My Great Strides Story
From MOM:
Leah is awesome! She is loving soccer and has scored a few goals for her team. She has
been in good health and has been starting to take charge. She still needs several reminders
but she’s making improvements in the right direction. She is down to doing 1 treatment a
day and is highly enjoying that. She is also participating in film club at school with Isaac and
is learning a lot. Leah has made her first quilt. With the help of my mom, her and my mom
made a beautiful quilt. Great job Leah. She is taking charge of her ADHD and speaks up for
herself and telling someone when she is struggling. She finished her clinical trial and was
such a rockstar. She is active in scouts and is working hard. She will be going to scout
camp at Bartle for the first time this summer with Rachel and Dad. Something Leah and the
rest of the family are excited about is that Leah got her Make a Wish trip approved. We are
headed to HAWAII!! We can’t wait. She’s excited to snorkel, swim with the dolphins, attend
a luau, etc.
The Cystic Fibrosis Foundation has made extraordinary progress — including fostering the development of more than a dozen CF treatments — but these treatments are not a cure and not everyone can benefit from them. We must keep going.
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By donating to my fundraising goal, you will help advance our mission for a cure for all. Please consider joining us and helping make CF stand for Cure Found.
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IMPORTANT NOTE ON ATTENDANCE AT FOUNDATION EVENTS:
Updated July 5th, 2023
The CF Foundation is committed to ensuring the health and wellbeing of individuals attending Foundation events. Individuals attending CF Foundation events must abide by the Foundation's Event Attendance Policy www.cff.org/attendancepolicy, which includes guidance for event attendees living with cystic fibrosis.