I couldn’t put it down. I found myself going though a kaleidescope of emotions as I read your journey of Angela’s life and death. It moved me to realize the challenges of those who quietly fight for life each day, while others take it for granted.” -Jennifer
“Your efforts to honor your beautiful daughter are touching many lives.” -Cynthia
“I read your book in three nights and cried every night I was reading. I too share in the loss of someone so dear to CF…my very best friend whom I had known since I was five. Charlie, died while awaiting a double lung transplant at the age of 38. Reading your story of the many long days and nights spent in the ICU “family room” brought back many memories…many days where family and friends would wait around the clock, sleeping on the floor and on chairs of the ICU waiting room which people had started to refer to as Camp Charlie…waiting with hope that lungs would arrive in time, waiting for our miracle. Thank you for sharing your story so that those of us who never got a chance to meet Angela to love her through your book and we can now hold her close in our hearts too.” -Kathryn
“Somehow it is a little easier to go through knowing someone else has gone through it too.” -Ruth
“Your love for Angie shines through on every page.” -LeeAnn
“Not just those afflicted with CF or [with CF] within their families, EVERYONE should read this book! The love of this family and the courage of one heck of a fighter to move beyond the limitations. I feel like I know Angie and I would have loved to be an older person with CF mentoring her through life. Now I have been mentored by her story of zest for life and love. Her story inspired me in a way, to keep shooting for the stars!
We bought many copies of the book as it is a great educational tool to help people understand that CF is an invisible illness. When you look at the average CF person, including myself, we do not look sick. However, the maintenance required to “look” and “feel” as good as we do is constant and energy draining, yet we do it because we want to live! I will continue fighting where Angie left off!
The love between [Angie and Don] reminds me of my relationship with my own father and how lucky I am and to never take time for granted. I read the book in two days, I could not put it down, and even read through a few meals. Angie and [my] stories are similar in many ways and it makes me sad to lose a sister to this illness, yet I know to keep preserving, have a good attitude and love others along the way. Thank you for sharing your heart, Don!” -Kelly, adult with cystic fibrosis
“The love and devotion of you and your wife for Angela was apparent. What a beautiful person–inside and out. It was enlightening to hear about the waiting room experience. [Nurses] get so busy on the unit that not enough thought is given to that “worry room,” as you so aptly coined it. There is forever the struggle to balance the emotional needs with the tasks that must be carried out. How could Angela not be pleased and honored with the projects you have initiated in her memory? You are an inspiration.” -Sue, RN
“Your book is amazing, and of course, heartbreaking. I want my family members and close friends to read it – so they can really know what we have gone through in the last 17 years, and what kind of special people CF parents are, and what extraordinary people CF patients are. There are many similarities in your book that are like my story (so far). Your book has renewed my life, and I am once again ready to fight this awful disease with [my children]. When things are going well, you don’t really dwell on CF, and you start getting kind of lazy and not doing that last Neb because it’s late. Well, no more of that! I have fought for 17 years and will continue until God says “that’s it!”" -Terri, mother of two children with CF




