The Kemp Legacy Foundation, Inc.

09/13/2026

Check this out if you are facing a rare disease or if you are supporting a loved one facing a rare disease. https://www.facebook.com/share/p/1EovzyuV7X/

rare disease community — we’re coming to Fort Lauderdale! 🌴

Registration is now open for NORD's free Living Rare, Living Stronger event on Friday, Dec. 4, at the Broward Center for the Performing Arts.

This free event brings patients and caregivers together for a day of education, connection, and community building. Attendees will learn from experts, connect with others on similar journeys, discover local resources, and explore opportunities to get involved in advocacy.

Register today: https://livingrare.org/florida/

07/19/2026

❤️ Sometimes hope begins with a single conversation.

Recently, we had the privilege of meeting Brittney Sunser, a devoted single mother of three, breast cancer survivor, and a woman who continues to face chronic ongoing medical challenges with remarkable strength and faith.

After learning about Brittney's journey, our Board was honored to provide charitable assistance to help ease some of the burden her family is experiencing.

When Brittney shared her testimony with us, these words reminded us exactly why our Foundation exists:

"I was looking for more than financial assistance—I was looking for people who understand that sometimes one act of kindness can
give someone the strength to keep moving forward. I am so grateful to have gotten that from speaking with Jennifer Kemp!"

Those words are a reminder that sometimes the greatest gift we can give someone is knowing they are seen, heard, and not alone.

Today, we invite our community to continue walking alongside Brittney and her family.

If you feel led to help, you can make a donation directly to support Brittney Sunser and her family. Please use the link below and include "Brittney Sunser" in the memo or comments section so your gift is designated specifically for her family's ongoing needs.

🔗 https://givebutter.com/the-kemp-legacy-foundation-inc?fbclid=IwY2xjawPKYJdleHRuA2FlbQIxMABicmlkETFGclJzS0Z0Y21DM3RyWndrc3J0YwZhcHBfaWQQMjIyMDM5MTc4ODIwMDg5MgABHgzkwyiX7AfIE3G9AgeHQrU1UUZ376-sVpPOMsof2c69ieX17yIKplM1BwU3_aem_XV9t24lLtf8eqj0CrIAazA

Every act of kindness—whether it's a donation, a prayer, or sharing this post—can remind someone that hope is still alive.

Thank you for helping us fulfill our mission of bringing Faith. Community. Service. Perseverance. Hope.

To learn more about The Kemp Legacy Foundation click the link here: https://thekemplegacyfoundation.org/

07/13/2026

07/02/2026

Only the Zebras will understand… Let’s change that!

Many zebras live with more than ‘just’ Ehlers Danlos Syndrome. A common combo you’ll hear about is the EDS + POTS + MCAS trifecta.
EDS – a connective tissue disorder that affects joints, skin, organs, and more
POTS – a form of dysautonomia where standing can cause rapid heart rate, dizziness, nausea, and even fainting
MCAS – Mast Cell Activation Syndrome, where mast cells release chemicals in the wrong way, causing allergy like reactions, flushing, GI issues, and more
These conditions can overlap and flare together, creating a web of symptoms that is exhausting to manage. If you live with any part of this trifecta, you are not ‘too much’ — your body is just dealing with a lot.

05/24/2026

A negative Lyme test does not always rule out Lyme disease.

In this video from Johns Hopkins Medicine Rheumatology, experts discuss the limitations of current Lyme disease testing and why clinical symptoms and patient history matter. Many patients facing chronic or complex illness are dismissed after a negative test result, but the science is more nuanced than that.

We believe awareness, education, and early recognition are critical for patients and families navigating Lyme disease and infection-triggered conditions.

Watch the full video on the Limitations of Lyme Disease Antibody Tests at https://youtu.be/r56kk66LfRc?si=mImxwgHXTQf5Zdug

04/04/2026

03/28/2026

🐾✨ URGENT PLEASE SHARE: Let’s Help Brittni ✨🐾

For 35 years, Brittni Flemming has been a tireless advocate for shelter animals — always fighting for those without a voice.

Now, she needs ours.

Brittni is currently seeking a living kidney donor. After living most of her life with one kidney, it is now failing. She is also the sole support system for her disabled adult son and is determined to be here for him.

She has begun the transplant process at Memorial Transplant Institute in Hollywood, FL and is actively searching for a donor.

If you’ve ever considered becoming a living donor — or know someone who might — please take a moment to learn more:
👉 MHS.donorscreen.org

Sharing this post could save her life. Please help us spread the word.

Let’s show Brittni the same love and dedication she has shown so many others. ❤️🐾

03/27/2026

We had the honor of supporting St. Jude at an unforgettable evening at The Glazer Hall, where music became hope. 💛

Dame Marina’s performance was breathtaking, but the moment that truly stayed with me was when she dedicated “Somewhere Over the Rainbow” and “Bridge Over Troubled Water” to the children of St. Jude. It brought tears to my eyes.

It reminded me why we created The Kemp Foundation—to be a bridge for families facing the unimaginable.

I’ve always loved “Bridge Over Troubled Water,” but last night gave it new meaning. It may just become the heart song of our foundation.

Grateful to attend a cause that gives families hope when they need it most. 💛

03/18/2026

Hi friends,

We have a local who is in need of a kidney. We are asking that you please continue to share this post in hopes a donor will be found.

It just takes a second to share!