From Cystic Fibrosis Foundation <[email protected]>
Subject Together: a Community Update
Date December 18, 2025 9:12 PM
  Links have been removed from this email. Learn more in the FAQ.
  Links have been removed from this email. Learn more in the FAQ.
Time is running out to make a difference


([link removed])


# December 18, 2025



Time is Running Out to Make a Difference

The clock is ticking to make a gift in 2025. While significant progress has been made in cystic fibrosis research and care, people still struggle with this disease. Families still face the heartbreak of watching loved ones get infections and fight complications, and lives are still being lost. Your support today can help change that.
Make your year-end gift now ([link removed])
and help fuel our mission, generating scientific breakthroughs that make a big difference for people with CF.


Give now » ([link removed])


([link removed])




Now on YouTube: North American Cystic Fibrosis Conference (NACFC) Highlights Webinar and Q+A

In case you missed it, the recording from our NACFC Highlights Webinar with CF research experts is now
available on YouTube ([link removed]). Among other research and care news, you can hear about how CFTR modulators affect the body, aging issues with CF, and the outlook on treatments for CF. A Spanish version of this recording will be available soon.

Watch the recording » ([link removed])


([link removed])




Protect Yourself Against Germs

It can be difficult to stay healthy during the winter months, especially for people with cystic fibrosis. There are
steps you can take to reduce your risk of illness ([link removed]), including thorough hand washing and ensuring that you always clean and disinfect your nebulizer. Explore eight ways to protect yourself from germs in your everyday life.



Reduce your risk of getting sick » ([link removed])


([link removed])






From the CF Community Blog: What I Wish I Knew Before Moving With Cystic Fibrosis

Michelle Bowers and her family thought they were prepared for their move from Oklahoma to Oregon, but they didn't expect a lapse in insurance coverage when her husband started his new job. This put her son's cystic fibrosis treatments in jeopardy. Luckily, they were able to lean on their support system to find help during this time. On the CF Community Blog, Michelle shares
tips for anyone moving with cystic fibrosis ([link removed]).


Read the full blog » ([link removed])


([link removed])






Support ([link removed])

Get Involved ([link removed])

CF Community Blog ([link removed])



([link removed])


www.cff.org ([link removed])

www.cff.org en español ([link removed])


4550 Montgomery Avenue, Suite 1100N | Bethesda, MD 20814 US


[if mso]> <![endif] ([link removed])


([link removed])
([link removed])
% link:[link removed] name="[link removed]" content="" %]
% link:[link removed] name="[link removed]" content="" %]


This email was sent to [email protected]

Got this as a forward? [Sign up]([link removed]) to receive our future emails.

[]([link removed] "Manage your subscription")[Manage your subscription]([link removed] "Manage your subscription")

[Opt out]([link removed]) of this mailing list |
Opt out of ALL ([link removed])
CF Foundation emails


cff.org ([link removed])
Screenshot of the email generated on import

Message Analysis