Jamie Pepin Martin/Carol Jackson Please donate in the name of Carol Jackson or Jamie Pepin, 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 Dawn Gebben The family of Dawn Gebben wants to raise awareness and funds for 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

Jean Schwarz Our mom was the epitome of grace under pressure as she battled this disease. Please donate in the name of Jean Schwarz, so that a cure and/or treatments to prolong life for sufferers of this terrible disease can be found. Thank you for your thoughtfulness. Your generosity and support is greatly appreciated. -Ingrid, Blanche, Joe, Paul and Carl Schwarz Families 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. If you have any questions please contact Jake Meding at jmeding@pulmonaryfibrosis.org or (312)854-2627

Anne Stone In April of 2022, Anne went to the doctor because she'd been experiencing shortness of breath. Her regular physician was concerned that it was a pulmonary embolism; instead, after several days in the hospital and a variety of tests, we learned it was idiopathic pulmonary fibrosis. "Idiopathic" means they're unable to pinpoint a cause. "Pulmonary fibrosis" means that it's a permanent, progressive scarring of her lungs. Anne tried two different experimental medications intended to stop the progression of her disease, but unfortunately it continued to advance. At the end of June 2023, her doctor indicated that it was time to begin hospice. On October 1, 2023 she passed away. Anne was an incredible mother, always advocating for her children and grandchildren, as well as a beloved sister and friend. She is deeply loved and missed. Please consider donating to help find a cure for this disease, so that no other families have to suffer through this unfortunate journey in the future. 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 have any questions please contact Jake Meding at jmeding@pulmonaryfibrosis.org or (312)854-2627

John Jenkins Please donate in the name of John Jenkins, 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. John Lester Jenkins, 59, fortified with the Sacraments of Holy Mother Church on Tuesday, October 12, 2021.The beloved husband of Tammy Jenkins (nee Thomason) for 25 years; cherished son of Barbara Jenkins (nee Veidt) and the late Lester Jenkins; dear brother of James (Michele) Jenkins and Paul (Lisa) Jenkins; treasured uncle of Angela Jenkins, Adam Jenkins, Laura, Sarah and Simon Jenkins, Graham Thomason, Samantha Thomason, Josh Thomason and Anna Thomason; loving brother-in-law of Joe (Michelle) Thomason and son-in-law of Sandy and Ron Thomason.John played soccer when he was younger and continued his enjoyment for sports throughout his life. He will be remembered for being a very genuine and kind-hearted man and will be greatly missed by his family and many friends.

Marilynne Ann Mancini was a kind, loving, considerate, and witty mother, wife, sister, daughter, friend, and grandmother. She passed away on May 23rd after fighting an arduous battle with pulmonary fibrosis. She lived for her grandchildren and her grandchildren adored her. We were all blessed to have known her and have her in our lives. We have chosen to support this organization because her kind heart would want to rid others of suffering. We hope to find a cure and support others suffering from pulmonary fibrosis. Marilynne’s memories and influence to do good for the world will live on in the lives of her loved ones. Her husband, Frank, her brother, Richard, her children, Ann, Michael, Jim, and Jenny, her grandchildren, Danny, Abby, Luca, Crosby, Holden, Ada, and Enza, along with many others that loved her, would like to thank you for your kind thoughts and prayers. Heaven is so lucky to have gained a new angel.

Terry Lovaas Please donate in the name of Terry Lovaas, 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

Steven L. Buenning Please donate in the memory of Steve, so that a cure and/or treatments to prolong life for sufferers of this terrible disease can be found. Steve was diagnosed in 2016, just after retiring from a 41 year teaching career. He refused to let IPF define him, so he kept this diagnosis private and lived as full a life possible even when he began to need oxygen. His family is heartbroken and he fought valiantly to be with us as long as possible, but the lung damage was just too great to overcome. 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

Nancy Scanlan-Laya Please donate in memory of Nancy Scanlan-Laya, 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 Gary Wodder, the most wonderful husband, father, and friend. On December 24, 2022, my father lost his battle with Pulmonary Fibrosis, a rare and horrendous disease that slowly stole his capacity to do what is most basic to all of us- to breath. My Dad lived his life with passion and zest. He was a wonderful husband, father, and friend; an athlete, reader, traveler, and lover of nature and animals. He touched the lives of many people and meant the world to us. Please consider donating to the research for a cure of pulmonary fibrosis. No person should have to suffer from this vile illness, and no family should have to lose precious time and memories with their loved ones. Thank you from the bottom of 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

Dick Koblinski Please donate in the name of Dick Koblinski. Dick was a man who lived life to the fullest and should have enjoyed a longer one if not for this disease. So please help us find a cure so that other families will not have to watch a loved one suffer in the name of this 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

Ashok Diwaker Please donate in the name of Ashok Diwaker, 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

Ray Anderson Please donate in the name of Ray Anderson, 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

Duane Crumb Duane Edwin Crumb of Townsend, WI, passed away early Monday morning, March 2nd near his home in North Myrtle Beach from complications of Idiopathic Pulmonary Fibrosis. He is survived by his wife of 31 years, Suzanne (Sue) Halko-Crumb.Duane was born in Binghamton, NY but grew up in the Chicagoland area and split his time between North Myrtle Beach, SC and Townsend, WI. He spent many years as a Land Surveyor with his dad, Ron. He then moved into Collectibles and even had a “Beanie Baby” hot line! Duane loved life and even more his family. He never complained or had a bad word to say about anyone. Duane loved fishing, traveling, cooking, gardening and golf. His nickname given by the golfers was “Pony” since Roy, his father-in-law was called the “Horse”! He was also fondly known as Dewy! Duane was a Chicago sports fan - Hawks, Bulls, Bears but especially the Cubs. In fact, Opening Day in 1987, Duane jumped onto the field and ran the bases, slid into home base and went into the Cubs dugout and took a drink out of the water fountain. Andy Frain Security proceeded to escort him out of the park :) He enjoyed classic rock, board games and collected little rubber ducks. At one point, Duane was proud to achieve the status of being "The Online World-Wide Cribbage Champion!" Duane was an all around FUN guy! Duane is survived by his mother Shirley Crumb; siblings Anne Marie Hughes (Rocky), Deborah Keller-Shultz and Carol Vajgert; Mother-in-law Margaret Aldworth; Sister-in-law Laura Halko; Nieces and Nephews George, Billy, RoseAnne, James, Daniel, Eric, Adam, Savannah, Hunter, Jonah and Tallulah. He is preceded in death by Father Ronald Crumb;Brother Thomas Crumb; Father-in-law Roy Halko; Nephew Elijah Vajgert. The Duane Crumb Farewell Tour: June 4Surf Golf & Beach Club 1701 Springland Lane2:00 - 4:00 pm August 9The Langford’s HomeOs351 East St. (Next to East Street Park)Winfield, IL 2:00 - 4:00 pm July 19McCauslin Brook Golf Course17067 Club House LaneLakewood, WI4:00 - 6:00 pm Please send cards or sentiments to:Sue Crumb4505 S Ocean Blvd - Unit 7ANorth Myrtle Beach, SC 29582 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

Bernard "Dino" Fantozzi Please donate in the name of Bernard "Dino" Fantozzi, 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

Emil FerrariniEmil B. Ferrarini 88, of Elmhurst, IL. Beloved husband of the late Patricia nee Corrigan. Loving father of Bill, Margaret (Ken) Bartels, Katie (Patrick) Byrne and Marty (Patti). Cherished grandfather of Amy Hatfield, Joe (Rachel) Ferrarini, Nicole (Jay) Filas, Brittany (Phil) Dorjath, Jake (Annice) Meding, Mike (Emma) Ferrarini, Jennifer Ferrarini, Bridget Byrne, Nick Ferrarini, and Frank Ferrarini. Great grandfather of 7. Fond brother of the late Eddie, Jack, Mello, Tom, Anthony, Marianna and Teddy. Uncle and great uncle of many.Family and friends may gather for a 9:30 a.m. Memorial Mass on Saturday, Feb 16, 2019, at Mary Queen of Heaven Church 426 N. West Ave, Elmhurst, IL. 60126. Please donate in the name of Emil Ferrarini, 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

Please donate in the name of Foster Sullivan, 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. Foster J. Sullivan - Of Huntington, on June 10, 2021, 71 years of age. Born in Chicago in 1949, Foster served in the US Army in Vietnam; married his high school sweetheart during the summer of ’69; spent decades selling spoons and plates around the world; and took the most pride in his role as father and grandfather to more than just his own. He was a loyal friend to many and although he is missed dearly, the tenor of his roguish laugh will remain forever etched in the minds and hearts of those who knew and loved him. Loving husband of Debbie Sullivan. Loving father of Ryan (Kit) Sullivan and Lindsay (Zachary) Sullivan. Cherished grandfather of Phoebe Sullivan, Foster Sullivan, and Cyrus Smith-Sullivan. Dear brother of Larry Sullivan, Debbie Duda, the late James Sullivan, and the late Lynn Sullivan. Private cremation.

Rory Samberg Please donate in the name of Rory Samberg, 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

Arthur J Mac Lean Please donate in the name of Arthur J Mac Lean, 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 Jewell Please donate in the name of Jack Jewell, 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 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 Kenneth George Friedman, 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 Farwell Please donate in the name of Robert Farwell, 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

While fighting this disease himself, Kevin Krambeer became active in the Pulmonary Fibrosis Foundation advocating for others also fighting this disease. Your donation in Kevin's name will help to find a cure and/or treatments to prolong life for sufferers of this terrible 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 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. If you have any questions please contact Jake Meding at jmeding@pulmonaryfibrosis.org or (312)854-2627

Our beloved Dad, Sridhar, was diagnosed with Idiopathic Pulmonary Fibrosis in June of 2021 from a chest x-ray ordered by his primary care provider when he complained of a dry cough. The diagnosis was shocking since he had no family history and was otherwise very healthy. He quickly established care with a pulmonologist and was started on a trial medication in hopes to halt progression of the scarring in his lungs. At the time of his diagnosis, he was still very active and independent. Within 6 months, he needed portable oxygen upon movement and his O2 requirements continued to increase. He researched so much about this disease and despite the grim prognosis, he was extremely optimistic. He was hopeful that he would be a candidate for a lung transplant and was eagerly awaiting his transplant evaluation in July of 2022. Unfortunately, a few days before his lung transplant evaluation, he had an exacerbation which led to a month long hospitalization. He fought so extremely hard but ultimately suffered complications during his stay that led to his passing on August 16, 2022. We are blessed beyond measure to be our Father’s daughters – he was the best Dad, best Husband to our Mom, and the absolute best Grandpa to our kids. We hope to continue sharing his story to bring more awareness towards this heartbreaking disease. Lung Transplant continues to be the only cure for IPF but for many that’s not an option due to age and underlying comorbidities. It will be our continuous endeavor to support and advocate for this organization that contributes to research and helps educate others in navigating their own PF journey. Please donate in the name of our Dad, Sridhar Angarai Srinivasan, 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

Derek Edward McLane Please donate in the name of Derek Edward McLane, 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 of a life well-lived. Beloved and loving wife, mom, grandmother, sister and friend, Marcia passed peacefully in her sleep, surrounded by her family, on October 5th, 2021. Born in Joliet, Illinois on May 24th, 1952, Marcia lived the majority of her life in the Chicago area before retiring in 2015 and realizing her dream of a life at the beach in Myrtle Beach. Marcia loved her family more than anything, but a close second was a project. Knitting, basket-making, quilting, painting, wallpapering - you name it, she'd dive headfirst into it. We are so lucky to have so many useful things made by her hands that will remain in our lives for years to come. Marcia is survived by her husband of nearly 49 years, Paul, as well as her sons Ryan and Aaron, her daughter-in-law Abby, grandchildren Hannah and Connor and grandpets Bjügaarhæd (aka Booger) and Sherman. 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. 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

RussWatson Please donate in the name of RussWatson, 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

Joseph Ciarcia Please donate in the name of Joseph Ciarcia, 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

Ali Mazaheri 10/01/1945 - 03/12/2023 Over the last 4 years, Ali courageously battled lung cancer and pulmonary fibrosis. At the time of his passing, he had been cancer free for 9 months, but pulmonary fibrosis doesn't have a cure and results in death. Ali lived an extraordinary life filled with amazing adventures and passion. He was loving, hard working, intelligent, witty, wise, and grateful. He loved poetry, Rumi, reading, story telling, growing fruit trees, animals, and his ranch. But above all else, he loved his wife, children, and grandchildren. He was a loving husband, an incredible father and an amazing grandfather. This page is set up for those who wish to donate 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

Larry Wayne Johnson, 65, of Minot, ND, died Monday, August 8, 2022, in a Minot hospital with his loving family surrounding him. Larry was born on May 23, 1957, in Kenmare, ND, to LeRoy and Lorna (Rasmusson) Johnson. He was raised in Minot with his sister, Carol, and brother, Wayne. Larry’s loving family includes his wife, Becky and sons, Drew and Lucas. Larry thoroughly enjoyed the time he spent visiting and socializing with family and friends. Along with Becky, Larry acquired a large family of people who loved him and welcomed him into their lives. If he could lend a helping hand to anyone, he was more than willing to do so. Larry will be missed, respected, and loved for the person he was. We will cherish the precious memories we have. Please donate in the name of Larry Johnson, 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