Tom Nate has the honor of succeeding Jane Kurz, who did a phenomenal job as Second Wind President from 2019 – 2020.
A two-time double lung transplant survivor, Tom was diagnosed with Kartageners Syndrome and bronchiectasis as a child. After learning of his need for a transplant, Tom relocated from San Antonio to St Louis, where in May 2007 he received a bilateral lung transplant. After returning home and to work, he was diagnosed with chronic rejection in 2008, and listed for a 2nd bilateral lung transplant. Once again he relocated to St. Louis and, following a very challenging two-year wait, Tom was re-transplanted in September 2010. He’s been blessed with relatively few issues since that surgery.
Tom received a BBA degree in Marketing from Sam Houston State University in Huntsville, TX in 1980. After a 25-year career in sales management in the Petroleum Marketing industry with Texaco, Star Enterprise, Motiva and Shell Oil Companies, he started his own company, a property insurance inspection business.
In addition to Second Wind, Tom volunteers with several other organizations. He is a past president and current member of the National Educational Foundation board of Pi Sigma Epsilon National Fraternity in Marketing Sales Management & Selling. He serves locally with the Texas Organ Sharing Alliance of San Antonio and Donate Life Texas. Tom is also a transplant mentor with the Barnes Jewish Hospital and the Lung Transplant Foundation Mentor programs.
Tom and his amazing wife and caregiver, Irma, reside in Boerne, TX and have a son, Joshua who is a freshman and track athlete at Dallas Baptist University,
Jane M. Kurz,Ph.d, rn
Jane holds a professional membership with the Second Wind Lung Transplant Association, Inc. and has since January of 1997. One of the first ways Jane served the Second Wind Community was as speaker at the Third Annual Educational Conference; Lung Transplant “The New Millennium”.
Jane Kurz has worked as a critical care nurse and nurse educator for more than 40 years. Her doctoral dissertation examined the lived experience of spouses of individuals waiting for lung transplantation. She has used qualitative and quantitative methods to explore stressors, coping and quality of life in other studies involving heart/lung transplant candidates, recipients and spouses with national samples. Other research interests include family dynamics in the presence of acute and chronic illness, marital support and adolescent health. She is the author of several articles on the application of nursing research in clinical practice.
Jane is currently a professor of Nursing at LaSalle University in Philadelphia, PA. In the past she was a faculty member and administrator at Temple University in Pennsylvania. She writes that she recognizes this organization’s wonderful work and she wants to be a part of the group that supports all those involved in this transplant journey. She has served on the board since 2011 and as president from 2019 until January 2021.
FRANK SHIELDS – Vice President
In September 2010, I had emergency gall bladder surgery. After a two week stay in the hospital, I was diagnosed with Idiopathic Pulmonary Fibrosis and was placed on supplemental oxygen 24/7. After my in- home recovery, I entered the pulmonary rehab program at Christ Hospital in Oak Lawn IL. As time went by, I required an incremental amount of oxygen. Routine daily activities became challenging at best.
My doctors then recommended the formal evaluation process to determine if I could be a viable lung transplant candidate. I was subsequently approved and was listed for a double lung transplant. After a five month wait, I underwent a successful bilateral lung transplant at the University of Chicago Medical Center in July 2012.
I received my BSBA degree at Roosevelt University and graduated with departmental honors in Finance. I was Senior Business Analyst at Spiegel Inc. and its subsidiaries for 30 plus years, having worked primarily with Credit Systems and Functions, I served on the board of directors of the International Credit Association of Greater Chicago and was listed in Who’s Who of Credit Card Management. I currently am a member of Organ Transplant Support and also attend the monthly Easy Breathers Support Group at Christ Hospital Medical Center. I was also fortunate to attend April’s Organ and Tissue Awareness event at The University of Chicago Medical Center.
Like all other board members who volunteer their time and energy, we strive to provide education, support and information not only to lung transplant candidates but to transplant recipients and those with other pulmonary issues. I consider it a privilege to be able to serve on the board of Second Wind Lung Transplant Association, Inc. He has served on the board since 2014 as a director and as Vice-President since 2016.
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Gary Bland – dIRECTOR
Gary received his B.S. in Business degree from Kansas State University in 1966 and his MBA degree from Webster University – San Diego in 1987. He worked for a Fortune 500 company in the canned food business for 33 years and retired in 2008. Gary held several positions with this company including Accounting Manager, Plant Controller, Financial Analyst, and was VP of Logistics when he retired. He worked in several locations throughout the U.S. and did a great deal of world traveling.
Gary was diagnosed with Idiopathic Pulmonary Fibrosis in 2005 and had a lung biopsy in 2007 to determine the lung disease was in fact IPF. He went on supplemental oxygen 24/7 immediately after the biopsy. Gary was evaluated for a lung transplant in March, 2009 and received a sequential bilateral transplant on April 7, 2009 at UCSD – San Diego after a very brief period of time on the transplant wait list.
He has been very active with the lung transplant group at UCSD – San Diego, actively participating in group meetings and discussions at UCSD-Thornton hospital. About one year ago, a group of lung transplant patients and other professionals decided that we were so grateful for all that has happened to us that we wanted to help others that may not be so blessed with their health and financial situation. We formed a non-profit 501 (c) (3) corporation which is has a website that is active. Gary is Treasurer of this non-profit company.
Gary joined Second Wind in May 2009 and in January, 2013 became a board member of Second Wind and has been elected to the position of Treasurer.
He has been married for 40 years and has 2 adult children and 2 grandchildren.
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Patrick Henry- editor, AirWays
You can reach Patrick with any information by clicking Here
Patrick Henry is a retired public servant and author (www.jpatrickhenry.net) who, as a result of a diagnosis of end-stage emphysema, received a single lung transplant at the Cleveland Clinic in August, 2015.
It was there that he learned of Second Wind from a gentleman who acts as the organization’s liaison to CC, and he became a member immediately upon his release.
In late 2017 he read an article in the Second Wind newsletter, “Airways”, by past Board President Cheryl Keeler in which she highlighted the organization’s serious need for new board members. Having long admired Second Wind’s dedication to serving the needs of pre and post-transplant lung patients, he felt an obligation to become part of this effort and joined the board in early 2018. Now in his second year on the board, he has accepted responsibility for leading the Financial Assistance Program Committee, and the role of Secretary to the Board.
Patrick is proud to be a part of this board, pleased to serve along side a group of highly motivated and dedicated people who volunteer their considerable time and energies to assure that Second Wind can continue to fulfill its mission.
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ERIC HARNED – Director
Eric is previously married and the father of a 26 year old son who’s an engineer at Honda, and a 21 year old daughter who is attending OSU in dental Hygiene. He is recently engaged to Lyn but a date has not officially been set for their wedding. Eric is a graduate of Ashland University in Ashland, Ohio and grew up in a small town, Hayesville not far from there. He has spent his entire career in Business Development/sales/Management and worked in several different industries. He also is back umpiring baseball for his 9th season, and it’s not uncommon for him to do over 100 games a season.
Eric also serves as a trustee on several committees: The FNCCC which is an area zoning development organization. He is also Past President of his neighborhood community and acting VP currently. He is active in his church and sang for many years in the church choir. He is an active Ambassador Speaker for Lifeline of Ohio, helping educate high school health class students the importance of organ donation, as well as speaking at OSU nursing meeting and student classes involved with Pulmonary rehab – all as a means of giving back after his transplant.
Eric was first diagnosed with scarring in his lungs – bronchiectasis – after a freak fall from a roof peak while hanging Christmas lights in 2006 – after x-rays were taken to confirm if his ribs were broken. Over the next 8 years his lung condition and ability to breathe continued to worsen till his right lung collapsed and he was rushed to the hospital failing to breath in early September 2014.. After two surgeries to correct the collapsed lung, further x-rays and a biopsy were done and he was told without a transplant he had 4-6 months to live. He had less than 20% lung capacity and went on oxygen 24/7. He was listed for Transplant – Dec. 18th, 2014 and three days later, he received THE CALL and a double lung transplant was completed the morning of Dec. 22nd. Since that time Eric has celebrated two years of great health, no complications, has returned to work full time, is also umpiring again, and remaining active in all the afore mentioned interests and commitments. He thanks his surgeons, the nurses and God for his second chance.
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Damian Neuberger, B.S., M.S., Ph.D.-Director
I was diagnosed with Idiopathic Pulmonary Fibrosis (IPF) in 1983. I never smoked, drank, nor did drugs, however Mayo clinic in 1991 suggested my exposure to some chemical issue fixatives while working on my degrees may have triggered a predisposition to the disease, as my paternal grandfather died in his 40s in 1924 and was described as having had weak lungs. In 1983, the life expectancy was on average only 3-5 years and lung transplants were not an option. I did well until 1996 when I traveled in January and got a bad case of the flu. My pulmonologist who was studying IPF at Northwestern University put me on oxygen in June and in September saw changes in my lung function and arranged for my lung transplant evaluation. I was listed on November 14, 1996 (my birthday) and, after an 11-month wait, was transplanted on October 19, 1997 with two great lungs at Loyola University Medical Center in Maywood, IL. I recovered quickly, and returned to work 6 weeks after transplant, as a senior research scientist at Baxter Healthcare. Within 8 months I was traveling for work and vacations. Life had returned to a normal family life with my wife, Judy, and 2 adult children. I worked until 2004 when I reached retirement age.
I am forever indebted to my donor, a 19-year-old young man, whose parents made this generous gift to me. I immediately wrote a thank you letter and during my six-week recovery I got a letter back from my donor’s mom. Sadly, my donor gave all his organs so that others could live, and yet, I was the only one to ever write a thank you letter. We finally met in December 2000 and have continued to correspond and visit with each other. Over the years, we have attend weddings of my donor’s cousins and they and others of the family attended my wife Judy and my 40th wedding anniversary celebration thinking that making 50th was unlikely; we are now 55 years married.
Fourteen years after my lung transplant, it was necessary to seek a kidney transplant at the University of Wisconsin Hospital, where I was put at the bottom of a living donor chain. I received my kidney transplant on October 19, 2011, 6.5 months after being put on the chain. Now, every October 19th I remember my bilateral lung transplant donor and his family and my anonymous living kidney donor from out in California.
My good health is a result of care from excellent transplant teams and “my following the rules while living my life”. As best as I can recollect, I have been a member of Second Wind since 1996 and served on the Board of Directors since 2005. I was editor of Airways starting with the November 2005, 25th Anniversary issue until 2011, and again from 2015 until late in 2019.
Melissa Burke, msn, crnp – Director
Melissa has over a decade of nursing experience specializing in the fields of cardiac surgery, trauma and emergency room, and currently in lung transplantation. She obtained her Bachelor of Nursing at James Madison University in 2006 and completed her Masters of Nursing at the University of Pennsylvania in 2015. She has been a Nurse Practitioner for the last 4 years specializing in the care of pre- and post-transplant patients in both the inpatient and outpatient settings. Her areas of specialty include kidney health in patients after lung transplantation, primary graft dysfunction, care of patients with pulmonary disease awaiting organ transplantation, CMV viremia treatment and prevention, and palliative care. In addition to her clinical work, she is a part-time faculty member at the University of Pennsylvania Nursing School where she mentors Nurse Practitioner students at clinical sites and as a faculty in a physical exam lab. She loves her job at Penn because she has the honor to work with an amazing team of dedicated nurses, advance practice providers, physicians, surgeons, nutritionists, physical therapist, and speech and swallow therapists. She enjoys working with lung transplant patients and she is inspired by their strength and resilience when facing a critical illness
I was born and raised in South Africa where I also received my education. My husband, daughter and I came to Los Angeles in February of 1977. In 2005, because of a change in the health of my nails, I went to see my doc who sent me for a chest X-ray. He confirmed that I had Interstitial lung disease and wanted me to get tested further. I was puzzled because, as a weight loss counselor for more than twenty years, I exercised regularly and was pretty fit. I ate very healthily and maintained my goal weight.
After a lung biopsy confirmed that I had Idiopathic Pulmonary Fibrosis I went on the usual regimen of meds. Things were stable until we went to Mexico and I returned in bad health. I was put on oxygen, which I believed was to be temporary. Wrong!
My health continued to decline until my doctor said I should consider a lung transplant. We didn’t hesitate and I was put on the list in June 2008. Nine short days later I got The Call. I received a pair of lungs from a male donor.
I had a very troubling start. During the transplant, my right lung received a reperfusion injury and the doctors thought I wasn’t going to make it. I was in ICU for almost 30 days! It was a very slow recovery, but I was compliant in my care and slowly evolved into the active person I am today.
We have travelled extensively through Europe and so I’m forever grateful to my donor and family for this amazing gift of life. I’d like to help other transplant recipients to have the support needed to get through this amazing journey.
I have my incredibly amazing husband for the past 43 years and two beautiful daughters, my son-in-law and two teenage grandkids whose support and encouragement make my life so much richer.
MIKE KILMER – DIRECTOR
Mike, who resides in Spearfish, South Dakota with his wife of nineteen
years, is a candidate for lung transplant, and currently under the care of doctors at
the National Jewish Health Center in Denver, Colorado.
He brings a variety of critical skills to the Board, including experience in
Information Technology, Graphic Arts, Marketing and Brand recognition.
In his Board application he noted, “The reason I am applying to be
considered for the board is that I have my personal experience in dealing with not
having the oxygen to do things I would like and thought I would be able to add to
Cathy Cuenin – DIRECTOR
Cathy is a retired nurse, therapist, and acupressure practitioner and now writes poetry and one book—so far (The Way I Walk, From Tugboat to Transplant), paints, quilts, and camps with her husband, Loren. She received a double lung transplant in 2004, six years after learning of her respiratory disease, Lymphangioleiomyomatosis, or LAM. That was in September of 1997 and it would be 1998 before her lung would return to its inflated position essential for breathing.
She and Loren left their home in Juneau, Alaska to await a transplant, leaving behind family, friends, and a land they loved. The couple was aided tremendously by the LAM Foundation in those early, frightening days and months after diagnosis of this rare disease. So, too, finding Second Wind since transplant for fellowship and support has been invaluable.
With seventeen years post-transplant and hundreds of hours of listening practice as a nurse or therapist, Cathy is well-suited to answer Second Wind’s Help Line. She enjoys listening and educating callers who are frightened or overwhelmed. She loves the stories about other transplant recipients in the Airways newsletter and really appreciates the e-mail support group. She has long been grateful for the work put in by board member volunteers and so she figured it was time she added a small part. She joined the board in 2021.
Cathy received her transplant at UC San Francisco and transferred her care to UWMC in Seattle when she and her husband relocated there. They live in Suquamish, Washington, a small community a ferry’s ride from downtown Seattle.
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Tom Nate, President
Frank Shields, Vice President
Phone: (773) 925-9782
Patrick Henry, 2nd Vice President
Sarah Ridder, Treasurer
Ruth Magnus, Secretary
Damian Neuberger, Director
Gary Bland, Director
Jane Kurz, Ph.D., R.N., Director
Eric Harned, Director
Mike Kilmer, Director
Melissa Burke, Director
Cathy Cuenin, Director