Abby's Army marches again! It is that time of year again when we ask you to dig into your pockets and help support our fundraising efforts to raise money to help us find a cure for cystic fibrosis. Abby's Army is marching for the thirteenth (!!) time, and every year we are absolutely blown away by the support you show. While we feel your love and support all year long, it is this time every year when we ask that you support us through fundraising and through dollars donated. We are truly humbled by your support, and how you give year after year to help us make a better life for our little girl.
Abby continues to fight CF like the champion she is. She does breathing treatments for at least an hour and a half every day, takes 13 enzyme pills to help her digest her food, and takes various other medications to deal with all of the other havoc that CF wreaks on her body, including her sinuses, stomach, and liver. Before anyone else sees her in the morning, she's already spent at least an hour taking care of her medical needs. This is every single day. She had sinus surgergy earlier this year, the third in her life. And, this cold and flu season has been a tough one, taking her to the doctor every couple of weeks and skirting a few hospital admissions by the skin of her teeth.
We long for the day when a medication will be available to treat the underlying cause of the disease and not just the symptoms. We need a real game changer here and we are so happy to say that there may be one on the market to help Abby as early as next year. But, it will not be a cure and there is no guarantee that it will help her to a great degree. We need a cure and we need it fast. We say it every year, but it bears repeating: Abby is in a race against time.
When the CF Foundation was founded, life expectancy for children with CF was only five years old. Many didn't make it to kindergarten. In large part, due to donors like yourself, the median life expectancy is now 41 and rising. But CF is mean and heartless, and often doesn't play fair. There are still children and young adults that are taken from us well before that age. Many of those fighting CF into adulthood waste far too much of their valuable time and energy in simply staying alive. We long for the day when these amazing adults can just live without fighting for every breath. That is why we continue, day after day, to fight CF. That is why we continue, year after year, to ask you to donate to our cause.
Abby's Army means so much to Abby. If you are able to walk with us, Abby is walking in Huntington Beach on May 18. Kids and adults are all welcome, and there is no minimum amount required to raise. Your support in both time and/or money would mean the world to us.
Foundation-Sponsored Indoor and Outdoor Events and Gatherings
The Foundation is closely following the evolving coronavirus outbreak. We will continue to monitor coronavirus guidance from the Centers for Disease Control and Prevention and assess whether we need to change any scheduled events.
To reduce the risk of getting and spreading germs at CF Foundation-sponsored events, we ask that everyone follow basic best practices by regularly cleaning your hands with soap and water or with an alcohol-based hand gel, covering your cough or sneeze with a tissue or your inner elbow, and maintaining a safe 6-foot distance from anyone with a cold or infection. Medical evidence shows that germs may spread among people with CF through direct and indirect contact, as well as through droplets that travel short distances when a person coughs or sneezes. These germs can lead to worsening symptoms and speed decline in lung function.
To further help reduce the risk of cross-infection, the Foundation's attendance policy recommends inviting only one person with CF to attend the indoor portion of a Foundation-sponsored event at a specific time. For the outdoor portion, the Foundation recommends that all people with CF maintain a safe 6-foot distance from each other at all times.