Support Logan's Fight Against AGTPBP1

This fundraiser is going towards therapy sessions and other medical devices that are needed for a special little boy named Logan who was born with a rare disease. Please continue reading and donate to the sweetest, most deserving child I know.

As most of you know, my twin sister Teresa has a special needs son named Logan with a genetic mutation (AGTPBP1). It is an extremely rare neurodegenerative disease. They basically say it's ALS for children. There is very little information available about this particular genetic mutation because of how rare it is (less than 25 known cases), but we do know that this disease is known to be fatal in early childhood.

However, we are huge believers that God is in control. We believe that He is in the midst of this terrible diagnosis and we aren't going to lose faith. Logan has already surpassed other children with this same disease. We are going to push Logan to be his best self every day. We are going to teach him to be strong and to work hard. We are all going to fight right along with this beautiful, precious baby boy and stand in belief that there is a miracle breakthrough coming his way.

My sister and her husband (Teresa and Anthony) have been through so much and have pushed for answers and searched for the best help out there for their son. They have been putting their son through some intensive physical therapy sessions that are, unfortunately, not covered by insurance. These sessions cost thousands of dollars for just one week of therapy.

I'm starting this Go Fund Me as a way to help this wonderful family, and even more important, to help Logan. I'm hoping we can help give Logan at least two more weeks of his DMI Intensive Physical Therapy sessions with the program he attends called All Kids Are Perfect.

If you are able to help in any amount at all it will be so appreciated. We love this little boy so much. He deserves this. He deserves a chance to be his best self and live his best life.