Why I Do What I Do: Spotlight on Michael Levine, NephCure Vice President October 2, 2017 by Lauren Eva Michael with his son, Matthew. NKI: How did you first find out about NephCure? How did you get involved? Michael Levine: I think my wife Dana found NephCure on the internet. That was 12 and half years ago, when my son Matthew was first diagnosed with FSGS. I think it was a few months after the diagnosis that we got connected. The first event we got involved with was probably the Countdown to a Cure gala, with Ron Cohen and everybody from New York. NKI: You’ve been involved both directly as a chair for so many of our events, like Countdown to a Cure New York and All In For a Cure on Long Island. What’s been your favorite NephCure event? Michael: Well, each one is different. Quite frankly I love them all, because they all serve a purpose: to create awareness all over the country and the world, and to bring exposure to NephCure, FSGS and Nephrotic Syndrome. And obviously, the events raise dollars to try and create this miracle of a cure. I guess my favorite event is Countdown to a Cure, because NephCure gets to put its best foot forward to so many people. Over 500 people attend, we raise over $600,000, and it’s just a very classy, professional event that is seen by so many families and patients around the country. It gives these patients and families hope. Seeing what NephCure does with that dinner, and meeting families from all over the world, it gives everybody so much hope that if we could do more events like that, a miracle of a cure is attainable. (L-R) Michael’s wife Dana Levine, special guest Cuba Gooding Jr, and Michael at the 2014 Countdown to a Cure gala. NKI: You have raised an incredible amount of money in the 12 years that you have been volunteering with NephCure, on the NephCure board, and chairing for so many events. Does asking for money get any easier with experience? Michael: It never does. The only thing that gets any easier is the knowledge of what we’re doing. Talking about what NephCure does and what our goals and dreams are, that gets easier because I talk about it so much. And telling my story gets easier only because it’s so engrained and enveloped in me. But for me, asking for money is not something that gets any easier. It’s very hard for me to do because I’ve never been a person who is big on asking for help. Many of the fundraising experts say that it should get easier, because you’re asking for money for a very good reason: you’re asking for money to fund a cure and save lives. But for myself personally, it never gets easier. NKI: Is there anything that you think to yourself just before you initiate that first conversation that helps you get past that feeling that it’s going to be tough to ask for money? Michael: Well every time I ask, I say to myself, “Think about all the warriors around the country and around the world battling FSGS and Nephrotic Syndrome.” All the people who reach out to me on Facebook with their families’ and children’s stories. All of the Humans of NephCure stories on Facebook, which I read every single week. You know, sometimes it’s not easy. Sometimes it’s overwhelming. And there are some days that I say, I can’t do this anymore. But then I think about all the families and children that are battling this horrible disease, and I don’t want them to go through the same living hell that my family has gone through over the past 12 years. So that’s my motivation. There are two phrases that I always carry around when I do this. First of all, when I find out that somebody has made a donation to NephCure for an event that I’m a part of, I always write back to them, “You’re an angel on our shoulders. You allow us to dream that a miracle of a cure is possible. You give us hope against the greatest odds, and you give us the strength to fight every day.” I write that to everybody. Matthew Levine, Yankees Manager Joe Girardi, and Michael at a Yankees pre-game press conference this year. I also often write to people, “We are delivering dreams, miracles, wishes, and cures to the warriors around the world battling two devastating kidney diseases, FSGS and Nephrotic Syndrome. These diseases have no cure, and destroy kidneys, families, and lives in their path.” Whenever I think of those things—that’s what motivates me to tell my story to ten people a day, and to ask people for help and to donate money, and to ask people to attend all these events around the country. NKI: What kind of advice would you give someone who wanted to do a big event, like a gala, for NephCure? Michael: The first year is the toughest. You just have to get through that. After the first year, when people see how heartfelt you are and see that you’re trying to deliver dreams, miracles, wishes, and cures, it will get easier. NephCure, FSGS and Nephrotic Syndrome need a ton of awareness and exposure and a ton of dollars. So grab some friends, family and business associates, and say, “I want to save some lives today. I want to create a miracle of a cure for the children and adults battling FSGS and Nephrotic Syndrome.” Whether it’s a bowling tournament, a sporting event, a golf outing, a lemonade stand, a gala, a dinner, just grab some people, form a committee, start having some meetings, and have that committee invite their friends, family, and business associates to the event. It’s like a mushroom, or a plant—it will grow. After you get through the first year, everyone who attends in year one will invite more people for year two, and it just expands. If you want to create a miracle of a cure for FSGS and Nephrotic Syndrome, just create an event. You can do it anywhere in the world. You might not raise that much money, awareness, or exposure in year one. But it’s the stepping stone to years 2, 3, 4, and 5. And maybe by year 4, 5, or 6 you could be like the Tampa Pig Jig, where they’re raising $800,000 and have 6,000 people attending their event. You can’t get discouraged; you just have to fight through it. Just get started. I think that’s the best advice I can give. NKI: You make something that might seem complex to someone who has never done it before seem very attainable and possible. Michael: It’s very possible. You could start an event anywhere, and every dollar you raise brings us one dollar closer to a cure. You’ll get so much out of it, knowing that, and all of your friends and your family can be involved in it with you. And when the event is over each year, the fulfillment of saving lives by doing an event is incredible. I would just like to add that NephCure has been a godsend to my family. With all the events that NephCure puts on—the Nephrotic Syndrome Symposia, the conference in Chicago, and all the walks and events and the visits to Capitol Hill—all these events bring awareness and exposure to the disease, and they allow us to dream that a miracle of a cure is possible. All these events allow us to participate in so much and know that we’re making a difference. The doctors that are involved, the scientific advisory board, everybody at NephCure—my family considers them angels on our shoulders because they give us hope that one day a miracle of a cure can be found. You really are making a difference. And I would just stress to people to get involved. People think NephCure just needs money. And we certainly do. But there are so many other ways to help—with your businesses or your workplace; it doesn’t always have to be money. Money is great, but people can also donate their time, goods, services, and supplies. They would be giving hope to so many people. Just get involved in some way. Michael and other NephCure board members and supporters ring the opening bell at the New York Stock Exchange on Aug. 15th, 2014. We are so grateful and lucky to have someone as committed as Michael on our board. Michael continues to devote an incredible amount of time and energy to NephCure each year. We salute you and your work, Michael! Thank you for your dedication to finding better treatments and a cure for all who suffer from FSGS and Nephrotic Syndrome. The Countdown to a Cure gala will be on Pier Sixty in Manhattan on Nov. 9th at 6pm. We invite you to attend, meet Michael, and help us change lives. You can visit the event page here. If you have any questions, please contact Lorraine Mackin at LMackin@NephCure.org.
Why I Do What I Do: Spotlight on Laci Weatherford, Volunteer Walk Leader August 1, 2017 by Lauren Eva Laci Weatherford is now in her 7th year as a volunteer leader for the St. Louis NephCure Walk. Her incredible efforts have helped grow the walk to a massive event, with more than 100 people in attendance and raising around $15,000 each year! We spoke to her recently to learn about her journey with FSGS and how she manages such a successful fundraiser. NKI: How did you become involved with NephCure? How long have you been involved? Laci at the St. Louis Walk in 2012. Laci: I believe the first time I found NephCure was in 2009 when I was diagnosed with FSGS. I researched on the internet and found the NephCure website. I must have provided my information and said I would like to get involved, because in 2011 I received an email saying they were going to have a walk in St Louis. The email asked if I would like to be on the committee. I said yes. The day I was on my first planning committee call, I discovered I was the committee, the only volunteer for the event that was about a month away. So that year I learned the very basics of putting together a walk and have been working on improving and growing our annual event ever since. NKI: Why do you devote your time and energy to this cause? If you feel comfortable explaining, what’s your personal connection to kidney disease? Laci: After I was diagnosed in 2009, I began my personal journey with FSGS and learned firsthand the terrible side effects of the drugs available and the lack thereof. I learned how precious the little things were and struggled to just get by day-to-day, enjoy my 2 year old baby, and take care of myself. I began to read more on the internet about this disease: sometimes it would be good and encouraging, sometimes not. It quickly became too overwhelming to read the stories from parents who had children struggling with these drugs and side effects. It broke my heart, and I felt it was so unfair. I had lived a good life up until my diagnosis; I enjoyed my childhood, but they were being robbed of simple joys. I received a referral for a specialist in NY and became so encouraged by his accomplishments and his knowledge of the disease. I have tremendous hope and belief the cure and proper treatments are out there. We just need the right people to have the right tools to make it happen. It takes a lot of work to put all the proper channels in motion, and I’m so grateful NephCure is there doing the work to keep progress in motion. I want to do what I can to help fund this process. Laci and members of Team Brayden at the 2016 St. Louis Walk. NKI: What’s the hardest part about being a walk leader? Laci: The hardest part is getting the word to participants. Since this is a rare disease, not many people have ever heard of FSGS or NephCure. Unless you or a loved one is personally impacted, then you are probably not looking for another charitable event to go to. I’ve got to find a way to find the patients and their families. Doctors aren’t willing to help most of the time because of HIPAA policies and various other reasons. NKI: What’s the best part? Laci: There is so much that warms my heart about the event. The first is my family. They drive 3 hours just to be in St. Louis with me on this special day. They also coordinate 75% of the activities and volunteer in any area I need. If it wasn’t for them, I literally couldn’t do this. Second is seeing the other patients. To see them smile and enjoy a day dedicated to them encourages me to keep going. I also love to see the growth in the event, which is the proof we are getting the word out there. My first walk had about 20 people and we raised around $2,400. The walk is now averaging between 100-120 people each year and we raise on average $15,000. That is just amazing to me. NKI: What has surprised you the most throughout your years of leading this walk? Laci: I’m surprised by how generous and easy is it to get donations. Most of the time all you have to do is ask. There are so many business that will gladly give you a gift card, services, or products to help you raise funds. There is no secret to fundraising or formula for getting donations—all you have to do is ask! Mostly likely you are going to get a yes. Laci, center, with family and friends at the 2016 St. Louis Walk. Congratulations and a big thank you to Laci and her supportive team for their incredible efforts each year! With their help, we are one step closer to finding better treatments and a cure for FSGS and Nephrotic Syndrome. We couldn’t do it without them! Interested in volunteering at a walk or creating a walk team? Great! Just email us at events@nephcure.org to get started.
Every gift has a story. November 23, 2015 by Lauren Eva Use new eCards to tell someone you love that you care about them.
2015 Countdown to a Cure – THANK YOU! November 20, 2015 by Lauren Eva We’ve said “hello” and “goodbye” to another Countdown to a Cure… From the beautiful scenery of New York City’s Chelsea Piers, to the heartfelt speeches delivered by NephCure’s beloved family, the Jones’ and honoree, Olympic athlete Aries Merritt, this event was truly the “Chance of a Lifetime” to make a difference in the fight against Nephrotic Syndrome. The success of Countdown has always been measured by the generosity of the many hundreds in attendance who consistently show support for NephCure and this year, our expectations were overwhelmingly exceeded, for which we could not be more grateful. You are changing the story. Energies were high and attendees were excited, lighting the way for one of the most successful galas in NephCure history. “Fund a Cure” donations blew expectations out of the water, bidding was at a high and the second annual game of “heads or tails,” brought a touch of silliness to an evening surrounding a very serious cause. Emcee, Moody McCarthy, along with “Asbury Fever,” a Bruce Springsteen Tribute band, kept the party going all night long with many moments filled with laughter, dancing and mingling. As always, we want to thank the committee who worked so hard to put this event together and the volunteers who generously gave up their time to help this event flourish into a huge success. The 2015 New York Countdown to a Cure raised over $750,000 and many left the event feeling inspired and hopeful. Finally, thanks to YOU. To each of you reading this who’ve decided to join us in this fight. We can’t do this alone. We need you, we’re grateful for you and we thank you.
NephCure Kidney International to Host First-Ever Fundraising Gala in Chicago October 8, 2015 by wpengine Chicago, IL (October 8, 2015) – Just one month until NephCure Kidney International’s (NKI) Chicago fundraising gala. This inaugural event will be held on Friday, November 6, 2015 from 7:30 PM to 11:30 PM at Architectural Artifacts, Inc., 4325 N. Ravenswood Ave, Chicago, IL. The event, themed “Crusade for a Cure” and sponsored by Rush University Medical Center, will bring together the most generous heroes of Chicago to raise money for research and finding a cure to the debilitating chronic kidney diseases Nephrotic Syndrome and Focal Segmental Glomerulosclerosis (FSGS). “We are thrilled to finally bring this fundraiser to Chicago,” said Jayne Drew, Regional Director for NephCure Kidney International. “The gala is in its 11th year in New York City and has raised more than $6 million. We believe we can have just as great of an impact here in Chicago.” Co-chairing the gala are Chicago natives and couple, Alap Patel and Amanda Schackart. “When Amanda was diagnosed with FSGS, our instant reaction was to learn as much as we can about the disease,” said Patel. “The problem, we soon realized, is that so little is actually known about it. This is why Amanda and I got involved with NephCure Kidney International. More research needs to be done on FSGS and Nephrotic Syndrome. More people need to be aware of these conditions, and the impact it has on millions of families across the US. We want to build a community where families affected by these diseases can know more and learn more from each other. We want to support a network of doctors who can discover more.” “We need more, we want more, and we want to give more!”, says Schackart. Nephrotic Syndrome and FSGS are conditions that affect the tiny filtering mechanisms in the kidneys. The result is that beneficial protein is spilled from the kidneys into the urine and is lost. Over time, this condition can result in renal failure and the need for dialysis or a kidney transplant. The cause of Nephrotic Syndrome and FSGS is not known, it can affect anyone, and there is no cure. FSGS is a leading cause of kidney failure in children. It is estimated that kidney disease affects 31 million people in the United States alone, with African Americans being 3 times more likely to experience kidney failure. Last year, 90,000 Americans were killed by kidney disease. More than breast cancer. More than prostate cancer. Tickets prices to the gala start at $125 per person, with VIP table options available, and include local cuisine, libations, raffle, as well as a silent auction. For more information about NephCure Kidney International, to purchase tickets or inquire about sponsorship opportunities, please visit the event website here CRUSADE, or by texting “CRUSADE” to 52182, or email Jayne Drew at jdrew@nephcure.org. About NephCure Kidney International NephCure Kidney International (NKI) is a 501(c)(3) tax-exempt public charity established in 1999. Comprised of patients, their families and friends, researchers, physicians and other healthcare professionals, NKI is the only organization committed exclusively to supporting research to identify the cause, improve the treatment, and find the cure of the two potentially debilitating kidney diseases, Nephrotic Syndrome and Focal Segmental Glomerulosclerosis (FSGS). ### Media Contact: Jayne Drew jdrew@nephcure.org 267-261-4918
Texas Clay Pigeon Shoot Fundraiser- Saturday May 9th in Lindale June 15, 2015 by Lauren Eva On Saturday May 9th, 2015, the Texas Clay Pigeon Shoot held by Baits, Balls & Clays raised $12,000 for Nephcure! Practice shooting and dinner with a live band (Bo Brumble) was held on Friday May 8th. The shoot was held on Saturday May 9th. Check out the photos below: Christian Family with Chad Grubbs (far right) Ashley Christian (Olivia’s mom) and Olivia Christian with Chad Grubbs talk to the crowd about Olivia’s struggles with FSGS [Best_Wordpress_Gallery id=”7″ gal_title=”Texas Clay Pigeon Shoot”] About Baits, Balls & Clays: In 2012 a group joined together to find a creative way to host multiple events that would help donate to charity. They called themselves Baits, Balls & Clays and the charity they selected was Nephcure. In their first year, Baits, Balls & Clays held a golf and fishing tournament, followed by the addition of a clay shooting tournament in the following year. Through their first 3 years Baits, Balls & Clays managed to raise around $20,000, which they donated to Nephcure. In 2013, a special little girl named Olivia was selected as an honorary member of Baits, Balls & Clays, becoming the face of the organization. About Olivia: Miss Olivia is 4 years old and a victim of a rare incurable kidney disease called FSGS. She and her twin sister were adopted into a family when they were young, gaining a mother, father, and 3 older brothers to watch out for them. Unfortunately, a few months after the adoption, when Olivia was only 16 months old, she was diagnosed with FSGS. Her illness caused the filters in her kidneys to stop working, spilling proteins into her body and causing massive swelling. The swelling had dire consequences for Olivia: she stopped walking, talking, playing, eating, smiling, and eventually stopped breathing on her own. In order to stay alive, Olivia went on dialysis and life support. Olivia was fortunate enough to survive with the help of a fighting spirit, and many supporters praying for her. Eventually with the help of various medications, she was stable enough to return home. Before her 3rd birthday, Olivia had undergone 7 surgeries and 12 hospitalizations. She has taken over 40 different medications in an attempt to treat her illness and keep her stable. Unfortunately, due to the lack of research regarding her rare disease, Olivia would be more likely to survive the most common form of childhood cancer than she would ESRD (End Stage Renal Disease), which is a common fatal outcome for patients like Olivia with FSGS. With supporters, Baits, Balls & Clays can continue to raise funds for desperately needed research through the Nephcure Foundation, which is committed to giving 9 out of every 10 dollars raised specifically to research for FSGS and its less aggressive form, Nephrotic Syndrome. Olivia and her family
Jet Food Stores – #Selfies4NephCure Contest May 29, 2015 by Lauren Eva On May 5th, Jet Food Stores hosted their annual NephCure Golf Classic at Twin City Country Club in Sandersville, Georgia. Over the past 12 years, this event has generated more than $350,000 for the NephCure mission. This year’s golf outing saw the introduction of the #Selfies4NephCure contest. Participants took “selfies” of themselves at the event and posted them to their social media pages. Jet Foods and NephCure are hoping that this social media awareness campaign will continue long after the golf outing. Anyone can join the fun and help us spread awareness – so take a picture of yourself, and post it with the hashtag on your Facebook, Twitter and Instagram pages with #Selfies4NephCure. NephCure board member and Jet Food Store President Charles Turner is the driving force behind the event. This cause is important to his family and their goal is to support research to discover and make available better treatments for all families dealing with these kidney conditions. Interested in hosting your own community fundraiser? Whether you’re running in a marathon, giving up your birthday for charity, doing a tribute, starting a walk in your town, or anything else; contact the events team at events@Nephcure.org to raise money for NephCure and make a real-life impact.
Support NephCure on #BTIGCharityDay – April 28, 2015 April 27, 2015 by Lauren Eva BTIG Commissions for Charity Day is Tuesday, April 28, 2015. SUPPORT NEPHCURE KIDNEY INTERNATIONAL on that day by asking your broker to trade through BTIG. Just ask that the trade support NephCure Kidney International. It will not cost you or your broker anything, commissions generated from the trades executed by BTIG on Charity Day are donated to charities nominated by BTIG clients. NKI is one of those charities! “BTIG Charity Day has grown into a global initiative. As a firm, we are passionate about the success of our annual event and are committed to supporting meaningful causes,” said Steven Starker, Co-Founder of BTIG. Since the event’s inception in 2003, BTIG’s clients, celebrity partners and employees throughout its U.S., London, Hong Kong, Singapore and Sydney offices, have raised more than US$30 million for hundreds of charitable organizations around the world, including over US$5 million from the May 2014 event last year. “We are always impressed by the number of well deserving organizations that our clients and celebrity partners support and bring to our attention each year. It’s an honor to be a part of an event that makes such a significant impact on improving opportunities for children and others worldwide,“ said Scott Kovalik, Co-Founder of BTIG. 2015 BTIG Charity Day Preview Video: https://vimeo.com/120527307 If you have questions about how to designate NKI as your beneficiary – please call NKI at 610-540-0186 ext. 24. About BTIG BTIG is a global financial services firm specializing in institutional trading, investment banking and related brokerage services. With an extensive global footprint and more than 475 employees, BTIG, LLC and its affiliates operate out of 13 cities in North America, Europe and Asia Pacific. BTIG offers execution, expertise and insights for equities, equity derivatives, ETFs, fixed income, futures, commodities, foreign exchange, interest rates, credit, and convertible and preferred securities. The company’s core capabilities include global sales, portfolio, electronic and outsource trading, investment banking, prime brokerage, capital introduction, corporate access, research and strategy, commission management and more. Disclaimer: https://www.btig.com/Disclosures.aspx
Countdown to a Cure ’14 – THANK YOU from NephCure! December 18, 2014 by Lauren Eva Another Countdown to a Cure has come and gone, but CDTAC 2014 was anything but ordinary. From the beautiful scenery of New York City’s Chelsea Piers, to the heartfelt dedication of NephCure’s inaugural Humanitarian of the Year award to Michael Levine, Countdown to a Cure 2014 was a night to remember. The real success of Countdown , however, has always been measured by the generosity of many hundreds in attendance who consistently show support for NephCure in our quest to accelerate research to find better treatments and a cure. Auction bidders were excited, Fund a Cure donations exceeded expectations and along with plenty of paddle raising, many participated in a game of “Heads or Tails,” willing to get a little silly for the cause. Those of us at NephCure are incredibly grateful, and we would never be able to express our gratitude enough. There are so many people, without whom, this night would not have been so successful. First, we would like to express heartfelt appreciation to Committee co-chairs Rich Genatt and Michael Levine. Michael and Rich are persistence personified, and their leadership of our Countdown committee is unmatched. Speaking of the Committee, a very special thanks to every member of our Countdown committee for your unique and invaluable contributions. Another thank you to the Milligan Family, our 2014 Fund a Cure Honorees. Jennifer and Jarrett, your unwavering determination to spread awareness and your passion for finding a cure for all those affected by Nephrotic Syndrome is the picture of strength and courage in the face of adversity. Congratulations! Joining us in kicking off the evening was Michelle Williams, Grammy award winning singing sensation and host of Oxygen’s Fix My Choir. Michelle graciously took the stage to welcome everyone in attendance. NephCure would like to thank Ms. Williams and congratulate her on the release of her fourth album, Journey to Freedom, as well as her nomination for a Stellar Music Award. We are thrilled to continue to work with Ms. Williams as a future Ambassador for NephCure. NephCure would also like to thank special guest Cuba Gooding Jr. The Oscar® award winning actor took the stage in supreme fashion and delivered a wonderfully vibrant dedication to Michael Levine, presenting him with his Humanitarian of the Year award with passion and enthusiasm. Thank you for your support of NephCure, Mr. Gooding, and best wishes and congratulations on both the upcoming release of Paramount Picture’s “Selma,” and your role as O.J. Simpson in FX’s American Crime Story. Finally, thanks to YOU. To each of you reading this who’ve decided to STAND UP & BE COUNTED to fight FSGS and Nephrotic Syndrome. We can’t do this alone. We need you, we’re grateful for you, we thank you. Watch Videos Here: [huge_it_videogallery id=”3″]
Cuba Gooding Jr. Partners with NephCure to Find a Cure! November 25, 2014 by Lauren Eva Cuba Gooding, Jr. may be best known for his roles as a high-energy football player, dedicated lawyer, or honor-bound solider. Off-camera the beloved actor and father of three is stepping into a new role: advocate and activist. The Academy Award® winning actor is partnering with NephCure Kidney International to raise awareness about kidney disease. “Kidney disease is the ninth leading cause of death in the United States, but is one of the most underfunded in research. FSGS (Focal Segmental Glomerulosclerosis) and Nephrotic Syndrome are some of the most devastating kidney diseases affecting children and adults. NephCure is the only organization in the world focused on raising money for research to get better treatments and a cure for these diseases. When I learned about these conditions I knew I had to do something. I’m proud to partner with NephCure to help them raise awareness,” Mr. Gooding said. Mr. Gooding will join NephCure at Countdown to a Cure, our Annual Fundraising Gala at New York’s Chelsea Piers on December 4. A select number of tickets are available for purchase until December 2 by clicking on this link. Can’t come to the event? You can still join the cause and support NephCure in their quest to end debilitating forms of kidney disease, FSGS and Nephrotic Syndrome. Simply text the word “CURE” along with your donation to 50155, or visit http://www.support.nephcure.org/TeamCuba to pledge your support today. To read the full press release, click here.