Jack McCullough Please donate in the name of Jack McCullough, 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

Thomas Howard Please donate in the name of Thomas Joel Howard, to raise awareness of Pulmonary Fibrosis and provide resources so that a cure or treatments to prolong life for sufferers of this disease can be found. Thank you for your love and support of this cause! 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

Milton Whitney A son, brother, husband, father and grandfather whose greatest love in life was his family and his farm. He enjoyed talking with people, telling stories, country fair food, and ice cream. He loved cutting wood in the winter and baling hay in the summer. He farmed alongside his own father behind a pair of horses. He put new life into old equipment and could fix anything. He passed on this passion to his own children and grandchildren. His perfect day would be morning coffee, talking and reading the newspaper (the stories of interest outloud), the outdoor chores of the season and a family dinner with all his kids and grandkids. In his older years he enjoyed keeping his bird feeders full, maintaining his farm, small engine repair for local townspeople, and visiting with family and friends. His spirit will be missed. Please donate in the name of Milton Whitney, 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

Kyungil "KC" Cho "The Mountains are calling, and I must go."KC cared deeply about people and always put others first. He loved his family, his home, his garden, and his neighborhood in OC. His greatest joy was being a grandfather after he retired from 30 years of public service, working for the State of California. He was proud of his Korean heritage, his alma mater (Seoul National University), and his service in the Korean Air Force.K.C. did not let IPF limit him from living life to the fullest. He was passionate about the outdoors and was true to the philosophy of John Muir who wrote, “The Mountains are calling, and I must go.” He hiked and skied until his last year with small oxygen tanks on his back. Up until his last month, he walked an hour a day on the beach, swam in a pool with his oxygen tanks on floats, and exercised with a personal trainer. KC used a portable oxygen machine to travel and spent his last year adventuring... driving across America to see the national parks, hiking in the footsteps of Charles Darwin in the Galapagos Islands, and becoming a Hawaiian "native,” enjoying stunning Maui sunsets with his toes in the sand. We hope his story encourages other patients with IPF to stay active.Please donate in his name so that treatments or a cure can be developed to improve life for sufferers of this terrible disease. All proceeds go to: • 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. 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. Your generosity and support is greatly appreciated.If you have any questions please contact Jake Meding at jmeding@pulmonaryfibrosis.org or (312) 854-2627

On September 7, 2020, father, grandfather, brother, uncle and friend, Edwin Gordon “Buck” Pohlmann, 73, passed away peacefully in the presence of loved ones. Buck, lovingly known as “Gator Buck” to his family, lived a full life and was well loved by his spouse, Catherine O’Donnell “Katy” Pohlmann, two children, six grandchildren, one sister, two brothers and many nieces and nephews. Gator will be greatly missed by his family, friends, and so many others whose lives he touched. In late 2013, Buck was diagnosed with Pulmonary Fibrosis and, as a result, he underwent a double-lung transplant on May 5, 2014 at the Cleveland Clinic. Under the care of Loyola University Medical Center in Chicago, Buck was able to enjoy six more joy filled years with his family and friends. 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. 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 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

Lynda Myers Please donate in the name of Lynda Myers, 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

Carl Cosola Please donate in the name of Carl Cosola, 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 honor and memory of William Gurin, who recently passed away after a hard-fought battle with PF, we have set up this donation page. A lifelong New Yorker and graduate of Brooklyn Law, Bill immediately went into public service, volunteering his time during his first years as an attorney to pro bono work representing victims of napalm and Agent Orange exposure in lawsuits against the government. He dedicated his career to serving justice as a nationally respected prosecutor, representing the interests of the people at the Brooklyn District Attorney's office and as an Assistant US Attorney in the Eastern District of New York, before turning his attention back to the state and city levels in his work at the New York State Workers' Compensation Board and New York City Health + Hospitals Corporation. He was a Vietnam veteran, avid baseball fan and eternal Mets optimist, personal rideshare service for his children and their friends years before Uber, and compulsive consumer of news whose thirst for knowledge was unmatched and whose brilliant mind and dry, incisive wit illuminated everything around him. Most importantly, he was a loving husband of 40 years to Merryl and devoted father to his daughters, Merette and Lindsey. We love him without end and will miss him dearly. He liked to joke that he was the straw that stirred the drink, but truly the ripple effects of his life stretch far and wide. He left the world a better place than he found it. We hope he is breathing easy and taking a break from checking the weather for blizzards and thunderstorms. He will always be in our hearts. 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

Peter "Takis" Economopoulos Please donate in the name of Takis Economopoulos, 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

Doug Jones Please donate in the name of Doug Jones, 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

Robert L Ruple Please donate in the name of Robert L Ruple, so that a cure and/or treatments to prolong life for sufferers of this terrible disease can be found. Robert dedicated his career to help life science companies manufacture the highest quality pharmaceutical and medical products to ensure safety for patients. 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

PeterFrench Please donate in the name of PeterFrench, so that a cure and/or treatments to prolong life for sufferers of this terrible disease can be found. Pete was a huge advocate for this disease, educating others with his knowledge throughout his journey. He always maintained the hope that a cure would be found for this gruesome disease. 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

Josephine Cometti As you look at all the wonderful photographs of the life of Josie Cometti, you will notice something - there are virtually no portraits of her by herself. Our family looked through thousands of photos for her funeral and memorial services and we found that in nearly every picture we have, over the course of her 75 years, Josie is always captured with someone else - her husband, her children, her friends, her grandchildren. This is because Josie was a welcoming and loving person who was much happier when she was with people and not alone. She was always talking, chatting, cooking, painting, playing cards, volunteering, working, dancing. She was always part of a community, even if she had to create that community herself. Have you ever noticed that in every neighborhood, there’s always one house where the kids always seem to congregate? That one house where the refrigerator door never gets to close, because everyone is in and out of it, and yet the fridge also never seems to ever run out of food? That was her home, and that was based on her effort and her hospitality. She was a woman of contradictions. She was born in Italy - moving over when she was only 20 years old. But she was fiercely proud of being American. With her husband Mario, she traveled all over the country, visiting and living everywhere from coastal Maine to Indian reservations in the badlands of South Dakota. She embraced her adopted country, and she raised her children as Americans, showing them an endless supply of love and patience. But this picture of an extrovert doesn’t tell the whole story. She was, in some less obvious ways, very shy and sensitive. Josie spent much of her childhood in a convent, being raised by nuns, due to illnesses she suffered through in the poverty of post-war Italy. When she was healthy enough to go home, her parents and siblings were like strangers to her. She adjusted, but the experience left her with a sense that family and friends and indeed life itself, were all things to be clutched closely as if they could be lost at any moment. It made her wary of loss but also determined to grab life and opportunity by the throat. At 19, when she met a dashing American medical student who asked her to marry him and move to another country, she set aside her worries and embraced the kind of change very few of us are brave enough to attempt. The world was bigger then - moving to the USA meant she wouldn’t see her family for many years. A different language, a different culture. But she took the chance, despite not speaking a word of English when she first arrived. She made it work, through sheer determination and with good humor. She could take a joke and she could deal one out too. The only thing she didn’t like was if you made fun of her accent - that might earn you a whack. She loved her husband and they became immediately inseparable from the day they met until the day they parted. They spent nearly 56 years together, going out dancing together every Saturday night. They even worked together, with Josie managing Dr. Mario’s office. They raised four children, lost one to illness and were lucky enough to be blessed with six grandchildren. She was tireless. Josie and Mario were always the first ones out on the dance floor and the last to leave. She was tough, stubborn even. When the doctors told her she had pulmonary fibrosis and gave her 2 to 5 years to live, she metaphorically shook her fist at them: “I’ll show you!.” She held out for eight years, thanks mostly to the amazing dedication of her husband’s care - but anyone who knew her wouldn’t have been surprised if she had been able to hold out for several years more, just out of sheer willpower. But when her illness took a turn for the worse, her family gathered around and she was able to finally let go. One of her grandchildren, unaccustomed to the idea of death, asked: “Does this mean I can never see her again?” Josie’s presence was so strong that it was hard to imagine she wouldn’t be here - even after her passing. We do feel her loss, and unfortunately, we won’t see her again, not in the same way as before. But she lives on, in her children and grandchildren, in the values she passed on to them, and she lives on in our hearts. Her presence has not diminished, it has only changed. She will be remembered by the many people whose lives she has touched. She would not have wanted memories of her to evoke sadness. She would have wanted her friends and family instead to continue to embrace life as she did - to laugh, to eat, to chat… to dance. Let us be together, not alone - as a community - the community she helped to make, and let us celebrate a life that was lived with determination, pluck and an endless supply of affection and kindness for the people she cared about. Please donate in the name of Josie, 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 Brian McEnany, 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. 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(Jack) Connerty Please donate in the name of John(Jack) Connerty, of Ogunquit, Maine 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

Betty Jones Please donate in the name of Betty Jones, 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

SteveCarney Please donate in the name of SteveCarney, 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 loving memory of the sweetest grandfather Please donate in the name of The Varoqua Family so that a cure and 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. 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

Dr. Dilipkumar Gor Please donate in the name of Dr. Dilipkumar Gor, 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

Robert Moore Robert (Bob) was a beloved husband, father, grandfather, brother, uncle, and friend. He fought a difficult battle with pulmonary fibrosis with great courage. He remained hopeful even in the final days of his fight. We want to honor his spirit and legacy with a gift to support research in pulmonary fibrosis. Please donate in the name of Robert Moore. 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. Your generosity and support is greatly appreciated.If you have any questions please contact Jake Meding at jmeding@pulmonaryfibrosis.org or (312)854-2627

Thank you for the outpouring of compassion and love that has been shown throughout Brian's journey with pulmonary fibrosis and since his passing. If you wish to express sympathy and/or take action in remembrance of Brian, in lieu of flowers or other gifts, please consider making a donation to the Pulmonary Fibrosis Foundation by clicking on the Make Donation button on the upper right side of this page. 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 All donations are tax-deductible and every dollar raised goes to help support the mission of the Pulmonary Fibrosis Foundation. Thank you again for your thoughtfulness. If you have any questions please contact Jake Meding at jmeding@pulmonaryfibrosis.org or (312)854-2627

Kenneth Berntsen Please donate in the name of Kenneth Berntsen, 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

JamesMarsh Please donate in the name of JamesMarsh, 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

Janet Zacharias Please donate in the name of Janet Zacharias, 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 A. Silva Please donate in the name of John A. Silva, 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

William Hunt died peacefully at the age of 74. He was beloved by his family, friends, and many others he met along the way. A stellar athlete, Bill led a very active life, frequently traveling the world and enjoying tennis, football, golf and most recently, pickleball! His family and friends always enjoyed his sense of humor, original take on politics, and wide-ranging intellect. William is survived by his wife, Dana, children Alicia and Bryan (Kelly), brothers Phil (Andrea) and Don (Carla), nephew Matthew, mother-in-law Elaine, and sister-in-laws Sharon and Marlene. To honor Bill's legacy, please consider a donation to the Pulmonary Fibrosis Foundation 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. 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 Joe Crawford Joe Crawford, age 66, was an active member of Pinckneyville, IL and cared deeply about the town and its residents. He was a long-time member of United Methodist Men, the Pinckneyville Chamber of Commerce, and the Pinckneyville Optimist Club. On Sundays, he could be found at the United Methodist Church of Pinckneyville, usually followed by a lunch at Red Hawk Country Club with his family. During the week, Joe could be found at the bank, smiling and laughing with those who walked through its doors. To Joe, it didn’t matter if you were there as a customer, worked there for a day or your entire career; to him, you were family. Joe’s other full-time job was being a father to son, Brian, daughter, Julie, and grandfather to his precious granddaughter, Tallulah. He enjoyed many years of family reunions and vacations and rarely missed a ballgame, band concert, or play. Joe was an avid sports fan and loved his favorite teams; the Pinckneyville Panthers, the Fighting Illini, the SIU Salukis, the St. Louis Cardinals, and the St. Louis Rams. For many years, he could be found most winter Friday and Saturday nights in Thomas Gymnasium cheering on the Panthers with his family. Throughout his life he was an avid golfer and fan of the PGA, the highlight of which was attending the 2018 PGA Championship with his son. Joe lived with his pulmonary fibrosis diagnosis for over a year. While he did not let the disease stop him from doing what he loved, he lost his battle on January 16, 2020. He lived a joyous life with a full heart, but left far too soon. Please donate in the name of Joe Crawford, 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

As my 45th birthday approaches, I realize I don’t need gifts. What I do need is to make sure future generations of my family don’t suffer from pulmonary fibrosis like my dad did. I would love it if you could donate to the PF Foundation in honor of my dad. Please donate in the name of Bob Keaton, 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 Joy Please donate in the name of Laura Joy, 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

Nayana Patel Please donate in the name of Nayana Patel, 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. 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