lorwalleye2024

Available for Purchase

COMING SOON

Browse, Bid & Buy

VIEW ITEMS

Sign Up to Participate

Frequently Asked Questions

Donate Now

Help our cause by contributing to our fundraising efforts.

No act of generosity is too small to make a difference.

$50

$100

$250

$500

$1,000

$2,500

Donor & Payment Information

Already have an account? Sign in

Email required

Select from the payment options below:

Terms and Conditions required

I have read and agree to the Terms and Conditions and Privacy Policy and give my consent to Milestone Radio, LLC to process my personal data. I understand I can revoke this consent at any time.

Donor approves the payments of any charitable donations and/or purchases to Milestone Radio, LLC in the amount set forth therein.

Subtotal:

Transaction Fees:

0.0

Total:

I will pay the fees

By paying the transaction fee, you ensure more money goes to your organization’s mission.

Your credit card statement will reflect charges from ‘BOB-FM’

Cancel

A 4 nights lodging, 3 day guided fishing trip that includes your meals for just $600 per person. You'll arrive Thursday, August 8th and depart on Monday, August 12th.

BOB FM has teamed up the owners of Life of Riley Resort, Josh and Jessica Gillson, to offer this exclusive vacation as a way to raise funds for the newly founded nonprofit, George's Pompe Pals.

Josh and Jessica's son George was born with a form of Muscular Dystrophy (MD) called Pompe Disease. Pompe disease is a rare genetic condition that causes muscle weakness that gets worse over time. It can have a serious effect on many of the body's systems. Pompe disease happens because of a mutation in a gene that helps make an enzyme called acid alpha-glucosidase. This enzyme breaks down a type of glucose called glycogen . When the enzyme is not made properly, glycogen builds up in the body's cells. This stops the cells - especially those in the body's muscles, including the heart - from working as they should.

undefined

In the past, many infants with Pompe disease lived only into early childhood. But today those odds are improving. Enzyme replacement therapy can extend the lives of babies with infantile-onset Pompe disease. It also helps people with late-onset disease. Getting care from a team of medical specialists helps many children with Pompe disease live well into adulthood.

The Gillson family is currently setting up a nonprofit called George's Pompe Pals to assist other families with children similar to George that are struggling getting their child to life saving treatments.