Egg My Yard for a Cure 2026

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Egg my Yard for a Cure 2026
Fight Cystic Fibrosis

Event Info

Date: April 4, 2026

Location: Richland Twp., Geistown Boro, Westmont Boro, Southmont Boro & Conemaugh Valley School District (CVSD)

Contact: Nancie Seifert


You're invited to our Egg My Yard for a Cure for Cystic Fibrosis fundraising event to help make CF stand for 'Cure Found'.

Beginning at 7pm on the evening of Saturday, April 4, 2026, volunteer Bunnies will silently hide surprise filled eggs in your front yard so your children will wake to our Easter egg hunt!

Please read ALL "RULES" below and then click on the BUY TICKETS button above to reserve your spot. If you would like to donate in addition to your order, please click on the “+Add Donation” button at the bottom of the order form.

If you would like to make a donation without having eggs delivered, please click on the DONATE button above.

RULES:

** All deliveries MUST be to homes within Richland Twp, Geistown Boro, Westmont Boro, Southmont Boro or CVSD, as we have volunteers located in these areas. Pick-ups are available for all other locations. Donations CANNOT be refunded to any orders outside of the delivery areas.

** For any areas outside of the Richland Twp, Geistown Boro, Westmont Boro, Southmont Boro or CVSD areas, pick-ups are available. After purchasing your eggs through the BUY TICKETS button, email TeamLuciaPalmer@gmail.com to discuss pick-up.

** A minimum of 25 eggs must be ordered. We will deliver 25 eggs for $25.00, 50 eggs for $45.00 and 75 eggs for $70.00. For 100 eggs, order two $45.00 tickets.


** A special egg with a simple note from the Easter Bunny can also be delivered for $5.00 (only one per home). 

** Eggs will be filled with candy and stickers. Children should only open eggs under the supervision of an adult.

** Please ensure your children are not in view of the front yard and all pets are secured beginning at 6:45pm.

** If the weather is inclement, eggs will be left in a bag on the front porch.


** If the yard being egged is different from the billing address, please email  TeamLuciaPalmer@gmail.com to provide appropriate delivery address.

** Spots are limited and reservations end on 3/30/2026, at midnight.

Make sure the Easter Bunny doesn't miss your yard with this EGG-cellent event!


The 3 little cuties in the picture above are Lucia & Palmer Santichen and Ehva Arendas.

My husband, Karl and I, are lucky enough to be the proud grandparents of Lucia & Palmer! They are rambunctious little 5 year old identical twins with one of the rarest forms of CF. Upon birth, they were life-flighted to Children's Hospital of Pittsburgh (CHP), a two hour drive from home, where they spent their first 104 days in the NICU. They endured several surgeries and had a few close calls. The girls are underweight but currently doing well. They each take 7 pills before every meal and 4 before a snack. This medication isn’t a cure or even therapeutic. It simply allows them to absorb nutrients needed to survive. They also spend 30 minutes 3 times a day completing rigorous airway clearance via a vest and compressor in addition to 2 medications in a nebulizer. Every two months, Mom, Dad and the girls travel to CHP where Palmer and Lucia meet their CF team of doctors to maintain their health.  In 2025, Palmer was lucky enough to escape the typically annual 14-day "tune-up" hospital visit! Lucia was not so lucky. On January 1, 2025, Lucia was taken by ambulance to CHP where a portion of her right lung was removed due to bronchiectasis damage. She ran into complications and ended up spending 9 days in the PICU and 7 days in a regular room. It was a month long recovery and she is thriving now.

Ehva Arendas 

In America, approximately 40,000 children and adults have CF. Three thousand of them have rare variants that do not respond to the therapeutic medications that are currently available. Of this 3,000, only 10 others have the same variant as Lucia and Palmer. Money for research, medication, clinical trials and a cure is needed for the 3,000 individuals with rare variants, as well as for all people with cystic fibrosis.

Our fundraising efforts have amounted to over $11,000 in 2023, over $21,000 in 2024 and over $45,000 in 2025, all with the help of two matching partners and other various corporate donations. This year, we hope to raise a total of $50,000 with the help of our matching partners and other various corporate donations.

Your participation in this fun and "EGG-citing" event is most appreciated. Please share our site with your neighbors and local businesses!!

We won’t stop until CF stands for "Cure Found”!