. He was diagnosed with dementia at 52. He’s 74 now, and Liz has been a fierce advocate for him and for other former players and family members navigating suspected CTE.

On April 23, Liz is hosting our 3rd Annual Race to End CTE Chicago Reception. It’s a night to honor those we’ve lost and stand with families impacted by CTE and push research forward.

Learn more and support our Chicago event at https://give.concussionandcte.org/event/3rd-annual-chicago-race-to-end-cte-reception/e776435

We join the global rugby community in mourning the loss of former New Zealand professional rugby player Shane Christie, ...
04/04/2026

We join the global rugby community in mourning the loss of former New Zealand professional rugby player Shane Christie, following the confirmation of advanced-stage CTE at just 39 years old. He is the third New Zealand rugby player to be publicly confirmed with the disease, following his close friend and teammate Billy Guyton, and Justin Jennings.

Shane represented the Highlanders, the Māori All Blacks, and the All Blacks Sevens during his career, before retiring in 2017 after repeated concussions. In retirement, he became a powerful advocate, sharing the reality of living with suspected CTE. In 2023, he co-founded the Billy Guyton Foundation to support players living with brain injury and to raise awareness of the long-term consequences of repeated head trauma. He also worked closely with our organization’s chapter in Australia, serving on its advisory committee and advocating for meaningful, systemic change in how rugby approaches player welfare.

Shane died by su***de in 2025. His loved ones hope that his final act of generosity, donating his brain to research, will help advance understanding of CTE and continue the mission he so passionately championed.

We stand with our colleagues in Australia in calling on all sporting codes and governing bodies to acknowledge the causal relationship between repetitive head impacts and CTE, implement CTE prevention protocols, and increase funding for research and athlete support services.

140.6 miles is a long way to go, but Matt Manahan says it’s nothing compared to the isolation he faced with an “invisibl...
04/03/2026

140.6 miles is a long way to go, but Matt Manahan says it’s nothing compared to the isolation he faced with an “invisible injury.”

As a high school hockey player, Matt faced a grueling six-month battle with PCS after multiple concussions in the same season. Adding to the physical pain, he says the hardest part was feeling unheard by doctors and frozen out by teammates who didn’t believe he was still suffering from persistent symptoms.

It’s why Matt and the MCY Foundation are going the distance for the Concussion & CTE Foundation — dedicating every mile they swim, bike, and run to our HelpLine.

As Matt and four friends train for this month’s IronMan Texas, they’ve already raised over $10,000 to keep our HelpLine free and make sure athletes know where to run for support during concussion recovery.

Head to the link on our stories to read more about Matt’s PCS journey and help Miles for a Cause reach its fundraising goal for our HelpLine.

Caroline Souza knew she was born to play soccer. Her childhood dream of playing in college came true when she was offere...
04/01/2026

Caroline Souza knew she was born to play soccer. Her childhood dream of playing in college came true when she was offered a scholarship to Chico State University in California.

Then a series of concussions forced her to make a difficult call: step away from the sport she loved to protect her health.

Caroline shared her story with us to help other athletes. Not to sugarcoat reality, but to show what’s still possible. A full life, and a hopeful path forward that doesn’t sacrifice your future.

➡️ Read her full story on our Inspiring Stories webpage or at the link in our bio.

03/31/2026

We’re excited to bring you another episode of Invisible Impact, our post-concussion podcast! 🎙️🧠 This week, we’re joined by actress, model, and content creator .

Noelle witnessed concussions firsthand in the wrestling world growing up with her father, Hall of Fame wrestler Mick Foley. But after she suffered one herself in 2019 she realized how each and every brain injury is unique, and recovery doesn’t have to look like anyone else’s to be real.

Noelle has been living with daily headaches & post-concussion syndrome (PCS) since 2019. In our new episode, she shares an honest look at the challenges and realities of navigating life after a brain injury.
📺 Watch on YouTube
🎧 Listen on Spotify or Apple Podcasts

03/31/2026

Jaedan Brown wants to world to understand what living with a parent suffering from CTE symptoms is like. Her father is a former NFL player and coach. She and her siblings sat down with our team last year to bravely share their story.

Today, that documentary is being recognized as a Webby Honoree at the 30th Annual Webby Awards, the leading international awards organization honoring excellence on the Internet. 🎬

This distinction places us in the top 25% of all submissions worldwide, an incredible honor and a testament to the power of the stories we are dedicated to telling.

“Unrecognizable: The Cost of Football for Corwin Brown’s Family” explores the long-term effects of repetitive head impacts and the toll it can take not just on the athlete, but an entire family.

We’re deeply grateful to the Brown family for trusting us with their story, and to everyone who collaborated to bring this project to life.

Narrated by: Bob Costas
Producer/Director:
Director of Photography:
Post-production:
Audio mixer:
Gaffer:

🎥 Watch the full documentary at the link in our bio.

03/28/2026

Unlike a broken bone, there isn’t a simple scan or test that can clearly show a concussion or PCS. The often “invisible” nature of the symptoms can make them harder to understand, for both the person experiencing them and the people around them. That doesn’t make them any less real.

You know your body best. If something feels off, speak up. Ask questions. Share all of your symptoms, even the ones that seem small or unrelated. If you feel dismissed, it’s okay to seek a second opinion or ask for further evaluation.

Healing isn’t always linear, and symptoms don’t have to be constant or severe to matter. Keep track of what you’re experiencing, advocate for the care you need, and don’t minimize what your body is telling you.

If you want to hear what this can look like in real life, shares her firsthand experience on Episode 6 of Invisible Impact: a Post-Concussion Podcast.
📺 Watch on YouTube
🎧 Listen on Spotify or Apple Podcasts

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