Join team Not So Plain Jane to Cure Cystic Fibrosis
Not So Plain Jane
Fundraising for Huntsville Great Strides 2026
Not So Plain Jane
2026 is our 5th year at Great Strides!
Wow! It is hard for us to believe that this year will be our 5th year attending Great Strides. We feel so honored to have our friends and family walking with us through this journey for the last (almost) 5 years!
On May 16th, we will be gathering at the Campus 805 Green Space (Butler Green) for Huntsville’s Great Strides.
If you have been to Great Strides with us in years past, then you know that it is mostly a tailgate with a side of breakfast, lawn games, and lots of love for Jane sprinkled on top. We’d love for you to be there to show Jane how much we love her and how we will always support her on her Cystic Fibrosis journey!
Jane lives every day with CF- a life shortening genetic disease that primarily affects lungs and digestive system.
*We continue to teach Jane more and more about cystic fibrosis as she grows older and gains independence, but we have chosen not to talk with her about the life expectancy aspect. As you can imagine, that is a heavy mental load for a child to carry. Please do not mention this part to your child when you are educating them on cystic fibrosis.
There is no cure. However, thanks to generous donations and research funding, major progress is happening! Jane now takes a CF “miracle medicine” that was developed around the time she as born and is potentially adding years onto her life!
The money we raise is making a difference in the lives of those affected by Cystic Fibrosis, and we are eternally grateful for your contributions to improve their lives.
On May 16th, we will be gathering at the Campus 805 Green Space (Butler Green) for Huntsville’s Great Strides.
If you have been to Great Strides with us in years past, then you know that it is mostly a tailgate with a side of breakfast, lawn games, and lots of love for Jane sprinkled on top. We’d love for you to be there to show Jane how much we love her and how we will always support her on her Cystic Fibrosis journey!
Jane lives every day with CF- a life shortening genetic disease that primarily affects lungs and digestive system.
*We continue to teach Jane more and more about cystic fibrosis as she grows older and gains independence, but we have chosen not to talk with her about the life expectancy aspect. As you can imagine, that is a heavy mental load for a child to carry. Please do not mention this part to your child when you are educating them on cystic fibrosis.
There is no cure. However, thanks to generous donations and research funding, major progress is happening! Jane now takes a CF “miracle medicine” that was developed around the time she as born and is potentially adding years onto her life!
The money we raise is making a difference in the lives of those affected by Cystic Fibrosis, and we are eternally grateful for your contributions to improve their lives.
So here’s your official invite:
Where: Campus 805 Butler Green
When: Saturday, May 16th 9:00-11:00(ish) am
You are welcome to come and go if you have other things scheduled that day. Group photo will be around 9:30.
What to Expect: Tailgating, yard games, breakfast, coffee, a short walk, music, and fellowship!
Please sign up to join us. Think of it as your RSVP (and please include family members’ names at the end when prompted). It is better to RSVP and not attend than not RSVP at all.
This day if very near and dear to our family every year. It is a physical example of the love and support we feel for Jane. Thank you thank you thank you for your continued support!
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