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Support Molly's LOL4CFF Campaign
Molly Barker
Molly Barker
Hello Beautiful Friends!
I can't believe I'm doing this, but here we are! I am stepping WAY OUTSIDE MY COMFORT ZONE (yes I wrote that in all caps) and am trying stand‑up comedy for the first time (!!) and I need your support.
I’m participating in LOL4CFF, a comedy competition featuring first‑time stand‑up comedians, where I’ll perform a five‑minute set to raise funds for the Cystic Fibrosis Foundation.
Nine other brave souls are on this journey with me. Over the summer and into the fall, we are meeting with comedy coaches, crafting our routines, and practicing them with each other.
Look for me to regularly post on my progress. I might even see if a few of you would be game for meeting up with me. While the thought of this is terrifying, I will definitely need to practice before I get on stage in front of 500 people!
I'll also be introducing you to some folks directly impacted by Cystic Fibrosis and others involved on the research side of things.
I'm really proud to raise funds for this noble organization and keeping my fingers crossed that you will feel proud too.
There are several easy ways you can help:
Attend the show – Join me at LOL4CFF on Friday, October 2, 2026, at The Casey in Charlotte. Tickets include a seated dinner, beer & wine—and you can vote for me to win!
Buy a table for the show - Your company can buy a table! If you'd like to learn more about how this will bring visibility to you and your company email me at molly@mollybarkerspeaks.com.
Donate – Any amount makes an impact and is greatly appreciated. Your gift will be credited directly to my fundraising goal.
Contribute to the event’s silent or live auction – Learn more and donate here: Auction - LOL4CFF 2026
Let's creatively partner - I don't know what that looks like, but I have lots of creative friends, so let's brainstorm!
Spread the word – PLEASE share my link with friends, family, or colleagues and invite them to support this cause.
Why It Matters
Cystic fibrosis is a genetic disease that causes thick mucus to build up in the lungs, pancreas, and other organs, leading to chronic infections and life‑threatening complications.
Thanks to the Cystic Fibrosis Foundation, life expectancy for people with CF has doubled over the past 30 years. Still, many individuals do not benefit from existing therapies. Our goal is a cure for every person with CF—and a life free from this disease.
You are a vital part of that progress. Together, let’s make CF stand for Cure Found.
Learn more at www.cff.org.
I can't believe I'm doing this, but here we are! I am stepping WAY OUTSIDE MY COMFORT ZONE (yes I wrote that in all caps) and am trying stand‑up comedy for the first time (!!) and I need your support.
I’m participating in LOL4CFF, a comedy competition featuring first‑time stand‑up comedians, where I’ll perform a five‑minute set to raise funds for the Cystic Fibrosis Foundation.
Nine other brave souls are on this journey with me. Over the summer and into the fall, we are meeting with comedy coaches, crafting our routines, and practicing them with each other.
Look for me to regularly post on my progress. I might even see if a few of you would be game for meeting up with me. While the thought of this is terrifying, I will definitely need to practice before I get on stage in front of 500 people!
I'll also be introducing you to some folks directly impacted by Cystic Fibrosis and others involved on the research side of things.
I'm really proud to raise funds for this noble organization and keeping my fingers crossed that you will feel proud too.
There are several easy ways you can help:
Attend the show – Join me at LOL4CFF on Friday, October 2, 2026, at The Casey in Charlotte. Tickets include a seated dinner, beer & wine—and you can vote for me to win!
Buy a table for the show - Your company can buy a table! If you'd like to learn more about how this will bring visibility to you and your company email me at molly@mollybarkerspeaks.com.
Donate – Any amount makes an impact and is greatly appreciated. Your gift will be credited directly to my fundraising goal.
Contribute to the event’s silent or live auction – Learn more and donate here: Auction - LOL4CFF 2026
Let's creatively partner - I don't know what that looks like, but I have lots of creative friends, so let's brainstorm!
Spread the word – PLEASE share my link with friends, family, or colleagues and invite them to support this cause.
Why It Matters
Cystic fibrosis is a genetic disease that causes thick mucus to build up in the lungs, pancreas, and other organs, leading to chronic infections and life‑threatening complications.
Thanks to the Cystic Fibrosis Foundation, life expectancy for people with CF has doubled over the past 30 years. Still, many individuals do not benefit from existing therapies. Our goal is a cure for every person with CF—and a life free from this disease.
You are a vital part of that progress. Together, let’s make CF stand for Cure Found.
Learn more at www.cff.org.
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