National Kidney Foundation

Hi everyone, my name is Marc Perez. I’m currently undergoing dialysis and in urgent need of a kidney transplant. I’m sharing my journey to raise awareness about living organ donation—and to support the incredible work of the National Kidney Foundation, an organization fighting to transform kidney care and save lives. 

If you are interested in becoming a living organ donor, or know someone who is interested, please visit this link to learn more and sign up: https://nkr.org/QLU857

The National Kidney Foundation is leading the charge to eliminate preventable kidney disease, drive innovation in patient care, and tackle the inequities that affect so many in need of dialysis and transplants.

Every donation—no matter the size—makes a real difference. If you’re unable to give right now, simply sharing this page can help reach someone who can.

From the bottom of my heart, thank you for your support. Your generosity means the world to me.

Want to join me in making a difference? I'm raising money to benefit National Kidney Foundation, and any donation will help make an impact. Thanks in advance for your contribution to this cause that means so much to me.

More information about National Kidney Foundation: The National Kidney Foundation is the leading organization in the U.S. dedicated to the awareness, prevention and treatment of kidney disease for hundreds of thousands of healthcare professionals, millions of patients and their families, and tens of millions of Americans at risk.

On November 4th 2022 I was admitted to hospital with pneumonia and hypertension. 2 weeks later I left with a diagnosis of chronic end stage kidney failure. Facing a life on dialysis or death my only hope was a transplant.

Step forward my brother Declan and one year later my life has changed in ways I could’ve never imagined. We faced months of testing together with many ups and downs along the way. With the help of Jess, my sister Susan and close family, I survived. 

Only 4% of the millions of people dealing with this disease are as lucky as me. There are over 100,000 people currently on the transplant list awaiting a deceased or living donor. 

I would like to try and give a little back by fundraising and volunteering as a peer mentor with the NKF giving guidance to those recently diagnosed with renal failure. 

Your donation is tax deductible and will go directly to the NKF. It will help people on dialysis as well as furthering research and making transplants more accessible.

December 7th, 2021….that is the day JJ Jeffries officially became an #organdonor, donating a left #kidney to one of his best friends, Jey Yokeley. To say the least, it was a day they will never forget. An early morning wake up in Winston Salem at Wake Forest Baptist Medical - to which Jey and JJ being former athletes (and their wives) referred to as “Game Day”.

That day, aside from July 2022 when we married our wives, was by far the most single impactful day of our lives. Everything, and I mean everything, instantly became noise. The fragility of life became real. The importance of family, friendship, and relationship became ever so more powerful. The day was here, where we would literally become blood brothers and form a bond that could never be explained by words.

When people inevitably found out after the surgery, it took many by shock - and understandably so. We ourselves before this day would have thought the same thing. It’s not every day you hear stories of an living organ donor….but often times we thought, “why not?” So it got us thinking….”JJ, why aren’t you advocating?” Why aren’t you helping change the narrative, that more people out there just like you could literally help save a life?"

According to the #NationalKidneyFoundation, on average the transplant waitlist (for a deceased kidney) is 3-5 years, and much longer in some areas of the country. However, if you have an approved living donor that clears the medical tests required, the wait can literally be days. It’s a game changer for someone in need, with little to no change whatsoever in lifestyle post recovery. Yes, #Donating can seem daunting and far from reality, with the countless questions and tests, but JJ and Jey are living proof that there are THOUSANDS out there that could save the life of someone in need - helping eradicate the waitlist as it stands today for many of those in dire need.

I’m sure many of you in your networks have a friend or loved one that has been impacted by kidney disease; and if so, we encourage you to support them, as many of you do already. But don’t rule out donating - to give the gift of life. That day JJ realized he forever changed Jey’s life, but Jey forever changed his. It reminded them both that our days are counted and it matters how we live them. Be bold. You will never regret that decision.

A special thanks to the amazing surgeons and team Wake Forest Baptist for such a successful surgery. To our wives Jordan and Dani for standing by our side every step of the way, and our incredible support system of family, friends, colleagues, and two outstanding companies in Capco and TransImpact that stood behind us through this entire journey.

If you or someone you know if going through this similar journey, please do not hesitate to reach out. Support is just around the corner!

-JJ & Jey

Thanks in advance for your contribution to this cause which means so much to us.

More information about the National Kidney Foundation: The National Kidney Foundation is the leading organization in the U.S. dedicated to the awareness, prevention and treatment of kidney disease for hundreds of thousands of healthcare professionals, millions of patients and their families, and tens of millions of Americans at risk.

Hi, I'm Alexis Dulle, and I'm raising funds for the National Kidney Foundation. This incredible organization is dedicated to saving lives by fighting preventable kidney disease, enhancing patient experiences, and addressing inequities in kidney care and transplantation. Together, we can make a significant impact in the lives of those affected by kidney disease.

Your support helps the National Kidney Foundation make a difference by contributing towards efforts like:

Every donation, no matter the size, brings us closer to a world where kidney disease is manageable and preventable. Let's join forces to support the vital work of the National Kidney Foundation. Thank you for your generosity!

a little about my story: Last April, I found out that I have polycystic kidney disease. This took us as a suprise that up to that point other than my past eating disorders I had been a healthy kid. But they found many cysts and engagement of my kidneys making me the 8th in my family to obtain this disease. My mom is currently the only other living one left, but she is at stage 4 kidney failure working to be put on the kidney transplant list in hopes to avoid doing dialysis and finding an alternative. With this disease most of the other diseased members have been through dialysis and we’re able to recieve a kidney through transplant. Recently, I started having my own problems with blood pressure and have been put on a medication to maintain it. Now, my next step is to be put on medication to slow down the process as I am a young patient to have PCK at only 19. This past year, I have been selected to be on the national kidney foundation committee and am in the process of putting word out there and finding support in many ways. As a committee member, my goal is that raise atleast $500 and create my own team for the foundation walk in Toledo, OH.

If you are interested in joined our team or even donating to help other Kinsey patients and related people who are just like me and my mom, then please feel free to donate or contact me at [phone redacted] if you want to join our team. The walk with be held on septemember 7th and will be a blast of a time with many events, acitivities, food, and drawings to take place. Join us in honoring those who are in need of your support.

My name is Nic Carter and since it is National Kidney Month I am asking people to donate. I received a kidney transplant on 4/29/2025 after 5 years of dialysis. Even $1 will be greatly appreciative. God Bless. Thank you!!!

Help Me Raise $25,000 for PKD Research – Let’s Make an Impact!

I’m reaching out because this mission is personal—not just for me, but for the 500,000 people diagnosed with Polycystic Kidney Disease (PKD) each year. PKD is a rare genetic condition that affects only 1 in 1,000 adults, yet its impact is devastating.

The significance of this fundraiser is deeply personal to me because of my close bond with my grandfather. He was my best friend, my protector, and the very first person to hold me as a baby. He was always there to keep me out of trouble, and his love and guidance shaped who I am today. This mission is especially meaningful because PKD is a hereditary disease—one that my grandfather carried and, unfortunately, was passed down to me. While he peacefully succumbed to renal disease, I was diagnosed far earlier than most, as PKD typically remains undetected until a person’s 40s or 50s. Because of this, I feel it is my purpose to advocate for those affected by PKD—for people like my grandfather and myself. This fundraiser is not just about raising money; it’s about carrying on his legacy and finishing the fight he started—to find relief, resources, and ultimately, a cure for PKD.

So, What is Polycystic Kidney Disease (PKD)?

PKD causes fluid-filled cysts to grow on the kidneys, leading to enlargement, organ damage, and eventually kidney failure. In severe cases—like mine—both kidneys are affected, which means a single or double kidney transplant could be in my future. There are two types of PKD caused by genetic mutations:

ADPKD (Autosomal Dominant PKD) – The most common form, inherited from a parent.

ARPKD (Autosomal Recessive PKD) – A rarer, more severe form passed on when both parents carry the gene.

There is no cure for PKD. But with research, we can change that.

How You Can Help:

My goal is to raise $25,000 for the National Kidney Foundation to support PKD research, treatment advancements, and patient resources.

If just 250 people donate $50, we will reach our goal and make a real impact!

Every donation brings us one step closer to better treatments and a cure for PKD.

To make a difference for individuals like me, please donate to this cause so I and others can thrive in life without this terrible disease!

Supporting My Pageant Journey:

In addition to fighting for a cure, I am also fundraising for my journey to the Universe United Miss pageant! I need support for lodging, travel, wardrobe, and pageant fees to ensure I can compete at my best while advocating for PKD awareness on an international stage.

Support My Pageant Fund Here: https://gofund.me/190830f2

I cannot do this alone, but together, we can create change. Whether you donate, sponsor, or simply share this message, you are making a difference. Thank you from the bottom of my heart for supporting me in this fight for a cure—let’s bring this title AND awareness for PKD home!

With love & gratitude,

Asiana Swift-Miller

Universe United Ms. Tennessee 2025

Hi,

I'm Janvee.

In 2020, I lost my dad, RAJ to kidney failure. His journey through dialysis and the challenges he faced showed me the importance of supporting those with kidney disease. I’m now raising funds for the National Kidney Foundation in his memory, so that others battling kidney disease can receive the care and support they deserve.

Every donation will help provide vital resources for dialysis treatments, awareness programs, and patient support. Your contribution, big or small, will make a significant difference in the lives of those who are struggling with kidney failure.

Please join me in supporting kidney patients and helping save lives. Thank you for your kindness and generosity.