OUR WORK

Since the Cystic Dreams Fund started in 2011, we've been able to make over 160 grants throughout 39 states because of the generous donations from people like you! These grants have gone to adults and children with CF and their families to assist with costs associated with managing their disease.

We'd like to share with you some of the stories of those folks we've been able to help with the funds we've raised and the generous donations we've received.

• Megan D is a 27 year old living on her own who developed a bacteria infection. Despite being employed and having insurance she incurred over $3000 in hospital visits she was struggling to pay. The Cystic Dreams Fund was able to assist by granting her funds paid directly to her hospital to offset her debt.

• Caleb was diagnosed shortly after birth when he developed an intestinal blockage. He was hospitalized in the NICU 39 days. His mother was not able to return to work and this parents where struggling with mounting medical bills. We were happy to lend financial assistance.

• Tina has two children with cystic fibrosis. Her un-­insulated home required enormous amounts of electricity to heat last winter. When she could not pay the entire amount owed, her power was turned off. We were able to help her get power restored. There have been several cases of other families having difficulty paying for electricity which is essential for keeping medications cooled and doing inhalation treatments.

• Kristy needed help with post-‐transplant expenses. We know how costly those drugs can be, and were happy to help her.

• Jayla is the youngest of five children, and the only girl! Her parents  needed help with her medical expenses after she had several hospitalizations.

• Some parents have more than one child with cystic fibrosis. Even with good insurance, expenses mount. That’s why we helped Emily's and Joshua’s parents with a medical grant.

• Denise needed funds for her double lung transplant as she had to travel a great distance to get the surgery. We were happy to contribute to her transplant fund.

• Many requests have come from cf patients needing air purifiers. We are pleased to have been able to help Melissa, Mark and Shannon, among others.


2020 UPDATE

COVID-19 is devastating for the cf community. Job losses because of economic shrinkage coupled with the fear of bringing the virus home to a vulnerable family member creates economic distress for many families.

Thanks to our generous donors, we were able to assist 40 cystic fibrosis patients and their families in 2020. Please help us continue this important work by making a contribution. we need your help now more than ever!











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Here's how your support directly impacts lives.

"Your support allows me to financially afford treatments and medications while trying to pursue a career and enjoy life! I am so grateful - thank you for this blessing." 

"I appreciate what your foundation has done for me! Even with my insurance it's hard to pay medical expenses for my condition. Without
foundations like yours we would be drowning in bills. Thank You from the bottom of my heart!!"

"Hello CDF, I wanted to express (socially) my heartfelt thanks to you for the grant I received in today's mail. I read your letter and shouted Merry Christmas to me! Thank you for relieving some of my financial burden."

"My husband and I received the very generous check and CD today. I wanted to thank you from the bottom of my heart for the much needed help. That money will be put to good use in buying Madison's meds and paying for her doctors appts. Thank you does not even do justice for the gratitude I feel for your foundation! I am so sorry for the loss of your son Paul, what you are doing in his honor is beyond amazing! I am looking forward to listening to his CD later today."