Hatsuko Stutz Hatsuko Stutz October 5th 1934 - October 2nd 2019 Hatsuko Stutz, age 84, passed away peacefully on October 2nd 2019 after a courageous battle with pulmonary fibrosis at the Aspirus Hospital in Wausau, Wisconsin. She will always be remembered for having a smile, regardless of her situation. Born in Kumamoto, Japan, she is a descendant from a Noble Samurai family named Kudo, whose history in Japan goes back nearly 1000 years. Hatsuko was the last surviving Princess of the Kudo family, but her young life was a constant struggle. The last vestige of their land was swindled from the Kudo’s by a corrupt government official before the start of World War II, and the family wound up destitute and living in the barn of their former estate. Her father died in an accident, and her new step-father sold Hatsuko, at 10 years old, and her younger brother into involuntary servitude at nearby farms. During the War at 11 years of age, while eating a potato on a hill, Hatsuko witnessed the firebombing by B29's resulting in the complete destruction of Kumamoto City. Even at such a young age, she never looked upon the American Armed Forces as enemies and instead as liberators from her oppression. At 15 years old, during the early days of the United States occupation of Japan, she escaped her captivity. She worked as a textile factory worker for a few years, and then as a cabaret dancer. She met her first husband, United States Army 11th airborne division sergeant Rinaldo Campise at a dance hall, and they fell in love. Hatsuko and first sergeant Campise were married shortly thereafter. After the end of the Korean War, Hatsuko and sergeant Campise, now with the 101st airborne division, moved to Fort Campbell, KY and had their first daughter Deborah. While stationed in Germany, they had two more children, Ronald and Karen. Hatsuko lost her first husband from injuries received after his return from the Vietnam War while deployed with the 82nd airborne division. In 1967 Hatsuko moved with her three children to Los Angeles, CA. They encountered many hardships but she worked hard. She independently raised them to be strong capable people. Fulfilling a lifelong dream, she graduated college with a degree in fashion design in 1981. Hatsuko then met her second husband Carlos Stutz. The now Hatsuko Stutz worked in the fashion industry until her husband Carlos passing in 1991. She then opened her own business, along with her daughters in El Segundo, CA. There she designed and marketed her own line of clothing. In 1998, Hatsuko purchased her first loom and developed a passion for weaving. She was an innovative and prolific weaver of fabric, rugs and clothing. Hatsuko’s love of textiles was woven into the remainder of her life. Hatsuko moved to Phillips, Wisconsin in 2014 with her youngest daughter Karen and husband James Murphy. In February of 2018 Hatsuko was diagnosed with terminal pulmonary fibrosis of the lungs. Having fought to the very end, Hatsuko Stutz lost her battle with her illness. Hatsuko passed away from this world and entered into eternal goodness and light while hearing the earnest prayers of her children. Hatsuko is survived by her son Ronald Campise (Lisa) from Los Angeles who is a veteran technical crime scene supervisor with the Los Angeles Police Department’s Detective Bureau, her daughter Karen Murphy (James) who is an antique dealer, her four grandchildren Chelseah, Connor, Alex and Brian, and her step-grandsons Ian and Justin. Her first born daughter, Deborah Campise, preceded her in death on October 16, 2018 of cancer. Hatsuko Stutz, the last Princess from the Noble Kudo family from southern Japan, left this World a much better place. Thoughts and prayers are welcome. In lieu of flowers, the family wishes that a donation instead be made to the Pulmonary Fibrosis Foundation. https://app.mobilecause.com/vf/PFFTribute/HatsukoStutz Please donate in the name of Hatsuko Stutz, 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

Gary Yeiter Please donate in the name of Gary Yeiter , 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

Gias & Suraiya Tarek Please donate in memory of our parents, who both suffered from this devastating disease. Our hope is 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

Jean Bateman Please donate in the name of Jean Bateman, 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

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

This tribute page has been created in remembrance of John Anthony Perri (Giovanni Antonio Perri), 89, of Walnut Creek, California. He loved and adored his family and friends and we all adored him in return. He had a distinquished career in high tech, receiving 13 patents and many awards for his work. He was best known by family and friends as a great cook who hosted many wonderful parties and family gatherings. He was a wonderful story teller sharing experiences of a life well lived. We miss you dearly Dad…Grandpa....Uncle….. Brother…..Great Friend! 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

Hello! My aunt, Tisha Gordon passed away suddenly due to a mix of health issues but one of the main problems that prevented her from getting better was her fight with pulmonary fibrosis. She passed three weeks shy of my 20th birthday, while that broke my heart I chose to see this as an opportunity to use my birthday as a way to help fight this disease towards one of the diseases that took my amazingly strong aunt from us so suddenly. So this year for my birthday, I am asking for donations to the Pulmonary Fibrosis Foundation rather than gifts. Thank you so much for your help in anyway its shown! Please donate in the name of Tisha Gordon, 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.

Greg Hicks Please donate in the name of Greg Hicks, 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

Martin Albert Hayes Marty lived an active and varied life with many interests. His main interests included acting in local theater productions, building and battling R/C warships and sailing R/C Sailboats. Marty was always a leader in whatever organization he joined. Marty retired from Westinghouse. Marty served in the Air Force and with the Civil Air Patrol. Marty was a lifetime learner and continued to take classes after he received his Masters Degree from the University of Baltimore. Marty will be missed by his family and friends far and wide. Please donate in the memory of Martin Albert Hayes, so that a cure and/or treatments 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 Bagby Please donate in the name of Michael Bagby , 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 Wilbur Schnatz Please donate in the name of Thomas Wilbur Schnatz, 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

Richard Buck Please donate in the name of Richard Buck, 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 Alice C. Johnson On November 21, 2019, this disease claimed the life of our beautiful, sweet, Alice. Despite the pain of our loss, we know how lucky we have been to have her in our lives. We also know the devastation and hopelessness of having a loved one that has been diagnosed with pulmonary fibrosis. Please donate in her name, so that other sufferers of this terrible disease might one day know a cure, or have the chance to live a longer healthier life. Thank you for your thoughtfulness. Your generosity and support is greatly appreciated. With love and gratitude, The Family and Friends of Alice C. Johnson 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. If you have any questions please contact Jake Meding at jmeding@pulmonaryfibrosis.org or (312)854-2627

Steve Rodick There is currently no cure for Pulmonary Fibrosis, which claimed Steve's lungs and nearly his life in 2013. A lung transplant allowed him to thrive for nearly 7 more years and meet his grandchildren. His family encourages everyone to register as an organ donor. For those wishing to contribute sooner, donations to the Pulmonary Fibrosis foundation are 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 register as an organ donor and share this page with those who might wish to contribute. 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

Ken Kerley Please donate in the name of Ken Kerley, 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, Arthur L. Rosa, Sr. 1936-2020 A devoted husband, loving father, caring grandfather, and amazing friend to all. You will be missed immensely. Heaven has gained one heck on an Angel and we know you are up there making jokes, fishing, boating, playing sports, visiting with our dear departed, and most of all watching down over us all. Arthur was first diagnosed with Idiopathic Pulmonary Fibrosis in 2007. His doctors gave him a 3-5 year life expectancy from that point. Just like the strong and determined person he was, he fought and stayed with us on this Earth for another 13 years. During those years, lots of quality family time was taken advantage of, more wisdom and advice was passed on, many sports games were viewed, and countless hours were spent laughing, joking, and making memories. However, not all of this time was happy. As this terrible disease continued to run its course with currently no cure known, it began to wear on Arthur's health; more specifically his lungs. In sparing the sorrowful and painful details, Arthur was able to spend his last months on this Earth in his own home on Hospice surrounded by those he loved most. He passed peacefully and comfortably, with family by his side. Now, we celebrate a truly beautiful man who lived and loved well. Rest In Peace Arthur L. Rosa, Sr. Family and friends, please donate in the name of Arthur L. Rosa, 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 if you can 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 share this link on social media. Every donation or share counts in the effort to spread awareness. Thank you for your thoughtfulness. Your generosity and support is greatly appreciated, The Rosa Family

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

Please donate in the name of Debra Baldwin, so that a cure and/or treatments to prolong life for sufferers of this terrible disease can be found. The Pulmonary Fibrosis Foundation was dear to her heart. In lieu of flowers please consider donating to PFF. -Amber 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 Gladys Stones Gladys was a vibrant & energetic 92-year-old Great Grandmother, who sadly slipped away on Friday, January 31st. surrounded by her loving family after suffering from Pulmonary Fibrosis. We know she is now reunited with her ever-loving husband of 53 years, Stan. Gladys is survived by her loving Daughter Alison and Son John. In lieu of flowers or other tributes, we would be grateful if you would instead make a donation in the name of Gladys Stones, 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. 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 call (312)854-2627

In Memory of Connie Haning Please donate in the name of Connie Haning, so that a cure and/or treatments to prolong life for sufferers of this terrible disease can be found. Her life touched many and we want to find a way to give back so others may live long and fruitful lives and not be plagued by this awful disease. Please consider making a small donation. 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. Please share away. The family of Connie thank you greatly.If you have any questions please contact Jake Meding at jmeding@pulmonaryfibrosis.org or (312)854-2627

Dear Friends and Family, Please donate in the name of Joe Mann, 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

Mary Lou Banaszak Please donate in the name of Mary Lou Banaszak, 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

Juan Garza My Father, Juan Garza passed away on March 10, 2020. Please consider a donation in the name of Juan Garza, 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

Jeanette Nelson Please donate in the name of Jeanette Nelson, 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

Jose "Guido" Betancourt Please donate in the name of Jose "Guido" Betancourt, 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

Ronald "RJ" Pohl Please donate in the name of Ronald Pohl, 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

Mari Ann Johnson Please donate in the name of Mari Ann 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

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