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LymeLight Foundation

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LymeLight Foundation

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LymeLight Foundation, founded in 2011 is dedicated to providing treatment grants to help with Lyme!

lymelightfoundation.org/grants
lymelightfoundation.org/get-involved
lymelightfoundation.org/social-media-policy
linktr.ee/lymelightfoundation The Foundation awards grants to eligible children and young adults through 25 years of age. It is the goal and the hope of the Foundation that through these grants children can receive proper treatment and medications in their fight against Lyme disease. The LymeLight Foundation is recognized by both the IRS and State of California Franchise Tax Board as a tax-exempt 501 (c) 3 organization. Contributions to the LymeLight Foundation are tax-deductible as allowed by law.

10/19/2026

After 15 wonderful years of hosting our Dart for Art annual fundraiser we are taking an event pause in 2027. Dart for Art has been an amazing success over the years, and we are taking time to celebrate all that has been accomplished, refresh our team and reinvigorate the event.

Since its beginning, Dart for Art has raised an INCREDIBLE $2.8 million and funded 282 full treatment grants for children and young adults battling Lyme disease.

We are deeply grateful to the artists, attendees, sponsors, patrons, and supporters who have made this event so meaningful over the years. Your generosity and belief in our mission have helped bring hope and healing to so many young people and their families.

As the event takes a pause, our mission does not. Together, we can keep lighting the way for the next child in need. 💚
Give the gift of health (also linked in bio): lymelightfoundation.org/donate

10/14/2026

ONE MONTH TO GO! 🌴✨ Come Join us on the beach, under the stars!

On November 13th, LymeLight Foundation will be the beneficiary of the 2026 LymeBytes Symposium Beachfront Gala in Fort Lauderdale, and we can’t wait for this special evening under the stars. This unique and fun gala will bring together the Lyme community for a night of connection, music, dancing, and excitement all while supporting LymeLight’s mission to provide treatment grants to children and young adults battling Lyme disease. We hope you’ll join us in Fort Lauderdale! 💚

🌊 Beachfront views
🍹 Cocktails at sunset
🔥 Fire pits on the beach
🍽️ Gourmet organic, gluten-free and dairy-free food
🎶 Live music and dancing
🏖️ Beach games
✨ A community coming together to make a difference

We’re so grateful to Dr. Myriah Hinchey () and the LymeBytes team for choosing LymeLight as this year’s beneficiary.

🎟️ Tickets are available for the BEACHFRONT DINNER and the SYMPOSIUM at shop.lymebytes.com and through the link in our bio.

10/12/2026

Our LymeLight Grant Recipient Gianna is proudly showing off the artwork she created at our summer Grant Recipient Reception. 💚

“Gianna was so happy to be included in the reception, and she was especially proud of herself for having the courage to say 'hi’ during the gathering. Afterward, she couldn’t wait for me to take a picture of her coloring page so we could send it to you! Thank you again for your generosity, kindness, and for making our family feel so welcome. We are truly grateful!”
— Kristi, mother of LymeLight Grant Recipient Gianna

Her beautiful smile reflects the joy of getting back to simply being a kid again, thanks to the amazing support of our incredible donors. YOU are giving LymeLight Grant Recipients across the nation access to treatment and healing from Lyme disease so they can move forward with lives filled with HOPE! 🪁🌈✨

10/07/2026

LymeLight Grant Recipient sisters Vada and Sloane give us HOPE through their positivity, friendship, and gratitude. 💚🌈✨

“Since Lyme disease affects every person differently, including the way they heal, it was so hard to figure out what the best treatments would be. I can confidently say we tried sooooo many things to help our daughters get better that would not have been possible without the grant funding. Nearly everything that we were interested in trying was costly and wasn’t covered by insurance.

I am so thankful to LymeLight for the grants that made healing possible for our kiddos. I can say they are both now functioning normally and able to just be kids. We still have some hurdles to cross, but I have HOPE because of LymeLight.”

– Kelleen, mother of LymeLight Grant Recipients Vada and Sloane

10/05/2026

THANK YOU to all who have hosted Facebook, Instagram and other inspiring fundraisers to help children battling Lyme disease! We are touched by the outpouring of support that has been raised so far in 2026 by Aimee, Teri, Kristle, Andrea, La, Dana, Troy, Brandi, Janell, Liza, Stephanie, Veronica, Maria, Cynthia, Sylvette, Kat, Kaleigh, Shelley, Karen, Robin, Ian, Yukiko, Serita, Theresa, Meg, Troy, Kay, Jake, Lisa and Iyesha.🌟⭐🌟⭐ Your passion combined with your generosity is an example of HOPE IN ACTION! LymeLight is incredibly grateful for your belief and support of our vital mission. Thank you and keep up the great work 💚

100% of ALL FUNDS RAISED to benefit LymeLight Foundation go directly toward treatment grants for children and young adults!!! Want to be a part of making a POSITIVE difference? Turn your passion into impact and host your own fundraiser - here are a few ideas to get you started:

💚 Marathons/5Ks/Other Athletic Adventures
💚 Concerts
💚 Art Nights
💚 Bake Sales
💚 Awareness Booths
💚 Fraternity/Sorority Fundraisers
💚 And many more! Any passion/talent can be turned into purpose!

Ready to host your own event? Visit our events page to learn more (also linked in bio): lymelightfoundation.org/auxiliary-events-collection

10/03/2026

LymeLight Foundation is honored to stand with the Center for Lyme Action, Bay Area Lyme Foundation, Project Lyme, Alpha-gal Alliance Action Fund, Global Lyme Alliance, and The LivLyme Foundation in applauding the Executive Order to accelerate action against tickborne diseases. Together, we recognize the importance of continued collaboration, innovation, and investment to turn promising research into meaningful solutions for patients and families.

“For families facing Lyme disease, innovation cannot come soon enough,” said Phyllis Bedford, Co-Founder and Executive Director of LymeLight Foundation. “We see every day how devastating this disease can be for children and young adults and how urgently families need better options. We are encouraged by this Executive Order’s focus on accelerating research, innovation, prevention, and solutions for tick-borne diseases. Building on the Lyme Disease Moonshot and LymeX efforts can help turn promising ideas into meaningful advances for patients and families who have been waiting far too long.”

You can read the full release here (and linked in bio): einpresswire.com/article/946626367/leading-tickborne-disease-organizations-applaud-executive-order-to-accelerate-action-against-tickborne-diseases

09/30/2026

A very exciting update from our LymeLight Grant Recipient, Luca and his twin, Hudson! 🎾

Despite the many ups and downs grant recipient Luca has faced throughout his Lyme disease journey, his perseverance and stamina continue to amaze us! This summer, Luca took first place, and his twin brother, Hudson, took second place at the Green Dot 10U Masters tournament, where the top eight tennis players compete at the end of the season! 🏆 Congratulations, boys!

“Lyme has taken so much from them and our family, but somehow, Luca continues to surprise us. We are always so grateful for this foundation and all it has afforded us. Four weeks before the tournament, Luca was at the hospital three days a week for two weeks getting plasmapheresis with a Permacath surgically implanted for the procedure. Thanks to this grant, Luca is getting better, and while the journey is still ongoing, we are most grateful for the ability to receive treatments that most people don’t have access to or can’t afford.”

— Brittani, mother of LymeLight grant recipient Luca and his twin brother, Hudson

09/29/2026

It’s been one week since an incredible night of music, community, and Lyme awareness in Central Park! 💚🎶

LymeLight team member Katie Tessier joined the thousands of people who came together to enjoy the music while also learning more about Lyme and tick-borne diseases, tick prevention, and how to stay safe outdoors.

We were proud to support Music for Action at SummerStage NYC, featuring Young the Giant and St. Lucia and to collaborate with other Lyme organizations, advocates, patients, and supporters to help spread awareness and reach people who may not otherwise be familiar with Lyme disease.

A huge thank you to , , , and everyone who helped make this special night possible.

With fellow support from: Steven & Alexandra Cohen Foundation Global Lyme Alliance Project Lyme The Quiet Epidemic Bay Area Lyme Foundation

09/28/2026

We’re excited to share that LymeLight Foundation has been selected as the beneficiary of the 2026 LymeBytes Symposium Beachfront Gala! Dance barefoot under the stars, and help a child heal 🌴🕯️

Taking place November 13–14 in Fort Lauderdale, the LymeBytes Symposium is the premier functional medicine conference on complex, chronic infection-driven illnesses. The weekend features a special Beachfront Gala on November 13, with proceeds benefiting LymeLight’s mission to provide hope and healing through treatment grants to children and young adults battling Lyme disease!

🌊 The ocean just steps away
🍹 Cocktails at sunset
🔥 Fire pits glowing on the beach
🍽️ Gourmet organic, gluten-free & dairy-free food
🎶 Live music & dancing
🏖️ Beach games
✨ And an incredible community coming together under the stars

We’re incredibly grateful to Dr. Myriah Hinchey () and the LymeBytes team for this amazing opportunity. Together we are Lighting the Way! 💚

🎟️ Want to attend? Come join us there. Get your tickets here for the BEACHFRONT DINNER and for the SYMPOSIUM (also linked in bio): shop.lymebytes.com

09/25/2026

In a powerful new commentary for the Times Union, investigative journalist and author Mary Beth Pfeiffer highlights how inadequate testing, limited treatment options, and severe underfunding continue to obscure the true impact of Lyme and other tick-borne diseases.

“The future of children playing in the outdoors, and leading lives free of chronic tick-induced illness, depends on it.”

It is time for greater awareness, stronger research, accurate diagnostics, and the investment patients deserve.

Read the full article (also linked in bio): bit.ly/TBDBlindSpotByMBPeiffer

Address

1229 Burlingame Avenue, Ste 205
Burlingame, CA
94010

Opening Hours

Monday	9am - 5pm
Tuesday	9am - 5pm
Wednesday	9am - 5pm
Thursday	9am - 5pm
Friday	9am - 5pm

Telephone

+16503485509

Website

http://lymelightfoundation.org/

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