Morgan, Logan, Heidi, Inga, Gary's Page

Dana Point 2018

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Raised: $4,900.00

Goal: $300.00

My Great Strides Story

Dear Family & Friends Near and Far,

It is that time again for our Cystic Fibrosis fundraiser for our son Morgan (aka MoJo) and children everywhere with Cystic Fibrosis. For those that don't know, our family has been very active in supporting the Cystic Fibrosis Foundation ever since our son was diagnosed at age 4. CF is a genetic disorder that affects the lungs and pancreas with potentially life threatening consequences. But that is where the Foundation comes in. The donations we have collected over the years really are making a difference. We can personally see how the new therapies have indeed improved the health and life of our own active fun loving son. For example, the New Tobi Podhaler (1 of several inhaled meds) has gone from 50 mins per day to less than 5 mins per day. That is huge in an active 17 year old's life. That is almost an hour taken off of his 2-3 hrs of treatments per day. Yeehaw, Thanks everyone!!

We know we are all bombarded with requests of our time and resources and forgive us for putting this out there once again. But our family won't stop supporting the Cystic Fibrosis Foundation until there is a cure for our MoJo's life and all of the CF kids everywhere. 

If you'd like to walk with us, the Great Strides event for our Team MoJo will be at a NEW LOCATION at the Marine Ocean Institute in Dana Point Harbor, CA on Sat. May 19, 9:00AM and we'd be honored to have you. If you'd like to donate, ANY (and we mean ANY!) amount is welcome and VERY appreciated! Click on the link below and your donation will go directly to the Cystic Fibrosis Foundation in support of our Team MoJo. And finally, if you'd just like to pray for MoJo and all of the kids afflicted with CF, that might just be the best gift of all.

If you do wish to help us in our quest to finally find a cure for CF, remember your gift is 100% tax deductible. We send our sincerest gratitude for reading this and lending your support. As the CF Foundation often reminds us, they/we won't stop until CF stands for...Cure Found!

Thank You from the bottom of our hearts,

The Johnson Family (Gary, Inga, Heidi, Logan & MoJo)


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