Second Wind: Other first-person accounts

  • Armalius, Tabetha-Lyn. Letter to the editor. CF Roundtable, Autumn 1995, 10.
  • “Amy’s Story.” Second Wind website, arthouse.com/secondwind/amysstory.htm, accessed 8/26/97.
  • Ballard, Katey. “My Transplant Journey and My Walk With God.” AirWays 13, no. 4 (July 2006): 10-12.
  • Balsam, David C. “Two years later, his pre-transplant memories of CF are fading away.” CF Roundtable, Spring 1992, 9.
  • Borowski, Barbara. “My Three Caregivers.” AirWays 10, no. 3 (May 2002): 7-10.
  • Broom, Jan. “Thank You For Our Miracles.” LifeNet Donor Family Tributes, lifenet.org/donor/donor_donorfam_t4.html, accessed July 11, 2003.
  • Cathy [no last name given]. “Net Notes.” AirWays 17, no. 1 (March 2009): 12.
  • Carlsen, Mary E. “A Mother’s Perspective.” CF Roundtable, Fall 1993, 5.
  • Chattin, Jonathan M. “My Son, The Best Boy.” Aneurysm and AVM Support, Brain Aneurysm Narratives, westga.edu/~wmaples/chattin.html, accessed July 11, 2003.
  • Couture, Karen. “Listed for Life,” Second Wind Lung Transplant Association website, 2ndwind.org/members/karen_couture.html, accessed July 27, 2002.
  • Cuenin, Cathy. “Moment to Moment.” AirWays 13, no. 3 (May 2006): 7, 12.
  • DelCimmuto, Bob. “Jessica’s Story.” Second Wind website, arthouse.com/secondwind/jessicas.htm, accessed August 26, 1997.
  • Donahue, Ruth. “What a Roller Coaster Ride Life Can Deal You!” AirWays 10, number 5 (September 2002): 1-5.
  • “Dreams are like clouds…floating through a sky blue mind.” AirWays 7, no. 4 (July 1999): 5-7.
  • Edwards, Sylvia. “Up Up and Away…Shooing COPD Blues Away.” Living with COPD website. http://www.papapoo.com/copd-sylvia.htm, accessed 2/1/00.
  • Ferranti-Mehal, Rosina. “She exits CF valley for a new peak in life.” CF Roundtable, Summer 1992, 4.
  • Flipse, Alex. Patient Diary. PH Central website, pulmonary-hypertension-diaries.phcentral.org/coping/diaries/Alex/asc/1, accessed July 23, 2002.
  • Flynn, Kathryn. “My Transplant Story.” AirWays 10, number 2 (March 2002): 14.
  • Gibson, Beatrice. “I Held My Son’s Hand.” Airways, 7, number 4 (July 1999): 15.
  • Graham, Walter. “The ‘Yin and Yang’ of UNOS; A personal retrospective on UNOS’ first two decades.” UNOS Update, May-June 2008, 4-5. UNOS website, unos.org/docs/Update_MayJune08_YinYang.pdf, accessed October 29, 2008.
  • Hardy, James D. Interview conducted by William S. Stoney, Jackson, Mississippi, August 10, 1999. In Pioneers of Cardiac Surgery, edited by William S. Stoney, 446-459. Nashville: Vanderbilt University Press, 2008.
  • Hardy, Mary. “Meeting My Amish Donor Family.” AirWays 14, no. 3 (July 2007): 10-11.
  • Hawkins, Don. “Experiencing the Decision.” AirWays 7, number 6 (November 1999): 1-3.
  • Hoilman, B. J. “COPD Like a Fish Out of Water.” Living with COPD website, http://papapoo.com/copd-fish.htm, accessed 2/1/00.
  • Holbert, Lori. “Perfect Lungs at the Perfect Time.” CF Roundtable, Spring 2002, 1, 20-1.
  • Jarrett, Dana. ”No Age is a Good Age to be Diagnosed with CF.” CF Roundtable, Autumn 1995, 1, 16.
  • Jennings, Max. “I Had a Heart and Lung Transplant.” The Ladies’ Home Journal 98 (October 1981), 39-47.
  • Jones, Glenda. “Waiting and Writing.” Living with COPD website, http://www.papapoo.com/copd-glenda.html, accessed 2/1/00.
  • Keeler, Cheryl. “Peer Support Program.” AirWays 15, no. 1 (March 2008): 2-3.
  • Kessinger,Janice. “A Sister’s Perspective.” CF Roundtable, Fall 1993, 6.
  • Ledbetter, Pat. “My Daughter’s Heart.” LifeGift Organ Donor Center Donor Stories, lifegift.org/do_sto.htm, accessed July 11, 2003.
  • Lon [no last name provided], “Waiting.” AirWays 6, no. 6 (November 1998): 12-13.
  • McDonough, Lisa Malia. “Tune-ups, with some creativity, can be handled.” CF Roundtable, Summer 1992, 6-7.
  • McNeill, Charles. “Waiting Was Hard But Worth It.” CF Roundtable, Winter 1996, 8.
  • Memorial to Jay Bullock. University of Michigan Transplant Center Transweb. http://www.transweb.org/stories/memorials/jbullock.shtml, accessed July 29, 2009.
  • Memorial to Lisa Cortese Davis, Transweb Memorials to Organ and Tissue Donors, http://www.transweb.org/stories/memorials/ldavis.shtm, accessed July 11, 2003.
  • Memorial to Lisa Smith, Transweb Memorials to Organ and Tissue Donors, http://www.transweb.org/stories/memorials/lsmith.shtml, accessed July 11, 2003.
  • Memory Quilt Story for Kayla Rack. New York Organ Donor Network, Donors and Their Families. nyodn.org/gift/memory_details2_14.html, accessed July 11, 2003.
  • Moran, Mickey. Patient Diary. PH Central website, pulmonary-hypertension-diaries.phcentral.org/coping/diaries/mmoran-inactive/asc/1, accessed July 9, 2002.
  • Murphy, Joni. “My life – the way I live it!” CF Roundtable, Fall 93, 14.
  • Neuberger, Damian. “A Rose for Chad.” AirWays 13, no. 6 (January 2007): 10-11.
  • O’Brien, Ken. “Conception rules begin to change.” CF Roundtable, Fall 1992, 7.
  • Penick, Heather. “Living Donor Double-Lung Transplant – A Gift of Life,” Patient Perspective.” , The Transplant Center at Fairview-University Medical Center, March 2001, fairviewtransplant.org/giftoflife.asp, accessed July 9, 2003.
  • Pennewell, Louise. Patient Diary. PH Central website, pulmonary-hypertension-diaries.phcentral.org/coping/diaries/Louise/asc/1, accessed July 23, 2002.
  • Pierson, Melody Masha. “Matchmaker, Matchmaker, Make Me a Match.” AirWays 16, no. 4 (September 2008): 4.
  • Pollack, Lynn. Letter to the editor. AirWays 9, number 4 (July 2001): 4-6.
  • Post, Pammie. “Vestibular Dysfunction.” CF Roundtable, Summer 1993, 11.
  • “The Right Thing to Do,” LifeNet Donor Family Tributes, lifenet.org/donor/donor_donorfam_t7.html accessed July 11, 2003.
  • Rothenberg, Laura. “My So-Called Lungs.” In Stories of Illness and Healing; Women Write Their Bodies, edited by Sayantani DasGupta and Marsha Hurst, 39-44. Kent, OH: Kent State University Press, 2007.
  • Schum, Joanne. “To My Surprise – I Have Been Part of Transplantation Numerous Times!!” Airways 10, no. 1 (January 2002), 5-11.
  • Shepherd, Brenda L. P. “Living with CF – A Wife’s Perspective.” CF Roundtable, Fall 1993, 1.
  • Shepard, Carol L. “Twin boys a gift for this CF mom.” CF Roundtable, Fall 1992, 11.
  • Steenland, Mary. “A Donor Mother’s Story.” Multiple Organ Retrieval and Exchange Program of Ontario website, Donor Stories, web.idirect.com/~more/donors_stories_1f.html, accessed July 10, 2003.
  • Stevens, Roger. “My IPF Story.” Roger Stevens’ Idiopathic Pulmonary Fibrosis homepage. http://www.ipfinfo.com, accessed July 27, 2002.
  • Tate, Janie. “CF often influenced her in college.” CF Roundtable, Winter 1991, 9-10.
  • “Turning Tragedy into Triumph.” Multiple Organ Retrieval and Exchange Program of Ontario website, Donor Stories, web.idirect.com/~more/donors_stories_2f.html, accessed July 10, 2003.
  • Vanderford, Kathy., “Miracles Still Happen.” AirWays 9, number 4 (July 2001): 8, 13-18.
  • Vernon, John. “Two Days in My Life I’ll Never Forget.” AirWays 10, no. 3 (May 2002): 1-4.
  • Wall, Donna. “That ‘Other Lady’ Is Gone Forever.” Living with COPD website. http://papapoo.com/copd-donna.html, accessed 2/1/00.
  • Weber, Carlene E. “College education prepares her for the long run.” CF Roundtable, Winter 1991, 7.
  • Wenrich, Philip. “Attitude about CF influences his life.” CF Roundtable, Fall 1992, 7.
  • Williams, Mike. “Keep death in perspective when dealing with it.” CF Roundtable, Fall 1992, 3.
  • Willis, Kristie. “Hometown college is stepping stone to university.” CF Roundtable, Winter 1991, 11.