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• 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. Compression vests are essential for treating cystic fibrosis. They are extremely expensive even with insurance help. We have helped countless families with vest payments.
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.
2021 UPDATE
Although we were unable to host any fundraising events in 2021, the requests kept rolling in. Thanks to our very generous donors, we offered grants to 35 individuals and families impacted by cystic fibrosis. Many thanks to those who support The Cystic Dreams Fund which qualified this year for the GuideStar Silver Transparency Shield.
2022 UPDATE
The threat of COVID still loomed over us, preventing us from planning and executing a major fundraising event. We did appear at a Northeast Comic-Con event in March to raise funds and spread awareness of cystic fibrosis. This, plus the kindness of our donors allowed us to make 31 grants this year. Thank you for supporting our important work.
2023 UPDATE
The Cystic Dreams Fund made an appearance at the North East Comic-Con focusing on awareness. We also secured many donations. An online auction was generated on Bidding Owl featuring gift certificates, theater tickets and even a timeshare week at Cape Cod!
2024 UPDATE
No events this year, but plans are underway for “Mahjong Madness” in 2025 combined with another Bidding Owl auction! Stay tuned!!!
• 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. Compression vests are essential for treating cystic fibrosis. They are extremely expensive even with insurance help. We have helped countless families with vest payments.
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.
2021 UPDATE
Although we were unable to host any fundraising events in 2021, the requests kept rolling in. Thanks to our very generous donors, we offered grants to 35 individuals and families impacted by cystic fibrosis. Many thanks to those who support The Cystic Dreams Fund which qualified this year for the GuideStar Silver Transparency Shield.
2022 UPDATE
The threat of COVID still loomed over us, preventing us from planning and executing a major fundraising event. We did appear at a Northeast Comic-Con event in March to raise funds and spread awareness of cystic fibrosis. This, plus the kindness of our donors allowed us to make 31 grants this year. Thank you for supporting our important work.
2023 UPDATE
The Cystic Dreams Fund made an appearance at the North East Comic-Con focusing on awareness. We also secured many donations. An online auction was generated on Bidding Owl featuring gift certificates, theater tickets and even a timeshare week at Cape Cod!
2024 UPDATE
No events this year, but plans are underway for “Mahjong Madness” in 2025 combined with another Bidding Owl auction! Stay tuned!!!
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."