Spotlight on: Allison Kostiuk, NephCure’s Manager, Volunteer Programs March 26, 2019 by Kylie Karley A dedicated volunteer herself, now managing our ever-expanding nationwide army of NephCure supporters, Allison Kostiuk is leading the pack of our Regional Volunteer Communities. Our newest regional initiative is a massive undertaking, but one which Allison sees as an amazing opportunity to help empower people, get patients quicker access to expert care, and ultimately raise more awareness for Nephrotic Syndrome. Allison, NephCure’s Manager of Volunteer Programs, makes it look easy. Find out what makes her job so unique and learn more about our new Regional Volunteer Communities that are changing the game for NephCure. NephCure: How long have you worked for NephCure? Allison Kostiuk: From February 2015 to September 2016, I was the Regional Manager for the Eastern Region. I returned to NephCure in March 2018 as a Patient Engagement Manager, and in August 2018 I took on the exciting role of Manager of Volunteer Programs. NephCure: You’ve recently been involved with creating, managing, and recruiting our volunteer communities. What has that experience been like? Allison: This has allowed me to be entrepreneurial in my way of doing my day-to-day job, as we have never had this structure before. I love the creativity and the “learning by doing” at times. It has also allowed me to meet some amazing volunteers who have always been supporters of NephCure—when asked to step up and do more, they raised their hands and said “Pick me!” Amazing! NephCure: Why are volunteers so valuable to an organization like NephCure? Allison: Volunteers bring such depth to an organization like NephCure, as they bring not only their time and expertise, but first-hand knowledge of living with Nephrotic Syndrome. NephCure: Can you tell us more about the structure of the volunteer regional communities? Allison: For this first year, we have 12 Regions in the United States, some bigger than others, but this is a place to start. Each region has a Volunteer Leader, a Regional CEO if you will. The leader will work to manage, motivate and recognize the volunteers while meeting our goals and objectives as an organization. Then we have lead volunteers in Advocacy, Fundraising, Marketing/Communications, Patient Engagement/Support, and Voice of Patient. As new patient families meet us and indicate they want to get involved, a short training per area will occur and they will be introduced to their area lead. Each volunteer will play a role in that region in that area. We are also working to create regions internationally. NephCure: What excites you most about the future at NephCure? Allison: This larger corps of volunteers to help us meet our missional goals as an organization and to connect to more folks locally so that they don’t feel so isolated. NephCure: What are some challenges have you faced with this major task of the regional volunteer communities? Allison: Some regions are very big geographically, but like I stated above, we had to start some place this first year. Eventually, we would love to see a Regional Leader in each state, with a smaller geographic area to connect. International Regions will also be a challenge, but it is a great need to help connect these families to NephCure. NephCure: How will these volunteers have an impact on the way NephCure is run? Allison: NephCure’s biggest asset has always been our volunteers. This new structure will ensure our volunteers feel equipped, supported and recognized for their important roles. This structure can also address local needs more efficiently. If you would like to get involved and volunteer for NephCure, the best way is to reach out to me is via email: akostiuk@nephcure.org. NephCure: When you’re not focused on volunteers and NephCure, what are you doing? Allison: Spending time cheering on my four athletic kids and coach husband. I am also a runner and try and get out as much as possible to “get away” from my loud house. I am a volunteer outside of NephCure as well, and because of that, I can truly thank our volunteers for their passion, expertise and hours they dedicate to this cause, to NephCure. I spend my days thanking people. It’s priceless.
Advocating for Awareness: One Mother’s Quest to Save Her Daughter’s Life March 25, 2019 by Kylie Karley Kidney disease advocacy is something no parent plans to be exceptional at. In fact, kidney health wasn’t even a blip on Marlene Botta’s radar until her 14-year-old daughter, Jacqueline, was diagnosed with Nephrotic Syndrome on February 28, 2016. It’s a day Botta has a hard time describing. “My stomach just dropped to the floor, and I felt like throwing up. My first reaction was, ‘This is going to be bad,’” she said. After an original misdiagnosis and an entire week anxiously spent in the hospital, Jacqueline began taking steroids to try to treat her protein-spilling kidneys. “That was probably the most frightening and traumatic time in her life, because she blew up so big, so fast overnight. She didn’t want to go to school, she didn’t want anybody to see her,” Botta said. For six more months Jacqueline proceeded with high dosage steroids, however her body resisted the treatment. The Bottas ultimately made the decision to start a search for a different doctor; one who had dealt with and specialized in Nephrotic Syndrome cases. “I was hysterical and desperate, and I felt like there was no urgency to find a cocktail of drugs that worked; that’s when I sent a crazy message to NephCure,” Botta said. With support from NephCure Kidney International, Botta found an alternative doctor and connected with other patient families in her local community. Jacqueline tried many other drugs, including tacrolimus and prednisone, all of which were unsuccessful in slowing her declining kidneys. The next step: clinical trials. “Although the drugs ended up not really help Jacqueline, the trial that we were in was comprehensive and probably the best care that she could’ve gotten. The amount of care that you get in a trial is totally different than what you would get in a regular visit. With a regular care plan you see your nephrologist every 2-3 months, in a drug trial you’re seeing them every week or every other week,” Botta described. While Jacqueline’s first biopsy displayed Minimal Change Disease, her second biopsy proved otherwise. It wasn’t until June 2018 that she was officially diagnosed with focal segmental glomerulosclerosis (FSGS). “And I just cried and cried again,” Botta wept. The change in diagnosis also caused a change in applicable clinical trials. Jacqueline switched into the Sparsentan study, which offered glimmers of hope and simultaneously brought along a new set of challenges. Amid the fog of the doctor’s appointments, hospital visits, and medications, Botta immediately knew what she was called to do. “I couldn’t sleep one night, and I just said, ‘There’s got to be a better way.’ So, I got in touch with other families, saw there was a walk, and wanted to get involved so that I wasn’t so alone,” Botta recalled. It was at that first walk on Long Island, New York where Botta truly caught the ‘Advocacy bug’. She wanted to make the walk even better and her involvement quickly became a lifestyle. Botta plastered her entire town with pictures and posters, sharing her daughter’s story with anyone who would listen. She quickly was asked to take on the Chairperson role of the Long Island Walk. Her involvement the past several years promptly increased the overall fundraising efforts—last year the Long Island Walk raised $61,000. “My first year as Chairperson, I invited a bunch of elected officials to the walk. Every single one of them came and every single one of them knew someone at the walk,” Botta said. In her experience, getting your story out is the key when it comes to advocacy. To make change at a state level, Botta stresses the importance of working with your elected officials. “Contact your elected officials, meet with them personally. Take your speaking points with you, but always remember your family’s story is what they want to hear. Be persistent. If you get a ‘no,’ go back until you get a ‘yes.’ Don’t let anybody tell you that you can’t do it,” she advised. Botta had previous work experience in public relations at the state capital in Albany, which provided her a wealth of knowledge when it came to understanding who she needed to speak with in order to get an entire Day of Awareness for the state of New York. She worked with various elected officials for roughly two years to secure a proclamation that was passed first in the State Assembly. This year that proclamation was presented to the Senate, officially making March 27, 2019 Nephrotic Syndrome Awareness Day in New York state. Because of this work, New York State Senator Shelley Mayer has now offered to partner with the other elected officials to create a permanent resolution, in the near future, that would make March 27th Nephrotic Syndrome Awareness Day every year. Another recent accomplishment was starting the first ever Rare Disease Day at the New York Police Department Headquarters in Manhattan, attended by more than 20 rare disease groups and 300 patient advocates. Botta’s husband, Anthony, has worked for the NYPD for 17 years, but it wasn’t until October 2018 that she got the idea to include the entire department in a day of awareness. “The pink was overwhelming,” Botta recalled. The idea sparked after she noticed an abundance of pink breast cancer awareness ribbons plastered on police cars and the building—it lit a fire inside her. Through her diligence and close work with the NYPD Deputy Commissioner of Administration, she was able to start Rare Disease Day; an afternoon where families within the department who have children with rare diseases come together and learn more about each other and the resources available to help them. “It really is all about persistence, persistence, persistence. Never let anyone tell you it can’t be done,” Botta shared. As far as future projects and goals, Botta has been named the NephCure Community Lead in the New York region. She’ll be responsible for overseeing all events, welcoming new patients, overseeing advocacy, and more. Botta is also working towards getting a documentary made to share her story and overall mission. “It’s on the horizon, 2020. Even if I have to mortgage my house,” Botta joked. Below is a list of helpful tips curated by Botta to help you reach out and provide change in your community:
Tackling Chronic Disease with Medication and Unwavering Hope: Geeta Moreau’s Journey March 8, 2019 by Kylie Karley Geeta Moreau first went into kidney failure in 2005—an extremely tough situation to handle for anyone, but especially for an independent and successful woman like herself. Throughout her triumphs and struggles, Geeta has remained true to her core of positivity and optimism. We asked Geeta to share her experiences and inspirational story to help others who may find themselves in similar situations. If there ever was a time to look within for hope and sheer will to live, it’s when I relapsed with Focal Segmental Glomerulosclerosis (FSGS) last summer. It was May 1, 2018, two weeks before Mother’s Day. I feared a relapse may happen considering I was recovering from a divorce and rebuilding a new chapter in me and my son’s life. And there it was fear realized—I thought about who would take care of my son. It was different the first time I went through kidney issues, but one symptom was the same: the edema. The sudden swelling to indicate the something was happening, 30 pounds of edema. I went through stage four kidney failure in September 2005. I lost all independence to care for myself. My lesson to learn and allow loved ones to care for me was humbling and uncomfortable at times. I didn’t know how to handle all the side effects from my various medications. I also didn’t socialize much because I was so acute and didn’t want people to see me sick. I wanted to be remembered a certain way. This time around I’m working hard, taking care of my son and myself, I’m working toward a better life. Although FSGS is not as acute as kidney failure, other factors come to mind: parenting, career, but most of all health. I’m a single mother and want to see my son grow up. I’m continuing to work in my field through my chronic illness, although it is a struggle at certain times. Another thing I encountered was a sudden onset of 30 pounds of edema. The physical weight was also a metaphor for the weight of the stress I was feeling. I had no idea how or what I was going to do, but I knew it was going to be looking forward to things in the future to stay alive. It was survival mode. I had read somewhere that when you’re sick make future plans, it helps the mind to look forward to something and betters your chance for survival. The most cathartic part of this process is I’m starting to share my story in hopes of helping others gain hope and resilience to fight for their own health. It’s difficult to share my personal experience of living with FSGS. I’ve always been a friendly person, but remain fiercely private at the same time. Anything I could do to keep a glimpse of optimism, I do it. Meditation, drawing, practicing guitar and music. My son’s a great reminder of the art of play and playing in the present is such a healer. I’m reminded daily the possibilities of the impossible. I also know how to better manage my own self-care, how to handle the side effects from the medications, but back in 2005 I was in a much more acute state. I went into a full remission in 2007/2008. I was on high doses of prednisone, cyclosporine, and other medications to keep my body systems in check as everything is affected when my kidneys were not functioning correctly. To say it’s difficult physically and mentally is an understatement. Life does have its consequences. The medications that saved my kidneys affected my bones. In 2009, I was diagnosed with avascular necrosis of the hip, bilateral in 2010. Bone death. I walked with a cane for two years. Lived with chronic pain and limited mobility. In 2011, I got married, honeymooned and had hip replacement surgery. Then it was ‘getting my health back’ mode. I wanted to get off the pain medications to try to have a baby. I was hopeful yet realistic. I did get pregnant and had a miscarriage in the 9th week in 2013. Though I had read it was common for that to occur, it was a sad time that I worked through. I kept thinking that my body is receptive to conceiving. Within two months I was pregnant again, and I had a healthy pregnancy. In November 2014, I delivered a beautiful baby boy naturally with a hip replacement. I thought a c-section was inevitable, but my perinatologist advised me to be in good shape, pay attention to my body and well-being. Motherhood is the best thing that ever happened to me; it reminds me every day how life is possible. I did have a ten-year remission after all. These recent days, my kidneys are responding to the medications within nine months. I have not been on dialysis or had a transplant. I’ve always felt fortunate to be able to tackle this chronic disease with medications. Acupuncture helps me tremendously, balancing my mind and body. Optimism has always been in my nature, even before I fell ill. But when I got sick and lost all independence to work and care for myself, optimism became a practice. It was a matter of survival, life or death. My tendency is to look forward. I don’t ask why this chronic condition is happening, rather I channel the energy to eat right, exercise, and work toward gaining kidney health. I do what I can control, and the rest I keep the faith and spirit of positivity close to my heart. It’s not easy, but it’s a will to not only survive, but to thrive. I hope to be in a full remission again. I remain optimistic because I’m grateful to be alive. – Geeta Moreau
NephCure Kidney International Announces Addition of Three New Members to its Scientific Advisory Board March 8, 2019 by Kylie Karley (KING OF PRUSSIA, PA – MARCH 8, 2019) NephCure Kidney International (NephCure) is proud to announce the addition of three new members to its Scientific Advisory Board (SAB). Joining the distinguished SAB are Laura Barisoni, MD; Alessia Fornoni, MD, PhD; and Marva Moxey-Mims, MD. “Our Scientific Advisory Board is made up of leading basic science and translational researchers, all of whom have made great strides in pushing glomerular disease research forward. We are thrilled to welcome Drs. Barisoni, Fornoni and Moxey-Mims to this esteemed group,” Irving Smokler, PhD, Board President of NephCure announced. NephCure’s CEO, Joshua Tarnoff, added, “All three of our newest Scientific Advisory Board members bring diverse expertise and experiences that embody the spirit of our NephCure community. We are very fortunate to welcome them to our team, as 2019 is a pivotal year for clinical research and bringing forward new and effective treatments.” The chairman of NephCure’s SAB, Martin Pollack, MD, also congratulated and welcomed the new members, “We are thrilled to welcome Drs. Fornoni, Barisoni, and Moxey-Mims to the Scientific Advisory Board. All three are outstanding and dedicated physician-investigators who are committed to improving our ability to care for individuals with glomerular disease.” Laura Barisoni, MD Laura Barisoni, MD is currently a Professor of Pathology and Medicine at Duke University Medical School. She is an accomplished diagnostic pathologist and an internationally recognized expert in the field of digital nephropathology and the use of digital image recognition as a diagnostic tool, particularly for glomerular diseases. Dr. Barisoni is the current President of the Renal Pathology Society, where she previously served for four years on the Board of Directors. Actively involved in NIH-sponsored grants on podocytopathies and clinical trials on Nephrotic Syndrome and Fabry’s disease, Dr. Barisoni also has remarkable teaching experience at numerous national and international courses in renal pathology. Alessia Fornoni, MD, PhD Alessia Fornoni, MD, PhD is a tenured Professor of Medicine and Molecular and Cellular Pharmacology at the University of Miami Miller School of Medicine. She is also the Chief of the Katz Family Division of Nephrology and Hypertension and serves as Director and Chair of the Peggy and Harold Katz Drug Discovery Center. Dr. Fornoni’s lab was the first to report an important role of sphingolipids and cholesterol in the modulation of podocyte function in focal segmental glomerulosclerosis. Her internationally recognized research findings, which are now being translated into humans with novel therapeutic applications, have challenged existing paradigms. Dr. Fornoni’s vision is one that brings industry, investors and not-for-profit organizations around the table with the intent to match science with innovation and patients’ motivation to find a cure for kidney diseases. Marva Moxey-Mims, MD Marva Moxey-Mims, MD is a Professor of Pediatrics at the George Washington School of Medicine and the Chief of the Division of Nephrology at Children’s National Health System in Washington, DC, where her focus is on clinical research to improve the care of children with kidney disease. She was most recently at the National Institute of Diabetes, and Digestive, and Kidney Diseases at the National Institutes of Health in Bethesda, MD, where she served as deputy director for clinical science in the Division of Kidney, Urologic and Hematologic Diseases. Two of the studies Dr. Moxey-Mims initiated are the ongoing Chronic Kidney Disease in Children (CKiD) study, the largest study of pediatric chronic kidney disease ever conducted in North America, and the Randomized Intervention for Children with Vesicoureteral Reflux (RIVUR) trial, the primary results of which were published in the New England Journal of Medicine. NephCure Kidney International’s Scientific Advisory Board includes: Gerald Appel, MD, PhD Daniel C. Cattran, MD Friedhelm Hildebrandt, MD Lawrence B. Holzman, MD Frederick Kaskel, MD, PhD Jeffrey B. Kopp, MD Matthias Kretzler, MD Peter Mundel, MD Martin R. Pollak, MD Jochen Reiser, MD, PhD Andrey S. Shaw, MD Karl Tryggvason, MD, PhD Roger Wiggins, MB, BChir *Michelle P. Winn, MD Posthumous Emeritus NephCure Kidney International’s mission is to accelerate research for effective treatments for rare forms of Nephrotic Syndrome, and to provide education and support that will improve the lives of those affected by these protein-spilling kidney diseases. Specifically, NephCure is focused on glomerular diseases such as: FSGS, IgA Nephropathy, Minimal Change Disease, Membranous Nephropathy, C3 Glomerulopathy, and Membranoproliferative Glomerulonephritis. NephCure is headquartered in King of Prussia, Pennsylvania. For more information about the organization, visit NephCure.org or call 1-866-637-4287.
Dr. Ahmed Awad: Why Participating in Trials Helps Patients Most of All February 4, 2019 by Kylie Karley NephCure Kidney International recently sat down with Dr. Ahmed Awad, a nephrologist in Kansas City, Missouri, to learn more about his company, Clinical Research Consultants, and find out why he believes clinical trial participation is so important. He also delves deeper into the DUPLEX study (specifically for FSGS patients), breaking down what participants can expect, how to get involved, and what the near future may hold for those diagnosed with Nephrotic Syndrome. Dr. Ahmed Awad, CEO and Principal Investigator at Clinical Research Consultants NephCure Kidney International: You founded a company, Clinical Research Consultants, specifically to help support clinical research. Why is that so important to you? Dr. Awad: I started back in 2008-2009 when there were more normal drugs coming on the market to specifically treat kidney disease. Up until about 2010, the majority of our treatment had not been specific to a particular disease. But I thought, “In the next 5-7 years, we will have more medications coming on the market that can treat a specific glomerular disease or a specific kidney disease, for a specific patient, rather than just giving them a general treatment with prednisone.” We did not have enough armaments in our hands to treat kidney disease, but I knew the future was coming, and that’s why I wanted to be more involved in clinical research. NephCure: Why is it important for patients to participate in clinical research, or to take control of their disease early in their disease journey? Dr. Awad: I do believe patients who participate in clinical trials get better care than when they only see their primary care physician or their regular nephrologist. In the real world, out there in the clinic, patients would typically be seen once every 3-4 months, and there’s not much education—labs can vary from one month to another. Whereas when a patient participates in clinical research, they would be seen by the specialist and study coordinator more frequently: between once a week to once a month. And the patient gets more in-tune with the disease process because they’re getting this reinforcement of seeing the study coordinator and seeing the study physician very frequently. They seem to be more in tune with their disease, and can learn more about living with their disease. Which means, in my experience, they seem to really do much better in the clinical trial than when they just see their specialist once every 3-4 months. NephCure: What’s the biggest obstacle patients face when enrolling in a clinical trial? Dr. Awad: Awareness. I think patients do not know there are clinical trials for these different types of kidney disease, and also, the physician may not be offering them. The physician may not even know that there are so many clinical trials out there to help with chronic kidney disease. NephCure: One of the studies you’re involved in enrolling patients in is the DUPLEX study for FSGS patients. What’s unique about this trial? Dr. Awad: It has a unique mechanism of action. It is a dual treatment—it not only works as an angiotensin receptor blockade, but also is an antecedent. It inhibits the antecedent from getting vasoconstricted, meaning clamping the blood vessels. So it has a dual mechanism of action in reducing protein in the urine, and we know, historically, that reduction of protein in the urine delays the progression to end stage renal disease. That’s the beauty about the DUPLEX trial with Sparsentan. The dual mechanism of action is not only an angiotensin receptor blockade, but it also has an antecedent activity. NephCure: So this is a drug that could potentially help all FSGS patients, whether they’re steroid-resistant, steroid-dependent, or not responsive to other treatments? Dr. Awad: Definitely, because it has the potential. We saw in the Phase II clinical trial, called the DUET study, that this drug, regardless of their FSGS’s resistance to steroids or not, showed a reduction of proteinuria. That’s why there’s now a Phase III clinical trial for this drug. NephCure: What’s involved for patients that want to participate in this study? Dr. Awad: It is an oral tablet. The trial is for about 2 years. The patient will visit us once every two weeks for the first two months, then once every four weeks for the next few months, and then after that, once every 3 months. Every time they come in, we check their bloodwork, and we check the amount of protein in their urine. NephCure: What would you say to someone who’s on the fence about participating in a trial, or in this trial specifically? Dr. Awad: Our motto here at Clinical Research Consultants is “Helping you, helping others.” I always tell my patients, if it wasn’t for people like you who participate in these kinds of clinical trials, we wouldn’t have the medication we are giving you right now, or one that has been approved by the FDA. Any patient who participates in a clinical trial is contributing to society by helping others, as well as themselves. NephCure: Do you have any final thoughts you’d like to add? Dr. Awad: I think we’re on the verge of a true treatment for glomerular diseases, more specifically the different types of kidney disease. It is not going to be a general treatment for all of them, it’s going to be a specific treatment for a specific disease. We know now the pathophysiology, the specific pathway in the development of this, and we even know what gene that can turn on or turn off the process of kidney disease. And there are so many medications, so many clinical trials undergoing to treat these different types of kidney disease. We will have treatments in the next 3-5 for all types of kidney disease. We encourage you to learn more about the DUPLEX Trial and other studies that might be right for you at kidneyhealthgateway.com.
Spotlight On: Meredith Wilson, National Events Manager at NephCure February 3, 2019 by Kylie Karley Meet Meredith Wilson, the woman behind the elaborate NephCure Kidney International events taking place across the entire country. Her meticulous planning and detail-oriented eye has made for many successful galas, walks, conferences, and more. This Disney-obsessed National Events Manager is celebrating her 5th anniversary with NephCure this year. We sit down with Meredith to learn more about her crucial role at NephCure and find out what she’s planning in the near future. NephCure: Can you believe you’ve been at NephCure Kidney International for 5 years? Meredith Wilson: My first day at NephCure was May 27, 2014, I started as an intern and never thought I’d still be working here almost 5 years later. NC: How did you originally get involved with NephCure? MW: I was unsure what direction I wanted to take after graduating college and thought it’d be interesting to try out something completely new. A friend of mine was working for NephCure at the time and mentioned to me they were looking for a summer intern. The experience was great, and I was curious to see how a nonprofit is run. NC: What different roles have you held during your time at the organization? MW: I’ve had many different roles during my time here at NephCure. Like I mentioned earlier, I started as a Special Events Intern assisting with our golf outings and galas. I then became a Regional Walks Manager on both the East and West coasts. After that, I stepped into the Regional Events Manager role, planning all of our East Coast events. And finally, I was promoted to the National Events Manager—which is my current title. That role has shifted a lot over the past few years as we continue to add more and more new NephCure events across the country. I’ve taken on roles from other departments when needed, like Operations and Conference Management, in addition to coordinating all of the administrative and logistical tasks for every fundraising event. NC: Which one has been your favorite? MW: My favorite role has been planning the annual NephCure Leadership Summit where all our top volunteer leaders come together to discuss their journeys, share their tips, and learn about NephCure’s new initiatives. It’s a great event, and I love planning it because it involves input from every department—the organization works as a whole to put together a fun and educational weekend for our volunteers. NC: What do you like most about working for NephCure? MW: There’s always something new to plan. I love starting a new project and then watching it come to life from beginning to end. It’s very rewarding. We have a great staff and it’s been a pleasure working alongside my colleagues, especially the ones who have been here as long as I have and have watched the organization grow and adapt to changes in the industry as well as the work space. NC: What is it like to plan such big events like a Countdown to a Cure gala? How much work really goes into it all? MW: Endless amounts of work! Every year I always say I wish I had more time! Countdown to a Cure, in particular, is a massive event that requires so many moving parts behind the scenes to ensure a successful experience for each of the attendees. NC: What things are you most excited for in NephCure’s future? MW: I think I’m most excited about the magnitude of new events we have coming up this year. In total, NephCure will have 4 brand new events in 2019! This is most new events we’ve ever had at this level. And none of it would be possible without the dedicated, hard working volunteers that have a passion for helping NephCure. They always bring new ideas to the table and it’s so fascinating to see their hard work come to life! NC: When you’re not at work, what are you most likely doing? MW: I might be at Disney World! I’ve been four times in the past year. I love all things Disney, especially Tinkerbell! Outside of that, I’ve recently joined the Young Professional’s Board for Uplift Center for Grieving Children. We are volunteers who promote the Center’s mission, run fundraising events, and assist the center in any way to ease their workload. It’s a wonderful opportunity to give back through another organization and network with local professionals.
Naturopathic Remedies for Kidney Disease: How Dr. Henderson’s Own Diagnosis is Helping Others January 17, 2019 by Kylie Karley Twenty six years ago, in 1993, Dr. Jenna Henderson’s life was forever altered by her focal segmental glomerulosclerosis (FSGS) diagnosis. Rather than breaking her down, her shocking Nephrotic Syndrome battle gave her a burst of motivation to promote change. After years of experimenting with mainstream medicine, Henderson turned to natural supplements to try and reverse her kidney damage. “FSGS can be an incredibly persistent condition. When you’re not getting the results you hoped for, you have to dig deeper, research more and try new things,” Henderson explained. Struggling to find answers at first, she was able to scrape together research and discover alternative medicine that worked. In the midst of battling her own kidney disease, Henderson enrolled into naturopathic medical school. “The naturopathic practice grew out of my experience and search for answers,” Henderson said. Now, she’s helping patients of all ages explore natural options to manage their prognosis. “Some kidney patients are afraid that they will have to stop their prescription medications if they look to natural medicine, but this is not the case. Often times we can decrease the need for medication and gradually step down from some prescriptions one at a time, which is a long-term goal for many,” Henderson said. She is taking things a step further and hoping to help even more people affected by Nephrotic Syndrome, by speaking at NephCure’s Nephrotic Syndrome Family Wellness Day on January 20th in Los Angeles, Ca. There she plans to speak with individuals about the ever-evolving research for glomerular diseases. “We’re going to look at novel agents that help reduce proteinuria. We’re also going to consider why do kidney patients feel cold easily and why do so many of us have insomnia,” Henderson stated. Henderson hopes after hearing from her at the Family Wellness Day, patients and families walk away knowing the importance of staying optimistic when it comes to new developments in medicine. “There’s information out now I wish someone had told me about in 1993, but you try to make things better for the next patient. Certainly, my journey was much easier than my cousin’s facing kidney problems in the ‘80s,” Henderson said. If you would like to hear more from Dr. Henderson at her Nephrotic Syndrome Family Wellness Day presentation, you can register for the free event here. For those who are not located in Southern California, Dr. Henderson advises visiting her website and contacting her there. To see a livestream of Dr. Henderson’s presentation as well as her slides on Natural Medicine and Kidney Disease, click here.
Connecticut Candle Company Brings Light to Nephrotic Syndrome, Donating Profits to NephCure December 18, 2018 by Kylie Karley How one diagnosis is helping change the lives of thousands affected by Nephrotic Syndrome A budding business in West Haven, Connecticut is creating candles for a cause. Jordan Crooms and Jennifer Lowe started A Little Soy Candle Company in March 2018, but there’s more than just wax and wicks consuming their lives. Before they became entrepreneurs, the couple was focused primarily on raising their child. In October 2015, their daughter Tatum was born. Just before her second birthday, Crooms and Lowe started noticing their once healthy baby girl now appeared more swollen than before. “We thought we were feeding her too much. At one point we asked, ‘Are we giving her too much juice?’” Crooms said. After several misdiagnoses, Tatum was correctly diagnosed with Nephrotic Syndrome in August 2017. “Your job as a parent is to do everything you can for your child, but there was nothing at that time that we could have done, and it was just defeating,” Crooms recalled. Initially Tatum was given steroids, but after several relapses she was put on CellCept (Mycophenolate Mofetil MMF). One thing both Tatum’s parents and doctors think contribute to her Nephrotic Syndrome, and relapses, is her sensitive skin. After Tatum’s diagnoses, Crooms and Lowe ripped through their home throwing away anything containing harsh chemicals. They swapped cleaning supplies for vinegar, and traditional paraffin wax candles for soy ones. “I did some research and noticed that they [traditional candles] are basically made from oil-refining by-products,” Crooms said. That didn’t sit well with them, and it’s ultimately what ushered the two to start their own soy candle company. Selling the candles to family members at first, the couple was able to branch out and grow business within months. They welcomed this unique opportunity to inform people about Nephrotic Syndrome, all while raising money. “Our core mission is to not only sell candles, but to work with NephCure and help support in any way that we can,” Crooms said. A Little Soy Candle Company is committed to finding a cure for all who suffer from Nephrotic Syndrome. They are donating 20% of their profits to NephCure Kidney International, but their vision by 2030 is to be able to give 80% of profits to help find a cure. “It’s a very bold mission, but I think we can do it,” Crooms conveyed. This year alone, the company has made nearly $7,000 in sales and is set to donate roughly $1,000 to NephCure. Since starting the candle company, Crooms and Lowe began to realize just how many people were affected by Nephrotic Syndrome in their area alone. They’ve connected with other families through candle sales and hope to build a community together. Hand delivering locally has allowed the couple to meet customers face-to-face and share the details of Nephrotic Syndrome. “When we deliver, it’s crazy because most of the people come out and say, ‘Our son has Nephrotic Syndrome.’ There’s just so many people,” Lowe explained. A Little Soy Candle Company has their products in several retail spaces in Connecticut, as well as a boutique in Missouri. “Our long-term goal is to really make this not just about candles, but a vehicle for people to help NephCure, help the families, and really just build a community around it,” Crooms said. For more information about A Little Soy Candle Company, or to place orders, head to their website or Facebook page.