Glenn Logue Please donate in the name of Glenn Logue, 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

Gloria (Rothermel) Glass Please donate in the name of Gloria (Rothermel) Glass, 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

Gloria Diaz Please donate in the name of Gloria Diaz, 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 Gloria O'Neill - beloved sister, wife, mother, grandmother, and great-grandmother. Please donate in the name of Gloria O'Neill, 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

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

GovindaReddyChukkalore Please donate in the name of GovindaReddyChukkalore, 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

Grace Sowle Please donate in the name of Grace Sowle, 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 honor of Grady Kuhn. Proceeds go towards finding effective treatments and someday a cure for pulmonary fibrosis. Please post this on your Facebook and Twitter pages and forward to friends and family who know what a great person Grady is and what a blessing he is to his family, his friends and his community. 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. Thank you for your thoughtfulness, your generosity and your support.If you have any questions please contact Jake Meding at jmeding@pulmonaryfibrosis.org or (312)854-2627

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

Greg Hykes Please donate in the name of Greg Hykes, 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

Greg Mueller Please donate in the name of Greg Mueller, so that a cure and/or treatments for sufferers of Pulmonary Fibrosis 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

Greg Thomas Please donate in the name of Greg Thomas, so that a cure and/or treatments to prolong life for sufferers of this terrible disease can be found. Greg's Daughter, Dr. Maggie Thomas Freeberg is doing research at Virginia Commonwealth University to help find a cure for Pulmonary Fibrosis! And every dollar we raise helps her and other researchers move their science forward. Community service was a way of life for Greg. In 1969, he became one of the earliest VISTA volunteers. He was a long time volunteer with the Boy Scouts, Meals-on-Wheels, Genesee Waterways Center, and the Red Cross (including providing hands-on aid to the victims of Katrina and many other disasters). Even while dealing with Pulmonary Fibrosis, he was involved with Rochester Community Bikes and Empty Bowls, and became a contributor to Rochester’s Sanctuary Village. Greg was the founder of Breathe Easy Rochester, a support group for people with Pulmonary Fibrosis and their caregivers. 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 Greg was devastating, yet I am reminded every day – how lucky I was to have been to know and loved him. Thank you for your thoughtfulness. Your generosity and support is truly appreciated. Mary PollockIf you have any questions please contact Jake Meding at jmeding@pulmonaryfibrosis.org or (312)854-2627

Gregoire Hamon Please donate in the name of Gregoire Hamon, 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

Gregory "Greg" Thomarios Please donate in the name of Gregory "Greg" Thomarios, 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

Gregory Reed Lockhart (May 30, 1944-September 22, 2019) Greg was a Loving Son, Brother, Father to Ian and Shannon, Grandfather to Jaden and an Amazing Friend and Mentor to many. He enjoyed traveling the world with the Love of his life Cindy and together, along with their band of friends, broke bread and immersed themselves in the arts and cycling. As many of you know Greg had the unfortunate diagnoses of IPF (Idiopathic Pulmonary Fibrosis). This debilitating disease robbed him of being able to live the active life he had grown accustomed to. It Literally took his breath away! The occurrence of this disease has doubled in the last decade. IPF has no known cure at this time but there are promising trials suggesting that there are effective drugs on the horizon. We want to Help! In honor of Greg, we will be accepting donations for the IPF Foundation the evening of the memorial. Our Family thanks you for all the Love and Support you have showered us with and that we continue to receive.

Guillermo Campero Martinez Please donate in the Memory of Guillermo Campero Martinez, 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

Gunvanti Gamadia Please donate in the name of Gunvanti Gamadia, 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

H. Michael Cunningham Please donate in the name of H. Michael Cunningham , so that a cure and/or treatments to prolong life for sufferers of this terrible disease can be found. https://www.fulwoodfuneralservice.com/obituary/Harry-Cunningham 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

Haeng Ju Kong 9/04/50 - 2/28/21 Born in South Korea, Haeng Ju Kong was the spirited, smart second son of DukJong Kong and DuSoon (Bae) Kong and a graduate of Yonsei University. One of his favorite memories of his university days was participating in the theatre. In 1978, he immigrated to the U.S with his wife, Cindy (Park) Kong and located in Riverdale, NY just in time for the birth of his son, Andrew Kong. In 1980, he welcomed his daughter, Juliet (Kong) Stiehl. Throughout his life, HJ was a vivacious, funny dad who tirelessly worked several jobs, with the goal of ensuring that his children were afforded every educational opportunity and the chance to achieve the "American Dream." While our childhood was filled with piano and violin lessons and, of course, laser focus on our schooling, it was also filled with family vacations, with my Dad driving all of us in his beloved minivan to Niagara Falls, the Cape and Florida. Dad was very committed to bringing us to various amusement parks and riding roller coasters with us. He was always there to champion our performances at our games, concerts and competitions. He also loved to play cards, eat Korean food and sushi (the joke is that "when the fish in the ocean could hear HJ coming, they would swim away"), sing karaoke and watch his Korean TV shows. And of course, he loved family trips to Vegas! He was both outgoing and welcoming and in that vein, he embraced both his son-in-law, George, and daughter-in-law, Joan to our family. But in his life, nothing seemed to bring him more joy than being with his grandchildren: James Stiehl (10), Charlotte Stiehl(6), Matthew Kong (9) and Elizabeth Kong (3). He was "fun harahbuhgee" who would play hide and seek and get in light saber fights with his grandsons. He would let Charlotte paint his nails and clap loudly while she performed her impromptu dance routines. He told my brother, Andrew, that his proudest moment as a father was when my brother adopted my niece, Elizabeth. And that is the core of Dad's heart. So it is with deep sadness that we say goodbye to this loving, cheerful husband, father, father-in-law and grandfather. We mourn the loss of your presence in our future, but we also are thankful for the memories we have. We love you and we already so greatly miss you, Apah. Dad's last few years were a challenge due to pulmonary fibrosis. Pulmonary Fibrosis is a general diagnosis when there is scarring of the lung tissue, which can never be regenerated or healed and ultimately impact one's ability to breathe and supply oxygen to one's body. It can cause great suffering for those who are diagnosed with it. And so, we ask that those who wish to do something for our family, please consider donating to the Pulmonary Fibrosis Foundation. Donations in honor of my father will go to: • Finding effective treatments and a cure for pulmonary fibrosis• Advocating for the pulmonary fibrosis community • Promoting disease awareness • Providing a compassionate environment for patients and their families Please donate and together we can help those living with pulmonary fibrosis 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

Hannah Kirkland Please donate in the name of Hannah Kirkland, 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

Harriet Fuchs Please donate in the name of Harriet Fuchs, 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

Harry Holt Please donate in the name of Harry Holt, 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

Harry Rumler Please donate in the name of Harry Rumler, 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

Harvey Davis was a loving and very giving husband, beloved father, and friend. He retired from the Navy, Army, oil delivery, Philadelphia Fire Department (as a Lieutenant) after many years. In his retirement, he started a new job as a public transportation bus driver. Always working and caring for his family and others it came as a shock that he was diagnosed with the rare lung disease "pulmonary fibrosis." Tje doctors had an inkling that this diagnosis could very possibly be due to his service in many chemical and smoke based jobs. Harvey leaves behind a loving wife, 2 daughters, 2 sons and 6 loving grandchildren. Please donate in the name of Harvey Davis, 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 Hasmita Patel of Atlanta, GA who sadly passed away at the age of 61. Hasmita was born in Kampala, Uganda and raised in London, United Kingdom. She will be lovingly remembered by her husband, Mukesh (Mike); children: Ayesha and Rishi; as well as numerous relatives and friends in the United States, United Kingdom, Fiji, and Australia. While we will be laying Hasmita’s beautiful soul to rest soon, we encourage those that knew her to remember all the precious and good times she influenced. We have likewise been overwhelmed with all the beautiful messages of sympathies and fond memories from friends and family close and far, and it’s humbling to see how much love, selflessness, kindness, and generosity one person could have. Hasmita was full to the brim with all of these characteristics, and unfortunately, that was too much for this world. She will forever be remembered as our angel that left us too soon. In lieu of flowers, the family asks that you consider making a donation in her honor to the Pulmonary Fibrosis Foundation. All proceeds go towards: • Finding effective treatments and a cure for pulmonary fibrosis• Advocating for the pulmonary fibrosis community • Promoting disease awareness • Providing a compassionate environment for patients and their families Please donate and together we can help those living with pulmonary fibrosis and the families of those we have lost. All donations are tax-deductible and every dollar raised goes to help support the mission of the Pulmonary Fibrosis Foundation. 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

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

Heather Bartlett Please donate in the name of Heather Bartlett, 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

Helen Mae Bateman Please donate in the name of Helen Mae 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

Helen Maslankowski Please donate in the name of Helen Maslankowski, 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

Helen Sydney Klostermann Helen Sydney “Syd” Klostermann passed away on May 10, 2019. Sydney was born July 15, 1941 in St. Louis to Harry and Helen Gleditsch. She had one sibling, Harry Richard. She attended Bishop Du Bourg High School graduating in 1959. After graduation, Sydney worked in several positions, most notably The Knights of Columbus, Anheuser-Busch (crowned Miss Budweiser in 1966), and Famous-Barr for over nineteen years. In 1966, Sydney married Roy Klostermann of St. Louis and together raised three children - Kimberly Stewart of Town & Country; Kirk of Chesterfield; and Keith of O’Fallon. Sydney has eight wonderful grandchildren. Sydney will be best remembered for her generosity, thoughtful spirit, and unending desire to put the needs of others ahead of her own. Whether it be raising three beautiful children who follow her example of being warm-hearted, caring, and trustworthy; caring for her brother, father, and aunt for over twenty years; hosting and cooking many holiday dinners; and shuttling grandchildren to dance competitions, cheerleading, sports events, etc. Sydney gave her heart and soul to her family and friends. She will be sorely missed for her passion and dedication to her mother and grandmother roles; love of her children and grandchildren; sage advice; stamina and perseverance; kind and loving words and thoughts. We cherish the day when we will see her again in perfect health and happiness! Services: Visitation will be held this Thursday from 4-8 p.m. at Kutis Funeral Home in Affton located at 10151 Gravois Road, St. Louis 63123. Mass will be held at St. Gabriel the Archangel on Friday at 11 a.m. located at 6303 Nottingham, St. Louis 63109. In lieu of flowers, donations can be made to the Pulmonary Fibrosis Foundation at Pulmonaryfibrosis.org. 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