Peter J. DeVito Peter DeVito fought the toughest battle of his life and was called Home to God on December 10, 2010. In his honor, we will support the fight on Pulmonary Fibrosis. All proceeds go towards: • Finding effective treatments and a cure for pulmonary fibrosis• Advocating for the pulmonary fibrosis community • Promoting disease awareness • Providing a compassionate environment for patients and their families Please donate and together we can help those living with pulmonary fibrosis and the families of those we have lost. All donations are tax-deductible and every dollar raised goes to help support the mission of the Pulmonary Fibrosis Foundation. If you cannot make a donation at this time, please forward this e-mail and link to everyone you know. Post this on your Facebook and Twitter pages. Every donation counts, no matter what the amount. The loss of a loved one is devastating. Yet, we are always reminded by our hearts – how lucky we have been to know those that we love even in our loss. Thank you for your thoughtfulness. Your generosity and support is greatly appreciated.If you have any questions please contact Jake Meding at jmeding@pulmonaryfibrosis.org or (312)854-2627

John M. O'Meara Please donate in the name of John M. O'Meara, so that a cure and/or treatments to prolong life for sufferers of this terrible disease can be found. All proceeds go towards: • Finding effective treatments and a cure for pulmonary fibrosis• Advocating for the pulmonary fibrosis community • Promoting disease awareness • Providing a compassionate environment for patients and their families Please donate and together we can help those living with pulmonary fibrosis and the families of those we have lost. All donations are tax-deductible and every dollar raised goes to help support the mission of the Pulmonary Fibrosis Foundation. If you cannot make a donation at this time, please forward this e-mail and link to everyone you know. Post this on your Facebook and Twitter pages. Every donation counts, no matter what the amount. The loss of a loved one is devastating. Yet, we are always reminded by our hearts – how lucky we have been to know those that we love even in our loss. Thank you for your thoughtfulness. Your generosity and support is greatly appreciated.If you have any questions please contact Jake Meding at jmeding@pulmonaryfibrosis.org or (312)854-2627

Sally and Bo Willis Dear Family and Friends, As many of you know, my wonderful Mom, Sally Willis passed away in May 2014. She was my hero, my rock, and my best friend. I want very much to honor her life, legacy, and indomitable spirit by raising money and awareness for Pulmonary Fibrosis, a cause very near and dear to Mom’s heart. On New Year’s Eve 2008, Mom lost the love of her life, Bo Willis, my incredible Dad, to Pulmonary Fibrosis. Her life was never the same. Over 30,000 people worldwide are diagnosed with PF every year. It is a progressive and severely debilitating lung disease, which slowly robs people of their livelihood and independence. It kills most patients within 3 years of initial diagnosis. Currently, there is no cure. This fall, I want to unite my love of the great outdoors: (mountains and hiking to be exact!) with finding a cure for PF, a cause that was incredibly meaningful to my Mom, especially during the difficult years following my Dad’s death. On September 8th, I will be lacing up my smelly hiking boots and over the course of the next 12 days, I will circumnavigate Mont Blanc, the highest mountain in the Alps. My journey will take me through 3 countries and over 100 miles. I hope you will consider honoring my Mom and her love for my Dad by sponsoring me $1 per mile or any other multiple of 100 that you feel is appropriate and make a donation in the name of Sally and Bo Willis to the Pulmonary Fibrosis Foundation. PFF is non-profit organization dedicated to offering care and support for those suffering from this deadly disease. I am proud to say I served on PFF’s board for over 6 years. All donations are tax-deductible and every dollar raised goes to help support the mission of the Pulmonary Fibrosis Foundation. Any amount will be greatly appreciated. This will be bittersweet trip for me. Not having my Mom and Dad in my life anymore is deeply sad for me. However, incredible beauty of the mountains will be a source of great comfort and a gentle reminder that my parents are still with me. Thank you. JulieIf you have any questions please contact Jake Meding at jmeding@pulmonaryfibrosis.org or (312)854-2627

In Memory of Dr. Reginald Howard Thanks for visiting our page. I am Jordan Howard, Running Back for the Chicago Bears. My father, Dr. Reginald B. Howard, was diagnosed with Pulmonary Fibrosis disease when I was only 3 years old. My father was an active athletic man in the prime of his life when he was diagnosed with Pulmonary Fibrosis. The diagnosis did not stop him from being a loving father and did not prevent him from helping prepare me for life and the game of football. I believe his diagnosis inspired him to enjoy life and his family even more. I watched him live with this disease for 9 years. I can still remember the not so good days when he didn't feel like fighting with the disease but continued to fight not just for himself but for his children. Pulmonary Fibrosis did not win with my daddy. Daddy fought until the very end but on January 31, 2007 he decided to move on to a better life at the age of 52. I am raising awareness and funds for the mission of the Pulmonary Fibrosis Foundation. All proceeds go towards: • Finding effective treatments and a cure for pulmonary fibrosis• Advocating for the pulmonary fibrosis community• Promoting disease awareness• Providing a compassionate environment for patients and their familiesPlease donate and together we can help those living with pulmonary fibrosis and the families of those we have lost. All donations are tax-deductible and every dollar raised goes to help support the mission of the Pulmonary Fibrosis Foundation.If you cannot make a donation at this time, please forward this e-mail and link to everyone you know. Post this on your Facebook and Twitter pages. Every donation counts, no matter what the amount.The loss of a loved one is devastating. Yet, we are always reminded by our hearts – how blessed we have been to know those that we love even in our loss.Thank you for your thoughtfulness. Your generosity and support is greatly appreciated.Jordan Howard If you have any questions please contact Jake Meding at jmeding@pulmonaryfibrosis.org or (312)854-2627

Please donate in the name of James B. McWethy, so that a cure and/or treatments to prolong life for sufferers of this terrible disease can be found. James B. McWethy, age 76, of Downers Grove, IL, passed away peacefully on June 22, 2020, with his loving family at his side. Jim was the beloved husband of Susan McWethy (née Wasilkoff), the loving father of Todd (Krista Loomis) McWethy and Gretchen (Chris) Hupke, and the cherished grandfather of Sophia and Molly McWethy and Will and Kate Hupke. Jim was born on Chicago’s South Side to his loving parents, James D. McWethy and Muriel McWethy (née Berry), and raised in Beverly and in Palos Heights, IL. He was a proud graduate of Cornell College, Class of 1965, and earned a Master’s Degree in Economics from Indiana University, where he then became a Professor of Economics. Jim later returned home to the Chicago area and began his accomplished professional career. While working at the First National Bank of Chicago, he met Susan, his wife of 51 years. Jim dedicated many years to Berry Bearing Company, founded by his entrepreneur grandfather, Les Berry, where he further developed and perfected his dedication to business, a strong work ethic, and a commitment to impeccable service. After retiring from Berry Bearing, Jim eventually became the owner and operator of Mistwood Golf Club, McWethy’s Tavern, and the Mistwood Golf Dome, along with numerous other business ventures. Jim’s love and pride for Mistwood and love of the game of golf were only surpassed by his immense love and dedication to his family. He was quite possibly the kindest, most humble, and generous man to have blessed this world. To know Jim was to respect and love him. Jim will be missed dearly by his family, friends, and all who had the privilege of knowing him. A celebration of life will be planned for a future date. In the meantime, Jim’s family kindly requests that any memories, stories, or tributes be sent directly to the family. All proceeds go towards: • Finding effective treatments and a cure for pulmonary fibrosis• Advocating for the pulmonary fibrosis community • Promoting disease awareness • Providing a compassionate environment for patients and their families Please donate and together we can help those living with pulmonary fibrosis and the families of those we have lost. All donations are tax-deductible and every dollar raised goes to help support the mission of the Pulmonary Fibrosis Foundation. If you cannot make a donation at this time, please forward this e-mail and link to everyone you know. Post this on your Facebook and Twitter pages. Every donation counts, no matter what the amount. The loss of a loved one is devastating. Yet, we are always reminded by our hearts – how lucky we have been to know those that we love even in our loss. Thank you for your thoughtfulness. Your generosity and support is greatly appreciated.If you have any questions please contact Jake Meding at jmeding@pulmonaryfibrosis.org or (312)854-2627

Please donate in the name of Valerie Coleman, so that a cure and/or treatments to prolong life for sufferers of this terrible disease can be found. Late in the afternoon of Monday, August 21, 2023, Valerie Anne Coleman of McLean, VA passed away peacefully after being surrounded by her loved ones over her final days. Valerie was the beloved wife of Daniel J. Coleman; mother of Stephanie Linnartz (Darren), Leslie Rose (Jason), Andrew Coleman (Anne), Brendan Coleman (Tara), Gavin Coleman (Alexandra), and Colin Coleman (Kara Pazik); grandmother of Aidan and Heidi Linnartz, Olivia, Charlotte, and Eloise Rose, Madeline Coyte, Molly, James, Samantha, and Winnie Coleman, Grady and Grayson Sullivan, Cooper and Piper Coleman, Henry, Taylor, and Peter Coleman; sister of Frank, Michael, and John O’Connell, Louise Stone, Karen Connor, and the late Kevin O’Connell; and best friend of Linda Rosecan. Valerie was an extraordinary sister, friend, wife, mom and grandmother. She was a remarkable woman who will never be forgotten and loved forever by those listed here and so many more. Relatives and friends may call at St. Aloysius Gonzaga Church, 900 North Capitol Street NW, Washington, DC, on Friday, September 15 from 5 p.m. until 7 p.m. when a prayer service will be held. Mass of Christian Burial at St. Aloysius on Saturday, September 16 at 12 noon. Interment Private. In lieu of flowers, the family requests that donations be made in Valerie’s name to the Pulmonary Fibrosis Foundation. All proceeds go towards: • Finding effective treatments and a cure for pulmonary fibrosis• Advocating for the pulmonary fibrosis community • Promoting disease awareness • Providing a compassionate environment for patients and their families Please donate and together we can help those living with pulmonary fibrosis and the families of those we have lost. All donations are tax-deductible and every dollar raised goes to help support the mission of the Pulmonary Fibrosis Foundation. If you cannot make a donation at this time, please forward this e-mail and link to everyone you know. Post this on your Facebook and Twitter pages. Every donation counts, no matter what the amount. The loss of a loved one is devastating. Yet, we are always reminded by our hearts – how lucky we have been to know those that we love even in our loss. Thank you for your thoughtfulness. Your generosity and support is greatly appreciated.If you have any questions please contact Jake Meding at jmeding@pulmonaryfibrosis.org or (312)854-2627

Meena Khandpur Please donate in the name of Meena Khandpur, so that a cure and/or treatments to prolong life for sufferers of this terrible disease can be found. Johnson & Johnson is a proud sponsor of the Pulmonary Fibrosis Foundation in memory of Meena Khandpur All proceeds go towards: • Finding effective treatments and a cure for pulmonary fibrosis• Advocating for the pulmonary fibrosis community • Promoting disease awareness • Providing a compassionate environment for patients and their families Please donate and together we can help those living with pulmonary fibrosis and the families of those we have lost. All donations are tax-deductible and every dollar raised goes to help support the mission of the Pulmonary Fibrosis Foundation. If you cannot make a donation at this time, please forward this e-mail and link to everyone you know. Post this on your Facebook and Twitter pages. Every donation counts, no matter what the amount. The loss of a loved one is devastating. Yet, we are always reminded by our hearts – how lucky we have been to know those that we love even in our loss. Thank you for your thoughtfulness. Your generosity and support is greatly appreciated.If you have any questions please contact Jake Meding at jmeding@pulmonaryfibrosis.org or (312)854-2627

In Loving Memory of Marion & Chuck Sehlke There was not a thing in this world that Chuck loved more than his family. Even after her passing, Chuck continued to love Marion by advocating for and supporting the Pulmonary Fibrosis Foundation (PFF). The PFF is an organization that is dedicated to helping find a cure for the disease that took Marion's life. Please consider donating in Chuck's honor and in memory of him and Marion. Please donate in the name of Marion & Chuck Sehlke, so that a cure and/or treatments to prolong life for sufferers of this terrible disease can be found. All proceeds go towards: • Finding effective treatments and a cure for pulmonary fibrosis• Advocating for the pulmonary fibrosis community • Promoting disease awareness • Providing a compassionate environment for patients and their families Please donate and together we can help those living with pulmonary fibrosis and the families of those we have lost. All donations are tax-deductible and every dollar raised goes to help support the mission of the Pulmonary Fibrosis Foundation. If you cannot make a donation at this time, please forward this e-mail and link to everyone you know. Post this on your Facebook and Twitter pages. Every donation counts, no matter what the amount. The loss of a loved one is devastating. Yet, we are always reminded by our hearts – how lucky we have been to know those that we love even in our loss. Thank you for your thoughtfulness. Your generosity and support is greatly appreciated.If you have any questions please contact Jake Meding at jmeding@pulmonaryfibrosis.org or (312)854-2627

Sharon Cirilli In February 2014, Sharon was diagnosed with a genetic form of Pulmonary Fibrosis, an autoimmune disorder that causes lung tissue to become damaged and scarred over time. As Pulmonary Fibrosis worsens, those who are affected become progressively short of breath, with their quality of life greatly decreasing. Currently, the lung damage caused by this disease can not be repaired, but medications and therapies are prescribed with the hope to ease the various symptoms and side effects. In the grand scheme of things, very little is known about this deadly disease, its progression, and whether or not there are specific genetic markers for the 200+ variations. Sharon ultimately passed from complications of pneumonia due to her Pulmonary Fibrosis. Over only a year and a half, her family and friends watched the disease become increasingly visible and rapidly deteriorate her health. At 63 years old, she went from a happy, new retiree with big plans of relaxing, and traveling with her husband to someone who was imprisoned to an oxygen machine, day and night, struggling to breathe on her own.Sharon was more than just a caring person--she was an amazing wife and mother to three beautiful children. Not to mention, she touched the lives of thousands throughout her 38 year teaching career. She was an extremely gifted sewer and spent much of her time crafting bags, dresses, and pillowcases to donate to Little Dresses for Africa, St. Judes, and Warm-Up America (among others). Her life was full of compassion, her sense of humor was contagious, and her kind heart was truly felt by everyone who knew her.In Sharon's honor, her family and friends are seeking to raise $25,000 to donate to The Pulmonary Fibrosis Foundation. Donations will benefit those who have succumbed to the disease, are currently fighting it, and will face Pulmonary Fibrosis in the future. Sharon is survived by her high school sweetheart and husband of 39 years, Alan Cirilli, as well as her three children (Alan II, Anthony, and Ashley M.) and daughter in law (Ashley E.). All proceeds go towards: • Finding effective treatments and a cure for pulmonary fibrosis• Advocating for the pulmonary fibrosis community • Promoting disease awareness • Providing a compassionate environment for patients and their families Please donate and together we can help those living with pulmonary fibrosis and the families of those we have lost. All donations are tax-deductible and every dollar raised goes to help support the mission of the Pulmonary Fibrosis Foundation. If you cannot make a donation at this time, please forward this e-mail and link to everyone you know. Post this on your Facebook and Twitter pages. Every donation counts, no matter what the amount. The loss of a loved one is devastating. Yet, we are always reminded by our hearts – how lucky we have been to know those that we love even in our loss. Thank you for your thoughtfulness. Your generosity and support is greatly appreciated.If you have any questions please contact Jake Meding at jmeding@pulmonaryfibrosis.org or (312)854-2627

Please donate in the name of Marion Sehlke, so that a cure and/or treatments to prolong life for sufferers of this terrible disease can be found. All proceeds go towards: • Finding effective treatments and a cure for pulmonary fibrosis• Advocating for the pulmonary fibrosis community • Promoting disease awareness • Providing a compassionate environment for patients and their families Please donate and together we can help those living with pulmonary fibrosis and the families of those we have lost. All donations are tax-deductible and every dollar raised goes to help support the mission of the Pulmonary Fibrosis Foundation. If you cannot make a donation at this time, please forward this e-mail and link to everyone you know. Post this on your Facebook and Twitter pages. Every donation counts, no matter what the amount. The loss of a loved one is devastating. Yet, we are always reminded by our hearts – how lucky we have been to know those that we love even in our loss. Thank you for your thoughtfulness. Your generosity and support is greatly appreciated.If you have any questions please contact Jake Meding at jmeding@pulmonaryfibrosis.org or (312)854-2627

Karen Stuart Please donate in the name of Karen Stuart, so that a cure and/or treatments to prolong life for sufferers of this terrible disease can be found. All proceeds go towards: • Finding effective treatments and a cure for pulmonary fibrosis• Advocating for the pulmonary fibrosis community • Promoting disease awareness • Providing a compassionate environment for patients and their families Please donate and together we can help those living with pulmonary fibrosis and the families of those we have lost. All donations are tax-deductible and every dollar raised goes to help support the mission of the Pulmonary Fibrosis Foundation. If you cannot make a donation at this time, please forward this e-mail and link to everyone you know. Post this on your Facebook and Twitter pages. Every donation counts, no matter what the amount. The loss of a loved one is devastating. Yet, we are always reminded by our hearts – how lucky we have been to know those that we love even in our loss. Thank you for your thoughtfulness. Your generosity and support is greatly appreciated.If you have any questions please contact Jake Meding at jmeding@pulmonaryfibrosis.org or (312)854-2627

John Pohlen Please donate in the name of John Pohlen, so that a cure and/or treatments to prolong life for sufferers of this terrible disease can be found. All proceeds go towards: • Finding effective treatments and a cure for pulmonary fibrosis• Advocating for the pulmonary fibrosis community • Promoting disease awareness • Providing a compassionate environment for patients and their families Please donate and together we can help those living with pulmonary fibrosis and the families of those we have lost. All donations are tax-deductible and every dollar raised goes to help support the mission of the Pulmonary Fibrosis Foundation. If you cannot make a donation at this time, please forward this e-mail and link to everyone you know. Post this on your Facebook and Twitter pages. Every donation counts, no matter what the amount. The loss of a loved one is devastating. Yet, we are always reminded by our hearts – how lucky we have been to know those that we love even in our loss. Thank you for your thoughtfulness. Your generosity and support is greatly appreciated.If you have any questions please contact Jake Meding at jmeding@pulmonaryfibrosis.org or (312)854-2627

In Memory of John Albino Moglia More photos hereIt is difficult to believe that the love of my life, my soul mate passed on 10 years ago. John Albino Moglia died Friday, 8/10/12 at 2:08AM of Pulmonary Fibrosis. As we mark this day let’s remember the man, the good times, the not so good but always his spirit, his loyalty to family and friends, his wit, laughter and humor. I know we all miss John terribly but his spirit continues on through Tina, John A., Bailey, and Oliver. John continually said that “every day on this side of the ground is a good one”, so make this day and the ones ahead count. September is Pulmonary Fibrosis month, please find it in your heart to contribute to John’s tribute page by the end of September. Wear blue during the month to bring awareness to the cause. Let’s once again celebrate his legacy with a donation to the Pulmonary Fibrosis Foundation. For anyone who wishes, a donation to the Pulmonary Fibrosis Foundation will help: •Funding and supporting new research•Providing educational materials to the medical and lay communities •Obtaining Congressional Support to increase funding of the NIH to find a cure for Pulmonary Fibrosis •Convincing the drug companies to initiate additional studies to find an effective treatment •Raising funds so that Medical and Scientific Researchers can devote their time exclusively to finding a cure and not have to be diverted from these tasks to seek financial support •Providing support groups, information and reassuranceAll donations are tax-deductible and every dollar raised goes to help support the mission of the Pulmonary Fibrosis Foundation. The loss of a loved one is devastating. Yet, we are always reminded by our hearts – how lucky we have been to know those that we love even in our loss.Thank you for your thoughtfulness. Your generosity and support is greatly appreciated. Love you all, Elena Moglia If you have any questions please contact Jake Meding at jmeding@pulmonaryfibrosis.org or (312)854-2627

James Hodge Please donate in the name of James Hodge, so that a cure and/or treatments to prolong life for sufferers of this terrible disease can be found. All proceeds go towards: • Finding effective treatments and a cure for pulmonary fibrosis• Advocating for the pulmonary fibrosis community • Promoting disease awareness • Providing a compassionate environment for patients and their families Please donate and together we can help those living with pulmonary fibrosis and the families of those we have lost. All donations are tax-deductible and every dollar raised goes to help support the mission of the Pulmonary Fibrosis Foundation. If you cannot make a donation at this time, please forward this e-mail and link to everyone you know. Post this on your Facebook and Twitter pages. Every donation counts, no matter what the amount. The loss of a loved one is devastating. Yet, we are always reminded by our hearts – how lucky we have been to know those that we love even in our loss. Thank you for your thoughtfulness. Your generosity and support is greatly appreciated.If you have any questions please contact Jake Meding at jmeding@pulmonaryfibrosis.org or (312)854-2627

Laura Sauber Please donate in the name of Laura Sauber , so that a cure and/or treatments to prolong life for sufferers of this terrible disease can be found. All proceeds go towards: • Finding effective treatments and a cure for pulmonary fibrosis• Advocating for the pulmonary fibrosis community • Promoting disease awareness • Providing a compassionate environment for patients and their families Please donate and together we can help those living with pulmonary fibrosis and the families of those we have lost. All donations are tax-deductible and every dollar raised goes to help support the mission of the Pulmonary Fibrosis Foundation. If you cannot make a donation at this time, please forward this e-mail and link to everyone you know. Post this on your Facebook and Twitter pages. Every donation counts, no matter what the amount. The loss of a loved one is devastating. Yet, we are always reminded by our hearts – how lucky we have been to know those that we love even in our loss. Thank you for your thoughtfulness. Your generosity and support is greatly appreciated.If you have any questions please contact Jake Meding at jmeding@pulmonaryfibrosis.org or (312)854-2627

Lawrence C. Hesse Sr Please donate in the name of Lawrence C. Hesse Sr, so that a cure and/or treatments to prolong life for sufferers of this terrible disease can be found. All proceeds go towards: • Finding effective treatments and a cure for pulmonary fibrosis• Advocating for the pulmonary fibrosis community • Promoting disease awareness • Providing a compassionate environment for patients and their families Please donate and together we can help those living with pulmonary fibrosis and the families of those we have lost. All donations are tax-deductible and every dollar raised goes to help support the mission of the Pulmonary Fibrosis Foundation. If you cannot make a donation at this time, please forward this e-mail and link to everyone you know. Post this on your Facebook and Twitter pages. Every donation counts, no matter what the amount. The loss of a loved one is devastating. Yet, we are always reminded by our hearts – how lucky we have been to know those that we love even in our loss. Thank you for your thoughtfulness. Your generosity and support is greatly appreciated.If you have any questions please contact Jake Meding at jmeding@pulmonaryfibrosis.org or (312)854-2627

Dear Friends and Family, In Liu of flowers which while lovely we hope we can use your gifts to find better ways care for people with this terrible disease Please donate in the name of Linda Cimachowicz, so that a cure and/or treatments to prolong life for sufferers of this terrible disease can be found. All proceeds go towards: • Finding effective treatments and a cure for pulmonary fibrosis• Advocating for the pulmonary fibrosis community • Promoting disease awareness • Providing a compassionate environment for patients and their families Please donate and together we can help those living with pulmonary fibrosis and the families of those we have lost. All donations are tax-deductible and every dollar raised goes to help support the mission of the Pulmonary Fibrosis Foundation. If you cannot make a donation at this time, please forward this e-mail and link to everyone you know. Post this on your Facebook and Twitter pages. Every donation counts, no matter what the amount. The loss of a loved one is devastating. Yet, we are always reminded by our hearts – how lucky we have been to know those that we love even in our loss. Thank you for your thoughtfulness. Your generosity and support is greatly appreciated.If you have any questions please contact Jake Meding at jmeding@pulmonaryfibrosis.org or (312)854-2627

If on mobile, please click "read more" below to see full tribute JANA LARMON KOCH1956 - 2021 In memory of our mother, Jana Koch, we her children hope to raise $10,000 in her honor. Any contribution, no matter the size, is greatly appreciated, so that together we can get one step closer to finding a cure for this terrible disease. All donations are tax-deductible and every dollar raised goes to help support the mission of the Pulmonary Fibrosis Foundation. Thank you for your thoughtfulness, generosity and support. Our Beloved Reggie - A Tribute We lost our beloved mother, Jana, or “Reggie,” a nickname we fondly called her and which she lovingly embraced, on May 20th, 2021. Though strong in mind and spirit, her health declined rapidly over the past six months, the result of a lifelong battle she did not even know she was fighting, against a vicious cycle whereby intestinal blockages caused by a rare birth defect were making her aspirate into her lungs. (Throughout her life, she would frequently experience episodes of stomach upset, nausea and vomiting, but ignorant of the cause, would incorrectly attribute them to food poisoning.) Over time, these aspirations damaged and scarred her lung tissue, which cumulatively led to the onset of a terminal lung disease called pulmonary fibrosis. A non-smoker who was perpetually committed to making responsible dietary and nutritional choices, her untimely death was all the more tragic because, apart from the freak nature of these digestive and respiratory ailments, her mind and body were otherwise strong and resilient. We lost our beloved Reggie well before her time. Our mom was a strong, spirited woman with a big personality and an even bigger heart. She was a colorful character who loved flowers, but a wallflower she was not. She had such charisma, and a great sense of humor! Wherever she went, and whomever she met, chances are she made friends, and regardless always made an impression. She loved to chat, and was always eager to help, and ready to lend a hand, or an ear, depending on what was needed. She frequently donated her time, money, clothing, and other possessions to charity, often at the expense of her own bills. As an artist, she loved the joy of creative expression. She had a spunky energy and vitality that was as charming and endearing as it was invigorating and life-affirming. And nowhere was this spunk and energy more evident than in the zest with which she approached motherhood, and the sheer delight she took in being a mom, and later a grandmother. "Love" is truly the operative word to use when describing our Reggie. Her mission in life was simply to be the best mom she could be, and she was tireless in her dedication and devotion to us. Always active, never passive, she would relentlessly advocate for us and champion our causes. She took great pride in us and would tell our life story to anyone who would listen. While this embarrassed us at the time, it also revealed the limitless depth of her love for us, which was truly unconditional. As we reflect on our childhood, there are so many wonderful memories and stories that illustrate her love and devotion to us as our mother. Here are just a few that help paint the picture of the extraordinary woman and mother she was: At just 24 years old, our mom faced months of extreme anxiety when Lyla, the second of her four kids, was born prematurely with a severely dysfunctional heart, and was given a 5% chance of seeing her first birthday. Thanks to our mom’s love and tireless advocacy for Lyla, and the help of some extraordinary doctors, Lyla at age one month became the youngest, smallest person in the world to receive a pacemaker and survive. Because our mom refused to give up on Lyla, she is now 40 years old and happily married with three beautiful kids. Throughout our childhood, our mom encouraged wholesome outdoor activities, and among the first we can remember was gardening. While we (and anyone that saw the amazing gardens she grew throughout her life) wish we had her green thumb, we remember vividly how she taught us as children to plant any and everything from seasonal flowers to complete vegetable and herb gardens. She taught us at an early age to respect nature, telling us to be gentle with earthworms and rebury them so they could aerate the soil. Our mom always had the most impressive gardens (occasionally bordering on jungles) with exotic flowers, tropical fruits, towering bamboo, palm trees, and enough fresh Italian herbs to supply the dinner tables of the entire neighborhood. The smell of wild oregano and gardenias will always remind us of her and our wonderful childhood years. For every performance, award ceremony, or graduation, she would never fail to be the first parent there to reserve front row seats for our family. Whenever one of us was in a school play, we would notice our mom on the edge of her seat, wide-eyed with a huge smile, subconsciously mouthing all of the lines or lyrics, which she had invariably memorized while helping us to rehearse in the many nights leading up to the big event. Because she wasn’t visible to whichever sibling was on stage, it was clear that this truly endearing habit of hers was completely subconscious and born from pure, unadulterated delight in seeing each of her kids perform. Like most children, we were picky eaters. But our mom took it in stride and for fifteen years straight, she would get up at dawn to prepare four different breakfasts so that none of us would go to school hungry. Pumpkin muffins, banana bread, pecan pound cake, peach kuchen… you name it, our mom could bake it! For every birthday, our mom would go out of her way to make us feel special. In the early years, it was homemade cakes in the shape of our favorite character or toy - Garfield, Minnie Mouse, a fire truck - her creativity was limitless. As we got older, we moved on to cookie cakes. Every year, there would be a different theme according to our interests at the time. From Bart Simpson to soccer to Tweety Bird to fishing or gymnastics, she was perfectly in tune with each of our constantly changing interests, and she always nailed it year after year. When it came to the holidays, Charles Dickens himself could not have dreamed of a better Christmas celebration! Every December, there were Christmas songs and movies being played, homemade fresh pine wreathes (made by Reggie herself), Christmas lights, decorations, and heavenly aromas coming from her kitchen. Thanks to her, we’re all Christmas fanatics and will always celebrate the joyous Christmas season to the fullest. Each of us kids went through an awkward phase during our adolescence, but our mom’s intuition could always tell when something was bothering us. So, in addition to making us a homemade lunch, she would frequently include a handwritten note in our lunchboxes, containing words of encouragement, love, and advice. For every single soccer game, hockey game, basketball game, track meet, or gymnastics event we ever participated in, Reggie was always there, rain or shine. Whenever we were on the team bus, we would see her car following the bus to all of our away games, no matter how far away they were. For the final 100 meters of every race, Reggie would position herself right by the finish line, hanging her head out over the fence, cheering for us as we sprinted to the end. We will never forget hearing her shout, with vocal cords strained from overuse, “Go Hans! Go Lyla! Go Jake! Go Lara!” We can still hear these shouts of encouragement in our heads, as loud and as clear as when they boomed out thunderously from the stands. When the boys took up hockey, she didn’t think twice when they asked her to move her magnificent rose garden so we could expand our driveway for street hockey. This selfless act made our driveway the neighborhood hotspot for street hockey games. And when we accidentally broke a window pane, she quickly painted a sun whose rays emanated out along the exact path of the web of shattered glass, so our dad wouldn’t notice. As a result, it went undiscovered for years. She always had our backs. Throughout our schooling, our mom was always dedicated to ensuring our success (while reminding us to enjoy life too, for a “B does not stand for ‘bad’ at Berkeley”). From choir trips to Scandinavia, to Spanish immersions in Costa Rica and Mexico, to class trips to NYC and DC, Environmental science trips to the Galapagos, our mom was certainly a ready and willing chaperone! Beyond the great adventures she shared with us on school trips near and far, she made our everyday schooling just as fun. From dressing up as the artist Georges Seurat to teach 4th graders pointillism in a “Meet the Masters” series (she even cut a piece of her own hair to fashion as a mustache for the occasion!), to teaching middle school students how to sew boxer shorts and scrunchies, to creating a full year’s course for 2nd graders in Gifted Literature – at no charge to the Florida public school system – when she found out Lara’s school only offered gifted math and science… our Reggie stopped at nothing to make sure her 4 children continued to grow academically, while never losing sight of the fun in learning. Nearly every Friday night we went out as a family to our favorite sushi restaurant. Not only did she get us permanently addicted to sushi, family dinners like those were part of her routine to help keep our family close. At home, she would cook elaborate meals five days a week to ensure, no matter how busy our schedules got, that we always broke bread together as a family each night. When our childhood dog, Floppy, was deathly ill, we all resigned ourselves to her fate and prepared for the worst. But Reggie, unbeknownst to us, took her to various specialists to see what could be done. After school one day, Reggie surprised us by telling us to look in the backseat of the family station wagon, where we found a bandaged-up but happy and tail-wagging Floppy, who had just received lifesaving surgery. This beautiful act of maternal intervention prevented our hearts from being broken at young ages, and bought us five more years with our family dog. Year after year, sibling after sibling, she helped us move into and out of our college dorms. She bought sofas at thrift stores and rented a U-Haul truck to drive them all the way up to us. In many a telephone conversation, she would frequently ask if “our ears were burning today,” because she had been bragging about our accomplishments. All the way to the end, our mom was one of the strongest people we have ever known. The doctors told us that her lung capacity was no more than the size of a juice box, and that her breathing was so labored, she was essentially experiencing the sensation of drowning at all times of day. Confined to a hospital bed, she was able to endure this state of perpetual misery for six long months. Her ability to stay sane, let alone hopeful and positive, through this ordeal was nothing short of superhuman. During her final days, it was obvious that her sole motivation to go on was her love for us and her desire to keep us from being hurt. The incredible strength she exhibited throughout her life and especially in her final days will always inspire us to be as strong and as loving as she was. To give a final sense of who our beloved Reggie was, we wish to share a portion of the epitaph she wrote, which we found among her things after her passing: She had the Soul of a GypsyThe Heart of a HippieThe Spirit of a Fairy Please donate my body to medical research. Celebrate my life with a big party telling Reggie stories and LAUGHING. Think about your favorite Reggie times! Laugh! Know that I will always be watching over you! I don’t know how, YET, but you know Reggie ALWAYS FINDS A WAY!! Talk to me when you have a problem; I’ll do my best to get some ideas to resolve it into your head! Reggie, we love you more than words can say. You were the best mom we could’ve asked for. You taught us how to love unconditionally with our whole hearts. And we are committed to carrying that torch forward, now and always.

Victor Kraker Please donate in the name of Victor Kraker, so that a cure and/or treatments to prolong life for sufferers of this terrible disease can be found. Vic Kraker was a loving, thoughtful, creative and innovative father, husband, son, brother and uncle whom we lost on April 25,2008 to Pulmonary Fibrosis. We remember and miss him every day. We are trying to help others with this terrible disease by helping the Pulmonary Fibrosis foundation raise money for research. All proceeds go towards: • Finding effective treatments and a cure for pulmonary fibrosis• Advocating for the pulmonary fibrosis community • Promoting disease awareness • Providing a compassionate environment for patients and their families Please donate and together we can help those living with pulmonary fibrosis and the families of those we have lost. All donations are tax-deductible and every dollar raised goes to help support the mission of the Pulmonary Fibrosis Foundation. If you cannot make a donation at this time, please forward this e-mail and link to everyone you know. Post this on your Facebook and Twitter pages. Every donation counts, no matter what the amount. The loss of a loved one is devastating. Yet, we are always reminded by our hearts – how lucky we have been to know those that we love even in our loss. Thank you for your thoughtfulness. Your generosity and support is greatly appreciated.If you have any questions please contact Jake Meding at jmeding@pulmonaryfibrosis.org or (312)854-2627

Ralph Howard Ralph Howard, suave and stalwart champion of Broadway Belts and husband of Julie Halston, passed away after several months of declining health. Ralph's battle with IPF and his journey with Julie through the aftermath were what brought us together for our first event in 2011: BB4PFF and its efforts on behalf of the Pulmonary Fibrosis Foundation would not exist were it not for both of them. You can read more about Howard's amazing life here: https://www.broadwayworld.com/article/Ralph-Howard-Veteran-Radio-Newscaster-And-Husband-Of-Julie-Halston-Dies-At-77-20180808 Please take time out of your day and make a donation to the Pulmonary Fibrosis Foundation in memory of Ralph. With your support we can help those living with pulmonary fibrosis and the families of those we have lost. All donations are tax-deductible and every dollar raised goes to help support the mission of the Pulmonary Fibrosis Foundation.If you cannot make a donation at this time, please forward this e-mail and link to everyone you know. Post this on your Facebook and Twitter pages. Every donation counts, no matter what the amount.The loss of a loved one is devastating. Yet, we are always reminded by our hearts – how lucky we have been to know those that we love even in our loss.Join all of us in sending deepest condolences to Ralph's and Julie's family.Thank you for your thoughtfulness. Your generosity and support is greatly appreciated. If you have any questions please contact Jake Meding at jmeding@pulmonaryfibrosis.org or (312)854-2627

Connie Nagle Please donate in the name of Connie Nagle, so that a cure and/or treatments to prolong life for sufferers of this terrible disease can be found. All proceeds go towards: • Finding effective treatments and a cure for pulmonary fibrosis• Advocating for the pulmonary fibrosis community • Promoting disease awareness • Providing a compassionate environment for patients and their families Please donate and together we can help those living with pulmonary fibrosis and the families of those we have lost. All donations are tax-deductible and every dollar raised goes to help support the mission of the Pulmonary Fibrosis Foundation. If you cannot make a donation at this time, please forward this e-mail and link to everyone you know. Post this on your Facebook and Twitter pages. Every donation counts, no matter what the amount. The loss of a loved one is devastating. Yet, we are always reminded by our hearts – how lucky we have been to know those that we love even in our loss. Thank you for your thoughtfulness. Your generosity and support is greatly appreciated.If you have any questions please contact Jake Meding at jmeding@pulmonaryfibrosis.org or (312)854-2627

Joan Justus Please donate in the name of Joan Justus, so that a cure and/or treatments to prolong life for sufferers of this terrible disease can be found. All proceeds go towards: • Finding effective treatments and a cure for pulmonary fibrosis• Advocating for the pulmonary fibrosis community • Promoting disease awareness • Providing a compassionate environment for patients and their families Please donate and together we can help those living with pulmonary fibrosis and the families of those we have lost. All donations are tax-deductible and every dollar raised goes to help support the mission of the Pulmonary Fibrosis Foundation. If you cannot make a donation at this time, please forward this e-mail and link to everyone you know. Post this on your Facebook and Twitter pages. Every donation counts, no matter what the amount. The loss of a loved one is devastating. Yet, we are always reminded by our hearts – how lucky we have been to know those that we love even in our loss. Thank you for your thoughtfulness. Your generosity and support is greatly appreciated.If you have any questions please contact Jake Meding at jmeding@pulmonaryfibrosis.org or (312)854-2627

Parthasarathi Kadambi In honor and memory of Partha Kadambi, who passed away after a hard-fought battle with PF. He was a devoted son, husband, loving father, brother, uncle, nephew, cousin, neighbor and a friend to countless many. He was a strong, courageous, gentle soul. He loved and adored his family and community, and they adored him in return. You will be missed by one and all. Please donate in the name of Parthasarathi Kadambi, so that a cure and/or treatments to prolong life for sufferers of this terrible disease can be found. All proceeds go towards: • Finding effective treatments and a cure for pulmonary fibrosis• Advocating for the pulmonary fibrosis community • Promoting disease awareness • Providing a compassionate environment for patients and their families Please donate and together we can help those living with pulmonary fibrosis and the families of those we have lost. All donations are tax-deductible and every dollar raised goes to help support the mission of the Pulmonary Fibrosis Foundation. If you cannot make a donation at this time, please forward this e-mail and link to everyone you know. Post this on your Facebook and Twitter pages. Every donation counts, no matter what the amount. The loss of a loved one is devastating. Yet, we are always reminded by our hearts – how lucky we have been to know those that we love even in our loss. Thank you for your thoughtfulness. Your generosity and support is greatly appreciated.If you have any questions please contact Jake Meding at jmeding@pulmonaryfibrosis.org or (312)854-2627

Charles E. Lindsey More photos My father had an engaging smile and the most kind and generous soul. All who met him left feeling better about themselves. His life was well-lived with pride, dignity and respect for everyone. Unfortunately, his life was cut short by Pulmonary Fibrosis, a horrible and devastating disease with no effective treatment or cure. My father faced his illness with determination, strength and courage. Always hoping for a cure, he continued to research creative treatments on his own until the day he died. On that day he said, " We do what is possible. It's the impossible that takes a little longer."Together we can make the impossible possible by finding a cure for Pulmonary Fibrosis.I am raising awareness and funds for the mission of the Pulmonary Fibrosis Foundation. All proceeds go towards: • Finding effective treatments and a cure for pulmonary fibrosis• Advocating for the pulmonary fibrosis community• Promoting disease awareness• Providing a compassionate environment for patients and their familiesAll donations are tax-deductible and every dollar raised goes to help support the mission of the Pulmonary Fibrosis Foundation.If you cannot make a donation at this time, please forward this e-mail and link to others. You can also post this on your Facebook and Twitter pages. Every donation counts, no matter what the amount.Thank you for your thoughtfulness and consideration. Your generosity and support is greatly appreciated. If you have any questions please contact Jake Meding at jmeding@pulmonaryfibrosis.org or (312)854-2627

Gopal Shenoy Please donate in the name of Gopal Shenoy, so that a cure and/or treatments to prolong life for sufferers of this terrible disease can be found. All proceeds go towards: • Finding effective treatments and a cure for pulmonary fibrosis• Advocating for the pulmonary fibrosis community • Promoting disease awareness • Providing a compassionate environment for patients and their families Please donate and together we can help those living with pulmonary fibrosis and the families of those we have lost. All donations are tax-deductible and every dollar raised goes to help support the mission of the Pulmonary Fibrosis Foundation. If you cannot make a donation at this time, please forward this e-mail and link to everyone you know. Post this on your Facebook and Twitter pages. Every donation counts, no matter what the amount. The loss of a loved one is devastating. Yet, we are always reminded by our hearts – how lucky we have been to know those that we love even in our loss. Thank you for your thoughtfulness. Your generosity and support is greatly appreciated.If you have any questions please contact Jake Meding at jmeding@pulmonaryfibrosis.org or (312)854-2627

Please donate in the name of Margo Lion, so that a cure and/or treatments to prolong life for sufferers of this terrible disease can be found. All proceeds go towards: • Finding effective treatments and a cure for pulmonary fibrosis• Advocating for the pulmonary fibrosis community • Promoting disease awareness • Providing a compassionate environment for patients and their families Please donate and together we can help those living with pulmonary fibrosis and the families of those we have lost. All donations are tax-deductible and every dollar raised goes to help support the mission of the Pulmonary Fibrosis Foundation. If you cannot make a donation at this time, please forward this e-mail and link to everyone you know. Post this on your Facebook and Twitter pages. Every donation counts, no matter what the amount. The loss of a loved one is devastating. Yet, we are always reminded by our hearts – how lucky we have been to know those that we love even in our loss. Thank you for your thoughtfulness. Your generosity and support is greatly appreciated.If you have any questions please contact Jake Meding at jmeding@pulmonaryfibrosis.org or (312)854-2627

Jack and Ronald Severson Please donate in the name of Jack and Ronald Severson, so that a cure and/or treatments to prolong life for sufferers of this terrible disease can be found. Jack Severson was born in Milwaukee, WI on December 3, 1932 and passed away on April 20, 2010 from Pulmonary Fibrosis. He is mourned by his wife Peggy and children Chris, Paula, Albert and Lisa. He joined his infant son Mark in heaven. He is further survived by his grandchildren Ross, Christy, Miles and Mark. He never met his great grandchildren Liam, Dash, Avery, Erica, Amina, and Emmet Jack. He was very family oriented and close to his siblings Fay, Oran, Oral, Beverly and Ron. His youngest brother Ron has just been diagnosed with Pulmonary Fibrosis and this has been devastating news for our family. On April 13, 2015, Ron lost his battle to Pulmonary Fibrosis. He is survived by his wife Carol, his children Renee, Russ, Randy, Sheila, Stephanie, Sue, Jason and Amy. He will be dearly missed by his 16 grandchildren: Tim, Kellen, Christian, Jake, Taylor, Hunter, Mackenzie, Sarah, Molly, Jansen, Nicholas, Laura, Ansley, Matt, Olivia and Alex and infant great- grandchild Elena. We are raising awareness and funds for the Pulmonary Fibrosis Foundation. All proceeds go towards:•Funding and supporting new research•Providing educational materials to the medical and lay communities •Obtaining Congressional Support to increase funding of the NIH to find a cure for Pulmonary Fibrosis •Convincing the drug companies to initiate additional studies to find an effective treatment •Raising funds so that Medical and Scientific Researchers can devote their time exclusively to finding a cure and not have to be diverted from these tasks to seek financial support •Providing support groups, information and reassurancePlease help me help those living with pulmonary fibrosis and those we lost by donating. All donations are tax-deductible and every dollar raised goes to help support the mission of the Pulmonary Fibrosis Foundation. If you cannot make a donation at this time, please forward this e-mail and link to everyone you know. Post this on your Facebook and Twitter pages. Every donation counts, no matter what the amount. The loss of a loved one is devastating. Yet, we are always reminded by our hearts – how lucky we have been to know those that we love even in our loss.Thank you for your thoughtfulness. Your generosity and support is greatly appreciated. If you have any questions please contact Jake Meding at jmeding@pulmonaryfibrosis.org or (312)854-2627

Chris Clarke Please donate in the name of Chris Clarke, so that a cure and/or treatments to prolong life for sufferers of this terrible disease can be found. Few of us are lucky enough to have had a man like Chris Clarke in our lives. He was a friend, brother, brother-in-law, neighbor, uncle, beloved son-in-law, father, and husband who formed deep and lasting impressions on everyone he knew found. As a way of honoring and remembering Chris, your support of the Pulmonary Fibrosis Foundation is very much appreciated. All proceeds go towards: • Finding effective treatments and a cure for pulmonary fibrosis• Advocating for the pulmonary fibrosis community • Promoting disease awareness • Providing a compassionate environment for patients and their families Please donate and together we can help those living with pulmonary fibrosis and the families of those we have lost. All donations are tax-deductible and every dollar raised goes to help support the mission of the Pulmonary Fibrosis Foundation. If you cannot make a donation at this time, please forward this e-mail and link to everyone you know. Post this on your Facebook and Twitter pages. Every donation counts, no matter what the amount. The loss of a loved one is devastating. Yet, we are always reminded by our hearts – how lucky we have been to know those that we love even in our loss. Thank you for your thoughtfulness. Your generosity and support is greatly appreciated.If you have any questions please contact Jake Meding at jmeding@pulmonaryfibrosis.org or (312)854-2627

Joel Richard Kroells Please donate in the name of Joel Kroells, so that a cure and/or treatments to prolong life for sufferers of this terrible disease can be found. All proceeds go towards: • Finding effective treatments and a cure for pulmonary fibrosis• Advocating for the pulmonary fibrosis community • Promoting disease awareness • Providing a compassionate environment for patients and their families Please donate and together we can help those living with pulmonary fibrosis and the families of those we have lost. All donations are tax-deductible and every dollar raised goes to help support the mission of the Pulmonary Fibrosis Foundation. If you cannot make a donation at this time, please forward this e-mail and link to everyone you know. Post this on your Facebook and Twitter pages. Every donation counts, no matter what the amount. The loss of a loved one is devastating. Yet, we are always reminded by our hearts – how lucky we have been to know those that we love even in our loss. Thank you for your thoughtfulness. Your generosity and support is greatly appreciated.If you have any questions please contact Jake Meding at jmeding@pulmonaryfibrosis.org or (312)854-2627

Bhim Madan Please donate in the name of Bhim Madan, so that a cure and/or treatments to prolong life for sufferers of this terrible disease can be found. Bhim S. Madan, a longtime resident of Brockport, passed away peacefully on Thursday January 1, 2015, in Arlington, Virginia. Born in India in 1934, Bhim immigrated to the United States in 1957 with his wife Raj, after completing his undergraduate degree in Mathematics. He then attended the University of Missouri, and received a B.S. in Mechanical Engineering, and M.S. in Industrial Engineering. Bhim’s professional career as a Mechanical & Industrial Engineer began in New York City in 1961. In 1965, he accepted a position at General Electric in Brockport. Thereafter, he worked at Delco Products (and its successors ITT and Valeo) in Rochester, NY, until his retirement. He participated in a number of golf leagues with his colleagues, and developed deep roots in the community. He is survived by his wife and best friend of 57 years, Raj Madan, sons Ajay (Allison) and Neal, grandchildren Connor and Jacob, his sister and two brothers, dozens of very close relatives on both sides of his family, and dear friends. In lieu of a public ceremony, condolences may be sent to the family at 501 North Lombardy Street, Arlington, VA 22203, and memorial gifts may be made to the Pulmonary Fibrosis Foundation online or by mail to 230 E. Ohio Street, Suite 500 Chicago, IL 60611. If you have any questions please contact Jake Meding at jmeding@pulmonaryfibrosis.org or (312)854-2627