Elizabeth Anne (Nana) Copp Our beloved wife, mom and Nana passed away peacefully after an 18 month battle with pulmonary fibrosis, Jan 4th 2019, the evening of her 77th birthday. Anne found comfort in PFF 's telephone based support group. Please donate in her name so that a cure and/or treatment for sufferers of this terrible disease may 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

EDILAINE SILVA Please donate in the name of EDILAINE 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

Alden 'AW' Jackson On April 2, 2019, artist, educator, and family man, Alden 'AW' Jackson, 93, passed away peacefully in the presence of his spouse and daughter in his home in Capitol Heights, MD after a multi-year battle with Idiopathic Pulmonary Fibrosis. AW is survived by his spouse, Deanna Burruss Jackson, two children, two grandchildren, and many nieces and nephews. AW was born in Charlottesville, VA in 1925. He was the son of John Andrew and Otelia Love Jackson, and a brother to John Andrew (II), Gloria, Ellard, George Franklin, Love, and Elwood Jackson, who all preceded him in death. AW entered the Army in 1943 and served in the Pacific until 1945. After returning from WWII, he completed his Bachelor’s degree at North Carolina Central University. After graduating, he returned to Charlottesville, VA, where he took care of his aging parents and volunteered as the Scoutmaster for a local Boy Scout Troop. Here, he met his lifelong friend, Oliver Anderson, a co-worker in a local frame shop. It’s also where he met his spouse, Deanna Burruss. They married in 1960 and were soon blessed with their first child. The family moved to Orangeburg, SC, where AW’s sister Gloria lived. With her help, he secured a job at South Carolina State College. Soon after they were blessed with their second child. In mid-1965, the family moved to the Washington, DC area, which became his long term home. From the Frame Restoration department of the Smithsonian Institution's National Gallery of Art to teaching art at the Mildred Green Elementary School, to decorating his church, St. Margaret of Scotland, for every major liturgical holiday for over 20 years, AW’s life was infused with his artistic talent and his desire to give to the community. His volunteer work also spanned his life, including being the Cubmaster for the church's Cub Scout Troop and organizing a meal stability project for the community at his church. After retiring from the DC Public Schools, AW attended ceramic classes (his favorite medium) at Prince George’s Community College, enjoying the community and the freedom to explore his own creative path. AW was also prolific gardener, indoors and out. His home was a veritable greenhouse and his gardens included a fish pond. AW’s vegetable gardens always produced a bounty, and he generously donated the surplus to the St. Margaret’s community. Through everything, AW’s family was central in his life. Married almost 60 years, he was extremely proud that his children had earned Ph.D.’s and were accomplished in their respective fields. He was a loving grandparent, always with a kind word of support. His nieces and nephews kept in touch with him as if he were their parent. His warmth and generosity also extended to his children’s friends, to whom he opened his home and heart. AW will be greatly missed by his family, friends, and so many others whose lives he touched. 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 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 are greatly appreciated.If you have any questions please contact Jake Meding at jmeding@pulmonaryfibrosis.org or (312)854-2627

Lenoard Wright Please donate in the name of Lenoard Wright, 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

Russel Wyckoff Please donate in the name of Russel Wyckoff, 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 Ezykowich On September 7, 2019, I watched my Dad go peacefully and be free from all of his suffering. He was diagnosed with Idiopathic Pulmonary fibrosis about 10 years ago and I watched his health decline gradually. In its simplest sense, pulmonary fibrosis (PF) means scarring in the lungs. Over time, the scar tissue can destroy the normal lung and make it hard for oxygen to get into your blood. Low oxygen levels (and the stiff scar tissue itself) can cause you to feel short of breath, particularly when walking and exercising. Pulmonary fibrosis isn’t just one disease. It is a family of more than 200 different lung diseases that all look very much alike. The PF family of lung diseases falls into an even larger group of diseases called the interstitial lung diseases (also known as ILD), which includes all of the diseases that have inflammation and/or scarring in the lung. I remember reading about this disease and the life expectancy was 3-5 years. In 2016, he received the gift of life through a lung transplant. Watching him breathe without oxygen and without struggle was the biggest blessing, and something we had imagined for so long. The post transplant life was not easy. After a few short months of good days, he started to have lousy ones again. The months & years that followed were filled with trips to the hospital for stints of pneumonia and infections. Each trip to the hospital would be more of a setback, and in 2018 a stroke bringing on even more issues. The last year, he spent almost 7/12 months in the hospital for different things. My mom didn’t leave his side for one single second - a true testament to their marriage and love. Watching my father pass was one of the hardest things, but knowing he is free from the suffering he endured for so long is providing us comfort during this time. I am a huge supporter of transplants, as that allowed me borrowed time with my Dad, but ultimately, we need to find a cure for pulmonary fibrosis. It’s devastating and heartbreaking. My Dad was a fighter, Superman, a PF warrior, and the greatest man I will ever know. Please donate in the name of Robert Ezykowich, 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 Jorge E. Devia On December 11, 2019, we lost Jorge to this terrible disease. We know how devastating this disease can be to not only to the person affected by it, but also to family and friends. Thank you for your thoughtfulness. Your generosity and support is greatly 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

Geeta Aroon Mankad, 75, of Blue Bell, Pennsylvania passed away on Wednesday, July 8, 2020 with her family by her side after a prolonged battle with pulmonary fibrosis. It would be wrong to say that Geeta lost her battle with pulmonary fibrosis because she remained strong and never stopped fighting. No matter the challenge, she was determined to live her life on her terms and to the fullest extent – she traveled the world, and most recently completed the Chardham Yatra and visited Pashupathinath Temple in Nepal (over 11,000 feet in elevation) to fulfill her religious aspiration and lifelong dream of visiting all of the 12 holiest Hindu sites devoted to Lord Shiva. The place where she was most at peace was at the Dattatreya Mandir in Nareshwar, to which she would visit on every trip to India. It is by her example that we learned what resilience, perseverance and kindness truly look like. She was officially diagnosed with pulmonary fibrosis almost 10 years ago. She fought bravely and outlived the normal prognosis of 3-5 years. Unfortunately, pulmonary fibrosis has no cure and there are very limited treatment options available for patients with this disease. To celebrate her life and legacy - we ask that in lieu of flowers, donations be made to the Pulmonary Fibrosis Foundation (PFF). A donation to PFF will help to raise awareness, provide money for research and support for families managing this disease. If you have other causes to support, consider this a reminder to make that donation. Thank you for your love, support and thoughtfulness. If you have any questions please contact Jake Meding at jmeding@pulmonaryfibrosis.org or (312)854-2627

Rip Kirby Please donate in the name of Lawrence Rip Kirby, so that a cure and/or treatments to prolong life for sufferers of this terrible disease can be found. Lawrence “Rip” Kirby of Rutland, Vermont passed away Saturday, January 4th, 2020 at age 59, surrounded by those he held dearest. Rip was born on October 21, 1960 in Watertown, NY to Lawrence and Yolanda Kirby, and spent most of his childhood in Chazy, NY. He earned his Bachelor’s degree in electrical engineering from Clarkson University in 1984, and worked at Central Hudson Gas and Electric in Poughkeepsie, NY until he moved to Rutland, VT in 1988. There, he worked as an electrical engineer for VELCO until 2001, and then CVPS/GMP until his retirement in 2017, during which time he earned his Professional Engineering (P.E.) licensure. He then worked as the electrical engineer for the State of Vermont Department of Public Service until his passing. Rip was a captivating and engaging presence. In his free time, he enjoyed playing scrabble and doing crossword puzzles, cooking chili for charity, and writing when a topic moved him. He collected guns and loved classic cars; he prided himself on his ability to recognize the make, model, and year of almost any classic car, and loved to chew the fat with a fellow owner at various regional car shows. He was a wealth of knowledge and had an unmatched sense of humor; he enjoyed nothing more than getting a room full of people laughing. He was a generous, gentle, loving man who will be missed dearly by many. 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. 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 Please donate in the name of Socorro Ramirez, 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 Lewis Case Jack is a dear friend and I created this page for others to give as a memorial contribution. We love you Jack, you will be missed. Rest In Peace. Please donate in the name of Jack Case, 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 Mike (Ghasem) Setork to help find a cure for those suffering of Idiopathic Pulmonary Fibrosis (IPF). Although we are devastated by Mike's loss, we are always reminded by our hearts – how lucky we have been to know him and the everlasting impact he had on all of us. Thank you for your thoughtfulness. Your generosity and support is greatly 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 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.

Char Terpsma Charlotte A. Terpsma (Oppenhuizen), age 67, of Kentwood, went home to be with her Lord on her birthday, Saturday, March 21, 2020. Born in Grand Rapids in 1953, Char attended Grand Rapids Central Christian High School. She enjoyed singing, gardening, and bicycling-holding a record (1990) for the 24-hour challenge. She really loved spending time with her family and had a special place in her heart for her grandchildren. Char worked as a Credit Administrator at Pleune Service Company where she was employed for the past 15 years. She was the president of the National Association of Women in Construction from 2012-2014. Char will be lovingly remembered by her children, Michelle Wright, Rachel and Tony Thampan, Jeremy and Melissa Terpsma, and Elizabeth and Ted Mosies; her five grandchildren, Gabriela, Caleb, and Anna Thampan, Jeremy Terpsma Jr., and Samantha Mosies; She will be greatly missed by her former husband David Terpsma; her brothers, Don and Shirley Oppenhuizen, Roger and Lois Oppenhuizen; her sisters, Marie and Tom Rogers, Karen and Sonny Garber; former sister-in-law, Sally Terpsma; former brother-in-law, Dan Terpsma, former mother-in-law, Mary Terpsma, along with many cousins, nieces and nephews. Char was predeceased by her parents Engelus (Oppie) and Gladys Oppenhuizen, former father-in-law Peter Terpsma, and former brother-in-law Peter Terpsma. A Celebration of Char’s life will be held at a future date. Memorial contributions can be made 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 All donations are tax-deductible. 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

Philip Hottle Please donate in the name of Philip Hottle, 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 Richard Hideo Yamada We thank you for all of the love and support you have given over the years and know that Richard is in a peaceful place. 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

Phillip Lee Monaghan, Jr. Phillip Lee Monaghan, Jr., age 75, resident of Mastic Beach, New York, passed away on May 22, 2021 after a long battle with Idiopathic Pulmonary Fibrosis. He is survived by Patricia Ann Monaghan, his wife of 49 years, his children Ellen Marie Rios (husband Kevin) and Stephen Phillip Monaghan (wife Julie) and was blessed with five grandchildren: Jordan (16), Connor (16), Meghan (13), Jessica (13), and Emma (9). Phil is also survived by his brothers Bob and Pat, and his sister Cindy. Phil is a Vietnam veteran and had a long and rewarding career in the medical field after an honorable discharge from the U.S. Navy. He will always be in our hearts. Please donate in the name of Phil Monaghan, 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. 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 Robert "Bob" Shaw, 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

Di Watts Please donate in the name of Di Watts, 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 Miller Jr. Please donate in the name of Arthur Miller Jr., 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

Claudia Heflin Please donate in the name of Claudia Heflin, 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

Jack Lambert Please donate in the name of Jack Lambert, 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

Ricky D. Henderson June 27, 1960 – July 3, 2022 Ricky D. Henderson, 62, of Marshall, died Sunday, July 3, 2022, at his home. Born June 27, 1960, in Marshall, Rick was the youngest child of Virgie Irene (Payton) and Joseph Lee Henderson. On July 25, 1978, Rick married his high-school sweetheart and soulmate, Lori (Johnson). Rick and Lori lived lovingly and loyally hand in hand for 44 years. In addition to his grieving widow, Rick will be deeply missed by his daughter, Trisha Henderson-Brown, and her husband, Jay Brown, of Columbia. Rick is also survived by a son, Jason Henderson of Cassville. Rick lived in Marshall most of his life, graduating from Marshall High School before serving as a sergeant in the U.S. Air Force. After being stationed as a construction equipment operator for the next seven years in such places as Grand Forks, N.D., and Wichita, Kan., Rick was honorably discharged. Rick then worked for around 10 years as a sandblaster and dedicated 20 years to the wire-rope industry. Additional survivors include three sisters, Mary Canon of Sedalia, Carolyn Riley of Marshall, and Virginia “Jenny” Henderson of Sedalia; three brothers, Wayne Henderson of Marshall, Dale Henderson of Marysville, Kan., Bobby Henderson of Zephyrhills, Fla.; a mother-in-law, Norma Johnson of Sedalia; a sister-in-law, Lisa Bridges of rural Marshall; a brother-in-law, Mike Johnson of Marshall; and several nieces, nephews, and cousins. In addition to his parents, Rick was preceded in death by two brothers, Lavern Henderson and Gene Henderson. __________________________________ Please donate in the name of Rick Henderson, 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

Jeffrey Knoop Please donate in the name of Jeffrey Knoop, 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

Michael Stryker Please donate in the name of Michael Stryker, 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 Afaf Mahfouz Schieren - beloved spouse, sister, aunt, friend (& adoptive mother) 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. If you have any questions please contact Jake Meding at jmeding@pulmonaryfibrosis.org or (312) 854-2627

Gene Harrott If you wish to please donate in the name of Gene Harrott, so that a cure and/or treatments to prolong life for sufferers of this terrible disease can be found. It is a terrible disease and he fought it like a champ! 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. 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

What a beautiful soul, what an awful disease! Lili fought for 7 long years and sadly the toolbox was empty at the end. Perhaps with your donation, there might be more available tools to save the life of another beautiful soul. 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 Thank you for your thoughtfulness. Your generosity and support is greatly appreciated. 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

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

Rene J. Fernandez del Valle 05/07/1951-07/03/2023 Rene was diagnosed with Pulmonary Fibrosis since February 2019. He lived an extraordinary life full of amazing adventures! He was a loving husband, father, grandfather, brother and cousin.He was intense with his work, intelligent, witty and never forgot were he was born. His love for Cuba to be free, was his greatest passion in life. Please donate in the name of Rene J. Fernandez del Valle, 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