In Support of Lincoln's Journey
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Hello family and friends!
We want to share Lincoln's journey with you. At just 8 months old, Lincoln was diagnosed with a rare gene mutation called GRIN1, which leads to various neurodevelopmental disorders. It has been a tough road, but Lincoln's resilience has shone through, and he has made significant strides. Unfortunately, after experiencing an episode of epilepsy and spending a month in the hospital to manage his seizures, some of his progress was set back. Lincoln is incredibly strong and has the potential to make progress once more, but he needs the right therapies and equipment to do so. These essential resources are expensive and not covered by insurance. Our family is committed to doing everything we can for Lincoln, but we need the support of our community to help him with specialized equipment like a suitable wheelchair, braces, and intensive therapies.
We invite you to support Lincoln's Journey. Together, we can give Lincoln the opportunities that every child deserves – the freedom of movement. Please consider helping the Jones family reach their $10,000 goal to make all this possible. Lincoln's family will keep everyone updated on his progress, so be sure to follow along!
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Updates
Keep up to date as needs change.
Mar 14, 2025
Lincoln got a new medical chair!
We have been working really hard to get Lincoln into a new medical ...
Dec 30, 2024
Lincoln is back to therapy after the holiday
Lincoln was off for the holiday, but is back at physical therapy to...
Dec 24, 2024
Merry Christmas Eve!
We wish everyone a very Merry Christmas Eve! Lincoln is enjoying th...
Gift Cards
- Created Dec 16, 2024
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