Lyla's Laps for Life

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Lyla's Laps for Life We aim to raise funds for Cystic Fibrosis. We hope that CF will soon stand for Cure Found.

The donations continue to pour in!  We'd like to thank Executive Swim Club, Kathy Holton, Angela Poppalardo, Louisa Maho...
07/08/2025

The donations continue to pour in!

We'd like to thank Executive Swim Club, Kathy Holton, Angela Poppalardo, Louisa Mahoney, Tara Jewett, Stacey Miller and Niamh Doherty for your support. 💜💜💜💜💜💜💜

💜July 28, 2025💜
31/07/2025

💜July 28, 2025💜

The numbers are in for 2025:🏊🏼‍♀️ 40+ swimmers🏊🏼‍♀️ 2,604 laps🏊🏼‍♀️39.4 miles💜 $12,000+ raised to find a cure for Cystic...
30/07/2025

The numbers are in for 2025:
🏊🏼‍♀️ 40+ swimmers
🏊🏼‍♀️ 2,604 laps
🏊🏼‍♀️39.4 miles
💜 $12,000+ raised to find a cure for Cystic Fibrosis

These swimmers have grown over the years!
30/07/2025

These swimmers have grown over the years!

2025 Swimmimg Crew
30/07/2025

2025 Swimmimg Crew

29/07/2025

Tonight was amazing! Thank you to all the swimmers and all the donors. We’re exhausted from our laps but will share more later. Going to bed with a grateful heart. 💜

What’s life like for individuals with Cystic Fibrosis?💜The number one priority is to keep them healthy and away from ger...
25/07/2025

What’s life like for individuals with Cystic Fibrosis?

💜The number one priority is to keep them healthy and away from germs! From a young age Lyla has been willing to wear a mask and stay away from others when they’re sick.

💜Regular doctor’s appointments: Lyla goes to her CF clinic every 3 months; that’s 4 times a year when she’s healthy! These appointments can last hours as she visits with multiple members of her medical team. She often has blood drawn, completes breathing tests and has X-rays taken frequently.

💜Daily airway clearance therapy and nebulizer treatments: she spends at least 20 minutes 2-3 times a day with her nebulizer and vest, when she’s not trying to pawn it off on her brothers to do for her! The vest vibrates her chest so the thick mucus in her lungs doesn’t settle.

We are thankful to research and medicine for all that Lyla and others with CF have access to.

We’re also thankful for all of you who have supported our fundraiser: https://passion.cff.org/lylas-laps-for-life?fbclid=IwQ0xDSwLtFLNleHRuA2FlbQIxMQABHsPdUZuIGvbo2UOBrZRp-xni2tceI1BAfvtiAT3nDZyhsMq4b-7VDEk1Cu2i_aem_INaRs3VequpuXrcVAuMmvA

Here are the pictures from 2019 and 2024. Can’t wait to snap this year’s picture on Monday night!
25/07/2025

Here are the pictures from 2019 and 2024. Can’t wait to snap this year’s picture on Monday night!

💜Thank you so much for your donations. 💜We greatly appreciate your support: Meri Buono, Carol Costello, Lisa Drobinski, ...
16/07/2025

💜Thank you so much for your donations. 💜

We greatly appreciate your support: Meri Buono, Carol Costello, Lisa Drobinski, Chris Nolli, Heather Jackson and the Camell Family!

Are you planning to attend the event?  Please help us prepare by RSVPing here:
15/07/2025

Are you planning to attend the event? Please help us prepare by RSVPing here:

Please help us plan for this year's event by completing this form if you or your family plans to attend the swim-a-thon on Monday, July 28th, 6-8 pm.

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